线虫中醛酮还原酶的系统发育和转录组学研究以及氟苯咪唑对它们的诱导作用

IF 4.1 2区 医学 Q1 PARASITOLOGY
Karolína Štěrbová, Lucie Raisová Stuchlíková, Nikola Rychlá, Kateřina Kohoutová, Markéta Babičková, Lenka Skálová, Petra Matoušková
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引用次数: 0

摘要

醛酮还原酶(AKRs)是一种依赖 NADP(H)的超家族氧化还原酶,可催化多种生物和异生物醛酮的氧化还原。在哺乳动物体内,AKRs 在激素和异生物代谢、氧化应激和耐药性方面发挥着重要作用,但人们对寄生线虫中的这些酶却知之甚少。在本研究中,研究人员调查了寄生线虫基因组中的 22 个 AKR 基因,并与秀丽隐杆线虫、绵羊和人类的 AKR 基因进行了系统发育分析和比较。研究人员测量了所有 AKRs 在虫卵、幼虫和成虫中的组成转录水平,并比较了它们在药物敏感株(ISE)和通过施加苯并咪唑选择压力从敏感株衍生的苯并咪唑抗性株(IRE)中的表达情况。此外,还测试了在体外将变形杆菌成虫暴露于苯并咪唑类抗虫药氟苯咪唑中诱导 AKR 的可能性。系统发育分析表明,轮虫中的大多数 AKR 基因在绵羊基因组中缺乏同源物,这一发现有利于将 AKR 作为潜在的药物靶点。观察到单个 AKR 的表达水平差异很大,其中 AKR1、AKR3、AKR8 和 AKR10 在大多数发育阶段的表达水平最高。在生命周期中,AKRs 的表达发生了显著变化,并发现了明显的性别差异。比较 IRE 和 ISE 品系,在成年期有三个 AKR 上调,七个 AKR 下调。此外,在 ISE 株系的成虫中,氟苯咪唑会诱导三个 AKRs 的表达。基于这些结果,AKR1、AKR2、AKR3、AKR5、AKR10 和 AKR19 尤其值得进一步研究,并确定其功能特征,以了解它们在 H. contortus 的药物生物转化和抗寄生虫药耐药性中的潜在参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phylogenetic and transcriptomic study of aldo-keto reductases in Haemonchus contortus and their inducibility by flubendazole

Phylogenetic and transcriptomic study of aldo-keto reductases in Haemonchus contortus and their inducibility by flubendazole

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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来源期刊
CiteScore
7.90
自引率
7.50%
发文量
31
审稿时长
48 days
期刊介绍: The International Journal for Parasitology – Drugs and Drug Resistance is one of a series of specialist, open access journals launched by the International Journal for Parasitology. It publishes the results of original research in the area of anti-parasite drug identification, development and evaluation, and parasite drug resistance. The journal also covers research into natural products as anti-parasitic agents, and bioactive parasite products. Studies can be aimed at unicellular or multicellular parasites of human or veterinary importance.
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