Shi-Gan International College of Science and Technology, Tribhuvan University, Kathmandu, Nepal.
Central Department of Microbiology, Tribhuvan University, Kathmandu, Nepal.
J Infect Dev Ctries. 2024 Jul 29;18(7):1010-1019. doi: 10.3855/jidc.17743.
Methicillin-resistant Staphylococcus aureus (MRSA) expresses the Panton-Valentine leukocidin (PVL) virulence gene, which is associated with community and hospital-acquired severe MRSA infections. The objective of this study was to determine the prevalence and antibiotic susceptibility profile with a focus on the presence of the PVL gene among MRSA isolates in healthcare settings.
A total of 1,207 clinical specimens and 304 hospital environment swabs were collected in a tertiary care hospital in Nepal, and investigated following basic microbiological techniques. S. aureus was confirmed with the coagulase test. An antibiotic susceptibility test (AST) was performed by the Kirby-Bauer method and screening for MRSA was carried out by the cefoxitin disc diffusion method guided by the Clinical and Laboratory Standards Institute (CLSI), 2020. DNA was extracted and used in a polymerase chain reaction (PCR) to detect mecA and PVL genes.
Of the 1,511 samples, 45 (2.9%) S. aureus (23 clinical and 22 environmental) were isolated. Among them, 69.6% (16/23) and 27.3% (6/22) were MRSA in clinical and environmental isolates, respectively. Twelve (52.2%) clinical isolates and seven (31.8%) environmental isolates were multidrug resistant. The majority of isolates were susceptible to vancomycin and linezolid. The PVL gene was detected in 18.2% (n = 4/22) of the MRSA isolates, of which three were from clinical sources and one was from an environmental swab.
The prevalence of MRSA, and PVL-producing S. aureus were higher in the hospital setting. Hence, immediate and urgent implementation of infection control and sanitation measures are needed in the hospital.
耐甲氧西林金黄色葡萄球菌(MRSA)表达杀白细胞素(PVL)毒力基因,与社区和医院获得性严重 MRSA 感染有关。本研究的目的是确定医疗保健环境中 MRSA 分离株中 PVL 基因的流行情况和抗生素敏感性谱,重点关注其存在情况。
在尼泊尔的一家三级保健医院共采集了 1207 份临床标本和 304 份医院环境拭子,并采用基本微生物学技术进行了调查。采用凝固酶试验确认金黄色葡萄球菌。采用 Kirby-Bauer 法进行抗生素敏感性试验(AST),并根据临床和实验室标准协会(CLSI),2020 年的头孢西丁纸片扩散法进行 MRSA 的筛选。提取 DNA 并用于聚合酶链反应(PCR)检测 mecA 和 PVL 基因。
在 1511 份样本中,分离出 45 株(2.9%)金黄色葡萄球菌(23 株临床分离株和 22 株环境分离株)。其中,临床分离株和环境分离株中的 MRSA 分别占 69.6%(16/23)和 27.3%(6/22)。12 株(52.2%)临床分离株和 7 株(31.8%)环境分离株为多药耐药株。大多数分离株对万古霉素和利奈唑胺敏感。在 22 株 MRSA 分离株中检测到 18.2%(n=4/22)的 PVL 基因,其中 3 株来自临床标本,1 株来自环境拭子。
医院环境中 MRSA 和产 PVL 金黄色葡萄球菌的流行率较高。因此,医院需要立即采取紧急的感染控制和卫生措施。