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acr-23 编码线虫中敏化于莫能菌素的通道。

acr-23 Encodes a monepantel-sensitive channel in Caenorhabditis elegans.

机构信息

Novartis Centre de Recherche Santé Animale, St. Aubin, Switzerland.

出版信息

PLoS Pathog. 2013;9(8):e1003524. doi: 10.1371/journal.ppat.1003524. Epub 2013 Aug 8.

DOI:10.1371/journal.ppat.1003524
PMID:23950710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3738477/
Abstract

Monepantel is a member of the recently identified class of anthelmintics known as the amino-acetonitrile derivatives (AADs). Monepantel controls all major gastro-intestinal nematodes in sheep including those that are resistant to the classical anthelmintics. Previous studies have shown that the Caenorhabditis elegans acr-23 and the Haemonchus contortus Hco-mptl-1 genes may be prominent targets of monepantel. With this discovery it became possible to investigate the mode of action of monepantel in nematodes at the molecular level. In the present study, we show that a C. elegans mutant acr-23 strain is fully rescued by expressing the wild-type acr-23 gene. Moreover, we present a new mutant allele, and characterize acr-23 alleles genetically. We also show that acr-23 is expressed in body wall muscle cells, and provide therefore a possible explanation for the paralysis caused by monepantel. Furthermore, genetic evidence suggests that the chaperone RIC-3 is required for expression of full monepantel resistance. Finally, we present reconstitution of the C. elegans ACR-23 receptor in Xenopus laevis oocytes and provide direct evidence of its modulation by monepantel. Conversely, co-injection of the chaperone RIC-3 had no impact for channel reconstitution in X. laevis oocytes. These results reinforce the involvement of the ACR-23 family in the mode of action of monepantel and advance our understanding of this new class of anthelmintics.

摘要

苯并咪唑是一类新发现的驱虫药,称为氨基乙腈衍生物(AADs)。苯并咪唑可控制绵羊体内所有主要的胃肠道线虫,包括对经典驱虫药有耐药性的线虫。先前的研究表明,秀丽隐杆线虫 acr-23 和捻转血矛线虫 Hco-mptl-1 基因可能是苯并咪唑的主要靶标。这一发现使得能够在分子水平上研究苯并咪唑在线虫中的作用机制。在本研究中,我们表明,表达野生型 acr-23 基因可完全挽救 acr-23 突变体线虫。此外,我们还提出了一个新的突变等位基因,并对 acr-23 等位基因进行了遗传特征分析。我们还表明,acr-23 在体壁肌肉细胞中表达,这为苯并咪唑引起的麻痹提供了可能的解释。此外,遗传证据表明,伴侣蛋白 RIC-3 是表达完全苯并咪唑抗性所必需的。最后,我们在非洲爪蟾卵母细胞中重建了秀丽隐杆线虫 ACR-23 受体,并提供了苯并咪唑对其调节的直接证据。相反,伴侣蛋白 RIC-3 的共注射对非洲爪蟾卵母细胞中通道的重建没有影响。这些结果增强了 ACR-23 家族在苯并咪唑作用机制中的作用,并加深了我们对这一新类驱虫药的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/d9f9f8f62ef7/ppat.1003524.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/646ba6c662dd/ppat.1003524.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/e004d96f57a2/ppat.1003524.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/74c6f2a1d16c/ppat.1003524.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/db39fbfee0be/ppat.1003524.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/d9f9f8f62ef7/ppat.1003524.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/646ba6c662dd/ppat.1003524.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/e004d96f57a2/ppat.1003524.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/74c6f2a1d16c/ppat.1003524.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/db39fbfee0be/ppat.1003524.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a384/3738477/d9f9f8f62ef7/ppat.1003524.g005.jpg

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