水传播病原体的生物膜形成和抗生素耐药性概况

IF 2.5 4区 生物学 Q3 MICROBIOLOGY
Kursat Koskeroglu, Mukaddes Barel, Harun Hizlisoy, Yeliz Yildirim
{"title":"水传播病原体的生物膜形成和抗生素耐药性概况","authors":"Kursat Koskeroglu,&nbsp;Mukaddes Barel,&nbsp;Harun Hizlisoy,&nbsp;Yeliz Yildirim","doi":"10.1016/j.resmic.2023.104056","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Water sources (surface water, drinking water, rivers, and ponds) are significant reservoirs for transmitting antibiotic-resistant bacteria. In addition, these waters are an important public health problem because they are suitable environments for transferring antibiotic resistance genes between bacterial species. Our study aimed to assess the prevalence of Extended-spectrum beta-lactamase (ESBL) producing isolates in water samples, the susceptibility of the isolates to the specified antibiotics, the determination of biofilm ability, antibiotic resistance genes, and the molecular typing of the isolates. For this purpose, </span>Polymerase chain reaction (PCR) and Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analyses were used. Out of 70 isolates, 15 (21%) were ESBL producing, and sent for the MALDI-TOF analysis, where </span><span><span><em>Escherichia coli, </em><em>Acinetobacter calcoaceticus</em><em>, </em></span><em>Enterobacter</em><span><span><em> bugandensis, Acinetobacter pittii, </em><em>Pseudomonas aeruginosa</em><em>, </em></span><em>Acinetobacter junii</em><span><em>, </em><em>Pseudomonas oleovorans</em><em>,</em></span></span></span> and <em>Enterobacter ludwigigii</em><span> were identified. Moreover, colistin resistance genes (</span><em>mcr 1/2/6, mcr 4, mcr 5, mcr 3/7</em>, and <em>mcr 8</em>), ESBL-encoding genes (<em>bla</em><sub>SHV</sub><em>, bla</em><sub>TEM</sub>, and <em>bla</em><sub>CTX-M</sub>) and carbapenemase genes (<em>bla</em><sub>NDM</sub>, <em>bla</em><sub>OXA-48</sub>, and <em>bla</em><sub>KPC</sub>) using molecular analysis (PCR) were confirmed. The colistin resistance gene was detected at 80% (12/15) in the isolates obtained. The distribution of these isolates according to resistance genes was found as <em>mcr 1/2/6</em> 4 (20%), <em>mcr 3/7</em> 3 (13%), and <em>mcr 5</em> (40%). Additionally, the isolates harbored <em>bla</em><sub>SHV</sub>(6.6%) and <em>bla</em><sub>TEM</sub> (6.6%) genes. However, <em>bla</em><sub>NDM</sub>, <em>bla</em><sub>OXA-48</sub>, <em>bla</em><sub>KPC</sub>, and <em>bla</em><sub>CTX-M</sub> genes were not detected in any isolates. According to the Congo red agar method, seven (46.6%) isolates showed negative biofilm ability, and eight (53.3%) showed moderate biofilm ability. However, the microplate method detected weak biofilm in 53.3% of the isolates. In conclusion, this study provides evidence for the existence of multidrug-resistant bacteria that co-exist with <em>mcr</em> and ESBL genes in water sources. These bacteria can migrate to other environments and pose increasing threats to public health.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Biofilm formation and antibiotic resistance profiles of water-borne pathogens\",\"authors\":\"Kursat Koskeroglu,&nbsp;Mukaddes Barel,&nbsp;Harun Hizlisoy,&nbsp;Yeliz Yildirim\",\"doi\":\"10.1016/j.resmic.2023.104056\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Water sources (surface water, drinking water, rivers, and ponds) are significant reservoirs for transmitting antibiotic-resistant bacteria. In addition, these waters are an important public health problem because they are suitable environments for transferring antibiotic resistance genes between bacterial species. Our study aimed to assess the prevalence of Extended-spectrum beta-lactamase (ESBL) producing isolates in water samples, the susceptibility of the isolates to the specified antibiotics, the determination of biofilm ability, antibiotic resistance genes, and the molecular typing of the isolates. For this purpose, </span>Polymerase chain reaction (PCR) and Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analyses were used. Out of 70 isolates, 15 (21%) were ESBL producing, and sent for the MALDI-TOF analysis, where </span><span><span><em>Escherichia coli, </em><em>Acinetobacter calcoaceticus</em><em>, </em></span><em>Enterobacter</em><span><span><em> bugandensis, Acinetobacter pittii, </em><em>Pseudomonas aeruginosa</em><em>, </em></span><em>Acinetobacter junii</em><span><em>, </em><em>Pseudomonas oleovorans</em><em>,</em></span></span></span> and <em>Enterobacter ludwigigii</em><span> were identified. Moreover, colistin resistance genes (</span><em>mcr 1/2/6, mcr 4, mcr 5, mcr 3/7</em>, and <em>mcr 8</em>), ESBL-encoding genes (<em>bla</em><sub>SHV</sub><em>, bla</em><sub>TEM</sub>, and <em>bla</em><sub>CTX-M</sub>) and carbapenemase genes (<em>bla</em><sub>NDM</sub>, <em>bla</em><sub>OXA-48</sub>, and <em>bla</em><sub>KPC</sub>) using molecular analysis (PCR) were confirmed. The colistin resistance gene was detected at 80% (12/15) in the isolates obtained. The distribution of these isolates according to resistance genes was found as <em>mcr 1/2/6</em> 4 (20%), <em>mcr 3/7</em> 3 (13%), and <em>mcr 5</em> (40%). Additionally, the isolates harbored <em>bla</em><sub>SHV</sub>(6.6%) and <em>bla</em><sub>TEM</sub> (6.6%) genes. However, <em>bla</em><sub>NDM</sub>, <em>bla</em><sub>OXA-48</sub>, <em>bla</em><sub>KPC</sub>, and <em>bla</em><sub>CTX-M</sub> genes were not detected in any isolates. According to the Congo red agar method, seven (46.6%) isolates showed negative biofilm ability, and eight (53.3%) showed moderate biofilm ability. However, the microplate method detected weak biofilm in 53.3% of the isolates. In conclusion, this study provides evidence for the existence of multidrug-resistant bacteria that co-exist with <em>mcr</em> and ESBL genes in water sources. These bacteria can migrate to other environments and pose increasing threats to public health.</p></div>\",\"PeriodicalId\":21098,\"journal\":{\"name\":\"Research in microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Research in microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0923250823000311\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research in microbiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0923250823000311","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

水源(地表水、饮用水、河流和池塘)是传播抗生素耐药性细菌的重要蓄水池。此外,这些水域是一个重要的公共卫生问题,因为它们是在细菌物种之间转移抗生素耐药性基因的合适环境。我们的研究旨在评估水样中产超广谱β-内酰胺酶(ESBL)分离株的患病率、分离株对特定抗生素的易感性、生物膜能力的测定、抗生素耐药性基因以及分离株的分子分型。为此,使用聚合酶链式反应(PCR)和基质辅助激光解吸电离飞行时间(MALDI-TOF)分析。在70个分离株中,有15个(21%)产生ESBL,并被送去进行MALDI-TOF分析,其中鉴定出大肠杆菌、钙酸不动杆菌、布甘德肠杆菌、皮氏不动菌、铜绿假单胞菌、杜松不动细菌、油卵假单胞菌和鲁氏肠杆菌。此外,使用分子分析(PCR)确认了粘菌素抗性基因(mcr 1/2/6、mcr 4、mcr 5、mcr 3/7和mcr 8)、ESBL编码基因(blaSHV、blaTEM和blaCTX-M)和碳青霉烯酶基因(blaNDM、blaOXA-48和blaKPC)。在所获得的分离株中,粘菌素抗性基因的检出率为80%(12/15)。根据抗性基因,这些分离株的分布为mcr1/2/64(20%)、mcr3/73(13%)和mcr5(40%)。此外,分离株携带blaSHV(6.6%)和blaTEM(6.6%。然而,在任何分离株中都没有检测到blaNDM、blaOXA-48、blaKPC和blaCTX-M基因。根据刚果红琼脂法,7个(46.6%)分离株显示出阴性生物膜能力,8个(53.3%)显示出中等生物膜能力。然而,微板法在53.3%的分离株中检测到弱生物膜。总之,本研究为水源中存在与mcr和ESBL基因共存的耐多药细菌提供了证据。这些细菌可以迁移到其他环境中,并对公众健康构成越来越大的威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biofilm formation and antibiotic resistance profiles of water-borne pathogens

Water sources (surface water, drinking water, rivers, and ponds) are significant reservoirs for transmitting antibiotic-resistant bacteria. In addition, these waters are an important public health problem because they are suitable environments for transferring antibiotic resistance genes between bacterial species. Our study aimed to assess the prevalence of Extended-spectrum beta-lactamase (ESBL) producing isolates in water samples, the susceptibility of the isolates to the specified antibiotics, the determination of biofilm ability, antibiotic resistance genes, and the molecular typing of the isolates. For this purpose, Polymerase chain reaction (PCR) and Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) analyses were used. Out of 70 isolates, 15 (21%) were ESBL producing, and sent for the MALDI-TOF analysis, where Escherichia coli, Acinetobacter calcoaceticus, Enterobacter bugandensis, Acinetobacter pittii, Pseudomonas aeruginosa, Acinetobacter junii, Pseudomonas oleovorans, and Enterobacter ludwigigii were identified. Moreover, colistin resistance genes (mcr 1/2/6, mcr 4, mcr 5, mcr 3/7, and mcr 8), ESBL-encoding genes (blaSHV, blaTEM, and blaCTX-M) and carbapenemase genes (blaNDM, blaOXA-48, and blaKPC) using molecular analysis (PCR) were confirmed. The colistin resistance gene was detected at 80% (12/15) in the isolates obtained. The distribution of these isolates according to resistance genes was found as mcr 1/2/6 4 (20%), mcr 3/7 3 (13%), and mcr 5 (40%). Additionally, the isolates harbored blaSHV(6.6%) and blaTEM (6.6%) genes. However, blaNDM, blaOXA-48, blaKPC, and blaCTX-M genes were not detected in any isolates. According to the Congo red agar method, seven (46.6%) isolates showed negative biofilm ability, and eight (53.3%) showed moderate biofilm ability. However, the microplate method detected weak biofilm in 53.3% of the isolates. In conclusion, this study provides evidence for the existence of multidrug-resistant bacteria that co-exist with mcr and ESBL genes in water sources. These bacteria can migrate to other environments and pose increasing threats to public health.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Research in microbiology
Research in microbiology 生物-微生物学
CiteScore
4.10
自引率
3.80%
发文量
54
审稿时长
16 days
期刊介绍: Research in Microbiology is the direct descendant of the original Pasteur periodical entitled Annales de l''Institut Pasteur, created in 1887 by Emile Duclaux under the patronage of Louis Pasteur. The Editorial Committee included Chamberland, Grancher, Nocard, Roux and Straus, and the first issue began with Louis Pasteur''s "Lettre sur la Rage" which clearly defines the spirit of the journal:"You have informed me, my dear Duclaux, that you intend to start a monthly collection of articles entitled "Annales de l''Institut Pasteur". You will be rendering a service that will be appreciated by the ever increasing number of young scientists who are attracted to microbiological studies. In your Annales, our laboratory research will of course occupy a central position, but the work from outside groups that you intend to publish will be a source of competitive stimulation for all of us."That first volume included 53 articles as well as critical reviews and book reviews. From that time on, the Annales appeared regularly every month, without interruption, even during the two world wars. Although the journal has undergone many changes over the past 100 years (in the title, the format, the language) reflecting the evolution in scientific publishing, it has consistently maintained the Pasteur tradition by publishing original reports on all aspects of microbiology.
×
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