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Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence

BACKGROUND: Sialic acid has been shown to be a major virulence determinant in the pathogenesis of otitis media caused by the bacterium Haemophilus influenzae. This study aimed to characterise the expression of genes required for the metabolism of sialic acid and to investigate the role of these gene...

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Autores principales: Jenkins, Gaynor A, Figueira, Marisol, Kumar, Gaurav A, Sweetman, Wendy A, Makepeace, Katherine, Pelton, Stephen I, Moxon, Richard, Hood, Derek W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836998/
https://www.ncbi.nlm.nih.gov/pubmed/20158882
http://dx.doi.org/10.1186/1471-2180-10-48
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author Jenkins, Gaynor A
Figueira, Marisol
Kumar, Gaurav A
Sweetman, Wendy A
Makepeace, Katherine
Pelton, Stephen I
Moxon, Richard
Hood, Derek W
author_facet Jenkins, Gaynor A
Figueira, Marisol
Kumar, Gaurav A
Sweetman, Wendy A
Makepeace, Katherine
Pelton, Stephen I
Moxon, Richard
Hood, Derek W
author_sort Jenkins, Gaynor A
collection PubMed
description BACKGROUND: Sialic acid has been shown to be a major virulence determinant in the pathogenesis of otitis media caused by the bacterium Haemophilus influenzae. This study aimed to characterise the expression of genes required for the metabolism of sialic acid and to investigate the role of these genes in virulence. RESULTS: Using qRT-PCR, we observed decreased transcriptional activity of genes within a cluster that are required for uptake and catabolism of 5-acetyl neuraminic acid (Neu5Ac), when bacteria were cultured in the presence of the sugar. We show that these uptake and catabolic genes, including a sialic acid regulatory gene (siaR), are highly conserved in the H. influenzae natural population. Mutant strains were constructed for seven of the nine genes and their influence upon LPS sialylation and resistance of the bacteria to the killing effect of normal human serum were assessed. Mutations in the Neu5Ac uptake (TRAP transporter) genes decreased virulence in the chinchilla model of otitis media, but the attenuation was strain dependent. In contrast, mutations in catabolism genes and genes regulating sialic acid metabolism (siaR and crp) did not attenuate virulence. CONCLUSION: The commensal and pathogenic behaviour of H. influenzae involves LPS sialylation that can be influenced by a complex regulatory interplay of sialometabolism genes.
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spelling pubmed-28369982010-03-12 Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence Jenkins, Gaynor A Figueira, Marisol Kumar, Gaurav A Sweetman, Wendy A Makepeace, Katherine Pelton, Stephen I Moxon, Richard Hood, Derek W BMC Microbiol Research article BACKGROUND: Sialic acid has been shown to be a major virulence determinant in the pathogenesis of otitis media caused by the bacterium Haemophilus influenzae. This study aimed to characterise the expression of genes required for the metabolism of sialic acid and to investigate the role of these genes in virulence. RESULTS: Using qRT-PCR, we observed decreased transcriptional activity of genes within a cluster that are required for uptake and catabolism of 5-acetyl neuraminic acid (Neu5Ac), when bacteria were cultured in the presence of the sugar. We show that these uptake and catabolic genes, including a sialic acid regulatory gene (siaR), are highly conserved in the H. influenzae natural population. Mutant strains were constructed for seven of the nine genes and their influence upon LPS sialylation and resistance of the bacteria to the killing effect of normal human serum were assessed. Mutations in the Neu5Ac uptake (TRAP transporter) genes decreased virulence in the chinchilla model of otitis media, but the attenuation was strain dependent. In contrast, mutations in catabolism genes and genes regulating sialic acid metabolism (siaR and crp) did not attenuate virulence. CONCLUSION: The commensal and pathogenic behaviour of H. influenzae involves LPS sialylation that can be influenced by a complex regulatory interplay of sialometabolism genes. BioMed Central 2010-02-16 /pmc/articles/PMC2836998/ /pubmed/20158882 http://dx.doi.org/10.1186/1471-2180-10-48 Text en Copyright ©2010 Jenkins et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Jenkins, Gaynor A
Figueira, Marisol
Kumar, Gaurav A
Sweetman, Wendy A
Makepeace, Katherine
Pelton, Stephen I
Moxon, Richard
Hood, Derek W
Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title_full Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title_fullStr Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title_full_unstemmed Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title_short Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
title_sort sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in haemophilus influenzae and its effect on virulence
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836998/
https://www.ncbi.nlm.nih.gov/pubmed/20158882
http://dx.doi.org/10.1186/1471-2180-10-48
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