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Inhibition of virulence potential of Vibrio cholerae by natural compounds

The rise in multi-drug resistant Vibrio cholerae strains is a big problem in treatment of patients suffering from severe cholera. Only a few studies have evaluated the potential of natural compounds against V. cholerae. Extracts from plants like ‘neem’, ‘guazuma’, ‘daio’, apple, hop, green tea and e...

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Autores principales: Yamasaki, Shinji, Asakura, Masahiro, Neogi, Sucharit Basu, Hinenoya, Atsushi, Iwaoka, Emiko, Aoki, Shunji
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089057/
https://www.ncbi.nlm.nih.gov/pubmed/21415500
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author Yamasaki, Shinji
Asakura, Masahiro
Neogi, Sucharit Basu
Hinenoya, Atsushi
Iwaoka, Emiko
Aoki, Shunji
author_facet Yamasaki, Shinji
Asakura, Masahiro
Neogi, Sucharit Basu
Hinenoya, Atsushi
Iwaoka, Emiko
Aoki, Shunji
author_sort Yamasaki, Shinji
collection PubMed
description The rise in multi-drug resistant Vibrio cholerae strains is a big problem in treatment of patients suffering from severe cholera. Only a few studies have evaluated the potential of natural compounds against V. cholerae. Extracts from plants like ‘neem’, ‘guazuma’, ‘daio’, apple, hop, green tea and elephant garlic have been shown to inhibit bacterial growth or the secreted cholera toxin (CT). However, inhibiting bacterial growth like common antimicrobial agents may also impose selective pressure facilitating development of resistant strains. A natural compound that can inhibit virulence in V. cholerae is an alternative choice for remedy. Recently, some common spices were examined to check their inhibitory capacity against virulence expression of V. cholerae. Among them methanol extracts of red chili, sweet fennel and white pepper could substantially inhibit CT production. Fractionation of red chili methanol extracts indicated a hydrophobic nature of the inhibitory compound(s), and the n-hexane and 90 per cent methanol fractions could inhibit >90 per cent of CT production. Purification and further fractionation revealed that capsaicin is one of the major components among these red chili fractions. Indeed, capsaicin inhibited the production of CT in various V. cholerae strains regardless of serogroups and biotypes. The quantitative reverse transcription real-time PCR assay revealed that capsaicin dramatically reduced the expression of major virulence-related genes such as ctxA, tcpA and toxT but enhanced the expression of hns gene that transcribes a global prokaryotic gene regulator (H-NS). This indicates that the repression of CT production by capsaicin or red chili might be due to the repression of virulence genes transcription by H-NS. Regular intake of spices like red chili might be a good approach to fight against devastating cholera.
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spelling pubmed-30890572011-05-16 Inhibition of virulence potential of Vibrio cholerae by natural compounds Yamasaki, Shinji Asakura, Masahiro Neogi, Sucharit Basu Hinenoya, Atsushi Iwaoka, Emiko Aoki, Shunji Indian J Med Res Review Article The rise in multi-drug resistant Vibrio cholerae strains is a big problem in treatment of patients suffering from severe cholera. Only a few studies have evaluated the potential of natural compounds against V. cholerae. Extracts from plants like ‘neem’, ‘guazuma’, ‘daio’, apple, hop, green tea and elephant garlic have been shown to inhibit bacterial growth or the secreted cholera toxin (CT). However, inhibiting bacterial growth like common antimicrobial agents may also impose selective pressure facilitating development of resistant strains. A natural compound that can inhibit virulence in V. cholerae is an alternative choice for remedy. Recently, some common spices were examined to check their inhibitory capacity against virulence expression of V. cholerae. Among them methanol extracts of red chili, sweet fennel and white pepper could substantially inhibit CT production. Fractionation of red chili methanol extracts indicated a hydrophobic nature of the inhibitory compound(s), and the n-hexane and 90 per cent methanol fractions could inhibit >90 per cent of CT production. Purification and further fractionation revealed that capsaicin is one of the major components among these red chili fractions. Indeed, capsaicin inhibited the production of CT in various V. cholerae strains regardless of serogroups and biotypes. The quantitative reverse transcription real-time PCR assay revealed that capsaicin dramatically reduced the expression of major virulence-related genes such as ctxA, tcpA and toxT but enhanced the expression of hns gene that transcribes a global prokaryotic gene regulator (H-NS). This indicates that the repression of CT production by capsaicin or red chili might be due to the repression of virulence genes transcription by H-NS. Regular intake of spices like red chili might be a good approach to fight against devastating cholera. Medknow Publications 2011-02 /pmc/articles/PMC3089057/ /pubmed/21415500 Text en © The Indian Journal of Medical Research http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Yamasaki, Shinji
Asakura, Masahiro
Neogi, Sucharit Basu
Hinenoya, Atsushi
Iwaoka, Emiko
Aoki, Shunji
Inhibition of virulence potential of Vibrio cholerae by natural compounds
title Inhibition of virulence potential of Vibrio cholerae by natural compounds
title_full Inhibition of virulence potential of Vibrio cholerae by natural compounds
title_fullStr Inhibition of virulence potential of Vibrio cholerae by natural compounds
title_full_unstemmed Inhibition of virulence potential of Vibrio cholerae by natural compounds
title_short Inhibition of virulence potential of Vibrio cholerae by natural compounds
title_sort inhibition of virulence potential of vibrio cholerae by natural compounds
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089057/
https://www.ncbi.nlm.nih.gov/pubmed/21415500
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