Whole-Genome Sequencing of Resistance, Virulence and Regulation Genes in Extremely Resistant Strains of Pseudomonas aeruginosa.

Q1 Medicine
Nerlis Pajaro-Castro, Erick Diaz-Morales, Kenia Hoyos, Cristhian Ibañez-Bersinger
{"title":"Whole-Genome Sequencing of Resistance, Virulence and Regulation Genes in Extremely Resistant Strains of <i>Pseudomonas aeruginosa</i>.","authors":"Nerlis Pajaro-Castro, Erick Diaz-Morales, Kenia Hoyos, Cristhian Ibañez-Bersinger","doi":"10.3390/medsci13010006","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/objectives: </strong><i>Pseudomonas aeruginosa</i> is a clinically significant opportunistic pathogen, renowned for its ability to acquire and develop diverse mechanisms of antibiotic resistance. This study examines the resistance, virulence, and regulatory mechanisms in extensively drug-resistant clinical strains of <i>P. aeruginosa</i>.</p><p><strong>Methods: </strong>Antibiotic susceptibility was assessed using the Minimum Inhibitory Concentration (MIC) method, and whole-genome sequencing (WGS) was performed on the Illumina NovaSeq platform.</p><p><strong>Results: </strong>The analysis demonstrated a higher prevalence of virulence genes compared to resistance and regulatory genes. Key virulence factors identified included secretion systems, motility, adhesion, and biofilm formation. Resistance mechanisms observed comprised efflux pumps and beta-lactamases, while regulatory systems involved two-component systems, transcriptional regulators, and sigma factors. Additionally, phenotypic profiles were found to correlate with resistance genes identified through genotypic analysis.</p><p><strong>Conclusions: </strong>This study underscores the significant resistance and virulence of the clinical <i>P. aeruginosa</i> strains analyzed, highlighting the urgent need for alternative strategies to address infections caused by extensively drug-resistant bacteria.</p>","PeriodicalId":74152,"journal":{"name":"Medical sciences (Basel, Switzerland)","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11755660/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical sciences (Basel, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/medsci13010006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background/objectives: Pseudomonas aeruginosa is a clinically significant opportunistic pathogen, renowned for its ability to acquire and develop diverse mechanisms of antibiotic resistance. This study examines the resistance, virulence, and regulatory mechanisms in extensively drug-resistant clinical strains of P. aeruginosa.

Methods: Antibiotic susceptibility was assessed using the Minimum Inhibitory Concentration (MIC) method, and whole-genome sequencing (WGS) was performed on the Illumina NovaSeq platform.

Results: The analysis demonstrated a higher prevalence of virulence genes compared to resistance and regulatory genes. Key virulence factors identified included secretion systems, motility, adhesion, and biofilm formation. Resistance mechanisms observed comprised efflux pumps and beta-lactamases, while regulatory systems involved two-component systems, transcriptional regulators, and sigma factors. Additionally, phenotypic profiles were found to correlate with resistance genes identified through genotypic analysis.

Conclusions: This study underscores the significant resistance and virulence of the clinical P. aeruginosa strains analyzed, highlighting the urgent need for alternative strategies to address infections caused by extensively drug-resistant bacteria.

铜绿假单胞菌极耐药菌株耐药、毒力及调控基因的全基因组测序。
背景/目的:铜绿假单胞菌是一种临床上重要的机会性病原体,以其获得和发展多种抗生素耐药机制的能力而闻名。本研究探讨了广泛耐药的铜绿假单胞菌临床菌株的耐药性、毒力和调控机制。方法:采用最低抑菌浓度法(MIC)评估抗生素敏感性,在Illumina NovaSeq平台上进行全基因组测序(WGS)。结果:分析表明,毒力基因的流行率高于抗性基因和调控基因。确定的关键毒力因素包括分泌系统、运动性、粘附和生物膜形成。观察到的耐药机制包括外排泵和β -内酰胺酶,而调节系统涉及双组分系统、转录调节因子和sigma因子。此外,表型谱与通过基因型分析鉴定的抗性基因相关。结论:本研究强调了所分析的临床铜绿假单胞菌菌株的显著耐药性和毒力,强调了迫切需要替代策略来解决广泛耐药细菌引起的感染。
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
CiteScore
9.00
自引率
0.00%
发文量
0
审稿时长
6 weeks
×
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