{"title":"The CueR-regulated transporters CopA and CusFABC coordinate copper detoxification in <i>Vibrio parahaemolyticus</i>.","authors":"Chengkun Zheng, Yimeng Zhai, Mengxian Wang, Zhengzhong Xu, Yunzeng Zhang, Xiaohui Zhou, Xiang Chen, Xinan Jiao","doi":"10.1080/21505594.2025.2545557","DOIUrl":null,"url":null,"abstract":"<p><p><i>Vibrio parahaemolyticus</i> is a zoonotic pathogen that poses a serious threat to shrimp aquaculture and public health worldwide. Copper (Cu) serves as a catalytic cofactor and structural element in bacteria but is toxic in excess. Herein, we report that the CueR-regulated transporters CopA and CusFABC coordinate Cu detoxification in <i>V. parahaemolyticus</i>. Through RNA sequencing, we show that most genes in the CueR and Fur regulons are significantly upregulated during <i>V. parahaemolyticus</i> response to external Cu. Quantitative real-time PCR (qRT-PCR) showed that <i>copA</i> and <i>cusA</i> are strongly induced by Cu. Growth curve analyses and spot dilution assay revealed that CopA and CusFABC protect <i>V. parahaemolyticus</i> against Cu-induced bactericidal effects. Inductively coupled plasma-mass spectrometry revealed that CopA and CusFABC are involved in maintaining Cu and Fe homoeostasis. Additionally, CopA promotes <i>V. parahaemolyticus</i> resistance to pyrithione. In a competitive-infection assay, the <i>copA</i> and <i>cusFABC</i> double mutant, but not the single mutants, was significantly attenuated in colonization of the zebrafish intestine. Lastly, qRT-PCR, RNA sequencing, β-galactosidase activity, and AIDmut-Seq analyses revealed that CueR can bind to the promoters of <i>copA</i> and <i>cusFABC</i>, and positively regulate their expression. Collectively, <i>V. parahaemolyticus</i> utilizes the CueR-regulated transporters CopA and CusFABC to coordinate Cu detoxification and colonization of the zebrafish intestine.</p>","PeriodicalId":23747,"journal":{"name":"Virulence","volume":" ","pages":"2545557"},"PeriodicalIF":5.4000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12341060/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virulence","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/21505594.2025.2545557","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/11 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Vibrio parahaemolyticus is a zoonotic pathogen that poses a serious threat to shrimp aquaculture and public health worldwide. Copper (Cu) serves as a catalytic cofactor and structural element in bacteria but is toxic in excess. Herein, we report that the CueR-regulated transporters CopA and CusFABC coordinate Cu detoxification in V. parahaemolyticus. Through RNA sequencing, we show that most genes in the CueR and Fur regulons are significantly upregulated during V. parahaemolyticus response to external Cu. Quantitative real-time PCR (qRT-PCR) showed that copA and cusA are strongly induced by Cu. Growth curve analyses and spot dilution assay revealed that CopA and CusFABC protect V. parahaemolyticus against Cu-induced bactericidal effects. Inductively coupled plasma-mass spectrometry revealed that CopA and CusFABC are involved in maintaining Cu and Fe homoeostasis. Additionally, CopA promotes V. parahaemolyticus resistance to pyrithione. In a competitive-infection assay, the copA and cusFABC double mutant, but not the single mutants, was significantly attenuated in colonization of the zebrafish intestine. Lastly, qRT-PCR, RNA sequencing, β-galactosidase activity, and AIDmut-Seq analyses revealed that CueR can bind to the promoters of copA and cusFABC, and positively regulate their expression. Collectively, V. parahaemolyticus utilizes the CueR-regulated transporters CopA and CusFABC to coordinate Cu detoxification and colonization of the zebrafish intestine.
期刊介绍:
Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication.
Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.