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首页> 外文期刊>Parasites Vectors >Exposure to amitraz, fipronil and permethrin affects cell viability and ABC transporter gene expression in an Ixodes ricinus cell line
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Exposure to amitraz, fipronil and permethrin affects cell viability and ABC transporter gene expression in an Ixodes ricinus cell line

机译:暴露于线虫,氟虫腈和苄氯菊酯会影响蓖麻线虫细胞系中的细胞活力和ABC转运蛋白基因表达

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Abstract BackgroundOver-expression of ATP-binding cassette (ABC) transporter proteins has been implicated in resistance of ticks to acaricides. Tick cell lines are useful for investigating resistance mechanisms, as development of an in vitro model for the study of acaricide resistance would contribute to improving knowledge of the molecular basis behind drug processing and exclusion in ticks. In the present study, cultures of the Ixodes ricinus -derived cell line IRE/CTVM19 were treated with the acaricides amitraz, permethrin or fipronil to determine modulation of ABC transporter gene expression. Cells were treated with different drug concentrations (25, 50, 100, 150 μM) and incubated for ten days. Cell morphology, viability, metabolic activity and relative expression of ABC (B1, B6, B8 and B10) genes were determined at day 10 post-treatment.ResultsCell morphology determined by light microscopy was altered following treatment with all drugs, but only at high concentrations, while total cell numbers decreased with increasing drug dose. Cell viability determined by trypan blue exclusion was not significantly different from untreated controls ( P 0.1) following treatment with amitraz and permethrin, but high concentrations of fipronil caused decrease (up to 37%, P 0.01) in viability. At all drug concentrations, fipronil and permethrin induced dose-dependent reduction in cell metabolic activity measured by MTT assay ( P 0.01). Quantitative RT-PCR showed that the drugs significantly affected expression of ABC genes. In particular, fipronil treatment downregulated ABCB1 ( P 0.001) and upregulated ABCB6, ABCB8 and ABCB10 ( P 0.01); amitraz treatment down regulated ABCB1 (significant difference between 25 and 150 μM, P 0.001) and upregulated ABCB8 and ABCB10 at lower concentrations (25 and 50 μM, P 0.05); and permethrin upregulated ABCB6, ABCB8 and ABCB10 only at 150 μM ( P 0.01).ConclusionsThe adverse effects on cell viability and metabolic activity, and changes in expression of different ABC transporter genes, detected in IRE/CTVM19 cells following treatment with amitraz, permethrin and fipronil, support the proposed application of tick cell lines as in vitro models for the study of resistance to these acaricides in ticks.
机译:摘要背景ATP结合盒(ABC)转运蛋白的过表达与壁虱对杀螨剂的抗性有关。 ick虫细胞系可用于研究抗药性机制,因为开发用于研究杀螨剂抗药性的体外模型将有助于提高对药物加工和tick虫排斥的分子基础的了解。在本研究中,用杀螨剂阿米特拉,苄氯菊酯或氟虫腈处理源自蓖麻短螺旋体的细胞系IRE / CTVM19的培养,以确定对ABC转运蛋白基因表达的调节。用不同的药物浓度(25、50、100、150μM)处理细胞,并孵育十天。在治疗后第10天测定细胞形态,活力,代谢活性和ABC(B1,B6,B8和B10)基因的相对表达。结果在用所有药物治疗后,通过光学显微镜确定的细胞形态发生了改变,但仅在高浓度下,而总细胞数则随着药物剂量的增加而减少。用锥虫蓝和苄氯菊酯处理后,通过锥虫蓝排除法测定的细胞活力与未处理的对照组相比无显着差异(P> 0.1),但是高浓度的氟虫腈导致活力降低(最高37%,P <0.01)。在所有药物浓度下,氟虫腈和苄氯菊酯诱导的剂量依赖性降低的细胞代谢活性均通过MTT法测定(P <0.01)。定量RT-PCR显示,这些药物显着影响ABC基因的表达。特别是氟虫腈治疗下调了ABCB1(P <0.001),上调了ABCB6,ABCB8和ABCB10(P <0.01);在较低浓度(25和50μM,P <0.05)下,甲酰胺治疗降低了ABCB1的上调(25和150μM之间的显着差异,P <0.001),并上调了ABCB8和ABCB10。氯菊酯和苄氯菊酯仅在150μM时才上调ABCB6,ABCB8和ABCB10(P <0.01)。和氟虫腈,支持拟议中的壁虱细胞系的应用作为体外模型,用于研究壁虱对这些杀螨剂的抗性。

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