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急性病抗原 A(adaA)染色体区域在查询(Q)热病原体柯克斯体伯氏菌中的微进化。

Microevolution of the chromosomal region of acute disease antigen A (adaA) in the query (Q) fever agent Coxiella burnetii.

机构信息

Bundeswehr Institute of Microbiology, Munich, Germany.

出版信息

PLoS One. 2013;8(1):e53440. doi: 10.1371/journal.pone.0053440. Epub 2013 Jan 3.

Abstract

The acute disease antigen A (adaA) gene is believed to be associated with Coxiella burnetii strains causing acute Q fever. The detailed analysis of the adaA genomic region of 23 human- and 86 animal-derived C. burnetii isolates presented in this study reveals a much more polymorphic appearance and distribution of the adaA gene, resulting in a classification of C. burnetii strains of better differentiation than previously anticipated. Three different genomic variants of the adaA gene were identified which could be detected in isolates from acute and chronic patients, rendering the association of adaA positive strains with acute Q fever disease disputable. In addition, all adaA positive strains in humans and animals showed the occurrence of the QpH1 plasmid. All adaA positive isolates of acute human patients except one showed a distinct SNP variation at position 431, also predominant in sheep strains, which correlates well with the observation that sheep are a major source of human infection. Furthermore, the phylogenetic analysis of the adaA gene revealed three deletion events and supported the hypothesis that strain Dugway 5J108-111 might be the ancestor of all known C. burnetii strains. Based on our findings, we could confirm the QpDV group and we were able to define a new genotypic cluster. The adaA gene polymorphisms shown here improve molecular typing of Q fever, and give new insights into microevolutionary adaption processes in C. burnetii.

摘要

急性病抗原 A(adaA)基因被认为与引起急性 Q 热的柯克斯体菌株有关。本研究对 23 个人源和 86 个动物源的柯克斯体分离株的 adaA 基因组区域进行了详细分析,结果表明 adaA 基因的多态性和分布更为复杂,从而可以更好地区分柯克斯体菌株。鉴定出 adaA 基因的三种不同基因组变异型,可在急性和慢性患者的分离株中检测到,这使得 adaA 阳性菌株与急性 Q 热疾病的关联变得值得怀疑。此外,在人类和动物中所有 adaA 阳性菌株都显示出 QpH1 质粒的存在。除了一个之外,所有急性人类患者的 adaA 阳性分离株在位置 431 处都表现出明显的 SNP 变异,这在绵羊菌株中也很普遍,这与绵羊是人类感染的主要来源的观察结果相符。此外,adaA 基因的系统发育分析显示了三个缺失事件,并支持了 Dugway 5J108-111 菌株可能是所有已知柯克斯体菌株的祖先的假说。基于我们的发现,我们可以确认 QpDV 组,并能够定义一个新的基因型簇。这里显示的 adaA 基因多态性可改善 Q 热的分子分型,并为柯克斯体的微观进化适应过程提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cd2/3536764/8df248c70bfa/pone.0053440.g001.jpg

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