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Streptococcus pneumoniae early response genes to human lung epithelial cells

BACKGROUND: Streptococcus pneumoniae infection starts from colonization of the host respiratory tract where interaction with host respiratory tract epithelial cells occurs. To investigate pneumococcal genes that are involved in the early stage of interaction with host epithelial cells, transcription...

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Detalles Bibliográficos
Autores principales: Song, Xin-Ming, Connor, Wayne, Hokamp, Karsten, Babiuk, Lorne A, Potter, Andrew A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527573/
https://www.ncbi.nlm.nih.gov/pubmed/18710517
http://dx.doi.org/10.1186/1756-0500-1-64
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author Song, Xin-Ming
Connor, Wayne
Hokamp, Karsten
Babiuk, Lorne A
Potter, Andrew A
author_facet Song, Xin-Ming
Connor, Wayne
Hokamp, Karsten
Babiuk, Lorne A
Potter, Andrew A
author_sort Song, Xin-Ming
collection PubMed
description BACKGROUND: Streptococcus pneumoniae infection starts from colonization of the host respiratory tract where interaction with host respiratory tract epithelial cells occurs. To investigate pneumococcal genes that are involved in the early stage of interaction with host epithelial cells, transcriptional responses of an encapsulated pathogenic pneumococcal strain TIGR4 upon exposure to human lung epithelial cells A549 for 0.5 h and 1 h time periods were investigated by using TIGR (JCVI) microarray technology. Gene expression changes were validated by quantitative real-time PCR (qRT-PCR) analysis. FINDINGS: We observed different transcriptional profiles at two incubation time periods in which most gene expressions were down-regulated at 0.5 h but up-regulated at 1 h. Many genes associated with ribonucleotide biosynthesis were down-regulated at both time points, whereas the genes associated with cell envelope, energy metabolism, transport and protein synthesis were mostly up-regulated at 1 h. Furthermore, these profiles were compared to the transcriptomes of a TIGR4-derived strain in response to human macrophages for the same time periods. We found one set of genes that exhibited similar expression changes upon exposure to both types of host cells, including cell envelope-associated bgaA (SP0648) and nanA (SP1693), and uncharacterized gene clusters such as SP1677–SP1680 and SP1688–SP1690. CONCLUSION: These data indicate that at the early stage of interaction with host epithelial cells, a complex gene regulation and expression change occur in bacteria. Some of them might play an essential role during pathogen-host interactions and for the establishment of infection.
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spelling pubmed-25275732008-09-02 Streptococcus pneumoniae early response genes to human lung epithelial cells Song, Xin-Ming Connor, Wayne Hokamp, Karsten Babiuk, Lorne A Potter, Andrew A BMC Res Notes Short Report BACKGROUND: Streptococcus pneumoniae infection starts from colonization of the host respiratory tract where interaction with host respiratory tract epithelial cells occurs. To investigate pneumococcal genes that are involved in the early stage of interaction with host epithelial cells, transcriptional responses of an encapsulated pathogenic pneumococcal strain TIGR4 upon exposure to human lung epithelial cells A549 for 0.5 h and 1 h time periods were investigated by using TIGR (JCVI) microarray technology. Gene expression changes were validated by quantitative real-time PCR (qRT-PCR) analysis. FINDINGS: We observed different transcriptional profiles at two incubation time periods in which most gene expressions were down-regulated at 0.5 h but up-regulated at 1 h. Many genes associated with ribonucleotide biosynthesis were down-regulated at both time points, whereas the genes associated with cell envelope, energy metabolism, transport and protein synthesis were mostly up-regulated at 1 h. Furthermore, these profiles were compared to the transcriptomes of a TIGR4-derived strain in response to human macrophages for the same time periods. We found one set of genes that exhibited similar expression changes upon exposure to both types of host cells, including cell envelope-associated bgaA (SP0648) and nanA (SP1693), and uncharacterized gene clusters such as SP1677–SP1680 and SP1688–SP1690. CONCLUSION: These data indicate that at the early stage of interaction with host epithelial cells, a complex gene regulation and expression change occur in bacteria. Some of them might play an essential role during pathogen-host interactions and for the establishment of infection. BioMed Central 2008-08-12 /pmc/articles/PMC2527573/ /pubmed/18710517 http://dx.doi.org/10.1186/1756-0500-1-64 Text en Copyright © 2008 Song et al; licensee BioMed Central Ltd. 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 Short Report
Song, Xin-Ming
Connor, Wayne
Hokamp, Karsten
Babiuk, Lorne A
Potter, Andrew A
Streptococcus pneumoniae early response genes to human lung epithelial cells
title Streptococcus pneumoniae early response genes to human lung epithelial cells
title_full Streptococcus pneumoniae early response genes to human lung epithelial cells
title_fullStr Streptococcus pneumoniae early response genes to human lung epithelial cells
title_full_unstemmed Streptococcus pneumoniae early response genes to human lung epithelial cells
title_short Streptococcus pneumoniae early response genes to human lung epithelial cells
title_sort streptococcus pneumoniae early response genes to human lung epithelial cells
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527573/
https://www.ncbi.nlm.nih.gov/pubmed/18710517
http://dx.doi.org/10.1186/1756-0500-1-64
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