The periplasmic protein HslJ is the first-line of defense against oxidative stress in Acinetobacter baumannii.

IF 4.3 2区 生物学 Q1 BIOLOGY
Daniela Scribano, Martina Pasqua, Dolores Limongi, Lucia Nencioni, Anna Teresa Palamara, Cecilia Ambrosi
{"title":"The periplasmic protein HslJ is the first-line of defense against oxidative stress in Acinetobacter baumannii.","authors":"Daniela Scribano, Martina Pasqua, Dolores Limongi, Lucia Nencioni, Anna Teresa Palamara, Cecilia Ambrosi","doi":"10.1186/s40659-025-00584-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Acinetobacter baumannii poses a significant threat globally, causing infections primarily in healthcare settings, with high mortality rates. Its adaptability to antibiotic resistance and tolerance to various stresses, including reactive oxygen species (ROS), contribute to its persistence in healthcare environments. Previous evidence suggested that the periplasmic heat shock protein, HslJ-like protein (ABUW_2868), could be involved in oxidative stress defense in A. baumannii. In this study, we demonstrate the pivotal function of HslJ as the first line of defense against oxidative damage induced by hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>).</p><p><strong>Methods: </strong>An isogenic site-specific hslJ mutant of A. baumannii AB5075 was used to evaluate its sensitivity to H<sub>2</sub>O<sub>2</sub>, survival rate in human macrophages, biofilm, cell surface hydrophobicity, and motility. Additionally, the hslJ expression profile was measured under stress conditions and its OxyR-dependent regulation was assessed both in vitro and in a heterologous host.</p><p><strong>Results: </strong>Herein, we report that HslJ is under the positive regulatory control of OxyR, which upregulates its expression in response to imipenem (IMP) and H<sub>2</sub>O<sub>2</sub>, thereby underscoring its importance in A. baumannii survival strategy. In addition, our findings revealed that the hslJ mutant displayed abrogated surface-associated motility accompanied by increased cell surface hydrophobicity (CSH), indicating also a role in maintaining cell membrane properties.</p><p><strong>Conclusions: </strong>This comprehensive understanding of HslJ multifaceted role not only enriches our knowledge of A. baumannii stress response mechanisms but also provides valuable insights for developing targeted strategies to eradicate this deadly resilient pathogen in healthcare settings.</p>","PeriodicalId":9084,"journal":{"name":"Biological Research","volume":"58 1","pages":"2"},"PeriodicalIF":4.3000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11724541/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s40659-025-00584-8","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Acinetobacter baumannii poses a significant threat globally, causing infections primarily in healthcare settings, with high mortality rates. Its adaptability to antibiotic resistance and tolerance to various stresses, including reactive oxygen species (ROS), contribute to its persistence in healthcare environments. Previous evidence suggested that the periplasmic heat shock protein, HslJ-like protein (ABUW_2868), could be involved in oxidative stress defense in A. baumannii. In this study, we demonstrate the pivotal function of HslJ as the first line of defense against oxidative damage induced by hydrogen peroxide (H2O2).

Methods: An isogenic site-specific hslJ mutant of A. baumannii AB5075 was used to evaluate its sensitivity to H2O2, survival rate in human macrophages, biofilm, cell surface hydrophobicity, and motility. Additionally, the hslJ expression profile was measured under stress conditions and its OxyR-dependent regulation was assessed both in vitro and in a heterologous host.

Results: Herein, we report that HslJ is under the positive regulatory control of OxyR, which upregulates its expression in response to imipenem (IMP) and H2O2, thereby underscoring its importance in A. baumannii survival strategy. In addition, our findings revealed that the hslJ mutant displayed abrogated surface-associated motility accompanied by increased cell surface hydrophobicity (CSH), indicating also a role in maintaining cell membrane properties.

Conclusions: This comprehensive understanding of HslJ multifaceted role not only enriches our knowledge of A. baumannii stress response mechanisms but also provides valuable insights for developing targeted strategies to eradicate this deadly resilient pathogen in healthcare settings.

质周蛋白HslJ是鲍曼不动杆菌抗氧化应激的第一道防线。
背景:鲍曼不动杆菌在全球范围内构成重大威胁,主要在卫生保健机构引起感染,死亡率高。它对抗生素耐药性的适应性和对各种应激的耐受性,包括活性氧(ROS),有助于其在医疗保健环境中的持久性。先前的证据表明,鲍曼不动杆菌的质周热休克蛋白hslj样蛋白(ABUW_2868)可能参与氧化应激防御。在这项研究中,我们证明了HslJ作为抗过氧化氢(H2O2)诱导的氧化损伤的第一道防线的关键功能。方法:采用鲍曼不动杆菌hslJ等基因位点特异性突变体AB5075,评价其对H2O2的敏感性、在人巨噬细胞中的存活率、生物膜、细胞表面疏水性和运动性。此外,我们还测量了应激条件下hslJ的表达谱,并在体外和异源宿主中评估了其依赖于oxyr的调控。结果:本文报道了HslJ受OxyR的正调控,在亚胺培南(IMP)和H2O2的作用下,HslJ的表达上调,从而强调了其在鲍曼不动杆菌生存策略中的重要性。此外,我们的研究结果显示,hslJ突变体表现出与表面相关的运动性减弱,并伴有细胞表面疏水性(CSH)的增加,这也表明它在维持细胞膜特性方面发挥作用。结论:对HslJ多方面作用的全面了解不仅丰富了我们对鲍曼不饱和杆菌应激反应机制的了解,而且为制定有针对性的策略根除这种致命的弹性病原体提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biological Research
Biological Research 生物-生物学
CiteScore
10.10
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Biological Research is an open access, peer-reviewed journal that encompasses diverse fields of experimental biology, such as biochemistry, bioinformatics, biotechnology, cell biology, cancer, chemical biology, developmental biology, evolutionary biology, genetics, genomics, immunology, marine biology, microbiology, molecular biology, neuroscience, plant biology, physiology, stem cell research, structural biology and systems biology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信