سامانه پشتیبانی خدمات اطلاعات

  اخبار و اعلانات

 آمار

تعداد نشریات163
تعداد شماره‌ها6,772
تعداد مقالات72,961
تعداد مشاهده مقاله132,341,205
تعداد دریافت فایل اصل مقاله103,795,819
ابراهیم زاده موسوی, حسینعلی, Mousavi, Ebrahimzadeh, Shayan, parviz, Soltani, Mehdi, Ebrahimzadeh, Elahe, Rostami, Mina. (1390). Detection of single Dactylogyrus spp. in DNA extracted from infected gill tissue of fishes using Polymerase Chain Reaction. , 5(2), 77-80. doi: 10.22059/ijvm.2011.23100
حسینعلی ابراهیم زاده موسوی; Ebrahimzadeh Mousavi; parviz Shayan; Mehdi Soltani; Elahe Ebrahimzadeh; Mina Rostami. "Detection of single Dactylogyrus spp. in DNA extracted from infected gill tissue of fishes using Polymerase Chain Reaction". , 5, 2, 1390, 77-80. doi: 10.22059/ijvm.2011.23100
ابراهیم زاده موسوی, حسینعلی, Mousavi, Ebrahimzadeh, Shayan, parviz, Soltani, Mehdi, Ebrahimzadeh, Elahe, Rostami, Mina. (1390). 'Detection of single Dactylogyrus spp. in DNA extracted from infected gill tissue of fishes using Polymerase Chain Reaction', , 5(2), pp. 77-80. doi: 10.22059/ijvm.2011.23100
ابراهیم زاده موسوی, حسینعلی, Mousavi, Ebrahimzadeh, Shayan, parviz, Soltani, Mehdi, Ebrahimzadeh, Elahe, Rostami, Mina. Detection of single Dactylogyrus spp. in DNA extracted from infected gill tissue of fishes using Polymerase Chain Reaction. , 1390; 5(2): 77-80. doi: 10.22059/ijvm.2011.23100

Detection of single Dactylogyrus spp. in DNA extracted from infected gill tissue of fishes using Polymerase Chain Reaction

Iranian Journal of Veterinary Medicine
مقاله 1، دوره 5، شماره 2 - شماره پیاپی 586579، شهریور 2011، صفحه 77-80    اصل مقاله (229.62 K)
شناسه دیجیتال (DOI): 10.22059/ijvm.2011.23100
نویسندگان
حسینعلی ابراهیم زاده موسوی1؛ Ebrahimzadeh Mousavi1؛ parviz Shayan2؛ Mehdi Soltani1؛ Elahe Ebrahimzadeh2؛ Mina Rostami1
1گروه بهداشت و بیماریهای آبزیان
2گروه انگل شناسی
چکیده
Dactylogyrus spp. are monogenean worms found mostly as ectoparasites on the gills of several fish species, including carp and goldfish. These parasites are commonly detected by microscopic analysis of the gill lamellae, but this is time-consuming and technically difficult. In contrast to this conventional method, molecular techniques provide specific, sensitive and safe detection of parasites. In the present study, polymerase chain reaction (PCR) and subsequent DNA sequencing were used to detect Dactylogyrus spp. Specific common primers were designed to amplify the ITS-1 region of the rRNA gene of Dactylogyrus spp. Dactylogyrus worms were collected from 100 goldfishes and identified using a dissection microscope. Then, single worms were used for DNA extraction. To evaluate the PCR, a single parasite was added to a parasite-free gill, which then had its DNA extracted. Subsequently, the PCR products were purified and sequenced. Comparison of the nucleotide sequences of the PCR products with GenBank sequences showed that there was 100% homology with sequences from two Dactylogyrus spp., namely Dactylogyrus vastator and Dactylogyrus dulkeiti (registered under accession numbers AJ 564159 and AJ 564126, respectively). The results obtained from sequence analyses were consistent with species identification by microscopy. Therefore, the results show that it is possible to develop a sensitive and precise PCR method for the detection of Dactylogyrus-infected fish using DNA extracted from the whole gill.
کلیدواژه‌ها
ITS-1؛ PCR
آمار
تعداد مشاهده مقاله: 2,751
تعداد دریافت فایل اصل مقاله: 2,513





سامانه مدیریت نشریات علمی. قدرت گرفته از سیناوب