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从加纳阿散蒂地区分离出的多重耐药菌的敏感性模式、质粒图谱及克隆相关性

Sensitivity Patterns, Plasmid Profiles and Clonal Relatedness of Multi-Drug Resistant Isolated From the Ashanti Region, Ghana.

作者信息

Odoi Hayford, Boamah Vivian Etsiapa, Duah Boakye Yaw, Dodoo Cornelius Cecil, Agyare Christian

机构信息

Department of Pharmaceutical Microbiology, School of Pharmacy, University of Health and Allied Sciences, Ho, Volta Region, Ghana.

Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

Environ Health Insights. 2022 Feb 14;16:11786302221078117. doi: 10.1177/11786302221078117. eCollection 2022.

Abstract

is a major cause of most opportunistic nosocomial infections in Ghana. The study sought to characterize isolates from market environments, poultry farms and clinical samples of patients from 2 district hospitals in the Ashanti region of Ghana. The genetic relatedness, plasmid profiles and antimicrobial sensitivity of the isolates were investigated. Culture based isolation and gene amplification were used to confirm the identity of the isolates. Susceptibility testing was conducted using the Kirby Bauer disk diffusion method. Random whole genome typing of the strains was done using Enterobacterial repetitive-intergenic consensus based (ERIC) PCR assay. The most active agents against isolates were ceftazidime (90%), piperacillin (85%), meropenem, cefipeme and ticarcillin/clavulanic acid (81.6%). The isolates were most resistant to gentamycin (69%), ciprofloxacin (62.1%), ticarcillin (56.3%) and aztreonam (25%). About 65% (n = 38) of the multi-drug resistant (MDR) isolates harbored 1 to 5 plasmids with sizes ranging from 2 to 116.8 kb. A total of 27 clonal patterns were identified. Two major clones were observed with a clone showing resistance to all the test antipseudomonal agents. There is therefore a need for continued intensive surveillance to control the spread and development of resistant strains.

摘要

是加纳大多数机会性医院感染的主要原因。该研究旨在对来自加纳阿散蒂地区2家district医院的市场环境、家禽养殖场及患者临床样本中的分离株进行特征分析。对分离株的遗传相关性、质粒图谱及抗菌敏感性进行了研究。采用基于培养的分离方法和基因扩增来确认分离株的身份。使用 Kirby Bauer 纸片扩散法进行药敏试验。采用基于肠杆菌重复基因间共识(ERIC)的PCR 检测法对菌株进行随机全基因组分型。对分离株最有效的药物是头孢他啶(90%)、哌拉西林(85%)、美罗培南、头孢吡肟和替卡西林/克拉维酸(81.6%)。分离株对庆大霉素(69%)、环丙沙星(62.1%)、替卡西林(56.3%)和氨曲南(25%)耐药性最强。约65%(n = 38)的多重耐药(MDR)分离株携带1至5个质粒,大小在2至116.8 kb之间。共鉴定出27种克隆模式。观察到两个主要克隆,其中一个克隆对所有测试的抗假单胞菌药物均耐药。因此,需要持续进行强化监测,以控制耐药菌株的传播和发展。

原文中“district”未翻译,可能是特定名称未给出准确中文,可根据实际情况补充完整准确的中文表述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3faa/8854229/451d82b1d290/10.1177_11786302221078117-fig1.jpg

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