Egyir Beverly, Bentum Jeannette, Attram Naiki, Fox Anne, Obeng-Nkrumah Noah, Appiah-Korang Labi, Behene Eric, Kumordjie Selassie, Yeboah Clara, Agbodzi Bright, Bentil Ronald Essah, Tagoe Rhodalyn, Kofi Adu Tabi Blessing, Owusu Felicia, Dayie Nicholas T K D, Donkor Eric S, Nsaful Josephine, Asah-Opoku Kwaku, Nyarko Edward, Asumanu Edward, Larsen Anders Rhod, Wolfe David M, Letizia Andrew G
Bacteriology Department, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra 00233, Ghana.
Naval Medical Research Unit-Three, Ghana Detachment, Accra 00233, Ghana.
Pathogens. 2021 Feb 12;10(2):196. doi: 10.3390/pathogens10020196.
( is a common cause of surgical site infections (SSIs) globally. Data on the occurrence of methicillin-susceptible (MSSA) as well as methicillin-resistant (MRSA) among patients with surgical site infections (SSIs) in sub-Saharan African are scarce. We characterized from SSIs in Ghana using molecular methods and antimicrobial susceptibility testing (AST). Wound swabs or aspirate samples were collected from subjects with SSIs. was identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF-MS); AST was performed by Kirby-Bauer disk diffusion, and results were interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guideline. Detection of , and genes was performed by polymerase chain reaction (PCR). Whole-genome sequencing (WGS) was done using the Illumina MiSeq platform. Samples were collected from 112 subjects, with 13 isolates recovered. Of these, 92% were sensitive to co-trimoxazole, 77% to clindamycin, and 54% to erythromycin. Multi-drug resistance was detected in 5 (38%) isolates. The four gene-positive MRSA isolates detected belonged to ST152 ( = 3) and ST5 ( = 1). In total, 62% of the isolates were positive for the Panton-Valentine leukocidin () toxin gene. This study reports, for the first time, a -positive ST152-t355 MRSA clone from SSIs in Ghana. The occurrence of multi-drug-resistant epidemic clones suggests that continuous surveillance is required to monitor the spread and resistance trends of in hospital settings in the country.
在全球范围内是手术部位感染(SSIs)的常见病因。关于撒哈拉以南非洲地区手术部位感染(SSIs)患者中耐甲氧西林金黄色葡萄球菌(MSSA)以及耐甲氧西林金黄色葡萄球菌(MRSA)发生情况的数据稀缺。我们采用分子方法和抗菌药物敏感性试验(AST)对加纳手术部位感染的金黄色葡萄球菌进行了特征分析。从手术部位感染的受试者中收集伤口拭子或抽吸样本。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)鉴定金黄色葡萄球菌;采用 Kirby-Bauer 纸片扩散法进行 AST,并根据临床和实验室标准协会(CLSI)指南解释结果。通过聚合酶链反应(PCR)检测 mecA、lukS-PV 和 lukF-PV 基因。使用 Illumina MiSeq 平台进行全基因组测序(WGS)。从112名受试者中收集样本,共分离出13株金黄色葡萄球菌。其中,92%对复方新诺明敏感,77%对克林霉素敏感,54%对红霉素敏感。在5株(38%)分离株中检测到多重耐药性。检测到的4株mecA基因阳性MRSA分离株属于ST152(n = 3)和ST5(n = 1)。总共62%的分离株Panton-Valentine杀白细胞素(PVL)毒素基因呈阳性。本研究首次报告了来自加纳手术部位感染的PVL阳性ST152-t355 MRSA克隆。多重耐药金黄色葡萄球菌流行克隆的出现表明,需要持续监测以监控该国医院环境中金黄色葡萄球菌的传播和耐药趋势。