High-Level Expression of Cell-Surface Signaling System Hxu Enhances Pseudomonas aeruginosa Bloodstream Infection
- Authors
- Yang, Fan; Zhou, Yuchen; Chen, Peishan; Cai, Zeqiong; Yue, Zhuo; Jin, Yongxin; Cheng, Zhihui; Wu, Weihui; Yang, Liang; Ha, Un-Hwan; Bai, Fang
- Issue Date
- 20-10월-2022
- Publisher
- AMER SOC MICROBIOLOGY
- Keywords
- ECF sigma factor; Hxu; Pseudomonas aeruginosa; Rnf; bloodstream infections; cell-surface signaling
- Citation
- INFECTION AND IMMUNITY, v.90, no.10
- Indexed
- SCIE
SCOPUS
- Journal Title
- INFECTION AND IMMUNITY
- Volume
- 90
- Number
- 10
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/145662
- DOI
- 10.1128/iai.00329-22
- ISSN
- 0019-9567
- Abstract
- Bloodstream infections (BSIs) caused by Pseudomonas aeruginosa are associated with a high mortality rate in the clinic. However, the fitness mechanisms responsible for the evolution of virulence factors that facilitate the dissemination of P. aeruginosa to the bloodstream are poorly understood. In this study, a transcriptomic analysis of the BSI-associated P. aeruginosa clinical isolates showed a high-level expression of cell-surface signaling (CSS) system Hxu. Whole-genome sequencing and comparative genomics of these isolates showed that a mutation in rnfE gene was responsible for the elevated expression of the Hxu-CSS pathway. Most importantly, deletion of the hxuIRA gene cluster in a laboratory strain PAO1 reduced its BSI capability while overexpression of the HxuIRA pathway promoted BSI in a murine sepsis model We further demonstrated that multiple components in the blood plasma, including heme, hemoglobin, the heme-scavenging proteins haptoglobin, and hemopexin, as well as the iron-delivery protein transferrin, could activate the Hxu system. Together, these studies suggested that the Hxu-CSS system was an important signal transduction pathway contributing to the adaptive pathogenesis of P. aeruginosa in BSI.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Biotechnology and Bioinformatics > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.