Division of Avian Immunosuppressive Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institutegrid.38587.31, Chinese Academy of Agricultural Sciences, Harbin, China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou University, Yangzhou, China.
J Virol. 2022 Mar 23;96(6):e0011322. doi: 10.1128/jvi.00113-22. Epub 2022 Feb 2.
Infectious bursal disease virus (IBDV), which targets bursa B lymphocytes, causes severe immunosuppressive disease in chickens, inducing huge economic losses for the poultry industry. To date, the functional receptor for IBDV binding and entry into host cells remains unclear. This study used mass spectrometry to screen host proteins of chicken bursal lymphocytes interacting with VP2. The chicken transmembrane protein cluster of differentiation 44 (chCD44) was identified and evaluated for its interaction with IBDV VP2, the major capsid protein. Overexpression and knockdown experiments showed that chCD44 promotes replication of IBDV. Furthermore, soluble chCD44 and the anti-chCD44 antibody blocked virus binding. The results of receptor reconstitution indicated that chCD44 overexpression conferred viral binding capability in nonpermissive cells. More important, although we found that IBDV could not replicate in the chCD44-overexpressed nonpermissive cells, the virus could enter nonpermissive cells using chCD44. Our finding reveals that chCD44 is a cellular receptor for IBDV, facilitating virus binding and entry in target cells by interacting with the IBDV VP2 protein. Infectious bursal disease virus (IBDV) causes severe immunosuppressive disease in chickens, inducing huge economic losses for the poultry industry. However, the specific mechanism of IBDV invading host cells of IBDV was not very clear. This study shed light on which cellular protein component IBDV is used to bind and/or enter B lymphocytes. The results of our study revealed that chCD44 could promote both the binding and entry ability of IBDV in B lymphocytes, acting as a cellular receptor for IBDV. Besides, this is the first report about chicken CD44 function in viral replication. Our study impacts the understanding of the IBDV binding and entry process and sets the stage for further elucidation of the infection mechanism of IBDV.
传染性法氏囊病病毒(IBDV)靶向法氏囊 B 淋巴细胞,导致鸡严重的免疫抑制性疾病,给家禽业造成巨大的经济损失。迄今为止,IBDV 结合和进入宿主细胞的功能性受体仍不清楚。本研究使用质谱法筛选与 VP2 相互作用的鸡法氏囊淋巴细胞的宿主蛋白。鉴定并评估了鸡跨膜蛋白 CD44 簇(chCD44)与 IBDV 主要衣壳蛋白 VP2 的相互作用。过表达和敲低实验表明 chCD44 促进了 IBDV 的复制。此外,可溶性 chCD44 和抗 chCD44 抗体阻断了病毒结合。受体重建结果表明,chCD44 过表达赋予了非允许细胞病毒结合能力。更重要的是,尽管我们发现 IBDV 不能在 chCD44 过表达的非允许细胞中复制,但病毒可以通过 chCD44 进入非允许细胞。我们的发现表明 chCD44 是 IBDV 的细胞受体,通过与 IBDV VP2 蛋白相互作用促进病毒在靶细胞中的结合和进入。