Balasubramanian N, Pounpandi P, Varatharaju G, Shanmugaiah V, Balakrishnan K, Thirunarayan M A
Department of Immunology, School of Biological Sciences, Madurai Kamaraj University, Madurai 625021, India.
Department of Immunology, School of Biological Sciences, Madurai Kamaraj University, Madurai 625021, India.
Colloids Surf B Biointerfaces. 2023 Mar;223:113151. doi: 10.1016/j.colsurfb.2023.113151. Epub 2023 Jan 18.
This study included 21 newly isolated clinical samples of Streptococcus agalactiae (Group B Streptococcus) screened in patients (six male, fifteen female) from various states of India with different infections (urinary tract infections, blood, pus and eye infections). All isolates were identified as Group B Streptococcus (GBS) using hemolytic properties, serogrouping and MALDI-TOF-MS analysis. Six virulence genes, cfb (100%), cylE (90.4%), lmp (85.7%), bca (71.4%), rib (38%) and bac (4.7%) were detected via polymerase chain reaction (PCR). Distribution studies of these six genes revealed five isolates containing five virulence genes (23.8%), followed by ten isolates containing four virulence genes (47.6%). The twenty GBS isolates selected on the glass surface included non-biofilm producers (n = 6, 30%), weak (n = 11, 55%) and moderate biofilm producers (n = 3, 15%). On the polystyrene surface, weak (n = 4, 20%), moderate (n = 2, 10%) and strong (n = 14, 70%) biofilm producers were detected. Live-dead cell staining revealed that more viable cells accumulated in the S. ag 7420 isolate than in the AH1 isolate. Scanning electron microscope (SEM) biofilm analysis showed S. ag AH1 cells appeared as chain-like structures, whereas the S. ag 7420 isolate biofilm cells appeared as fork-like structures on the glass surface. Biofilm elements were analyzed using Energy Dispersive X-Ray Analysis (EDAX) for both isolates and 13 elements with different orders of composition were found. Thus, virulence gene detection, distribution and biofilm formation by these new clinical isolates suggested the virulent nature of these pathogens, which might cause different levels of disease severity in humans.
本研究纳入了21份新分离的无乳链球菌(B组链球菌)临床样本,这些样本来自印度不同邦患有不同感染(尿路感染、血液感染、脓液感染和眼部感染)的患者(6名男性,15名女性)。所有分离株均通过溶血特性、血清分型和基质辅助激光解吸电离飞行时间质谱分析鉴定为B组链球菌(GBS)。通过聚合酶链反应(PCR)检测到6个毒力基因,分别为cfb(100%)、cylE(90.4%)、lmp(85.7%)、bca(71.4%)、rib(38%)和bac(4.7%)。对这6个基因的分布研究显示,5株分离株含有5个毒力基因(23.8%),其次是10株分离株含有4个毒力基因(47.6%)。在玻璃表面挑选出的20株GBS分离株包括非生物膜形成菌(n = 6,30%)、弱生物膜形成菌(n = 11,55%)和中度生物膜形成菌(n = 3,15%)。在聚苯乙烯表面,检测到弱生物膜形成菌(n = 4,20%)、中度生物膜形成菌(n = 2,10%)和强生物膜形成菌(n = 14,70%)。活死细胞染色显示,与AH1分离株相比,ag 7420分离株中积累的活细胞更多。扫描电子显微镜(SEM)生物膜分析显示,ag AH1细胞呈链状结构,而ag 7420分离株的生物膜细胞在玻璃表面呈叉状结构。对两种分离株均使用能量色散X射线分析(EDAX)对生物膜成分进行分析,发现了13种组成顺序不同的元素。因此,这些新的临床分离株的毒力基因检测、分布和生物膜形成表明了这些病原体的毒性本质,它们可能会在人类中引起不同程度的疾病严重程度。