Yousef Naserzadeh, Насерзаде Юсеф, E. Pakina, Пакина Елена Николаевна, A. M. Nafchi, Нафчи Абдорреза Мохаммади, A. Gadzhikurbanov, Гаджикурбанов Анвар Шихрагимович
{"title":"黑腹果蝇PCR特异性鉴定方法","authors":"Yousef Naserzadeh, Насерзаде Юсеф, E. Pakina, Пакина Елена Николаевна, A. M. Nafchi, Нафчи Абдорреза Мохаммади, A. Gadzhikurbanov, Гаджикурбанов Анвар Шихрагимович","doi":"10.22363/2312-797x-2020-15-2-134-141","DOIUrl":null,"url":null,"abstract":"D. melanogaster is one of the most harmful citrus fruit flies having a large number of host plants. The molecular diagnostic method has been created for identification the D. melanogaster from another non-quarantine species Drosophila spp. The proposed method for differentiation is to use the mitochondrial DNA cytochrome oxidase I gene region 709-bp. We amplified samples of DNA with primers Droso-S391 and Droso-A381 by D. melanogaster, D. suzukii, and D. Simulans collections in the laboratory samples from many countries and contrasted with sequences of other GenBank Drosophila taxa. The findings of a polymerase chain reaction (PCR) based on DNA sequence polymorphisms showed that these primers accurately identify the area of the gene as well as the unique primers of Drosophila melanogaster.","PeriodicalId":53086,"journal":{"name":"RUDN Journal of Agronomy and Animal Industries","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Specific Identification Method based on PCR for Drosophila melanogaster\",\"authors\":\"Yousef Naserzadeh, Насерзаде Юсеф, E. Pakina, Пакина Елена Николаевна, A. M. Nafchi, Нафчи Абдорреза Мохаммади, A. Gadzhikurbanov, Гаджикурбанов Анвар Шихрагимович\",\"doi\":\"10.22363/2312-797x-2020-15-2-134-141\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"D. melanogaster is one of the most harmful citrus fruit flies having a large number of host plants. The molecular diagnostic method has been created for identification the D. melanogaster from another non-quarantine species Drosophila spp. The proposed method for differentiation is to use the mitochondrial DNA cytochrome oxidase I gene region 709-bp. We amplified samples of DNA with primers Droso-S391 and Droso-A381 by D. melanogaster, D. suzukii, and D. Simulans collections in the laboratory samples from many countries and contrasted with sequences of other GenBank Drosophila taxa. The findings of a polymerase chain reaction (PCR) based on DNA sequence polymorphisms showed that these primers accurately identify the area of the gene as well as the unique primers of Drosophila melanogaster.\",\"PeriodicalId\":53086,\"journal\":{\"name\":\"RUDN Journal of Agronomy and Animal Industries\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RUDN Journal of Agronomy and Animal Industries\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22363/2312-797x-2020-15-2-134-141\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RUDN Journal of Agronomy and Animal Industries","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22363/2312-797x-2020-15-2-134-141","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Specific Identification Method based on PCR for Drosophila melanogaster
D. melanogaster is one of the most harmful citrus fruit flies having a large number of host plants. The molecular diagnostic method has been created for identification the D. melanogaster from another non-quarantine species Drosophila spp. The proposed method for differentiation is to use the mitochondrial DNA cytochrome oxidase I gene region 709-bp. We amplified samples of DNA with primers Droso-S391 and Droso-A381 by D. melanogaster, D. suzukii, and D. Simulans collections in the laboratory samples from many countries and contrasted with sequences of other GenBank Drosophila taxa. The findings of a polymerase chain reaction (PCR) based on DNA sequence polymorphisms showed that these primers accurately identify the area of the gene as well as the unique primers of Drosophila melanogaster.