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Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition

Prodigiosin, a red linear tripyrrole pigment, has long been recognised for its antimicrobial property. However, the physiological contribution of prodigiosin to the survival of its producing hosts still remains undefined. Hence, the aim of this study was to investigate the biological role of prodigi...

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Autores principales: Yip, Chee-Hoo, Mahalingam, Sobina, Wan, Kiew-Lian, Nathan, Sheila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221495/
https://www.ncbi.nlm.nih.gov/pubmed/34161391
http://dx.doi.org/10.1371/journal.pone.0253445
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author Yip, Chee-Hoo
Mahalingam, Sobina
Wan, Kiew-Lian
Nathan, Sheila
author_facet Yip, Chee-Hoo
Mahalingam, Sobina
Wan, Kiew-Lian
Nathan, Sheila
author_sort Yip, Chee-Hoo
collection PubMed
description Prodigiosin, a red linear tripyrrole pigment, has long been recognised for its antimicrobial property. However, the physiological contribution of prodigiosin to the survival of its producing hosts still remains undefined. Hence, the aim of this study was to investigate the biological role of prodigiosin from Serratia marcescens, particularly in microbial competition through its antimicrobial activity, towards the growth and secreted virulence factors of four clinical pathogenic bacteria (methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus faecalis, Salmonella enterica serovar Typhimurium and Pseudomonas aeruginosa) as well as Staphylococcus aureus and Escherichia coli. Prodigiosin was first extracted from S. marcescens and its purity confirmed by absorption spectrum, high performance liquid chromatography (HPLC) and liquid chromatography-tandem mass spectrophotometry (LC-MS/MS). The extracted prodigiosin was antagonistic towards all the tested bacteria. A disc-diffusion assay showed that prodigiosin is more selective towards Gram-positive bacteria and inhibited the growth of MRSA, S. aureus and E. faecalis and Gram-negative E. coli. A minimum inhibitory concentration of 10 μg/μL of prodigiosin was required to inhibit the growth of S. aureus, E. coli and E. faecalis whereas > 10 μg/μL was required to inhibit MRSA growth. We further assessed the effect of prodigiosin towards bacterial virulence factors such as haemolysin and production of protease as well as on biofilm formation. Prodigiosin did not inhibit haemolysis activity of clinically associated bacteria but was able to reduce protease activity for MRSA, E. coli and E. faecalis as well as decrease E. faecalis, Salmonella Typhimurium and E. coli biofilm formation. Results of this study show that in addition to its role in inhibiting bacterial growth, prodigiosin also inhibits the bacterial virulence factor protease production and biofilm formation, two strategies employed by bacteria in response to microbial competition. As clinical pathogens were more resistant to prodigiosin, we propose that prodigiosin is physiologically important for S. marcescens to compete against other bacteria in its natural soil and surface water environments.
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spelling pubmed-82214952021-07-07 Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition Yip, Chee-Hoo Mahalingam, Sobina Wan, Kiew-Lian Nathan, Sheila PLoS One Research Article Prodigiosin, a red linear tripyrrole pigment, has long been recognised for its antimicrobial property. However, the physiological contribution of prodigiosin to the survival of its producing hosts still remains undefined. Hence, the aim of this study was to investigate the biological role of prodigiosin from Serratia marcescens, particularly in microbial competition through its antimicrobial activity, towards the growth and secreted virulence factors of four clinical pathogenic bacteria (methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus faecalis, Salmonella enterica serovar Typhimurium and Pseudomonas aeruginosa) as well as Staphylococcus aureus and Escherichia coli. Prodigiosin was first extracted from S. marcescens and its purity confirmed by absorption spectrum, high performance liquid chromatography (HPLC) and liquid chromatography-tandem mass spectrophotometry (LC-MS/MS). The extracted prodigiosin was antagonistic towards all the tested bacteria. A disc-diffusion assay showed that prodigiosin is more selective towards Gram-positive bacteria and inhibited the growth of MRSA, S. aureus and E. faecalis and Gram-negative E. coli. A minimum inhibitory concentration of 10 μg/μL of prodigiosin was required to inhibit the growth of S. aureus, E. coli and E. faecalis whereas > 10 μg/μL was required to inhibit MRSA growth. We further assessed the effect of prodigiosin towards bacterial virulence factors such as haemolysin and production of protease as well as on biofilm formation. Prodigiosin did not inhibit haemolysis activity of clinically associated bacteria but was able to reduce protease activity for MRSA, E. coli and E. faecalis as well as decrease E. faecalis, Salmonella Typhimurium and E. coli biofilm formation. Results of this study show that in addition to its role in inhibiting bacterial growth, prodigiosin also inhibits the bacterial virulence factor protease production and biofilm formation, two strategies employed by bacteria in response to microbial competition. As clinical pathogens were more resistant to prodigiosin, we propose that prodigiosin is physiologically important for S. marcescens to compete against other bacteria in its natural soil and surface water environments. Public Library of Science 2021-06-23 /pmc/articles/PMC8221495/ /pubmed/34161391 http://dx.doi.org/10.1371/journal.pone.0253445 Text en © 2021 Yip et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yip, Chee-Hoo
Mahalingam, Sobina
Wan, Kiew-Lian
Nathan, Sheila
Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title_full Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title_fullStr Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title_full_unstemmed Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title_short Prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
title_sort prodigiosin inhibits bacterial growth and virulence factors as a potential physiological response to interspecies competition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221495/
https://www.ncbi.nlm.nih.gov/pubmed/34161391
http://dx.doi.org/10.1371/journal.pone.0253445
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