Raza Ali, Kopp Steven R, Bagnall Neil H, Jabbar Abdul, Kotze Andrew C
CSIRO Agriculture, Queensland Bioscience Precinct, University of Queensland, Brisbane, Australia; School of Veterinary Science, University of Queensland, Gatton, Australia.
School of Veterinary Science, University of Queensland, Gatton, Australia.
Int J Parasitol Drugs Drug Resist. 2016 Aug;6(2):103-15. doi: 10.1016/j.ijpddr.2016.03.001. Epub 2016 Mar 23.
This study investigated the interaction of ATP binding cassette (ABC) transport proteins with ivermectin (IVM) and levamisole (LEV) in larvae of susceptible and resistant isolates of Haemonchus contortus in vitro by measuring transcription patterns following exposure to these anthelmintics. Furthermore, we studied the consequences of drug exposure by measuring the sensitivity of L3 to subsequent exposure to higher drug concentrations using larval migration assays. The most highly transcribed transporter genes in both susceptible and resistant L3 were pgp-9.3, abcf-1, mrp-5, abcf-2, pgp-3, and pgp-10. The resistant isolate showed significantly higher transcription of pgp-1, pgp-9.1 and pgp-9.2 compared to the susceptible isolate. Five P-gp genes and the haf-6 gene showed significantly higher transcription (up to 12.6-fold) after 3 h exposure to IVM in the resistant isolate. Similarly, five P-gp genes, haf-6 and abcf-1 were transcribed at significantly higher levels (up to 10.3-fold) following 3 h exposure to LEV in this isolate. On the other hand, there were no significant changes in transcriptional patterns of all transporter genes in the susceptible isolate following 3 and 6 h exposure to IVM or LEV. In contrast to these isolate-specific transcription changes, both isolates showed an increase in R-123 efflux following exposure to the drugs, suggesting that the drugs stimulated activity of existing transporter proteins in both isolates. Exposure of resistant larvae to IVM or LEV resulted, in some instances, in an increase in the proportion of the population able to migrate at the highest IVM concentrations in subsequent migration assays. The significant increase in transcription of some ABC transporter genes following 3 h exposure to both IVM and LEV in the resistant isolate only, suggests that an ability to rapidly upregulate protective pathways in response to drugs may be a component of the resistance displayed by this isolate.
本研究通过测量感染柔线虫的敏感和抗性分离株幼虫在体外接触这些驱虫药后的转录模式,研究了ATP结合盒(ABC)转运蛋白与伊维菌素(IVM)和左旋咪唑(LEV)之间的相互作用。此外,我们通过幼虫迁移试验测量L3对随后暴露于更高药物浓度的敏感性,研究了药物暴露的后果。在敏感和抗性L3中,转录水平最高的转运蛋白基因是pgp-9.3、abcf-1、mrp-5、abcf-2、pgp-3和pgp-10。与敏感分离株相比,抗性分离株中pgp-1、pgp-9.1和pgp-9.2的转录水平显著更高。在抗性分离株中,暴露于IVM 3小时后,五个P-糖蛋白基因和haf-6基因的转录水平显著升高(高达12.6倍)。同样,在该分离株中,暴露于LEV 3小时后,五个P-糖蛋白基因、haf-6和abcf-1的转录水平显著升高(高达10.3倍)。另一方面,敏感分离株在暴露于IVM或LEV 3小时和6小时后,所有转运蛋白基因的转录模式均无显著变化。与这些分离株特异性的转录变化相反,两种分离株在接触药物后R-123外排均增加,这表明药物刺激了两种分离株中现有转运蛋白的活性。在某些情况下,抗性幼虫暴露于IVM或LEV后,在随后的迁移试验中,能够在最高IVM浓度下迁移的群体比例增加。仅在抗性分离株中,暴露于IVM和LEV 3小时后,一些ABC转运蛋白基因的转录显著增加,这表明快速上调对药物的保护途径的能力可能是该分离株所表现出的抗性的一个组成部分。