Pakistan Council of Scientific and Industrial Research Laboratories Complex, Karachi, Pakistan.
Microb Pathog. 2013 Aug-Sep;61-62:66-72. doi: 10.1016/j.micpath.2013.05.002. Epub 2013 May 25.
A total of 180 food borne isolates of methicillin resistant Staphylococcus aureus (MRSA) (oxacillin MICs 864 μg/ml) were used in the present study to investigate the effect of oxacillin on biofilm formation and its detachment process. Majority (98.3%) of these isolates were found to carry icaA gene. Out of 180 isolates 35.5% were identified as MRSA and 64.4% were methicillin sensitive S. aureus (MSSA). Biofilm studies by con-red agar and tube methods revealed that 57% of the MRSA isolates were biofilm producers. Polymerase chain reaction studies suggested that all of the biofilm positive MRSA isolates belong to SCCmec type IV and carry agr type II. This showed the strong association of SCCmec IV agr type II and biofilm formation in food borne MRSA. Conversely, only 13.7% of the MSSA isolates were biofilm positive and majority was found to carry agr type II. It has been noticed that oxacillin has regulatory effect on icaA expression and induce the icaA dependent polysaccharide intracellular adhesin (PIA) production and biofilm formation. This was confirmed by Real Time PCR studies of MRSA and MSSA isolates. Quantitative analysis showed that most of the MRSA isolates started biofilm formation after 24 h of incubation in the presence of sub-inhibitory concentration of oxacillin and achieved highest adhesion on glass slide after 48 h. The control in the absence of oxacillin showed slow conversion from planktonic to biofilm mode of growth (Table 1). Another novel feature of most of these biofilm producing isolates is the reduction in (Optical Density) OD, which is noticed after 48 h of incubation. Possibly, after 48 h oxacillin loses its toxicity or consumed the cells re-adapt to the planktonic state, possibly, by the activation of accessory gene regulator A (agrA) which has an important role in biofilm dispersal.
本研究共使用了 180 株耐甲氧西林金黄色葡萄球菌(MRSA)(苯唑西林 MIC864μg/ml)的食源性病原体分离株,以研究苯唑西林对生物膜形成及其脱落过程的影响。这些分离株中,大多数(98.3%)携带icaA 基因。在 180 株分离株中,35.5%被鉴定为 MRSA,64.4%为甲氧西林敏感金黄色葡萄球菌(MSSA)。通过 con-red 琼脂和管方法进行的生物膜研究表明,57%的 MRSA 分离株是生物膜产生者。聚合酶链反应研究表明,所有生物膜阳性的 MRSA 分离株均属于 SCCmec 类型 IV,并携带 agr 类型 II。这表明 SCCmec IV agr 类型 II 与食源性病原体 MRSA 的生物膜形成密切相关。相反,只有 13.7%的 MSSA 分离株是生物膜阳性,且大多数携带 agr 类型 II。研究人员注意到,苯唑西林对 icaA 表达具有调节作用,并诱导 icaA 依赖性多糖细胞内黏附素(PIA)的产生和生物膜的形成。这一点通过对 MRSA 和 MSSA 分离株的实时 PCR 研究得到了证实。定量分析表明,大多数 MRSA 分离株在亚抑菌浓度的苯唑西林存在下孵育 24 小时后开始生物膜形成,并在 48 小时后在玻片上达到最高黏附。在没有苯唑西林的情况下,对照组显示出从浮游生物到生物膜生长模式的缓慢转化(表 1)。这些产生物膜的分离株的另一个新特征是在孵育 48 小时后(光密度)OD 的降低。可能是在 48 小时后,苯唑西林失去了毒性或被消耗,细胞重新适应浮游状态,可能是通过辅助基因调节剂 A(agrA)的激活,agrA 在生物膜分散中起重要作用。