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由Flv控制的小鼠对黄病毒感染的固有抗性不依赖于一氧化氮。

Innate resistance to flavivirus infection in mice controlled by Flv is nitric oxide-independent.

作者信息

Silvia Ondine J, Shellam Geoffrey R, Urosevic Nadezda

机构信息

Department of Microbiology, University of Western Australia, Nedlands, WA 6907, Australia1.

出版信息

J Gen Virol. 2001 Mar;82(Pt 3):603-607. doi: 10.1099/0022-1317-82-3-603.

Abstract

Innate resistance to flaviviruses in mice is active in the brain where it restricts virus replication. This resistance is controlled by a single genetic locus, FLV, located on mouse chromosome 5 near the locus encoding the neuronal form of nitric oxide synthase (Nos1). Since nitric oxide (NO) has been implicated in antiviral activity, its involvement in natural resistance to flaviviruses has been hypothesized. Here we present data on NO production before and during flavivirus infection in both brain tissue and peritoneal macrophages from two flavivirus-resistant (FLV(r)) and one congenic susceptible (FLV(s)) mouse strains. This study provides evidence that NO is not involved in the expression of flavivirus resistance controlled by FLV since: (a) there is no difference in brain tissue NO levels between susceptible and resistant mice, and (b) lipopolysaccharide-induced NO does not abrogate the difference in flavivirus replication in peritoneal macrophages from susceptible and resistant mice.

摘要

小鼠对黄病毒的先天抗性在大脑中起作用,它能限制病毒复制。这种抗性由位于小鼠5号染色体上靠近编码神经元型一氧化氮合酶(Nos1)基因座的单个基因座FLV控制。由于一氧化氮(NO)与抗病毒活性有关,因此有人推测它参与了对黄病毒的天然抗性。在这里,我们展示了来自两种抗黄病毒(FLV(r))和一种同基因易感(FLV(s))小鼠品系的脑组织和腹腔巨噬细胞在感染黄病毒之前和期间NO产生的数据。这项研究提供了证据,表明NO不参与由FLV控制的黄病毒抗性表达,原因如下:(a)易感小鼠和抗性小鼠的脑组织NO水平没有差异;(b)脂多糖诱导的NO不会消除易感小鼠和抗性小鼠腹腔巨噬细胞中黄病毒复制的差异。

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