Role of yceA-cybB-yceB operon in oxidative stress tolerance, swimming motility and antibiotic susceptibility of Stenotrophomonas maltophilia

Author:

Liao Chun-Hsing12ORCID,Ku Ren-Hsuan3,Li Li-Hua45ORCID,Wu Cheng-Mu3,Yang Tsuey-Ching3

Affiliation:

1. Division of Infectious Diseases, Far Eastern Memorial Hospital , New Taipei City, Taiwan , Republic of China

2. Departmentof Medicine, National Yang Ming Chiao Tung University , Taipei, Taiwan , Republic of China

3. Department of Biotechnology and Laboratory Science in Medicine, National Yang Ming Chiao Tung University , Taipei, Taiwan , Republic of China

4. Department of Pathology and Laboratory Medicine, Taipei Veterans General Hospital , Taipei, Taiwan , Republic of China

5. School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University , Taipei, Taiwan , Republic of China

Abstract

Abstract Background Stenotrophomonas maltophilia is ubiquitous in the environment and is an important MDR opportunistic pathogen. Oxidative stress is an inevitable challenge to an aerobic bacterium. Accordingly, S. maltophilia has many capabilities to face variable oxidative stress. Some of the oxidative stress alleviation systems cross-protect bacteria from antibiotics. In our recent RNA-sequencing transcriptome analysis, we documented the increased expression of a three-gene cluster, yceA-cybB-yceB, in the presence of hydrogen peroxide (H2O2). The YceI-like, cytochrome b561 and YceI-like proteins encoded by yceA, cybB and yceB are located in the cytoplasm, inner membrane and periplasm, respectively. Objectives To characterize the role of the yceA-cybB-yceB operon of S. maltophilia in oxidative stress tolerance, swimming motility and antibiotic susceptibility. Methods The presence of the yceA-cybB-yceB operon was verified by RT–PCR. The functions of this operon were revealed by in-frame deletion mutant construction and complementation assay. Expression of the yceA-cybB-yceB operon was assessed by quantitative RT–PCR. Results The yceA, cybB and yceB genes form an operon. Loss of function of the yceA-cybB-yceB operon compromised menadione tolerance, enhanced swimming motility and increased susceptibility to fluoroquinolone and β-lactam antibiotics. The expression of the yceA-cybB-yceB operon was up-regulated by oxidative stress, such as H2O2 and superoxide, and not impacted by antibiotics, such as fluoroquinolone and β-lactams. Conclusions The evidence strongly supports the view that the physiological function of the yceA-cybB-yceB operon is to alleviate oxidative stress. The operon provides an additional example that oxidative stress alleviation systems can cross-protect S. maltophilia from antibiotics.

Funder

National Science and Technology Council of Taiwan

National Yang Ming Chiao Tung University

Far Eastern Memorial Hospital

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Reference43 articles.

1. Biogenesis of respiratory cytochromes in bacteria;Thony-Meyer;Microbiol Mol Biol Rev,1997

2. A unique aromatic residue modulates the redox range of a periplasmic multiheme cytochrome from Geobacter metallireducens;Portela;J Biol Chem,2021

3. Structure and sequence relationships in the lipocalins and related proteins;Flower;Protein Sci,1993

4. Functions and regulation of lipocalin-2 in gut-origin sepsis: a narrative review;Lu;Crit Care,2019

5. The bacterial lipocalins;Bishop;Biochim Biophys Acta,2000

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3