检测临床分离的金黄色葡萄球菌的生物膜生成和抗生素敏感性模式。

IF 1.1 Q4 MICROBIOLOGY
Journal of Pathogens Pub Date : 2024-05-06 eCollection Date: 2024-01-01 DOI:10.1155/2024/2342468
Sushant Pokhrel, Namrata Sharma, Suraj Aryal, Rachita Khadka, Tika Bahadur Thapa, Pawan Pandey, Govardhan Joshi
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引用次数: 0

摘要

目的:抗生素耐药性和在医疗器械中形成生物膜的能力不断增强,已成为金黄色葡萄球菌(S. aureus)引起严重感染的主要原因。由于生活在生物膜中的细菌对抗生素的耐药性可增加 10 到 1000 倍,并会引发慢性传染病,因此检测金黄色葡萄球菌形成生物膜的能力对于管理、减少和有效治疗由其引起的感染具有重要意义。本研究旨在比较试管培养法和组织培养法检测 MRSA 和 MSSA 的生物膜生成和抗生素敏感性:通过菌落形态学检查、革兰氏染色和各种生化测试对分离出的金黄色葡萄球菌进行鉴定。根据 CLSI 指南的建议,采用改良柯比鲍尔盘扩散法对所有分离菌株进行抗菌药敏感性检测。使用头孢西丁圆片(30 微克)对 MRSA 进行表型筛选。使用 D 试验检测分离株的诱导耐药性,并使用两种表型方法检测生物膜的形成:结果:在 982 份非重复临床标本中,有 103 份(10.48%)分离出金葡菌。在 103 例临床分离的金黄色葡萄球菌中,54 例(52.42%)为 MRSA,49 例(47.57%)为 MSSA。在 54 个 MRSA 分离物中,有 23 个/54 个(42.59%)观察到可诱导的 MLSB 表型,D 测试结果呈阳性。根据 TCP 方法,26 株(48.1%)MRSA 分离物具有较强的生物膜生成能力,而在所有 MSSA 分离物中,只有 6 株(12.2%)具有较强的生物膜生成能力:结论:与 MSSA 相比,MRSA 具有较强的生物膜生成能力。结论:与 MSSA 相比,MRSA 具有较强的生物膜产生能力。TCP 法是检测金黄色葡萄球菌分离物中生物膜的可靠推荐方法,TM 法可用于常规临床实验室筛选金黄色葡萄球菌的生物膜产生情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Biofilm Production and Antibiotic Susceptibility Pattern among Clinically Isolated Staphylococcus aureus.

Aim: The increasing antibiotic resistance and the ability to form biofilms in medical devices have become the leading cause of severe infections associated with Staphylococcus aureus (S. aureus). Since the bacteria living in biofilms can exhibit 10- to 1,000-fold increase in antibiotic resistance and implicate chronic infectious diseases, the detection of S. aureus ability to form biofilms is of great importance for managing, minimizing, and effectively treating infections caused by it. This study aimed to compare the tube and tissue culture methods to detect biofilm production and antibiotic susceptibility in MRSA and MSSA.

Materials and methods: The S. aureus isolates were identified by the examination of the colony morphology, Gram staining, and various biochemical tests. Antimicrobial susceptibility testing of all isolates was performed by the modified Kirby-Bauer disc diffusion method as recommended by CLSI guidelines. MRSA screening was performed phenotypically using a cefoxitin disc (30 µg). Isolates were tested for inducible resistance using the D-test, and two phenotypic methods detected biofilm formation.

Results: Among 982 nonrepeated clinical specimens, S. aureus was isolated from 103 (10.48%). Among 103 clinical isolates of S. aureus, 54 (52.42%) isolates were MRSA, and 49 (47.57%) were MSSA. Among 54 MRSA isolates, the inducible MLSB phenotype was observed in 23/54 (42.59%) with a positive D-test. By TCP method, 26 (48.1%) MRSA isolates were strong biofilm producers, whereas, among all MSSA isolates, only 6 (12.2%) were strong biofilm producers.

Conclusion: MRSA showed strong biofilm production in comparison with MSSA. The TCP method is a recommended reliable method to detect the biofilm among S. aureus isolates, and the TM method could be useful for the screening of biofilm production in S. aureus in the routine clinical laboratory.

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Journal of Pathogens
Journal of Pathogens MICROBIOLOGY-
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