Department of Biomedical Science, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia.
Faculty of Health Sciences, Universiti Sultan Zainal Abidin, 21300, Kuala Nerus, Terengganu, Malaysia.
Int Microbiol. 2023 Nov;26(4):841-849. doi: 10.1007/s10123-023-00335-3. Epub 2023 Feb 20.
Methicillin-susceptible Staphylococcus aureus (MSSA) is an important nosocomial pathogen worldwide. This study aims to investigate the in vitro biofilm-forming ability of clinical MSSA isolated from various sources in the main public tertiary referral hospital in Terengganu, Malaysia and to detect the presence of biofilm-associated and regulatory genes among these isolates. A total of 104 MSSA isolates [pus (n = 75), blood (n = 24), respiratory secretions (n = 2), eye (n = 2), and urine (n = 1)] were investigated for slime production and biofilm formation using Congo red agar and crystal violet microtitre plate, respectively. Fifteen MSSA isolates with varying degrees of biofilm formation were selected for validation via a real-time cell analyser. All isolates were screened for microbial surface components recognising adhesive matrix molecules (MSCRAMM) and accessory gene regulator (agr) using polymerase chain reaction assay. A total of 76.0% (79/104) isolates produced slime layer, while all isolates developed biofilm as follows: 52.8% (55/104) strong biofilm producers, 40.4% (42/104) intermediate biofilm producers, and 6.7% (7/104) weak biofilm producers. A total of 98.1% (102/104) isolates carried at least one of the screened MSCRAMM gene(s) with the eno gene detected at the highest rate (87.5%, 91/104), while the sasG gene was significantly associated with strong biofilm production (p = 0.015). Three agr groups, 1, 2, and 3, were detected among the MSSA isolates with a predominance of agr-3 (32.7%, 34/104). In conclusion, biofilm formation varied greatly among clinical MSSA isolates, and the presence of sasG gene and agr-1 may play important role in initiating MSSA infections via biofilm formation.
耐甲氧西林金黄色葡萄球菌(MSSA)是一种重要的全球医院获得性病原体。本研究旨在调查从马来西亚登嘉楼州主要公立三级转诊医院的各种来源分离的临床 MSSA 的体外生物膜形成能力,并检测这些分离株中生物膜相关和调节基因的存在。总共研究了 104 株 MSSA 分离株[脓液(n = 75),血液(n = 24),呼吸道分泌物(n = 2),眼睛(n = 2)和尿液(n = 1)],以分别使用刚果红琼脂和结晶紫微量滴定板检测粘液产生和生物膜形成。选择了 15 株具有不同程度生物膜形成的 MSSA 分离株通过实时细胞分析仪进行验证。使用聚合酶链反应(PCR)检测所有分离株对微生物表面成分识别粘附基质分子(MSCRAMM)和辅助基因调节剂(agr)的筛查。76.0%(79/104)的分离株产生粘液层,而所有分离株均形成生物膜:52.8%(55/104)强生物膜生产者,40.4%(42/104)中间生物膜生产者和 6.7%(7/104)弱生物膜生产者。总共 98.1%(102/104)的分离株携带至少一种筛选的 MSCRAMM 基因,其中 eno 基因的检出率最高(87.5%,91/104),而 sasG 基因与强生物膜产生显著相关(p = 0.015)。在 MSSA 分离株中检测到三个 agr 组,1、2 和 3,其中 agr-3 占主导地位(32.7%,34/104)。总之,临床 MSSA 分离株的生物膜形成差异很大,sasG 基因和 agr-1 的存在可能通过生物膜形成在引发 MSSA 感染中起重要作用。