二氧化钛纳米颗粒在小鼠诺如病毒感染期间引起促炎反应,尽管对病毒复制的影响很小。

Sudhakar Agnihothram, Lisa Mullis, Todd A Townsend, Fumiya Watanabe, Thikra Mustafa, Alexandru Biris, Mugimane G Manjanatha, Marli P Azevedo
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引用次数: 4

摘要

诺如病毒(NoV)对胃肠道(GI)具有增强的趋向性,是人类非细菌性胃肠炎的主要原因。二氧化钛(TiO2)纳米颗粒(NPs)被用作食品添加剂、膳食补充剂和化妆品,在胃肠道中积累。通过小鼠诺如病毒(MNV-1)感染RAW 264.7巨噬细胞,研究锐钛矿型TiO2 NPs对病毒感染过程中NoV复制和宿主反应的影响。20 μg/ml锐钛酶NPs预处理显著降低巨噬细胞单独或病毒感染期间的活力,但不改变病毒复制。相比之下,2 μg/ml锐钛酶NPs在48小时内将病毒复制减少了5倍。在MNV-1感染期间,锐钛酶NPs的存在引起了促炎症反应,通过检测细胞因子表达的显著增加,包括IL-6、IFN-γ、TNFα和TGFβ1。在MNV-1感染期间,没有检测到锐钛矿型TiO2 NPs单独或存在的基因毒性损伤。本研究强调了诺如病毒或其他食源性病毒感染者胃肠道NP暴露相关的重要安全考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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.

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