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July 17th, 2025
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Sydney School of Veterinary Science, Faculty of Science, The University of Sydney, Australia
genomics
biorxiv

Characterisation of β-tubulin isotypes in Uncinaria stenocephala and implications for benzimidazole resistance in hookworms

Stocker, T.Open in Google Scholar•Slapeta, J.Open in Google Scholar

Uncinaria stenocephala is a widespread hookworm of dogs across Europe, Canada, southern Australia, and other temperate regions, where it often outnumbers infections caused by Ancylostoma caninum. Although a putative {beta}-tubulin isotype-1 mutation associated with resistance has been detected in U. stenocephala, clinical resistance to benzimidazoles has not yet been confirmed. Benzimidazole resistance is linked to single nucleotide polymorphisms (SNPs) in the {beta}-tubulin isotype-1 gene; however, the {beta}-tubulin genes of U. stenocephala have not been fully characterised. We aimed to identify {beta}-tubulin genes and confirm the coding sequences for key residues (Q134, F167, E198, and F200) in the {beta}-tubulin isotype-1 gene of the U. stenocephala genome. Two U. stenocephala specimens were subjected to Illumina sequencing, and species identity was confirmed through morphological and molecular analysis using ITS rDNA and cox-1 markers. Genome assembly revealed the presence of {beta}-tubulin isotype-1 (10 exons) and isotype-2 (9 exons), both homologous to {beta}-tubulins from other hookworms (A. caninum, A. ceylanicum, A. duodenale and Necator americanus). The {beta}-tubulin isotype-1 protein sequence of U. stenocephala contained two variable residues (S37Q and G441A) compared to other hookworm sequences. While the isotype-2 protein sequence was conserved among Ancylostoma species, U. stenocephala exhibited six distinct polymorphisms (E39D, T40S, N115S, L130I, A287S, T439G). The benzimidazole-susceptible residues (Q134, F167, E198, F200) were present in the {beta}-tubulin isotype-1 protein sequence. Characterisation of the complete coding regions of {beta}-tubulin isotypes 1 and 2 enables population-level screening for benzimidazole resistance-associated SNPs and provides a foundation for future epidemiological studies in U. stenocephala.

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