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首页> 外文期刊>Advanced Biomedical Research >Identification of genotypes of Giardia duodenalis human isolates in Isfahan, Iran, using polymerase chain reaction - Restriction Fragment Length polymorphism
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Identification of genotypes of Giardia duodenalis human isolates in Isfahan, Iran, using polymerase chain reaction - Restriction Fragment Length polymorphism

机译:使用聚合酶链反应-限制性片段长度多态性鉴定伊朗伊斯法罕的十二生虫(Giardia duodenalis)人类分离株的基因型

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Background : Giardia duodenalis is one of the most prevalent intestinal parasites of human. It also infects a wide range of mammals.Two genotype of G.duodenalis (A and B) were commonly reported among humans with different frequency of distribution in different geographical locations. This work was conducted to discriminate genotypes of Giardia duodenalis human isolates in Isfahan city using PCR- RFLP. This is the first molecular study on human isolates of G.duodenalis in the area. Methods: Samples were collected from different health centers of Isfahan city during June 2011 and February 2012. From 175 Giardia positive stool samples 67 specimens were selected randomly. Cysts of Giardia positive samples were concentrated by flotation sucrose. Extraction of genomic DNA from trophozoite and cysts was performed using QIAamp Stool Mini kit with a modified protocol. PCR- RFLP method was used to amplify a fragment of 458bp at the glutamate dehydrogenase locus, and restriction enzymes BspLI and RsaI differentiated human genotypes A and B and their subgroups. Results: PCR - RFLP assay of 67 isolates showed 40(59.7%) isolates as Genotype A group II, 23(34.32%) samples as Genotype B Group III and two (2.98%) sample as Genotype B group IV. Mixed genotype of (AII and B) was detected only in two isolates (2.98%). Conclusions: PCR - RFLP assay targeting gdh locus is a sensitive tool and discriminates genotypes, sub genotypes and mixed type of G.duodenalis . Results of our study suggest both anthroponotic and zoonotic origins for the infections respectively.
机译:背景:贾第鞭毛虫是人类最普遍的肠道寄生虫之一。它也感染了广泛的哺乳动物。人类中普遍报告了十二指肠球菌的两个基因型(A和B),它们在不同地理位置的分布频率不同。使用PCR-RFLP进行这项工作以区分伊斯法罕市的十二生贾第鞭毛虫人类分离株的基因型。这是该地区人类十二指肠球菌的首次分子研究。方法:2011年6月至2012年2月,从伊斯法罕市不同卫生中心收集样本。从175例贾第虫阳性粪便样本中随机抽取67份样本。浮选蔗糖浓缩贾第虫阳性样品的囊肿。使用改良的QIAamp Stool Mini试剂盒从滋养体和囊肿中提取基因组DNA。 PCR-RFLP方法用于在谷氨酸脱氢酶基因座扩增458bp的片段,限制性酶BspLI和RsaI区分了人类基因型A和B及其亚型。结果:PCR-RFLP分析的67个分离株显示40个(59.7%)分离株为基因型A组,23个(34.32%)样品为基因型B组,两个(2.98%)样品为基因型B组。 (AII和B)的混合基因型仅在两个分离株(2.98%)中检测到。结论:靶向gdh基因座的PCR-RFLP检测是一种敏感工具,可区分十二指肠球菌的基因型,亚基因型和混合型。我们的研究结果表明,感染分别是人为和人畜共患的。

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