The role of lysosomes as intermediates in betacoronavirus PHEV egress from nerve cells

IMPORTANCE: Betacoronaviruses, including severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and mouse hepatitis virus (MHV), exploit the lysosomal exocytosis pathway for egress. However, whether all betacoronaviruses members use the same pathway to exit cells remains unknown. Here, we demonstrated that porcine hemagglutinating encephalomyelitis virus (PHEV) egress occurs by Arl8b-dependent lysosomal exocytosis, a cellular egress mechanism shared by SARS-CoV-2 and MHV. Notably, PHEV acidifies lysosomes and activates lysosomal degradative enzymes, while SARS-CoV-2 and MHV deacidify lysosomes and limit the activation of lysosomal degradative enzymes. In addition, PHEV release depends on V-ATPase-mediated lysosomal pH. Furthermore, this is the first study to evaluate βCoV using lysosome for spreading through the body, and we have found that lysosome played a critical role in PHEV neural transmission and brain damage caused by virus infection in the central nervous system. Taken together, different betacoronaviruses could disrupt lysosomal function differently to exit cells.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:97

Enthalten in:

Journal of virology - 97(2023), 12 vom: 21. Dez., Seite e0133823

Sprache:

Englisch

Beteiligte Personen:

Wang, Zhenzhen [VerfasserIn]
He, Wenqi [VerfasserIn]
Li, Caili [VerfasserIn]
Chen, Yuzhu [VerfasserIn]
Li, Zi [VerfasserIn]
Jiao, Yubo [VerfasserIn]
Zhang, Jing [VerfasserIn]
Shi, Junchao [VerfasserIn]
Wang, Gaili [VerfasserIn]
Guan, Jiyu [VerfasserIn]
Zhao, Kui [VerfasserIn]
Song, Deguang [VerfasserIn]
Gao, Feng [VerfasserIn]
Lan, Yungang [VerfasserIn]

Links:

Volltext

Themen:

Betacoronaviruses
CNS
Comparative Study
EC 3.6.1.-
Journal Article
Lysosome
PHEV
V-ATPase
Vacuolar Proton-Translocating ATPases
Virus egress

Anmerkungen:

Date Completed 03.01.2024

Date Revised 03.01.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1128/jvi.01338-23

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM365011258