Hampton Naomi, Smith Vicki, Brewer Matthew T, Jesudoss Chelladurai Jeba R J
Department of Diagnostic Medicine/Pathobiology, Kansas State University College of Veterinary Medicine, Manhattan, KS, United States of America.
Department of Veterinary Pathology, Iowa State University College of Veterinary Medicine, Ames, Iowa, United States of America.
PLoS One. 2024 Jul 17;19(7):e0307261. doi: 10.1371/journal.pone.0307261. eCollection 2024.
The increase in reports of resistance to macrocyclic lactones in the canine heartworm, Dirofilaria immitis is alarming. While DNA based tests have been well-validated, they can be expensive. In a previous study, we showed that two biochemical tests adapted to a 96- well plate format and read in a spectrophotometer could detect differences among lab validated D. immitis isolates. The two tests- Resazurin reduction and Hoechst 33342 efflux-detect metabolism and P-glycoprotein activity respectively in microfilariae isolated from infected dog blood.
Our objective was to optimize the two assays further by testing various assay parameters in D. immitis isolates not tested previously. We tested microfilarial seeding density, incubation time and the effect of in vitro treatment with ivermectin and doxycycline in five other D. immitis isolates-JYD-34, Big Head, Berkeley, Georgia III and LOL. All assays were performed in 3 technical replicates and 2-4 biological replicates. To understand the molecular basis of the assays, we also performed qPCR for selected drug metabolism and elimination associated genes of the ABC transporter and cytochrome P450 gene families.
Metabolism and ABC transporter activity as detected by these assays varied between strains. Anthelmintic status (resistant or susceptible) did not correlate with metabolism or P-gp efflux. Basal transcriptional variations were found between strains in ABC transporter and cytochrome P450 genes.
These assays provide a greater understanding of the biochemical variation among isolates of D. immitis, which can be exploited in the future to develop in vitro diagnostic tests capable of differentiating susceptible and resistant isolates.
犬心丝虫(犬恶丝虫)对大环内酯类药物耐药性的报告增加,令人担忧。虽然基于DNA的检测方法已经得到充分验证,但成本可能很高。在之前的一项研究中,我们表明,两种适用于96孔板格式并通过分光光度计读取的生化检测方法,可以检测实验室验证的犬恶丝虫分离株之间的差异。这两种检测方法——刃天青还原法和Hoechst 33342外排法——分别检测从感染犬血液中分离出的微丝蚴的代谢和P-糖蛋白活性。
我们的目标是通过在之前未检测过的犬恶丝虫分离株中测试各种检测参数,进一步优化这两种检测方法。我们在另外五种犬恶丝虫分离株——JYD-34、大头、伯克利、佐治亚III和LOL中,测试了微丝蚴接种密度、孵育时间以及伊维菌素和强力霉素体外处理的效果。所有检测均进行3次技术重复和2-4次生物学重复。为了了解这些检测方法的分子基础,我们还对ABC转运蛋白和细胞色素P450基因家族中选定的药物代谢和消除相关基因进行了qPCR。
这些检测方法检测到的代谢和ABC转运蛋白活性在不同菌株之间存在差异。驱虫状态(耐药或敏感)与代谢或P-糖蛋白外排无关。在ABC转运蛋白和细胞色素P450基因的菌株之间发现了基础转录差异。
这些检测方法有助于更深入地了解犬恶丝虫分离株之间的生化差异,未来可利用这些差异开发能够区分敏感和耐药分离株的体外诊断检测方法。