Detection and Molecular Characterization of ESBLs in E. coli Isolates from a Tertiary Care Hospital in North India with Special Attention to CTX-M-27

N. Anand, A. Asthana, M. Madan
{"title":"Detection and Molecular Characterization of ESBLs in E. coli Isolates from a Tertiary Care Hospital in North India with Special Attention to CTX-M-27","authors":"N. Anand, A. Asthana, M. Madan","doi":"10.9734/bmrj/2016/27860","DOIUrl":null,"url":null,"abstract":"Background: Extended spectrum beta-lactamases are the main cause of resistance to beta lactam antibiotics in members of Enterobacteriaceae. ESBL associated infections are on a rise worldwide and have become a serious public health problem. We aimed to investigate the molecular epidemiology of ESBL producing E. coli isolates recovered from various clinical specimens at a tertiary care hospital and to determine the antibiotic sensitivity profile of ESBL positive isolates. Methodology: A total of 300 isolates of E. coli were collected from various clinical specimens between the study period of 2011 to 2014. Antimicrobial susceptibility testing was done. ESBL detection was carried out by CLSI Phenotypic confirmatory method. Molecular typing of ESBLs was performed by uniplex PCR among 100 ESBL isolates. The bla CTX-M strains were genotyped by sequencing of PCR product. Nucleotide sequences were submitted to Gen Bank and accession numbers were obtained. Results: 61% isolates were found to be ESBL producers. ESBL and non-ESBL producers compared among in- and out-patients gave statistically significant result ( P value=0.002 ). All ESBL isolates (100%) were sensitive to imipenem. Overall 93.9% ESBL producers and 67.5% non-Original ESBLs were Multi Drug Resistant (Resistance to 3 or more class of antibiotics). The difference was statistically significant ( P value=0.001). Majority of the typeable isolates harboured two or more ESBL genes (52%). Sequencing was done for 10 randomly selected bla CTX-M PCR products and majority (90%) were identified as CTXM-15 belonging to CTX-M Cluster-1 while 1 0f 10 (10%) was identified as CTX-M- 27 belonging to CTX-M Cluster-9 on blast analysis. Deduced nucleotide sequences were submitted to Gen Bank. The accession numbers obtained from Gen Bank are KU946005-KU946009. Conclusion: Our study shows high ESBL occurrence among E.coli isolates and highlights the incidence CTX-M-27 for the first time from North India.","PeriodicalId":9269,"journal":{"name":"British microbiology research journal","volume":"42 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British microbiology research journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/bmrj/2016/27860","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Extended spectrum beta-lactamases are the main cause of resistance to beta lactam antibiotics in members of Enterobacteriaceae. ESBL associated infections are on a rise worldwide and have become a serious public health problem. We aimed to investigate the molecular epidemiology of ESBL producing E. coli isolates recovered from various clinical specimens at a tertiary care hospital and to determine the antibiotic sensitivity profile of ESBL positive isolates. Methodology: A total of 300 isolates of E. coli were collected from various clinical specimens between the study period of 2011 to 2014. Antimicrobial susceptibility testing was done. ESBL detection was carried out by CLSI Phenotypic confirmatory method. Molecular typing of ESBLs was performed by uniplex PCR among 100 ESBL isolates. The bla CTX-M strains were genotyped by sequencing of PCR product. Nucleotide sequences were submitted to Gen Bank and accession numbers were obtained. Results: 61% isolates were found to be ESBL producers. ESBL and non-ESBL producers compared among in- and out-patients gave statistically significant result ( P value=0.002 ). All ESBL isolates (100%) were sensitive to imipenem. Overall 93.9% ESBL producers and 67.5% non-Original ESBLs were Multi Drug Resistant (Resistance to 3 or more class of antibiotics). The difference was statistically significant ( P value=0.001). Majority of the typeable isolates harboured two or more ESBL genes (52%). Sequencing was done for 10 randomly selected bla CTX-M PCR products and majority (90%) were identified as CTXM-15 belonging to CTX-M Cluster-1 while 1 0f 10 (10%) was identified as CTX-M- 27 belonging to CTX-M Cluster-9 on blast analysis. Deduced nucleotide sequences were submitted to Gen Bank. The accession numbers obtained from Gen Bank are KU946005-KU946009. Conclusion: Our study shows high ESBL occurrence among E.coli isolates and highlights the incidence CTX-M-27 for the first time from North India.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
北印度一家三级医院大肠杆菌分离株ESBLs的检测和分子特征,特别关注CTX-M-27
背景:广谱β -内酰胺酶是肠杆菌科细菌对β -内酰胺类抗生素产生耐药性的主要原因。ESBL相关感染在世界范围内呈上升趋势,已成为一个严重的公共卫生问题。我们的目的是研究从三级保健医院的各种临床标本中回收的产生ESBL的大肠杆菌分离株的分子流行病学,并确定ESBL阳性分离株的抗生素敏感性谱。方法:2011 - 2014年从临床各类标本中采集大肠杆菌300株。进行药敏试验。采用CLSI表型验证法进行ESBL检测。采用单链PCR对100株ESBL进行分子分型。对bla CTX-M菌株进行PCR产物测序分型。将核苷酸序列提交到genbank并获得加入号。结果:61%的分离株为ESBL生产者。ESBL和非ESBL生产者在住院和门诊患者中比较,结果有统计学意义(P值=0.002)。所有ESBL分离株(100%)对亚胺培南敏感。总体而言,93.9%的ESBL生产者和67.5%的非原始ESBL生产者多重耐药(对3类或3类以上抗生素耐药)。差异有统计学意义(P值=0.001)。大多数可分型分离株含有两个或多个ESBL基因(52%)。随机选择10个bla CTX-M PCR产物进行测序,大多数(90%)鉴定为CTXM-15,属于CTX-M Cluster-1, 10个(10%)鉴定为CTX-M- 27,属于CTX-M Cluster-9。推断出的核苷酸序列提交给Gen Bank。从Gen Bank获得的登录号为KU946005-KU946009。结论:本研究显示大肠杆菌分离株中ESBL发生率较高,并首次在北印度发现CTX-M-27。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Isolation and Molecular Detection of Pathogenic Vibrio Species among Economic Fish from Red Sea in Egypt Methicillin Resistant Staphylococcus aureus in Wound Swabs of Patients Attending a Public Hospital in Warri Delta State, Nigeria Role of Three Different Laboratory Tests in Demonstrating Sensitization to Various Allergens in Common Atopic Disorders Molecular Identification, Bioactivity Screening and Metabolic Fingerprinting of the Actinomycetes of Chenab River Sediments Antibacterial Activity of Lactobacillus spp and Lactococcus spp Isolated from Various Parts of Pebbly Fish, Alestes baremoze
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1