利用PCR-RFLP和DNA测序技术鉴定人和动物肝吸虫种类

Vilya Shwan Othman, Abdullah A. Hama, Dana Taib Garib, Rostam Hama Zorab
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引用次数: 0

摘要

筋膜吸虫是吸虫(吸虫)的一种,通常被称为肝吸虫,它们是影响人类和动物肝脏的极具致病性的寄生虫,如今,大多数实验室和研究机构都使用基于分子的技术来识别和描述筋膜吸虫。分子诊断标记物,如聚合酶链式反应(PCR)、限制性片段长度多态性(RFLP)和PCR-RFLP方法比免疫学和显微镜方法准确且更具特异性。肝吸虫种类的鉴定将为筋膜炎的治疗和控制提供新的线索。本研究的目的是找到苏莱曼尼市从人和动物中分离的筋膜属的分子特征。使用内窥镜技术从人类和苏莱曼尼新屠宰场屠宰的牲畜中分离出吸虫,从不同宿主中收集了48只肝吸虫;2021年10月至2022年4月期间,人类(n=3)、牛(n=20)、绵羊(n=20个)和山羊(n=5个)。使用核糖体脱氧核糖核酸(rDNA)通用引物,对PCR产物进行限制性片段多态性(RFLP)分析,用限制性内切酶DraII消化PCR产物,并对引物细胞色素氧化酶亚单位1(COX1)的PCR产物进行DNA测序。28s rDNA的PCR-RFLP结果显示,吸虫之间存在遗传多态性,并观察到肝吸虫和巨大吸虫的两种RFLP模式,COX1部分基因的序列分析表明,分离的吸虫属于肝吸虫和大吸虫,具有一定的遗传变异,并且序列的结果以以下登录号存储在基因库中;巨型F.gigantica(OP718780和OP718781)和肝吸虫F.hepatica(OP7187 82、OP718783和OP7187 84)。本研究的结论是F。肝吸虫和巨型吸虫都是伊拉克库尔德斯坦地区人和动物吸虫病的罪魁祸首,因此,RFLP技术和DNA测序是一种可靠的、鉴别肝吸虫种类和基因分型的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liver Fluke Species Identification Isolated From Humans and Animals Using PCR-RFLP and DNA Sequencing
Fasciola species are a member of flatworms belonging to the trematodes (flukes), commonly known as liver fluke, they are extremely pathogenic parasites that affect the liver of humans and animals, nowadays, most laboratories and research facilities use molecular-based techniques for identifying and describing Fasciola species. The molecular diagnostic markers such as polymerase chain reaction (PCR), restriction fragment length polymorphism (RFLP), and PCR-RFLP methods are accurate and more specific than the immunological and microscopical methods. The identification of the species of liver flukes will give a new clue for the treatment and control of fascioliasis. The aim, of this study, is to find the molecular characterization of Fasciola spp. isolated from humans and animals in Sulaimani city. The flukes were isolated from humans using endoscopic techniques and from slaughtered livestock at the new slaughterhouse of Sulaimani, 48 liver flukes were collected from different hosts; human (n = 3), cattle (n = 20), sheep (n = 20), and goats (n = 5) from October 2021 to April 2022. The uinversal primers ribosomal Deoxy Ribo Nuclic Acid (rDNA) were used, then the PCR products were subjected to restriction fragment polymorphism (RFLP) assay and The PCR Product was digested with restriction enzymes DraII, also the DNA sequencing was used for the PCR product of the primer Cytochrome Oxidase subuint 1 (COX1). The results of the PCR-RFLP of the 28s rDNA show the genetic polymorphisms among the flukes and two patterns of RFLP were observed F. hepatica, and F. gigantica, also the sequence analysis of the partial gene of the COX1 showed the isolated flukes belonged to F. hepatica and F. gigantica with some genetic variation, and the result of the sequences was deposited in the Gene Bank under the following Accession numbers; F. gigantica (OP718780 and OP718781) and F. hepatica (OP718782, OP718783, and OP718784). The present study concludes thatF. hepatica and F. gigantica are both responsible for human and animal Fasciolasis in Kurdistan-Iraq, Therefore, RFLP techniques and DNA sequencing are a reliable, and differential method for species and genotyping identification of liver fluke.
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