Antibiogram profiling and detection of icaA and blaZ genes from Staphylococcus aureus and coagulase-negative Staphylococcus spp. of healthy bovine raw milk sample origin.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2024-06-19 eCollection Date: 2024-06-01 DOI:10.5455/javar.2024.k795
Asmaul Husna, Md Arefin Kallol, Farhana Binte Ferdous, Khudaza Akter Lima, Zannatul Haque Tumpa, Mohammad Ferdousur Rahman Khan, Marzia Rahman
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引用次数: 0

Abstract

Objective: This study focused on the antibiogram profiling of Staphylococcus aureus and coagulase-negative Staphylococcus spp. (CoNS) and the detection of icaA and blaZ genes from bovine raw milk samples.

Materials and methods: Bovine milk samples were collected from dairy farms, and Staphylococcus spp. were isolated and identified via conventional and molecular screening. Disk diffusion test (DDT) was implemented to determine the resistance pattern. Biofilm and β-lactamase-producing Staphylococcus spp. were identified via amplification of the icaA and blaZ genes. Methicillin-resistant Staphylococcus aureus and CoNS were identified by DDT and PCR of the mecA gene.

Results: From 63 samples, 35 were confirmed as Staphylococcus spp., of which 16 (25.39%) S. aureus isolates were coagulase-positive, while 19 (30.16%) were negative. PCR confirmed that 50% (8/16) of S. aureus and 36.84% (7/19) of CoNS possessed the icaA gene. All S. aureus isolates were found resistant to penicillin-G (P) both phenotypically and genotypically. The isolates were also resistant to erythromycin (ERY) and oxytetracycline (TET). While CoNS showed high to reduced resistance against P, TET, ERY, and azithromycin, no S. aureus isolates were resistant to sulfamethoxazole, while 10.53% of CoNS isolates were. All S. aureus and CoNS isolates were susceptible to vancomycin and gentamicin. MR was exhibited by 37.5% of S. aureus and 42.10% of CoNS isolates. Moreover, S. aureus and CoNS had 56.25% and 52.63% multidrug-resistant (MDR) isolates, respectively.

Conclusion: The present study revealed the presence of a biofilm-producing, MDR staphylococcal strain in milk that might endanger consumers. Routine surveillance and monitoring, along with antimicrobial resistance learning, can reduce risks.

金黄色葡萄球菌和凝固酶阴性葡萄球菌的抗生素图谱分析及icaA 和 blaZ 基因检测
研究目的本研究的重点是金黄色葡萄球菌和凝固酶阴性葡萄球菌(CoNS)的抗生素谱分析以及牛生乳样品中 icaA 和 blaZ 基因的检测:从奶牛场采集牛乳样本,通过传统和分子筛选方法分离和鉴定葡萄球菌。采用盘扩散试验(DDT)确定耐药性模式。通过扩增 icaA 和 blaZ 基因,确定了产生物膜和产β-内酰胺酶的葡萄球菌属。耐甲氧西林金黄色葡萄球菌和 CoNS 通过 DDT 和 mecA 基因的 PCR 鉴定:结果:在 63 份样本中,35 份被确认为葡萄球菌属,其中 16 份(25.39%)金黄色葡萄球菌分离株凝固酶阳性,19 份(30.16%)阴性。聚合酶链式反应证实 50%(8/16)的金黄色葡萄球菌和 36.84%(7/19)的 CoNS 具有 icaA 基因。所有分离出的金黄色葡萄球菌在表型和基因型上都对青霉素-G(P)具有耐药性。这些分离物还对红霉素(ERY)和土霉素(TET)具有抗药性。虽然 CoNS 对 P、TET、ERY 和阿奇霉素的耐药性从高到低不等,但没有金黄色葡萄球菌分离物对磺胺甲噁唑具有耐药性,而 10.53% 的 CoNS 分离物对磺胺甲噁唑具有耐药性。所有金黄色葡萄球菌和 CoNS 分离物均对万古霉素和庆大霉素敏感。37.5%的金黄色葡萄球菌和 42.10%的 CoNS 分离物表现出 MR。此外,金黄色葡萄球菌和 CoNS 分别有 56.25% 和 52.63% 的多重耐药(MDR)分离株:本研究揭示了牛奶中存在可产生生物膜的 MDR 葡萄球菌菌株,这可能会危及消费者。常规监测和监控以及抗菌药耐药性学习可降低风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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