dc.contributor.author | Safa, AH | |
dc.contributor.author | Harandi, MF | |
dc.contributor.author | Tajaddini, M | |
dc.contributor.author | Rostami-Nejad, M | |
dc.contributor.author | Mohtashami-Pour, M | |
dc.contributor.author | Pestehchian, N | |
dc.date.accessioned | 2018-08-26T09:33:20Z | |
dc.date.available | 2018-08-26T09:33:20Z | |
dc.date.issued | 2016 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57528 | |
dc.description.abstract | High-resolution melting (HRM) is a reliable and sensitive scanning method to detect variation in DNA sequences. We used this method to better understand the epidemiology and transmission of Echinococcus granulosus. We tested the use of HRM to discriminate the genotypes of E. granulosus and E. canadensis. One hundred forty-one hydatid cysts were collected from slaughtered animals in different parts of Isfahan-Iran in 2013. After DNA extraction, the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene was amplified using PCR coupled with the HRM curve. The result of HRM analysis using partial the sequences of cox1 gene revealed that 93, 35, and 2 isolates were identified as G1, G3, and G6 genotypes, respectively. A single nucleotide polymorphism (SNP) was found in locus 9867 of the cox1 gene. This is a critical locus for the differentiation between the G6 and G7 genotypes. In the phylogenictree,thesamplewithaSNPwaslocatedbetween the G6 and G7 genotypes, which suggest that this isolate has a G6/G7 genotype. The HRM analysis developed in the present study provides a powerful technique for molecular and epidemiological studies on echinococcosis in humans and animals. é 2016, National Institute of Health. All rights reserved. | |
dc.language.iso | English | |
dc.relation.ispartof | Japanese Journal of Infectious Diseases | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | Article | |
dc.subject | cox1 gene | |
dc.subject | DNA extraction | |
dc.subject | DNA sequence | |
dc.subject | echinococcosis | |
dc.subject | Echinococcus granulosus | |
dc.subject | Elodea canadensis | |
dc.subject | gene frequency | |
dc.subject | genotype | |
dc.subject | goat | |
dc.subject | high resolution melting analysis | |
dc.subject | nonhuman | |
dc.subject | nucleotide sequence | |
dc.subject | phylogeny | |
dc.subject | polymerase chain reaction | |
dc.subject | real time polymerase chain reaction | |
dc.subject | sheep | |
dc.subject | single nucleotide polymorphism | |
dc.subject | animal | |
dc.subject | bioassay | |
dc.subject | bovine | |
dc.subject | classification | |
dc.subject | DNA denaturation | |
dc.subject | echinococcosis | |
dc.subject | Echinococcus | |
dc.subject | Echinococcus granulosus | |
dc.subject | gene locus | |
dc.subject | genetics | |
dc.subject | Iran | |
dc.subject | isolation and purification | |
dc.subject | parasitology | |
dc.subject | single nucleotide polymorphism | |
dc.subject | veterinary | |
dc.subject | cytochrome c oxidase | |
dc.subject | helminth DNA | |
dc.subject | helminth protein | |
dc.subject | Animals | |
dc.subject | Biological Assay | |
dc.subject | Cattle | |
dc.subject | DNA, Helminth | |
dc.subject | Echinococcosis | |
dc.subject | Echinococcus | |
dc.subject | Echinococcus granulosus | |
dc.subject | Electron Transport Complex IV | |
dc.subject | Genetic Loci | |
dc.subject | Genotype | |
dc.subject | Goats | |
dc.subject | Helminth Proteins | |
dc.subject | Iran | |
dc.subject | Nucleic Acid Denaturation | |
dc.subject | Phylogeny | |
dc.subject | Polymerase Chain Reaction | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Sheep | |
dc.title | Rapid identification of Echinococcus granulosus and E. canadensis using high-resolution melting (HRM) analysis by focusing on a single nucleotide polymorphism | |
dc.type | Article | |
dc.citation.volume | 69 | |
dc.citation.issue | 4 | |
dc.citation.spage | 300 | |
dc.citation.epage | 305 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.7883/yoken.JJID.2015.161 | |