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Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence
Phospholipase C (PLC) enzymes are key virulence factors in several pathogenic bacteria. Burkholderia pseudomallei, the causative agent of melioidosis, possesses at least three plc genes (plc1, plc2 and plc3). We found that in culture medium plc1 gene expression increased with increasing pH, whilst e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648637/ https://www.ncbi.nlm.nih.gov/pubmed/33159122 http://dx.doi.org/10.1038/s41598-020-76186-z |
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author | Srinon, Varintip Withatanung, Patoo Chaiwattanarungruengpaisan, Somjit Thongdee, Metawee Meethai, Chatruthai Stevens, Joanne M. Titball, Richard W. Korbsrisate, Sunee |
author_facet | Srinon, Varintip Withatanung, Patoo Chaiwattanarungruengpaisan, Somjit Thongdee, Metawee Meethai, Chatruthai Stevens, Joanne M. Titball, Richard W. Korbsrisate, Sunee |
author_sort | Srinon, Varintip |
collection | PubMed |
description | Phospholipase C (PLC) enzymes are key virulence factors in several pathogenic bacteria. Burkholderia pseudomallei, the causative agent of melioidosis, possesses at least three plc genes (plc1, plc2 and plc3). We found that in culture medium plc1 gene expression increased with increasing pH, whilst expression of the plc3 gene was pH (4.5 to 9.0) independent. Expression of the plc2 gene was not detected in culture medium. All three plc genes were expressed during macrophage infection by B. pseudomallei K96243. Comparing B. pseudomallei wild-type with plc mutants revealed that plc2, plc12 or plc123 mutants showed reduced intracellular survival in macrophages and reduced plaque formation in HeLa cells. However, plc1 or plc3 mutants showed no significant differences in plaque formation compared to wild-type bacteria. These findings suggest that Plc2, but not Plc1 or Plc3 are required for infection of host cells. In Galleria mellonella, plc1, plc2 or plc3 mutants were not attenuated compared to the wild-type strain, but multiple plc mutants showed reduced virulence. These findings indicate functional redundancy of the B. pseudomallei phospholipases in virulence. |
format | Online Article Text |
id | pubmed-7648637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76486372020-11-12 Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence Srinon, Varintip Withatanung, Patoo Chaiwattanarungruengpaisan, Somjit Thongdee, Metawee Meethai, Chatruthai Stevens, Joanne M. Titball, Richard W. Korbsrisate, Sunee Sci Rep Article Phospholipase C (PLC) enzymes are key virulence factors in several pathogenic bacteria. Burkholderia pseudomallei, the causative agent of melioidosis, possesses at least three plc genes (plc1, plc2 and plc3). We found that in culture medium plc1 gene expression increased with increasing pH, whilst expression of the plc3 gene was pH (4.5 to 9.0) independent. Expression of the plc2 gene was not detected in culture medium. All three plc genes were expressed during macrophage infection by B. pseudomallei K96243. Comparing B. pseudomallei wild-type with plc mutants revealed that plc2, plc12 or plc123 mutants showed reduced intracellular survival in macrophages and reduced plaque formation in HeLa cells. However, plc1 or plc3 mutants showed no significant differences in plaque formation compared to wild-type bacteria. These findings suggest that Plc2, but not Plc1 or Plc3 are required for infection of host cells. In Galleria mellonella, plc1, plc2 or plc3 mutants were not attenuated compared to the wild-type strain, but multiple plc mutants showed reduced virulence. These findings indicate functional redundancy of the B. pseudomallei phospholipases in virulence. Nature Publishing Group UK 2020-11-06 /pmc/articles/PMC7648637/ /pubmed/33159122 http://dx.doi.org/10.1038/s41598-020-76186-z Text en © The Author(s) 2020 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/. |
spellingShingle | Article Srinon, Varintip Withatanung, Patoo Chaiwattanarungruengpaisan, Somjit Thongdee, Metawee Meethai, Chatruthai Stevens, Joanne M. Titball, Richard W. Korbsrisate, Sunee Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title | Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title_full | Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title_fullStr | Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title_full_unstemmed | Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title_short | Functional redundancy of Burkholderia pseudomallei phospholipase C enzymes and their role in virulence |
title_sort | functional redundancy of burkholderia pseudomallei phospholipase c enzymes and their role in virulence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648637/ https://www.ncbi.nlm.nih.gov/pubmed/33159122 http://dx.doi.org/10.1038/s41598-020-76186-z |
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