Characteristics of Staphylococcus aureus Isolated From Clinical Specimens in a Tertiary Care Hospital, Kathmandu, Nepal.

Microbiology insights Pub Date : 2020-11-11 eCollection Date: 2020-01-01 DOI:10.1177/1178636120972695
Shesh Narayan Kandel, Nabaraj Adhikari, Binod Dhungel, Upendra Thapa Shrestha, Khadga Bikram Angbuhang, Gayatri Karki, Bipin Adhikari, Megha Raj Banjara, Komal Raj Rijal, Prakash Ghimire
{"title":"Characteristics of <i>Staphylococcus aureus</i> Isolated From Clinical Specimens in a Tertiary Care Hospital, Kathmandu, Nepal.","authors":"Shesh Narayan Kandel,&nbsp;Nabaraj Adhikari,&nbsp;Binod Dhungel,&nbsp;Upendra Thapa Shrestha,&nbsp;Khadga Bikram Angbuhang,&nbsp;Gayatri Karki,&nbsp;Bipin Adhikari,&nbsp;Megha Raj Banjara,&nbsp;Komal Raj Rijal,&nbsp;Prakash Ghimire","doi":"10.1177/1178636120972695","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Methicillin resistant <i>Staphylococcus aureus</i> (MRSA) is a major human pathogen associated with nosocomial and community infections. <i>mec</i>A gene is considered one of the important virulence factors of <i>S. aureus</i> responsible for acquiring resistance against methicillin. The main objective of this study was to explore the prevalence, antibiotic susceptibility pattern, and <i>mec</i> A gene.</p><p><strong>Methods: </strong>A total of 39 isolates of <i>S. aureus</i> were isolated from 954 clinical specimens processed in Microbiology laboratory of Himal Hospital, Kathmandu. Antimicrobial susceptibility test (AST) was performed by Kirby-Bauer disc diffusion method using cefoxitin, and performed Polymerase Chain Reaction (PCR) for amplification of <i>mecA</i> gene in MRSA isolates.</p><p><strong>Results: </strong>Out of 954 clinical samples, (16.2%; 153/954) samples had bacterial growth. Among 153 culture positive isolates, 25.5% (39/153) were positive for <i>S. aureus.</i> Among 39 <i>S. aureus</i> (61.5%; 24/39) were multiple drug resistant (MDR). On AST, amoxicillin was detected as the least effective while vancomycin was the most effective. The prevalence of methicillin resistance was 46% (18/39) of which 72.2% (13/18) were positive for <i>mecA</i> gene in PCR assay.</p><p><strong>Conclusion: </strong>One in 4 culture positive isolates from the clinical specimens were <i>S. aureus</i>, of which almost two-thirds were MDR. Around half of the MDR showed MRSA and significant proportion of them were positive for <i>mecA</i> gene. This study concludes that the <i>mecA</i> gene is solely dependent for methicillin resistance in <i>S. aureus</i> but the presence of gene is not obligatory. PCR detection of the <i>mec</i>A gene is reliable, valid and can be suggested for the routine use in diagnostic laboratories.</p>","PeriodicalId":74187,"journal":{"name":"Microbiology insights","volume":"13 ","pages":"1178636120972695"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1178636120972695","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology insights","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/1178636120972695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

Abstract

Introduction: Methicillin resistant Staphylococcus aureus (MRSA) is a major human pathogen associated with nosocomial and community infections. mecA gene is considered one of the important virulence factors of S. aureus responsible for acquiring resistance against methicillin. The main objective of this study was to explore the prevalence, antibiotic susceptibility pattern, and mec A gene.

Methods: A total of 39 isolates of S. aureus were isolated from 954 clinical specimens processed in Microbiology laboratory of Himal Hospital, Kathmandu. Antimicrobial susceptibility test (AST) was performed by Kirby-Bauer disc diffusion method using cefoxitin, and performed Polymerase Chain Reaction (PCR) for amplification of mecA gene in MRSA isolates.

Results: Out of 954 clinical samples, (16.2%; 153/954) samples had bacterial growth. Among 153 culture positive isolates, 25.5% (39/153) were positive for S. aureus. Among 39 S. aureus (61.5%; 24/39) were multiple drug resistant (MDR). On AST, amoxicillin was detected as the least effective while vancomycin was the most effective. The prevalence of methicillin resistance was 46% (18/39) of which 72.2% (13/18) were positive for mecA gene in PCR assay.

Conclusion: One in 4 culture positive isolates from the clinical specimens were S. aureus, of which almost two-thirds were MDR. Around half of the MDR showed MRSA and significant proportion of them were positive for mecA gene. This study concludes that the mecA gene is solely dependent for methicillin resistance in S. aureus but the presence of gene is not obligatory. PCR detection of the mecA gene is reliable, valid and can be suggested for the routine use in diagnostic laboratories.

Abstract Image

Abstract Image

Abstract Image

尼泊尔加德满都一家三级医院临床标本分离金黄色葡萄球菌的特征
简介:耐甲氧西林金黄色葡萄球菌(MRSA)是一种与医院和社区感染相关的主要人类病原体。mecA基因被认为是金黄色葡萄球菌对甲氧西林产生耐药性的重要毒力因子之一。本研究的主要目的是探讨mec A的患病率,抗生素敏感性模式和基因。方法:从加德满都Himal医院微生物实验室处理的954份临床标本中分离出39株金黄色葡萄球菌。用头孢西丁进行Kirby-Bauer圆盘扩散法抗菌药敏试验(AST),并采用聚合酶链反应(PCR)扩增MRSA分离株mecA基因。结果:954份临床样本中,(16.2%;153/954)样品有细菌生长。153株培养阳性菌株中金黄色葡萄球菌阳性的占25.5%(39/153)。39株金黄色葡萄球菌占61.5%;24/39例为多重耐药(MDR)。在AST上,阿莫西林效果最差,万古霉素效果最好。甲氧西林耐药率为46%(18/39),其中PCR检测mecA基因阳性的占72.2%(13/18)。结论:临床标本培养阳性分离物1 / 4为金黄色葡萄球菌,其中近2 / 3为耐多药菌株。大约一半的耐多药患者表现为MRSA,其中相当一部分人的mecA基因呈阳性。本研究得出结论,金黄色葡萄球菌的甲氧西林耐药性完全依赖于mecA基因,但该基因的存在并非强制性的。PCR检测mecA基因是可靠、有效的,可建议在诊断实验室常规使用。
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
自引率
0.00%
发文量
0
审稿时长
8 weeks
×
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