Literature DB >> 22535222

Putative type VI secretion systems of Vibrio parahaemolyticus contribute to adhesion to cultured cell monolayers.

Ying Yu1, Hong Yang, Jun Li, Peipei Zhang, Beibei Wu, Binglin Zhu, Yan Zhang, Weihuan Fang.   

Abstract

Analysis of the genome sequence of Vibrio parahaemolyticus reveals two IcmF family genes in putative type VI secretion system (vpT6SS) clusters in chromosomes 1 (icmF1) and 2 (icmF2). The icmF1 gene is present in majority of clinical isolates (87.5 %), but has a low fraction (25.0 %) in environmental isolates. However, icmF2 is contained in all strains of both clinical and environmental sources. Deletion of either icmF1 or hcp1 significantly reduced bacterial adhesion to Caco-2 cells or HeLa monolayers. However, the ΔicmF2 and Δhcp2 mutants showed decreased adhesion only to HeLa monolayers. Western blot analysis showed that Hcp2 was present both in the supernatant and pellet samples in the wild-type strain, but only in the pellet of the ΔicmF2 mutant, indicating that Hcp2 is a translocon of T6SS2. Although vpT6SS1 might be functional in cellular adhesion, the putative translocon Hcp1 was not detectable. Quantitative PCR revealed 10-fold and 17-fold less transcripts of hcp1 and icmF1 mRNA than those of hcp2 and icmF2 accordingly. Thus, we postulate that the putative vpT6SS systems contribute to adhesion of V. parahaemolyticus to host cells.

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Year:  2012        PMID: 22535222     DOI: 10.1007/s00203-012-0816-z

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  44 in total

1.  Acute Hepatopancreatic Necrosis Disease-Causing Vibrio parahaemolyticus Strains Maintain an Antibacterial Type VI Secretion System with Versatile Effector Repertoires.

Authors:  Peng Li; Lisa N Kinch; Ann Ray; Ankur B Dalia; Qian Cong; Linda M Nunan; Andrew Camilli; Nick V Grishin; Dor Salomon; Kim Orth
Journal:  Appl Environ Microbiol       Date:  2017-06-16       Impact factor: 4.792

2.  Genomic Features of Environmental and Clinical Vibrio parahaemolyticus Isolates Lacking Recognized Virulence Factors Are Dissimilar.

Authors:  J Ronholm; N Petronella; C Chew Leung; A W Pightling; S K Banerjee
Journal:  Appl Environ Microbiol       Date:  2015-12-04       Impact factor: 4.792

3.  De Novo Sequencing Provides Insights Into the Pathogenicity of Foodborne Vibrio parahaemolyticus.

Authors:  Jianfei Liu; Kewei Qin; Chenglin Wu; Kaifei Fu; Xiaojie Yu; Lijun Zhou
Journal:  Front Cell Infect Microbiol       Date:  2021-05-14       Impact factor: 5.293

Review 4.  New Insights into the Mechanism of Action of PirAB from Vibrio Parahaemolyticus.

Authors:  Sonia A Soto-Rodriguez; Rodolfo Lozano-Olvera; Gabriela Ramos-Clamont Montfort; Edgar Zenteno; José Luis Sánchez-Salgado; Norberto Vibanco-Pérez; Karla G Aguilar Rendón
Journal:  Toxins (Basel)       Date:  2022-03-30       Impact factor: 5.075

5.  The pathogenesis, detection, and prevention of Vibrio parahaemolyticus.

Authors:  Rongzhi Wang; Yanfang Zhong; Xiaosong Gu; Jun Yuan; Abdullah F Saeed; Shihua Wang
Journal:  Front Microbiol       Date:  2015-03-05       Impact factor: 5.640

Review 6.  Roles of thermostable direct hemolysin (TDH) and TDH-related hemolysin (TRH) in Vibrio parahaemolyticus.

Authors:  Pendru Raghunath
Journal:  Front Microbiol       Date:  2015-01-22       Impact factor: 5.640

7.  A novel adhesive factor contributing to the virulence of Vibrio parahaemolyticus.

Authors:  Ming Liu; Sheng Chen
Journal:  Sci Rep       Date:  2015-09-24       Impact factor: 4.379

8.  Genomic Comparison of Translocating and Non-Translocating Escherichia coli.

Authors:  Nathan L Bachmann; Mohammad Katouli; Adam Polkinghorne
Journal:  PLoS One       Date:  2015-08-28       Impact factor: 3.240

9.  Hemolysin Co-regulated Family Proteins Hcp1 and Hcp2 Contribute to Edwardsiella ictaluri Pathogenesis.

Authors:  Safak Kalindamar; Hossam Abdelhamed; Adef O Kordon; Lesya M Pinchuk; Attila Karsi
Journal:  Front Vet Sci       Date:  2021-06-02

10.  Vibrio parahaemolyticus type VI secretion system 1 is activated in marine conditions to target bacteria, and is differentially regulated from system 2.

Authors:  Dor Salomon; Herman Gonzalez; Barrett L Updegraff; Kim Orth
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

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