Allele specific PCR for a major marker of levamisole resistance in Haemonchus contortus.


Journal

International journal for parasitology. Drugs and drug resistance
ISSN: 2211-3207
Titre abrégé: Int J Parasitol Drugs Drug Resist
Pays: Netherlands
ID NLM: 101576715

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 11 04 2022
revised: 04 08 2022
accepted: 04 08 2022
pubmed: 16 8 2022
medline: 15 12 2022
entrez: 15 8 2022
Statut: ppublish

Résumé

Haemonchus contortus is a haematophagous parasitic nematode that infects small ruminants and causes significant animal health concerns and economic losses within the livestock industry on a global scale. Treatment primarily depends on broad-spectrum anthelmintics, however, resistance is established or rapidly emerging against all major drug classes. Levamisole (LEV) remains an important treatment option for parasite control, as resistance to LEV is less prevalent than to members of other major classes of anthelmintics. LEV is an acetylcholine receptor (AChR) agonist that, when bound, results in paralysis of the worm. Numerous studies implicated the AChR sub-unit, ACR-8, in LEV sensitivity and in particular, the presence of a truncated acr-8 transcript or a deletion in the acr-8 locus in some resistant isolates. Recently, a single non-synonymous SNP in acr-8 conferring a serine-to-threonine substitution (S168T) was identified that was strongly associated with LEV resistance. Here, we investigate the role of genetic variation at the acr-8 locus in a controlled genetic cross between the LEV susceptible MHco3(ISE) and LEV resistant MHco18(UGA2004) isolates of H. contortus. Using single worm PCR assays, we found that the presence of S168T was strongly associated with LEV resistance in the parental isolates and F3 progeny of the genetic cross surviving LEV treatment. We developed and optimised an allele-specific PCR assay for the detection of S168T and validated the assay using laboratory isolates and field samples that were phenotyped for LEV resistance. In the LEV-resistant field population, a high proportion (>75%) of L

Identifiants

pubmed: 35970104
pii: S2211-3207(22)00018-5
doi: 10.1016/j.ijpddr.2022.08.001
pmc: PMC9399269
pii:
doi:

Substances chimiques

Levamisole 2880D3468G
Anthelmintics 0
Receptors, Cholinergic 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-26

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T020733/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors report that they have no conflict of interest.

Auteurs

Alistair Antonopoulos (A)

School of Veterinary Medicine, University of Glasgow, Glasgow, Scotland, United Kingdom; Institute of Biodiversity, Animal Health, & Comparative Medicine, University of Glasgow, Glasgow, Scotland, United Kingdom. Electronic address: Alistair.Antonopoulos@glasgow.ac.uk.

Stephen R Doyle (SR)

Wellcome Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.

David J Bartley (DJ)

Moredun Research Institute, Penicuik, Scotland, United Kingdom.

Alison A Morrison (AA)

Moredun Research Institute, Penicuik, Scotland, United Kingdom.

Ray Kaplan (R)

St. George's University, Grenada.

Sue Howell (S)

Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, USA.

Cedric Neveu (C)

Institut National de la Recherche Agronomique, Nouzilly, France.

Valentina Busin (V)

School of Veterinary Medicine, University of Glasgow, Glasgow, Scotland, United Kingdom.

Eileen Devaney (E)

Institute of Biodiversity, Animal Health, & Comparative Medicine, University of Glasgow, Glasgow, Scotland, United Kingdom.

Roz Laing (R)

Institute of Biodiversity, Animal Health, & Comparative Medicine, University of Glasgow, Glasgow, Scotland, United Kingdom. Electronic address: Rosalind.Laing@glasgow.ac.uk.

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Classifications MeSH