脾脏
免疫抑制
马尔尼菲青霉菌
生物
免疫学
菌落形成单位
环磷酰胺
微生物学
细菌
人类免疫缺陷病毒(HIV)
化疗
遗传学
共感染
作者
Lixiang Chen,Gang Wang,Wudi Wei,Hong Zhang,Jinhao He,Qiang Luo,Xiuli Bao,Yuxuan Liu,Baili Zhan,Xiao-Tao He,Hao Liang,Junjun Jiang,Li Ye
标识
DOI:10.1016/j.micpath.2023.106358
摘要
To establish a murine model of Talaromyces marneffei (T. marneffei) latent infection and reactivation, providing a foundation for exploring the molecular mechanisms underlying disease relapse.BALB/c mice were tail vein injected with T. marneffei at 0 days post-infection (dpi) and treated with cyclophosphamide (CTX) intraperitoneally every four days, starting from 21 dpi or 42 dpi. Mice were observed for body weight changes, liver and spleen indices, histological characteristics of liver and spleen, fungal load detection in liver and spleen, and Mp1p qualitation in liver and spleen to assess T. marneffei infection severity.T. marneffei-infected mice exhibited a trend of initial weight loss followed by recovery and a subsequent decrease in weight after CTX injection throughout the observation period. Liver and spleen indices, as well as tissue damage, significantly increased during infection but later returned to normal levels, with a gradual rise observed after immunosuppression. Fungal load analysis revealed positive T. marneffei cultures in the liver and spleen at 7 dpi and 14 dpi, followed by negative T. marneffei cultures from 21 dpi until day 21 post-immunosuppression (42 dpi or 63 dpi); however, the spleen remained T. marneffei-cultured negative, consistent with the trend observed in Mp1p detection results.A latent infection and reactivation model of T. marneffei in mice was successfully established, with the liver likely serving as a key site for latent T. marneffei.
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