Next Article in Journal
Photosynthesis in Hydrogen-Dominated Atmospheres
Next Article in Special Issue
Pilin Processing Follows a Different Temporal Route than That of Archaellins in Methanococcus maripaludis
Previous Article in Journal
Function and Regulation of Ferredoxins in the Cyanobacterium, Synechocystis PCC6803: Recent Advances
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Viruses of Haloarchaea

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia
Department of Microbiology, The Chinese University of Hong Kong, Sha Tin, Hong Kong, China
Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269-3125, USA
Author to whom correspondence should be addressed.
Life 2014, 4(4), 681-715;
Received: 11 September 2014 / Revised: 23 October 2014 / Accepted: 24 October 2014 / Published: 13 November 2014
(This article belongs to the Special Issue Archaea: Evolution, Physiology, and Molecular Biology)


In hypersaline environments, haloarchaea (halophilic members of the Archaea) are the dominant organisms, and the viruses that infect them, haloarchaeoviruses are at least ten times more abundant. Since their discovery in 1974, described haloarchaeoviruses include head-tailed, pleomorphic, spherical and spindle-shaped morphologies, representing Myoviridae, Siphoviridae, Podoviridae, Pleolipoviridae, Sphaerolipoviridae and Fuselloviridae families. This review overviews current knowledge of haloarchaeoviruses, providing information about classification, morphotypes, macromolecules, life cycles, genetic manipulation and gene regulation, and host-virus responses. In so doing, the review incorporates knowledge from laboratory studies of isolated viruses, field-based studies of environmental samples, and both genomic and metagenomic analyses of haloarchaeoviruses. What emerges is that some haloarchaeoviruses possess unique morphological and life cycle properties, while others share features with other viruses (e.g., bacteriophages). Their interactions with hosts influence community structure and evolution of populations that exist in hypersaline environments as diverse as seawater evaporation ponds, to hot desert or Antarctic lakes. The discoveries of their wide-ranging and important roles in the ecology and evolution of hypersaline communities serves as a strong motivator for future investigations of both laboratory-model and environmental systems.

Graphical Abstract

1. Introduction

Viruses infect all three domains of life, with viruses of Archaea being the least studied. Currently, around 100 viruses infecting Archaea (archaeoviruses) have been described, compared to around 6200 bacteriophages [1,2,3]. Nevertheless, research into archaeoviruses has increased in recent years, and in the same ways that studies of Archaea uncovered unique traits about their cellular adaptation, ecology and evolution [4], there is no doubt that archaeoviruses are engendering high levels of interest.
Haloarchaea are members of the Archaea that live in hypersaline environments ranging from 10% salinity to salt saturation (~36% salinity) [5]. Haloarchaea are found in a wide range of environments that differ in their geography, climate, limnology and chemistry, and include salt lakes, soda lakes and artificially formed seawater evaporation ponds. Haloarchaea tend to be the dominant cellular forms in hypersaline environments above 15% NaCl, with halophilic bacteria typically contributing less than a quarter of the population [2,6,7]. Eucarya tend to be even less abundant, but may be diverse [8,9,10], with the phototrophic green alga, Dunaliella spp. being an important primary-producer and source of nutrients [2,6,7]. A general feature of hypersaline environments is that the communities tend to have low complexity. Relative to other aquatic systems, they can also sustain high concentrations of viruses, with virus-like particles per mL reaching up to 1.3 × 1010 [11,12].
Viruses infecting haloarchaea, haloarchaeoviruses [1,13], were first discovered in 1974, several years before Archaea were described as a lineage of life distinct from Bacteria and Eucarya [4,14,15]. By 2003, fifteen haloarchaeoviruses were described, and methods for the isolation and cultivation of haloarchaeoviruses were published in 2006 [16,17]. In 2012, two large studies on haloarchaeoviruses were performed, one culture-dependent [2], the other culture-independent [12], contributing to a total of 33 haloarchaeoviruses, and another 34 putative haloarchaeoviruses which either are not yet genome sequenced, or were constructed from metaviromes, but not yet confirmed with laboratory isolation.
Forty years since the first discovery of haloarchaeoviruses, relatively few have been investigated in great detail, and many studies have been discontinued after initial attempts [6,18]. This is due in part to difficulties in isolating and cultivating haloarchaea hosts, and to date, the majority of research performed on haloarchaeoviruses has been with strains of Halorubrum spp. and Haloarcula spp., which tend to be amenable to laboratory manipulation.

2. Classification

In hypersaline environments, virus-like particles with a variety of different morphotypes have been described, including head-tailed, spindle-shaped, spherical and filamentous, ranging from 40 to 100 nm in diameter [11,19,20,21,22]. During microscopy examinations, filamentous forms may be interpreted as being bacteriophages because this morphology has not been described for many archaeoviruses, an exception being the prevalence of filamentous forms that infect thermophilic Archaea [23]. In some hypersaline environments, spherical forms are the most abundant, with spindle-shaped forms increasing in abundance with increasing salinity [6,11]. In environments close to salt saturation, spindle-shaped virus-like particles appear to be the most abundant, followed by spherical forms, with head-tailed forms representing a minority of up to 1% in some systems [19,21,22].
Traditionally, viruses/phage have been classified into only two modes of infection: virulent and temperate. Virulent viruses perform a lytic cycle and form progeny within their host after infection, and do not form stable lysogens with their hosts. Temperate viruses do have the capacity to form stable lysogens with their hosts, in addition to being able to undergo a lytic cycle. This classification is inadequate to describe all haloarchaeoviruses, as many are more aptly described as having persistent infection. Persistent infection differs from temperate infection by host cells not containing viral DNA in a provirus form (i.e., integrated in the host chromosome) [24]. Persistent infection also differs from virulent infection by viruses forming unstable carrier states and continuously producing and releasing progeny at a low rate without causing host cell lysis [25,26,27].
For all cellular life, taxonomic classification and phylogeny can be inferred by comparing universally conserved marker genes, typically small subunit ribosomal RNA genes. However, as universal marker genes are not present in viruses, inferring viral lineages is inherently more difficult. Below we briefly consider how viral lineages can be interpreted, in order to rationalize a satisfactory means of classifying haloarchaeoviruses.

Viral Lineages

Haloarchaeoviruses that infect taxonomically diverse hosts have viral capsids with very similar structures and protein motifs, but do not have many detectable genetic sequence similarities. One explanation is that while there is scope to diversify gene sequence and gene content, there are only a limited number of plausible structures for viruses, and therefore there is a structural convergence of virus form [28,29]. The lack of sequence identity would be consistent with a polyphyletic origin for viruses [28]. If certain lineages of viruses existed before the last universal common ancestor of cellular life, viruses could have diverged to evolve with distinct host types [30,31]. Certain genes, such as structural and assembly genes, could be vertically inherited if strong evolutionary constraints restrict their divergence. If these genes are conserved, viruses infecting different hosts would have similar structures. In comparison, genes for replication, host interaction and virus release could have less evolutionary constraint, thereby enabling recombination events to be more readily inherited and detected more frequently than for non-structural genes. A relatively high level of permissive recombination for these genes would lead to the ability of viruses to evolve and maintain effective interactions with hosts.
Because all viruses do not share a universal marker gene, viruses have traditionally been classified based on their genome types, sequence similarities and general morphology. However, genomic similarity may not provide the best measure of phylogeny [28], or inference of host type [32]. Viral communities may represent a pool of DNA that overlaps and can be exchanged with their hosts, thereby underpinning a phylogenetic web of lateral and vertical inheritance, rather than supporting a coherent virus phylogenetic tree [33,34]. Therefore traditional classification may not accurately define the evolutionary relationships of viruses or be suitable for assigning viruses to higher order taxa [29,35,36]. Instead, it has been argued that comparison of coat protein structures and virion architecture may be better for approximating phylogenetic classification of viruses, with a structure-based determination of viral lineages applying universally to viruses infecting different domains of life [29,32,36,37].
Support for the validity of this type of classification comes from the viral lineage proposed for head-tailed viruses (caudoviruses) containing conserved Hong Kong 97 (HK97)-like main capsid proteins [38]. The HK97 protein fold was found in viruses infecting all three domains, including seven bacteriophages, the eucaryovirus herpes simplex virus type 1, and recently haloarchaeovirus HSTV-1 [38]. Within the Archaea, a viral lineage has been proposed that encompasses all short-tailed spindle-shaped viruses, which infect both archaeal kingdoms Crenarchaeota and Euryarchaeota [39].
A second line of support relates to the proposed vertical β-barrel superlineage of viruses [30,40]. This superlineage comprises of two sublineages; PRD1-type viruses with double β-barrel capsid proteins which infect all three domains of life, and halosphaerovirus SH1 and bacteriophage P23-77 with single β-barrel capsid proteins [30,40,41,42,43]. If viruses are restricted by structural constraints, there is likely to be a limited number of unique viral coat proteins, and therefore a limited number of structure-based viral lineages to be discovered [29].
Archaeovirus morphologies have previously been reviewed and classified into eight morphotypes, with 15 families described by 2012 [1,3]. In this review, described haloarchaeoviruses are classified into four morphotypes (Table 1), and many are classified into six families (Figure 1). While it is impossible to know if all extant viruses had a common ancestor, it seems reasonable to classify haloarchaeoviruses based on viral lineages that incorporate subdivisions based primarily on morphology and virion architecture, with genomic information being used to refine classification (e.g.,further subdivision).
Table 1. Characteristics of haloarchaeoviruses (adapted from [44]).
Table 1. Characteristics of haloarchaeoviruses (adapted from [44]).
Virus 1Host 2Mode of Infection 3SourceMorphology 4Size/nmGenome TypeGenome Size/kbG + C mol% pI References
HATV-1Haloarcula sp.VirulentSaltern, ThailandHead-tailed (contractile)-----[2]
HATV-2Har. sp., Halorubrum. sp.VirulentSaltern, IsraelHead-tailed (contractile)-----[2]
HF1Halobacterium salinarum, Haloferax volcaniiPersistentSaltern, AustraliaHead-tailed (contractile)Head 67.8 ± 3, Tail 90 ± 2Linear dsDNA75.955.8<5[25,45]
HF2Halorubrum coriense, Halorubrum saccharovorumPersistentSaltern, AustraliaHead-tailed (contractile)Head 58, Tail 94Linear dsDNA77.755.8<5[25,45,46]
HGTV-1Halogranum sp.VirulentSaltern, ThailandHead-tailed (contractile)-Linear dsDNA143.950.4-[2,47]
HJTV-1Haloarcula japonicaVirulentSaltern, ItalyHead-tailed (contractile)-----[2]
HJTV-2Har. JaponicaVirulentSaltern, ThailandHead-tailed (contractile)-----[2]
HRTV-1Hrr. sp.-Saltern, ItalyHead-tailed (contractile)Head 50, Tail 87----[48]
HRTV-2Hrr. sp.VirulentSaltern, ItalyHead-tailed (contractile)-----[2]
HRTV-3Hrr. sp.VirulentSaltern, ItalyHead-tailed (contractile)-----[2]
HRTV-5Hrr. sp.VirulentSaltern, ItalyHead-tailed (contractile)-Linear dsDNA76.156.4-[2,47]
HRTV-6Hrr. sp.VirulentSaltern, ItalyHead-tailed (contractile)-----[2]
HRTV-7Hrr. sp.VirulentSaltern, ItalyHead-tailed (contractile)-Linear dsDNA69.059.6-[2,47]
HRTV-8Hrr. sp.VirulentSaltern, ThailandHead-tailed (contractile)-Linear dsDNA74.557.1-[2,47]
HRTV-9Hrr. sp.VirulentSaltern, IsraelHead-tailed (contractile)-----[2]
HRTV-10Hrr. sp.VirulentSaltern, IsraelHead-tailed (contractile)-----[2]
HRTV-11Hrr. sp.VirulentSaltern, IsraelHead-tailed (contractile)-----[2]
HRTV-12Hrr. sp.VirulentSaltern, SpainHead-tailed (contractile)-----[2]
Hs1Hbt. SalinarumPersistentHbt. salinarum cultures from salted codfishHead-tailed (contractile)Head 50, Tail 120----[14,49]
HSTV-2Halorubrum. SodomenseVirulentSaltern, IsraelHead-tailed (contractile)Head 60, Tail 101 ± 5Linear dsDNA68.260.0-[2,50]
HSTV-3Hrr. sodomenseVirulentSaltern, IsraelHead-tailed (contractile)-----[2]
Ja1Hbt. SalinarumVirulentSalt ponds, JamaicaHead-tailed (contractile)Head 90, Tail 150----[5]
ΦCh1Natrialba magadiiTemperateNab. magadii cultureHead-tailed (contractile)Head 70, Tail 130Linear dsDNA58.561.9<5.2[51,52,53]
ΦHHbt. SalinarumTemperateHbt. salinarum cultureHead-tailed (contractile)Head 64, Tail 170Linear dsDNA59.065.0-[54,55,56,57,58,59,60,61]
S5100Hbt. salinarumPersistentSalt ponds, JamaicaHead-tailed (contractile)-dsDNA---[62]
BJ1Hrr. sp.TemperateSalt lake, MongoliaHead-tailed (non-contractile)Head 56, Tail 71Linear dsDNA42.364.0<5[63]
HCTV-1Haloarcula californiaeVirulentSaltern, ItalyHead-tailed (non-contractile)Head 63, Tail 80Linear dsDNA103.257.0-[47,48]
HCTV-2Har. californiaeVirulentSaltern, ThailandHead-tailed (non-contractile)-Linear dsDNA54.368.1-[2,47]
HCTV-5Har. californiaeVirulentSaltern, ThailandHead-tailed (non-contractile)-Linear dsDNA102.157.6-[2,47]
Hh-1Hbt. salinarumPersistentAnchovy sauce, PhilippinesHead-tailed (non-contractile)Head 60, Tail 100dsDNA32.767.1-[64,65]
Hh-3Hbt. salinarumPersistentAnchovy sauce, PhilippinesHead-tailed (non-contractile)Head 75, Tail 50dsDNA29.462.2-[64,65]
HHTV-1Haloarcula hispanicaVirulentSaltern, ItalyHead-tailed (non-contractile)Head 50, Tail 110Linear dsDNA49.156.5-[47,48]
HHTV-2Har. hispanicaVirulentSaltern, ThailandHead-tailed (non-contractile)-Linear dsDNA52.666.6-[2,47]
HRTV-4Hrr. sp.VirulentSaltern, ItalyHead-tailed (non-contractile)-Linear dsDNA35.759.5-[2,47]
HVTV-1Haloarcula vallismortisVirulentSaltern, ThailandHead-tailed (non-contractile)Head 70, Tail 73 ± 5Linear dsDNA101.758.0-[2,50]
ΦNHbt. salinarumVirulentHbt. salinarum NRL/JW culturesHead-tailed (non-contractile)Head 55, Tail 85Linear dsDNA56.070.0-[66]
S45Hbt. salinarumVirulentSalt ponds, JamaicaHead-tailed (non-contractile)Head 40, Tail 70dsDNA---[67]
HSTV-1Haloarcula sinaiiensis, Har. vallismortisVirulentSaltern, ItalyHead-tailed (short)Head 60, Tail 40Circular dsDNA32.260.0-[2,38]
EHP-2Putative Haloquadratum walsbyi-Saltern, SpainPutative head-tailed-Linear dsDNA27.243.9-[12]
EPH-11Putative Halorubrum lacusprofundi-Saltern, SpainPutative head-tailed-Linear dsDNA33.558.5-[12]
HGPV-1Halogeometricum sp.PersistentSaltern, SpainPleomorphic55.5 ± 5.2Circular dsDNA9.761.6-[2,26,68]
HHPV-1Har. hispanicaPersistentSaltern, ItalyPleomorphic51.7 ± 4.0Circular dsDNA8.155.8-[26,35,48,69]
His2Har. hispanicaPersistentSalt lake, AustraliaPleomorphic70.6 ± 3.6Linear dsDNA16.139.0–40.0<7[24,26,70]
HRPV-1Hrr. sp.PersistentSaltern, ItalyPleomorphic41.1 ± 2.2Circular ssDNA7.054.2-[26,69]
HRPV-2Hrr. sp.PersistentSaltern, ThailandPleomorphic54.0 ± 4.3ssDNA10.763.7-[2,26]
HRPV-3Hrr. sp.PersistentArtificial salt pond, IsraelPleomorphic67.2 ± 5.2Circular dsDNA8.858.3-[2,26,68]
HRPV-6Hrr. sp.PersistentSaltern, ThailandPleomorphic48.5 ± 2.7Circular ssDNA8.562.7-[26,68]
SH1Har. hispanicaPersistentSalt lake, AustraliaSpherical70Linear dsDNA30.968.4<5[70,71,72,73,74]
HHIV-2Har. hispanica, Har. vallismortis, Har. japonicaVirulentSaltern, ItalySpherical80Linear dsDNA30.666.5-[2,75]
PH1Har. hispanicaPersistentSalt lake, AustraliaSpherical51Linear dsDNA28.167.6-[27]
SNJ1Natrinema sp.TemperateNnm. sp. (mitomycin C induction)Spherical67Circular dsDNA16.348.8-69.7<6[76,77]
His1Har. hispanicaPersistentSalt lake, AustraliaSpindleHead 44 × 77, Tail 7Linear dsDNA16.539-40<7[24,39,78]
Notes: 1 Viruses in bold have been studied in more detail, with both culture-dependent and culture-independent methods; 2 Strains previously designated as Halobacterium halobium, Hbt. cutirubrum and Hbt. salinarium were proposed to be corrected to Hbt. salinarum [79]; Haloferax volcanii was previously known as Halobacterium volcanii. Genus name abbreviations used are based on those proposed by the subcommittee on the taxonomy of the family Halobacteriaceae; the complete list: Haladaptatus (Hap.), Halalkalicoccus (Hac.), Haloarcula (Har.), Halobacterium (Hbt.), Halobaculum (Hbl.), Halobiforma (Hbf.), Halococcus (Hcc.), Haloferax (Hfx.), Halogeometricum (Hgm.), Halomicrobium (Hmc.), Halopiger (Hpg.), Haloplanus (Hpn.), Haloquadratum (Hqr.), Halorhabdus (Hrd.), Halorubrum (Hrr.), Halosimplex (Hsx.), Halostagnicola (Hst.), Haloterrigena (Htg.), Halovivax (Hvx.), Natrialba (Nab.), Natrinema (Nnm.), Natronobacterium (Nbt.), Natronococcus (Ncc.), Natronolimnobius (Nln.), Natronomonas (Nmn.), Natronorubrum (Nrr.) [80]; 3 The modes of infection listed here are tentative, with classifications of virulent infection possibly being persistent; 4 Proposed viral families were assigned based on morphology, with head-tailed (contractile), head-tailed (non-contractile), head-tailed (short), pleomorphic, spherical and spindle morphotypes assigned to Myoviridae, Siphoviridae, Podoviridae, Pleolipoviridae, Sphaerolipoviridae and Fuselloviridae, respectively. Pleolipoviridae and Sphaerolipoviridae families, and the classification of many haloarchaeoviruses into existing families, have not yet been formally accepted by the International Committee on Taxonomy of Viruses; “-”, not determined.
Figure 1. Morphotypes of haloarchaeoviruses. Blue lines represent protein and red dotted lines represent lipids. Proposed viral families are included. Note that Pleolipoviridae and Sphaerolipoviridae families, and the classification of many haloarchaeoviruses into existing families, have not yet been formally accepted by the International Committee on Taxonomy of Viruses. Haloarchaeoviruses of each morphotype are listed except for head-tailed viruses with undetermined tail morphologies. Electron micrographs show isolates representing each morphotype, head-tailed (contractile) ΦCh1 [51]; head-tailed (non-contractile) BJ1 [63]; head-tailed (short) HSTV-1 [38]; pleomorphic HRPV-1 [69]; spherical SH1 [17]; spindle-shaped His1 [39]. Scale bars represent 100 nm.
Figure 1. Morphotypes of haloarchaeoviruses. Blue lines represent protein and red dotted lines represent lipids. Proposed viral families are included. Note that Pleolipoviridae and Sphaerolipoviridae families, and the classification of many haloarchaeoviruses into existing families, have not yet been formally accepted by the International Committee on Taxonomy of Viruses. Haloarchaeoviruses of each morphotype are listed except for head-tailed viruses with undetermined tail morphologies. Electron micrographs show isolates representing each morphotype, head-tailed (contractile) ΦCh1 [51]; head-tailed (non-contractile) BJ1 [63]; head-tailed (short) HSTV-1 [38]; pleomorphic HRPV-1 [69]; spherical SH1 [17]; spindle-shaped His1 [39]. Scale bars represent 100 nm.
Life 04 00681 g001

3. Morphotypes

3.1. Head-Tailed Caudoviruses

Head-tailed viruses (Caudovirales) comprise 96% of known bacteriophages and have been well studied compared to other viral morphotypes [3]. Head-tailed viruses are non-enveloped, and contain an icosahedral head which encapsidates the viral genome and is attached to a flexible hollow tail by a connector [81]. The head, known as the capsid, is composed of capsomer subunits, formed by main capsid proteins (MCPs).
Head-tailed viruses adsorb to cells by their tails and inject their DNA into the host. After transcription, translation and DNA replication, the virus capsid is assembled with scaffold proteins, DNA is packaged into the capsid, and the tail is added to the head. In some head-tailed viruses, the scaffold function is performed by a separate domain of the MCP or prohead protease, with this scaffold component removed from the capsid after assembly is completed [82,83,84]. The host cell is then lysed to release progeny viruses. Unlike head-tailed bacteriophages [81], mechanisms underpinning the life cycles of haloarchaeoviruses have not been well described. One major difference to the typical lytic cycle mechanism of bacteriophages is that some head-tailed haloarchaeoviruses are able to exit hosts without causing lysis (also see “Virulent and persistent infection” below).
Microscopic examination of environmental samples revealed that head-tailed viruses are the least abundant morphotype, comprising only 1% in some environments, yet the majority of isolated haloarchaeoviruses are head-tailed viruses [6,11,19,21,22]. This bias in part reflects the limitations imposed by difficulties in host cultivation, and virus isolation methods favouring lytic viruses that can be observed through the formation of plaques.
Head-tailed haloarchaeoviruses are morphologically and genetically similar to bacteriophage families, and are proposed to be assigned to the families Myoviridae, Siphoviridae and Podoviridae, which possess long contractile tails, long non-contractile tails and short tails, respectively [1,2,13,47,84,85]. Because archaeal caudoviruses carry many genes with homologues to bacterial genes, and the occurrence of head-tailed archaeoviruses is rare, it was suggested that caudoviruses did not evolve independently in Bacteria and Archaea, but instead were introduced to haloarchaea by interdomain spreading from halophilic bacterial hosts [13,22,84]. However, it has also been proposed that the presence of homologous genes in viruses from across the three domains of life is unlikely to be a consequence of inter-domain horizontal gene transfer due to the large evolutionary distances between cellular hosts [86]. Instead, homologous genes between archaeoviruses and bacteriophages have been regarded as derived from a primordial viral gene pool that predated the divergence of the three domains [86]. Head-tailed viruses (including distinct myoviruses and siphoviruses) could have been present at the very beginning of Archaea [87]. However, the evolution of head-tail viruses in haloarchaea might be complex and consist of vertical descent from a shared ancestor with bacterial caudoviruses along with subsequent inter-domain horizontal gene transfer, with the latter possibly occurring via recombination between intracellular archaeoviral genomes and provirus-containing exogenous bacterial DNA taken up by archaeal cells [87].
For the 17 head-tailed haloarchaeoviruses with sequenced genomes, a further subdivision has been made into groups including HF2-like myoviruses, HRTV-7-like myoviruses, HCTV-1-like siphoviruses, and “singletons” based on genome, structural and protein similarities [88]. Not all head-tail viruses have been classified into Myoviridae, Siphoviridae or Podoviridae because insufficient information is known about their tail structures (Table 1).
A total of 58 head-tailed haloarchaeoviruses have been described, although not all have been studied both morphologically and genomically. Head diameters range from 40 to 100 nm, and all three tail types have been characterized. With two recent culture-independent studies, the number of known haloarchaeoviruses had almost tripled [2,12]. A total of 42 viral genomes were retrieved by metagenomic sequencing using fosmid clones [12]. Of these, 17 genomes are almost complete and tentatively identified as head-tailed viruses due to the presence of terminase genes which are commonly used in caudoviruses for DNA packaging into capsids. Through culture-dependent methods, 26 new head-tail haloarchaeoviruses were identified from salterns and salt ponds in Italy, Thailand, Israel and Spain [2].

3.2. Pleolipoviruses

Recently, the seven pleomorphic haloarchaeoviruses were reviewed and proposed to be classified into a new group called pleolipoviruses (family Pleolipoviridae) due to their unique lipid envelope and protein similarities [26]. The members of this group are not restricted to Archaea; based on their structural features, this viral lineage is proposed to include the pleomorphic mycoplasma virus L172 [69,85,89,90]. However, there is currently no genome sequence data available for L172 to confirm this proposed relationship [85].
Pleolipoviruses have shapes ranging from elongated to round, and they possess a random distribution of spikes decorating their surfaces [26,69]. In contrast to most pleomorphic bacteriophages, pleolipoviruses contain no major structural proteins associated with their genomes, indicating that they have no nucleocapsids [26]. However, pleolipoviruses all contain two or three major structural proteins: at least one spike protein (usually one, although His2 has two), which appears to be important for host infection; and one or two membrane proteins, which may interact with the genome during virion assembly [26,85,89]. Post-translation modification of spike proteins has been shown for HGPV-1 and His2 (lipid modification) and HRPV-1 (glycosylation) [26,89].
Pleolipoviruses have a persistent mode of infection, and virions are released continuously from the host cell without lysis [2,26,69]. They are likely to be released from the cell by vesicle formation and budding, with nonselective acquisition of lipids from the host cell membrane [26,35,89]. In this respect, pleolipoviruses differ from the halosphaerovirus SH1, in which the lipid membrane underlies the icosahedral protein capsid (see “Lipids”, below) and lipids are acquired selectively from the host lipid pool, likely as a result of the geometrical constraints within the icosahedral protein capsid [71]. Described as “sloppy” assembly, this results in asymmetric virion structures, and varied genome types and genome packaging densities [26]. Accordingly, pleolipoviruses have a variety of genome types, including circular and linear, dsDNA and ssDNA [26,68].
Pleolipoviruses have been classified into two sets of subgroups, one based on virion structure dissociation, and the other based on genomic similarities (Table 2). These two subgroups do not fully correspond, indicating that the genetic material and replication strategies do not link to virion architecture. For the genomic set, the first two subgroups can form putative proviruses or proviral remnants (also see “Haloarchaeovirus genome variation” below).
Table 2. Pleolipovirus subgroups.
Table 2. Pleolipovirus subgroups.
Subgroups Based on Protein Fragmentation After Virion Dissociation [26]Subgroups Based on Genome Organization and Replication [68]
(1) Soluble fragments only(1) Use rolling circle replication and contain the replication initiation protein (Rep)
  • HHPV-1, His2, HRPV-1
  • HHPV-1, HRPV-1, HRPV-2, HRPV-6
(2) Soluble fragments and one membrane-associated fragment(2) Use rolling circle replication and do not contain Rep
  • HRPV-2, HRPV-6
  • HGPV-1, HRPV-3
(3) Membrane-associated fragments only(3) Use protein-primed replication and have linear genomes
  • HGPV-1, HRPV-3
  • His2

3.3. Spherical/Icosahedral Halosphaeroviruses

Four spherical, tailless haloarchaeoviruses (family Sphaerolipoviridae) have been described; SH1, HHIV-2 and PH1 from Har. hispanica and SNJ1 from Nnm. sp. [27]. Two genera were proposed, separating SH1, PH1 and HHIV-2 into Alphasphaerolipovirus, and SNJ1 into Betasphaerolipovirus [91]. Halosphaeroviruses are structurally similar to the bacterial family Tectiviridae, suggesting that they may belong to the same evolutionary viral lineage [13,71,85]. However, SH1 has been proposed to represent a novel and early divergent lineage of viruses and virus-like genetic elements infecting halophilic archaea and thermophilic bacteria [42]. Recent evidence suggests that bacteriophages infecting thermophilic Thermus thermophilus, P23-77 and IN93, have similar morphologies, protein structure and conserved core genes, and should be included within the same family under the genus Gammasphaerolipovirus [91].
The viral particles range from 51 to 80 nm in diameter, and contain a capsid with an internal lipid membrane. SH1 has spike structures on the capsid, and putative spike proteins appear to be present in HHIV-2 and PH1 [27,43,71,73,75,77]. SH1, HHIV-2 and PH1 contain linear dsDNA with terminal proteins [27]. In contrast, SNJ1 contains circular dsDNA [77].

3.4. Spindle-Shaped/Lemon-Shaped Salterproviruses

The His1 virus is the only spindle-shaped haloarchaeovirus isolated to date, despite this morphotype being the most abundant in several hypersaline environments [6,19]. His2 was originally classed as spindle-shaped based on morphological similarities to His1. However, His2 has a different protein profile, and no gene synteny with His1, and was later identified to be pleomorphic, belonging to the pleolipoviruses [26,39].
The spindle-shape morphotype is unique to archaeoviruses and has not been described in bacteriophages or eucaryoviruses [78,92]. His1 has similar morphology to the archaeovirus family Fuselloviridae. However, genomic differences has established His1 as the type species of the new genus Salterprovirus [24]. Recently it has been proposed that all spindle-shaped viruses can be segregated into the families Fuselloviridae and Bicaudaviridae, and based on related capsid proteins and overlapping gene content, salterprovirus His1 should also be included within the Fuselloviridae family [92].
Flexibility is a common feature of spindle-shaped viruses, and in His1 this is due to lipid modification of the virion capsid proteins [39,92]. His1 was also observed to undergo structural transformation to form elongated particles [39,78,92]. These larger particles may contain more than one copy of the genome, or a less densely packaged genome [39]. Electron micrographs indicate the presence of a very short tail on His1 particles, although His1 is referred to both as short-tailed and tailless depending on the publication source [24,39,78,92].
Flexibility of virions has also been observed for spindle-shaped viruses infecting hyperthermophilic Archaea. Acidianus two-tailed virus (ATV), the only member of the family Bicaudaviridae, was shown to develop long tails at each pointed end of the spindle-shaped particle, after being released from the host cell [93]. The mechanism is driven by conformational changes and rearrangements of proteins within the virus particle [94]. The large spindle-shaped viruses of Sulfolobus tengchongensis, spindle-shaped virus 1 and 2 (STSV1 and STSV2), exhibit a single tail, with a “nose-like” structure at the opposite end of the spindle. The length of the tails of different virions varies between 20 and 500 nm [95,96], and the range of sizes may reflect the mechanism of virion release which may be via a budding mechanism involving host lipids [96]. The morphological similarities between the spindle-shaped archaeoviruses from hyperthermophiles and haloarchaeoviruses illustrate there is a great deal to be learned about the evolutionary relationships of this virus morphotype.

4. Macromolecules

4.1. Genomes

The majority of viruses listed in Table 1 have had their genomes sequenced, and a quarter of currently known haloarchaeoviruses were discovered by genome reconstruction of metagenome data from hypersaline environments [12]. In recent studies, 140 viral genomes were reconstructed from Lake Tyrrell (Australia) and were determined to have partial sequence similarities to previously sequenced haloarchaeoviruses BJ1, EHP-1 and φCh1 [97,98]. However, it was undetermined whether these sequences belonged to archaeoviruses or bacteriophages, and therefore they have not been discussed in this review. The sequenced haloarchaeoviruses all contain DNA, and genome size ranges from 7.0 to 103.2 kb (HCTV-1) [44,69]. The majority of genomes sequenced are linear, and all are dsDNA, except for HRPV-1 and HRPV-6 which are circular ssDNA [26,69].
Most open reading frames (ORFs) of haloarchaeoviruses lack significant matches to sequences in databases; for example, HF1 has 102 unique ORFs out of a total of 117 [25]. For genes with annotated functions, associations were made to organisms from all three domains of life, as well as viruses infecting all three domains of life, indicating that that haloarchaeoviruses have been involved in the exchange of genetic material that has originated from a very broad range of taxa [95]. One apparent consequence of this transfer and recombination is that many haloarchaeoviruses have mosaic genomes [47,50,99,100].
Because viruses use host replication machinery, it may be expected that their G + C mol% would be similar. In sequenced haloarchaeoviruses, the G + C mol% mostly ranges from 55% to 70%, which is similar to the host haloarchaea (60% to 70%) [12]. The G + C mol% of Hqr. walsbyi is lower than other haloarchaea, at 47.9%. Viral genome reconstruction from metagenome data identified 14 new haloarchaeoviruses with a relatively low G + C mol% of 43% to 46%, therefore possibly indicating they infect Hqr. walsbyi [12,101]. They may also infect members of a new order of haloarchaea which have low G + C mol% and were identified recently using metagenomics [102,103] and single cell sorting [104].
However, the G + C mol% of haloarchaeoviruses does not always reflect their hosts, and this may impact translation efficiency via changes in codon usage. HF2 has 10% lower G + C mol% than its hosts Hrr. coriense and Hrr. saccharovorum, but contains five putative tRNA sequences, which are thought to compensate for differences in codon usage [99]. Similarly, putative tRNA for phenylalanine is encoded in BJ1, and tRNA for glutamine in HSTV-2 and HVTV-1 [50,63]. In contrast, while His1 and His2 have G + C mol% ~ 20% lower than their host Har. hispanica, they do not appear to encode tRNAs [24]. This may indicate that His1 and His2 infect other (unknown) hosts with a lower G + C mol%. Interestingly, HGTV-1 encodes 36 tRNAs, covering all universal genetic code amino acids, but the significance of this is yet to be determined as the G + C mol% for its host (Halogranum sp. SS5–1) has not been established [47].
Matching their haloarchaeal hosts, the majority of haloarchaeovirus proteins predicted from genome sequences have predicted isoelectric points (pI) that are acidic (below pH 6). Haloarchaea accumulate high concentrations of intracellular salt (KCl). The low pI of proteins results in a negative charge which is thought to facilitate salt bridge formation and attract water molecules thereby forming hydration shells around proteins [105]. This property would enable haloarchaeovirus proteins to be compatible with both the high intracellular and extracellular salt environments [106]. The low pI combined with covalent cross-linking of structural components may promote protein stability more broadly, enabling haloarchaeoviruses to cope with environmental changes, such as transient low concentrations of salt [52] (also see “Salinity, infection and evolutionary strategy” below). As the extremely halophilic bacterium, Salinibacter ruber has protein pI values, DNA G + C mol%, and intracellular KCl concentrations similar to haloarchaea [107], the bacteriophages that infect S. ruber may have similar stability properties to haloarchaeoviruses.

4.2. Lipids

From the limited analyses of lipids in haloarchaeoviruses it has been determined that caudoviruses typically do not contain lipid membranes, pleolipoviruses contain an outer lipid envelope, halosphaeroviruses contain a lipid membrane inside the protein capsid, and salterprovirus His1 and some halosphaeroviruses contain lipid-modified proteins [108]. The presence of an outer lipid envelope, such as in pleolipoviruses, allows virus particles to have mechanical flexibility, thereby enabling exit from host cells without causing lysis [26] (also see “Spindle-shaped/lemon-shaped salterproviruses” above). The His1 salterprovirus does not contain a lipid bilayer, but the lipid-modified capsid protein also appears to enable virion flexibility and persistent infection of host cells [39] (also see “Virulent and persistent infection” below).
Viral lipids are generally acquired from the host lipid pool. Pleolipoviruses show nonselective incorporation of host lipids, and appear to be released from the host cell by budding [26,35,89]. In contrast, halosphaeroviruses selectively acquire lipid components from the host cell membrane [71,77]. The halosphaerovirus SH1 contains only negatively charged phospholipids as an inner lipid membrane beneath the capsid, which may help to neutralize and stabilize the membrane, thereby facilitating membrane-DNA interactions [43].

4.3. Structural Proteins of Head-Tailed Haloarchaeoviruses

The majority of known haloarchaeoviruses have head-tail morphology, similar in structure to head-tailed bacteriophages (Caudovirales) [1,13]. The virus particle/virion consists of the head (capsid) which houses the genetic material of the virus, and a tail which is responsible for host attachment.

4.3.1. Capsid Proteins

Several novel capsid structures have been observed in haloarchaeoviruses. In order to expand the capsid size to accommodate more genetic material, three main mechanisms are employed by bacteriophages; increasing the number of protomers, i.e., increasing the triangulation number (T-number); increasing the size of each MCP; or assuming an elongated, prolate structure rather than icosahedral [50]. In HSTV-2, a fourth solution was discovered: using minor capsid proteins to form trimeric structures in between protomers to expand the construct of the capsid [50]. Hence the genome size of HSTV-2 is much larger than the expected size for a capsid structure of T = 7. Similar capsid constructs possibly also occur in HF1 and HF2 [50].
Some haloarchaeovirus capsids contain additional proteins. HVTV-1 contains decorative trimeric structures in the center of each MCP hexamer to increase capsid stability [50]. HSTV-1 has large, cone-shaped tower structures extending from the surface, but the function of these is not known [38]. Some halosphaeroviruses such as SNJ1 and SH1 have two major capsid proteins [71,77]. SH1 was also found to have an unusual capsid architecture of T = 28 with horn-like spikes which decorate and stabilize capsomers that constitute the capsid [43]. The capsid of SH1 is composed of proteins with single vertical β-barrel folds, and this structure provides a possible “missing link” in the evolution to double β-barrel folds which are commonly present in viruses infecting all three domains of life [43].

4.3.2. Tail Proteins

The tail length of bacteriophage λ is determined by the tail tape measure protein [109]. Putative tail tape measure proteins were identified in the genome sequences of ten head-tailed haloarchaeoviruses, suggesting a common mechanism for determining tail lengths [47]. The caudoviruses HF1 and HF2, which are nearly identical in the first 48 kb of their genome, have many changes in the last 28 kb [25]. The structural proteins for virion assembly appear to be highly conserved whereas other proteins such as tail fibers are highly variable [25]. This offers an explanation for the different host ranges of these two viruses despite being so similar morphologically and genetically.
ΦCh1 exhibits phase variation in tail fiber proteins, thereby enabling constant changes to be manifested in tails produced [53]. This may overcome host defenses to improve attachment and infection [53] (also see “Host defense” below). Tail fiber proteins in ΦCh1 are encoded by the genes ORF34 and ORF36, which are separated by ORF35, and are oriented with their 3’ ends facing ORF35 (Figure 2). ORF35 codes for recombinase and is invertible, causing variations in the 3’ ends of ORF34 and ORF36. The resulting tail fiber proteins have variable lengths and C-terminal regions [100]. ΦCh1 that is able to infect Nab. magadii only has ORF35 in the negative orientation, and ORF34 expressed. The tail fiber proteins commonly contain a galactose-binding domain in the C-terminal region. This may facilitate attachment to the host as galactose residues are present in the S-layer and flagella of Nab. magadii.
Figure 2. Schematic representation of the inversion of ORF35 and its effects on ORF34 and ORF36 in ΦCh1. ORF34 and ORF36 code for tail fiber proteins and ORF35 is invertible and codes for a recombinase. The black arrows indicate the orientation of the ORFs. The white arrows symbolize an inversion of ORF35, after which the ends of ORF34 and ORF36 are swapped, causing variations in resulting tail fiber proteins. Adapted from [100].
Figure 2. Schematic representation of the inversion of ORF35 and its effects on ORF34 and ORF36 in ΦCh1. ORF34 and ORF36 code for tail fiber proteins and ORF35 is invertible and codes for a recombinase. The black arrows indicate the orientation of the ORFs. The white arrows symbolize an inversion of ORF35, after which the ends of ORF34 and ORF36 are swapped, causing variations in resulting tail fiber proteins. Adapted from [100].
Life 04 00681 g002

5. Life Cycles

5.1. Adsorption and DNA Ejection

Spikes which are present on the surfaces of pleolipoviruses and some halosphaeroviruses, have been characterized in detail in HRPV-1 and SH1, respectively, and their function has been linked to infectivity and host adsorption [26,43,89]. Haloarchaeoviruses studied have adsorption rates ranging from 1.2 × 10−10 to 2.9 × 10−13 mL/min, which is low compared to 10−9 mL/min for bacteriophage λ [48,64,110]. It was suggested that such low adsorption rates may be due to differences in surface structures of Bacteria and Archaea making it more difficult for haloarchaeoviruses to attach [48]. The low adsorption rates may reflect an evolutionary adaptation to aspects of host growth dynamics; in particular, long generation times which may deplete total host numbers if rapid adsorption (and hence infection) rates occurred [48]. Alternatively, it has been hypothesized that the changing salinity conditions of some hypersaline environments may have selected for slow-adsorbing viruses that can adsorb effectively over a range of salt concentrations [111] (also see “Salinity, infection and evolutionary strategy” below).
Very limited information is available on archaeovirus DNA ejection, and the first in depth study was performed in 2013 on His1 [112]. His1 DNA ejection into the host is dependent on osmotic pressure, and the ejection rate is reduced with increased external pressure [112]. Due to the stabilizing effect of charge screening, increases in external positive ion concentration decreases the number of ejections and the length of ejected DNA [112]. Additionally, it was suggested that cellular processes are required to complete the DNA transfer, as in vitro ejections were found to not be complete [112]. DNA ejection was directional, and occurred at a mean rate of 144 ± 72 kbp/s in His1 compared to 60 kbp/s in bacteriophage λ [112,113]. The ejection of DNA was stepwise, and seemingly random stops and starts in the process were attributed to conformational changes or deformations of the capsid [112].

5.2. Replication and Assembly

The mechanisms of replication and assembly of haloarchaeoviruses have mainly been inferred from genetic analyses. Both rolling-circle replication (HHPV-1 and HRPV-1) and protein-primed replication (His2, SH1, HHIV-2, ΦN and PH1) have been proposed [24,27,35,66,75]. The genomes of HF2, HSTV-2, HCTV-1, HCTV-5, HRTV-5, HRTV-7 and HRTV-8 contain terminal repeats, suggesting replication occurs through concatameric intermediates [46,47,50]. In contrast, the closely related ΦH, ΦN and ΦCh1 viruses, and HCTV-2, HHTV-1, HHTV-2, HRTV-4 and HSTV-1 have partially circularly permuted, terminally redundant genomes indicating they are likely to be packed by a headful mechanism [38,47,54,66].
A number of haloarchaeoviruses, including His2, SH1, HHIV-2, ΦN and PH1, contain proteins covalently-bound to the termini of their linear genomes that may be involved in protein-primed replication [24,27,66,75]. His2 also encodes genes with similarity to DNA polymerases from viruses and plasmids known to replicate via protein priming, thereby providing support for this hypothesis [24]. Interestingly, the 5’ termini of His2 and SH1 genomes must be protein bound in order for the viral DNA to be successfully artificially introduced into host cells [70]. However, terminal proteins might function by end-patching genomic DNA after replication, rather than in primary replication [27].
The members of pleolipoviruses and members of halosphaeroviruses have different genome forms and methods of replication [26,27]. For example, the pleolipoviruses HHPV-1 and HRPV-1 have ssDNA and dsDNA, respectively, but they share sequence homology and synteny for genes related to host integration, replication and virus assembly functions [35]. Because these viruses acquire host cell membrane lipids and are released from the host by budding, the form of the genome does not appear to be important to the assembly process [26].

5.3. Temperate Infection

Only three temperate haloarchaeoviruses have so far been discovered: ΦCh1, SNJ1 and ΦH [51,76,110]. HCTV-5, HRTV-5, HRTV-7 and HRTV-8 encode putative integrases, but have not been found to form lysogens [47]. Based on the turbidity of its plaques and the presence of putative integrase genes in the genome, BJ1 may be a lysogen, but further study is required to assess this [63]. The lack of isolation of temperate haloarchaeoviruses is consistent with metagenomic analyses of a seawater evaporation pond in the Santa Pola saltern (Spain) which identified the presence of integrases in only 2 out of 42 viral fosmids [12].
ΦCh1 integrates into the genome of Nab. magadii, while SNJ1 in Nnm. sp. and ΦH in Hbt. salinarum exist as a lysogen in a non-integrated circular form [51,76,114]. ΦCh1 contains a putative site-specific λ-like integrase which probably facilitates integration [52]. Non-integrated, circular forms of viruses/phage are often described as plasmids because they are semi-autonomous, extrachromosomal DNA that replicate in a similar fashion to plasmids, such as Escherichia coli phage P1 [115].
The circular form of SNJ1 (referred to as plasmid pHH205) confers to its host resistance to superinfection [76,77]. ΦH circularizes either as a full-length form, or just the L segment (referred to plasmid pΦHL) [114] (also see “Gene regulation” below). Although ΦH does not integrate into the host chromosome, recombination with other plasmids containing homologous segments can occur, and ΦH variants with insertions, deletions and inversions have been identified [54,116].
Two putative head-tailed proviruses, Hlac-Pro1 and Nmag-Pro1, were identified in the genomes of Hrr. lacusprofundi and Nab. magadii, respectively [84]. Both putative proviruses share sequence similarities with head-tailed haloarchaeovirus BJ1, which infects Hrr. sp., and Hlac-Pro1 appears to be defective [63,84]. Viral sequences matching to BJ1 were also detected in the metagenome of Deep Lake (Antarctica), the hypersaline system where Hrr. lacusprofundi was isolated from and represents about 10% of the cellular community [117].
Putative proviruses in haloarchaea relating to sphaerolipoviruses have been described. HalaPauP1 from Haladaptatus paucihalophilus and HaloLacP1 from Halobiforma lacisalsi have homologous genes to alphasphaerolipoviruses, while HaloMukP1 and HaloMukP2 from Halomicrobium mukohataei, and integrated Haloarcula provirus (IHP) from Haloarcula marismortui shares genes with betasphaerolipovirus SNJ1 [91].
Putative pleomorphic proviruses were also found as extrachromosomal genetic elements in Hfx. volcanii and Hrr. spp. [2,118,119]. The sequence of plasmid pHK2 from Hfx. volcanii and a chromosomal region of Hfx. volcanii have considerable identity to pleomorphic viruses HHPV-1 and HRPV-1. The chromosomal region of Hfx. volcanii and pHK2 contain putative integrases, suggesting that it is a virus that can both integrate and replicate extrachromosomally [35]. Similarly, plasmid pHRDV1 from Hrr. sp. has a genome organization and protein homology linking it to pleomorphic viruses HRPV-3 and HGPV-1 [119]. Although pHK2 and pHRDV1 have not been shown experimentally to form extracellular viruses, these findings suggest that temperate haloarchaeoviruses may be more prevalent than is currently recognized.

5.4. Virulent and Persistent Infection

The majority of head-tailed haloarchaeoviruses are described as virulent (see Table 1), but the label may be inappropriate for many, since most haloarchaeoviruses do not portray the normal characteristics expected of virulent viruses (also see “CLASSIFICATION” above). In pleolipoviruses, salterprovirus His1 and some halosphaeroviruses and head-tailed haloarchaeoviruses, progeny can be produced continuously without lysing host cells, and are described as causing persistent (or chronic) infections [111]. Those presently characterized as persistent include head-tailed HF1, HF2, Hs1, Hh-1, Hh-3 and S5100, all known pleolipoviruses, halosphaerovirus SH1 and PH1, and salterprovirus His1 (Table 1).
By using a budding mechanism, pleolipoviruses are released to the extracellular environment while the host continues to grow [69,89]. As haloarchaea lack a rigid exterior, such as the peptidoglycan layer present in many bacterial cell walls, haloarchaeoviruses with protein capsids may enter and exit haloarchaea without disrupting the integrity of the cell envelope [64]. For His1, His2 and SH1, virus particles are continually liberated from host cells without cell lysis, but cells eventually die and lyse [24,72,111]. During persistent infections, host cells continue to multiply at a slightly slower growth rate than when non-infected, and cells are not immune to superinfection by heterogeneous viruses, eventually lysing when the cell membrane is compromised by continual entry and egress of viruses [24,25,64,111]. Regulation of transitions from persistent to lytic states is not well understood, but for His1 and S5100, salinity has been shown to be a controlling environmental factor [49,62] (also see “Salinity, infection and evolutionary strategy” below). For lytic haloarchaeal caudoviruses, the precise mechanism causing host lysis is unclear, as they lack known lysin or holin genes (as described for many bacteriophages). RTX toxins, which are inferred to be cytolytic, have been annotated in the genomes of certain haloarchaea (e.g., a putative Hqr. walsbyi virus [12]). Genes for zeta toxins have been identified in a number of head-tailed haloarchaeoviruses (e.g., HVTV-1, HCTV-1), but their role in the life cycle of the virus is not known [50]. It has not been determined if haloarchaeovirus encoded RTX or zeta toxins play a role in host cell lysis.

6. Genetic Manipulation and Gene Expression

6.1. Genetic Manipulation

A method to artificially introduce ΦH DNA into Hbt. salinarum was developed using polyethylene glycol and spheroplasts [120]. This was extended to Hfx. volcanii which was otherwise unable to be infected by ΦH particles [121]. The DNA of several other haloarchaeoviruses, including His2 and SH1, has also been successfully introduced into hosts [70]. The successful introduction of viral DNA by artificial means, and subsequent generation of virus progeny, highlights the relatively broad range of hosts that are capable of sustaining haloarchaeovirus replication.
The broad host-range ability has been recognized for its potential to facilitate the development of ΦH-based shuttle vectors for haloarchaea [70]. Using the replicon region of ΦH, plasmid vectors were developed for transforming Hbt. salinarum, enabling studies of gene regulation via experiments using transposon mutagenesis [122]. However, in Hfx. volcanii, while the recombinant plasmids were able to replicate they tended to be lost from the host. The outcomes of these studies to date provide a strong basis for further development of genetic manipulation systems for haloarchaea.

6.2. Gene Regulation

To date, in-depth molecular studies of gene regulation in haloarchaeoviruses have only been performed on ΦH and ΦCh1, revealing complex mechanisms of gene regulation. In Hbt. salinarum, ΦH appears to have evolved mechanisms to regulate host abundance and protect itself during unfavorable growth conditions (e.g., changes in salinity) [57]. ΦH is temperate and exists either as a 57 kb circular, extrachromosomal provirus, or as a 12 kb L circular form which only comprises the L region of the ΦH genome. The presence of either confers host immunity against lysis by ΦH.
The L region encodes the majority of viral regulatory functions, and carries genes responsible for influencing whether lytic or lysogenic cycles occur [59] (Figure 3). In the L region, the T4 gene is required for lytic growth, and is located back-to-back with the repressor rep gene [57]. Expression of T4 is very effectively turned off by the product of the rep gene, which binds to the T4 promoter region. T4 and rep transcription seem to be mutually exclusive, as rep transcription is also repressed by T4 transcription [61]; a phenomenon reminiscent of CI and Cro proteins in E. coli λ phage. Expression of T4 would maintain lysogeny of ΦH and cause immunity by preventing infecting ΦH-like viruses from expressing genes necessary for entering the lytic cycle. The per (promotes efficiency of rep) gene enhances the effect of the Rep protein tenfold [59]. However, the host immunity conferred by the L form can be overcome by some ΦH mutants, such as ΦHL, which have an ISH23 inserted element between the T4 and rep genes [57]. This separates the repression binding site (operator region) from the promoter region of T4, thereby rendering Rep activity null [57].
Figure 3. Schematic map of the genetic region between transcripts T6 and T1 in ΦH. Boxes represent ORFs. Adapted from [59].
Figure 3. Schematic map of the genetic region between transcripts T6 and T1 in ΦH. Boxes represent ORFs. Adapted from [59].
Life 04 00681 g003
An additional mechanism for immunity in hosts is through post-transcriptional processing by host endonucleases of the transcript from the early lytic gene, T1 [59] (Figure 3). Antisense RNA is transcribed from the Tant gene located at the end of the T1 gene, expressed from the complementary strand in the opposite direction to T1 [58]. Binding of the antisense RNA makes T1 susceptible to specific host RNAses which cleave ribosomal binding sites from the first ORF, but interestingly does not digest the products [58].
In the temperate virus ΦCh1, ORF49 is regulated by the rep gene, which encodes the winged-helix repressor Rep protein [123]. Proteins Gp43 and Gp44 encoded by ORF43 and ORF44, respectively, partially relieve rep-mediated repression as they bind to the same site as the Rep protein, but at a lower specificity.
While gene regulation studies are limited, the parallels to control mechanisms in head-tail bacteriophages, such as E. coli λ, are notable. Such mechanisms have not been discovered in viruses infecting thermophilic archaea, which may indicate that head-tail haloarchaeoviruses have more in common with bacteriophages.

7. Host-Virus Responses

7.1. Host Defense

In the ongoing struggle between viruses and hosts, hosts develop mechanisms to defend against viruses while viruses evolve to evade host defenses. One well studied mechanism used by bacterial hosts against bacteriophages is restriction-modification systems [124]. Many haloarchaeoviruses have a lack of, or low incidence of, the sequence GATC and its inverse CTAG, which may relate to the tetranucleotide sequences being commonly targeted by restriction endonucleases [124]. This phenomenon occurs in all groups of haloarchaeoviruses, including caudoviruses BJ1, HF1, HF2, pleolipovirus HHIV-2, halosphaerovirus His2, PH1 and SH1, and salterprovirus His1 [24,27,46,63,99]. Furthermore, HF2 possesses AT rich sequences which may also help to circumvent host defense mechanisms as haloarchaeal restriction systems mainly target G + C mol% rich regions [46]. Additionally, some haloarchaeoviruses have been observed to carry modified bases, including methylated cytosines in ΦN and HRPV-3 and methylated adenine in ΦCh1 and HGPV-1, which may reduce susceptibility of their DNA to host endonucleases during infection [51,66,68]; methylation could arise from host- or virus-encoded methylases. However, the motif GATC is 50% G + C mol%, and the majority of haloarchaea have >65% G + C mol% with the third codon position reaching >90%, while Hqr. walsbyi, has G + C mol% < 50% with the third codon position reaching down to 42%. The observation that haloarchaeoviruses do not tend to contain the sequence GATC may therefore relate to their biased G + C mol% content.
Genomic and metagenomic data have provided evidence that hosts evade haloarchaeovirus invasion by expressing cell envelope proteins which have sequence variation. This has been observed for Hqr. walsbyi [125] and within haloarchaea communities [12], and similar observations were made for the bacterium S. ruber, based on metagenome data from seawater evaporation ponds of Chula Vista salterns (USA) [107]. In Har. marismortui, the subunit (archaellin) composition of the flagellum (archaellum) is known to vary, possibly as a mechanism to facilitate archaellin switching in order to evade viruses that target archaella [126].
Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins form a CRISPR/Cas system that functions as a defense mechanism against invading foreign nucleic acid [127,128] (Figure 4). CRISPR/Cas systems have been reported in about 80% of Archaea and 50% of Bacteria examined [127,128], and have similarities to the RNA interference systems of Eucarya [129]. The CRISPR/Cas systems differ to other defense systems of Archaea and Bacteria by being dynamic and responsive to new invading DNA, and being sequence specific [130].
Figure 4. Schematic of the CRISPR-Cas adaptive immune system [131].
Figure 4. Schematic of the CRISPR-Cas adaptive immune system [131].
Life 04 00681 g004
Detailed CRISPR/Cas reviews have been published [131,132,133,134,135], some with more emphasis on archaeal systems [136,137,138]. Briefly, the system consists of three stages; adaptation (or acquisition), expression and interference, which involve different Cas proteins (Figure 4). In the adaptation stage, small fragments of foreign nucleic acids termed protospacers are recognized as non-self, and the corresponding sequences incorporated into a host genome CRISPR locus as spacers in between short direct repeat sequences. Short sequences called protospacer adjacent motifs (PAMs), directly upstream of protospacers, are essential for the selection of new sequences to be incorporated as spacers. In the expression stage, the CRISPR locus is expressed to generate pre-CRISPR RNAs (pre-crRNAs), which are processed into mature crRNAs. In the interference stage, crRNAs are used to recognize invasion by the same foreign nucleic acid elements for subsequent destruction or silencing.
Type I and type II CRISPR/Cas systems have been identified in Archaea, with type I-B mainly observed in haloarchaea (most studies have been performed on Hfx. spp.) [127]. Hfx. volcanii strain H119 contains a type I-B CRISPR/Cas system with eight Cas proteins and three CRISPR loci with a total of 74 spacers, which are constitutively transcribed and processed [130,139]. Similar CRISPR repeat sequences were found in 20 of 32 haloarchaeal genomes [130,139,140], and CRISPR/Cas systems were identified in about two thirds of sequenced haloarchaeal genomes [127,128]. In Haloferax mediterranei, six CRISPR loci were identified, and the CRISPR/Cas system components and mechanisms were different from other type I-B systems in methanogens and Clostridium spp., suggesting that haloarchaea may have unique features in their CRISPR/Cas systems [141].
In contrast to the multiple loci in Hfx. mediterranei, a recent study of Hrr. spp. phylogroups reported that the distribution of CRISPRs was variable within phylogroup A and the genus as a whole, and phylogroup B members appeared to lack CRISPRs entirely [142].
In studies identifying CRISPR/Cas systems in haloarchaeal genomes, only few haloarchaea spacers matched to haloarchaeovirus sequences [127,128]. In a metagenomic study of Lake Tyrrell (Australia), ~ 8000 unique spacer sequences were identified, but the vast majority had no matches to viral contigs from the same sample, and the spacers with matches to viruses did not match sequences in archaeal genomes from the same environmental sample [98]. In a separate study of ten haloarchaeovirus genomes, no matches were identified to CRISPR spacers in haloarchaeal genomes [47].
The low level of match between spacers (haloarchaea genome sequences) and protospacers (haloarchaeovirus sequences) may be due to CRISPR/Cas systems successfully maintaining viral populations at low abundances, therefore rendering most of the invading viruses undetectable in metavirome data [98]. It is also possible that only few haloarchaeovirus sequences are available, and viruses have fast rates of evolution, and therefore protospacer-spacer matches may not be recognized in database searches [130,139,140].
However, the CRISPR/Cas systems may not be the primary resistance mechanism against viruses in haloarchaea [47,142]. Some CRISPR systems require precise matches between spacer and invading proto-spacer [143], and the cost of maintaining the system may outweigh the benefit [142]. Moreover, haloarchaea are able to form heterodiploids and exchange long tracts of DNA [144], and exchange has been observed in environmental communities even between distinct haloarchaea genera [117]. As CRISPR/Cas systems function by degrading incoming DNA, if DNA exchange benefits the community (and is therefore positively selected), it is unclear what role CRISPR/Cas systems would perform and how they would be regulated in response to self, similar or dissimilar “invading” DNA. Overall, the defense systems observed in haloarchaea may reflect a dynamic balance between CRISPRs and other defense systems (e.g., restriction/modification systems, cell surface variation) and the selection pressures related to the nature and functionality of those systems in response to the cost/benefit of the invading DNA.

7.2. Host-Range

Assessments of host-range are limited by the ability to cultivate hosts and successfully infect and propagate haloarchaeoviruses using available hosts. Moreover, if plaque formation is used to assay infection, persistent or temperate infection is difficult to assess and therefore interpret host-range. Most haloarchaeoviruses have been reported to have a narrow host range, and this has been attributed to the small receptor range of virus attachment proteins rather than due to DNA restriction barriers [45]. However, in a study of infectivity, host-range and biogeography, myoviruses were found to be most readily isolated on a Hrr. sp. host, yet cross-testing revealed the ability of some of the isolated myoviruses to infect Har. sp., Halosarcina sp., Hgm. sp., Halogranum sp. and two unclassified isolates [2,12]. While host-range varied with virus type (e.g., myoviruses had a wider host range than siphoviruses), the study highlighted that, given the opportunity, haloarchaeovirus-mediated exchange of host and viral material is likely to be able to occur between diverse members of communities that are from distinct geographic locations [2,12].

7.3. Haloarchaeovirus Genome Variation

As an extension to the concept of ecotypes and niche adaptation which allows a population to adapt to differences or changes in environmental parameters, the term “ecoviriotypes” was proposed to describe viruses which have different but very closely related genomes (e.g., single nucleotide polymorphisms-SNPs) [141]. Metagenomic and metatranscriptomic analyses of haloarchaeoviruses in a seawater evaporation pond in a multi-pond solar saltern in Santa Pola (Spain) determined that the mutation frequency was 7.7 × 10−3 substitutions per nucleotide, with 24% higher mutation frequency in coding regions than non-coding regions [101,145]. As mutation rates of DNA bacteriophages were reported to be between 10−8 to 10−6 substitutions per nucleotide [146], this indicates that haloarchaeoviruses can have abnormally high mutation rates and those populations require high adaptive potential [101]. Such high rates of mutation may contribute to the generation of phenotypic variation in haloarchaeoviruses (e.g., tail proteins), with variant forms selected in response to host evasion mechanisms, such as hosts expressing variant forms of cell envelope proteins (see “Host defense” above).
The term virus and plasmid related elements (ViPREs) was coined to describe virus or plasmid integrants in the host genome which form gene cassettes that can move between viruses during recombination, thus allowing novel virus genomes to be generated by re-assortment [27]. Such recombination events have been proposed to explain the fact that viruses in closely related groups (within halosphaeroviruses or pleolipoviruses) often have similar capsid proteins but different genomic characteristics and methods of replication [26,27,147]. The first ViPREs were described in Hqr. walsbyi and subsequently described in Hmc. mukohataei and Hfx. spp. [27]. These findings indicate that ViPREs are involved in recombination not only between virus species, but also across host species. By enabling extensive recombination between viruses, plasmids and hosts, ViPREs represent mobile collections of capsid and replication genes from different sources, which may allow rapid evolution of haloarchaeoviruses and hosts.

7.4. Salinity, Infection and Evolutionary Strategy

Due to their proportionally high numbers, viruses have the potential to provide strong selective pressures on hosts [28]. To some extent this may be counterbalanced by haloarchaeoviruses tending to adopt persistent, rather than lytic, infection of hosts (also see “Virulent and persistent infection” above). While virus exploitation of their hosts may drive the selection of defense mechanisms, viruses may benefit host populations by acting as agents of genetic exchange and therefore influencing populations in positive ways [19,69,148]. As a measure of viral impact, one study of the microbial loop demonstrated that production by Archaea and Bacteria exceeded losses caused by viral lysis [6]. Viral concentrations have also been linked to growth responses of hosts in response to environmental conditions, such as levels of salinity [11,19,48].
As freshwater input can cause major changes to salinity in hypersaline environments, numerous studies have examined the effects of salinity on virus-host interactions. Membrane-containing viruses were found to be more sensitive to low ionic strength environments compared to head-tailed viruses [48]. In particular, enveloped pleolipoviruses were more sensitive than halosphaeroviruses with internal membranes [48]. Nevertheless, all haloarchaeoviruses have been shown to be able to withstand wider variations in salinity than their hosts [5,48,64]. In fact, His1 can maintain a constant titer for 24 h at 0.02% salinity, and HHIV-2 can maintain infectivity in as low as 0.006% NaCl [64,78]. Furthermore, HHTV-1, HCTV-1, HRTV-1, ΦN and SH1 are reported to maintain 50% infectivity in distilled water [48,66]. The ability to endure exposure to low salinity allows haloarchaeoviruses to survive influxes of freshwater that would be lethal to hosts, offering a possible evolutionary advantage to the viruses [64].
The infectivity of HVTV-1 and HSTV-2 is salt-dependent and low salinity causes reversible inactivation of the virus [50]. As a result, the level of active viruses varies with the numbers of viable hosts and the chance of host extinction is reduced. These findings are corroborated by studies of communities in Sfax solar salterns (Tunisia) where viral concentration and virus-to-cell ratios increased along a salinity gradient [11].
In contrast, for other haloarchaeoviruses, such as ΦCh1, the opposite occurs and virus population densities are lowest during high salinity when host populations are high, and highest during low salinity when host populations are low [51]. His1 and S5100 engage in persistent infection when salinities are above the optimum for their hosts, and lyse host cells when salinity is low [49,62]. This may be a strategy for viruses to exit the hosts in order to avoid becoming decimated when host cells are stressed and die [111]. Alternatively, viruses may recognize and attack hosts that are not likely to contribute genes to future generations, and therefore virus growth and lysis in low salinity would not contribute to selection because the hosts will inevitably die [51].
The interpretations of responses to changes in salinity are relevant to broader considerations of virus-host relationships. It has been proposed that low virulence may contribute to how hosts evolve [148]. Viruses with low virulence would maintain a low density thereby posing less threat to the host, and therefore not prompt hosts to evolve mechanisms of defense. Temperate or persistent infection would enable viruses to grow stably with the host, with increased viral infectivity and lytic growth under conditions when the host will die (e.g., low salinity). Under these conditions, the virus may benefit by limiting the evolution of host defense systems. The host may also benefit by having viruses carry, preserve and transfer its cellular DNA to suitable hosts when the cellular population has reestablished after a period of decline.

8. Conclusions

Although it has been almost 40 years since haloarchaeoviruses were discovered, there has been relatively little research compared to bacteriophages and eucaryoviruses, in part due to the difficulty in cultivating haloarchaea. However, from studies so far, a great deal of novelty has been documented about certain haloarchaeoviruses. This includes the unique spindle-shaped morphology, capsid structures unseen in other viruses, and a different mode of host infection that challenges the traditional virus dichotomy of temperate versus virulent. In addition, the majority of predicted protein-coding genes have no significant matches in current databases. This opens up the possibility of discovering a whole new arena of protein structure and function.
As there is at least one order of magnitude more viruses than hosts, cellular life has been described as bathing in a virtual sea of viruses [28]. Gene transfer agents that are known to package and transfer random pieces of cellular genomic DNA in bacteria and the archaeon Methanococcus voltae [149,150], may function in equivalent ways in haloarachaea. Viral infection and recombination appears to generate the mosaic genomes of haloarchaeoviruses and ViPREs, as well as contributing to the evolution of cellular lineages. By facilitating horizontal gene transfer and recombination, variation is bestowed upon populations, enabling adaptation to environmental changes and continuation of speciation [151]. As haloarchaea are relatively slow-growing but demonstrate high levels of genetic variation, haloarchaeoviruses may play an important role in their continuing evolution.
With the majority of haloarchaeoviruses having persistent infection, transfer of genetic material between host haloarchaea may be facilitated without causing harm to the hosts. Whereas viruses have traditionally been considered to primarily have predator-prey relationships with their hosts, haloarchaoviruses may have more of a mutualistic association with haloarchaea. Moreover, while higher trophic predators such as protozoa tend to have low abundance in hypersaline systems compared to haloarchaea [2,19,20], diversity of Eucarya can be high and the eucaryotes can feed on the haloarchaea [8,9,10]. Research-into and modelling-of predator-prey relationships therefore needs to take into account the possible ecological relevance of mutualistic association of haloarchaeoviruses with their hosts, as well as protozoan grazing on hosts.
The fact that viruses have not yet been successfully isolated infecting Hqr. walsbyi, an abundant member of many halophilic communities, illustrates a challenge in the field. Much in the field remains to be discovered, especially to improve the depth of knowledge about morphology, host attachment, host entry, replication and assembly. While some research on horizontal gene transfer has been performed, selective pressures on hosts and regulation of host cell densities, the full diversity of haloarchaeoviruses, their ecological roles, and the details of their “love-hate” relationship with their hosts remain to be determined.
Advances in DNA sequencing technologies continue to expand the capacity to perform meta/genomics, as do DNA sequencing and mass spectrometry technologies for meta/transcriptomic and meta/proteomic analyses, thereby offering powerful and cost effective avenues for rapidly learning about virus-host interactions, ecology and evolution. Equally so, physiological and biochemical studies of isolates, and particularly importantly, infection and isolation studies of haloarchaeoviruses, must be undertaken; for example, persistent infection would not have been discovered without the use of laboratory, culture-dependent approaches. Based on progress to date and trajectory of the field, the future of haloarchaeovirus research looks to continue to bloom.


Research in RC’s group is supported by the Australian Research Council (DP140100582, LP0776387), and the Australian Antarctic Science program. RTP is funded by the National Science Foundation (Grants DEB-0830024), the US-Israel Binational Science Foundation (Grant number 2013061) and NASA Astrobiology: Exobiology and Evolutionary Biology (Grant Number NNX12AD70G). SE is funded by an EMBO Long-term Fellowship (ALTF 188-2014) co-funded by the European Commission (EMBOCOFUND2012, GA-2012-600394) support from Marie Curie Actions.

Conflicts of Interest

The authors declare no conflict of interest.


  1. Pina, M.; Bize, A.; Forterre, P.; Prangishvili, D. The archeoviruses. FEMS Microbiol. Rev. 2011, 35, 1035–1054. [Google Scholar] [CrossRef] [PubMed]
  2. Atanasova, N.S.; Roine, E.; Oren, A.; Bamford, D.H.; Oksanen, H.M. Global network of specific virus-host interactions in hypersaline environments. Environ. Microbiol. 2012, 14, 426–440. [Google Scholar] [CrossRef] [PubMed]
  3. Ackermann, H.W.; Prangishvili, D. Prokaryote viruses studied by electron microscopy. Arch. Virol. 2012, 157, 1843–1849. [Google Scholar] [CrossRef] [PubMed]
  4. Cavicchioli, R. Archaea-timeline of the third domain. Nat. Rev. Microbiol. 2011, 9, 51–61. [Google Scholar] [CrossRef] [PubMed]
  5. Wais, A.C.; Kon, M.; MacDonald, R.E.; Stollar, B.D. Salt dependent bacteriophage infecting Halobacterium cutirubrum and H. halobium. Nature 1975, 256, 314–315. [Google Scholar] [CrossRef] [PubMed]
  6. Guixa-Boixareu, N.; Calderón-Paz, J.I.; Heldal, M.; Bratbak, G.; Pedrós-Alió, C. Viral lysis and bacterivory as prokaryotic loss factors along a salinity gradient. Aquat. Microb. Ecol. 1996, 11, 215–227. [Google Scholar] [CrossRef]
  7. Oren, A. Diversity of halophilic microorganisms: Environments, phylogeny, physiology, and applications. J. Ind. Microbiol. Biotechnol. 2002, 28, 56–63. [Google Scholar] [CrossRef] [PubMed]
  8. Park, J.S.; Cho, B.C.; Simpson, A.G. Halocafeteria seosinensis gen. et sp. nov. (Bicosoecida), a halophilic bacterivorous nanoflagellate isolated from a solar saltern. Extremophiles 2006, 10, 493–504. [Google Scholar] [CrossRef] [PubMed]
  9. Park, J.S.; Kim, H.; Choi, D.H.; Cho, B.C. Active flagellates grazing on prokaryotes in high salinity waters of a solar saltern. Aquat. Microb. Ecol. 2003, 33, 173–179. [Google Scholar] [CrossRef]
  10. Casamayor, E.O.; Massana, R.; Benlloch, S.; Ovreas, L.; Diez, B.; Goddard, V.J.; Gasol, J.M.; Joint, I.; Rodriguez-Valera, F.; Pedros-Alio, C. Changes in archaeal, bacterial and eukaryal assemblages along a salinity gradient by comparison of genetic fingerprinting methods in a multipond solar saltern. Environ. Microbiol. 2002, 4, 338–348. [Google Scholar] [CrossRef] [PubMed]
  11. Boujelben, I.; Yarza, P.; Almansa, C.; Villamor, J.; Maalej, S.; Anton, J.; Santos, F. Virioplankton community structure in Tunisian solar salterns. Appl. Environ. Microbiol. 2012, 78, 7429–7437. [Google Scholar] [CrossRef] [PubMed]
  12. Garcia-Heredia, I.; Martin-Cuadrado, A.B.; Mojica, F.J.M.; Santos, F.; Mira, A.; Antón, J.; Rodriguez-Valera, F. Reconstructing viral genomes from the environment using fosmid clones: The case of haloviruses. PLoS One 2012, 7, e33802. [Google Scholar] [CrossRef]
  13. Prangishvili, D.; Forterre, P.; Garrett, R.A. Viruses of the archaea: A unifying view. Nat. Rev. Microbiol. 2006, 4, 837–848. [Google Scholar] [CrossRef] [PubMed]
  14. Torsvik, T.; Dundas, I.D. Bacteriophage of Halobacterium salinarium. Nature 1974, 248, 680–681. [Google Scholar] [CrossRef] [PubMed]
  15. Woese, C.R.; Kandler, O.; Wheelis, M.L. Towards a natural system of organisms: Proposal for the domains Archaea, Bacteria, and Eucarya. Proc. Natl. Acad. Sci. USA 1990, 87, 4576–4579. [Google Scholar] [CrossRef] [PubMed]
  16. Porter, K.; Dyall-Smith, M. The Isolation and Study of Viruses of Halophilic Microorganisms. In Extremophiles; Rainey, R.A., Oren, A., Eds.; Elsevier: Waltham, MA, USA, 2006; Volume 35, pp. 681–702. [Google Scholar]
  17. Dyall-Smith, M.; Tang, S.L.; Bath, C. Haloarchaeal viruses: How diverse are they? Res. Microbiol. 2003, 154, 309–313. [Google Scholar]
  18. Benlloch, S.; Acinas, S.G.; Anton, J.; Lopez-Lopez, A.; Luz, S.P.; Rodriguez-Valera, F. Archaeal biodiversity in crystallizer ponds from a solar saltern: Culture versus PCR. Microb. Ecol. 2001, 41, 12–19. [Google Scholar] [PubMed]
  19. Oren, A.; Bratbak, G.; Heldal, M. Occurrence of virus-like particles in the Dead Sea. Extremophiles 1997, 1, 143–149. [Google Scholar] [CrossRef] [PubMed]
  20. Santos, F.; Meyerdierks, A.; Peña, A.; Rosselló-Mora, R.; Amann, R.; Antón, J. Metagenomic approach to the study of halophages: The environmental halophage 1. Environ. Microbiol. 2007, 9, 1711–1723. [Google Scholar] [CrossRef] [PubMed]
  21. Bettarel, Y.; Bouvier, T.; Bouvier, C.; Carre, C.; Desnues, A.; Domaizon, I.; Jacquet, S.; Robin, A.; Sime-Ngando, T. Ecological traits of planktonic viruses and prokaryotes along a full-salinity gradient. FEMS Microbiol. Ecol. 2011, 76, 360–372. [Google Scholar] [CrossRef][Green Version]
  22. Sime-Ngando, T.; Lucas, S.; Robin, A.; Tucker, K.P.; Colombet, J.; Bettarel, Y.; Desmond, E.; Gribaldo, S.; Forterre, P.; Breitbart, M.; et al. Diversity of virus-host systems in hypersaline Lake Retba, Senegal. Environ. Microbiol. 2011, 13, 1956–1972. [Google Scholar] [CrossRef]
  23. Prangishvili, D.; Garrett, R.A. Viruses of hyperthermophilic Crenarchaea. Trends Microbiol. 2005, 13, 535–542. [Google Scholar] [CrossRef] [PubMed]
  24. Bath, C.; Cukalac, T.; Porter, K.; Dyall-Smith, M.L. His1 and His2 are distantly related, spindle-shaped haloviruses belonging to the novel virus group, Salterprovirus. Virology 2006, 350, 228–239. [Google Scholar]
  25. Tang, S.L.; Nuttall, S.; Dyall-Smith, M. Haloviruses HF1 and HF2: Evidence for a recent and large recombination event. J. Bacteriol. 2004, 186, 2810–2817. [Google Scholar] [CrossRef] [PubMed]
  26. Pietilä, M.K.; Atanasova, N.S.; Manole, V.; Liljeroos, L.; Butcher, S.J.; Oksanen, H.M.; Bamforda, D.H. Virion architecture unifies globally distributed pleolipoviruses infecting halophilic Archaea. J. Virol. 2012, 86, 5067–5078. [Google Scholar] [CrossRef] [PubMed]
  27. Porter, K.; Tang, S.L.; Chen, C.P.; Chiang, P.W.; Hong, M.J.; Dyall-Smith, M. Ph1: An archaeovirus of Haloarcula hispanica related to SH1 and HHIV-2. Archaea 2013, 2013, 456318. [Google Scholar] [CrossRef]
  28. Bamford, D.H. Do viruses form lineages across different domains of life? Res. Microbiol. 2003, 154, 231–236. [Google Scholar]
  29. Abrescia, N.G.; Bamford, D.H.; Grimes, J.M.; Stuart, D.I. Structure unifies the viral universe. Annu. Rev. Biochem. 2012, 81, 795–822. [Google Scholar] [CrossRef]
  30. Krupovič, M.; Bamford, D.H. Virus evolution: How far does the double β-barrel viral lineage extend? Nat. Rev. Microbiol. 2008, 6, 941–948. [Google Scholar]
  31. Jalasvuori, M; Bamford, J.K.H. Viruses and life: Can there be one without the other? J. Cosmol. 2010, 10, 3446–3454. [Google Scholar]
  32. Bamford, D.H.; Grimes, J.M.; Stuart, D.I. What does structure tell us about virus evolution? Curr. Opin. Struct. Biol. 2005, 15, 655–663. [Google Scholar] [CrossRef]
  33. Pedulla, M.L.; Ford, M.E.; Houtz, J.M.; Karthikeyan, T.; Wadsworth, C.; Lewis, J.A.; Jacobs-Sera, D.; Falbo, J.; Gross, J.; Pannunzio, N.R.; et al. Origins of highly mosaic mycobacteriophage genomes. Cell 2003, 113, 171–182. [Google Scholar] [CrossRef]
  34. Papke, R.T.; Doolittle, W.F. Phage evolution: New worlds of genomic diversity. Curr. Biol. 2003, 13, R606–R607. [Google Scholar] [CrossRef] [PubMed]
  35. Roine, E.; Kukkaro, P.; Paulin, L.; Laurinavičius, S.; Domanska, A.; Somerharju, P.; Bamford, D.H. New, closely related haloarchaeal viral elements with different nucleic acid types. J. Virol. 2010, 84, 3682–3689. [Google Scholar] [CrossRef] [PubMed]
  36. Krupovič, M.; Bamford, D.H. Order to the viral universe. J. Virol. 2010, 84, 12476–12479. [Google Scholar] [CrossRef]
  37. Benson, S.D.; Bamford, J.K.H.; Bamford, D.H.; Burnett, R.M. Does common architecture reveal a viral lineage spanning all three domains of life? Mol. Cell 2004, 16, 673–685. [Google Scholar]
  38. Pietilä, M.K.; Laurinmäki, P.; Russell, D.A.; Ko, C.C.; Jacobs-Sera, D.; Hendrix, R.W.; Bamford, D.H.; Butcher, S.J. Structure of the archaeal head-tailed virus HSTV-1 completes the HK97 fold story. Proc. Natl. Acad. Sci. USA 2013, 110, 10604–10609. [Google Scholar] [CrossRef] [PubMed]
  39. Pietilä, M.K.; Atanasova, N.S.; Oksanen, H.M.; Bamford, D.H. Modified coat protein forms the flexible spindle-shaped virion of haloarchaeal virus His1. Environ. Microbiol. 2013, 15, 1674–1686. [Google Scholar] [CrossRef] [PubMed]
  40. Jaatinen, S.T.; Happonen, L.J.; Laurinmaki, P.; Butcher, S.J.; Bamford, D.H. Biochemical and structural characterisation of membrane-containing icosahedral dsDNA bacteriophages infecting thermophilic Thermus thermophilus. Virology 2008, 379, 10–19. [Google Scholar] [CrossRef] [PubMed]
  41. Jalasvuori, M.; Jaatinen, S.T.; Laurinavicius, S.; Ahola-Iivarinen, E.; Kalkkinen, N.; Bamford, D.H.; Bamford, J.K. The closest relatives of icosahedral viruses of thermophilic Bacteria are among viruses and plasmids of the halophilic Archaea. J. Virol. 2009, 83, 9388–9397. [Google Scholar] [CrossRef] [PubMed]
  42. Jalasvuori, M.; Pawlowski, A.; Bamford, J.K. A unique group of virus-related, genome-integrating elements found solely in the bacterial family Thermaceae and the archaeal family Halobacteriaceae. J. Bacteriol. 2010, 192, 3231–3234. [Google Scholar] [CrossRef]
  43. Jäälinoja, H.T.; Roine, E.; Laurinmäki, P.; Kivelä, H.M.; Bamford, D.H.; Butcher, S.J. Structure and host-cell interaction of SH1, a membrane-containing, halophilic euryarchaeal virus. Proc. Natl. Acad. Sci. USA 2008, 105, 8008–8013. [Google Scholar] [CrossRef] [PubMed]
  44. Dyall-Smith, M. Halobacterial viruses (haloviruses) summary table. Available online: (accessed on 28 May 2013).
  45. Nuttall, S.D.; Dyall-Smith, M.L. HF1 and HF2: Novel bacteriophages of halophilic Archaea. Virology 1993, 197, 678–684. [Google Scholar] [CrossRef] [PubMed]
  46. Nuttall, S.D.; Dyall-Smith, M.L. Halophage HF2: Genome organization and replication strategy. J. Virol. 1995, 69, 2322–2327. [Google Scholar] [PubMed]
  47. Senčilo, A.; Jacobs-Sera, D.; Russell, D.A.; Ko, C.C.; Bowman, C.A.; Atanasova, N.S.; Os̈terlund, E.; Oksanen, H.M.; Bamford, D.H.; Hatfull, G.F.; et al. Snapshot of haloarchaeal tailed virus genomes. RNA Biol. 2013, 10, 803–816. [Google Scholar] [CrossRef] [PubMed]
  48. Kukkaro, P.; Bamford, D.H. Virus-host interactions in environments with a wide range of ionic strengths. Environ. Microbiol. Rep. 2009, 1, 71–77. [Google Scholar] [CrossRef] [PubMed]
  49. Torsvik, T.; Dundas, I.D. Persisting phage infection in Halobacterium salinarium str. 1. J. Gen. Virol. 1980, 47, 29–36. [Google Scholar] [CrossRef]
  50. Pietilä, M.K.; Laurinmäki, P.; Russell, D.A.; Ko, C.C.; Jacobs-Sera, D.; Butcher, S.J.; Bamford, D.H.; Hendrix, R.W. Insights into head-tailed viruses infecting extremely halophilic Archaea. J. Virol. 2013, 87, 3248–3260. [Google Scholar] [CrossRef] [PubMed]
  51. Witte, A.; Baranyi, U.; Klein, R.; Sulzner, M.; Luo, C.; Wanner, G.; Krüger, D.H.; Lubitz, W. Characterization of Natronobacterium magadii phage φCh1, a unique archaeal phage containing DNA and RNA. Mol. Microbiol. 1997, 23, 603–616. [Google Scholar] [CrossRef] [PubMed]
  52. Klein, R.; Baranyi, U.; Rössler, N.; Greineder, B.; Scholz, H.; Witte, A. Natrialba magadii virus φCh1: First complete nucleotide sequence and functional organization of a virus infecting a haloalkaliphilic archaeon. Mol. Microbiol. 2002, 45, 851–863. [Google Scholar] [CrossRef] [PubMed]
  53. Rössler, N.; Klein, R.; Scholz, H.; Witte, A. Inversion within the haloalkaliphilic virus φCh1 DNA results in differential expression of structural proteins. Mol. Microbiol. 2004, 52, 413–426. [Google Scholar] [CrossRef] [PubMed]
  54. Schnabel, H.; Zillig, W.; Pfäffle, M.; Schnabel, R.; Michel, H.; Delius, H. Halobacterium halobium phage øH. EMBO J. 1982, 1, 87–92. [Google Scholar] [PubMed]
  55. Schnabel, H.; Schramm, E.; Schnabel, R.; Zillig, W. Structural variability in the genome of phage φH of Halobacterium halobium. Mol. Gen. Genet. 1982, 188, 370–377. [Google Scholar] [CrossRef]
  56. Gropp, F.; Palm, P.; Zillig, W. Expression and regulation of Halobacterium halobium phage φH genes. Can. J. Microbiol. 1989, 35, 182–188. [Google Scholar] [CrossRef] [PubMed]
  57. Stolt, P.; Zillig, W. In vivo studies on the effects of immunity genes on early lytic transcription in the Halobacterium salinarium phage φH. Mol. Gen. Genet. 1992, 235, 197–204. [Google Scholar] [CrossRef] [PubMed]
  58. Stolt, P.; Zillig, W. Antisense RNA mediates transcriptional processing in an archaebacterium, indicating a novel kind of RNase activity. Mol. Microbiol. 1993, 7, 875–882. [Google Scholar] [CrossRef] [PubMed]
  59. Stolt, P.; Zillig, W. In vivo and in vitro analysis of transcription of the l region from the Halobacterium salinarium phage øH: Definition of a repressor-enhancing gene. Virology 1993, 195, 649–658. [Google Scholar] [CrossRef] [PubMed]
  60. Stolt, P.; Zillig, W. Gene regulation in halophage φH; more than promoters. Syst. Appl. Microbiol. 1994, 16, 591–596. [Google Scholar] [CrossRef]
  61. Stolt, P.; Zillig, W. Transcription of the halophage φH repressor gene is abolished by transcription from an inversely oriented lytic promoter. FEBS Lett. 1994, 344, 125–128. [Google Scholar] [CrossRef] [PubMed]
  62. Daniels, L.L.; Wais, A.C. Ecophysiology of bacteriophage S5100 infecting Halobacterium cutirubrum. Appl. Environ. Microbiol. 1990, 56, 3605–3608. [Google Scholar] [PubMed]
  63. Pagaling, E.; Haigh, R.D.; Grant, W.D.; Cowan, D.A.; Jones, B.E.; Ma, Y.; Ventosa, A.; Heaphy, S. Sequence analysis of an archaeal virus isolated from a hypersaline lake in inner Mongolia, China. BMC Genomics 2007, 8, 410. [Google Scholar] [CrossRef] [PubMed]
  64. Pauling, C. Bacteriophages of Halobacterium halobium: Isolation from fermented fish sauce and primary characterization. Can. J. Microbiol. 1982, 28, 916–921. [Google Scholar] [CrossRef] [PubMed]
  65. Rohrmann, G.F.; Cheney, R.; Pauling, C. Bacteriophages of Halobacterium halobium: Virion DNAs and proteins. Can. J. Microbiol. 1983, 29, 627–629. [Google Scholar] [CrossRef] [PubMed]
  66. Vogelsang-Wenke, H.; Oesterhelt, D. Isolation of a halobacterial phage with a fully cytosine-methylated genome. Mol. Gen. Genet. 1988, 211, 407–414. [Google Scholar] [CrossRef]
  67. Daniels, L.L.; Wais, A.C. Restriction and modification of halophage S45 in Halobacterium. Curr. Micriobiol. 1984, 10, 133–136. [Google Scholar] [CrossRef]
  68. Senčilo, A.; Paulin, L.; Kellner, S.; Helm, M.; Roine, E. Related haloarchaeal pleomorphic viruses contain different genome types. Nucleic Acids Res. 2012, 40, 5523–5534. [Google Scholar] [CrossRef]
  69. Pietilä, M.K.; Roine, E.; Paulin, L.; Kalkkinen, N.; Bamford, D.H. An ssDNA virus infecting Archaea: A new lineage of viruses with a membrane envelope. Mol. Microbiol. 2009, 72, 307–319. [Google Scholar] [CrossRef] [PubMed]
  70. Porter, K.; Dyall-Smith, M.L. Transfection of haloarchaea by the DNAs of spindle and round haloviruses and the use of transposon mutagenesis to identify non-essential regions. Mol. Microbiol. 2008, 70, 1236–1245. [Google Scholar] [CrossRef] [PubMed]
  71. Bamford, D.H.; Ravantti, J.J.; Ronnholm, G.; Laurinavicius, S.; Kukkaro, P.; Dyall-Smith, M.; Somerharju, P.; Kalkkinen, N.; Bamford, J.K. Constituents of SH1, a novel lipid-containing virus infecting the halophilic euryarchaeon Haloarcula hispanica. J. Virol. 2005, 79, 9097–9107. [Google Scholar] [CrossRef] [PubMed]
  72. Porter, K.; Kukkaro, P.; Bamford, J.K.H.; Bath, C.; Kivelä, H.M.; Dyall-Smith, M.L.; Bamford, D.H. SH1: A novel, spherical halovirus isolated from an Australian hypersaline lake. Virology 2005, 335, 22–33. [Google Scholar] [CrossRef] [PubMed]
  73. Kivelä, H.M.; Roine, E.; Kukkaro, P.; Laurinavičius, S.; Somerharju, P.; Bamford, D.H. Quantitative dissociation of archaeal virus SH1 reveals distinct capsid proteins and a lipid core. Virology 2006, 356, 4–11. [Google Scholar] [CrossRef] [PubMed]
  74. Porter, K.; Russ, B.E.; Yang, J.; Dyall-Smith, M.L. The transcription programme of the protein-primed halovirus SH1. Microbiology 2008, 154, 3599–3608. [Google Scholar] [CrossRef] [PubMed]
  75. Jaakkola, S.T.; Penttinen, R.K.; Vilén, S.T.; Jalasvuori, M.; Rönnholm, G.; Bamford, J.K.H.; Bamford, D.H.; Oksanen, H.M. Closely related archaeal Haloarcula hispanica icosahedral viruses HHIV-2 and SH1 have nonhomologous genes encoding host recognition functions. J. Virol. 2012, 86, 4734–4742. [Google Scholar] [CrossRef] [PubMed]
  76. Mei, Y.; Chen, J.; Sun, D.; Chen, D.; Yang, Y.; Shen, P.; Chen, X. Induction and preliminary characterization of a novel halophage SNJ1 from lysogenic Natrinema sp. F5. Can. J. Microbiol. 2007, 53, 1106–1110. [Google Scholar] [CrossRef] [PubMed]
  77. Zhang, Z.; Liu, Y.; Wang, S.; Yang, D.; Cheng, Y.; Hu, J.; Chen, J.; Mei, Y.; Shen, P.; Bamford, D.H.; et al. Temperate membrane-containing halophilic archaeal virus SNJ1 has a circular dsDNA genome identical to that of plasmid pHH205. Virology 2012, 434, 233–241. [Google Scholar] [CrossRef] [PubMed]
  78. Bath, C.; Dyall-smith, M.L. His1, an archaeal virus of the Fuselloviridae family that infects Haloarcula hispanica. J. Virol. 1998, 72, 9392–9395. [Google Scholar] [PubMed]
  79. Ventosa, A.; Oren, A. Halobacterium salinarum nom. corrig, a name to replace Halobacterium salinarium (elazari-volcani) and to include Halobacterium halobium and Halobacterium cutirubrum. Int. J. Syst. Bacteriol. 1996, 46, 347. [Google Scholar] [CrossRef]
  80. Euzeby, J.P. List of prokaryotic names with standing in nomenclature. Available online: (accessed on 5 September 2014).
  81. Ackermann, H.W. Tailed bacteriophages: The order Caudovirales. Adv. Virus. Res. 1998, 51, 135–201. [Google Scholar] [PubMed]
  82. Hendrix, R.W. Bacteriophage HK97: Assembly of the capsid and evolutionary connections. Adv. Virus. Res. 2005, 64, 1–14. [Google Scholar] [PubMed]
  83. Chang, J.R.; Spilman, M.S.; Rodenburg, C.M.; Dokland, T. Functional domains of the bacteriophage P2 scaffolding protein: Identification of residues involved in assembly and protease activity. Virology 2009, 384, 144–150. [Google Scholar] [CrossRef] [PubMed]
  84. Krupovič, M.; Forterre, P.; Bamford, D.H. Comparative analysis of the mosaic genomes of tailed archaeal viruses and proviruses suggests common themes for virion architecture and assembly with tailed viruses of Bacteria. J. Mol. Biol. 2010, 397, 144–160. [Google Scholar] [CrossRef] [PubMed]
  85. Pietilä, M.K.; Demina, T.A.; Atanasova, N.S.; Oksanen, H.M.; Bamford, D.H. Archaeal viruses and bacteriophages: Comparisons and contrasts. Trends Microbiol. 2014, 22, 334–344. [Google Scholar] [CrossRef] [PubMed]
  86. Prangishvili, D. The wonderful world of archaeal viruses. Annu. Rev. Microbiol. 2013, 67, 565–585. [Google Scholar] [CrossRef] [PubMed]
  87. Krupovic, M.; Spang, A.; Gribaldo, S.; Forterre, P.; Schleper, C. A thaumarchaeal provirus testifies for an ancient association of tailed viruses with archaea. Biochem. Soc. Trans. 2011, 39, 82–88. [Google Scholar] [CrossRef] [PubMed]
  88. Senčilo, A.; Roine, E. A glimpse of the genomic diversity of haloarchaeal tailed viruses. Front. Microbiol. 2014, 5, 84. [Google Scholar] [CrossRef] [PubMed]
  89. Pietilä, M.K.; Laurinavičius, S.; Sund, J.; Roine, E.; Bamford, D.H. The single-stranded DNA genome of novel archaeal virus Halorubrum pleomorphic virus 1 is enclosed in the envelope decorated with glycoprotein spikes. J. Virol. 2010, 84, 788–798. [Google Scholar] [CrossRef] [PubMed]
  90. Dybvig, K.; Nowak, J.A.; Sladek, T.L.; Maniloff, J. Identification of an enveloped phage, mycoplasma virus L172, that contains a 14-kilobase single-stranded DNA genome. J. Virol. 1985, 53, 384–390. [Google Scholar] [PubMed]
  91. Pawlowski, A.; Rissanen, I.; Bamford, J.K.; Krupovic, M.; Jalasvuori, M. Gammasphaerolipovirus, a newly proposed bacteriophage genus, unifies viruses of halophilic Archaea and thermophilic Bacteria within the novel family Sphaerolipoviridae. Arch. Virol. 2014, 159, 1541–1554. [Google Scholar] [CrossRef] [PubMed]
  92. Krupovic, M.; Quemin, E.R.; Bamford, D.H.; Forterre, P.; Prangishvili, D. Unification of the globally distributed spindle-shaped viruses of the Archaea. J. Virol. 2014, 88, 2354–2358. [Google Scholar] [CrossRef] [PubMed]
  93. Haring, M.; Vestergaard, G.; Rachel, R.; Chen, L.; Garrett, R.A.; Prangishvili, D. Virology: Independent virus development outside a host. Nature 2005, 436, 1101–1102. [Google Scholar] [CrossRef] [PubMed]
  94. Scheele, U.; Erdmann, S.; Ungewickell, E.J.; Felisberto-Rodrigues, C.; Ortiz-Lombardia, M.; Garrett, R.A. Chaperone role for proteins P618 and P892 in the extracellular tail development of Acidianus two-tailed virus. J. Virol. 2011, 85, 4812–4821. [Google Scholar] [CrossRef] [PubMed]
  95. Xiang, X.; Chen, L.; Huang, X.; Luo, Y.; She, Q.; Huang, L. Sulfolobus tengchongensis spindle-shaped virus STSV1: Virus-host interactions and genomic features. J. Virol. 2005, 79, 8677–8686. [Google Scholar] [CrossRef] [PubMed]
  96. Erdmann, S.; Chen, B.; Huang, X.; Deng, L.; Liu, C.; Shah, S.A.; Le Moine Bauer, S.; Sobrino, C.L.; Wang, H.; Wei, Y.; et al. A novel single-tailed fusiform Sulfolobus virus STSV2 infecting model Sulfolobus species. Extremophiles 2014, 18, 51–60. [Google Scholar] [CrossRef] [PubMed]
  97. Emerson, J.B.; Thomas, B.C.; Andrade, K.; Allen, E.E.; Heidelberg, K.B.; Banfielda, J.F. Dynamic viral populations in hypersaline systems as revealed by metagenomic assembly. Appl. Environ. Microbiol. 2012, 78, 6309–6320. [Google Scholar] [CrossRef] [PubMed]
  98. Emerson, J.B.; Andrade, K.; Thomas, B.C.; Norman, A.; Allen, E.E.; Heidelberg, K.B.; Banfield, J.F. Virus-host and CRISPR dynamics in Archaea-dominated hypersaline Lake Tyrrell, Victoria, Australia. Archaea 2013, 2013, 370871. [Google Scholar] [CrossRef] [PubMed]
  99. Tang, S.L.; Nuttall, S.; Ngui, K.; Fisher, C.; Lopez, P.; Dyall-Smith, M. HF2: A double-stranded DNA tailed haloarchaeal virus with a mosaic genome. Mol. Microbiol. 2002, 44, 283–296. [Google Scholar] [CrossRef] [PubMed]
  100. Klein, R.; Rössler, N.; Iro, M.; Scholz, H.; Witte, A. Haloarchaeal myovirus φCh1 harbours a phase variation system for the production of protein variants with distinct cell surface adhesion specificities. Mol. Microbiol. 2012, 83, 137–150. [Google Scholar] [CrossRef] [PubMed]
  101. Santos, F.; Yarza, P.; Parro, V.; Briones, C.; Anton, J. The metavirome of a hypersaline environment. Environ. Microbiol. 2010, 12, 2965–2976. [Google Scholar] [CrossRef] [PubMed]
  102. Narasingarao, P.; Podell, S.; Ugalde, J.A.; Brochier-Armanet, C.; Emerson, J.B.; Brocks, J.J.; Heidelberg, K.B.; Banfield, J.F.; Allen, E.E. De novo metagenomic assembly reveals abundant novel major lineage of Archaea in hypersaline microbial communities. ISME J. 2012, 6, 81–93. [Google Scholar] [CrossRef] [PubMed]
  103. Ghai, R.; Pasic, L.; Fernandez, A.B.; Martin-Cuadrado, A.B.; Mizuno, C.M.; McMahon, K.D.; Papke, R.T.; Stepanauskas, R.; Rodriguez-Brito, B.; Rohwer, F.; et al. New abundant microbial groups in aquatic hypersaline environments. Sci. Rep. 2011, 1. [Google Scholar] [CrossRef]
  104. Zhaxybayeva, O.; Stepanauskas, R.; Mohan, N.R.; Papke, R.T. Cell sorting analysis of geographically separated hypersaline environments. Extremophiles 2013, 17, 265–275. [Google Scholar] [CrossRef] [PubMed]
  105. Cavicchioli, R. Extremophiles and the search for extraterrestrial life. Astrobiology 2002, 2, 281–292. [Google Scholar] [CrossRef] [PubMed]
  106. DasSarma, S. Extreme halophiles are models for astrobiology. Microbe 2006, 1, 120–126. [Google Scholar]
  107. Pasic, L.; Rodriguez-Mueller, B.; Martin-Cuadrado, A.B.; Mira, A.; Rohwer, F.; Rodriguez-Valera, F. Metagenomic islands of hyperhalophiles: The case of Salinibacter ruber. BMC Genomics 2009, 10. [Google Scholar] [CrossRef] [PubMed]
  108. Roine, E.; Bamford, D.H. Lipids of archaeal viruses. Archaea 2012, 2012, 384919. [Google Scholar] [CrossRef] [PubMed]
  109. Katsura, I.; Hendrix, R.W. Length determination in bacteriophage lambda tails. Cell 1984, 39, 691–698. [Google Scholar] [CrossRef] [PubMed]
  110. Shao, Y.; Wang, I.N. Bacteriophage adsorption rate and optimal lysis time. Genetics 2008, 180, 471–482. [Google Scholar] [CrossRef] [PubMed]
  111. Porter, K.; Russ, B.E.; Dyall-Smith, M.L. Virus-host interactions in salt lakes. Curr. Opin. Microbiol. 2007, 10, 418–424. [Google Scholar] [CrossRef] [PubMed]
  112. Hanhijärvi, K.J.; Ziedaite, G.; Pietilä, M.K.; Hæggström, E.; Bamford, D.H. DNA ejection from an archaeal virus - a single-molecule approach. Biophys. J. 2013, 104, 2264–2272. [Google Scholar] [CrossRef] [PubMed]
  113. Grayson, P.; Han, L.; Winther, T.; Phillips, R. Real-time observations of single bacteriophage λ DNA ejections in vitro. Proc. Natl. Acad. Sci. USA 2007, 104, 14652–14657. [Google Scholar] [CrossRef] [PubMed]
  114. Schnabel, H. An immune strain of Halobacterium halobium carries the invertible L segment of phage φH as a plasmid. Proc. Natl. Acad. Sci. USA 1984, 81, 1017–1020. [Google Scholar] [CrossRef] [PubMed]
  115. Lobocka, M.B.; Rose, D.J.; Plunkett, G., III; Rusin, M.; Samojedny, A.; Lehnherr, H.; Yarmolinsky, M.B.; Blattner, F.R. Genome of bacteriophage P1. J. Bacteriol. 2004, 186, 7032–7068. [Google Scholar] [CrossRef] [PubMed]
  116. Schnabel, H.; Zillig, W. Circular structure of the genome of phage φH in a lysogenic Halobacterium halobium. Mol. Gen. Genet. 1984, 193, 422–426. [Google Scholar] [CrossRef]
  117. DeMaere, M.Z.; Williams, T.J.; Allen, M.A.; Brown, M.V.; Gibson, J.A.; Rich, J.; Lauro, F.M.; Dyall-Smith, M.; Davenport, K.W.; Woyke, T.; et al. High level of intergenera gene exchange shapes the evolution of haloarchaea in an isolated Antarctic lake. Proc. Natl. Acad. Sci. USA 2013, 110, 16939–16944. [Google Scholar] [CrossRef] [PubMed]
  118. Chen, S.; Wang, C.; Zhao, Z.; Yang, Z.L. Genome sequence of Halorubrum sp. strain T3, an extremely halophilic archaeon harboring a virus-like element. J. Bacteriol. 2012, 194, 6608–6609. [Google Scholar] [CrossRef] [PubMed]
  119. Chen, S.; Wang, C.; Xu, J.P.; Yang, Z.L. Molecular characterization of PHRDV1, a new virus-like mobile genetic element closely related to pleomorphic viruses in haloarchaea. Extremophiles 2014, 18, 195–206. [Google Scholar] [CrossRef] [PubMed]
  120. Cline, S.W.; Doolittle, W.F. Efficient transfection of the archaebacterium Halobacterium halobium. J. Bacteriol. 1987, 169, 1341–1344. [Google Scholar] [PubMed]
  121. Cline, S.W.; Lam, W.L.; Charlebois, R.L.; Schalkwyk, L.C.; Doolittle, W.F. Transformation methods for halophilic archaebacteria. Can. J. Microbiol. 1989, 35, 148–152. [Google Scholar] [CrossRef] [PubMed]
  122. Blaseio, U.; Pfeifer, F. Transformation of Halobacterium halobium: Development of vectors and investigation of gas vesicle synthesis. Proc. Natl. Acad. Sci. USA 1990, 87, 6772–6776. [Google Scholar] [CrossRef] [PubMed]
  123. Iro, M.; Klein, R.; Gálos, B.; Baranyi, U.; Rössler, N.; Witte, A. The lysogenic region of virus φCh1: Identification of a repressor-operator system and determination of its activity in halophilic Archaea. Extremophiles 2007, 11, 383–396. [Google Scholar] [CrossRef] [PubMed]
  124. Allers, T.; Mevarech, M. Archaeal genetics—the third way. Nat. Rev. Genet. 2005, 6, 58–73. [Google Scholar] [CrossRef] [PubMed]
  125. Cuadros-Orellana, S.; Martin-Cuadrado, A.B.; Legault, B.; D’Auria, G.; Zhaxybayeva, O.; Papke, R.T.; Rodriguez-Valera, F. Genomic plasticity in prokaryotes: The case of the square haloarchaeon. ISME J. 2007, 1, 235–245. [Google Scholar] [CrossRef] [PubMed]
  126. Pyatibratov, M.G.; Beznosov, S.N.; Rachel, R.; Tiktopulo, E.I.; Surin, A.K.; Syutkin, A.S.; Fedorov, O.V. Alternative flagellar filament types in the haloarchaeon Haloarcula marismortui. Can. J. Microbiol. 2008, 54, 835–844. [Google Scholar] [CrossRef] [PubMed]
  127. Grissa, I.; Vergnaud, G.; Pourcel, C. The CRISPRdb database and tools to display CRISPRs and to generate dictionaries of spacers and repeats. BMC Bioinform. 2007, 8, 172. [Google Scholar] [CrossRef]
  128. Rousseau, C.; Gonnet, M.; Le Romancer, M.; Nicolas, J. CRISPI: A CRIPSR interactive database. Bioinformatics 2009, 25, 3317–3318. [Google Scholar] [CrossRef] [PubMed][Green Version]
  129. Koonin, E.V.; Wolf, Y.I. Is evolution Darwinian or/and Lamarckian? Biol. Direct 2009, 4, 42. [Google Scholar] [CrossRef]
  130. Maier, L.K.; Fischer, S.; Stoll, B.; Brendel, J.; Pfeiffer, F.; Dyall-Smith, M.; Marchfelder, A. The immune system of halophilic Archaea. Mob. Genet. Elements 2012, 2, 228–232. [Google Scholar] [CrossRef] [PubMed]
  131. Van der Oost, J.; Westra, E.R.; Jackson, R.N.; Wiedenheft, B. Unravelling the structural and mechanistic basis of CRISPR-Cas systems. Nat. Rev. Microbiol. 2014, 12, 479–492. [Google Scholar] [CrossRef] [PubMed]
  132. Bhaya, D.; Davison, M.; Barrangou, R. CRISPR-Cas systems in Bacteria and Archaea: Versatile small RNAs for adaptive defense and regulation. Annu. Rev. Genet. 2011, 45, 273–297. [Google Scholar] [CrossRef] [PubMed]
  133. Barrangou, R.; Fremaux, C.; Deveau, H.; Richards, M.; Boyaval, P.; Moineau, S.; Romero, D.A.; Horvath, P. CRISPR provides acquired resistance against viruses in prokaryotes. Science 2007, 315, 1709–1712. [Google Scholar] [CrossRef] [PubMed]
  134. Garneau, J.E.; Dupuis, M.E.; Villion, M.; Romero, D.A.; Barrangou, R.; Boyaval, P.; Fremaux, C.; Horvath, P.; Magadán, A.H.; Moineau, S. The CRISPR/Cas bacterial immune system cleaves bacteriophage and plasmid DNA. Nature 2010, 468, 67–71. [Google Scholar] [CrossRef] [PubMed]
  135. Al-Attar, S.; Westra, E.R.; van der Oost, J.; Brouns, S.J. Clustered regularly interspaced short palindromic repeats (CRISPRs): The hallmark of an ingenious antiviral defense mechanism in prokaryotes. Biol. Chem. 2011, 392, 277–289. [Google Scholar] [CrossRef] [PubMed]
  136. Garrett, R.A.; Vestergaard, G.; Shah, S.A. Archaeal CRISPR-based immune systems: Exchangeable functional modules. Trends Microbiol. 2011, 19, 549–556. [Google Scholar] [CrossRef] [PubMed]
  137. Terns, M.P.; Terns, R.M. CRISPR-based adaptive immune systems. Curr. Opin. Microbiol. 2011, 14, 321–327. [Google Scholar] [CrossRef] [PubMed]
  138. Vestergaard, G.; Garrett, R.A.; Shah, S.A. CRISPR adaptive immune systems of Archaea. RNA Biol. 2014, 11, 156–167. [Google Scholar] [CrossRef] [PubMed]
  139. Fischer, S.; Maier, L.K.; Stoll, B.; Brendel, J.; Fischer, E.; Pfeiffer, F.; Dyall-Smith, M.; Marchfelder, A. An archaeal immune system can detect multiple protospacer adjacent motifs (PAMs) to target invader DNA. J. Biol. Chem. 2012, 287, 33351–33365. [Google Scholar] [CrossRef] [PubMed]
  140. Maier, L.K.; Stoll, B.; Brendel, J.; Fischer, S.; Pfeiffer, F.; Dyall-Smith, M.; Marchfelder, A. The ring of confidence: A haloarchaeal CRISPR/Cas system. Biochem. Soc. Trans. 2013, 41, 374–378. [Google Scholar] [CrossRef] [PubMed]
  141. Li, M.; Liu, H.; Han, J.; Liu, J.; Wang, R.; Zhao, D.; Zhou, J.; Xiang, H. Characterization of CRISPR RNA biogenesis and Cas6 cleavage-mediated inhibition of a provirus in the haloarchaeon Haloferax mediterranei. J. Bacteriol. 2013, 195, 867–875. [Google Scholar] [CrossRef] [PubMed]
  142. Fullmer, M.S.; Soucy, S.M.; Swithers, K.S.; Makkay, A.M.; Wheeler, R.; Ventosa, A.; Gogarten, J.P.; Papke, R.T. Population and genomic analysis of the genus Halorubrum. Front. Microbiol. 2014, 5. [Google Scholar] [CrossRef] [PubMed]
  143. Deveau, H.; Barrangou, R.; Garneau, J.E.; Labonte, J.; Fremaux, C.; Boyaval, P.; Romero, D.A.; Horvath, P.; Moineau, S. Phage response to CRISPR-encoded resistance in Streptococcus thermophilus. J. Bacteriol. 2008, 190, 1390–1400. [Google Scholar] [CrossRef] [PubMed]
  144. Naor, A.; Lapierre, P.; Mevarech, M.; Papke, R.T.; Gophna, U. Low species barriers in halophilic Archaea and the formation of recombinant hybrids. Curr. Biol. 2012, 22, 1444–1448. [Google Scholar] [CrossRef] [PubMed]
  145. Santos, F.; Moreno-Paz, M.; Meseguer, I.; López, C.; Rosselló-Mora, R.; Parro, V.; Antón, J. Metatranscriptomic analysis of extremely halophilic viral communities. ISME J. 2011, 5, 1621–1633. [Google Scholar] [CrossRef] [PubMed]
  146. Sanjuán, R.; Nebot, M.R.; Chirico, N.; Mansky, L.M.; Belshaw, R. Viral mutation rates. J. Virol. 2010, 84, 9733–9748. [Google Scholar] [CrossRef] [PubMed]
  147. Dyall-Smith, M.L.; Pfeiffer, F.; Klee, K.; Palm, P.; Gross, K.; Schuster, S.C.; Rampp, M.; Oesterhelt, D. Haloquadratum walsbyi: Limited diversity in a global pond. PLoS One 2011, 6, e20968. [Google Scholar] [CrossRef] [PubMed]
  148. Wais, A.C.; Daniels, L.L. Populations of bacteriophage infecting Halobacterium in a transient brine pool. FEMS Microbiol. Ecol. 1985, 31, 323–326. [Google Scholar] [CrossRef]
  149. Bertani, G. Transduction-like gene transfer in the methanogen Methanococcus voltae. J. Bacteriol. 1999, 181, 2992–3002. [Google Scholar] [PubMed]
  150. Lang, A.S.; Zhaxybayeva, O.; Beatty, J.T. Gene transfer agents: Phage-like elements of genetic exchange. Nat. Rev. Microbiol. 2012, 10, 472–482. [Google Scholar] [PubMed]
  151. Williams, D.; Gogarten, J.P.; Papke, R.T. Quantifying homologous replacement of loci between haloarchaeal species. Genome Biol. Evol. 2012, 4, 1223–1244. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Luk, A.W.S.; Williams, T.J.; Erdmann, S.; Papke, R.T.; Cavicchioli, R. Viruses of Haloarchaea. Life 2014, 4, 681-715.

AMA Style

Luk AWS, Williams TJ, Erdmann S, Papke RT, Cavicchioli R. Viruses of Haloarchaea. Life. 2014; 4(4):681-715.

Chicago/Turabian Style

Luk, Alison W. S., Timothy J. Williams, Susanne Erdmann, R. Thane Papke, and Ricardo Cavicchioli. 2014. "Viruses of Haloarchaea" Life 4, no. 4: 681-715.

Article Metrics

Back to TopTop