{"title":"Molecular Method to Diagnosis of some Strongylide Nematode of goats in Nyala Area South Darfur State- Sudan","authors":"S. Hassan","doi":"10.9790/2380-1004025456","DOIUrl":null,"url":null,"abstract":"A total of 100 positive faecal samples were examined using floatation technique to detect strongylide eggs, were confirmed by PCR technique, faecal samples were storage by frozen in -20 ° C and DNA extraction by using phenol/chloroform/isoamylalcohol protocol. PCR leading to amplify the region of the second internal transcribed spacer (ITS-2) of nuclear ribosomal DNA (r DNA) of strongylide species, amplification by three different primers in separate reactions, in each reaction used species specific primer forward and a universal reverse primer to srongylide species NC2. Haemonchus contortus, Trichostrongylus spp and Oesophagostomum columbianum prevalence rates were recorded as 47(47%), 4(4%) and (0%) respectively, Most commonly, small ruminants are affected by multiple strongylide nematodes, mixed infection between Haemonchus contortus and Trichostrongylus spp was recorded 3(3%) Keyword: Strongylide, PCR, ITS-2, NC2, goats, Sudan.","PeriodicalId":14496,"journal":{"name":"IOSR Journal of Agriculture and Veterinary Science","volume":"9 1","pages":"54-56"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IOSR Journal of Agriculture and Veterinary Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9790/2380-1004025456","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A total of 100 positive faecal samples were examined using floatation technique to detect strongylide eggs, were confirmed by PCR technique, faecal samples were storage by frozen in -20 ° C and DNA extraction by using phenol/chloroform/isoamylalcohol protocol. PCR leading to amplify the region of the second internal transcribed spacer (ITS-2) of nuclear ribosomal DNA (r DNA) of strongylide species, amplification by three different primers in separate reactions, in each reaction used species specific primer forward and a universal reverse primer to srongylide species NC2. Haemonchus contortus, Trichostrongylus spp and Oesophagostomum columbianum prevalence rates were recorded as 47(47%), 4(4%) and (0%) respectively, Most commonly, small ruminants are affected by multiple strongylide nematodes, mixed infection between Haemonchus contortus and Trichostrongylus spp was recorded 3(3%) Keyword: Strongylide, PCR, ITS-2, NC2, goats, Sudan.