Stein A, Kruszewska D, Gouvernet J, Raoult D
Faculté de Médecine, Unité des Rickettsies, Marseille, France.
Eur J Epidemiol. 1997 Jun;13(4):471-5. doi: 10.1023/a:1007389315808.
The complete 16S-23S ribosomal DNA (rDNA) internal transcribed spacer (ITS) of 22 isolates of the obligate intracellular bacterium Coxiella burnetii, the agent of Q fever, were amplified by the polymerase chain reaction (PCR) and sequenced using an automated laser fluorescent DNA sequencer. The ITS measured 497 base pairs (bp) and encoded isoleucine-tRNA and alanine-tRNA. The comparison of the sequence alignments of the 22 C. burnetii strains revealed very high levels of sequence similitary (> 99%) although they had different geographic origins and phenotypic characteristics. Sequencing of the 16S-23S rDNA ITS of C. burnetii could be utilized for identification of the bacterium but is not applicable to studies of epidemiology, virulence and taxonomy.
通过聚合酶链反应(PCR)扩增了22株专性细胞内细菌伯氏考克斯体(Q热病原体)的完整16S - 23S核糖体DNA(rDNA)内部转录间隔区(ITS),并使用自动激光荧光DNA测序仪进行测序。ITS长度为497个碱基对(bp),编码异亮氨酸 - tRNA和丙氨酸 - tRNA。尽管22株伯氏考克斯体菌株具有不同的地理来源和表型特征,但它们的序列比对显示出非常高的序列相似性(> 99%)。伯氏考克斯体16S - 23S rDNA ITS测序可用于该细菌的鉴定,但不适用于流行病学、毒力和分类学研究。