Characterization of a Clostridioides difficile ST-293 isolate from a recurrent infection in Argentina

IF 1.8 4区 生物学 Q4 MICROBIOLOGY
P. Cecilia Soldavini Pelichotti , Daniela Cejas , Liliana Fernández-Caniggia , Fernando M. Trejo , Pablo F. Pérez
{"title":"Characterization of a Clostridioides difficile ST-293 isolate from a recurrent infection in Argentina","authors":"P. Cecilia Soldavini Pelichotti ,&nbsp;Daniela Cejas ,&nbsp;Liliana Fernández-Caniggia ,&nbsp;Fernando M. Trejo ,&nbsp;Pablo F. Pérez","doi":"10.1016/j.ram.2022.09.004","DOIUrl":null,"url":null,"abstract":"<div><p><em>Clostridioides difficile</em> is an opportunistic spore-forming pathogen responsible for antibiotic-associated diarrhea in humans. <em>C. difficile</em> produces two main toxins: TcdA and TcdB as well as a third toxin named binary toxin (CDT) that is also involved in virulence. The present study aimed at characterizing the <em>C. difficile</em> isolate ALCD3 involved in a relapse episode of nosocomial infection. Molecular characterization showed that isolate ALCD3 belongs to toxinotype 0/v and the MLST analysis demonstrated allelic profile <em>adk:91</em>, <em>atpA:1</em>, <em>dxr:2</em>, <em>glyA: 1</em>, <em>recA:27</em>, <em>sodA: 1</em> and <em>tpi:1</em> which corresponds to ST293 (MLST clade: 1). During growth, isolate ALCD3 showed an early increase in the sporulation ratio as well as maximal values of heat resistant forms after 2 days of incubation. Both sporulation kinetics and production of heat resistant forms were faster for isolate ALCD3 than for the reference strain VPI 10463. Germination in the presence of the natural germinant taurocholate was faster for isolate ALCD3 than for strain VPI 10463, which indicates that isolate ALCD3 starts cortex hydrolysis earlier than strain VPI 10463. Furthermore, the co-germinant glycine, induces rapid release of dipicolinic acid (DPA) in isolate ALCD3. These findings indicate that isolate ALCD3 is particularly efficient in both sporulation and germination. The present work represents the first report of the circulation of <em>C. difficile</em> ST293 in Argentina. The ability of isolate ALCD3 to produce toxins and its high sporulation/germination capacity are key features compatible with a microorganism with high dissemination potential and the possibility of inducing recurrent infections.</p></div>","PeriodicalId":21163,"journal":{"name":"Revista Argentina de microbiologia","volume":null,"pages":null},"PeriodicalIF":1.8000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Argentina de microbiologia","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S032575412200102X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Clostridioides difficile is an opportunistic spore-forming pathogen responsible for antibiotic-associated diarrhea in humans. C. difficile produces two main toxins: TcdA and TcdB as well as a third toxin named binary toxin (CDT) that is also involved in virulence. The present study aimed at characterizing the C. difficile isolate ALCD3 involved in a relapse episode of nosocomial infection. Molecular characterization showed that isolate ALCD3 belongs to toxinotype 0/v and the MLST analysis demonstrated allelic profile adk:91, atpA:1, dxr:2, glyA: 1, recA:27, sodA: 1 and tpi:1 which corresponds to ST293 (MLST clade: 1). During growth, isolate ALCD3 showed an early increase in the sporulation ratio as well as maximal values of heat resistant forms after 2 days of incubation. Both sporulation kinetics and production of heat resistant forms were faster for isolate ALCD3 than for the reference strain VPI 10463. Germination in the presence of the natural germinant taurocholate was faster for isolate ALCD3 than for strain VPI 10463, which indicates that isolate ALCD3 starts cortex hydrolysis earlier than strain VPI 10463. Furthermore, the co-germinant glycine, induces rapid release of dipicolinic acid (DPA) in isolate ALCD3. These findings indicate that isolate ALCD3 is particularly efficient in both sporulation and germination. The present work represents the first report of the circulation of C. difficile ST293 in Argentina. The ability of isolate ALCD3 to produce toxins and its high sporulation/germination capacity are key features compatible with a microorganism with high dissemination potential and the possibility of inducing recurrent infections.

阿根廷一次复发性感染难辨梭菌ST-293分离株的鉴定
艰难梭菌是一种机会性孢子形成病原体负责抗生素相关性腹泻在人类。艰难梭菌产生两种主要毒素:TcdA和TcdB,以及第三种被称为二元毒素(CDT)的毒素,它也参与毒性。本研究旨在描述难辨梭菌分离ALCD3与院内感染复发的关系。分子鉴定结果表明,ALCD3菌株属于0/v型毒素,MLST分析显示,等位基因序列adk:91, atpA:1, dxr:2, glyA: 1, recA:27, sodA: 1和tpi:1与ST293 (MLST分支:1)相对应。在生长过程中,ALCD3菌株的产孢率在培养2天后早期增加,耐热形态的最大值也在培养2天后出现。与参考菌株VPI 10463相比,分离菌株ALCD3的产孢动力学和耐热型的产生速度都更快。在天然发芽剂牛牛胆酸盐存在下,ALCD3的萌发速度比菌株VPI 10463快,这表明ALCD3比菌株VPI 10463更早开始皮层水解。此外,共生发甘氨酸诱导分离ALCD3快速释放二吡啶酸(DPA)。这些发现表明,分离ALCD3在产孢和萌发中都特别有效。目前的工作是阿根廷首次报道艰难梭菌ST293的传播。分离ALCD3产生毒素的能力及其高产孢/萌发能力是与具有高传播潜力和诱导复发感染可能性的微生物相容的关键特征。
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
3.30
自引率
0.00%
发文量
46
审稿时长
>12 weeks
期刊介绍: La Revista Argentina de Microbiología es una publicación trimestral editada por la Asociación Argentina de Microbiología y destinada a la difusión de trabajos científicos en las distintas áreas de la Microbiología. La Asociación Argentina de Microbiología se reserva los derechos de propiedad y reproducción del material aceptado y publicado.
×
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