Holberg-Petersen M, Steinbakk M, Figenschau K J, Jantzen E, Eng J, Melby K K
Ullevaal University Hospital, Oslo, Norway.
APMIS. 1999 Feb;107(2):231-9.
Twenty-one mycobacterial type strains and 334 clinical isolates of mycobacteria were identified by standardized sequence analysis using part of the gene encoding 16S rRNA. Apart from two clinical isolates, the resulting sequences corresponded to previously published sequences. The results of the molecular determinations of the type strains completely overlapped the identities obtained using conventional techniques (cultural characteristics, biochemical tests, commercial DNA probes, and gas chromatographic lipid profiles). Of 323 isolates conventionally identified as slow-growing mycobacteria, 318 (98.5%) were identified to the same species or group level by 16S rDNA sequence analysis, while 6 of the 11 strains of rapid growers obtained a corresponding identity with the two approaches. The sequencing protocol combined with a few cultural characteristics (i.e. growth rate, pigmentation and susceptibility testing) offers a rapid, reliable and usually definite identification of mycobacterial isolates.
使用编码16S rRNA的基因部分进行标准化序列分析,鉴定出了21株分枝杆菌标准菌株和334株分枝杆菌临床分离株。除了两株临床分离株外,所得序列与先前发表的序列一致。标准菌株的分子鉴定结果与使用传统技术(培养特征、生化试验、商业DNA探针和气相色谱脂质谱)获得的鉴定结果完全重叠。在323株传统上鉴定为生长缓慢的分枝杆菌分离株中,通过16S rDNA序列分析,318株(98.5%)被鉴定到相同的物种或组水平,而11株生长快速的菌株中有6株通过两种方法获得了相应的鉴定结果。结合一些培养特征(即生长速率、色素沉着和药敏试验)的测序方案能够快速、可靠且通常能明确地鉴定分枝杆菌分离株。