Assessment of the growth inhibition and anti-biofilm activity of aptamer (PmA2G02) against Proteus mirabilis 1429T

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Rajalakshmi Elumalai , Archana Vishwakarma , Anandkumar Balakrishnan , Mohandass Ramya
{"title":"Assessment of the growth inhibition and anti-biofilm activity of aptamer (PmA2G02) against Proteus mirabilis 1429T","authors":"Rajalakshmi Elumalai ,&nbsp;Archana Vishwakarma ,&nbsp;Anandkumar Balakrishnan ,&nbsp;Mohandass Ramya","doi":"10.1016/j.resmic.2023.104105","DOIUrl":null,"url":null,"abstract":"<div><p><span><em>Proteus </em><em>mirabilis</em></span><span> is known to cause Catheter-associated urinary tract infections (CAUTIs), which exhibit virulence factors linked to forming biofilms. Aptamers have recently been explored as potential anti-biofilm agents. This study demonstrates the anti-biofilm activity of aptamer (PmA2G02) targeting </span><em>P. mirabilis</em> 1429<sup>T</sup><span><span>, a pathogenic bacteria known to cause Catheter-associated urinary tract infections (CAUTIs). The studied aptamer inhibited biofilm formation, swarming motility<span>, and cell viability<span> at a concentration of 3 μM. The study also showed that the PmA2G02 had a binding affinity towards fimbrial </span></span></span>outer membrane usher protein (</span><em>PMI1466</em><span>), flagellin protein (</span><em>PMI1619</em>), and regulator of swarming behavior (<em>rsbA</em><span>), which are responsible for adhesion, motility, and quorum sensing, respectively. Crystal violet assay, SEM, and confocal imaging confirmed the effectiveness of the PmA2G02 as an anti-biofilm agent. Moreover, as verified by qPCR, the expression levels of </span><em>fimD</em>, <em>fliC2</em>, and <em>rsbA</em> were significantly reduced compared to the untreated group. This study suggests that aptamer may be a potential alternative to traditional antibiotics for the treatment of CAUTIs caused by <em>P. mirabilis</em>. These findings shed light on the mechanisms by which the aptamer inhibits biofilm formation.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0923250823000803","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Proteus mirabilis is known to cause Catheter-associated urinary tract infections (CAUTIs), which exhibit virulence factors linked to forming biofilms. Aptamers have recently been explored as potential anti-biofilm agents. This study demonstrates the anti-biofilm activity of aptamer (PmA2G02) targeting P. mirabilis 1429T, a pathogenic bacteria known to cause Catheter-associated urinary tract infections (CAUTIs). The studied aptamer inhibited biofilm formation, swarming motility, and cell viability at a concentration of 3 μM. The study also showed that the PmA2G02 had a binding affinity towards fimbrial outer membrane usher protein (PMI1466), flagellin protein (PMI1619), and regulator of swarming behavior (rsbA), which are responsible for adhesion, motility, and quorum sensing, respectively. Crystal violet assay, SEM, and confocal imaging confirmed the effectiveness of the PmA2G02 as an anti-biofilm agent. Moreover, as verified by qPCR, the expression levels of fimD, fliC2, and rsbA were significantly reduced compared to the untreated group. This study suggests that aptamer may be a potential alternative to traditional antibiotics for the treatment of CAUTIs caused by P. mirabilis. These findings shed light on the mechanisms by which the aptamer inhibits biofilm formation.

适体(PmA2G02)对奇异变形杆菌1429T的生长抑制和抗生物膜活性的评估。
奇异变形杆菌已知会引起导管相关尿路感染(CAUTIs),这种感染表现出与形成生物膜有关的毒力因子。适体最近被探索为潜在的抗生物膜剂。本研究证明了适体(PmA2G02)针对奇异紫外假单胞菌1429T的抗生物膜活性,奇异紫外菌株是一种已知引起导管相关尿路感染(CAUTIs)的病原菌。所研究的适体在3μM的浓度下抑制生物膜的形成、群集运动和细胞活力。研究还表明,PmA2G02对菌毛外膜引座蛋白(PMI1466)、鞭毛蛋白(PMI619)和群集行为调节因子(rsbA)具有结合亲和力,它们分别负责粘附、运动和群体感应。结晶紫分析、SEM和共聚焦成像证实了PmA2G02作为抗生物膜剂的有效性。此外,通过qPCR验证,与未治疗组相比,fimD、fliC2和rsbA的表达水平显著降低。这项研究表明,适体可能是传统抗生素的一种潜在替代品,可用于治疗奇异假单胞菌引起的CAUTI。这些发现揭示了适体抑制生物膜形成的机制。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
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