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捻转血矛线虫的P-糖蛋白:用于基因表达研究的实时PCR检测方法的开发

P-glycoproteins of Haemonchus contortus: development of real-time PCR assays for gene expression studies.

作者信息

Williamson S M, Wolstenholme A J

机构信息

Department of Infectious Diseases, College of Veterinary Medicine and Center for Tropical and Emerging Global Disease, University of Georgia, Athens, GA 30602, USA.

出版信息

J Helminthol. 2012 Jun;86(2):202-8. doi: 10.1017/S0022149X11000216. Epub 2011 Jun 1.

Abstract

P-glycoproteins (P-gps) are proteins that function as efflux pumps, removing lipophilic xenobiotic compounds from cells. There is evidence that P-gps play a role in the resistance of parasitic nematodes to anthelmintic drugs such as benzimidazoles and macrocyclic lactones. As anthelmintic resistance becomes more common, it is important to identify candidate resistance genes with the aim of understanding the molecular basis of resistance, and of developing assays to detect these resistance-associated changes. We identified several sequences from the genome of the parasite Haemonchus contortus with convincing homology to the known P-gp coding genes of the model nematode Caenorhabditis elegans. Nine of these sequences were successfully amplified by polymerase chain reaction (PCR) and shown to be most similar to the C. elegans sequences for pgp-1, pgp-2, pgp-3, pgp-4, pgp-9, pgp-10, pgp-11, pgp-12 and pgp-14. These partial P-gp sequences from H. contortus were used to design and optimize a quantitative real-time PCR assay to investigate potential changes in the expression levels of P-gp transcripts associated with drug resistance. No significant changes in P-gp mRNA expression levels were found in a rapidly selected ivermectin-resistant parasite isolate compared to its drug-sensitive parent, but the assay has the potential to be used on other isolates in the future to further investigate resistance-associated changes in P-gp gene expression.

摘要

P-糖蛋白(P-gps)是一种起外排泵作用的蛋白质,可将亲脂性外源性化合物从细胞中清除。有证据表明,P-gps在寄生线虫对苯并咪唑和大环内酯类等驱虫药物的抗性中发挥作用。随着驱虫抗性变得越来越普遍,识别候选抗性基因对于理解抗性的分子基础以及开发检测这些抗性相关变化的检测方法至关重要。我们从捻转血矛线虫的基因组中鉴定出了几个序列,它们与模式线虫秀丽隐杆线虫已知的P-gp编码基因具有令人信服的同源性。其中9个序列通过聚合酶链反应(PCR)成功扩增,并显示与秀丽隐杆线虫的pgp-1、pgp-2、pgp-3、pgp-4、pgp-9、pgp-10、pgp-11、pgp-12和pgp-14序列最为相似。这些来自捻转血矛线虫的部分P-gp序列被用于设计和优化定量实时PCR检测方法,以研究与耐药性相关的P-gp转录本表达水平的潜在变化。与对药物敏感的亲本相比,在快速选择的伊维菌素抗性寄生虫分离株中未发现P-gp mRNA表达水平有显著变化,但该检测方法未来有可能用于其他分离株,以进一步研究P-gp基因表达中与抗性相关的变化。

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