Journal Article

The Autonomous Fusion Activity of Human Cytomegalovirus Glycoprotein B Is Regulated by Its Carboxy-Terminal Domain

Kropff, Barbara, Mach, Michael, Britt, William J., Chen, Xiaohan, Sticht, Heinrich, Thomas, Marco, Reuter, Nina

2024

Overview

The human cytomegalovirus (HCMV) glycoprotein B (gB) is the viral fusogen required for entry into cells and for direct cell-to-cell spread of the virus. We have previously demonstrated that the exchange of the carboxy-terminal domain (CTD) of gB for the CTD of the structurally related fusion protein G of the vesicular stomatitis virus (VSV-G) resulted in an intrinsically fusion-active gB variant (gB/VSV-G). In this present study, we employed a dual split protein (DSP)-based cell fusion assay to further characterize the determinants of fusion activity in the CTD of gB. We generated a comprehensive library of gB CTD truncation mutants and identified two mutants, gB-787 and gB-807, which were fusion-competent and induced the formation of multinucleated cell syncytia in the absence of other HCMV proteins. Structural modeling coupled with site-directed mutagenesis revealed that gB fusion activity is primarily mediated by the CTD helix 2, and secondarily by the recruitment of cellular SH2/WW-domain-containing proteins. The fusion activity of gB-807 was inhibited by gB-specific monoclonal antibodies (MAbs) targeting the antigenic domains AD-1 to AD-5 within the ectodomain and not restricted to MAbs directed against AD-4 and AD-5 as observed for gB/VSV-G. This finding suggested a differential regulation of the fusion-active conformational state of both gB variants. Collectively, our findings underscore a pivotal role of the CTD in regulating the fusogenicity of HCMV gB, with important implications for understanding the conformations of gB that facilitate membrane fusion, including antigenic structures that could be targeted by antibodies to block this essential step in HCMV infection.

• Publisher: MDPI AG,MDPI
• Subject: Antibodies / Antigenic determinants / blocking fusion / Care and treatment / Cell Fusion / Cell Line / cell-cell fusion / Cells / Cytomegalovirus / Cytomegalovirus - genetics / Cytomegalovirus - physiology / Cytomegalovirus infections / Cytomegalovirus Infections - virology / Diagnosis / domain / Drug resistance / Fusion protein / gH/gL-independent fusion / giant cells / Giant Cells - virology / Glycoprotein B / Glycoproteins / Health aspects / herpesvirus / Human betaherpesvirus 5 / human cytomegalovirus / Humans / Infections / Membrane fusion / Monoclonal antibodies / Mortality / Mutagenesis, Site-Directed / Mutants / Plasmids / Protein Domains / Protein G / Proteins / Site-directed mutagenesis / Stomatitis / Syncytia / Vaccines / Vesiculovirus / Viral Envelope Proteins - chemistry / Viral Envelope Proteins - genetics / Viral Envelope Proteins - metabolism / Viral Fusion Proteins - chemistry / Viral Fusion Proteins - genetics / Viral Fusion Proteins - metabolism / Viral infections / Virus Internalization / viruses