Project Details
Abstract
Serratia marcescens is an opportunistic human pathogen and causes many nosocomial
infections. In our previous works, by using the transposon mutagenesis, a two
component system RssAB was identified and characterized to involve in the
regulation of swarming behavior and biofilm formation. Through the regulation of
flhDC, the virulence factor, hemolysin, is also impacted by RssAB and thus
RssAB-FlhDC-ShlBA serves as a critical role in pathogenesis of S. marcescens.
Subsequent investigation has identified at least 7 genes that are regulated by RssAB.
These gene products are homologous to some interesting proteins of other pathogens
such as QseBC and CcdAB. Thus in this proposal, we investigate the regulatory
mechanisms of multicelluar behaviors in S. marcescens including swarming, biofilm
formation, and quorum sensing system. We study how two sets of two-component
regulator regulate the swarming process and biofilm formation and to evaluate the
role of QseBC interplay in pathogenesis. In addition, we investigate the
toxin-antitoxin system, CcdAB and persister cells formation and thereby assess their
roles in antibiotics resistance. Furthermore, the proinflammatory effect of S.
marcescens virulence factors, autoinducers, biofilm matrix in host would be addressed.
We are wondering whether the RssAB and QseBC networks involve in the interaction
with macrophages. Hence, the inflammasomes activation by the S. marcescens
infection will be determined. This study will benefit us to develop well strategies to
prevent and control the S. marcescens infection.
Project IDs
Project ID:PC10108-0894
External Project ID:NSC101-2320-B182-023-MY3
External Project ID:NSC101-2320-B182-023-MY3
Status | Finished |
---|---|
Effective start/end date | 01/08/12 → 31/07/13 |
Keywords
- Serratia marcescens
- quorum sensing
- QseBC
- CcdAB
- persister
- biofilm
- inflammasome
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.