首页> 外文期刊>Bulgarian journal of veterinary medicine. >SEQUENCING AND PHYLOGENETIC ANALYSIS OF MITOCHONDRIAL COX1 AND NAD1 GENES IN?TOXOCARA CANIS?AND?TOXASCARIS LEONINA?ISOLATES FROM IRAN
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SEQUENCING AND PHYLOGENETIC ANALYSIS OF MITOCHONDRIAL COX1 AND NAD1 GENES IN?TOXOCARA CANIS?AND?TOXASCARIS LEONINA?ISOLATES FROM IRAN

机译:线粒体COX1和NAD1基因的测序和系统发育分析?Toxocara canis?和?Toxascaris Leonina?来自伊朗的分离物

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Toxocara canis and Toxascaris leonina are the most important ascaridoid nematodes of the family Toxocaridae. The present study was aimed to characterisation and analysis of genetic variation within and among T. canis and T. leonina isolates obtained from Iran by sequencing partial mitochondrial cytochrome c oxidase subunit 1 (pcox1) and partial NADH dehydrogenase subunit 1 (pnad1) genes. A total number of 134 adult nematodes belonging to Toxocaridae family were collected from stray dogs in Alborz province, Iran during 2015 and 2016. Polymerase chain reaction (PCR) was performed and products were sequenced. Sequences of two mitochondrial cox1 and nad1 genes were compared with other sequences in the GenBank, while multiple sequences alignment analysis was performed using the Bioedit and MEGA6 software and phylogenetic tree was plotted. For all isolates, amplicons of about 450 and 350 base pairs (bp) were successfully produced by PCR for cox1 and nad1, respectively. All sequences of T. canis isolates from present study were 100% homologous across the nad1 gene but not in the cox1 gene. The results indicate that the PCR method based on sequence of cox1 and nad1 genes is a suitable technique for the differentiation of T. canis and T. leonina species and that mtDNA regions could be used as genetic markers for the identification and differentiation of Toxocara species.
机译:Toxocara Canis和Toxascaris Leonina是毒素的最重要的蛔虫线虫。本研究旨在通过测序部分线粒体细胞色素C氧化酶亚基1(PCOX1)和部分NADH脱氢酶亚基1(PNAD1)基因来表征和分析从伊朗获得的遗传变异和T. in in in in in in in in in in in leanina分离物。在2015年和2016年伊朗的伊尔尔兹省的流浪狗收集了属于毒素的134名成人线虫。在2015年和2016年期间,进行聚合酶链式反应(PCR),并测序产物。将两个线粒体COX1和NAD1基因的序列与Genbank中的其他序列进行比较,而使用生物培训和Mega6软件和系统发育树进行多个序列对准分析。对于所有分离物,通过PCR分别通过PCR为COX1和NAD1成功产生约450和350个碱基对(BP)的扩增子。来自本研究的所有T. canis分离物的序列在NAD1基因上均为100%同源,但不在COX1基因中。结果表明,基于COX1和NAD1基因序列的PCR方法是一种合适的技术,用于分化T. canis和T.Leonina物种,并且MTDNA区可用作毒素物种的鉴定和分化的遗传标志物。

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