PREVALANCE AND MOLECULAR CHARACTERIZATION OF GIARDIA DUODENALIS IN LIVESTOCK IN VAN, TURKEY


Ayan A., ALIÇ URAL D., ERDOĞAN H., Kilinc O. O., GÜLTEKİN M., URAL K.

INTERNATIONAL JOURNAL OF ECOSYSTEMS AND ECOLOGY SCIENCE-IJEES, cilt.9, sa.2, ss.289-296, 2019 (ESCI) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 9 Sayı: 2
  • Basım Tarihi: 2019
  • Doi Numarası: 10.31407/ijees9208
  • Dergi Adı: INTERNATIONAL JOURNAL OF ECOSYSTEMS AND ECOLOGY SCIENCE-IJEES
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), CAB Abstracts, Environment Index, Veterinary Science Database
  • Sayfa Sayıları: ss.289-296
  • Van Yüzüncü Yıl Üniversitesi Adresli: Evet

Özet

Giardia duodenalis (Giardia lambia, Giardia intestinalis), a flagellated parasite, is a gastrointestinal pathogen that affects public health worldwide. There are limited studies on the epidemiology and molecular characterization of G. duodenalis in farm animals in Turkey. Molecular characterization is requited to determine the zoonotic potential of Giardia infection. In the present study, 71 calf 50 lamb, and 66 goat fecal stool samples were obtained from the animal rectum using a disposable latex glove and the samples were transferred to the laboratory. Then, the presence of cysts was examined with a microscope using of saturated zinc sulfate flotation method (ZnSO4; 33%). Afterwards, the samples were scanned with ELISA-based rapid diagnostic test kits for diagnosis. Then, DNA was extracted with QIAamp DNA Stool Mini Kit (Qiagen, Germany). Nested PCR was then conducted with the corresponding primers. DNA sequence analysis was conducted on beta-giardin gene region of each PCR positive samples. Then, sequence analyses were blasted and compared with the access numbers in the gene bank (M36728 for sub-genotype A1, AY072723 for sub-genotype A2, for AY072724 sub-genotype A3, AY072725 for subgenotype B1, AY072726 for sub-genotype B2, AY072727 for sub-genotype B3, AY072728 for sub-genotype B4). In the microscopic examination, Giardia cysts were identified in 41 calves, 18 lambs, and 23 goats. Positivity was determined with rapid test kits in 38 calves, 16 lambs, and 20 goats. In nested PCR results, specific bands (511 bp) were obtained in 46 calves, 21 lambs and 24 goats. Sequencing findings demonstrated Assemblage A and subgenotype A3 presence in all animal samples. The importance of treatment and the need to take protective measures due to its zoonotic importance were emphasized.