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

机译:二氧化钛纳米粒子在小鼠诺如病毒感染期间引起促炎反应尽管对病毒复制影响最小

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摘要

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.
机译:诺如病毒(NoV)具有增强的胃肠道(GI)嗜性,是人类非细菌性胃肠炎的主要原因。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)积聚在胃肠道中。我们使用鼠诺如病毒(MNV-1)感染RAW 264.7巨噬细胞,研究了锐钛矿型TiO2 NPs在病毒感染过程中对NoV复制和宿主反应的影响。用20μg/ ml锐钛矿NP进行的预处理显着降低了单独或在病毒感染期间巨噬细胞的活力,但并未改变病毒复制。相反,与2μg/ ml锐钛矿NP一起预孵育在48小时将病毒复制降低了五倍。 MNV-1感染期间锐钛矿NPs的存在引起了促炎反应,这通过细胞因子(包括IL-6,IFN-γ,TNFα和TGFβ1)表达的显着增加来衡量。没有检测到仅由于锐钛矿型TiO2 NP或由于它们在MNV-1感染期间的存在而引起的遗传毒性损伤。这项研究强调了感染诺如病毒或其他食源性病毒的个人与胃肠道NP暴露相关的重要安全考虑。

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