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两栖动物()巨噬细胞在慢性蛙病毒 3 感染中的作用。

The Roles of Amphibian () Macrophages during Chronic Frog Virus 3 Infections.

机构信息

Department of Biological Sciences, George Washington University, Washington, DC 20052, USA.

出版信息

Viruses. 2021 Nov 18;13(11):2299. doi: 10.3390/v13112299.

Abstract

Infections by Frog Virus 3 (FV3) and other ranavirus genus members are significantly contributing to global amphibian decline. The frog is an ideal research platform upon which to study the roles of distinct frog leukocyte populations during FV3 infections. Frog macrophages (MΦs) are integrally involved during FV3 infection, as they facilitate viral dissemination and persistence but also participate in immune defense against this pathogen. In turn, MΦ differentiation and functionality depend on the colony-stimulating factor-1 receptor (CSF-1R), which is ligated by CSF-1 and iterleukin-34 (IL-34) cytokines. Our past work indicated that CSF-1 and IL-34 give rise to morphologically and functionally distinct frog MΦ subsets, and that these CSF-1- and IL-34-MΦs respectively confer susceptibility and antiviral resistance to FV3. Because FV3 targets the frog kidneys and establishes chronic infections therein, presently we examined the roles of the frog CSF-1- and IL-34-MΦs in seeding and maintaining these chronic kidney infections. Our findings indicate that the frog CSF-1-MΦs result in more prominent kidney FV3 infections, which develop into greater reservoirs of lingering FV3 marked by infiltrating leukocytes, fibrosis, and overall immunosuppressive states. Moreover, the antiviral effects of IL-34-MΦs are short-lived and are lost as FV3 infections progress.

摘要

蛙病毒 3(FV3)和其他蛙属 Ranavirus 成员的感染是导致全球两栖动物数量减少的重要原因。青蛙是研究 FV3 感染期间不同青蛙白细胞群体作用的理想研究平台。在 FV3 感染过程中,青蛙巨噬细胞(MΦ)起着至关重要的作用,因为它们促进了病毒的传播和持续存在,但也参与了针对这种病原体的免疫防御。反过来,MΦ 的分化和功能取决于集落刺激因子-1 受体(CSF-1R),该受体被 CSF-1 和白细胞介素-34(IL-34)细胞因子连接。我们过去的工作表明,CSF-1 和 IL-34 产生了形态和功能上不同的青蛙 MΦ 亚群,而这些 CSF-1 和 IL-34-MΦ 分别赋予了对 FV3 的易感性和抗病毒抗性。由于 FV3 靶向青蛙肾脏并在其中建立慢性感染,目前我们研究了青蛙 CSF-1 和 IL-34-MΦ 在播种和维持这些慢性肾脏感染中的作用。我们的研究结果表明,青蛙 CSF-1-MΦ 导致更明显的肾脏 FV3 感染,这些感染发展成更大的 FV3 潜伏储库,其特征是浸润白细胞、纤维化和整体免疫抑制状态。此外,IL-34-MΦ 的抗病毒作用是短暂的,随着 FV3 感染的进展而丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0149/8621048/cae40ca57e9c/viruses-13-02299-g001.jpg

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