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Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity

Pathogens adapted to sub‐lethal acidic conditions could increase the virulence and survival ability under lethal conditions. In the aquaculture industry, feed acidifiers have been used to increase the growth of aquatic animals. However, there is limited study on the effects of acidic condition on th...

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Autores principales: Gu, Dan, Wang, Kangru, Lu, Tianyu, Li, Lingzhi, Jiao, Xinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359830/
https://www.ncbi.nlm.nih.gov/pubmed/33831221
http://dx.doi.org/10.1111/jfd.13376
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author Gu, Dan
Wang, Kangru
Lu, Tianyu
Li, Lingzhi
Jiao, Xinan
author_facet Gu, Dan
Wang, Kangru
Lu, Tianyu
Li, Lingzhi
Jiao, Xinan
author_sort Gu, Dan
collection PubMed
description Pathogens adapted to sub‐lethal acidic conditions could increase the virulence and survival ability under lethal conditions. In the aquaculture industry, feed acidifiers have been used to increase the growth of aquatic animals. However, there is limited study on the effects of acidic condition on the virulence and survival of pathogens in aquaculture. In this study, we investigated the survival ability of Vibrio parahaemolyticus at lethal acidic pH (4.0) after adapted the bacteria to sub‐lethal acidic pH (5.5) for 1 hr. Our results indicated that the adapted strain increased the survival ability at lethal acidic pH invoked by an inorganic (HCl) or organic (citric) acid. RNA‐sequencing (RNA‐seq) results revealed that 321 genes were differentially expressed at the sub‐lethal acidic pH including cadC, cadBA and groES/groEL relating to acid tolerance response (ATR), as well as genes relating to outer membrane, heat‐shock proteins, phosphotransferase system and flagella system. Quantitative real‐time polymerase chain reaction (qRT‐PCR) confirmed that cadC and cadBA were upregulated under sub‐lethal acidic conditions. The CadC protein could directly regulate the expression of cadBA to modulate the ATR in V. parahaemolyticus. RNA‐seq data also indicated that 113 genes in the CadC‐dependent way and 208 genes in the CadC‐independent way were differentially expressed, which were related to the regulation of ATR. Finally, the motility and cytotoxicity of the sub‐lethal acidic adapted wild type (WT) were significantly increased compared with the unadapted strain. Our results demonstrated that the dietary acidifiers may increase the virulence and survival of V. parahaemolyticus in aquaculture.
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spelling pubmed-83598302021-08-17 Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity Gu, Dan Wang, Kangru Lu, Tianyu Li, Lingzhi Jiao, Xinan J Fish Dis Research Articles Pathogens adapted to sub‐lethal acidic conditions could increase the virulence and survival ability under lethal conditions. In the aquaculture industry, feed acidifiers have been used to increase the growth of aquatic animals. However, there is limited study on the effects of acidic condition on the virulence and survival of pathogens in aquaculture. In this study, we investigated the survival ability of Vibrio parahaemolyticus at lethal acidic pH (4.0) after adapted the bacteria to sub‐lethal acidic pH (5.5) for 1 hr. Our results indicated that the adapted strain increased the survival ability at lethal acidic pH invoked by an inorganic (HCl) or organic (citric) acid. RNA‐sequencing (RNA‐seq) results revealed that 321 genes were differentially expressed at the sub‐lethal acidic pH including cadC, cadBA and groES/groEL relating to acid tolerance response (ATR), as well as genes relating to outer membrane, heat‐shock proteins, phosphotransferase system and flagella system. Quantitative real‐time polymerase chain reaction (qRT‐PCR) confirmed that cadC and cadBA were upregulated under sub‐lethal acidic conditions. The CadC protein could directly regulate the expression of cadBA to modulate the ATR in V. parahaemolyticus. RNA‐seq data also indicated that 113 genes in the CadC‐dependent way and 208 genes in the CadC‐independent way were differentially expressed, which were related to the regulation of ATR. Finally, the motility and cytotoxicity of the sub‐lethal acidic adapted wild type (WT) were significantly increased compared with the unadapted strain. Our results demonstrated that the dietary acidifiers may increase the virulence and survival of V. parahaemolyticus in aquaculture. John Wiley and Sons Inc. 2021-04-08 2021-08 /pmc/articles/PMC8359830/ /pubmed/33831221 http://dx.doi.org/10.1111/jfd.13376 Text en © 2021 The Authors. Journal of Fish Diseases published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Gu, Dan
Wang, Kangru
Lu, Tianyu
Li, Lingzhi
Jiao, Xinan
Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title_full Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title_fullStr Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title_full_unstemmed Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title_short Vibrio parahaemolyticus CadC regulates acid tolerance response to enhance bacterial motility and cytotoxicity
title_sort vibrio parahaemolyticus cadc regulates acid tolerance response to enhance bacterial motility and cytotoxicity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359830/
https://www.ncbi.nlm.nih.gov/pubmed/33831221
http://dx.doi.org/10.1111/jfd.13376
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