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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.
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.
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Other Contributors
EPub Date
Publication Date
2023-01-26
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Article - AAM
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Abstract
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.
Citation
Beesley, N. J, Cwiklinski, K., Allen, K., Hoyle, R. C., Spithill, T. W., La Course E. J., Williams, D. J. L., Paterson, S., & Hodgkinson, J. E. (2023). A major locus confers triclabendazole resistance in Fasciola hepatica and shows dominant inheritance. PLoS Pathogens, 19(1), article-number e1011081. https://doi.org/10.1371/journal.ppat.1011081
Publisher
Public Library of Science
Journal
PLoS Pathogens
Research Unit
DOI
10.1371/journal.ppat.1011081
PubMed ID
PubMed Central ID
Type
Article
Language
Description
Series/Report no.
ISSN
1553-7366
EISSN
1553-7374
