Mechanisms of anthelmintic resistance in Cooperia oncophora, a nematode parasite of cattle

• Main Author: Njue, Annette Igandu
• Other Authors: Prichard, Roger (advisor)
• Format: Others
• Language: en
• Published: McGill University 2003
• Subjects: Cooperia.; Drug resistance.; Anthelmintics.; Ivermectin.; Chloride channels.; Cattle > Parasites.
• Online Access: http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=84302

Anthelmintic resistance is a major problem in livestock, and while it has been slower to emerge in cattle, there are reports of its occurrence. Three broad-spectrum anthelmintics are available for use, and one mechanism of resistance that is common to all is target site alteration. Glutamate-gated chloride channels (GluCls) are an important target for macrocyclic lactone anthelmintics (MLs), while beta-tubulin represents the benzimidazole (BZ) target. The objectives of this thesis were to determine whether GluCls are involved in ML resistance in the cattle parasite Cooperia oncophora , and whether beta-tubulin is involved in BZ and ML resistance. Two isolates of C. oncophora were used. In a fecal egg-count reduction test, ivermectin was found to be 100% effective against one isolate (IVS), and only 77.8% effective against the second isolate (IVR). Two full-length GluCl cDNAs, encoding GluClalpha3 and beta subunits, were cloned. These subunits share high sequence identity with similar GluCl subunits from Haemonchus contortus and Caenorhabditis elegans. Genetic variability analysis of the two genes showed significant differences in allele frequencies between IVS and IVR worms at the GluClalpha3 gene, but not the GluClbeta gene, suggesting that the GluClalpha3 gene is involved in ivermectin resistance. Sequencing of full-length GluCl subunit cDNAs from IVS and IVR worms revealed the presence of mutations in the N-terminal domains. Mutations in the GluClalpha3 caused modest but significant reductions in glutamate, ivermectin and moxidectin sensitivity, while mutations in the GluClbeta abolished glutamate sensitivity. Of the three mutations identified in the IVR GluClalpha3, the L256F mutation accounted for the difference in glutamate and ivermectin response between IVS and IVR GluClalpha3 channels. Two beta-tubulin isotypes cloned from C. oncophora were found to share a high homology with beta-tubulin isotypes from other trichostrongylids. Gen