RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens

Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dom...

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Veröffentlicht in:Infection and Immunity 2010-11, Vol.78 (11), p.4870-4881
Hauptverfasser: Lin, Chuan-Sheng, Horng, Jim-Tong, Yang, Chun-Hung, Tsai, Yu-Huan, Su, Lin-Hui, Wei, Chia-Fong, Chen, Chang-Chieh, Hsieh, Shang-Chen, Lu, Chia-Chen, Lai, Hsin-Chih
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container_end_page 4881
container_issue 11
container_start_page 4870
container_title Infection and Immunity
container_volume 78
creator Lin, Chuan-Sheng
Horng, Jim-Tong
Yang, Chun-Hung
Tsai, Yu-Huan
Su, Lin-Hui
Wei, Chia-Fong
Chen, Chang-Chieh
Hsieh, Shang-Chen
Lu, Chia-Chen
Lai, Hsin-Chih
description Serratia marcescens has long been recognized as an important opportunistic pathogen, but the underlying pathogenesis mechanism is not completely clear. Here, we report a key pathogenesis pathway in S. marcescens comprising the RssAB two-component system and its downstream elements, FlhDC and the dominant virulence factor hemolysin ShlBA. Expression of shlBA is under the positive control of FlhDC, which is repressed by RssAB signaling. At 37°C, functional RssAB inhibits swarming, represses hemolysin production, and promotes S. marcescens biofilm formation. In comparison, when rssBA is deleted, S. marcescens displays aberrant multicellularity favoring motile swarming with unbridled hemolysin production. Cellular and animal infection models further demonstrate that loss of rssBA transforms this opportunistic pathogen into hypervirulent phenotypes, leading to extensive inflammatory responses coupled with destructive and systemic infection. Hemolysin production is essential in this context. Collectively, a major virulence regulatory pathway is identified in S. marcescens.
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source American Society for Microbiology; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bronchi - cytology
Bronchi - microbiology
Cells, Cultured
Epithelial Cells - microbiology
Gene Expression Regulation, Bacterial
Hemolysin Proteins - genetics
Hemolysin Proteins - metabolism
Hemolysis
Humans
Male
Molecular Pathogenesis
Pneumonia, Bacterial - microbiology
Pneumonia, Bacterial - pathology
Rats
Rats, Sprague-Dawley
Serratia Infections - microbiology
Serratia Infections - pathology
Serratia marcescens
Serratia marcescens - genetics
Serratia marcescens - metabolism
Serratia marcescens - pathogenicity
Signal Transduction
Virulence
title RssAB-FlhDC-ShlBA as a Major Pathogenesis Pathway in Serratia marcescens
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