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Aliasghar Bahari

Aliasghar Bahari

Academic rank: Associate Professor
ORCID:
Education: PhD.
ScopusId:
HIndex:
Faculty: Faculty of Veterinary Medicine
Address: Department of Clinical Sciences, Bu-Ali Sina University, Felestin Sq., Hamedan IRAN Postal code: 6517658978 Tel: +98 81 34227350 Fax: +98 81 34227475 Mob: +98 9188130710 E-mail: aliasghar.bahari@basu.ac.ir E-mail: bahariaa@gmail.com http://vm.basu.ac.ir/en/~aliasghar.bahari
Phone: 08134227350

Research

Title
Molecular study of benzimidazole resistance in Teladorsagia circumcincta isolated from sheep in north of Iran
Type
JournalPaper
Keywords
Sheep; Anthelmintic resistance; Teladorsagia; Single nucleotide polymorphism; SNP; β-tubulin
Year
2019
Journal Iranian Journal of Parasitology
DOI
Researchers ، Aliasghar Bahari ، Pezhman Mahmoodi ، ALIREZA SAZMAND

Abstract

Background: Resistance to benzimidazole (BZ) compounds is common in Teladorsagia circumcincta populations in sheep and goats worldwide. Given the importance of anthelmintic resistance and shortage of information on single nucleotide polymorphisms (SNPs) in this prevalent nematode in Iran, this study was conducted. Methods: From June to September 2016, abomasa of 139 sheep of different sexes and ages in Amol City slaughterhouse, northern Iran were examined for isolation of nematodes. Totally 45 male T. circumcincta confirmed by both microscopical and nested-PCR-RFLP methods were included in this study. Susceptibility or resistance of each single T. circumcincta worm to benzimidazoles was assessed using allele-specific PCR. Results: Frequency of genotypes in the present study were 33.33% heterozygote BZ and 66.67% BZ homozygote sensitive. No homozygote resistant worm was found. Conclusion: Resistance against BZs in T. circumcincta of sheep has occurred at a low prevalence in the north of Iran. However, mutated genes might get dominant under drug selection in future. Hence, periodic investigations for early detection of mutated alleles in nematode populations using accurate and sensitive molecular methods such as PCR-RFLP is recommended.