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线虫配体门控氯离子通道:对其在大环内酯抗性中的作用评估及开发分子标记的前景

Nematode ligand-gated chloride channels: an appraisal of their involvement in macrocyclic lactone resistance and prospects for developing molecular markers.

作者信息

McCavera S, Walsh T K, Wolstenholme A J

机构信息

Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.

出版信息

Parasitology. 2007;134(Pt 8):1111-21. doi: 10.1017/S0031182007000042.

Abstract

SUMMARYLigand-gated chloride channels, including the glutamate-(GluCl) and GABA-gated channels, are the targets of the macrocyclic lactone (ML) family of anthelmintics. Changes in the sequence and expression of these channels can cause resistance to the ML in laboratory models, such as Caenorhabditis elegans and Drosophila melanogaster. Mutations in multiple GluCl subunit genes are required for high-level ML resistance in C. elegans, and this can be influenced by additional mutations in gap junction and amphid genes. Parasitic nematodes have a different complement of channel subunit genes from C. elegans, but a few genes, including avr-14, are widely present. A polymorphism in an avr-14 orthologue, which makes the subunit less sensitive to ivermectin and glutamate, has been identified in Cooperia oncophora, and polymorphisms in several subunits have been reported from resistant isolates of Haemonchus contortus. This has led to suggestions that ML resistance may be polygenic. Possible reasons for this, and its consequences for the development of molecular tests for resistance, are explored.

摘要

摘要

配体门控氯离子通道,包括谷氨酸门控氯离子通道(GluCl)和γ-氨基丁酸门控通道,是大环内酯类驱虫药的作用靶点。在实验室模型中,如秀丽隐杆线虫和黑腹果蝇,这些通道的序列和表达变化可导致对大环内酯类药物产生抗性。秀丽隐杆线虫中高水平的大环内酯类抗性需要多个GluCl亚基基因突变,这可能受间隙连接和化感器基因中的其他突变影响。寄生线虫具有与秀丽隐杆线虫不同的通道亚基基因组合,但包括avr-14在内的一些基因广泛存在。在牛古柏线虫中已鉴定出avr-14同源物中的一种多态性,该多态性使亚基对伊维菌素和谷氨酸的敏感性降低,并且从捻转血矛线虫的抗性分离株中报道了几个亚基中的多态性。这导致有人提出大环内酯类抗性可能是多基因的。本文探讨了其可能原因及其对耐药性分子检测发展的影响。

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