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Clone-based haplotyping of Giardia intestinalis assemblage B human isolates

机译:基于克隆的Giardia intestinalis组合B人类分离物的单倍型

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The level of genetic variability of Giardia intestinalis clinical isolates is an intensively studied and discussed issue within the scientific community. Our collection of G. intestinalis human isolates includes six in vitro-cultured isolates from assemblage B, with extensive genetic variability. Such variability prevents the precise genotype characterisation by the multi-locus genotyping (MLG) method commonly used for assemblage A. It was speculated that the intra-assemblage variations represent a reciprocal genetic exchange or true mixed infection. Thus, we analysed gene sequences of the molecular clones of the assemblage B isolates, each representing a single DNA molecule (haplotype) to determine whether the polymorphisms are present within individual haplotypes. Our results, which are based on the analysis of three standard genetic markers (bg, gdh, tpi), point to haplotype diversity and show numerous single nucleotide polymorphisms (SNPs) mostly in codon wobble positions. We do not support the recombinatory origin of the detected haplotypes. The point mutations tolerated by mismatch repair are the possible cause for the detected sequence divergence. The precise sub-genotyping of assemblage B will require finding more conservative genes, as the existing ones are hypervariable in most isolates and prevent their molecular and epidemiological characterisation.
机译:Giardia intestinalis临床分离株的遗传变异程度是科学界内的群体研究和讨论的问题。我们的G. Intestinalis人分离物包含来自组合B的六种体外培养的分离物,具有广泛的遗传变异性。这种可变性通过常用于组装A的多基因座基因分型(MLG)方法来防止精确的基因型表征A.试图有组装内变化代表往复遗传交换或真正的混合感染。因此,我们分析了组合B分离株的分子克隆的基因序列,每个分子克隆分离为单个DNA分子(单倍型)以确定多态性是否存在于单个单倍型内。我们的结果,基于对三种标准遗传标记(BG,GDH,TPI)的分析,指向单倍型多样性,并显示多种单一核苷酸多态性(SNP),主要是密码子摆动位置。我们不支持检测到的单倍型的重组起源。通过不匹配修复耐受的点突变是检测到的序列发散的可能原因。组合B的精确次基因分型将需要找到更保守的基因,因为现有的基因在大多数分离物中是过度变性的,并且预防其分子和流行病学表征。

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