Haemonchus contortus P-glycoprotein-2: in situ localisation and characterisation of macrocyclic lactone transport

- Functional Haemonchus contortus PGP-2 was stably expressed in mammalian cells.
- Avermectins inhibited Rhodamine 123 (Rho123) transport by Hco-PGP-2 in a saturable manner.
- Moxidectin showed low, non-saturable inhibition of Rho123 transport by Hco-PGP-2.
- Hco-PGP-2 is expressed in adult H. contortus in head structures and intestine.
- Hco-PGP-2 may regulate avermectin (AVM) levels, contributing to AVM resistance.

Haemonchus contortus is a veterinary nematode that infects small ruminants, causing serious decreases in animal production worldwide. Effective control through anthelmintic treatment has been compromised by the development of resistance to these drugs, including the macrocyclic lactones. The mechanisms of resistance in H. contortus have yet to be established but may involve efflux of the macrocyclic lactones by nematode ATP-binding-cassette transporters such as P-glycoproteins. Here we report the expression and functional activity of H. contortus P-glycoprotein 2 expressed in mammalian cells and characterise its interaction with the macrocyclic lactones, ivermectin, abamectin and moxidectin. The ability of H. contortus P-glycoprotein 2 to transport different fluorophore substrates was markedly inhibited by ivermectin and abamectin in a dose-dependent and saturable way. The profile of transport inhibition by moxidectin was markedly different. H. contortus P-glycoprotein 2 was expressed in the pharynx, the first portion of the worm's intestine and perhaps in adjacent nervous tissue, suggesting a role for this gene in regulating the uptake of avermectins and in protecting nematode tissues from the effects of macrocyclic lactone anthelmintic drugs. H. contortus P-glycoprotein 2 may thus contribute to resistance to these drugs in H. contortus.

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