{"title":"伊朗中部卡尚和阿拉克地区反刍家畜片形虫和双骨吸虫分离株的分子鉴定。","authors":"Mohsen Arbabi, Hossein Hooshyar, Mahdi Delavari","doi":"10.1007/s12639-024-01771-2","DOIUrl":null,"url":null,"abstract":"<p><p><i>Fascioliasis</i> and <i>Dicrocoeliasis</i> are important trematode infections that affect humans and ruminants worldwide. Molecular techniques have a conclusive role in detection of liver flukes. The purpose of the current study was to find outthe genotypic diversity of <i>Fasciola</i> and <i>Dicrocoelium</i> spp. isolated from different hosts in Iran. Totally, 160 and 200 adult <i>Fasciola</i> and <i>Dicrocoelium</i> spp. isolates were collected from infected cattle, sheep, and goatsfrom two abattoirs in the center of Iran.PCR-RFLP, and DNA sequences nuclear markers (18 S, 28 S, ITS) and the mitochondrial marker (ND1, CO1) were applied. PCR products of <i>Dicrocoelium</i> and <i>Fasciola</i> samples were subjected to digestion by <i>BfaI</i>, <i>Tru1I</i>, <i>BsrBI</i>, <i>ECO881</i>, and <i>Hind III</i> enzymes. DNA from 60 isolates of <i>Fasciola</i> and <i>Dicrocoelium</i> of different hosts were sequenced and evaluated. The PCR reaction showed the length of 18 S, 28 S, ND1, CO1 of <i>Fasciola</i> at 260 bp, 618 bp, 700 bp, and 500 bp, and the length of the ITS2 and 28 S of <i>Dicrocoelium</i> was 236 bp and 963 bp respectively. <i>D. dendriticum</i> has an RFLP pattern of 110, and 126 bp (ITS2), and 116, 293, 409 bp (28 S) using, <i>BfaI</i> and <i>Tru1I</i> restriction enzymes. <i>F. gigantica</i> has a profile of 333, and 285 bp (28 S) using <i>BsrBI</i> enzyme. The RFLP pattern of genotype <i>F</i>. <i>hepatica</i> was 73, 120, and 507 bp (ND1) and 119 and 381 bp (CO1) in size using <i>Hind III</i> and <i>ECO881</i> enzymes. Using the PCR-RFLP, two species of <i>Fasciola</i> (<i>F. hepatica</i> and <i>F. gigantica</i>), and one species of Dicrocoelium (<i>D. dendriticum</i>) were identified. To uncover the genetic population structure of liver flukes across the country, future studies are still required.</p>","PeriodicalId":16664,"journal":{"name":"Journal of Parasitic Diseases","volume":"49 2","pages":"453-464"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12126427/pdf/","citationCount":"0","resultStr":"{\"title\":\"Molecular identification of <i>Fasciola</i> and <i>Dicrocoelium</i> species isolates in ruminants livestock from Kashan and Arak in center of Iran.\",\"authors\":\"Mohsen Arbabi, Hossein Hooshyar, Mahdi Delavari\",\"doi\":\"10.1007/s12639-024-01771-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Fascioliasis</i> and <i>Dicrocoeliasis</i> are important trematode infections that affect humans and ruminants worldwide. Molecular techniques have a conclusive role in detection of liver flukes. The purpose of the current study was to find outthe genotypic diversity of <i>Fasciola</i> and <i>Dicrocoelium</i> spp. isolated from different hosts in Iran. Totally, 160 and 200 adult <i>Fasciola</i> and <i>Dicrocoelium</i> spp. isolates were collected from infected cattle, sheep, and goatsfrom two abattoirs in the center of Iran.PCR-RFLP, and DNA sequences nuclear markers (18 S, 28 S, ITS) and the mitochondrial marker (ND1, CO1) were applied. PCR products of <i>Dicrocoelium</i> and <i>Fasciola</i> samples were subjected to digestion by <i>BfaI</i>, <i>Tru1I</i>, <i>BsrBI</i>, <i>ECO881</i>, and <i>Hind III</i> enzymes. DNA from 60 isolates of <i>Fasciola</i> and <i>Dicrocoelium</i> of different hosts were sequenced and evaluated. The PCR reaction showed the length of 18 S, 28 S, ND1, CO1 of <i>Fasciola</i> at 260 bp, 618 bp, 700 bp, and 500 bp, and the length of the ITS2 and 28 S of <i>Dicrocoelium</i> was 236 bp and 963 bp respectively. <i>D. dendriticum</i> has an RFLP pattern of 110, and 126 bp (ITS2), and 116, 293, 409 bp (28 S) using, <i>BfaI</i> and <i>Tru1I</i> restriction enzymes. <i>F. gigantica</i> has a profile of 333, and 285 bp (28 S) using <i>BsrBI</i> enzyme. The RFLP pattern of genotype <i>F</i>. <i>hepatica</i> was 73, 120, and 507 bp (ND1) and 119 and 381 bp (CO1) in size using <i>Hind III</i> and <i>ECO881</i> enzymes. Using the PCR-RFLP, two species of <i>Fasciola</i> (<i>F. hepatica</i> and <i>F. gigantica</i>), and one species of Dicrocoelium (<i>D. dendriticum</i>) were identified. To uncover the genetic population structure of liver flukes across the country, future studies are still required.</p>\",\"PeriodicalId\":16664,\"journal\":{\"name\":\"Journal of Parasitic Diseases\",\"volume\":\"49 2\",\"pages\":\"453-464\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12126427/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Parasitic Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s12639-024-01771-2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/26 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Parasitic Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12639-024-01771-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/26 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 0
摘要
片形吸虫病和棘球绦虫病是影响全世界人类和反刍动物的重要吸虫感染。分子技术在肝吸虫检测中具有决定性作用。本研究的目的是了解伊朗不同寄主分离的片形吸虫和双星吸虫的基因型多样性。从伊朗中部两个屠宰场感染的牛、绵羊和山羊中分别采集到160株和200株成年片形吸虫和双骨吸虫分离株。应用PCR-RFLP和DNA序列分析核标记(18s、28s、ITS)和线粒体标记(ND1、CO1)。采用BfaI、Tru1I、BsrBI、ECO881和Hind III酶解双骨吸虫和片形吸虫样品的PCR产物。对来自不同宿主的60株片形吸虫和双骨吸虫的DNA进行了测序和评价。PCR反应显示,片形吸虫的18 S、28 S、ND1和CO1的长度分别为260 bp、618 bp、700 bp和500 bp,双骨吸虫的ITS2和28 S的长度分别为236 bp和963 bp。在使用BfaI和Tru1I限制性内切酶时,树突草的RFLP模式分别为110、126 bp (ITS2)和116、293、409 bp (28 S)。利用BsrBI酶,F. gigantica的基因谱为333 bp, 285bp (28s)。Hind III酶和ECO881酶的RFLP分别为73、120、507 bp (ND1)和119、381 bp (CO1)。PCR-RFLP鉴定出2种片形吸虫(肝片形吸虫和巨型片形吸虫)和1种树状吸虫(树突片形吸虫)。为了揭示全国范围内肝吸虫的遗传种群结构,还需要进一步的研究。
Molecular identification of Fasciola and Dicrocoelium species isolates in ruminants livestock from Kashan and Arak in center of Iran.
Fascioliasis and Dicrocoeliasis are important trematode infections that affect humans and ruminants worldwide. Molecular techniques have a conclusive role in detection of liver flukes. The purpose of the current study was to find outthe genotypic diversity of Fasciola and Dicrocoelium spp. isolated from different hosts in Iran. Totally, 160 and 200 adult Fasciola and Dicrocoelium spp. isolates were collected from infected cattle, sheep, and goatsfrom two abattoirs in the center of Iran.PCR-RFLP, and DNA sequences nuclear markers (18 S, 28 S, ITS) and the mitochondrial marker (ND1, CO1) were applied. PCR products of Dicrocoelium and Fasciola samples were subjected to digestion by BfaI, Tru1I, BsrBI, ECO881, and Hind III enzymes. DNA from 60 isolates of Fasciola and Dicrocoelium of different hosts were sequenced and evaluated. The PCR reaction showed the length of 18 S, 28 S, ND1, CO1 of Fasciola at 260 bp, 618 bp, 700 bp, and 500 bp, and the length of the ITS2 and 28 S of Dicrocoelium was 236 bp and 963 bp respectively. D. dendriticum has an RFLP pattern of 110, and 126 bp (ITS2), and 116, 293, 409 bp (28 S) using, BfaI and Tru1I restriction enzymes. F. gigantica has a profile of 333, and 285 bp (28 S) using BsrBI enzyme. The RFLP pattern of genotype F. hepatica was 73, 120, and 507 bp (ND1) and 119 and 381 bp (CO1) in size using Hind III and ECO881 enzymes. Using the PCR-RFLP, two species of Fasciola (F. hepatica and F. gigantica), and one species of Dicrocoelium (D. dendriticum) were identified. To uncover the genetic population structure of liver flukes across the country, future studies are still required.
期刊介绍:
The primary constituency of the Journal of Parasitic Diseases is parasitology. It publishes original research papers (pure, applied and clinical), which contribute significantly to any area of parasitology. Research papers on various aspects of cellular and molecular parasitology are welcome.