1. Academic Validation
  2. Inhibition of PIKFYVE kinase interferes ESCRT pathway to suppress RNA virus replication

Inhibition of PIKFYVE kinase interferes ESCRT pathway to suppress RNA virus replication

  • J Med Virol. 2023 Jan 25. doi: 10.1002/jmv.28527.
Zhen Luo 1 2 Yicong Liang 1 Mingfu Tian 3 Zhihui Ruan 1 2 Rui Su 4 5 Muhammad Adnan Shereen 4 6 Jialing Yin 1 Kailang Wu 4 Jun Guo 3 Qiwei Zhang 1 2 Yongkui Li 1 2 Jianguo Wu 1 2 3 4
Affiliations

Affiliations

  • 1 Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University, Guangzhou, 510632, China.
  • 2 Foshan Institute of Medical Microbiology, Foshan, 528315, China.
  • 3 Department of Cardiology, the First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.
  • 4 State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430072, China.
  • 5 Henan Key Laboratory of Immunology and Targeted Drug, School of Basic Medical Science, Xinxiang Medical University, Xinxiang, 453003, China.
  • 6 Department of Microbiology, Kohsar University Murree, Kashmir Point, 47150, Pakistan.
Abstract

ESCRT (Endosomal sorting complex required for transport) is essential in the functional operation of endosomal transport in envelopment and budding of enveloped RNA viruses. However, in non-enveloped RNA viruses such as enteroviruses of the Picornaviridae family, the precise function of ESCRT pathway in viral replication remains elusive. Here, we initially evaluated that ESCRT pathway is important for viral replication upon EV71 (Enterovirus 71) Infection. Furthermore, we discovered that YM201636, a specific inhibitor of PIKfyve (Phosphoinositide kinase, FYVE finger containing) kinase, significantly suppressed EV71 replication and virus-induced inflammation in vitro and in vivo. Mechanistically, YM201636 inhibits PIKfyve kinase to block ESCRT pathway and endosomal transport, leading to the disruption of viral entry and replication complex in subcellular components and ultimately repression of intracellular RNA virus replication and virus-induced inflammatory responses. Further studies found that YM201636 broadly represses the replication of other RNA viruses, including CVB3 (Coxsackievirus B3), PV1 (Poliovirus 1), E11 (Echovirus 11), ZIKV (Zika virus), and VSV (Vesicular stomatitis virus), rather than DNA viruses, including ADV3 (Adenovirus 3) and HBV (Hepatitis B virus). Our findings shed LIGHT on the mechanism underlying PIKFYVE-modulated ESCRT pathway involved in RNA virus replication, and also provide a prospective Antiviral therapy during RNA viruses infections. This article is protected by copyright. All rights reserved.

Keywords

Antiviral therapy; Endosomal sorting complex required for transport (ESCRT); Enveloped RNA viruses; Non-enveloped RNA viruses; Phosphoinositide kinase FYVE finger containing (PIKFYVE); RNA virus replication.

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