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Interactions between Prokaryotic Viruses and Their Hosts

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Microbiology".

Deadline for manuscript submissions: closed (31 July 2023) | Viewed by 4553

Special Issue Editors


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Guest Editor
CRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology and Microbial Technology Institute, Shandong University, Qingdao 266237, China
Interests: prokaryotic host-virus interactions; CRISPR-Cas immune systems; archaeal DNA damage repair; archaeal cell division regulation

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Guest Editor
Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Science, Jinan 250100, China
Interests: phage ecology; phage product development for diseases control and welfare of livestock
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Special Issue Information

Dear Colleagues,

Bacteria and archaea are major players in global biogeochemical cycles. These prokaryotes predominate the cellular form of life on Earth, and they coexist with their viruses, i.e., bacteriophages or phages and archaeal viruses, in all environments. Recent studies show that soils and sediments represent the richest sources of prokaryotic viruses where they outnumber their hosts by 2–3 orders of magnitude. Metagenomic analyses further reveal that many novel bacteriophages are present in the intestines of animals and human beings where the ratio of virus/host cells is estimated to be 1:1, a number that is doomed to increase due to the growth of ongoing research in the field. To date, 60–99% of viral genes in viromes generated from diverse biomes have unknown functions, and more than 99% of viral diversity remains to be explored. These viruses and their prokaryotic hosts interact with each other antagonistically and beneficially to influence nutrient cycling and ecological functions, but little has been found regarding their host–virus interactions. Furthermore, bacteria and archaea encode an arsenal of antiviral systems, many of which are novel. For example, focused research on model CRISPR-Cas systems have revealed that prokaryotic hosts deploy adaptive immunity to defend themselves from a virus invasion, whereas viruses encode anti-CRISPR systems to subvert CRISPR immunity. Since there is a great diversity both in CRISPR-Cas systems and anti-CRISPR systems, much more remains to be learned with regard to the arms race between prokaryotic hosts and their viruses. In addition, several pioneer research studies have revealed additional novel bacterial and archaeal antiviral systems, representing a new direction for prokaryotic virus research.

This Special Issue is dedicated to publishing research articles, reviews, perspectives and opinion articles with a focus on studying interactions between bacterial and archaeal hosts and their viruses. The article collection covers, but is not limited to, the following research areas:

  1. Identification and functional characterization of novel prokaryotic viruses including bacteriophages and archaeal viruses;
  2. Mechanisms of virus infection, such as identification of novel receptors for infection or revealing mechanisms of infection by novel viruses;
  3. Identification of global regulators controlling/modulating the expression of viral and host genes;
  4. The novel mechanism of antiviral defense by innate and adaptive immune systems as well as signaling systems and abortive infection, such as R-M systems, CRISPR-Cas systems, CBASS, etc.;
  5. The arms race between host-encoded antiviral systems and virus-encoded proteins that subvert the host immunity.

Prof. Dr. Qunxin She
Prof. Dr. Yuqing Liu
Guest Editors

Manuscript Submission Information

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Keywords

  • bacteriophages
  • archaeal viruses
  • mechanisms of virus infection
  • R-M systems
  • CRISPR-Cas systems
  • cOA signaling
  • abortive infection
  • anti-CRISPR
  • arms race
  • host–virus interactions

Published Papers (2 papers)

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Research

15 pages, 3571 KiB  
Article
Characterization and Genomic Analysis of a Novel Lytic Phage DCp1 against Clostridium perfringens Biofilms
by Zhaohui Tang, Xiaojing Li, Xinwei Wang, Can Zhang, Ling Zou, Huiying Ren and Wenhua Liu
Int. J. Mol. Sci. 2023, 24(4), 4191; https://doi.org/10.3390/ijms24044191 - 20 Feb 2023
Cited by 4 | Viewed by 1824
Abstract
Clostridium perfringens (C. perfringens) is one of the foremost pathogens responsible for diarrhea in foals. As antibiotic resistance increases, phages that specifically lyse bacteria are of great interest to us with regard to C. perfringens. In this study, a novel [...] Read more.
Clostridium perfringens (C. perfringens) is one of the foremost pathogens responsible for diarrhea in foals. As antibiotic resistance increases, phages that specifically lyse bacteria are of great interest to us with regard to C. perfringens. In this study, a novel C. perfringens phage DCp1 was isolated from the sewage of a donkey farm. Phage DCp1 had a non-contractile short tail (40 nm in length) and a regular icosahedral head (46 nm in diameter). Whole-genome sequencing indicated that phage DCp1 had a linear double-stranded DNA genome with a total length of 18,555 bp and a G + C content of 28.2%. A total of 25 ORFs were identified in the genome, 6 of which had been assigned to functional genes, others were annotated to encode hypothetical proteins. The genome of phage DCp1 lacked any tRNA, virulence gene, drug resistance gene, or lysogenic gene. Phylogenetic analysis indicated that phage DCp1 belonged to the family Guelinviridae, Susfortunavirus. Biofilm assay showed that phage DCp1 was effective in inhibiting the formation of C. perfringens D22 biofilms. Phage DCp1 could completely degrade the biofilm after 5 h of interaction. The current study provides some basic information for further research on phage DCp1 and its application. Full article
(This article belongs to the Special Issue Interactions between Prokaryotic Viruses and Their Hosts)
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6 pages, 1648 KiB  
Communication
Phage Engineering for Targeted Multidrug-Resistant Escherichia coli
by Jiaoyang Song, Zhengjie Liu, Qing Zhang, Yuqing Liu and Yibao Chen
Int. J. Mol. Sci. 2023, 24(3), 2459; https://doi.org/10.3390/ijms24032459 - 27 Jan 2023
Cited by 2 | Viewed by 2054
Abstract
The lytic bacteriophages have potential application value in the treatment of bacterial infections. However, the narrow host spectrum of these phages limits their range of clinical application. Here, we demonstrate the use of scarless Cas9-assisted recombination (no-SCAR) gene-editing technology to regulate phage–host range. [...] Read more.
The lytic bacteriophages have potential application value in the treatment of bacterial infections. However, the narrow host spectrum of these phages limits their range of clinical application. Here, we demonstrate the use of scarless Cas9-assisted recombination (no-SCAR) gene-editing technology to regulate phage–host range. We used phage PHB20 as the scaffold to create agents targeting different multidrug-resistant Escherichia coli by replacing its phage tail fiber gene (ORF40). The engineered phages were polyvalent and capable of infecting both the original host bacteria and new targets. Phage-tail fiber genes can be amplified by PCR to construct a recombinant phage PHB20 library that can deal with multidrug-resistant bacteria in the future. Our results provide a better understanding of phage–host interactions, and we describe new anti-bacterial editing methods. Full article
(This article belongs to the Special Issue Interactions between Prokaryotic Viruses and Their Hosts)
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