Wilkinson Richard, Law Christopher J, Hoey Elizabeth M, Fairweather Ian, Brennan Gerard P, Trudgett Alan
School of Biological Sciences, The Queen's University of Belfast, 97, Lisburn Road, Belfast BT9 7BL, N. Ireland, UK.
Mol Biochem Parasitol. 2012 Nov;186(1):69-72. doi: 10.1016/j.molbiopara.2012.08.008. Epub 2012 Sep 12.
Control of fasciolosis is threatened by the development of anthelmintic resistance. Enhanced triclabendazole (TCBZ) efflux by ABC transporters such as P-glycoprotein (Pgp) has been implicated in this process. A putative full length cDNA coding for a Pgp expressed in adult Fasciola hepatica has been constructed and used to design a primer set capable of amplifying a region encoding part of the second nucleotide binding domain of Pgp when genomic DNA was used as a template. Application of this primer set to genomic DNA from TCBZ-resistant and -susceptible field populations has shown a significant difference in the alleles present. Analysis of an allele occurring at a three-fold higher frequency in the "resistant" population revealed that it was characterised by a serine to arginine substitution at residue 1144. Homology modelling studies have been used to locate this site in the Pgp structure and hence assess its potential to modify functional activity.
抗蠕虫药耐药性的出现威胁着肝片吸虫病的防治。ABC转运蛋白(如P-糖蛋白,Pgp)介导的三氯苯达唑(TCBZ)外排增强与这一过程有关。构建了一个推测的全长cDNA,其编码在成年肝片吸虫中表达的Pgp,并用于设计一套引物。当以基因组DNA为模板时,该引物能够扩增编码Pgp第二个核苷酸结合结构域部分的区域。将这套引物应用于来自对TCBZ耐药和敏感的田间种群的基因组DNA,结果显示存在的等位基因有显著差异。对“耐药”种群中出现频率高三倍的一个等位基因的分析表明,它的特征是在第1144位残基处丝氨酸被精氨酸取代。同源建模研究已用于在Pgp结构中定位该位点,从而评估其改变功能活性的可能性。