Adair D M, Worsham P L, Hill K K, Klevytska A M, Jackson P J, Friedlander A M, Keim P
Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona 86011-5640, USA.
J Clin Microbiol. 2000 Apr;38(4):1516-9. doi: 10.1128/JCM.38.4.1516-1519.2000.
We have identified a tetranucleotide repeat sequence, (CAAA)(N), in the genome of Yersinia pestis, the causative agent of plague. This variable-number tandem repeat (VNTR) region has nine alleles and great diversity (calculated as 1 minus the sum of the squared allele frequencies) (diversity value, 0.82) within a set of 35 diverse Y. pestis strains. In contrast, the nucleotide sequence of the lcrV (low-calcium-response) gene differed only slightly among these strains, having a haplotype diversity value of 0.17. Replicated cultures, phenotypic variants of particular strains, and extensively cultured replicates within strains did not differ in VNTR allele type. Thus, while a high mutation rate must contribute to the great diversity of this locus, alleles appear stable under routine laboratory culture conditions. The classic three plague biovars did not have single identifying alleles, although there were allelic biases within biovar categories. The antiqua biovar was the most diverse, with four alleles observed in 5 strains, while the orientalis and mediaevalis biovars exhibited five alleles in 21 strains and three alleles in 8 strains, respectively. The CAAA VNTR is located immediately adjacent to the transcriptional promoters for flanking open reading frames and may affect their activity. This VNTR marker may provide a high-resolution tool for epidemiological analyses of plague.
我们在鼠疫耶尔森菌(鼠疫的病原体)的基因组中鉴定出一个四核苷酸重复序列,(CAAA)(N)。这个可变数目串联重复序列(VNTR)区域有9个等位基因,并且在35株不同的鼠疫耶尔森菌菌株中具有高度多样性(计算为1减去等位基因频率平方和)(多样性值为0.82)。相比之下,这些菌株中lcrV(低钙反应)基因的核苷酸序列差异很小,单倍型多样性值为0.17。复制培养物、特定菌株的表型变体以及菌株内广泛培养的重复样本在VNTR等位基因类型上没有差异。因此,虽然高突变率必定导致了该位点的高度多样性,但在常规实验室培养条件下,等位基因似乎是稳定的。经典的三种鼠疫生物变种没有单一的鉴别等位基因,尽管在生物变种类别内存在等位基因偏差。古典型生物变种最为多样,在5株菌株中观察到4个等位基因,而东方型和中世纪型生物变种在21株菌株中分别表现出5个等位基因和在8株菌株中表现出3个等位基因。CAAA VNTR紧邻侧翼开放阅读框的转录启动子,可能会影响它们的活性。这个VNTR标记可能为鼠疫的流行病学分析提供一个高分辨率工具。