Literature DB >> 27645387

Emergence of a Competence-Reducing Filamentous Phage from the Genome of Acinetobacter baylyi ADP1.

Brian A Renda1, Cindy Chan1, Kristin N Parent2, Jeffrey E Barrick3.   

Abstract

Bacterial genomes commonly contain prophage sequences as a result of past infections with lysogenic phages. Many of these integrated viral sequences are believed to be cryptic, but prophage genes are sometimes coopted by the host, and some prophages may be reactivated to form infectious particles when cells are stressed or mutate. We found that a previously uncharacterized filamentous phage emerged from the genome of Acinetobacter baylyi ADP1 during a laboratory evolution experiment. This phage has a genetic organization similar to that of the Vibrio cholerae CTXϕ phage. The emergence of the ADP1 phage was associated with the evolution of reduced transformability in our experimental populations, so we named it the competence-reducing acinetobacter phage (CRAϕ). Knocking out ADP1 genes required for competence leads to resistance to CRAϕ infection. Although filamentous bacteriophages are known to target type IV pili, this is the first report of a phage that apparently uses a competence pilus as a receptor. A. baylyi may be especially susceptible to this route of infection because every cell is competent during normal growth, whereas competence is induced only under certain environmental conditions or in a subpopulation of cells in other bacterial species. It is possible that CRAϕ-like phages restrict horizontal gene transfer in nature by inhibiting the growth of naturally transformable strains. We also found that prophages with homology to CRAϕ exist in several strains of Acinetobacter baumannii These CRAϕ-like A. baumannii prophages encode toxins similar to CTXϕ that might contribute to the virulence of this opportunistic multidrug-resistant pathogen. IMPORTANCE: We observed the emergence of a novel filamentous phage (CRAϕ) from the genome of Acinetobacter baylyi ADP1 during a long-term laboratory evolution experiment. CRAϕ is the first bacteriophage reported to require the molecular machinery involved in the uptake of environmental DNA for infection. Reactivation and evolution of CRAϕ reduced the potential for horizontal transfer of genes via natural transformation in our experiment. Risk of infection by similar phages may limit the expression and maintenance of bacterial competence in nature. The closest studied relative of CRAϕ is the Vibrio cholerae CTXϕ phage. Variants of CRAϕ are found in the genomes of Acinetobacter baumannii strains, and it is possible that phage-encoded toxins contribute to the virulence of this opportunistic multidrug-resistant pathogen.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2016        PMID: 27645387      PMCID: PMC5105901          DOI: 10.1128/JB.00424-16

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  56 in total

1.  CTX prophages in classical biotype Vibrio cholerae: functional phage genes but dysfunctional phage genomes.

Authors:  B M Davis; K E Moyer; E F Boyd; M K Waldor
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

2.  The CTXphi repressor RstR binds DNA cooperatively to form tetrameric repressor-operator complexes.

Authors:  Harvey H Kimsey; Matthew K Waldor
Journal:  J Biol Chem       Date:  2003-11-10       Impact factor: 5.157

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Review 4.  Bacteriophage resistance mechanisms.

Authors:  Simon J Labrie; Julie E Samson; Sylvain Moineau
Journal:  Nat Rev Microbiol       Date:  2010-03-29       Impact factor: 60.633

Review 5.  Opportunities for genetic investigation afforded by Acinetobacter baylyi, a nutritionally versatile bacterial species that is highly competent for natural transformation.

Authors:  David M Young; Donna Parke; L Nicholas Ornston
Journal:  Annu Rev Microbiol       Date:  2005       Impact factor: 15.500

6.  DNA uptake by the nosocomial pathogen Acinetobacter baumannii occurs during movement along wet surfaces.

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7.  Chitin induces natural competence in Vibrio cholerae.

Authors:  Karin L Meibom; Melanie Blokesch; Nadia A Dolganov; Cheng-Yen Wu; Gary K Schoolnik
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Authors:  Xiaoxue Wang; Younghoon Kim; Qun Ma; Seok Hoon Hong; Karina Pokusaeva; Joseph M Sturino; Thomas K Wood
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  7 in total

1.  New Shuttle Vectors for Real-Time Gene Expression Analysis in Multidrug-Resistant Acinetobacter Species: In Vitro and In Vivo Responses to Environmental Stressors.

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Journal:  Appl Environ Microbiol       Date:  2019-08-29       Impact factor: 4.792

Review 2.  Filamentous phages: masters of a microbial sharing economy.

Authors:  Iain D Hay; Trevor Lithgow
Journal:  EMBO Rep       Date:  2019-04-05       Impact factor: 8.807

3.  New Shuttle Vectors for Gene Cloning and Expression in Multidrug-Resistant Acinetobacter Species.

Authors:  Massimiliano Lucidi; Federica Runci; Giordano Rampioni; Emanuela Frangipani; Livia Leoni; Paolo Visca
Journal:  Antimicrob Agents Chemother       Date:  2018-03-27       Impact factor: 5.191

4.  Comparative Analysis of 37 Acinetobacter Bacteriophages.

Authors:  Dann Turner; Hans-Wolfgang Ackermann; Andrew M Kropinski; Rob Lavigne; J Mark Sutton; Darren M Reynolds
Journal:  Viruses       Date:  2017-12-24       Impact factor: 5.048

5.  Genome alterations associated with improved transformation efficiency in Lactobacillus reuteri.

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6.  Genome diversity of domesticated Acinetobacter baumannii ATCC 19606T strains.

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7.  Rapid and assured genetic engineering methods applied to Acinetobacter baylyi ADP1 genome streamlining.

Authors:  Gabriel A Suárez; Kyle R Dugan; Brian A Renda; Sean P Leonard; Lakshmi Suryateja Gangavarapu; Jeffrey E Barrick
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