Surve Manalee Vishnu, Anil Anjali, Kamath Kshama Ganesh, Bhutda Smita, Sthanam Lakshmi Kavitha, Pradhan Arpan, Srivastava Rohit, Basu Bhakti, Dutta Suryendu, Sen Shamik, Modi Deepak, Banerjee Anirban
Dept. of Biosciences and Bioengineering, Indian Institute of Technology-Bombay, Mumbai, India.
Molecular Biology Division, Bhabha Atomic Research Centre, Mumbai, India.
PLoS Pathog. 2016 Sep 1;12(9):e1005816. doi: 10.1371/journal.ppat.1005816. eCollection 2016 Sep.
Infection of the genitourinary tract with Group B Streptococcus (GBS), an opportunistic gram positive pathogen, is associated with premature rupture of amniotic membrane and preterm birth. In this work, we demonstrate that GBS produces membrane vesicles (MVs) in a serotype independent manner. These MVs are loaded with virulence factors including extracellular matrix degrading proteases and pore forming toxins. Mice chorio-decidual membranes challenged with MVs ex vivo resulted in extensive collagen degradation leading to loss of stiffness and mechanical weakening. MVs when instilled vaginally are capable of anterograde transport in mouse reproductive tract. Intra-amniotic injections of GBS MVs in mice led to upregulation of pro-inflammatory cytokines and inflammation mimicking features of chorio-amnionitis; it also led to apoptosis in the chorio-decidual tissue. Instillation of MVs in the amniotic sac also resulted in intrauterine fetal death and preterm delivery. Our findings suggest that GBS MVs can independently orchestrate events at the feto-maternal interface causing chorio-amnionitis and membrane damage leading to preterm birth or fetal death.
B族链球菌(GBS)是一种机会性革兰氏阳性病原体,其引起的泌尿生殖道感染与胎膜早破和早产有关。在这项研究中,我们证明GBS以血清型独立的方式产生膜泡(MVs)。这些MVs装载有毒力因子,包括细胞外基质降解蛋白酶和形成孔道的毒素。用MVs离体攻击小鼠绒毛蜕膜导致广泛的胶原蛋白降解,从而导致硬度丧失和机械强度减弱。MVs经阴道注入后能够在小鼠生殖道中进行顺行运输。向小鼠羊膜腔内注射GBS MVs导致促炎细胞因子上调以及模拟绒毛膜羊膜炎的炎症特征;这也导致绒毛蜕膜组织发生凋亡。向羊膜囊内注入MVs还导致宫内胎儿死亡和早产。我们的研究结果表明,GBS MVs可以独立地协调母胎界面处的事件,导致绒毛膜羊膜炎和胎膜损伤,进而导致早产或胎儿死亡。