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Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation

Ancylostoma caninum is an important zoonotic gastrointestinal nematode of dogs worldwide and a close relative of human hookworms. We recently reported that racing greyhound dogs in the USA are infected with A. caninum that are commonly resistant to multiple anthelmintics. Benzimidazole resistance in...

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Autores principales: Venkatesan, Abhinaya, Jimenez Castro, Pablo D., Morosetti, Arianna, Horvath, Hannah, Chen, Rebecca, Redman, Elizabeth, Dunn, Kayla, Collins, James Bryant, Fraser, James S., Andersen, Erik C., Kaplan, Ray M., Gilleard, John S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013918/
https://www.ncbi.nlm.nih.gov/pubmed/36862759
http://dx.doi.org/10.1371/journal.ppat.1011146
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author Venkatesan, Abhinaya
Jimenez Castro, Pablo D.
Morosetti, Arianna
Horvath, Hannah
Chen, Rebecca
Redman, Elizabeth
Dunn, Kayla
Collins, James Bryant
Fraser, James S.
Andersen, Erik C.
Kaplan, Ray M.
Gilleard, John S.
author_facet Venkatesan, Abhinaya
Jimenez Castro, Pablo D.
Morosetti, Arianna
Horvath, Hannah
Chen, Rebecca
Redman, Elizabeth
Dunn, Kayla
Collins, James Bryant
Fraser, James S.
Andersen, Erik C.
Kaplan, Ray M.
Gilleard, John S.
author_sort Venkatesan, Abhinaya
collection PubMed
description Ancylostoma caninum is an important zoonotic gastrointestinal nematode of dogs worldwide and a close relative of human hookworms. We recently reported that racing greyhound dogs in the USA are infected with A. caninum that are commonly resistant to multiple anthelmintics. Benzimidazole resistance in A. caninum in greyhounds was associated with a high frequency of the canonical F167Y(TTC>TAC) isotype-1 β-tubulin mutation. In this work, we show that benzimidazole resistance is remarkably widespread in A. caninum from domestic dogs across the USA. First, we identified and showed the functional significance of a novel benzimidazole isotype-1 β-tubulin resistance mutation, Q134H(CAA>CAT). Several benzimidazole resistant A. caninum isolates from greyhounds with a low frequency of the F167Y(TTC>TAC) mutation had a high frequency of a Q134H(CAA>CAT) mutation not previously reported from any eukaryotic pathogen in the field. Structural modeling predicted that the Q134 residue is directly involved in benzimidazole drug binding and that the 134H substitution would significantly reduce binding affinity. Introduction of the Q134H substitution into the C. elegans β-tubulin gene ben-1, by CRISPR-Cas9 editing, conferred similar levels of resistance as a ben-1 null allele. Deep amplicon sequencing on A. caninum eggs from 685 hookworm positive pet dog fecal samples revealed that both mutations were widespread across the USA, with prevalences of 49.7% (overall mean frequency 54.0%) and 31.1% (overall mean frequency 16.4%) for F167Y(TTC>TAC) and Q134H(CAA>CAT), respectively. Canonical codon 198 and 200 benzimidazole resistance mutations were absent. The F167Y(TTC>TAC) mutation had a significantly higher prevalence and frequency in Western USA than in other regions, which we hypothesize is due to differences in refugia. This work has important implications for companion animal parasite control and the potential emergence of drug resistance in human hookworms.
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spelling pubmed-100139182023-03-15 Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation Venkatesan, Abhinaya Jimenez Castro, Pablo D. Morosetti, Arianna Horvath, Hannah Chen, Rebecca Redman, Elizabeth Dunn, Kayla Collins, James Bryant Fraser, James S. Andersen, Erik C. Kaplan, Ray M. Gilleard, John S. PLoS Pathog Research Article Ancylostoma caninum is an important zoonotic gastrointestinal nematode of dogs worldwide and a close relative of human hookworms. We recently reported that racing greyhound dogs in the USA are infected with A. caninum that are commonly resistant to multiple anthelmintics. Benzimidazole resistance in A. caninum in greyhounds was associated with a high frequency of the canonical F167Y(TTC>TAC) isotype-1 β-tubulin mutation. In this work, we show that benzimidazole resistance is remarkably widespread in A. caninum from domestic dogs across the USA. First, we identified and showed the functional significance of a novel benzimidazole isotype-1 β-tubulin resistance mutation, Q134H(CAA>CAT). Several benzimidazole resistant A. caninum isolates from greyhounds with a low frequency of the F167Y(TTC>TAC) mutation had a high frequency of a Q134H(CAA>CAT) mutation not previously reported from any eukaryotic pathogen in the field. Structural modeling predicted that the Q134 residue is directly involved in benzimidazole drug binding and that the 134H substitution would significantly reduce binding affinity. Introduction of the Q134H substitution into the C. elegans β-tubulin gene ben-1, by CRISPR-Cas9 editing, conferred similar levels of resistance as a ben-1 null allele. Deep amplicon sequencing on A. caninum eggs from 685 hookworm positive pet dog fecal samples revealed that both mutations were widespread across the USA, with prevalences of 49.7% (overall mean frequency 54.0%) and 31.1% (overall mean frequency 16.4%) for F167Y(TTC>TAC) and Q134H(CAA>CAT), respectively. Canonical codon 198 and 200 benzimidazole resistance mutations were absent. The F167Y(TTC>TAC) mutation had a significantly higher prevalence and frequency in Western USA than in other regions, which we hypothesize is due to differences in refugia. This work has important implications for companion animal parasite control and the potential emergence of drug resistance in human hookworms. Public Library of Science 2023-03-02 /pmc/articles/PMC10013918/ /pubmed/36862759 http://dx.doi.org/10.1371/journal.ppat.1011146 Text en © 2023 Venkatesan et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Venkatesan, Abhinaya
Jimenez Castro, Pablo D.
Morosetti, Arianna
Horvath, Hannah
Chen, Rebecca
Redman, Elizabeth
Dunn, Kayla
Collins, James Bryant
Fraser, James S.
Andersen, Erik C.
Kaplan, Ray M.
Gilleard, John S.
Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title_full Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title_fullStr Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title_full_unstemmed Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title_short Molecular evidence of widespread benzimidazole drug resistance in Ancylostoma caninum from domestic dogs throughout the USA and discovery of a novel β-tubulin benzimidazole resistance mutation
title_sort molecular evidence of widespread benzimidazole drug resistance in ancylostoma caninum from domestic dogs throughout the usa and discovery of a novel β-tubulin benzimidazole resistance mutation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013918/
https://www.ncbi.nlm.nih.gov/pubmed/36862759
http://dx.doi.org/10.1371/journal.ppat.1011146
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