Stull T L, LiPuma J J, Edlind T D
Department of Pediatrics, Medical College of Pennsylvania, Philadelphia 19129.
J Infect Dis. 1988 Feb;157(2):280-6. doi: 10.1093/infdis/157.2.280.
We investigated the use of ribosomal RNA (rRNA) as a probe for molecular epidemiology of bacterial pathogens. The chromosomal DNA of Escherichia coli, Pseudomonas cepacia, and nontypable Haemophilus influenzae was digested with EcoRI. Agarose gel electrophoresis, Southern blotting, and hybridization by 32P-labeled rRNA revealed eight to 13 bands. The P. cepacia and H. influenzae banding patterns, observed by using an E. coli rRNA probe, were identical to those produced with homologous rRNA probes. Polymorphism of several hybridization bands distinguished all E. coli isolates, nine of 10 H. influenzae isolates, and seven of eight P. cepacia isolates. Two to four bands were common to all P. cepacia and E. coli isolates. The banding patterns of H. influenzae isolates cultured from the trachea and blood of an infant and from the mother's cervix were identical. These data demonstrate that this method is a widely applicable system for determining the molecular epidemiology of genetically diverse gram-negative organisms.
我们研究了将核糖体RNA(rRNA)用作细菌病原体分子流行病学探针的情况。用EcoRI消化大肠杆菌、洋葱伯克霍尔德菌和不可分型流感嗜血杆菌的染色体DNA。琼脂糖凝胶电泳、Southern印迹法以及用32P标记的rRNA进行杂交显示出8至13条带。使用大肠杆菌rRNA探针观察到的洋葱伯克霍尔德菌和流感嗜血杆菌的条带模式与使用同源rRNA探针产生的条带模式相同。几个杂交带的多态性区分了所有大肠杆菌分离株、10株流感嗜血杆菌分离株中的9株以及8株洋葱伯克霍尔德菌分离株中的7株。所有洋葱伯克霍尔德菌和大肠杆菌分离株有两到四条共同的带。从一名婴儿的气管和血液以及母亲宫颈培养的流感嗜血杆菌分离株的条带模式相同。这些数据表明,该方法是一种广泛适用的系统,可用于确定遗传多样性革兰氏阴性菌的分子流行病学。