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克氏锥虫基因分型:对检测方法的系统选择,可快速准确区分所有已知谱系。

Genotyping of Trypanosoma cruzi: systematic selection of assays allowing rapid and accurate discrimination of all known lineages.

机构信息

Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

出版信息

Am J Trop Med Hyg. 2009 Dec;81(6):1041-9. doi: 10.4269/ajtmh.2009.09-0305.

Abstract

Trypanosoma cruzi, the agent of Chagas disease, can be subdivided into six discrete typing units (DTUs), TcI, TcIIa, TcIIb, TcIIc, TcIId or TcIIe, each having distinct epidemiologically important features. Dozens of genetic markers are available to determine the DTU to which a T. cruzi isolate belongs, but there is no consensus on which should be used. We selected five assays: three polymerase chain reaction (PCR)-restriction fragment length polymorphisms based on single nucleotide polymorphisms (SNPs) in the HSP60, Histone H1, and GPI loci, and PCR product size polymorphism of the LSU rDNA and mini-exon loci. Each assay was tested for its capacity to differentiate between DTUs using a panel of 48 genetically diverse T. cruzi clones. Some markers allowed unequivocal identification of individual DTUs, however, only by using a combination of multiple markers could all six DTUs be resolved. Based upon the results we recommend a triple-assay comprising the LSU rDNA, HSP60 and GPI markers for reliable, rapid, low-cost DTU assignment.

摘要

克氏锥虫,恰加斯病的病原体,可以细分为六个离散的 typing units(DTUs),TcI、TcIIa、TcIIb、TcIIc、TcIId 或 TcIIe,每个都具有不同的流行病学重要特征。有数十种遗传标记可用于确定 T. cruzi 分离株所属的 DTU,但对于应该使用哪种标记尚无共识。我们选择了五个检测方法:三个基于 HSP60、组蛋白 H1 和 GPI 基因座中单个核苷酸多态性 (SNP) 的聚合酶链反应 (PCR)-限制性片段长度多态性,以及 LSU rDNA 和 mini-exon 基因座的 PCR 产物大小多态性。使用一组 48 个遗传多样化的 T. cruzi 克隆对每个检测方法进行了区分 DTUs 的能力测试。一些标记可以明确识别个别 DTU,但只有通过使用多种标记的组合才能区分所有六个 DTUs。根据结果,我们建议使用 LSU rDNA、HSP60 和 GPI 标记进行三重检测,以实现可靠、快速、低成本的 DTU 分配。

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