Weyant R S, Quinn F D, Utt E A, Worley M, George V G, Candal F J, Ades E W
Emerging Bacterial and Mycotic Disease Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333.
J Infect Dis. 1994 Feb;169(2):430-3. doi: 10.1093/infdis/169.2.430.
An in vitro cytotoxicity model that uses an immortalized human microvascular endothelial cell line (HMEC-1) differentiates Brazilian purpuric fever (BPF)-associated Haemophilus influenzae biogroup aegyptius (HAE) strains from non-BPF-associated HAE strains. Toxic strains produced a characteristic HMEC-1 phenotype at an MOI of < 1 bacterium/1000 tissue culture cells (TCC). Nontoxic strains required MOIs of > 1000 bacteria/TCC to produce an observable effect. The cytotoxic phenotype was characterized by the presence of large clumps of HMEC-1 cells, which detached from the monolayer within 48 h of inoculation by HAE cells. The cytotoxic phenotype was observed with 100% of BPF-associated HAE (40/40) and 14% of non-BPF-associated HAE (8/57; P < .001). The ability to study a BPF-associated phenotype in vitro using human microvascular cells should enhance our knowledge of BPF pathogenesis.
一种使用永生化人微血管内皮细胞系(HMEC-1)的体外细胞毒性模型,可将巴西紫癜热(BPF)相关的埃及嗜血杆菌生物群(HAE)菌株与非BPF相关的HAE菌株区分开来。毒性菌株在感染复数(MOI)<1个细菌/1000个组织培养细胞(TCC)时产生特征性的HMEC-1表型。无毒菌株需要MOI>1000个细菌/TCC才能产生可观察到的效应。细胞毒性表型的特征是存在大量HMEC-1细胞团块,这些细胞团块在HAE细胞接种后48小时内从单层中脱离。在100%的BPF相关HAE(40/40)和14%的非BPF相关HAE(8/57;P<.001)中观察到细胞毒性表型。利用人微血管细胞在体外研究BPF相关表型的能力应能增强我们对BPF发病机制的认识。