Comparison of the expression of small regulatory RNAs AS1974, AS2779, IGR2780 and the Hfq gene in carbapenem-resistant and susceptible clinical isolates of Pseudomonas aeruginosa.

IF 5.4 2区 生物学 Q2 MICROBIOLOGY
Fatemeh Keivanpour, Mohammad Hashemzadeh, Mohammad Savari
{"title":"Comparison of the expression of small regulatory RNAs AS1974, AS2779, IGR2780 and the Hfq gene in carbapenem-resistant and susceptible clinical isolates of Pseudomonas aeruginosa.","authors":"Fatemeh Keivanpour, Mohammad Hashemzadeh, Mohammad Savari","doi":"10.1186/s12866-026-05380-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Small regulatory RNAs regulate many physiological processes, such as quorum sensing, iron homeostasis, and biofilm formation in Pseudomonas aeruginosa. This study aimed to investigate the expressions of sRNAs AS1974, AS2779, IGR2780, and Hfq in carbapenem-resistant and susceptible clinical isolates of P. aeruginosa.</p><p><strong>Methods: </strong>Clinical isolates of P. aeruginosa were inoculated onto cetrimide agar and incubated for 24 h, and were identified using standard microbiology tests. Final confirmation of the bacteria was performed using PCR amplification of gyrB. The antibiotic resistance pattern was evaluated using disk diffusion method. The expressions of sRNAs AS1974, AS2779, IGR2780, and Hfq were assessed by real-time reverse transcription polymerase chain reaction.</p><p><strong>Results: </strong>Overall, 80 isolates of P. aeruginosa were confirmed by phenotypic tests and PCR of gyrB. The results showed that 25% (N = 20) and 75% (N = 60) isolates of P. aeruginosa were carbapenem-susceptible and carbapenem-resistant, respectively. The presence of sRNAs AS1974, AS2779, IGR2780, and Hfq genes were confirmed in 80 clinical isolates of P. aeruginosa using PCR. The expressions of sRNAs AS1974, AS2779, and IGR2780 were decreased in carbapenem-resistant isolates compared to susceptible isolates of P. aeruginosa. hfq had significant increase in expression in carbapenem-resistant isolates compared to susceptible isolates of P. aeruginosa.</p><p><strong>Conclusions: </strong>The results of our study confirmed the regulatory role of sRNAs in antibiotic resistance among clinical isolates of P. aeruginosa. Further studies are needed to verify and determine the details of this regulatory role.</p>","PeriodicalId":9233,"journal":{"name":"BMC Microbiology","volume":" ","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2026-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13647858/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12866-026-05380-2","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Small regulatory RNAs regulate many physiological processes, such as quorum sensing, iron homeostasis, and biofilm formation in Pseudomonas aeruginosa. This study aimed to investigate the expressions of sRNAs AS1974, AS2779, IGR2780, and Hfq in carbapenem-resistant and susceptible clinical isolates of P. aeruginosa.

Methods: Clinical isolates of P. aeruginosa were inoculated onto cetrimide agar and incubated for 24 h, and were identified using standard microbiology tests. Final confirmation of the bacteria was performed using PCR amplification of gyrB. The antibiotic resistance pattern was evaluated using disk diffusion method. The expressions of sRNAs AS1974, AS2779, IGR2780, and Hfq were assessed by real-time reverse transcription polymerase chain reaction.

Results: Overall, 80 isolates of P. aeruginosa were confirmed by phenotypic tests and PCR of gyrB. The results showed that 25% (N = 20) and 75% (N = 60) isolates of P. aeruginosa were carbapenem-susceptible and carbapenem-resistant, respectively. The presence of sRNAs AS1974, AS2779, IGR2780, and Hfq genes were confirmed in 80 clinical isolates of P. aeruginosa using PCR. The expressions of sRNAs AS1974, AS2779, and IGR2780 were decreased in carbapenem-resistant isolates compared to susceptible isolates of P. aeruginosa. hfq had significant increase in expression in carbapenem-resistant isolates compared to susceptible isolates of P. aeruginosa.

Conclusions: The results of our study confirmed the regulatory role of sRNAs in antibiotic resistance among clinical isolates of P. aeruginosa. Further studies are needed to verify and determine the details of this regulatory role.

小调控rna AS1974、AS2779、IGR2780和Hfq基因在铜绿假单胞菌碳青霉烯耐药和敏感临床分离株中的表达比较
背景:在铜绿假单胞菌中,小调控rna调节许多生理过程,如群体感应、铁稳态和生物膜形成。本研究旨在探讨sRNAs AS1974、AS2779、IGR2780和Hfq在绿脓杆菌碳青霉烯耐药和敏感临床分离株中的表达。方法:将临床分离的铜绿假单胞菌接种于头孢啶脂琼脂上孵育24 h,采用标准微生物学方法进行鉴定。利用gyrB的PCR扩增对细菌进行最终确认。采用纸片扩散法评价耐药模式。实时逆转录聚合酶链反应检测sRNAs AS1974、AS2779、IGR2780和Hfq的表达。结果:共分离得到80株铜绿假单胞菌。结果表明,25% (N = 20)的铜绿假单胞菌对碳青霉烯敏感,75% (N = 60)的菌株对碳青霉烯耐药。采用PCR方法,在80株铜绿假单胞菌临床分离株中检测到AS1974、AS2779、IGR2780和Hfq基因。与P. aeruginosa敏感株相比,碳青霉烯耐药株的sRNAs AS1974、AS2779和IGR2780的表达量降低。与P. aeruginosa敏感菌株相比,hfq在碳青霉烯耐药菌株中的表达显著增加。结论:我们的研究结果证实了sRNAs在铜绿假单胞菌临床分离株抗生素耐药性中的调节作用。需要进一步的研究来验证和确定这种调节作用的细节。
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
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
×
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:604180095
Book学术官方微信
小红书