Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile

<p>Abstract</p> <p>Background</p> <p><it>Staphylococcus epidermidis </it>has emerged as one of the most important nosocomial pathogens, mainly because of its ability to colonize implanted biomaterials by forming a biofilm. Extensive studies are focused on th...

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Main Authors: Yu Fangyou, Hu Jian, Wu Yang, Lou Qiang, Zhu Tao, Qu Di
Format: Article
Language:English
Published: BMC 2010-11-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/10/287
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author Yu Fangyou
Hu Jian
Wu Yang
Lou Qiang
Zhu Tao
Qu Di
author_facet Yu Fangyou
Hu Jian
Wu Yang
Lou Qiang
Zhu Tao
Qu Di
author_sort Yu Fangyou
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p><it>Staphylococcus epidermidis </it>has emerged as one of the most important nosocomial pathogens, mainly because of its ability to colonize implanted biomaterials by forming a biofilm. Extensive studies are focused on the molecular mechanisms involved in biofilm formation. The LytSR two-component regulatory system regulates autolysis and biofilm formation in <it>Staphylococcus aureus</it>. However, the role of LytSR played in <it>S. epidermidis </it>remained unknown.</p> <p>Results</p> <p>In the present study, we demonstrated that <it>lytSR </it>knock-out in <it>S. epidermidis </it>did not alter susceptibility to Triton X-100 induced autolysis. Quantitative murein hydrolase assay indicated that disruption of <it>lytSR </it>in <it>S. epidermidis </it>resulted in decreased activities of extracellular murein hydrolases, although zymogram showed no apparent differences in murein hydrolase patterns between <it>S. epidermidis </it>strain 1457 and its <it>lytSR </it>mutant. Compared to the wild-type counterpart, 1457<it>ΔlytSR</it> produced slightly more biofilm, with significantly decreased dead cells inside. Microarray analysis showed that <it>lytSR </it>mutation affected the transcription of 164 genes (123 genes were upregulated and 41 genes were downregulated). Specifically, genes encoding proteins responsible for protein synthesis, energy metabolism were downregulated, while genes involved in amino acid and nucleotide biosynthesis, amino acid transporters were upregulated. Impaired ability to utilize pyruvate and reduced activity of arginine deiminase was observed in 1457<it>ΔlytSR</it>, which is consistent with the microarray data.</p> <p>Conclusions</p> <p>The preliminary results suggest that in <it>S. epidermidis </it>LytSR two-component system regulates extracellular murein hydrolase activity, bacterial cell death and pyruvate utilization. Based on the microarray data, it appears that <it>lytSR </it>inactivation induces a stringent response. In addition, LytSR may indirectly enhance biofilm formation by altering the metabolic status of the bacteria.</p>
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spelling doaj.art-3dd3a5392d754a0292671da8c0fc67a52022-12-21T18:09:50ZengBMCBMC Microbiology1471-21802010-11-0110128710.1186/1471-2180-10-287Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profileYu FangyouHu JianWu YangLou QiangZhu TaoQu Di<p>Abstract</p> <p>Background</p> <p><it>Staphylococcus epidermidis </it>has emerged as one of the most important nosocomial pathogens, mainly because of its ability to colonize implanted biomaterials by forming a biofilm. Extensive studies are focused on the molecular mechanisms involved in biofilm formation. The LytSR two-component regulatory system regulates autolysis and biofilm formation in <it>Staphylococcus aureus</it>. However, the role of LytSR played in <it>S. epidermidis </it>remained unknown.</p> <p>Results</p> <p>In the present study, we demonstrated that <it>lytSR </it>knock-out in <it>S. epidermidis </it>did not alter susceptibility to Triton X-100 induced autolysis. Quantitative murein hydrolase assay indicated that disruption of <it>lytSR </it>in <it>S. epidermidis </it>resulted in decreased activities of extracellular murein hydrolases, although zymogram showed no apparent differences in murein hydrolase patterns between <it>S. epidermidis </it>strain 1457 and its <it>lytSR </it>mutant. Compared to the wild-type counterpart, 1457<it>ΔlytSR</it> produced slightly more biofilm, with significantly decreased dead cells inside. Microarray analysis showed that <it>lytSR </it>mutation affected the transcription of 164 genes (123 genes were upregulated and 41 genes were downregulated). Specifically, genes encoding proteins responsible for protein synthesis, energy metabolism were downregulated, while genes involved in amino acid and nucleotide biosynthesis, amino acid transporters were upregulated. Impaired ability to utilize pyruvate and reduced activity of arginine deiminase was observed in 1457<it>ΔlytSR</it>, which is consistent with the microarray data.</p> <p>Conclusions</p> <p>The preliminary results suggest that in <it>S. epidermidis </it>LytSR two-component system regulates extracellular murein hydrolase activity, bacterial cell death and pyruvate utilization. Based on the microarray data, it appears that <it>lytSR </it>inactivation induces a stringent response. In addition, LytSR may indirectly enhance biofilm formation by altering the metabolic status of the bacteria.</p>http://www.biomedcentral.com/1471-2180/10/287
spellingShingle Yu Fangyou
Hu Jian
Wu Yang
Lou Qiang
Zhu Tao
Qu Di
Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
BMC Microbiology
title Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
title_full Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
title_fullStr Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
title_full_unstemmed Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
title_short Impact of the <it>Staphylococcus epidermidis </it>LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile
title_sort impact of the it staphylococcus epidermidis it lytsr two component regulatory system on murein hydrolase activity pyruvate utilization and global transcriptional profile
url http://www.biomedcentral.com/1471-2180/10/287
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