Department of Microbiology and Hygiene, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh, Bangladesh.
Department of Microbiology and Public Health, Faculty of Veterinary Medicine and Animal Science, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur, Bangladesh.
PLoS One. 2024 Aug 5;19(8):e0308282. doi: 10.1371/journal.pone.0308282. eCollection 2024.
Biofilm development significantly enhances the virulence of methicillin-resistant Staphylococcus aureus (MRSA), leading to severe infections and decreased susceptibility to antibiotics, especially in strains associated with hospital environments. This study examined the occurrence of MRSA, their ability to form biofilms, agr typing, and the antibiotic resistance profiles of biofilm-forming MRSA strains isolated from environmental surfaces at Mymensingh Medical College Hospital (MMCH). From 120 swab samples, 86 (71.67%) tested positive for S. aureus. MRSA was identified in 86 isolates using the disk diffusion technique, and by polymerase chain reaction (PCR), 56 (65.1%) isolates were confirmed to carry the mecA gene. The Crystal Violet Microtiter Plate (CVMP) test revealed that 80.35% (45 isolates) were biofilm-forming and 19.6% (11 isolates) were non-biofilm-forming. Out of 45 biofilm producer isolates 37.5% and 42.9% isolates exhibited strong and intermediate biofilm-forming characteristics, respectively. Molecular analysis revealed that 17.78% of MRSA isolates carried at least one gene related to biofilm formation, specifically icaA, icaB, and icaD genes were discovered in 13.33%, 8.89%, 6.67% of the MRSA isolates, respectively. In agr typing, the most prevalent group was agr I (71.11%), followed by group III (17.78%) and group II (11.11%). Group IV was not detected. The distribution of agr gene groups showed a significant difference among biofilm-forming isolates (p < 0.05). In agr group I, 18.75% of isolates carried the icaA gene, 12.5% carried the icaB gene, and 9.37% carried the icaD gene. Biofilm-forming genes were not detected in any of the isolates from agr groups II or III. There are no statistically significant differences between agr groups and the presence of these genes (p > 0.05). Antibiotic resistance varied significantly among agr groups, with agr group I displaying the highest resistance, agr group II, and agr group III exhibiting the least resistance (p < 0.05). Seventy-three (73.3%) of the isolates were multi-drug resistant, with agr group I displaying nineteen MDR patterns. The occurrence of MRSA in hospital environments and their capacity to form biofilm raises concerns for public health. These findings support the importance of further research focused on agr quorum sensing systems as a basis for developing novel antibacterial agents.
生物膜的形成显著增强了耐甲氧西林金黄色葡萄球菌(MRSA)的毒力,导致严重感染和抗生素敏感性降低,特别是在与医院环境相关的菌株中。本研究检测了从孟加拉国迈门辛医学院医院(MMCH)环境表面分离的耐甲氧西林金黄色葡萄球菌(MRSA)的生物膜形成能力、agr 分型以及生物膜形成 MRSA 菌株的抗生素耐药谱。从 120 个拭子样本中,86 个(71.67%)检测出金黄色葡萄球菌呈阳性。使用圆盘扩散技术鉴定了 86 个分离株中的 MRSA,通过聚合酶链反应(PCR),56 个(65.1%)分离株证实携带 mecA 基因。结晶紫微量平板(CVMP)试验显示,80.35%(45 个分离株)为生物膜形成,19.6%(11 个分离株)为非生物膜形成。在 45 个生物膜产生分离株中,有 37.5%和 42.9%的分离株分别表现出强和中等生物膜形成特性。分子分析显示,MRSA 分离株中至少有一个与生物膜形成相关的基因,17.78%的 MRSA 分离株携带 icaA、icaB 和 icaD 基因,分别为 13.33%、8.89%和 6.67%。在 agr 分型中,最常见的组是 agr I(71.11%),其次是 agr III(17.78%)和 agr II(11.11%)。未检测到 agr IV 组。生物膜形成分离株中 agr 基因群的分布存在显著差异(p<0.05)。在 agr I 组中,18.75%的分离株携带 icaA 基因,12.5%的分离株携带 icaB 基因,9.37%的分离株携带 icaD 基因。agr 组 II 或 III 的任何分离株中均未检测到生物膜形成基因。agr 组与这些基因的存在之间没有统计学上的显著差异(p>0.05)。抗生素耐药性在 agr 组之间存在显著差异,agr I 组显示出最高的耐药性,agr II 组和 agr III 组显示出最低的耐药性(p<0.05)。73 株(73.3%)为多药耐药株,agr I 组显示 19 种 MDR 模式。医院环境中耐甲氧西林金黄色葡萄球菌的发生及其形成生物膜的能力引起了公众健康的关注。这些发现支持进一步研究 agr 群体感应系统作为开发新型抗菌药物基础的重要性。