4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Bacterial resistance to temperate phage is influenced by the frequency of lysogenic establishment

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Temperate phages can shape bacterial community dynamics and evolution through lytic and lysogenic life cycles. In response, bacteria that resist phage infection can emerge. This study explores phage-based factors that influence bacterial resistance using a model system of temperate P22 phage and Salmonella both inside and outside the mammalian host. Phages that remained functional despite gene deletions had minimal impact on lysogeny and phage resistance except for deletions in the immI region that substantially reduced lysogeny and increased phage resistance to levels comparable to that observed with an obligately lytic P22. This immI deletion does not make the lysogen less competitive but instead increases the frequency of bacterial lysis. Thus, subtle changes in the balance between lysis and lysogeny during the initial stages of infection can significantly influence the extent of phage resistance in the bacterial population. Our work highlights the complex nature of the phage-bacteria-mammalian host triad.

          Graphical abstract

          Highlights

          • Deletion of the P22 immunity region, ImmI, decreases its frequency of lysogeny in STm

          • Increased lysis by P22 mutants leads to greater phage resistance among STm

          • Increased phage resistance among STm is observed in culture and mice

          Abstract

          Virology; Microbiology; Viral microbiology

          Related collections

          Most cited references57

          • Record: found
          • Abstract: found
          • Article: not found

          One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products.

          We have developed a simple and highly efficient method to disrupt chromosomal genes in Escherichia coli in which PCR primers provide the homology to the targeted gene(s). In this procedure, recombination requires the phage lambda Red recombinase, which is synthesized under the control of an inducible promoter on an easily curable, low copy number plasmid. To demonstrate the utility of this approach, we generated PCR products by using primers with 36- to 50-nt extensions that are homologous to regions adjacent to the gene to be inactivated and template plasmids carrying antibiotic resistance genes that are flanked by FRT (FLP recognition target) sites. By using the respective PCR products, we made 13 different disruptions of chromosomal genes. Mutants of the arcB, cyaA, lacZYA, ompR-envZ, phnR, pstB, pstCA, pstS, pstSCAB-phoU, recA, and torSTRCAD genes or operons were isolated as antibiotic-resistant colonies after the introduction into bacteria carrying a Red expression plasmid of synthetic (PCR-generated) DNA. The resistance genes were then eliminated by using a helper plasmid encoding the FLP recombinase which is also easily curable. This procedure should be widely useful, especially in genome analysis of E. coli and other bacteria because the procedure can be done in wild-type cells.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Bacteriophage resistance mechanisms.

              Phages are now acknowledged as the most abundant microorganisms on the planet and are also possibly the most diversified. This diversity is mostly driven by their dynamic adaptation when facing selective pressure such as phage resistance mechanisms, which are widespread in bacterial hosts. When infecting bacterial cells, phages face a range of antiviral mechanisms, and they have evolved multiple tactics to avoid, circumvent or subvert these mechanisms in order to thrive in most environments. In this Review, we highlight the most important antiviral mechanisms of bacteria as well as the counter-attacks used by phages to evade these systems.
                Bookmark

                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                27 March 2024
                19 April 2024
                27 March 2024
                : 27
                : 4
                : 109595
                Affiliations
                [1 ]Department of Biological Sciences, Fralin Life Sciences Institute, Center for Emerging, and Zoonotic, Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA 24061, USA
                [2 ]Department of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, Irvine, CA, USA
                Author notes
                []Corresponding author bhsu@ 123456vt.edu
                [3]

                Lead contact

                Article
                S2589-0042(24)00817-4 109595
                10.1016/j.isci.2024.109595
                11016777
                38623331
                553daae7-34b4-404b-bdfc-81c87f795191
                © 2024 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 2 November 2023
                : 23 January 2024
                : 25 March 2024
                Categories
                Article

                virology,microbiology,viral microbiology
                virology, microbiology, viral microbiology

                Comments

                Comment on this article