Next Article in Journal
Acidisoma silvae sp. nov. and Acidisomacellulosilytica sp. nov., Two Acidophilic Bacteria Isolated from Decaying Wood, Hydrolyzing Cellulose and Producing Poly-3-hydroxybutyrate
Next Article in Special Issue
Genomic Analysis of Prophages from Klebsiella pneumoniae Clinical Isolates
Previous Article in Journal
Seasonal Characterization of the Endophytic Fungal Microbiome of Mulberry (Morus spp.) Cultivars Resistant and Susceptible to Sclerotiniosis
Previous Article in Special Issue
The Characterization of a Novel Phage, pPa_SNUABM_DT01, Infecting Pseudomonas aeruginosa
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Microorganisms
Volume 9
Issue 10
10.3390/microorganisms9102043
microorganisms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Genomic Characterization of a Prophage, Smhb1, That Infects Salinivibrio kushneri BNH Isolated from a Namib Desert Saline Spring

by
Israel Olonade
,
Leonardo Joaquim van Zyl
* and
Marla Trindade
Institute for Microbial Biotechnology and Metagenomics (IMBM), University of the Western Cape, Bellville, Cape Town 7535, South Africa
*
Author to whom correspondence should be addressed.
Microorganisms 2021, 9(10), 2043; https://doi.org/10.3390/microorganisms9102043
Submission received: 8 August 2021 / Revised: 27 August 2021 / Accepted: 28 August 2021 / Published: 28 September 2021
(This article belongs to the Special Issue Bacteriophage Genomics)
Browse Figures
Versions Notes

Abstract

:
Recent years have seen the classification and reclassification of many viruses related to the model enterobacterial phage P2. Here, we report the identification of a prophage (Smhb1) that infects Salinivibrio kushneri BNH isolated from a Namib Desert salt pan (playa). Analysis of the genome revealed that it showed the greatest similarity to P2-like phages that infect Vibrio species and showed no relation to any of the previously described Salinivibrio-infecting phages. Despite being distantly related to these Vibrio infecting phages and sharing the same modular gene arrangement as seen in most P2-like viruses, the nucleotide identity to its closest relatives suggest that, for now, Smhb1 is the lone member of the Peduovirus genus Playavirus. Although host range testing was not extensive and no secondary host could be identified for Smhb1, genomic evidence suggests that the phage is capable of infecting other Salinivibrio species, including Salinivibrio proteolyticus DV isolated from the same playa. Taken together, the analysis presented here demonstrates how adaptable the P2 phage model can be.

1. Introduction

With an estimate of ~1031 viral particles present in the environment, numbering from 107 to 109 per gram of soil or sediment [1,2] to 1010 per liter of sea water [3], bacteriophages (viruses that infect bacteria) are known to be widely distributed in nature. While the discovery of phages and the investigation of phage model systems have contributed to our understanding of molecular biology, only more recently has their impact on ecosystems been fully appreciated [4,5].
The range of interactions phages can have with their hosts suggests that they can play an important role in shaping microbial diversity and ecology [6,7,8]. Such roles include significant contributions to nutrient cycling in the ocean by being major predators of bacteria and archaea [9] and as major contributors to genetic exchange in the environment with phages estimated to transduce 1025 to 1028 base pairs of DNA per year in the marine environment alone [10].
Haloalkaline environments are considered to have the highest abundance and diversity of viruses of all types of environments, with the highest viral count documented to be 2 × 109 per mL in the hypersaline Mono Lake, California [11]. The impact phages can have on trophic levels was demonstrated in the East African Rift Valley lakes where a short food chain, involving cyanophages, the cyanobacterium Arthrospira fusiformis, and the Lesser Flamingo, exists [12].
The population of A. fusiformis can collapse drastically and unpredictably due to a cyanophage infection, and this fluctuation represents the major factor influencing the population and distribution of the Lesser Flamingo [13,14]. The study also made an interesting observation that, although the phage to bacteria ratio constantly fluctuated, the difference remained in the same order of magnitude. This suggests that phages are actively involved in keeping bacterial populations at a threshold.
The Namib Desert salt playas are unique environments with salinities in the range of 3–15% depending on the sampling depth, evaporation rate as a consequence of the time of the day, and the distance from the source [15,16,17,18]. The Eisfeld site explored here has a salinity range of 4.5–8.6% [19]. These values are relatively low in comparison to other saline environments, such as the moderately hypersaline Salton Sea (CA, USA), which has a salinity range of 5% (water table) to 11.8% (sediments) [20] or crystallizer ponds and solar salterns with a range from 13.8% to 37% [21,22].
Physico-chemical analysis also showed that the site has a pH range of 6.5 (source) to 8.5 (sink), a conductivity range of 66–180 mS/cm, and total dissolved solids (TDS) range of 42,000–115,000 ppm [15,18,19]. Temperatures have also been reported to reach up to 50 °C [15]. These parameters together with its unique, under sampled, geographic location suggests that it could be an environment that harbors novel halotolerant and halophilic bacteria, which could host potentially unique viruses.
A description of the virome data for the Eisfeld site was presented elsewhere [19] with the families Circoviridae, Microviridae, and Inoviridae found to comprise a significant portion of the viral diversity of the site. The genus Salinivibrio is comprised of halophilic, curved rod shaped, motile, facultative anaerobic, Gram-negative bacteria that, according to the genome taxonomy database classification, currently consists of seven species. Phages CW02, G3, and UTAK are the only phages known to infect the Salinivibrio species; however, only phage CW02 has been described in terms of general features and genomic architecture, while the host for UTAK may have been incorrectly reported [23,24].
Recent efforts by the bacterial and archaeal virus subcommittee of the ICTV has seen a large number of phages being classified and re-classified, and the P2-like viruses are no exception. Within the last four years, the subfamily has expanded from two genera/nineteen species in 2017 to thirty-one genera/seventy-six species in 2020 and a proposal in 2021 to elevate the subfamily to family status [25]. Here, we describe the isolation of a new P2-like phage, Smhb1, which infects a Salinivibrio species that, given the seeming rarity of Salinivibrio-infecting phages and its novel nucleotide sequence compared against newly classified P2-like viruses, makes it highly unique.

2. Materials and Methods

2.1. Sampling and Bacterial Isolation and Identification

Samples were collected from the Eisfield salt playa 21.5 km Northeast of Swakopmund (22°29’5.31” S; 14°34’17.88” E), Namibia. Fifty milliliters of the microbial mat suspended in spring water from the playa was shaken at 50 rpm for 2 h to encourage the dissociation of bacterial cells from biofilm debris. After a low-speed centrifugation (26.5× g for 10 min), 10 µL of the supernatant was spread on MHB agar plates containing the following per liter: 98 g NaCl (Cat. No. S9888), 20 g bacteriological agar, 10 g yeast extract, 5 g tryptone, 2 g KCl (Cat. No. P3911), 1 g D-glucose (Cat. No. SAAR2676020EM, Merck, Darmstadt, Germany), 1 g MgSO4·7H2O (Cat. No. M2773), 0.36 g CaCl2·6H2O (Cat. No. 442909), 0.23 g NaBr (Cat. No. 310506,), 0.06 g NaHCO3 (Cat. No. S6014), and 0.001 g FeCl3 (Cat. No. 157740).
Except for the yeast extract (Cat. No. HG000BX6.500), bacteriological agar (Cat. No. HG000BX1.500), and tryptone (Cat. No. HG000BX4.250) powder purchased from biolab (Merck, Modderfontein, South Africa), the other reagents were purchased from Sigma-Aldrich, St. Louis, MO, USA. The plates were incubated at 37 °C until colonies were observed. Colonies of varying morphologies were selected after visual inspection and Gram staining. Each isolate was purified by three rounds of re-streaking on fresh agar plates and stored in MHB broth supplemented with 50% glycerol at −80 °C until required.
The 16S rRNA gene from each isolate was amplified using the universal primers E9F (5′-GAGTTTGATCCTGGCTCAG-3′) [26] and U1510R (5′-GGTTACCTTGTTACGACTT-3′) [27]. DNA templates were prepared by re-suspending a loop-full of each isolate in 100 μL of PCR grade water and boiling at 85 °C for 5 min. Each PCR reaction contained 12.5 μL of KAPA Taq ReadyMix (Cat. No KK1006, Kapa Biosystems, Boulder, CO, USA), with a 0.5 µM final primer concentration and 2 μL of DNA template that was adjusted to a final volume of 25 μL with water.
The PCR conditions were an initial denaturation at 95 °C for 3 min, followed by 35 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 2 min, with a final extension at 72 °C for 2 min. DNA bands were excised and purified using the Nucleospin® Gel and PCR Clean-up kit (Cat. No. 740609.50, Macherey-Nagel, Dueren, Germany) according to the manufacturer’s instruction. The amplicon sequence was determined using an ABI PRISM® 377 automated DNA sequencer (Applied Biosystems, Thermo Scientific, Waltham, MA, USA) at the Central Analytical Facility of the University of Stellenbosch, South Africa.

2.2. Smhb1 Isolation and Transmission Electron Microscopy

During routine culturing of bacterial isolates identified as Salinivibrio species, culture lysis was observed for S. kushneri BNH, and epifluorescence microscopy confirmed the presence of virus-like particles in the culture supernatant. Plating a lawn of the culture also yielded individual plaques. Phage samples were prepared for imaging by centrifugation of the phage lysate at 27,200× g (Centrifuge Eppendorf 5417 R, Merck, Darmstadt, Germany) for 5 h and the phage pellet resuspended in 100 mM ammonium acetate, pH 6.5 and washed four times in this solution, according to [28].
Three microliters of the phage suspension were spotted onto glow-discharged (EMS100 Glow Discharge Unit, Electron Microscopy Sciences, Hatfield, PA, USA) 200-mesh carbon-coated copper grids (Cat. No. AGG2200C, Agar Scientific, Stansted, Essex, UK) and allowed to adsorb for 1 min. The grid was washed twice in sterile water and stained with 2% aqueous uranyl acetate (SPI Supplies, West Chester, PA, USA) for 30 s. The samples were viewed using a LEO 912 Omega TEM (Zeiss, Oberkochen, Germany) at 120 kV, and images were collected using a ProScan CCD camera (Cincinnati, OH, USA).

2.3. Genomic DNA Extractions

To extract phage genomic DNA, the supernatant of a 48-h 1 L culture of the bacterial host was cleared by centrifugation at 15,971× g for 30 min. Debris was further removed by passing it through a 0.22 μm filter (Cat. No. FJ25ANCCA002DD01, GVS, Bologna, Italy). Phage particles were concentrated by adding PEG 8000 (89510-1KG-F, Sigma-Aldrich, St. Louis, MO, USA) to a final concentration of 7% (wt/vol) and then incubated overnight at 4 °C. Viruses were pelleted at 9585× g for 15 min and resuspended in 1 mL SM buffer, and the DNA was extracted using a modified version of a published protocol [29]. Briefly, 1 mL of the resuspended viruses was transferred to a 15 mL Greiner centrifuge tube (T1943, Sigma-Aldrich, St. Louis, MO, USA) and 12.5 µL of 0.1 M MgCl2 was added to stabilize the DNA. Five microliters of DNAse I (1 U/uL, (Cat. No. EN0521, Fermentas, Vilnius, Lithuania) and 1 µL of RNAse A (10 mg/mL, (Cat. No. EN0531, Fermentas, Vilnius, Lithuania) were added, and the mixture incubated at 37 °C for one hour to digest the host DNA and RNA. The absence of contaminating DNA was confirmed by PCR amplification of the 16S rRNA gene as described above.
Proteinase K (final concentration 97.5 µg/mL, Cat. No. EO0491, Fermentas, Vilnius, Lithuania), 40 µL of 0.5 M EDTA and 50 µL of 10% SDS were added, and the mixture was incubated at 55 °C for 2 h with periodic mixing by gentle inversion. Complete lysis of the phage particles was confirmed by adding 1 µL of 10,000 × SYBR Gold (Cat. No. S11494, Invitrogen, Waltham, MA, USA) to 10 µL of the mixture with observation under a fluorescence microscope (Zeiss Axioplan 2, Zeiss, Oberkochen, Germany).
Viral DNA was extracted by adding an equal volume of Phenol: Chloroform: Isoamyl alcohol (25:24:1) and gently inverting the tubes. Phases were separated by centrifugation (Eppendorf 5810 R) for 5 min at 17,900× g at room temperature. The top aqueous layer was carefully removed and transferred to a sterile 2 mL Eppendorf tube. DNA was precipitated overnight at 4 °C by adding two volumes of absolute ethanol and 1/10 volume of 3 M NaOAc (pH 5.2), followed by pelleting at 17,900× g for 10 min. The DNA pellet was resuspended in 50 µL of TE buffer (pH 8).
Bacterial genomic DNA was extracted from the two Salinivibrio species (DV and BNH) isolated from the saline site. Five milliliters of an overnight culture of each strain in MHB broth was centrifuged at 2700× g for 5 min to collect bacterial cells. Genomic DNA was extracted from the bacterial pellets using a modified protocol [29]. Briefly, each pellet was resuspended in 950 µL of TE buffer and 50 µL of 10% SDS, and 5 µL of 20 mg/mL proteinase K (Fermentas) were added.
The suspension was incubated at 37 °C for 1 h. One hundred and eighty microliters of 5 M NaCl and 150 µL of CTAB/NaCl (10%/4% wt/vol) solution were added, mixed thoroughly, and incubated at 65 °C for 20 min. An equal volume of chloroform/isoamyl alcohol (24:1) was added. The solution was mixed gently and centrifuged at 20,800× g for 10 min at room temperature to separate the phases.
The DNA-containing supernatant was transferred to a fresh tube and extracted with an equal volume of phenol/chloroform/isoamyl alcohol, mixed gently, and centrifuged at 20,800× g for 10 min at room temperature. The clear upper phase was transferred to a new tube, 0.6 volume isopropanol was added, and the sample was gently mixed and centrifuged at 20,800× g for 10 min at room temperature. The pellet was washed with 70% ethanol, air dried, and resuspended in 200 µL of 1X TE buffer (pH 8).

2.4. Whole Genome Sequencing and Analysis

Prior to sequencing, the bacterial and phage genomic DNA was further cleaned using the Qiagen Gel Extraction kit (Qiaex II, Cat. No. 20021). Sequencing libraries were prepared using the Illumina Nextera XT library prep kit as per the manufacturer’s instructions, and sequencing was performed using the Illumina MiSeq Reagent kit V3, which included a 10% phiX V3 spike (Preparation guide, Part #15031942, May 2012 revision). This resulted in 2 × 300 bp paired end reads (forward and reverse). A de novo assembly was performed on reads using CLC Genomics version 7.5.1 (Qiagen, Venlo, Netherlands) at the default settings.
For the genomes of DV and BNH, annotation of the assembled contigs were carried out using the NCBI prokaryotic genome annotation pipeline (PGAP) [30]. Tetranucleotide usage deviation was calculated using TETRA in JSpeciesWS [31]. Phylogeny for bacterial genomes was established using GTDB-Tk through its implementation in K-Base [32,33]. Clustered regularly interspaced short palindromic repeats (CRISPRs) regions were scanned for using CRISPRFinder [34].
For phage Smhb1, the longest assembled contig was uploaded to the phage search tool PHASTER [35] for early identification of phage genes, followed by BLASTx comparison of non-coding segments against the NCBInr database. These were then manually curated using the CLC Genomics workbench and BLAST. Closely related phages were identified by examining data generated using VIRIDIC [36] and published in ICTV taxonomic proposal 2020.117B.R.Peduoviruses.
Comparison of genomic synteny was performed using Easyfig [37] using the tBLASTx function with the settings: min. length 35; max. e-value 0.001; min. identity value 0. VipTree [38] was used for comparison of Smhb1 proteins to those of other Peduoviruses. Direct repeats were identified using REPFIND [39] with a 10-bp minimum repeat length. tRNA genes were predicted using ARAGORN [40] and the tRNAscan-SE program [41,42]. Intron prediction was done using the RNAweasel server [43]. Transmembrane regions were predicted using the TMHMM server v2.0 [44].
For phylogenetic tree construction, the full-length amino acid sequences of selected terminase large subunit proteins were aligned using MUSCLE in MEGA7 [45], and the tree was constructed using the built-in program [46]. To determine amino acid usage profiles, the major capsid protein, terminase large and small subunits, sheath protein, head completion scaffold protein, and portal protein sequences were concatenated, and duplicate sequences removed using CD-HIT [47].
The sequences were aligned in MEGA 7 using MUSCLE and the alignment was manually curated to remove gaps (p-distance = 0.51). The aligned proteins were split into representatives from moderate halophiles (those infecting Vibrio sp., SMHB1 and C5a) and non-halophile infecting phages and these were used as “query” and “background” inputs to Composition Profiler, respectively [48].

3. Results and Discussion

3.1. Host Isolation and Sequencing; Smhb1 Morphological Characterization, and Host Range Testing

A number of bacteria (Halomonas caseinilytica, Halomonas eurihalina, Halomonas sinaiensis, Idiomarina loihiensis, Marinobacter xestospongiae, and Virgibacillus salarius) including two Salinivibrio species (designated DV and BNH throughout the manuscript) were isolated from dense microbial mats collected from the Eisfeld playa (Figure 1). Based on the spontaneous development of plaques when plating the BNH strain during routine culturing, we sought to investigate the presence of a prophage present in this isolate. Following lytic induction and washing to prepare the phage for TEM, the morphology was determined as a myovirus with a head-neck-contractile tail geometry [49] (Figure 2). The phage had a capsid diameter of approximately 56 nm, within the range of 30 to 60 nm reported for 65% of aquatic viruses [50], and a tail length of approximately 106 nm.
We assessed the sensitivity of the isolates mentioned above as well as the Vibrio/Salinivibrio species listed in Table S3 to Smhb1. Testing against the wider range of isolates from this site was done, as it has previously been demonstrated that some phages are capable of infecting across several bacteria phyla [51,52]. None of the isolates tested were found to be susceptible to Smhb1, including Salinivibrio DV.
To establish the phylogeny of the Salinivibrio isolates, to determine the features of the prophage in BNH, and possibly to explain why DV was resistant to Smhb1, the genomes of both Salinivibrio isolates were sequenced (Table S1). Analyzing the genomes using GTDB-Tk showed that they were two separate species (Salinivibrio kushneri BNH and Salinivibrio proteolyticus DV) belonging to phylogroup I and III, respectively, as defined by de la Haba [53]. Given the specificity of most phages for their cognate host, the inability of Smhb1 to infect DV might be expected; however, further analysis indicated another plausible reason for the inability of Smhb1 to infect the isolate DV (see Section 3.5). No other prophages were identified in the genomes of S. kushneri BNH and S. proteolyticus DV using PHASTER.

3.2. Basic Genome Characterization, Phylogeny and Prophage Integration

The genome of phage Smhb1 is 32,826 bp, within the average length for Peduovirus genomes (33776 bp ± 3800 bp), and has a GC content of 50.8%, close to that of its host (50.5%). Forty-nine putative open reading frames were predicted (Table S2), and no function could be assigned to twenty-three of these following BLASTp comparisons to genes of characterized phages. No introns or tRNAs were identified on the genome of phage Smhb1.
Tetranucleotide usage deviation analysis showed a Pearson correlation coefficient (PCC) of 0.77 between Smhb1 and the S. kushneri BNH genome and 0.75 between Smhb1 and S. proteolyticus DV. When using the TCS feature in JSpeciesWS, the highest correlation was to Salinivibrio sharmensis DSM 18,182 (PCC-0.776). Interestingly, many of the best hits were to Yersinia species; however, apart from phage L413C, Peduovirinae related phages that infect Yersinia sp. have only recently been deposited on the NCBI database (MT374855, MT374858, and MT374857). A search for prophages in some of these Yersinia genomes showed that each contained either a part of or a full Peduovirus prophage and, in some cases, multiple complete Peduovirinae phage genomes.
The phage was classified as part of the ICTVs efforts to name and classify the many new phage genomes discovered through next generation sequencing efforts. Smhb1 is currently the only member and, therefore, type species of the genus Playavirus, named for the geographic feature from which its host was isolated (https://tinyurl.com/saze2zth (accessed on 8 August 2021); 2020.117B.R.Peduoviruses).
Physical characterization of the Smhb1 genomic DNA consisted of digestion with restriction endonucleases (Figure S1) to establish the presence or absence of DNA modifications as a mechanism to avoid susceptibility to endonucleases encoded by BNH [54,55]. Such modifications usually involve the addition of a methyl or glycosyl group (Krüger & Bickle, 1983; Adams & Burdon, 1985). EcoRI (five sites), HindIII (five sites), HhaI (336 sites), and RsaI (61 sites) are insensitive to dam or dcm methylation and were able to digest the phage DNA.
MboI (71 sites) is sensitive to dam methylation, and the phage DNA remained uncut. While the related phages K139 and PV94 encode their own N6 adenine methylases [56], no equivalent enzyme could be identified on the Smhb1 genome. S. kushneri BNH does, however, encode a DNA (cytosine-5) methyltransferase (dcm) as well as a DNA adenine methylase (dam), which may explain why MboI digestion was blocked.
We further investigated the relation of Smhb1 to other Peduovirinae using VIRIDIC, which showed that, of the viruses on the NCBI virus database, Smhb1 was the most similar to the recently sequenced Vibrio alginolyticus prophage Valm-yong1 (MN56393) at the nucleotide level and sharing 26% identity over the length of their genomes. A prophage found in Salinivibrio siamensis KP-1, however, appears to be its closest relative at 56.3% identity.
ViPTree analysis and BLASTp was performed and showed that the majority of annotated proteins were similar to those of phages ValM-yong 1 (Vibrio alginolyticus), VD1 (Vibrio diazotrophicus), PV94 (Vibrio vulnificus), K139 (Vibrio cholerae), Kappa (Vibrio cholerae), 1.202.O._10N.222.45.E8, and VPUSM 8 (Vibrio cholerae) [57] (Figure S2). This was supported by the BLASTx analysis and alignment of these related genomes (Figure 3).
None of the Smhb1 encoded proteins shared any amino acid similarity to proteins encoded by the podovirus CW02, one of the three published Salinivibrio-infecting phages, which belongs to the T7-like supergroup [24]. The other two Salinivibrio-infecting phages that have been described are the myoviruses UTAK [23] and G3 [58]; however, the genomes are unavailable, and no comparisons can be made. UTAK is currently propagated on Vibrio hispanica in culture collections, while G3 displayed a remarkably wide host range [58,59] demonstrating that phages that are known to infect Salinivibrio species can exhibit a wide host range.
Smhb1 inserted into the S. kushneri BNH dusA gene (tRNA dihydrouridine synthase) involved in the post translational reduction of uridine, which serves as an integration site for prophages and genomic islands in over 200 bacteria [60,61]. The integrase encoded by Smhb1, therefore, belongs to the family of dusA-associated integrases. The only other Peduovirinae virus that encodes a similar integrase is Pseudoalteromonas phage C5a (73% identity), which adds to the repertoire of integrases encoded by the Peduovirinae [62].
Using the consensus attachment sequences reported for this family of integrases [61], we identified the attL and attR sites for Smhb1 consisting of imperfect direct repeats flanking the inserted phage with the attL sequence located inside the dusA gene encoded by S. kushneri BNH, while the second repeat constitutes the last 21 bp of a 30 amino acid fragment of the N-terminal of a non- BNH dusA gene (Figure 4A). Analysis of the integrated genome showed another conserved 12 bp direct repeat (CAGTCTCCCTAT) with one repeat 26 bps upstream of the integrase gene and the second downstream of the non-BNH 5′-dusA gene region mentioned above (Figure 4A).
These repeats lie roughly 180 bp apart on the phage genome as extracted from intact head particles and may have an undescribed role in phage integration. Investigation of the attR region showed that a small region between the crossover from the bacterial genome sequence and the start of Smhb1 genome appeared to harbor a 30 amino acid region of a dusA gene from a Salinivibrio strain other than DV or BNH. The arrangement of dusA fragments as depicted in Figure 4A is highly reminiscent of the arrangement seen by Farrugia and coworkers in Acinetobacter baumannii on the insertion of a genomic island [61].
The alignment of several complete dusA genes from Salinivibrio species indicated that the N-terminus can be grouped into two groups and that S. proteolyticus DV and S. kushneri BNH each fall into a different group with the dusA represented by the 30 amino acid stretch being in the second group (Figure 4B). This may be evidence to support that this phage has, in the past, infected a Salinivibrio species/strain other than S. proteolyticus DV or S. kushneri BNH (see CRISPR section below).
Immediately downstream of the dusA gene, we find the phage shock protein G (PspG) followed by a Fe3+-hydroxamate ABC substrate-binding protein. PspG is part of the phage shock response, a generalized membrane-related stress response system that is upregulated during phage infection [63,64], and the transporter is responsible for the uptake of hydroxamate siderophores. Iron uptake is one of the features identified as strongly downregulated when pspG is overexpressed [65].
The baseplate assembly proteins of P2-like phages incorporates iron ions, which served as examples when Bonnain, Breitbart, and Buck proposed their “Ferrojan hypothesis”, which was expanded on recently by Muratore and Weitz [66,67]. The predicted Smhb1 tail spike protein (gp49) does contain one H-T-H motif predicted to be the iron binding motif. In the Muratore and Weitz model, they considered the influence of iron availability on the ability of virus infection to change the host’s iron uptake strategies, and they concluded that viral infection and nutrient dynamics jointly shape the fate of microbial populations.
However, this was seen from a purely lytic perspective and more complex interactions might be observed as, in the case of Smhb1, where lysogenic conversion may affect iron uptake. S. kushneri BNH does not have genes associated with siderophore production but does encode a siderophore uptake protein and would, therefore, act as a “defector” host in the model [67]. The location of the pspG gene and siderophore uptake transporter relative to the integrated Smhb1 phage suggests that phage integration may lead to modulation of iron uptake through this ancillary aspect of the phage shock response and siderophore uptake protein.

3.3. Lysis/Lysogeny

Holin and endolysin-like ORFs were identified on the Smhb1 genome together with a lysogeny module. Nilsson and co-workers investigated the arrangement and evolution of P2-like phage lysogeny modules and found distinct P2-like and phage 186-like lysogeny modules [62]. The arrangement of genes within the lysogeny module of most P2 phages is thought to follow a similar pattern attL-integrase-C-cox/apl; however, Smhb1 shares a lysogeny module of the 186-type with the genes arranged as attL-integrase-cI-cox/apl-cII (Figure 3).
Apart from allowing the phage to escape host defenses, methylation, discussed earlier, may also be important for regulating the switch between lysis and lysogeny. Dalia and coworkers demonstrated that there are two undermethylated sites at the cI operator site located between the cI and cox genes in phage K139 and that binding of the cI repressor is likely responsible for undermethylation of these sites [68]. They further speculated that methylation of the site may not allow binding of cI, thereby, leading to lytic induction. We identified two canonical dam methylation sites in the region covering the cI gene and the intergenic space between cI and cox with one located 4 bp upstream of the translational start of cI and the other located 74 bp downstream of the translational start.
When compared with the NCBInr database, the Smhb1 endolysin, which contains a M15A peptidase motif, had higher similarity to endolysins from prophages in Photobacterium, Vibrio, Serpentinomonas, and Pseudomonas (>50% identity) and showed little homology to the proteins from K139, KP-1, PV94, and the Pasturella-infecting phage F108 with the closest Peduovirus encoded endolysin being that of Pseudoalteromonas phage C5a (32% identity). This likely demonstrates adaptation to a different cell wall structure of S. kushneri BNH.
The holin belongs to class I with three transmembrane domains and no dual start motif. Phage holins are known to display greater sequence diversity than endolysins [69], and the holin from Smhb1 is no exception. BLASTp comparison of the Smhb1 holin with homologs on the NCBI viral database showed that it was only found in Smhb1 with more distantly related homologs (<43% amino acid identity) in Vibrio phage vB_VchM_VP-3213, Vibrio phage LP.1, Oceanospirillum phage vB_OliS_GJ44, and Pseudomonas phage 14-1 among others.
Thus, the Smhb1 endolysin and holin are not conserved even among its closest relatives. One evolutionary requirement for holins is that they need to create a pore large enough to allow access of the cognate endolysin to the peptidoglycan layer in the cell wall [70]. It could be that the unique endolysin and holin of Smhb1 are co-evolved for effective lysis in S. kushneri BNH.

3.4. DNA Replication and Packaging

The model Peduovirinae phage, P2, replicates via a rolling circle mechanism following circularization of the genome through cohesive ends [71]. Replication is initiated by a phage encoded endonuclease (gpA) introducing a single stranded nick at the origin of replication (located within the gpA encoding ORF), which becomes covalently bound to the 5′ end of the nick site. The homologous protein in Smhb1 is encoded by gp15. Should replication in Smhb1 proceed as described for P2, we can expect the replication origin to be located within gp15.
Evidence that the origin of replication is located here is the presence of the conserved nick site (ori) sequence in gp15, which appears to be conserved among the Peduovirinae (Figure S3). Cumulative GC-skew analysis has been used to predict the origin and terminus of replication for several DNA species [72,73] and, in Smhb1, showed a local minimum (origin) at 18,101 bp and a maximum (terminus) at 2901 bp (Figure S4).
When assessing the cumulative GC-skew for the P2 phage, the tool predicts a local minimum at 29,401 bp, close to the experimentally determined origin (29,892 bp), suggesting an accurate prediction. Whether or not the local minimum in cumulative GC-skew identified for Smhb1 carries significance with respect to the role it might play in replication is yet to be determined.
The large and small subunit terminase genes are encoded by gp27 and gp30 and are responsible for the initiation of the packaging of viral DNA. The terminase large subunit is not only useful as a phylogenetic marker [74,75] but also as an indicator of the type of packaging mechanism employed by the phage [76,77]. This can be phage specific but generally follows one of a handful of models, and phages with similar terminase genes have been shown to package DNA in the same manner [76,77,78].
In P2, the phage genome replicates as a single copy through a rolling circle mechanism instead of replicating as concatenated genomes as with phages, such as lambda, and these single genomes serve as the substrate for packaging [79]. Comparison of the Smhb1 terminase to others suggests that the DNA packaging mechanism phage Smhb1 employs is similar to that of P2, 186 and related phages, being cos-dependent (Figure 5) [57,80].

3.5. Late Gene Expression and Virion Protein Features

In phage P2, the expression of late genes is controlled through autoregulation by the Zinc-finger containing protein Ogr (an ORF located between the integrase and late control D family gene) of its own promoter whereas, in phage 186, this role falls to cI [81,82,83]. In phage K139, the ogr homolog is located between the portal protein and replication endonuclease, which is also the case for Smhb1 (Figure 3) [56]. Once produced, Ogr acts as an inducer of late gene expression, and the location of the Ogr homolog in K139 and Smhb1 may suggest a different timing of late gene expression compared with the enterobacterial phages P2 and 186.
The genomic organization of the head and tail assembly modules of phage Smhb1 show a close relationship to phage K139 with 11 characterized genes showing significant homology (Table S2). The capsid of P2-like viruses is encoded by at least four genes [80]. In Smhb1, these are encoded by gp26 (P2 gpQ portal protein), gp28 (P2 gpO homolog), gp29 (P2 gpN homolog), and the gp30 (P2 gpL homolog). A BLASTp analysis of the gp29 protein identifies the Phage_cap_P2 domain conserved among Peduovirinae, including K139, HP1, and HP2, which have been shown to be highly conserved in similarity [56].
Kapfhammer describes the capsid of P2-like phages as a DNA container that requires little or no adaptation to different hosts, whereas the tail formation genes show greater divergence [56]. This is ignoring the fact that these viruses find themselves in a range of physicochemical environments and that all proteins making up the physical structure of the virus would be under selective pressure under these conditions.
A signature of halophilic protein adaptation is an increase in the use of Asp, Glu, Val, and Thr residues and a decrease in Lys, Ile, Met, Leu, and Cys as well as a reduction in the predicted pI value [84]. Analysis of the aligned concatenated moderate halophilic capsid, portal, head scaffolding, terminase large and small subunits, and sheath proteins compared against a non-redundant list of non-halophile Peduovirinae homologs did not show the same preference in amino acid usage or pI (Figures S5 and S6).
The moderately halophilic phage proteins appeared enriched for His, Trp, Lys, Met, and Asn. This could be due to Salinivibrio and Vibrio species not being extreme halophiles such as those analyzed by Paul et al. [84]. We did note substantially increased Ala and Arg content of Burkholderia infecting Peduovirinae phages. No other discernable patterns related to amino acid composition were identified (enriched for hydrophobic residues, solvation potential, etc.).

3.6. Smhb1 Resistance in S. proteolyticus DV

As mentioned earlier, the phage Smhb1 was unable to infect S. proteolyticus DV. One possible defense mechanism is the presence of CRISPR spacer regions targeted against the phage [85,86]. In microbial hosts, CRISPR loci usually contain a combination of CRISPR-associated (cas) genes and non-coding RNA elements, which are responsible for the target specificity of CRISPR-mediated nucleic acid cleavage [87,88]. Seven CRISPR regions were identified in S. proteolyticus DV and three regions in S. kushneri BNH (Table S4), including the largest CRISPR array found among the Vibrionaceae to date at 179 spacers [89].
BLASTn analysis of all the spacers identified in both bacteria against the phage Smhb1 genome showed that seven spacers from S. proteolyticus DV were perfect matches to the genome. The spacers target several genes involved in phage replication, packaging, and virion morphogenesis (tail tube and capsid), which should ensure that no functional progeny can be reproduced in vivo (Table S5).
As taxonomic classification of S. kushneri BNH and S. proteolyticus DV indicated that these are two distinct species, and this presents two scenarios for the presence of spacers targeting Smhb1 in S. proteolyticus DV [53]. According to McDonald et al. [89], many CRISPR arrays found in the Vibrionaceae are acquired through horizontal transfer and are found inside or on mobile elements (transposons, plasmids, and genomic islands). Thus, either the spacer regions targeting Smhb1 were inherited with the CRISPR array or Smhb1 can infect more than one species of Salinivibrio.

3.7. Accessory Genes

The K139 encoded G protein-like ORF, or Glo protein, is a secreted virulence factor of Vibrio cholerae [90]. gp4 on Smhb1 showed low but detectable homology (20% identity, 44% similarity) to the Glo protein from phages K139, VcP032, and VD1. The KP-1 prophage, PV94, and phage F108 have no such homologs. Although this could suggest that Salinivibrio species may act as reservoirs for phages harboring these virulence factors, the absence of a canonical CAAX motif at the C-terminal as was observed for the protein from φO18P. Apart from its role in virulence, the Glo protein was also shown to play a role in phage exclusion in K139, and gp4 may perform a similar function in Smhb1 [91].

4. Conclusions

We described phage Smhb1, a novel member of the family Peduovirinae. Despite being isolated from a unique habitat and having a unique nucleotide sequence, the conservation of amino acid sequences and P2-like modular layout of its genome demonstrates that the selective pressure to maintain P2-like features must be strong and present in the Eisfeld playa. The host range appears to be limited to Salinivibrio species; however, taken together, the data presented suggests that Smhb1-type phages could display a wide host range. Smhb1 serves to extend the adaptability window of the P2 phage model.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/microorganisms9102043/s1. Figure S1: Agarose gel electrophoresis of digested phage DNA. Lane one phage Lambda DNA cut with PstI used as a molecular marker, Figure S2: ViPTree analysis of Smhb1 encoded proteins compared with those of other Peduovirinae phages present on the Virus-Host DB: RefSeq release 93. The branch that Smhb1 (NC_047775.1) is on is highlighted in red, Figure S3: Alignment of origin of replication (ori) sequences from Smhb1 and related Peduoviruses. Only differences from the reference (Smhb1) are shown, Figure S4: GC skew analysis of the genome of phage Smhb1 and P2 to predict the putative replication origin (ori) and termination sites (ter) calculated using a window size of 1000 bp and a step size of 100 bp, Figure S5: Amino acid composition profiles comparing moderately halophilic Peduovirinae proteins to non-halophilic Peduovirinae encoded proteins ordered by observed difference, Figure S6: Predicted protein isoelectric point (pI) of selected Peduovirinae encoded proteins ranked from highest to lowest. Smhb1 predicted protein pI indicated in red and those of Vibrio infecting phages in green, Table S1: Summary of the sequence analysis report for the assembly of phage Smhb1, Table S2: CRISPRs and number of spacers identified in the genomes of Salinivibrio species DV and BNH using CRISPRFinder, Table S3: A summary of the BLASTx analysis of the ORFs of phage Smhb1. The + or – sign before the ORF number indicates on which strand the gene is found, Table S4: Number and sequence of CRISPR repeat regions identified in BNH and DV, Table S5: Sequence and genomic location of CRISPR spacers targeted against various ORFs on Smhb1 identified in DV.

Author Contributions

Conceptualization, I.O., L.J.v.Z. and M.T.; I.O. isolated bacteria and Smhb1 phage from playa biomass; I.O. performed DNA extraction and host-range experiments; I.O. performed TEM analyses; L.J.v.Z. performed genome sequencing and bioinformatic analyses; writing-original draft preparation, I.O. and L.J.v.Z.; writing-review and editing, I.O., L.J.v.Z. and M.T.; supervision, L.J.v.Z. and M.T.; funding acquisition, M.T. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Research Foundation (NRF) of South Africa.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets presented in this study can be found in online repositories. The genomes have been submitted to NCBI and can be found under the GenBank accession numbers MEBP00000000, MEBQ00000000 and NC_047775.

Acknowledgments

We wish to thank the researcher and management of the Gobabeb Desert research station for hosting us during sample collection. We also thank Mohammed Jaffer at the Electron Microscope Unit at the University of Cape Town for helping to capture TEM images.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Danovaro, R.; Serresi, M. Viral density and virus-to-bacterium ratio in deep-sea sediments of the Eastern Mediterranean. Appl. Environ. Microbiol. 2000, 66, 1857–1861. [Google Scholar] [CrossRef] [Green Version]
  2. Hewson, I.; O’Neil, J.M.; Fuhrman, J.A.; Dennison, W.C. Virus-like particle distribution and abundance in sediments and overlying waters along eutrophication gradients in two subtropical estuaries. Limnol. Oceanogr. 2001, 46, 1734–1746. [Google Scholar] [CrossRef] [Green Version]
  3. Bergh, O.; Børsheim, K.Y.; Bratbak, G.; Heldal, M. High abundance of viruses found in aquatic environments. Nature 1989, 340, 467–468. [Google Scholar] [CrossRef]
  4. Bogovazova, G.G.; Voroshilova, N.N.; Bondarenko, V.M. The efficacy of Klebsiella pneumoniae bacteriophage in the therapy of experimental Klebsiella infection. Zhurnal Mikrobiol. Epidemiol. Immunobiol. 1991, 4, 5–8. [Google Scholar]
  5. Hamilton, G. Phage and the Origins of Molecular Biology; Cairns, J., Stent, G.S., Watson, J.D., Eds.; Cold Spring Harbor Laboratory Press: New York, NY, USA, 1992; p. 366. [Google Scholar] [CrossRef]
  6. Fuhrman, J.A. Marine viruses and their biogeochemical and ecological effects. Nature 1999, 399, 541–548. [Google Scholar] [CrossRef] [PubMed]
  7. Clokie, M.R.; Millard, A.D.; Letarov, A.V.; Heaphy, S. Phages in nature. Bacteriophage 2011, 1, 31–45. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Ghannad, M.S.; Mohammadi, A. Bacteriophage: Time to re-evaluate the potential of phage therapy as a promising agent to control multidrug-resistant bacteria. Iran. J. Basic Med. Sci. 2012, 15, 693–701. [Google Scholar]
  9. Wilhelm, S.W.; Suttle, C.A. Viruses and nutrient cycles in the sea. BioScience 1999, 49, 781. [Google Scholar] [CrossRef] [Green Version]
  10. Paul, J.H. Microbial gene transfer: An ecological perspective. J. Mol. Microbiol. Biotechnol. 1999, 1, 45–50. [Google Scholar]
  11. Brum, J.; Steward, G.; Jiang, S.; Jellison, R. Spatial and temporal variability of prokaryotes, viruses, and viral infections of prokaryotes in an alkaline, hypersaline lake. Aquat. Microb. Ecol. 2005, 41, 247–260. [Google Scholar] [CrossRef] [Green Version]
  12. Peduzzi, P.; Gruber, M.; Gruber, M.; Schagerl, M. The virus’s tooth: Cyanophages affect an African flamingo population in a bottom-up cascade. ISME J. 2014, 8, 1346–1351. [Google Scholar] [CrossRef] [Green Version]
  13. Vareschi, E.; Jacobs, J. The ecology of Lake Nakuru. Oecologia 1985, 65, 412–424. [Google Scholar] [CrossRef] [PubMed]
  14. Krienitz, L.; Kotut, K. Fluctuating algal food populations and the occurrence of lesser flamingos (Phoeniconaias minor) in three Kenyan rift valley lakes. J. Phycol. 2010, 46, 1088–1096. [Google Scholar] [CrossRef]
  15. Day, J.A.; Seely, M.K. Physical and chemical conditions in an hypersaline spring in the Namib Desert. Hydrobiologia 1988, 160, 141–153. [Google Scholar] [CrossRef]
  16. Day, J.A. The major ion chemistry of some southern African saline systems. Hydrobiologia 1993, 267, 37–59. [Google Scholar] [CrossRef]
  17. Eckardt, F.D.; Drake, N.; Goudie, A.S.; White, K.; Viles, H. The role of playas in pedogenic gypsum crust formation in the Central Namib Desert: A theoretical model. Earth Surf. Process. Landf. 2001, 26, 1177–1193. [Google Scholar] [CrossRef]
  18. Eckardt, F.D.; Drake, N. Introducing the Namib Desert Playas. In Sabkha Ecosystems; Öztürk, M., Böer, B., Barth, H.J., Clüsener-Godt, M., Khan, M., Breckle, S.W., Eds.; Tasks for Vegetation Science; Springer: Dordrecht, The Netherlands, 2010; Volume 46, pp. 19–25. [Google Scholar]
  19. Adriaenssens, E.; van Zyl, L.; Cowan, D.; Trindade, M. Metaviromics of Namib Desert salt pans: A novel lineage of haloarchaeal salterproviruses and a rich source of ssDNA viruses. Viruses 2016, 8, 14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Swan, B.K.; Ehrhardt, C.J.; Reifel, K.M.; Moreno, L.I.; Valentine, D.L. Archaeal and bacterial communities respond differently to environmental gradients in anoxic sediments of a California hypersaline lake, the Salton Sea. Appl. Environ. Microbiol. 2010, 76, 757–768. [Google Scholar] [CrossRef] [Green Version]
  21. Santos, F.; Yarza, P.; Parro, V.; Briones, C.; Antón, J. The metavirome of a hypersaline environment. Environ. Microbiol. 2010, 12, 2965–2976. [Google Scholar] [CrossRef] [PubMed]
  22. Boujelben, I.; Yarza, P.; Almansa, C.; Villamor, J.; Maalej, S.; Antón, J.; Santos, F. Virioplankton community structure in Tunisian solar salterns. Appl. Environ. Microbiol. 2012, 78, 7429–7437. [Google Scholar] [CrossRef] [Green Version]
  23. Goel, U.; Kauri, T.; Kushner, D.J.; Ackermann, H.-W. A moderately halophilic Vibrio from a Spanish saltern and its lytic bacteriophage. Can. J. Microbiol. 1996, 42, 1015–1023. [Google Scholar] [CrossRef]
  24. Shen, P.S.; Domek, M.J.; Sanz-Garcia, E.; Makaju, A.; Taylor, R.M.; Hoggan, R.; Culumber, M.D.; Oberg, C.J.; Breakwell, D.P.; Prince, J.T.; et al. Sequence and structural characterization of great Salt Lake bacteriophage CW02, a member of the T7-Like supergroup. J. Virol. 2012, 86, 7907–7917. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Adriaenssens, E.M.; Sullivan, M.B.; Knezevic, P.; van Zyl, L.J.; Sarkar, B.L.; Dutilh, B.E.; Alfenas-Zerbini, P.; Łobocka, M.; Tong, Y.; Brister, J.R.; et al. Taxonomy of prokaryotic viruses: 2018–2019 update from the ICTV Bacterial and Archaeal Viruses Subcommittee. Arch. Virol. 2020, 165, 1253–1260. [Google Scholar] [CrossRef] [Green Version]
  26. Farrelly, V.; Rainey, F.A.; Stackebrandt, E. Effect of genome size and rrn gene copy number on PCR amplification of 16S rRNA genes from a mixture of bacterial species. Appl. Environ. Microbiol. 1995, 61, 2798–2801. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Reysenbach, A.; Pace, N. Reliable amplification of hyperthermophilic archaeal 16S rRNA genes by the polymerase chain reaction. In Archaea: A Laboratory Manual; Robb, F., Place, A., Eds.; Cold Spring Harbor Laboratory Press: New York, NY, USA, 1995; pp. 101–107. [Google Scholar]
  28. Ackermann, H.W. Bacteriophages. In Bacteriophages: Methods and Protocols; Clokie, M.R.J., Kropinski, A.M., Eds.; Humana Press: New York, NY, USA, 2009; pp. 113–126. [Google Scholar]
  29. Sambrook, J.; Fritsch, E.F.; Maniatis, T. Molecular cloning: A Laboratory Manual; Cold Spring Harbor Laboratory Press: New York, NY, USA, 1989; p. 626. [Google Scholar]
  30. Li, W.; O’Neill, K.R.; Haft, D.H.; DiCuccio, M.; Chetvernin, V.; Badretdin, A.; Coulouris, G.; Chitsaz, F.; Derbyshire, M.K.; Durkin, A.S.; et al. RefSeq: Expanding the Prokaryotic Genome Annotation Pipeline reach with protein family model curation. Nucleic Acids Res. 2021, 48, D1020–D1028. [Google Scholar] [CrossRef]
  31. Richter, M.; Rosselló-Móra, R.; Glöckner, F.O.; Peplies, J. JSpeciesWS: A web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 2016, 32, 929–931. [Google Scholar] [CrossRef] [PubMed]
  32. Arkin, A.; Cottingham, R.; Henry, C.; Harris, N.L.; Stevens, R.L.; Maslov, S.; Dehal, P.; Ware, D.; Perez, F.; Canon, S.; et al. KBase: The United States Department of Energy Systems Biology Knowledgebase. Nat. Biotechnol. 2018, 36, 566–569. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Chaumeil, P.-A.; Mussig, A.J.; Hugenholtz, P.; Parks, D.H. GTDB-Tk: A toolkit to classify genomes with the Genome Taxonomy Database. Bioinformatics 2020, 36, 1925–1927. [Google Scholar] [CrossRef]
  34. Grissa, I.; Vergnaud, G.; Pourcel, C. CRISPRFinder: A web tool to identify clustered regularly interspaced short palindromic repeats. Nucleic Acids Res. 2007, 35, W52–W57. [Google Scholar] [CrossRef] [Green Version]
  35. Arndt, D.; Grant, J.R.; Marcu, A.; Sajed, T.; Pon, A.; Liang, Y.; Wishart, D.S. PHASTER: A better, faster version of the PHAST phage search tool. Nucleic Acids Res. 2016, 44, W16–W21. [Google Scholar] [CrossRef] [Green Version]
  36. Moraru, C.; Varsani, A.; Kropinski, A.M. VIRIDIC—A novel tool to calculate the intergenomic similarities of prokaryote-infecting viruses. Viruses 2020, 12, 1268. [Google Scholar] [CrossRef]
  37. Sullivan, M.J.; Petty, N.K.; Beatson, S.A. Easyfig: A genome comparison visualizer. Bioinformatics 2011, 27, 1009–1010. [Google Scholar] [CrossRef]
  38. Nishimura, Y.; Yoshida, T.; Kuronishi, M.; Uehara, H.; Ogata, H.; Goto, S. ViPTree: The viral proteomic tree server. Bioinformatics 2017, 33, 2379–2380. [Google Scholar] [CrossRef] [PubMed]
  39. Betley, J.N.; Frith, M.C.; Graber, J.H.; Choo, S.; Deshler, J.O. A ubiquitous and conserved signal for RNA localization in chordates. Curr. Biol. 2002, 12, 1756–1761. [Google Scholar] [CrossRef] [Green Version]
  40. Laslett, D.; Canback, B. ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res. 2004, 32, 11–16. [Google Scholar] [CrossRef]
  41. Lowe, T.M.; Eddy, S.R. tRNAscan-SE: A program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 1997, 25, 955–964. [Google Scholar] [CrossRef]
  42. Schattner, P.; Brooks, A.N.; Lowe, T.M. The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res. 2005, 33, W686–W689. [Google Scholar] [CrossRef]
  43. Gautheret, D.; Lambert, A. Direct RNA motif definition and identification from multiple sequence alignments using secondary structure profiles. J. Mol. Biol. 2001, 313, 1003–1011. [Google Scholar] [CrossRef] [PubMed]
  44. Krogh, A.; Larsson, B.; von Heijne, G.; Sonnhammer, E.L.L. Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes. J. Mol. Biol. 2001, 305, 567–580. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Tamura, K.; Stecher, G.; Peterson, D.; Filipski, A.; Kumar, S. MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol. 2013, 30, 2725–2729. [Google Scholar] [CrossRef] [Green Version]
  46. Saitou, N.; Nei, M. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 1987, 4, 406–425. [Google Scholar]
  47. Fu, L.; Niu, B.; Zhu, Z.; Wu, S.; Li, W. CD-HIT: Accelerated for clustering the next generation sequencing data. Bioinformatics 2012, 28, 3150–3152. [Google Scholar] [CrossRef] [PubMed]
  48. Vacic, V.; Uversky, V.N.; Dunker, A.K.; Lonardi, S. Composition Profiler: A tool for discovery and visualization of amino acid composition differences. BMC Bioinform. 2007, 8, 211. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Ackermann, H.W. 5500 Phages examined in the electron microscope. Arch. Virol. 2007, 152, 227–243. [Google Scholar] [CrossRef] [PubMed]
  50. Wommack, K.E.; Colwell, R.R. Virioplankton: Viruses in aquatic ecosystems. MMBR 2000, 64, 69–114. [Google Scholar] [CrossRef] [Green Version]
  51. Malki, K.; Kula, A.; Bruder, K.; Sible, E.; Hatzopoulos, T.; Steidel, S.; Watkins, S.C.; Putonti, C. Bacteriophages isolated from Lake Michigan demonstrate broad host-range across several bacterial phyla. Virol. J. 2015, 12, 164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Zhang, X.; Wang, R.; Xie, X.; Hu, Y.; Wang, J.; Sun, Q.; Feng, X.; Tong, S.; Cui, Y.; Wang, M.; et al. Mining bacterial NGS data vastly expands the complete genomes of temperate phages. bioRxiv 2021. [Google Scholar] [CrossRef]
  53. de la Haba, R.R.; López-Hermoso, C.; Sánchez-Porro, C.; Konstantinidis, K.T.; Ventosa, A. Comparative Genomics and Phylogenomic Analysis of the Genus Salinivibrio. Front. Microbiol. 2019, 10, 2104. [Google Scholar] [CrossRef] [Green Version]
  54. Samson, J.E.; Magadán, A.H.; Sabri, M.; Moineau, S. Revenge of the phages: Defeating bacterial defences. Nat. Rev. Microbiol. 2013, 11, 675–687. [Google Scholar] [CrossRef]
  55. Vasu, K.; Nagaraja, V. Diverse functions of restriction-modification systems in addition to cellular defense. MMBR 2013, 77, 53–72. [Google Scholar] [CrossRef] [Green Version]
  56. Kapfhammer, D.; Blass, J.; Evers, S.; Reidl, J. Vibrio cholerae phage K139: Complete genome sequence and comparative genomics of related phages. J. Bacteriol. 2002, 184, 6592–6601. [Google Scholar] [CrossRef] [Green Version]
  57. Pryshliak, M.; Hammerl, J.A.; Reetz, J.; Strauch, E.; Hertwig, S. Vibrio vulnificus phage PV94 is closely related to temperate phages of V. cholerae and other Vibrio species. PLoS ONE 2017, 9, e94707. [Google Scholar] [CrossRef] [PubMed]
  58. Kauri, T.; Ackermann, H.W.; Goel, U.; Kushner, D.J. A bacteriophage of a moderately halophilic bacterium. Arch. Microbiol. 1991, 156, 435–438. [Google Scholar] [CrossRef]
  59. Ventosa, A.; Nieto, J.J.; Oren, A. Biology of moderately halophilic aerobic bacteria. Microbiol. Mol. Biol. Rev. 1998, 62, 504–544. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Kasprzak, J.M.; Czerwoniec, A.; Bujnicki, J.M. Molecular evolution of dihydrouridine synthases. BMC Bioinform. 2012, 13, 153. [Google Scholar] [CrossRef] [Green Version]
  61. Farrugia, D.N.; Elbourne, L.D.H.; Mabbutt, B.C.; Paulsen, I.T. A novel family of integrases associated with prophages and genomic islands integrated within the tRNA-dihydrouridine synthase A (dusA) gene. Nucleic Acids Res. 2015, 43, 4547–4557. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Nilsson, H.; Cardoso-Palacios, C.; Haggård-Ljungquist, E.; Nilsson, A.S. Phylogenetic structure and evolution of regulatory genes and integrases of P2-like phages. Bacteriophage 2011, 1, 207–218. [Google Scholar] [CrossRef] [Green Version]
  63. Lloyd, L.J.; Jones, S.E.; Jovanovic, G.; Gyaneshwar, P.; Rolfe, M.D.; Thompson, A.; Hinton, J.C.; Buck, M. Identification of a new member of the phage shock protein response in Escherichia coli, the phage shock protein G (PspG). J. Biol. Chem. 2004, 279, 55707–55714. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Flores-Kim, J.; Darwin, A.J. The Phage Shock Protein Response. Ann. Rev. Microbiol. 2016, 70, 83–101. [Google Scholar] [CrossRef] [PubMed]
  65. Jovanovic, G.; Lloyd, L.J.; Stumpf, M.P.H.; Mayhew, A.J.; Buck, M. Induction and function of the phage shock protein extracytoplasmic stress response in Escherichia coli. J. Biol. Chem. 2006, 281, 21147–21161. [Google Scholar] [CrossRef] [Green Version]
  66. Bonnain, C.; Breitbart, M.; Buck, K.M. The ferrojan horse hypothesis: Iron-Virus Interactions in the Ocean. Front. Mar. Sci. 2016, 3, 82. [Google Scholar]
  67. Muratore, D.; Weitz, J.S. Infect while the iron is scarce: Nutrient-explicit phage-bacteria games. Theor. Ecol. 2021. [Google Scholar] [CrossRef]
  68. Dalia, A.B.; Lazinski, D.W.; Camilli, A. Characterization of undermethylated sites in Vibrio cholerae. J. Bacteriol. 2013, 195, 2389–2399. [Google Scholar] [CrossRef] [Green Version]
  69. Young, R. Bacteriophage holins: Deadly diversity. J. Mol. Microbiol. Biotechnol. 2002, 4, 21–36. [Google Scholar] [PubMed]
  70. Catalão, M.J.; Gil, F.; Moniz-Pereira, J.; São-José, C.; Pimentel, M. Diversity in bacterial lysis systems: Bacteriophages show the way. FEMS Microbiol. Rev. 2013, 37, 554–571. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Weigel, C.; Seitz, H. Bacteriophage replication modules. FEMS Microbiol. Rev. 2006, 30, 321–381. [Google Scholar] [CrossRef]
  72. Grigoriev, A. Analyzing genomes with cumulative skew diagrams. Nucleic Acids Res. 1998, 26, 2286–2290. [Google Scholar] [CrossRef] [Green Version]
  73. Lu, J.; Salzberg, S.L. SkewIT: The Skew Index Test for large-scale GC Skew analysis of bacterial genomes. PLoS Comput. Biol. 2020, 16, e1008439. [Google Scholar] [CrossRef]
  74. Liu, R.; Zhang, P.; Pu, X.; Xing, X.; Chen, J.; Deng, X. Analysis of a prophage gene frequency revealed population variation of ‘Candidatus Liberibacter asiaticus’ from two citrus-growing provinces in China. Plant Dis. 2010, 95, 431–435. [Google Scholar] [CrossRef]
  75. Shan, J.; Patel, K.V.; Hickenbotham, P.T.; Nale, J.Y.; Hargreaves, K.R.; Clokie, M.R.J. Prophage carriage and diversity within clinically relevant strains of Clostridium difficile. Appl. Environ. Microbiol. 2012, 78, 6027–6034. [Google Scholar] [CrossRef] [Green Version]
  76. Black, L.W. DNA packaging and cutting by phage terminases: Control in phage T4 by a synaptic mechanism. BioEssays 1995, 17, 1025–1030. [Google Scholar] [CrossRef]
  77. Feiss, M.; Catalano, C.E. Bacteriophage Lambda terminase and the mechanism of viral DNA packaging. In Viral Genome Packaging Machines: Genetics, Structure, and Mechanism; Molecular Biology Intelligence Unit; Springer: Boston, MA, USA, 2005. [Google Scholar] [CrossRef]
  78. Hsiao, C.L.; Black, L.W. Head morphogenesis of bacteriophage T4 III. The role of gene 20 in DNA packaging. Virology 1978, 91, 26–38. [Google Scholar] [CrossRef]
  79. Taylor, K.; Węgrzyn, G. Replication of coliphage lambda DNA. FEMS Microbiol. Rev. 1995, 17, 109–119. [Google Scholar] [CrossRef]
  80. Linderoth, N.A.; Ziermann, R.; Haggård-Ljungquist, E.; Christie, G.E.; Calendar, R. Nucleotide sequence of the DNA packaging and capsid synthesis genes of bacteriophage P2. Nucleic Acids Res. 1991, 19, 7207–7214. [Google Scholar] [CrossRef] [PubMed]
  81. Dibbens, J.A.; Gregory, S.L.; Egan, J.B. Control of gene expression in the temperate coliphage 186. X. The cI repressor directly represses transcription of the late control gene B. Mol. Microbiol. 1992, 6, 2643–2650. [Google Scholar] [CrossRef] [PubMed]
  82. Portelli, R.; Dodd, A.B.; Xue, Q.; Egan, J.B. The late-expressed region of the temperate coliphage 186 genome. Virology 1998, 248, 117–130. [Google Scholar] [CrossRef]
  83. Christie, G.E.; Calendar, R. Bacteriophage P2. Bacteriophage 2016, 6, e1145782. [Google Scholar] [CrossRef] [Green Version]
  84. Paul, S.; Bag, S.K.; Das, S.; Harvill, E.T.; Dutta, C. Molecular signature of hypersaline adaptation: Insights from genome and proteome composition of halophilic prokaryotes. Genome Biol. 2008, 9, R70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Sorek, R.; Kunin, V.; Hugenholtz, P. CRISPR—A widespread system that provides acquired resistance against phages in bacteria and archaea. Nat. Rev. Microbiol. 2008, 6, 181–186. [Google Scholar] [CrossRef] [PubMed]
  86. Bondy-Denomy, J.; Pawluk, A.; Maxwell, K.; Davidson, A.R. Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system. Nature 2013, 493, 429–432. [Google Scholar] [CrossRef] [Green Version]
  87. Bikard, D.; Marraffini, L.A. Control of gene expression by CRISPR-Cas systems. F1000Prime Rep. 2013, 5, 47. [Google Scholar] [CrossRef]
  88. Rath, D.; Amlinger, L.; Rath, A.; Lundgren, M. The CRISPR-Cas immune system: Biology, mechanisms and applications. Biochimie 2015, 117, 119–128. [Google Scholar] [CrossRef] [PubMed]
  89. McDonald, N.D.; Regmi, A.; Morreale, D.P.; Borowski, J.D.; Boyd, E.F. CRISPR-Cas systems are present predominantly on mobile genetic elements in Vibrio species. BMC Genom. 2019, 20, 105. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Reidl, J.; Mekalanos, J.J. Characterization of Vibrio cholerae bacteriophage K139 and use of a novel mini-transposon to identify a phage-encoded virulence factor. Mol. Microbiol. 1995, 18, 685–701. [Google Scholar] [CrossRef] [PubMed]
  91. Nesper, J.; Blaß, J.; Fountoulakis, M.; Reidl, J. Characterization of the major control region of Vibrio cholerae bacteriophage K139: Immunity, exclusion, and integration. J. Bacteriol. 1999, 181, 2902–2913. [Google Scholar] [CrossRef] [Green Version]
Microorganisms 09 02043 g001 550
Figure 1. Microbial mat sample from the Eisfeld site.
Figure 1. Microbial mat sample from the Eisfeld site.
Microorganisms 09 02043 g001
Microorganisms 09 02043 g002 550
Figure 2. Electron micrographs of phage Smhb1. (A) Intact viral particles. (B) Phage with contracted tail and that has presumably ejected the genome. (C) Several phage particles bound to cell debris. Images in (A) and (B) are at 50,000× magnification, and the scale bar represents 50 nm.
Figure 2. Electron micrographs of phage Smhb1. (A) Intact viral particles. (B) Phage with contracted tail and that has presumably ejected the genome. (C) Several phage particles bound to cell debris. Images in (A) and (B) are at 50,000× magnification, and the scale bar represents 50 nm.
Microorganisms 09 02043 g002
Microorganisms 09 02043 g003 550
Figure 3. Genome organization and tBLASTx comparison of Smhb1 with its closest relatives.
Figure 3. Genome organization and tBLASTx comparison of Smhb1 with its closest relatives.
Microorganisms 09 02043 g003
Microorganisms 09 02043 g004 550
Figure 4. (A) Graphical representation of the integration site of the phage Smhb1 within the genome of the host, BNH. (B) Alignment of the N-terminal 32 amino acids of selected Salinivibrio DusA proteins showing the differences in the amino acid composition. Differences from the reference sequence (BNH top) are highlighted.
Figure 4. (A) Graphical representation of the integration site of the phage Smhb1 within the genome of the host, BNH. (B) Alignment of the N-terminal 32 amino acids of selected Salinivibrio DusA proteins showing the differences in the amino acid composition. Differences from the reference sequence (BNH top) are highlighted.
Microorganisms 09 02043 g004
Microorganisms 09 02043 g005 550
Figure 5. Phylogenetic tree comparing Smhb1 terminase large subunit to phage terminases for which the packaging mechanism is known. The evolutionary history was inferred using the Maximum Likelihood method based on the JTT matrix-based model. There was a total of 160 positions in the final dataset. The accession numbers for the top phage terminase hits are listed in supplementary data. The red star denotes the position of Smhb1 large terminase subunit in the tree.
Figure 5. Phylogenetic tree comparing Smhb1 terminase large subunit to phage terminases for which the packaging mechanism is known. The evolutionary history was inferred using the Maximum Likelihood method based on the JTT matrix-based model. There was a total of 160 positions in the final dataset. The accession numbers for the top phage terminase hits are listed in supplementary data. The red star denotes the position of Smhb1 large terminase subunit in the tree.
Microorganisms 09 02043 g005
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Olonade, I.; van Zyl, L.J.; Trindade, M. Genomic Characterization of a Prophage, Smhb1, That Infects Salinivibrio kushneri BNH Isolated from a Namib Desert Saline Spring. Microorganisms 2021, 9, 2043. https://doi.org/10.3390/microorganisms9102043

AMA Style

Olonade I, van Zyl LJ, Trindade M. Genomic Characterization of a Prophage, Smhb1, That Infects Salinivibrio kushneri BNH Isolated from a Namib Desert Saline Spring. Microorganisms. 2021; 9(10):2043. https://doi.org/10.3390/microorganisms9102043

Chicago/Turabian Style

Olonade, Israel, Leonardo Joaquim van Zyl, and Marla Trindade. 2021. "Genomic Characterization of a Prophage, Smhb1, That Infects Salinivibrio kushneri BNH Isolated from a Namib Desert Saline Spring" Microorganisms 9, no. 10: 2043. https://doi.org/10.3390/microorganisms9102043

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop