Cargando…

A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus

Vibrio parahaemolyticus is an important foodborne pathogen and its biofilm formation ability facilitates its colonization and persistence in foods by protecting it from stresses including environmental variation and antibiotic exposure. Several important proteins are involved in biofilm formation; h...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Fufeng, Lei, Tao, Wang, Zhi, He, Min, Zhang, Jumei, Wang, Juan, Zeng, Haiyan, Chen, Moutong, Xue, Liang, Ye, Qinghua, Pang, Rui, Wu, Shi, Gu, Qihui, Ding, Yu, Wu, Qingping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064395/
https://www.ncbi.nlm.nih.gov/pubmed/33897670
http://dx.doi.org/10.3389/fmicb.2021.656380
_version_ 1783682126833516544
author Jiang, Fufeng
Lei, Tao
Wang, Zhi
He, Min
Zhang, Jumei
Wang, Juan
Zeng, Haiyan
Chen, Moutong
Xue, Liang
Ye, Qinghua
Pang, Rui
Wu, Shi
Gu, Qihui
Ding, Yu
Wu, Qingping
author_facet Jiang, Fufeng
Lei, Tao
Wang, Zhi
He, Min
Zhang, Jumei
Wang, Juan
Zeng, Haiyan
Chen, Moutong
Xue, Liang
Ye, Qinghua
Pang, Rui
Wu, Shi
Gu, Qihui
Ding, Yu
Wu, Qingping
author_sort Jiang, Fufeng
collection PubMed
description Vibrio parahaemolyticus is an important foodborne pathogen and its biofilm formation ability facilitates its colonization and persistence in foods by protecting it from stresses including environmental variation and antibiotic exposure. Several important proteins are involved in biofilm formation; however, the identity and function of many remain unknown. In this study, we discovered a hypothetical protein, VP0610 that negatively regulates biofilm formation in Vibrio parahaemolyticus, and we found that the loss of vp0610 typically results in pleiotropic phenotypes that contribute toward promoting biofilm formation, including significantly increased insoluble exopolysaccharide production and swimming motility, decreased soluble exopolysaccharide production, and decreased bis-(3′-5′)-cyclic dimeric guanosine monophosphate production. Pull-down assays revealed that VP0610 can interact with 180 proteins, some of which (Hfq, VP0710, VP0793, and CyaA) participate in biofilm formation. Moreover, deleting vp0610 enhanced the expression of genes responsible for biofilm component (flaE), the sugar phosphotransferase system (PTS) EIIA component (vp0710 and vp0793), and a high-density regulator of quorum sensing (opaR), while reducing the expression of the bis-(3′-5′)-cyclic dimeric guanosine monophosphate degradation protein (CdgC), resulting in faster biofilm formation. Taken together, our results indicate that vp0610 is an integral member of the key biofilm regulatory network of V. parahaemolyticus that functions as a repressor of biofilm formation.
format Online
Article
Text
id pubmed-8064395
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-80643952021-04-24 A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus Jiang, Fufeng Lei, Tao Wang, Zhi He, Min Zhang, Jumei Wang, Juan Zeng, Haiyan Chen, Moutong Xue, Liang Ye, Qinghua Pang, Rui Wu, Shi Gu, Qihui Ding, Yu Wu, Qingping Front Microbiol Microbiology Vibrio parahaemolyticus is an important foodborne pathogen and its biofilm formation ability facilitates its colonization and persistence in foods by protecting it from stresses including environmental variation and antibiotic exposure. Several important proteins are involved in biofilm formation; however, the identity and function of many remain unknown. In this study, we discovered a hypothetical protein, VP0610 that negatively regulates biofilm formation in Vibrio parahaemolyticus, and we found that the loss of vp0610 typically results in pleiotropic phenotypes that contribute toward promoting biofilm formation, including significantly increased insoluble exopolysaccharide production and swimming motility, decreased soluble exopolysaccharide production, and decreased bis-(3′-5′)-cyclic dimeric guanosine monophosphate production. Pull-down assays revealed that VP0610 can interact with 180 proteins, some of which (Hfq, VP0710, VP0793, and CyaA) participate in biofilm formation. Moreover, deleting vp0610 enhanced the expression of genes responsible for biofilm component (flaE), the sugar phosphotransferase system (PTS) EIIA component (vp0710 and vp0793), and a high-density regulator of quorum sensing (opaR), while reducing the expression of the bis-(3′-5′)-cyclic dimeric guanosine monophosphate degradation protein (CdgC), resulting in faster biofilm formation. Taken together, our results indicate that vp0610 is an integral member of the key biofilm regulatory network of V. parahaemolyticus that functions as a repressor of biofilm formation. Frontiers Media S.A. 2021-04-09 /pmc/articles/PMC8064395/ /pubmed/33897670 http://dx.doi.org/10.3389/fmicb.2021.656380 Text en Copyright © 2021 Jiang, Lei, Wang, He, Zhang, Wang, Zeng, Chen, Xue, Ye, Pang, Wu, Gu, Ding and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jiang, Fufeng
Lei, Tao
Wang, Zhi
He, Min
Zhang, Jumei
Wang, Juan
Zeng, Haiyan
Chen, Moutong
Xue, Liang
Ye, Qinghua
Pang, Rui
Wu, Shi
Gu, Qihui
Ding, Yu
Wu, Qingping
A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title_full A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title_fullStr A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title_full_unstemmed A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title_short A Novel Gene vp0610 Negatively Regulates Biofilm Formation in Vibrio parahaemolyticus
title_sort novel gene vp0610 negatively regulates biofilm formation in vibrio parahaemolyticus
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8064395/
https://www.ncbi.nlm.nih.gov/pubmed/33897670
http://dx.doi.org/10.3389/fmicb.2021.656380
work_keys_str_mv AT jiangfufeng anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT leitao anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wangzhi anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT hemin anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT zhangjumei anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wangjuan anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT zenghaiyan anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT chenmoutong anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT xueliang anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT yeqinghua anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT pangrui anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wushi anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT guqihui anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT dingyu anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wuqingping anovelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT jiangfufeng novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT leitao novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wangzhi novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT hemin novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT zhangjumei novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wangjuan novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT zenghaiyan novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT chenmoutong novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT xueliang novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT yeqinghua novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT pangrui novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wushi novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT guqihui novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT dingyu novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus
AT wuqingping novelgenevp0610negativelyregulatesbiofilmformationinvibrioparahaemolyticus