Ramadass P, Meerarani S, Venkatesha M D, Senthilkumar A, Nachimuthu K
Department of Animal Biotechnology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, Tamil Nadu, India.
Int J Syst Bacteriol. 1997 Apr;47(2):575-6. doi: 10.1099/00207713-47-2-575.
Randomly amplified polymorphic DNA (RAPD) fingerprinting of 14 laboratory strains of leptospiral serovars (serovars australis, autumnalis, ballum, bataviae, canicola, grippotyphosa, hardjoprajitno, hebdomadis, icterohaemorrhagiae, javanica, pomona, pyrogenes, panama, and tarassovi) was carried out by using a pair of primers. Each serovar had a unique and distinct fingerprint pattern. DNAs of other bacterial species, including Escherichia coli, Pasteurella multocida, Salmonella spp., Pseudomonas spp., and Klebsiella spp., did not show any amplification. RAPD fingerprinting was found to be a rapid and sensitive method for serovar identification when it was compared to DNA restriction enzyme analysis, which produced a larger number of bands that made it more difficult to compare serovars.
使用一对引物对14种钩端螺旋体血清型(澳洲血清型、秋季血清型、拜伦血清型、巴达维亚血清型、犬血清型、七日热血清型、哈德乔普拉吉诺血清型、七日热血清型、出血性黄疸血清型、爪哇血清型、波摩那血清型、热原质血清型、巴拿马血清型和塔拉索夫血清型)的实验室菌株进行随机扩增多态性DNA(RAPD)指纹分析。每种血清型都有独特且明显的指纹图谱。其他细菌物种的DNA,包括大肠杆菌、多杀巴斯德菌、沙门氏菌属、假单胞菌属和克雷伯菌属,均未显示任何扩增。与DNA限制性酶切分析相比,RAPD指纹分析被发现是一种快速且灵敏的血清型鉴定方法,DNA限制性酶切分析产生的条带数量更多,使得血清型比较更加困难。