Cargando…

A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance

Fasciola hepatica infection is responsible for substantial economic losses in livestock worldwide and poses a threat to human health in endemic areas. The mainstay of control in livestock and the only drug licenced for use in humans is triclabendazole (TCBZ). TCBZ resistance has been reported on eve...

Descripción completa

Detalles Bibliográficos
Autores principales: Beesley, Nicola J., Cwiklinski, Krystyna, Allen, Katherine, Hoyle, Rebecca C., Spithill, Terry W., La Course, E. James, Williams, Diana J. L., Paterson, Steve, Hodgkinson, Jane E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904461/
https://www.ncbi.nlm.nih.gov/pubmed/36701396
http://dx.doi.org/10.1371/journal.ppat.1011081
_version_ 1784883618472001536
author Beesley, Nicola J.
Cwiklinski, Krystyna
Allen, Katherine
Hoyle, Rebecca C.
Spithill, Terry W.
La Course, E. James
Williams, Diana J. L.
Paterson, Steve
Hodgkinson, Jane E.
author_facet Beesley, Nicola J.
Cwiklinski, Krystyna
Allen, Katherine
Hoyle, Rebecca C.
Spithill, Terry W.
La Course, E. James
Williams, Diana J. L.
Paterson, Steve
Hodgkinson, Jane E.
author_sort Beesley, Nicola J.
collection PubMed
description Fasciola hepatica infection is responsible for substantial economic losses in livestock worldwide and poses a threat to human health in endemic areas. The mainstay of control in livestock and the only drug licenced for use in humans is triclabendazole (TCBZ). TCBZ resistance has been reported on every continent and threatens effective control of fasciolosis in many parts of the world. To date, understanding the genetic mechanisms underlying TCBZ resistance has been limited to studies of candidate genes, based on assumptions of their role in drug action. Taking an alternative approach, we combined a genetic cross with whole-genome sequencing to localise a ~3.2Mbp locus within the 1.2Gbp F. hepatica genome that confers TCBZ resistance. We validated this locus independently using bulk segregant analysis of F. hepatica populations and showed that it is the target of drug selection in the field. We genotyped individual parasites and tracked segregation and reassortment of SNPs to show that TCBZ resistance exhibits Mendelian inheritance and is conferred by a dominant allele. We defined gene content within this locus to pinpoint genes involved in membrane transport, (e.g. ATP-binding cassette family B, ABCB1), transmembrane signalling and signal transduction (e.g. GTP-Ras-adenylyl cyclase and EGF-like protein), DNA/RNA binding and transcriptional regulation (e.g. SANT/Myb-like DNA-binding domain protein) and drug storage and sequestration (e.g. fatty acid binding protein, FABP) as prime candidates for conferring TCBZ resistance. This study constitutes the first experimental cross and genome-wide approach for any heritable trait in F. hepatica and is key to understanding the evolution of drug resistance in Fasciola spp. to inform deployment of efficacious anthelmintic treatments in the field.
format Online
Article
Text
id pubmed-9904461
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-99044612023-02-08 A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance Beesley, Nicola J. Cwiklinski, Krystyna Allen, Katherine Hoyle, Rebecca C. Spithill, Terry W. La Course, E. James Williams, Diana J. L. Paterson, Steve Hodgkinson, Jane E. PLoS Pathog Research Article Fasciola hepatica infection is responsible for substantial economic losses in livestock worldwide and poses a threat to human health in endemic areas. The mainstay of control in livestock and the only drug licenced for use in humans is triclabendazole (TCBZ). TCBZ resistance has been reported on every continent and threatens effective control of fasciolosis in many parts of the world. To date, understanding the genetic mechanisms underlying TCBZ resistance has been limited to studies of candidate genes, based on assumptions of their role in drug action. Taking an alternative approach, we combined a genetic cross with whole-genome sequencing to localise a ~3.2Mbp locus within the 1.2Gbp F. hepatica genome that confers TCBZ resistance. We validated this locus independently using bulk segregant analysis of F. hepatica populations and showed that it is the target of drug selection in the field. We genotyped individual parasites and tracked segregation and reassortment of SNPs to show that TCBZ resistance exhibits Mendelian inheritance and is conferred by a dominant allele. We defined gene content within this locus to pinpoint genes involved in membrane transport, (e.g. ATP-binding cassette family B, ABCB1), transmembrane signalling and signal transduction (e.g. GTP-Ras-adenylyl cyclase and EGF-like protein), DNA/RNA binding and transcriptional regulation (e.g. SANT/Myb-like DNA-binding domain protein) and drug storage and sequestration (e.g. fatty acid binding protein, FABP) as prime candidates for conferring TCBZ resistance. This study constitutes the first experimental cross and genome-wide approach for any heritable trait in F. hepatica and is key to understanding the evolution of drug resistance in Fasciola spp. to inform deployment of efficacious anthelmintic treatments in the field. Public Library of Science 2023-01-26 /pmc/articles/PMC9904461/ /pubmed/36701396 http://dx.doi.org/10.1371/journal.ppat.1011081 Text en © 2023 Beesley 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
Beesley, Nicola J.
Cwiklinski, Krystyna
Allen, Katherine
Hoyle, Rebecca C.
Spithill, Terry W.
La Course, E. James
Williams, Diana J. L.
Paterson, Steve
Hodgkinson, Jane E.
A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title_full A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title_fullStr A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title_full_unstemmed A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title_short A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance
title_sort major locus confers triclabendazole resistance in fasciola hepatica and shows dominant inheritance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904461/
https://www.ncbi.nlm.nih.gov/pubmed/36701396
http://dx.doi.org/10.1371/journal.ppat.1011081
work_keys_str_mv AT beesleynicolaj amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT cwiklinskikrystyna amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT allenkatherine amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT hoylerebeccac amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT spithillterryw amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT lacourseejames amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT williamsdianajl amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT patersonsteve amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT hodgkinsonjanee amajorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT beesleynicolaj majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT cwiklinskikrystyna majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT allenkatherine majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT hoylerebeccac majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT spithillterryw majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT lacourseejames majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT williamsdianajl majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT patersonsteve majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance
AT hodgkinsonjanee majorlocusconferstriclabendazoleresistanceinfasciolahepaticaandshowsdominantinheritance