Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Moredun Research Institute, Pentlands Science Park, Edinburgh, United Kingdom.
Front Cell Infect Microbiol. 2017 Nov 6;7:452. doi: 10.3389/fcimb.2017.00452. eCollection 2017.
Resistance to anthelmintic drugs is a major problem in the global fight against parasitic nematodes infecting humans and animals. While previous studies have identified mutations in drug target genes in resistant parasites, changes in the expression levels of both targets and transporters have also been reported. The mechanisms underlying these changes in gene expression are unresolved. Here, we take a novel approach to this problem by investigating the role of small regulatory RNAs in drug resistant strains of the important parasite . microRNAs (miRNAs) are small (22 nt) non-coding RNAs that regulate gene expression by binding predominantly to the 3' UTR of mRNAs. Changes in miRNA expression have been implicated in drug resistance in a variety of tumor cells. In this study, we focused on two geographically distinct ivermectin resistant strains of and two lines generated by multiple rounds of backcrossing between susceptible and resistant parents, with ivermectin selection. All four resistant strains showed significantly increased expression of a single miRNA, , compared to the susceptible strain. This same miRNA is also upregulated in a multi-drug-resistant strain of the related nematode . is enriched in female worms, is likely to be located on the X chromosome and is restricted to clade V parasitic nematodes. Genes containing predicted binding sites for were identified computationally and refined based on differential expression in a transcriptomic dataset prepared from the same drug resistant and susceptible strains. This analysis identified three putative target mRNAs, one of which, a CHAC domain containing protein, is located in a region of the genome introgressed from the resistant parent. was shown to interact with the 3' UTR of this gene by dual luciferase assay. This study is the first to suggest a role for miRNAs and the genes they regulate in drug resistant parasitic nematodes. also has potential as a biomarker of resistance in different nematode species.
抗寄生虫药物的耐药性是全球对抗感染人类和动物的寄生线虫的主要问题。虽然以前的研究已经确定了耐药寄生虫中药物靶基因的突变,但也报道了靶基因和转运蛋白表达水平的变化。这些基因表达变化的机制尚未解决。在这里,我们通过研究重要寄生虫 中耐药株的小调控 RNA 的作用,为这个问题提供了一种新的方法。 microRNAs (miRNAs) 是小的(22nt)非编码 RNA,通过主要结合到 mRNA 的 3'UTR 来调节基因表达。miRNA 表达的变化与各种肿瘤细胞的耐药性有关。在这项研究中,我们专注于伊维菌素耐药株和两个通过易感和耐药亲本之间的多轮回交产生的两条线,并用伊维菌素进行选择。与敏感株相比,所有四个耐药株的单个 miRNA 表达均显著增加,。同样的 miRNA 在相关线虫的多药耐药株中也上调。 在雌性蠕虫中富集,可能位于 X 染色体上,并且局限于寄生虫线虫的 clade V。通过计算预测了包含 的结合位点的基因,并根据来自相同耐药性和敏感性株的转录组数据集的差异表达进行了细化。该分析确定了三个推定的靶 mRNA,其中一个 CHAC 结构域包含蛋白,位于从耐药亲本导入的 基因组的一个区域。通过双荧光素酶测定证明 与该基因的 3'UTR 相互作用。这项研究首次表明 miRNAs 及其调节的基因在耐药寄生线虫中起作用。 也有可能成为不同线虫物种耐药性的生物标志物。