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家蚕Akirin劫持了由BmCPV环状RNA编码的病毒肽vSP27,并激活ROS-NF-κB途径以抵抗病毒感染。

Bombyx mori Akirin hijacks a viral peptide vSP27 encoded by BmCPV circRNA and activates the ROS-NF-κB pathway against viral infection.

作者信息

Zhang Yunshan, Zhang Xing, Dai Kun, Zhu Min, Liang Zi, Pan Jun, Zhang Ziyao, Xue Renyu, Cao Guangli, Hu Xiaolong, Gong Chengliang

机构信息

School of Biology & Basic Medical Science, Soochow University, Suzhou 215123, China.

School of Biology & Basic Medical Science, Soochow University, Suzhou 215123, China; Agricultural Biotechnology Research Institute, Agricultural Biotechnology and Ecological Research Institute, Soochow University, Suzhou 215123, China.

出版信息

Int J Biol Macromol. 2022 Jan 1;194:223-232. doi: 10.1016/j.ijbiomac.2021.11.201. Epub 2021 Dec 5.

DOI:10.1016/j.ijbiomac.2021.11.201
PMID:34875309
Abstract

Bombyx mori cypovirus (BmCPV), a member of the family Reoviridae, is a model of Cypovirus, has a 10 segmented double-stranded RNA genome. However, so far, only one viral small peptide vSP27 with negative regulation on viral infection was identified; the mechanisms underlying host-BmCPV interaction are still unknown. Here, we identified that vSP27 was translated from a BmCPV derived circular RNA (circRNA-vSP27). Subsequently, results showed that vSP27 induced generation of ROS activated the NF-κB signaling pathway, induced the expression of antimicrobial peptides, and suppressed BmCPV infection. On the other hand, we identified a nuclear protein Akirin that could hijack vSP27, positively regulate the NF-κB pathway, and lead to inhibiting the viral infection. Altogether, our data suggested that BmCPV derived circRNA-vSP27 with small peptide translation activity may be employed by the host immunity in defense against the BmCPV infection.

摘要

家蚕质型多角体病毒(BmCPV)是呼肠孤病毒科的成员,是质型多角体病毒的一个模型,具有10个节段的双链RNA基因组。然而,到目前为止,仅鉴定出一种对病毒感染具有负调控作用的病毒小肽vSP27;宿主与BmCPV相互作用的潜在机制仍然未知。在此,我们鉴定出vSP27是从BmCPV衍生的环状RNA(circRNA-vSP27)翻译而来。随后,结果表明vSP27诱导活性氧的产生,激活NF-κB信号通路,诱导抗菌肽的表达,并抑制BmCPV感染。另一方面,我们鉴定出一种核蛋白Akirin,它可以劫持vSP27,正向调节NF-κB通路,并导致抑制病毒感染。总之,我们的数据表明,具有小肽翻译活性的BmCPV衍生circRNA-vSP27可能被宿主免疫系统用于抵御BmCPV感染。

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