File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Exploration of Anti-infectives From Mangrove-Derived Micromonospora sp. RMA46 to Combat Vibrio cholerae Pathogenesis

TitleExploration of Anti-infectives From Mangrove-Derived Micromonospora sp. RMA46 to Combat Vibrio cholerae Pathogenesis
Authors
Keywordsanti-infectives
anti-virulence
anti-biofilm
rare marine Actinobacteria
Micromonosporaspecies
Issue Date2020
PublisherFrontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/microbiology/
Citation
Frontiers in Microbiology, 2020, v. 11, p. article no. 1393 How to Cite?
AbstractVibrio cholerae, the etiological agent of cholera, employs quorum sensing (QS) pathways to control the expression of virulence factors, including the production of cholera toxin and biofilm formation. Acquired antibiotic resistance inV. choleraedraws attention to the development of novel therapeutics that counteract virulence, rather than the viability of the pathogen. In this context, we explored the anti-infective potential of rare marine Actinobacteria (RMA) from a mangrove ecosystem. Here, we report the effects ofMicromonosporasp. RMA46 againstV. cholerae in vitro. The RMA46 organic extract was non-bactericidal toV. choleraecells and non-cytotoxic to macrophage RAW264.7 cell lines. RMA46 inhibited the formation ofV. choleraebiofilms and downregulated the QS global switches LuxO and HapR, as well as other virulence genes includingct,tcp, andhapA.In silicomolecular docking simulation of RMA46 ethyl acetate extract with LuxO and HapR revealed that 2-methoxy-4-vinylphenol and hexahydro-3-(phenylmethyl)-pyrrolo[1,2-a]pyrazine-1,4-dione could interact with the active sites of LuxO and HapR and potentially inhibit them. This study highlightsMicromonosporasp. RMA46 as a potential source of anti-infectives againstV. cholerae.
Persistent Identifierhttp://hdl.handle.net/10722/297634
ISSN
2021 Impact Factor: 6.064
2020 SCImago Journal Rankings: 1.701
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSarveswari, HB-
dc.contributor.authorKalimuthu, S-
dc.contributor.authorShanmugam, K-
dc.contributor.authorNeelakantan, P-
dc.contributor.authorSolomon, AP-
dc.date.accessioned2021-03-23T04:19:42Z-
dc.date.available2021-03-23T04:19:42Z-
dc.date.issued2020-
dc.identifier.citationFrontiers in Microbiology, 2020, v. 11, p. article no. 1393-
dc.identifier.issn1664-302X-
dc.identifier.urihttp://hdl.handle.net/10722/297634-
dc.description.abstractVibrio cholerae, the etiological agent of cholera, employs quorum sensing (QS) pathways to control the expression of virulence factors, including the production of cholera toxin and biofilm formation. Acquired antibiotic resistance inV. choleraedraws attention to the development of novel therapeutics that counteract virulence, rather than the viability of the pathogen. In this context, we explored the anti-infective potential of rare marine Actinobacteria (RMA) from a mangrove ecosystem. Here, we report the effects ofMicromonosporasp. RMA46 againstV. cholerae in vitro. The RMA46 organic extract was non-bactericidal toV. choleraecells and non-cytotoxic to macrophage RAW264.7 cell lines. RMA46 inhibited the formation ofV. choleraebiofilms and downregulated the QS global switches LuxO and HapR, as well as other virulence genes includingct,tcp, andhapA.In silicomolecular docking simulation of RMA46 ethyl acetate extract with LuxO and HapR revealed that 2-methoxy-4-vinylphenol and hexahydro-3-(phenylmethyl)-pyrrolo[1,2-a]pyrazine-1,4-dione could interact with the active sites of LuxO and HapR and potentially inhibit them. This study highlightsMicromonosporasp. RMA46 as a potential source of anti-infectives againstV. cholerae.-
dc.languageeng-
dc.publisherFrontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/microbiology/-
dc.relation.ispartofFrontiers in Microbiology-
dc.rightsThis Document is Protected by copyright and was first published by Frontiers. All rights reserved. It is reproduced with permission.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectanti-infectives-
dc.subjectanti-virulence-
dc.subjectanti-biofilm-
dc.subjectrare marine Actinobacteria-
dc.subjectMicromonosporaspecies-
dc.titleExploration of Anti-infectives From Mangrove-Derived Micromonospora sp. RMA46 to Combat Vibrio cholerae Pathogenesis-
dc.typeArticle-
dc.identifier.emailNeelakantan, P: prasanna@hku.hk-
dc.identifier.authorityNeelakantan, P=rp02214-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3389/fmicb.2020.01393-
dc.identifier.pmid32765430-
dc.identifier.pmcidPMC7381277-
dc.identifier.scopuseid_2-s2.0-85088515031-
dc.identifier.hkuros321922-
dc.identifier.volume11-
dc.identifier.spagearticle no. 1393-
dc.identifier.epagearticle no. 1393-
dc.identifier.isiWOS:000555903700001-
dc.publisher.placeSwitzerland-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats