Division of Infectious Diseases, Department of Pediatrics, Childrens Hospital Los Angeles and Keck School of Medicine, University of Southern California, Los Angeles, California 90027, USA.
J Biol Chem. 2011 Jan 21;286(3):2183-93. doi: 10.1074/jbc.M110.178236. Epub 2010 Nov 11.
Outer membrane protein A (OmpA) has been implicated as an important virulence factor in several gram-negative bacterial infections such as Escherichia coli K1, a leading cause of neonatal meningitis associated with significant mortality and morbidity. In this study, we generated E. coli K1 mutants that express OmpA in which three or four amino acids from various extracellular loops were changed to alanines, and we examined their ability to survive in several immune cells. We observed that loop regions 1 and 2 play an important role in the survival of E. coli K1 inside neutrophils and dendritic cells, and loop regions 1 and 3 are needed for survival in macrophages. Concomitantly, E. coli K1 mutants expressing loop 1 and 2 mutations were unable to cause meningitis in a newborn mouse model. Of note, mutations in loop 4 of OmpA enhance the severity of the pathogenesis by allowing the pathogen to survive better in circulation and to produce high bacteremia levels. These results demonstrate, for the first time, the roles played by different regions of extracellular loops of OmpA of E. coli K1 in the pathogenesis of meningitis and may help in designing effective preventive strategies against this deadly disease.
外膜蛋白 A(OmpA)已被认为是几种革兰氏阴性细菌感染(如大肠杆菌 K1)的重要毒力因子,大肠杆菌 K1 是导致与高死亡率和发病率相关的新生儿脑膜炎的主要原因。在这项研究中,我们生成了表达 OmpA 的大肠杆菌 K1 突变体,其中来自各种细胞外环的三个或四个氨基酸被替换为丙氨酸,我们检查了它们在几种免疫细胞中存活的能力。我们观察到环区 1 和 2 在大肠杆菌 K1 在内中性粒细胞和树突状细胞中的存活中发挥重要作用,而环区 1 和 3 是在巨噬细胞中存活所必需的。同时,表达环 1 和 2 突变的大肠杆菌 K1 突变体在新生小鼠模型中无法引起脑膜炎。值得注意的是,OmpA 环 4 中的突变通过允许病原体在循环中更好地存活并产生高菌血症水平,从而增强了发病机制的严重程度。这些结果首次证明了大肠杆菌 K1 的 OmpA 细胞外环不同区域在脑膜炎发病机制中的作用,并可能有助于设计针对这种致命疾病的有效预防策略。