Phylogenetic and transcriptomic study of aldo-keto reductases in Haemonchus contortus and their inducibility by flubendazole
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38996597
PubMed Central
PMC11296255
DOI
10.1016/j.ijpddr.2024.100555
PII: S2211-3207(24)00036-8
Knihovny.cz E-zdroje
- Klíčová slova
- AKR, Drug-resistance, Drug-susceptibility, Expression profile, Haemonchus contortus, Phylogenetic analysis,
- MeSH
- aldehydreduktasa genetika metabolismus MeSH
- aldo-keto reduktasy * genetika metabolismus MeSH
- anthelmintika farmakologie MeSH
- benzimidazoly farmakologie MeSH
- Caenorhabditis elegans genetika účinky léků enzymologie MeSH
- fylogeneze * MeSH
- Haemonchus * genetika účinky léků enzymologie MeSH
- léková rezistence genetika MeSH
- lidé MeSH
- mebendazol * farmakologie analogy a deriváty MeSH
- ovce MeSH
- transkriptom MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aldehydreduktasa MeSH
- aldo-keto reduktasy * MeSH
- anthelmintika MeSH
- benzimidazoly MeSH
- flubendazole MeSH Prohlížeč
- mebendazol * MeSH
Aldo-keto reductases (AKRs), a superfamily of NADP(H)-dependent oxidoreductases, catalyze the oxidoreduction of a wide variety of eobiotic and xenobiotic aldehydes and ketones. In mammals, AKRs play essential roles in hormone and xenobiotic metabolism, oxidative stress, and drug resistance, but little is known about these enzymes in the parasitic nematode Haemonchus contortus. In the present study, 22 AKR genes existing in the H. contortus genome were investigated and a phylogenetic analysis with comparison to AKRs in Caenorhabditis elegans, sheep and humans was conducted. The constitutive transcription levels of all AKRs were measured in eggs, larvae, and adults of H. contortus, and their expression was compared in a drug-sensitive strain (ISE) and a benzimidazole-resistant strain (IRE) previously derived from the sensitive strain by imposing benzimidazole selection pressure. In addition, the inducibility of AKRs by exposure of H. contortus adults to benzimidazole anthelmintic flubendazole in vitro was tested. Phylogenetic analysis demonstrated that the majority of AKR genes in H. contortus lack orthologues in the sheep genome, which is a favorable finding for considering AKRs as potential drug targets. Large differences in the expression levels of individual AKRs were observed, with AKR1, AKR3, AKR8, and AKR10 being the most highly expressed at most developmental stages. Significant changes in the expression of AKRs during the life cycle and pronounced sex differences were found. Comparing the IRE and ISE strains, three AKRs were upregulated, and seven AKRs were downregulated in adults. In addition, the expression of three AKRs was induced by flubendazole exposure in adults of the ISE strain. Based on these results, AKR1, AKR2, AKR3, AKR5, AKR10 and AKR19 in particular merit further investigation and functional characterization with respect to their potential involvement in drug biotransformation and anthelmintic resistance in H. contortus.
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