Ryley H C, Millar-Jones L, Paull A, Weeks J
Department of Medical Microbiology, University of Wales College of Medicine, Heath Park, Cardiff.
J Med Microbiol. 1995 Dec;43(6):436-41. doi: 10.1099/00222615-43-6-436.
Polymerase chain reaction (PCR) ribotyping detects differences in the intergenic spacer between the 16S and 23SrRNA genes. This method was applied to Burkholderia cepacia isolates from 16 Welsh cystic fibrosis (CF) patients attending three different clinics. Amplification of the intergenic spacer followed by an additional digestion step with TaqI restriction endonuclease identified seven distinct electrophoretic patterns among the patient isolates. Each of the seven patterns was distinct from that of the so called "epidemic strain" commonly isolated from patients attending clinics elsewhere in the UK. Two environmental isolates from the hospital clinics and four NCTC reference strains gave different patterns. The simplicity of the method lends itself to use in a general microbiological laboratory.
聚合酶链反应(PCR)核糖体分型可检测16S和23S rRNA基因之间基因间隔区的差异。该方法应用于来自威尔士三家不同诊所的16名囊性纤维化(CF)患者的洋葱伯克霍尔德菌分离株。对基因间隔区进行扩增,随后用TaqI限制性内切酶进行额外的消化步骤,在患者分离株中鉴定出七种不同的电泳图谱。这七种图谱中的每一种都与通常从英国其他地方诊所的患者中分离出的所谓“流行菌株”的图谱不同。来自医院诊所的两个环境分离株和四个NCTC参考菌株呈现出不同的图谱。该方法操作简单,适用于普通微生物实验室。