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首页> 外文期刊>Parasitology Research >Geographical clustering of Trypanosoma cruzi I groups from Colombia revealed by low-stringency single specific primer-PCR of the intergenic regions of spliced-leader genes
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Geographical clustering of Trypanosoma cruzi I groups from Colombia revealed by low-stringency single specific primer-PCR of the intergenic regions of spliced-leader genes

机译:低严格性单特异性引物-剪接前导基因基因间区域的PCR揭示了哥伦比亚克氏锥虫I组的地理聚类

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A low-stringency single-primer polymerase chain reaction (LSSP-PCR) typing procedure targeted to the intergenic regions of spliced-leader genes (SL) was designed to profile Trypanosoma cruzi I stocks from endemic regions of Colombia. Comparison between SL-LSSP-PCR profiles of parasite DNA from vector faeces and cultures isolated from those faeces showed more conservative signatures than profiles using LSSP-PCR targeted to the minicircle variable regions (kDNA). This was also observed by analysing 15 parasite clones from one stock as well as serial samples of a same stock after in vitro culturing or inoculation into mice. Thus, SL-LSSP-PCR appears more appropriate than kDNA-LSSP-PCR for reliable typing of major T. cruzi I groups from in vitro cultured stocks and triatomine faeces. SL-LSSP-PCR grouped 46 of 47 T. cruzi I Colombian stocks according to their geographical procedences in four clusters: Cluster Cas from Casanare Department, Cluster Mg from Northern Magdalena department, Cluster Mom from Momposina Depression in Southern Magdalena and finally Cluster NW from northwestern Colombia, including Sucre, Chocó, Córdoba and Antioquia departments. Sequence analysis identified punctual mutations among amplicons from each cluster. Within Cluster Mg, sequence polymorphism allowed association with different sylvatic vector species. Novel SL sequences and LSSP-PCR profiles are reported from T. cruzi I infecting Eratyrus cuspidatus, Panstrongylus geniculatus and Rhodnius pallescens vectors.
机译:针对接合前导基因(SL)的基因间区域的低严格性单引物聚合酶链式反应(LSSP-PCR)分型程序旨在分析哥伦比亚流行地区的锥虫锥虫种群。来自载体粪便的寄生虫DNA的SL-LSSP-PCR谱和从这些粪便分离的培养物的SL-LSSP-PCR谱的比较显示,与使用针对小圆圈可变区(kDNA)的LSSP-PCR的谱相比,保守的签名更为保守。在体外培养或接种到小鼠中后,通过分析来自一种原种的15种寄生虫克隆以及同一原种的系列样品也观察到了这一点。因此,SL-LSSP-PCR似乎比kDNA-LSSP-PCR更适合于可靠地分选体外培养的原种和三松散粪便中的主要T. cruzi I组。 SL-LSSP-PCR按照地理顺序将47种哥伦比亚T. cruzi I种群中的46种按四类进行分组:Casanare部门的Cas集群,Magdalena北部的Mg集群,Magdalena南部的Momposina Depression的集群Mom和最后来自Magdalena的Cluster NW集群哥伦比亚西北部,包括苏克雷,乔科,科尔多瓦和安蒂奥基亚省。序列分析确定了每个簇的扩增子之间的守时突变。在簇镁中,序列多态性允许与不同的sylvatic载体物种关联。据报道,新的SL序列和LSSP-PCR图谱由克鲁维氏菌I感染了尖头鹰嘴豆,泛古斯潘提虫和淡色红球菌载体。

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