Effect of Baicalin on Bacterial Secondary Infection and Inflammation Caused by H9N2 AIV Infection in Chickens
文献类型: 外文期刊
作者: Zhang, Xinheng 1 ; Zhao, Qiqi 1 ; Ci, Xiaotong 1 ; Chen, Sheng 1 ; Chen, Liyi 1 ; Lian, Jiamin 1 ; Xie, Zi 1 ; Ye, Yaqion 1 ;
作者机构: 1.South China Agr Univ, Coll Anim Sci, Lingnan Guangdong Lab Modern Agr, Guangzhou 510642, Peoples R China
2.South China Agr Univ, Coll Anim Sci, Guangdong Prov Key Lab Agroanim Genom & Mol Breed, Guangzhou 510642, Peoples R China
3.Guangdong Engn Res Ctr Vector Vaccine Anim Virus, Guangzhou 510642, Peoples R China
4.South China Collaborat Innovat Ctr Poultry Dis Co, Guangzhou 510642, Peoples R China
5.Foshan Univ, Coll Life Sci & Engn, Foshan 528231, Peoples R China
6.Beijing Ctr Biol CO LTD, Beijing 100000, Peoples R China
7.ARS, USDA, Avian Dis & Oncol Lab, E Lansing, MI 48823 USA
期刊名称:BIOMED RESEARCH INTERNATIONAL ( 影响因子:3.411; 五年影响因子:3.62 )
ISSN: 2314-6133
年卷期: 2020 年 2020 卷
页码:
收录情况: SCI
摘要: H9N2 subtype avian influenza virus (H9N2 AIV) is a low pathogenic virus that is widely prevalent all over the world. H9N2 AIV causes immunosuppression in the host and often leads to high rates of mortality due to secondary infection with Escherichia. Due to the drug resistance of bacteria, many antibiotics are not effective in the treatment of secondary bacterial infection. Therefore, the purpose of this study is to find effective nonantibiotic drugs for the treatment of H9N2 AIV infection-induced secondary bacterial infection and inflammation. This study proves, for the first time, that baicalin, a Chinese herbal medicine, can regulate Lactobacillus to replace Escherichia induced by H9N2 AIV, so as to resolve the intestinal flora disorder. In addition, baicalin can effectively prevent intestinal bacterial translocation of SPF chickens' post-H9N2 AIV infection, thus inhibiting secondary bacterial infection. Furthermore, baicalin can effectively treat H9N2 AIV-induced inflammation by inhibiting intestinal structural damage, inhibiting damage to ileal mucus layer construction and tight junctions, improving antioxidant capacity, affecting blood biochemical indexes, and inhibiting the production of inflammatory cytokines. Taken together, these results provide a new theoretical basis for clinical prevention and control of H9N2 AIV infection-induced secondary bacterial infection and inflammation.
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