耐药性和毒力的守护者:从尼日利亚西南部的临床和食品样本中检测耐甲氧西林和耐万古霉素金黄色葡萄球菌中的 mec、femA、Van、pvl、hlg 和 spa 基因。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Folasade Muibat Adeyemi, Omotayo Opemipo Oyedara, Nana Aishat Yusuf-Omoloye, Olaoniye Habeebat Ajigbewu, Onyinye Lynda Ndaji, Maryam Kikelomo Adegbite-Badmus, Taiwo Samson Olumakinde, Timilehin Emmanuel Oluokun
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引用次数: 0

摘要

背景:金黄色葡萄球菌菌株毒性很强,与各种严重的院内感染和社区获得性感染有关:本研究评估了来自临床和即食(RTE)食品来源的耐甲氧西林和耐万古霉素金黄色葡萄球菌(MRSA/VRSA),筛查了抗生素耐药性,以及抗生素和毒力基因的分子决定因素:方法:通过传统微生物学技术分析了 465 份临床和即食食品样本,并通过 nuc 基因检测确认了金黄色葡萄球菌的身份。耐甲氧西林和耐万古霉素的表型筛选分别采用琼脂筛查和微滴稀释法,而抗生素药敏试验则采用碟片扩散技术。VanA/vanB/VanC1、femA、mecA/mecC、pvl/hlg 和 spa 基因通过聚合酶链反应进行检测:从表型上看,共分离出 211 株葡萄球菌,其中 138 株(65.4%)携带 nuc 基因--所有 138 株(100.0%)均为 VRSA,而 59/138 株(42.8%)从表型上看为 MRSA。总体而言,114/138(82.6%)、7/138(5.1%)和 6/138(4.3%)个分离株带有 femA、mecA 和 mecC 基因,只有 3 个(2.2%)分离株检测到 van 基因,分别有 8 个(5.8%)、10 个(7.2%)和 77 个(55.8%)分离株带有毒力决定因子 pvl、hlg 和 spa 基因。总共有 11.6% 的分离物携带抗药性相关基因,55.8% 的分离物携带毒力基因,12.3% 的分离物同时检测到抗药性基因和毒力基因。总体而言,96/138(69.6%)株具有多重耐药性(MDR),一株具有极端耐药性(XDR)。83.3%的分离株的MAR指数≥0.2:本研究强调了奥索博的 MRSA 和 VRSA 循环菌株的毒力水平,有助于对其进行持续监测,并为后续流行病学调查提供更多可用数据。本研究还报告了尼日利亚西南部从即食食品和人体样本中分离出的金黄色葡萄球菌中出现的 mecC 基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Guardians of resistance and virulence: detection of mec, femA, Van, pvl, hlg and spa genes in methicillin and vancomycin-resistant Staphylococcus aureus from clinical and food samples in Southwestern Nigeria.

Background: Staphylococcus aureus strains are highly virulent and associated with an eclectic range of severe nosocomial and community-acquired infections.

Objectives: This study assessed methicillin- and vancomycin-resistant Staphylococcus aureus (MRSA/VRSA) from clinical and ready-to-eat (RTE) food sources, screened for antibiotic resistance; and molecular determinants of antibiotic and virulence genes.

Methods: Altogether, 465 clinical and RTE food samples were analyzed via conventional microbiological techniques and S. aureus identification was confirmed by nuc gene detection. Phenotypic screening for methicillin and vancomycin-resistance was by agar-screen cum micro-broth dilution respectively, while antibiotic susceptibility testing was done by the disc-diffusion technique. VanA/vanB/VanC1, femA, mecA/mecC; pvl/hlg and spa gene detection was via Polymerase chain reaction.

Results: Phenotypically, 211 Staphylococcal isolates were recovered, 138 (65.4%) of them carrying the nuc gene - all 138 (100.0%) were VRSA, while 59/138 (42.8%) were MRSA phenotypically. Overall, 114/138 (82.6%), 7/138 (5.1%), and 6/138 (4.3%) of isolates had the femA, mecA, and mecC genes, while van genes were detected in only 3 (2.2%) isolates, with virulence determinants pvl, hlg, and spa gene carriage in 8 (5.8%), 10 (7.2%), and 77 (55.8%) isolates respectively. In all, 11.6% carried resistance-associated genes, 55.8% carried virulence genes, and co-detection of resistance and virulence genes was observed in 12.3%. Overall, 96/138 (69.6%) were multidrug-resistant (MDR), while one strain was extremely drug-resistant (XDR). MAR Indices ≥ 0.2 was observed in 83.3% of isolates.

Conclusion: This study highlights virulence levels of MRSA and VRSA circulating strains in Osogbo, contributing to their sustained surveillance, and improving available data for successive epidemiology investigations. This study also reports the occurrence of the mecC gene in S. aureus isolates from RTE foods and human samples in Southwestern Nigeria.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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