Prasadarao N V, Wass C A, Weiser J N, Stins M F, Huang S H, Kim K S
Division of Infectious Diseases, Childrens Hospital Los Angeles, California 90027, USA.
Infect Immun. 1996 Jan;64(1):146-53. doi: 10.1128/iai.64.1.146-153.1996.
Escherichia coli is the most common gram-negative bacteria causing meningitis during the neonatal period, but is unclear what microbial factors mediate traversal of E. coli across the blood-brain barrier. Outer membrane protein A (OmpA), a highly conserved 35-kDa protein, was examined for its role in E. coli K1 invasion of brain microvascular endothelial cells (BMEC). The invasive capability of the OmpA+ strains was 25- to 50-fold greater than that of OmpA- strains, and the invasive capability of OmpA- strains was restored to the level of the OmpA+ strain by complementation with the OmpA+ E. coli into BMEC. Two short synthetic peptides (a hexamer, Asn-27-Glu-32, and a pentamer, Gly-65-Asn-69) generated from the N-terminal amino acid sequence of OmpA exhibited significant inhibition of OmpA+ E. coli invasion, suggesting that these two sequences represent the OmpA domains involved in E. coli invasion of BMEC. These findings suggest that OmpA is the first microbial structure identified to enhance E. coli invasion of BMEC, an important event in the pathogenesis of E. coli meningitis.
大肠杆菌是新生儿期引起脑膜炎最常见的革兰氏阴性菌,但尚不清楚哪些微生物因素介导大肠杆菌穿越血脑屏障。外膜蛋白A(OmpA)是一种高度保守的35 kDa蛋白,研究了其在大肠杆菌K1侵袭脑微血管内皮细胞(BMEC)中的作用。OmpA+菌株的侵袭能力比OmpA-菌株高25至50倍,通过将OmpA+大肠杆菌互补到BMEC中,OmpA-菌株的侵袭能力恢复到OmpA+菌株的水平。从OmpA的N端氨基酸序列产生的两个短合成肽(一个六聚体,Asn-27-Glu-32,和一个五聚体,Gly-65-Asn-69)对OmpA+大肠杆菌的侵袭具有显著抑制作用,表明这两个序列代表了参与大肠杆菌侵袭BMEC的OmpA结构域。这些发现表明,OmpA是首个被鉴定出可增强大肠杆菌侵袭BMEC的微生物结构,这是大肠杆菌脑膜炎发病机制中的一个重要事件。