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寄生性桡足类 Caligus rogercresseyi 中的谷氨酸门控氯离子通道新家族:对伊维菌素激活具有抗性的亚基在异源寡聚体组装体中占优势。

A new family of glutamate-gated chloride channels in parasitic sea louse Caligus rogercresseyi: A subunit refractory to activation by ivermectin is dominant in heteromeric assemblies.

机构信息

Centro de Estudios Científicos (CECs), Valdivia, Chile.

Facultad de Ciencias para el Cuidado de la Salud, Universidad San Sebastián, Valdivia, Chile.

出版信息

PLoS Pathog. 2023 Mar 14;19(3):e1011188. doi: 10.1371/journal.ppat.1011188. eCollection 2023 Mar.

Abstract

Sea louse ectoparasitosis is a major threat to fish aquaculture. Avermectins such as ivermectin and emamectin have been effectively used against sea louse infestation, but the emergence of resistance has limited their use. A better understanding of the molecular targets of avermectins is essential to the development of novel treatment strategies or new, more effective drugs. Avermectins are known to act by inhibiting neurotransmission through allosteric activation of glutamate-gated chloride channels (GluCls). We have investigated the GluCl subunit present in Caligus rogercresseyi, a sea louse affecting aquaculture in the Southern hemisphere. We identify four new subunits, CrGluCl-B to CrGluCl-E, and characterise them functionally. CrGluCl-A (previously reported as CrGluClα), CrGluCl-B and CrGluCl-C all function as glutamate channel receptors with different sensitivities to the agonist, but in contrast to subunit -A and -C, CrGluCl-B is not activated by ivermectin but is rather antagonised by the drug. CrGluCl-D channel appears active in the absence of any stimulation by glutamate or ivermectin and CrGluCl-E does not exhibit any activity. Notably, the expression of CrGluCl-B with either -A or -C subunits gives rise to receptors unresponsive to ivermectin and showing altered response to glutamate, suggesting that coexpression has led to the preferential formation of heteromers to which the presence of CrGluCl-B confers the property of ivermectin-activation refractoriness. Furthermore, there was evidence for heteromer formation with novel properties only when coexpressing pairs E/C and D/B CrGluCl subtypes. Site-directed mutagenesis shows that three transmembrane domain residues contribute to the lack of activation by ivermectin, most crucially Gln 15' in M2, with mutation Q15'T (the residue present in ivermectin-activated subunits A and C) conferring ivermectin activation to CrGluCl-B. The differential response to avermectin of these Caligus rogercresseyi GluClsubunits, which are highly conserved in the Northern hemisphere sea louse Lepeophtheirus salmonis, could have an influence on the response of these parasites to treatment with macrocyclic lactones. They could serve as molecular markers to assess susceptibility to existing treatments and might be useful molecular targets in the search for novel antiparasitic drugs.

摘要

海虱外寄生虫病是水产养殖的主要威胁。伊维菌素和埃玛菌素等阿维菌素类药物已被有效用于防治海虱感染,但耐药性的出现限制了它们的使用。更好地了解阿维菌素类药物的分子靶标对于开发新的治疗策略或新的、更有效的药物至关重要。阿维菌素类药物通过别构激活谷氨酸门控氯通道(GluCls)来抑制神经传递。我们研究了影响南半球水产养殖的海虱 Caligus rogercresseyi 中存在的 GluCl 亚基。我们鉴定了四个新的亚基,CrGluCl-B 到 CrGluCl-E,并对它们进行了功能表征。CrGluCl-A(先前报道为 CrGluClα)、CrGluCl-B 和 CrGluCl-C 均作为谷氨酸通道受体发挥作用,对激动剂的敏感性不同,但与亚基-A 和亚基-C 不同,CrGluCl-B 不受伊维菌素激活,而是被该药物拮抗。CrGluCl-D 通道在没有任何谷氨酸或伊维菌素刺激的情况下似乎是活跃的,而 CrGluCl-E 则没有任何活性。值得注意的是,CrGluCl-B 与亚基-A 或亚基-C 的表达导致对伊维菌素无反应且对谷氨酸的反应改变的受体,表明共表达导致优先形成对伊维菌素激活的抗性赋予异源二聚体的性质。此外,只有在共表达新型特性的 E/C 和 D/B CrGluCl 亚基对时,才会出现具有新型特性的异源二聚体形成的证据。定点突变显示三个跨膜结构域残基有助于伊维菌素缺乏激活,最重要的是 M2 中的 Gln15',突变 Q15'T(存在于伊维菌素激活的亚基-A 和亚基-C 中的残基)使 CrGluCl-B 具有伊维菌素激活能力。这些 Caligus rogercresseyi GluCl 亚基对阿维菌素的不同反应,在北半球海虱 Lepeophtheirus salmonis 中高度保守,可能会影响这些寄生虫对大环内酯类药物治疗的反应。它们可以作为评估现有治疗方法敏感性的分子标记物,并且可能是寻找新型抗寄生虫药物的有用分子靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa5/10038264/bb9bbd75d3a9/ppat.1011188.g001.jpg

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