Higher replication potential of West Nile virus governs apoptosis induction in human neuroblastoma cells.

Abstract

The extent of neuronal cell damage caused by West Nile virus (WNV) infection governs the disease severity ranging from mild, febrile illness to fatal encephalitis. Availability of naturally occurring genetic variants is helpful to study viral factors governing differential pathogenesis. During WNV infection, apoptosis serves as a virulence determinant positively contributing to viral pathogenesis. We investigated the levels of apoptosis induced by a low neurovirulent WNV lineage 5 strain 804994 and a high neurovirulent lineage 1 strain 68856 in human neuroblastoma cells, IMR-32. Our investigations clearly show the correlation between higher multiplication capacities of 68856 with higher levels of cytopathology induced by apoptosis. We observed activation of both the extrinsic and intrinsic apoptotic pathways during WNV infection. Infection with higher neurovirulent strain resulted in higher upregulation of pro-apoptotic proteins including death receptors (DR), adaptor protein, BH3-only regulatory proteins and higher cleavage of initiator caspases of both pathways. These results suggest that the virulence of a WNV strain may correlate with its higher replication fitness and ability to cause more cellular damage.

• Authors: Sonal Mundhra, Vijay P Bondre
• Journal: Apoptosis : an international journal on programmed cell death (Apoptosis) Vol. 28 Issue 7-8 Pg. 1113-1127 (08 2023) ISSN: 1573-675X [Electronic] Netherlands
• PMID: 37186273 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Topics

• Humans
• West Nile virus (genetics)
• West Nile Fever (genetics, pathology)
• Apoptosis
• Virus Replication
• Neuroblastoma (genetics)