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黑狐蝠(Pteropus alecto)RIG-I 样解旋酶的分子特征。

Molecular characterisation of RIG-I-like helicases in the black flying fox, Pteropus alecto.

机构信息

CSIRO Livestock Industries, Australian Animal Health Laboratory, 5 Portarlington Rd, East Geelong, Victoria 3220, Australia.

出版信息

Dev Comp Immunol. 2012 Apr;36(4):657-64. doi: 10.1016/j.dci.2011.11.008. Epub 2011 Dec 4.

Abstract

The RIG-I like helicases, RIG-I, mda5 and LGP2 are an evolutionarily conserved family of cytosolic pattern recognition receptors important in the recognition of viral RNA, and responsible for the innate induction of interferons and proinflammatory cytokines upon viral infection. Bats are natural reservoir hosts to a variety of RNA viruses that cause significant morbidity and mortality in other species; however the mechanisms responsible for the control of viral replication in bats are not understood. This report describes the molecular cloning and expression analysis of RIG-I, mda5 and LGP2 genes in the fruit bat Pteropus alecto, and is the first description of RIG-I like helicases from any species of bat. Our results demonstrate that P. alecto RIG-I, mda5 and LGP2 have similar primary structures and tissue expression patterns to their counterparts in humans and other mammals. Stimulation of bat kidney cells with synthetic dsRNA (poly I:C) induced high levels of interferon β and rapid upregulation of all three helicases. These findings reveal that the cytoplasmic virus sensing machinery is present and intact in P. alecto. This study provides the foundation for further investigations into the interactions between bat RIG-I-like helicases and viruses to elucidate the mechanisms responsible for the asymptomatic nature of viral infections in bats.

摘要

RIG-I 样解旋酶、RIG-I、MDA5 和 LGP2 是一类进化上保守的胞质模式识别受体,在识别病毒 RNA 方面具有重要作用,负责在病毒感染时先天诱导干扰素和促炎细胞因子的产生。蝙蝠是多种 RNA 病毒的天然宿主,这些病毒在其他物种中引起严重的发病率和死亡率;然而,控制蝙蝠中病毒复制的机制尚不清楚。本报告描述了 RIG-I、MDA5 和 LGP2 基因在果蝠 Pteropus alecto 中的分子克隆和表达分析,这是首次描述蝙蝠中任何一种 RIG-I 样解旋酶。我们的结果表明,P. alecto 的 RIG-I、MDA5 和 LGP2 具有与人类和其他哺乳动物相似的一级结构和组织表达模式。用合成 dsRNA(poly I:C)刺激蝙蝠肾细胞可诱导高水平的干扰素 β,并迅速上调所有三种解旋酶。这些发现表明,细胞质病毒感应机制在 P. alecto 中存在且完整。本研究为进一步研究蝙蝠 RIG-I 样解旋酶与病毒之间的相互作用提供了基础,以阐明病毒感染在蝙蝠中无症状的机制。

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