Cargando…

Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba

Burkholderia pseudomallei, an etiological agent of melioidosis is an environmental bacterium that can survive as an intracellular pathogen. The biofilm produced by B. pseudomallei is crucial for cellular pathogenesis of melioidosis. The purpose of this investigation is to explore the role of biofilm...

Descripción completa

Detalles Bibliográficos
Autores principales: Bunma, Chainarong, Noinarin, Parumon, Phetcharaburanin, Jutarop, Chareonsudjai, Sorujsiri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547685/
https://www.ncbi.nlm.nih.gov/pubmed/37789212
http://dx.doi.org/10.1038/s41598-023-43824-1
_version_ 1785115107284484096
author Bunma, Chainarong
Noinarin, Parumon
Phetcharaburanin, Jutarop
Chareonsudjai, Sorujsiri
author_facet Bunma, Chainarong
Noinarin, Parumon
Phetcharaburanin, Jutarop
Chareonsudjai, Sorujsiri
author_sort Bunma, Chainarong
collection PubMed
description Burkholderia pseudomallei, an etiological agent of melioidosis is an environmental bacterium that can survive as an intracellular pathogen. The biofilm produced by B. pseudomallei is crucial for cellular pathogenesis of melioidosis. The purpose of this investigation is to explore the role of biofilm in survival of B. pseudomallei during encounters with Acanthamoeba sp. using B. pseudomallei H777 (a biofilm wild type), M10 (a biofilm defect mutant) and C17 (a biofilm-complemented strain). The results demonstrated similar adhesion to amoebae by both the biofilm wild type and biofilm mutant strains. There was higher initial internalisation, but the difference diminished after longer encounter with the amoeba. Interestingly, confocal laser scanning microscopy demonstrated that pre-formed biofilm of B. pseudomallei H777 and C17 were markedly more persistent in the face of Acanthamoeba sp. grazing than that of M10. Metabolomic analysis revealed a significant increased level of 8-O-4′-diferulic acid, a superoxide scavenger metabolite, in B. pseudomallei H777 serially passaged in Acanthamoeba sp. The interaction between B. pseudomallei with a free-living amoeba may indicate the evolutionary pathway that enables the bacterium to withstand superoxide radicals in intracellular environments. This study supports the hypothesis that B. pseudomallei biofilm persists under grazing by amoebae and suggests a strategy of metabolite production that turns this bacterium from saprophyte to intracellular pathogen.
format Online
Article
Text
id pubmed-10547685
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-105476852023-10-05 Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba Bunma, Chainarong Noinarin, Parumon Phetcharaburanin, Jutarop Chareonsudjai, Sorujsiri Sci Rep Article Burkholderia pseudomallei, an etiological agent of melioidosis is an environmental bacterium that can survive as an intracellular pathogen. The biofilm produced by B. pseudomallei is crucial for cellular pathogenesis of melioidosis. The purpose of this investigation is to explore the role of biofilm in survival of B. pseudomallei during encounters with Acanthamoeba sp. using B. pseudomallei H777 (a biofilm wild type), M10 (a biofilm defect mutant) and C17 (a biofilm-complemented strain). The results demonstrated similar adhesion to amoebae by both the biofilm wild type and biofilm mutant strains. There was higher initial internalisation, but the difference diminished after longer encounter with the amoeba. Interestingly, confocal laser scanning microscopy demonstrated that pre-formed biofilm of B. pseudomallei H777 and C17 were markedly more persistent in the face of Acanthamoeba sp. grazing than that of M10. Metabolomic analysis revealed a significant increased level of 8-O-4′-diferulic acid, a superoxide scavenger metabolite, in B. pseudomallei H777 serially passaged in Acanthamoeba sp. The interaction between B. pseudomallei with a free-living amoeba may indicate the evolutionary pathway that enables the bacterium to withstand superoxide radicals in intracellular environments. This study supports the hypothesis that B. pseudomallei biofilm persists under grazing by amoebae and suggests a strategy of metabolite production that turns this bacterium from saprophyte to intracellular pathogen. Nature Publishing Group UK 2023-10-03 /pmc/articles/PMC10547685/ /pubmed/37789212 http://dx.doi.org/10.1038/s41598-023-43824-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bunma, Chainarong
Noinarin, Parumon
Phetcharaburanin, Jutarop
Chareonsudjai, Sorujsiri
Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title_full Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title_fullStr Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title_full_unstemmed Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title_short Burkholderia pseudomallei biofilm resists Acanthamoeba sp. grazing and produces 8-O-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
title_sort burkholderia pseudomallei biofilm resists acanthamoeba sp. grazing and produces 8-o-4′-diferulic acid, a superoxide scavenging metabolite after passage through the amoeba
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547685/
https://www.ncbi.nlm.nih.gov/pubmed/37789212
http://dx.doi.org/10.1038/s41598-023-43824-1
work_keys_str_mv AT bunmachainarong burkholderiapseudomalleibiofilmresistsacanthamoebaspgrazingandproduces8o4diferulicacidasuperoxidescavengingmetaboliteafterpassagethroughtheamoeba
AT noinarinparumon burkholderiapseudomalleibiofilmresistsacanthamoebaspgrazingandproduces8o4diferulicacidasuperoxidescavengingmetaboliteafterpassagethroughtheamoeba
AT phetcharaburaninjutarop burkholderiapseudomalleibiofilmresistsacanthamoebaspgrazingandproduces8o4diferulicacidasuperoxidescavengingmetaboliteafterpassagethroughtheamoeba
AT chareonsudjaisorujsiri burkholderiapseudomalleibiofilmresistsacanthamoebaspgrazingandproduces8o4diferulicacidasuperoxidescavengingmetaboliteafterpassagethroughtheamoeba