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Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida
ABSTRACT: Carbohydrate metabolism of bacterial pathogens conducts crucial roles in regulating pathogenesis but the molecular mechanisms by which metabolisms and virulence are been modulated and coordinated remain to be illuminated. Here, we investigated in this regard Edwardsiella piscicida, a notor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881556/ https://www.ncbi.nlm.nih.gov/pubmed/35218391 http://dx.doi.org/10.1007/s00253-022-11848-8 |
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author | Mao, Qiaoqiao Jiang, Jihao Wu, Xiao Xu, Rongjing Ma, Yue Zhang, Yuanxing Shao, Shuai Wang, Qiyao |
author_facet | Mao, Qiaoqiao Jiang, Jihao Wu, Xiao Xu, Rongjing Ma, Yue Zhang, Yuanxing Shao, Shuai Wang, Qiyao |
author_sort | Mao, Qiaoqiao |
collection | PubMed |
description | ABSTRACT: Carbohydrate metabolism of bacterial pathogens conducts crucial roles in regulating pathogenesis but the molecular mechanisms by which metabolisms and virulence are been modulated and coordinated remain to be illuminated. Here, we investigated in this regard Edwardsiella piscicida, a notorious zoonotic pathogen previously named E. tarda that could ferment very few PTS sugars including glucose, fructose, mannose, N-acetylglucosamine, and N-acetylgalactosamine. We systematically characterized the roles of each of the predicted 23 components of phosphotransferase system (PTS) with the respective in-frame deletion mutants and defined medium containing specific PTS sugar. In addition, PtsH was identified as the crucial PTS component potentiating the utilization of all the tested PTS sugars. Intriguingly, we also found that PtsH while not Fpr was involved in T3SS gene expression and was essential for the pathogenesis of E. piscicida. To corroborate this, His15 and Ser46, the two established PtsH residues involved in phosphorylation cascade, showed redundant roles in regulating T3SS yields. Moreover, PtsH was shown to facilitate mannose uptake and transform it into mannose-6-phosphate, an allosteric substrate established to activate EvrA to augment bacterial virulence. Collectively, our observations provide new insights into the roles of PTS reciprocally regulating carbohydrate metabolism and virulence gene expression. KEY POINTS: • PTS components’ roles for sugar uptake are systematically determined in Edwardsiella piscicida. • PtsH is involved in saccharides uptake and in the regulation of E. piscicida’s T3SS expression. • PtsH phosphorylation at His15 and Ser46 is essential for the T3SS expression and virulence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11848-8. |
format | Online Article Text |
id | pubmed-8881556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-88815562022-02-28 Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida Mao, Qiaoqiao Jiang, Jihao Wu, Xiao Xu, Rongjing Ma, Yue Zhang, Yuanxing Shao, Shuai Wang, Qiyao Appl Microbiol Biotechnol Applied Genetics and Molecular Biotechnology ABSTRACT: Carbohydrate metabolism of bacterial pathogens conducts crucial roles in regulating pathogenesis but the molecular mechanisms by which metabolisms and virulence are been modulated and coordinated remain to be illuminated. Here, we investigated in this regard Edwardsiella piscicida, a notorious zoonotic pathogen previously named E. tarda that could ferment very few PTS sugars including glucose, fructose, mannose, N-acetylglucosamine, and N-acetylgalactosamine. We systematically characterized the roles of each of the predicted 23 components of phosphotransferase system (PTS) with the respective in-frame deletion mutants and defined medium containing specific PTS sugar. In addition, PtsH was identified as the crucial PTS component potentiating the utilization of all the tested PTS sugars. Intriguingly, we also found that PtsH while not Fpr was involved in T3SS gene expression and was essential for the pathogenesis of E. piscicida. To corroborate this, His15 and Ser46, the two established PtsH residues involved in phosphorylation cascade, showed redundant roles in regulating T3SS yields. Moreover, PtsH was shown to facilitate mannose uptake and transform it into mannose-6-phosphate, an allosteric substrate established to activate EvrA to augment bacterial virulence. Collectively, our observations provide new insights into the roles of PTS reciprocally regulating carbohydrate metabolism and virulence gene expression. KEY POINTS: • PTS components’ roles for sugar uptake are systematically determined in Edwardsiella piscicida. • PtsH is involved in saccharides uptake and in the regulation of E. piscicida’s T3SS expression. • PtsH phosphorylation at His15 and Ser46 is essential for the T3SS expression and virulence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11848-8. Springer Berlin Heidelberg 2022-02-26 2022 /pmc/articles/PMC8881556/ /pubmed/35218391 http://dx.doi.org/10.1007/s00253-022-11848-8 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Applied Genetics and Molecular Biotechnology Mao, Qiaoqiao Jiang, Jihao Wu, Xiao Xu, Rongjing Ma, Yue Zhang, Yuanxing Shao, Shuai Wang, Qiyao Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title | Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title_full | Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title_fullStr | Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title_full_unstemmed | Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title_short | Coordinate regulation of carbohydrate metabolism and virulence by PtsH in pathogen Edwardsiella piscicida |
title_sort | coordinate regulation of carbohydrate metabolism and virulence by ptsh in pathogen edwardsiella piscicida |
topic | Applied Genetics and Molecular Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881556/ https://www.ncbi.nlm.nih.gov/pubmed/35218391 http://dx.doi.org/10.1007/s00253-022-11848-8 |
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