Literature DB >> 33187995

Vibrio fischeri Amidase Activity Is Required for Normal Cell Division, Motility, and Symbiotic Competence.

Pat M Fidopiastis1, Vanessa Mariscal2, Jeanne-Marie McPherson2, Sarah McAnulty3, Anne Dunn4, Eric V Stabb5, Karen L Visick6.   

Abstract

N-Acetylmuramoyl-l-alanine amidases are periplasmic hydrolases that cleave the amide bond between N-acetylmuramic acid and alanine in peptidoglycan (PG). Unlike many Gram-negative bacteria that encode redundant periplasmic amidases, Vibrio fischeri appears to encode a single protein that is homologous to AmiB of Vibrio cholerae We screened a V. fischeri transposon mutant library for strains altered in biofilm production and discovered a biofilm-overproducing strain with an insertion in amiB (VF_2326). Further characterization of biofilm enhancement suggested that this phenotype was due to the overproduction of cellulose, and it was dependent on the bcsA cellulose synthase. Additionally, the amiB mutant was nonmotile, perhaps due to defects in its ability to septate during division. The amidase mutant was unable to compete with the wild type for the colonization of V. fischeri's symbiotic host, the squid Euprymna scolopes In single-strain inoculations, host squid inoculated with the mutant eventually became colonized but with a much lower efficiency than in squid inoculated with the wild type. This observation was consistent with the pleiotropic effects of the amiB mutation and led us to speculate that motile suppressors of the amiB mutant were responsible for the partially restored colonization. In culture, motile suppressor mutants carried point mutations in a single gene (VF_1477), resulting in a partial restoration of wild-type motility. In addition, these point mutations reversed the effect of the amiB mutation on cellulosic biofilm production. These data are consistent with V. fischeri AmiB possessing amidase activity; they also suggest that AmiB suppresses cellulosic biofilm formation but promotes successful host colonization.IMPORTANCE Peptidoglycan (PG) is a critical microbe-associated molecular pattern (MAMP) that is sloughed by cells of V. fischeri during symbiotic colonization of squid. Specifically, this process induces significant remodeling of a specialized symbiotic light organ within the squid mantle cavity. This phenomenon is reminiscent of the loss of ciliated epithelium in patients with whooping cough due to the production of PG monomers by Bordetella pertussis Furthermore, PG processing machinery can influence susceptibility to antimicrobials. In this study, we report roles for the V. fischeri PG amidase AmiB, including the beneficial colonization of squid, underscoring the urgency to more deeply understand PG processing machinery and the downstream consequences of their activities.
Copyright © 2021 American Society for Microbiology.

Entities:  

Keywords:  Euprymna scolopes; Vibrio fischeri; amidase; biofilm; cellulose; peptidoglycan

Mesh:

Substances:

Year:  2021        PMID: 33187995      PMCID: PMC7848909          DOI: 10.1128/AEM.02109-20

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  47 in total

1.  An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring.

Authors:  Desirée C Yang; Nick T Peters; Katherine R Parzych; Tsuyoshi Uehara; Monica Markovski; Thomas G Bernhardt
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-17       Impact factor: 11.205

2.  The CpxR/CpxA two-component system up-regulates two Tat-dependent peptidoglycan amidases to confer bacterial resistance to antimicrobial peptide.

Authors:  Natasha Weatherspoon-Griffin; Guang Zhao; Wei Kong; Ying Kong; Helene Andrews-Polymenis; Michael McClelland; Yixin Shi
Journal:  J Biol Chem       Date:  2010-12-13       Impact factor: 5.157

3.  Effective mutagenesis of Vibrio fischeri by using hyperactive mini-Tn5 derivatives.

Authors:  Noreen L Lyell; Anne K Dunn; Jeffrey L Bose; Susan L Vescovi; Eric V Stabb
Journal:  Appl Environ Microbiol       Date:  2008-09-19       Impact factor: 4.792

4.  The cell wall amidase AmiB is essential for Pseudomonas aeruginosa cell division, drug resistance and viability.

Authors:  Anastasiya A Yakhnina; Heather R McManus; Thomas G Bernhardt
Journal:  Mol Microbiol       Date:  2015-07-14       Impact factor: 3.501

5.  Cell separation in Vibrio cholerae is mediated by a single amidase whose action is modulated by two nonredundant activators.

Authors:  Andrea Möll; Tobias Dörr; Laura Alvarez; Michael C Chao; Brigid M Davis; Felipe Cava; Matthew K Waldor
Journal:  J Bacteriol       Date:  2014-09-02       Impact factor: 3.490

6.  Coordinated cyclic-di-GMP repression of Salmonella motility through YcgR and cellulose.

Authors:  Violeta Zorraquino; Begoña García; Cristina Latasa; Maite Echeverz; Alejandro Toledo-Arana; Jaione Valle; Iñigo Lasa; Cristina Solano
Journal:  J Bacteriol       Date:  2012-11-16       Impact factor: 3.490

7.  Rugosity in Grimontia hollisae.

Authors:  S K Curtis; M H Kothary; R J Blodgett; R B Raybourne; G C Ziobro; B D Tall
Journal:  Appl Environ Microbiol       Date:  2006-12-22       Impact factor: 4.792

8.  GroES/GroEL and DnaK/DnaJ have distinct roles in stress responses and during cell cycle progression in Caulobacter crescentus.

Authors:  Michelle F Susin; Regina L Baldini; Frederico Gueiros-Filho; Suely L Gomes
Journal:  J Bacteriol       Date:  2006-09-15       Impact factor: 3.490

9.  Effect of transposon-induced motility mutations on colonization of the host light organ by Vibrio fischeri.

Authors:  J Graf; P V Dunlap; E G Ruby
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

10.  Tools for Rapid Genetic Engineering of Vibrio fischeri.

Authors:  Karen L Visick; Kelsey M Hodge-Hanson; Alice H Tischler; Allison K Bennett; Vincent Mastrodomenico
Journal:  Appl Environ Microbiol       Date:  2018-07-02       Impact factor: 4.792

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