Low-Level Aflatoxin B-1 Promotes Influenza Infection and Modulates a Switch in Macrophage Polarization from M1 to M2
文献类型： 外文期刊
作者： Sun, Yuhang 1 ; Liu, Zixuan 1 ; Liu, Dandan 1 ; Chen, Jin 1 ; Gan, Fang 1 ; Huang, Kehe 1 ;
作者机构： 1.Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Jiangsu, Peoples R China
2.Nanjing Agr Univ, Inst Nutr & Metab Disorders Domest Anim & Fowls, Nanjing, Jiangsu, Peoples R China
3.Jiangsu Acad Agr Sci, Natl Res Ctr Engn & Technol Vet Biol, Nanjing, J
关键词： Aflatoxin B-1; Swine influenza virus; H1N1; Porcine alveolar macrophage; Polarization; Mouse
期刊名称：CELLULAR PHYSIOLOGY AND BIOCHEMISTRY （ 影响因子：5.5； 五年影响因子：4.354 ）
ISSN： 1015-8987
年卷期： 2018 年 49 卷 3 期
页码：
收录情况： SCI
摘要： Background/Aims: Swine influenza virus (SIV) is a major pathogen of both animals and humans. Aflatoxin B-1 (AFB(1)) is one of the most common mycotoxins in feed and food. However, the central contribution of AFB(1) to SIV infection remains unclear. Methods: Here, TCID50 assays, fluorescence-based quantitative real-time PCR, western blotting, immunofluorescence staining, histopathological examination, flow cytometry and scanning electron microscopy were performed to investigate the involvement and underlying mechanism of AFB(1) in SIV infection in vivo and in vitro using mouse models and porcine alveolar macrophage (PAM) models, respectively. Results: The in vivo study showed that low levels of AFB(1) promoted SIV infection and increased its severity, as demonstrated by the increased mRNA expression of viral matrix protein (M); by the increased protein expression of nucleoprotein (NP), matrix protein 1 and ion channel protein; and by animal weight loss, lung index and lung histologic damage. In addition, the increased occurrence of SIV infection accompanied by increases in the level of IL-10 in sera and lungs, in the spleen index and in the number of CD206-positive mouse alveolar macrophages but decreases in the level of TNF-alpha in sera and lungs, in the thymus index and in the number of CD80-positive mouse alveolar macrophages was observed in SIV-infected mice after low-level AFB(1) exposure. The in vitro study showed that low concentrations of AFB(1) promoted SIV infection, as demonstrated by the increases in viral titers and viral M mRNA and NP expression levels in SIV-infected PAMs as well as by the number of cells positive for NP protein expression. Furthermore, AFB(1) promoted the polarization of SIV-infected PAMs to the M1 phenotype at 8 hpi and to the M2 phenotype at 24 hpi, as measured by the increases in IL-10 expression and in the number of CD206-positive PAMs as well as by the morphological changes observed by scanning electron microscopy. The administration of the immune stimulant lipopolysaccharide (LPS) reversed the switch in PAM polarization from M2 to M1 and thereby counteracted the promotion of influenza virus infection induced by AFB(1). Conclusion: Our results are the first to confirm that low-level exposure to AFB(1) promotes SIV infection and modulates a switch in macrophage polarization from M1 to M2. The work reported here provides important data that point to a role for AFB(1) in SIV infection, and it opens a new field of study. (C) 2018 The Author(s) Published by S. Karger AG, Basel
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