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首页> 外文期刊>Iranian Journal of Parasitology. >Prevalence and Genotyping of Trichomonas vaginalis Infected to dsRNA Virus by PCR– Restriction Fragment Length Polymorphism (RFLP)
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Prevalence and Genotyping of Trichomonas vaginalis Infected to dsRNA Virus by PCR– Restriction Fragment Length Polymorphism (RFLP)

机译:PCR限制性片段长度多态性(RFLP)对DsRNA病毒感染DSRNA病毒的患病率和基因分型

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Background: Trichomonas vaginalis is a prevalent sexually transmitted infection cause trichomoniasis. In this study prevalence and genotype of Iranian isolates of T. vaginalis infected (dsRNA) viruses were evaluated by PCR-RFLP and obtained patterns were then confirmed by sequence analysis and genotype of these Iranian isolates confirmed again. Methods: Ten strains of T. vaginalis were collected from 1700 vaginal samples of women referred to hospitals associated with Iran University of Medical Sciences in Tehran, Iran during Feb 2016 to Jul 2017, evaluated in points of infection to T. vaginalis Virus (TVV-1) were used in a PCR-RFLP. All of ten isolates of T. vaginalis were examined by designed nested PCR for actin gene and then digestion patterns of three endonuclease enzymes of HindII, MseI and RsaI were evaluated and genotype of these isolates was defined. Results: By combination of fragments pattern of three enzymes of HindII, RsaI and MseI, three genotypes were found; six genotypes E, two genotypes G and two genotypes I. The most dominant genotypes were genotype E. Among four TVV infected isolates two genotype E, one genotype G and one genotype I were found, however among six uninfected T. vaginalis isolates to TVV-1, all of three genotypes were also found. Conclusion: Three genotypes E, G and I in T. vaginalis infected with dsRNA isolates were found, however, these three genotypes in T. vaginalis without virus were also observed. Further study is needed to evaluate genotypes of T. vaginalis, which infected virus in more great T. vaginalis population.
机译:背景:流动性传播感染的滴虫苗族病菌病导致滴虫病。在这项研究中,通过PCR-RFLP评估了阴道伊朗分离株的伊朗分离株的患病率和基因型,并通过PCR-RFLP评估病毒,然后通过这些伊朗分离物的序列分析和基因型证实得到的图案。方法:从1700年2月在2016年2月到2017年2月到2017年7月,从1700名妇女的阴道样本收集了10株妇女的阴道样本,从伊朗伊朗伊朗伊朗举行。 1)用于PCR-RFLP。通过设计嵌套PCR为肌动蛋白基因设计的所有10个分离株,然后评估了三种内切核酸酶的消化模式,并定义了这些分离株的基因型。结果:通过碎片模式的三种酶,RSAI和MSEI的组合,发现了三种基因型;六个基因型E,两个基因型G和两个基因型I.最显性的基因型是基因型E.四种TVV感染分离株两种基因型E,一种基因型E,一种基因型G和一种基因型,但是在六个未感染的T.阴道分离为TVV- 1,也发现了所有三种基因型。结论:发现了三种基因型E,G和I在T.阴道感染DSRNA分离株的阴道,然而,还观察到没有病毒的阴道中的这三种基因型。需要进一步研究来评估T.AvinAnisis的基因型,在更大的T.阴道人群中感染的病毒。

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