Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Role of envelope glycoprotein complexes in cell-associated spread of human cytomegalovirus

Weiler, Nina, Paal, Caroline, Adams, Kerstin, Calcaterra, Christopher, Fischer, Dina, Stanton, Richard James, Stöhr, Dagmar, Laib Sampaio, Kerstin and Sinzger, Christian 2021. Role of envelope glycoprotein complexes in cell-associated spread of human cytomegalovirus. Viruses 13 (4) , 614. 10.3390/v13040614

[thumbnail of viruses-13-00614-v2.pdf] PDF - Published Version
Available under License Creative Commons Attribution.

Download (5MB)

Abstract

The role of viral envelope glycoproteins, particularly the accessory proteins of trimeric and pentameric gH/gL-complexes, in cell-associated spread of human cytomegalovirus (HCMV) is unclear. We aimed to investigate their contribution in the context of HCMV variants that grow in a strictly cell-associated manner. In the genome of Merlin pAL1502, the glycoproteins gB, gH, gL, gM, and gN were deleted by introducing stop codons, and the mutants were analyzed for viral growth. Merlin and recent HCMV isolates were compared by quantitative immunoblotting for expression of accessory proteins of the trimeric and pentameric gH/gL-complexes, gO and pUL128. Isolates were treated with siRNAs against gO and pUL128 and analyzed regarding focal growth and release of infectious virus. All five tested glycoproteins were essential for growth of Merlin pAL1502. Compared with this model virus, higher gO levels were measured in recent isolates of HCMV, and its knockdown decreased viral growth. Knockdown of pUL128 abrogated the strict cell-association and led to release of infectivity, which allowed cell-free transfer to epithelial cells where the virus grew again strictly cell-associated. We conclude that both trimer and pentamer contribute to cell-associated spread of recent clinical HCMV isolates and downregulation of pentamer can release infectious virus into the supernatant.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Systems Immunity Research Institute (SIURI)
Publisher: MDPI
ISSN: 1999-4915
Funders: MRC, Wellcome Trust
Date of First Compliant Deposit: 7 April 2021
Date of Acceptance: 26 March 2021
Last Modified: 07 Apr 2021 13:30
URI: https://orca.cardiff.ac.uk/id/eprint/140299

Citation Data

Cited 8 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics