Special Issue "Phage Ecology"

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Bacterial Viruses".

Deadline for manuscript submissions: 30 June 2020.

Special Issue Editor

Prof. Stephen T. Abedon
E-Mail Website1 Website2
Guest Editor
Department of Microbiology, The Ohio State University, Mansfield, OH 44906, USA
Interests: bacteriophage; phage ecology; phage therapy; phage therapy pharmacology; phage history
Special Issues and Collections in MDPI journals

Special Issue Information

Dear Colleagues,

Ecology is the study of the interactions of organisms with their environments. This can be with environmental abiotic (non-living) components, environmental biotic (living) components, or in terms of organism distribution over space and time. We can describe these various interactions in terms of organismal ecology, physiological ecology, evolutionary ecology, behavioral ecology, population ecology, community ecology, ecosystem ecology, landscape ecology, mathematical ecology, and biogeography. Bacteriophages (phages) are the viruses of bacteria. Along with the conceptually related viruses of domain Archaea (archaeal viruses), phages generally make a living by finding and then infecting either individual cells or instead clumps of cells, the latter as making up cellular arrangements, microcolonies, and/or biofilms. Our interest is in the ecology, variously considered, of such viruses.

I have been studying phage ecology for ~30 years, with over 100 publications, most of which touch on this subject. My specific interests have been on phage adaptations and tradeoffs, the ecology of phage interactions with biofilms, and the ecology of phage use as antibacterial agents, otherwise described as phage-therapy pharmacology. I have authored, edited, or co-edited roughly 10 monographs or edited volumes including The Bacteriophages 2/e (Oxford University Press, 2006), Bacteriophage Ecology (Cambridge University Press, 2008), The ‘Nuts and Bolts’ of Phage Therapy (Current Pharmaceutical Biotechnology, 2010), Bacteriophages and Biofilms (Nova Science Publishers, 2011), and Viruses of Microorganisms (Caister, 2018). In addition, I founded in 1996 and continue to maintain phage.org, i.e., the Bacteriophage Ecology Group. See also abedon.phage.org as well as facebook.com/Bacteriophage-Ecology-Group-111721928901953/.

In this Special Issue we are inviting submissions on all aspects of phage ecology, from the basic to the applied, from the study of individual viruses to the viromics of environments, and everything in between. Each submission will be given a quick read and editing by myself, consisting of a pre-peer review, prior to submission for actual peer review. We look forward in these submissions to experiencing your passion and enthusiasm for the subject of phage ecology.

Prof. Stephen T. Abedon
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All papers will be peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Viruses is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2000 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • phages
  • bacteriophages
  • archaeal viruses
  • growth parameters
  • modeling
  • adaptation
  • population dynamics
  • predator-prey dynamics
  • antagonistic coevolution
  • transduction
  • trophic interactions
  • biogeochemistry
  • carbon cycle
  • productivity
  • viromics
  • metagenomics
  • microbiomes
  • environmental microbiology
  • biogeography
  • distribution

Published Papers (4 papers)

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Research

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Open AccessArticle
Promises and Pitfalls of In Vivo Evolution to Improve Phage Therapy
Viruses 2019, 11(12), 1083; https://doi.org/10.3390/v11121083 - 21 Nov 2019
Abstract
Phage therapy is the use of bacterial viruses (phages) to treat bacterial infections, a medical intervention long abandoned in the West but now experiencing a revival. Currently, therapeutic phages are often chosen based on limited criteria, sometimes merely an ability to plate on [...] Read more.
Phage therapy is the use of bacterial viruses (phages) to treat bacterial infections, a medical intervention long abandoned in the West but now experiencing a revival. Currently, therapeutic phages are often chosen based on limited criteria, sometimes merely an ability to plate on the pathogenic bacterium. Better treatment might result from an informed choice of phages. Here we consider whether phages used to treat the bacterial infection in a patient may specifically evolve to improve treatment on that patient or benefit subsequent patients. With mathematical and computational models, we explore in vivo evolution for four phage properties expected to influence therapeutic success: generalized phage growth, phage decay rate, excreted enzymes to degrade protective bacterial layers, and growth on resistant bacteria. Within-host phage evolution is strongly aligned with treatment success for phage decay rate but only partially aligned for phage growth rate and growth on resistant bacteria. Excreted enzymes are mostly not selected for treatment success. Even when evolution and treatment success are aligned, evolution may not be rapid enough to keep pace with bacterial evolution for maximum benefit. An informed use of phages is invariably superior to naive reliance on within-host evolution. Full article
(This article belongs to the Special Issue Phage Ecology)
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Open AccessArticle
A Novel Benthic Phage Infecting Shewanella with Strong Replication Ability
Viruses 2019, 11(11), 1081; https://doi.org/10.3390/v11111081 - 19 Nov 2019
Abstract
The coastal sediments were considered to contain diverse phages playing important roles in driving biogeochemical cycles based on genetic analysis. However, till now, benthic phages in coastal sediments were very rarely isolated, which largely limits our understanding of their biological characteristics. Here, we [...] Read more.
The coastal sediments were considered to contain diverse phages playing important roles in driving biogeochemical cycles based on genetic analysis. However, till now, benthic phages in coastal sediments were very rarely isolated, which largely limits our understanding of their biological characteristics. Here, we describe a novel lytic phage (named Shewanella phage S0112) isolated from the coastal sediments of the Yellow Sea infecting a sediment bacterium of the genus Shewanella. The phage has a very high replication capability, with the burst size of ca. 1170 phage particles per infected cell, which is 5–10 times higher than that of most phages isolated before. Meanwhile, the latent period of this phage is relatively longer, which might ensure adequate time for phage replication. The phage has a double-stranded DNA genome comprising 62,286 bp with 102 ORFs, ca. 60% of which are functionally unknown. The expression products of 16 ORF genes, mainly structural proteins, were identified by LC-MS/MS analysis. Besides the general DNA metabolism and structure assembly genes in the phage genome, there is a cluster of auxiliary metabolic genes that may be involved in 7-cyano-7-deazaguanine (preQ0) biosynthesis. Meanwhile, a pyrophosphohydrolase (MazG) gene being considered as a regulator of programmed cell death or involving in host stringer responses is inserted in this gene cluster. Comparative genomic and phylogenetic analysis both revealed a great novelty of phage S0112. This study represents the first report of a benthic phage infecting Shewanella, which also sheds light on the phage–host interactions in coastal sediments. Full article
(This article belongs to the Special Issue Phage Ecology)
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Open AccessArticle
A Quest of Great Importance-Developing a Broad Spectrum Escherichia coli Phage Collection
Viruses 2019, 11(10), 899; https://doi.org/10.3390/v11100899 - 26 Sep 2019
Abstract
Shigella ssp. and enterotoxigenic Escherichia coli are the most common etiological agents of diarrheal diseases in malnourished children under five years of age in developing countries. The ever-growing issue of antibiotic resistance and the potential negative impact of antibiotic use on infant commensal [...] Read more.
Shigella ssp. and enterotoxigenic Escherichia coli are the most common etiological agents of diarrheal diseases in malnourished children under five years of age in developing countries. The ever-growing issue of antibiotic resistance and the potential negative impact of antibiotic use on infant commensal microbiota are significant challenges to current therapeutic approaches. Bacteriophages (or phages) represent an alternative treatment that can be used to treat specific bacterial infections. In the present study, we screened water samples from both environmental and industrial sources for phages capable of infecting E. coli laboratory strains within our collection. Nineteen phages were isolatedand tested for their ability to infect strains within the ECOR collection and E. coli O157:H7 Δstx. Furthermore, since coliphages have been reported to cross-infect certain Shigella spp., we also evaluated the ability of the nineteen phages to infect a representative Shigella sonnei strain from our collection. Based on having distinct (although overlapping in some cases) host ranges, ten phage isolates were selected for genome sequence and morphological characterization. Together, these ten selected phages were shown to infect most of the ECOR library, with 61 of the 72 strains infected by at least one phage from our collection. Genome analysis of the ten phages allowed classification into five previously described genetic subgroups plus one previously underrepresented subgroup. Full article
(This article belongs to the Special Issue Phage Ecology)
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Review

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Open AccessReview
Look Who’s Talking: T-Even Phage Lysis Inhibition, the Granddaddy of Virus-Virus Intercellular Communication Research
Viruses 2019, 11(10), 951; https://doi.org/10.3390/v11100951 - 16 Oct 2019
Abstract
That communication can occur between virus-infected cells has been appreciated for nearly as long as has virus molecular biology. The original virus communication process specifically was that seen with T-even bacteriophages—phages T2, T4, and T6—resulting in what was labeled as a lysis inhibition. [...] Read more.
That communication can occur between virus-infected cells has been appreciated for nearly as long as has virus molecular biology. The original virus communication process specifically was that seen with T-even bacteriophages—phages T2, T4, and T6—resulting in what was labeled as a lysis inhibition. Another proposed virus communication phenomenon, also seen with T-even phages, can be described as a phage-adsorption-induced synchronized lysis-inhibition collapse. Both are mediated by virions that were released from earlier-lysing, phage-infected bacteria. Each may represent ecological responses, in terms of phage lysis timing, to high local densities of phage-infected bacteria, but for lysis inhibition also to locally reduced densities of phage-uninfected bacteria. With lysis inhibition, the outcome is a temporary avoidance of lysis, i.e., a lysis delay, resulting in increased numbers of virions (greater burst size). Synchronized lysis-inhibition collapse, by contrast, is an accelerated lysis which is imposed upon phage-infected bacteria by virions that have been lytically released from other phage-infected bacteria. Here I consider some history of lysis inhibition, its laboratory manifestation, its molecular basis, how it may benefit expressing phages, and its potential ecological role. I discuss as well other, more recently recognized examples of virus-virus intercellular communication. Full article
(This article belongs to the Special Issue Phage Ecology)
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