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二氧化钛纳米颗粒在小鼠诺如病毒感染期间引发促炎反应,尽管对病毒复制影响极小。

Titanium Dioxide Nanoparticles Evoke Proinflammatory Response during Murine Norovirus Infection Despite Having Minimal Effects on Virus Replication.

作者信息

Agnihothram Sudhakar, Mullis Lisa, Townsend Todd A, Watanabe Fumiya, Mustafa Thikra, Biris Alexandru, Manjanatha Mugimane G, Azevedo Marli P

机构信息

Division of Microbiology, Jefferson, Arkansas, 72079, USA.

Division of Genetic and Molecular Toxicology, Jefferson, Arkansas, 72079, USA.

出版信息

Int J Nanotechnol Eng Med. 2016 Dec;1(3):63-73. doi: 10.25141/2474-8811-2016-3.0063. Epub 2016 Dec 5.

Abstract

Noroviruses (NoV) have enhanced tropism for the gastrointestinal (GI) tract and are the major cause of nonbacterial gastroenteritis in humans. Titanium dioxide (TiO2) nanoparticles (NPs) used as food additives, dietary supplements, and cosmetics accumulate in the GI tract. We investigated the effect anatase TiO2 NPs on NoV replication and host response during virus infection, using murine norovirus (MNV-1) infection of RAW 264.7 macrophages. Pretreatment with 20 μg/ml anatase NPs significantly reduced the viability of macrophages alone or during virus infection, but did not alter virus replication. In contrast, pre-incubation with 2 μg/ml anatase NPs reduced virus replication fivefold at 48 h. The presence of anatase NPs during MNV-1 infection evoked a pro-inflammatory response, as measured by a significant increase in expression of cytokines, including IL-6, IFN-γ, TNFα and the TGFβ1. No genotoxic insults due to anatase TiO2 NPs alone or to their presence during MNV-1 infection were detected. This study highlights important safety considerations related to NP exposure of the GI tract in individuals infected with noroviruses or other foodborne viruses.

摘要

诺如病毒(NoV)对胃肠道(GI)具有更强的嗜性,是人类非细菌性肠胃炎的主要病因。用作食品添加剂、膳食补充剂和化妆品的二氧化钛(TiO2)纳米颗粒(NPs)会在胃肠道中蓄积。我们利用RAW 264.7巨噬细胞感染鼠诺如病毒(MNV-1),研究了锐钛矿型TiO2 NPs对病毒感染期间NoV复制和宿主反应的影响。用20μg/ml锐钛矿型NPs预处理可显著降低单独存在或病毒感染期间巨噬细胞的活力,但不改变病毒复制。相比之下,用2μg/ml锐钛矿型NPs预孵育48小时可使病毒复制降低五倍。MNV-1感染期间锐钛矿型NPs的存在引发了促炎反应,这可通过细胞因子(包括IL-6、IFN-γ、TNFα和TGFβ1)表达的显著增加来衡量。未检测到单独的锐钛矿型TiO2 NPs或其在MNV-1感染期间存在所导致的基因毒性损伤。这项研究突出了与感染诺如病毒或其他食源性病毒的个体胃肠道NP暴露相关的重要安全考虑因素。

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