Impact of viral telomeric repeat sequences on herpesvirus vector vaccine integration and persistence.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 22 03 2024
accepted: 14 05 2024
medline: 28 5 2024
pubmed: 28 5 2024
entrez: 28 5 2024
Statut: aheadofprint

Résumé

Marek's disease virus (MDV) vaccines were the first vaccines that protected against cancer. The avirulent turkey herpesvirus (HVT) was widely employed and protected billions of chickens from a deadly MDV infection. It is also among the most common vaccine vectors providing protection against a plethora of pathogens. HVT establishes latency in T-cells, allowing the vaccine virus to persist in the host for life. Intriguingly, the HVT genome contains telomeric repeat arrays (TMRs) at both ends; however, their role in the HVT life cycle remains elusive. We have previously shown that similar TMRs in the MDV genome facilitate its integration into host telomeres, which ensures efficient maintenance of the virus genome during latency and tumorigenesis. In this study, we investigated the role of the TMRs in HVT genome integration, latency, and reactivation in vitro and in vivo. Additionally, we examined HVT infection of feather follicles. We generated an HVT mutant lacking both TMRs (vΔTMR) that efficiently replicated in cell culture. We could demonstrate that wild type HVT integrates at the ends of chromosomes containing the telomeres in T-cells, while integration was severely impaired in the absence of the TMRs. To assess the role of TMRs in vivo, we infected one-day-old chickens with HVT or vΔTMR. vΔTMR loads were significantly reduced in the blood and hardly any virus was transported to the feather follicle epithelium where the virus is commonly shed. Strikingly, latency in the spleen and reactivation of the virus were severely impaired in the absence of the TMRs, indicating that the TMRs are crucial for the establishment of latency and reactivation of HVT. Our findings revealed that the TMRs facilitate integration of the HVT genome into host chromosomes, which ensures efficient persistence in the host, reactivation, and transport of the virus to the skin.

Identifiants

pubmed: 38805555
doi: 10.1371/journal.ppat.1012261
pii: PPATHOGENS-D-24-00610
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1012261

Informations de copyright

Copyright: © 2024 Denesvre et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

We have read the journal’s policy and the authors of this manuscript have the following competing interests: Zoltán Penzes is employed by and received a salary from Ceva Santé Animale. All other authors declare that they have no conflict of interest.

Auteurs

Caroline Denesvre (C)

INRAE, UMR1282 ISP, Equipe Biologie des Virus Aviaires, Nouzilly, France.

Yu You (Y)

Institute of Virology, Freie Universität Berlin, Berlin, Germany.

Sylvie Rémy (S)

INRAE, UMR1282 ISP, Equipe Biologie des Virus Aviaires, Nouzilly, France.

Tereza Vychodil (T)

Institute of Virology, Freie Universität Berlin, Berlin, Germany.

Katia Courvoisier (K)

INRAE, UMR1282 ISP, Equipe Biologie des Virus Aviaires, Nouzilly, France.

Zoltán Penzes (Z)

Ceva Santé Animale, Ceva-Phylaxia, Budapest, Hungary.

Luca D Bertzbach (LD)

Leibniz Institute of Virology (LIV), Department of Viral Transformation, Hamburg, Germany.

Ahmed Kheimar (A)

Institute of Virology, Freie Universität Berlin, Berlin, Germany.
Department of Poultry Diseases, Faculty of Veterinary Medicine, Sohag University, Sohag, Egypt.

Benedikt B Kaufer (BB)

Institute of Virology, Freie Universität Berlin, Berlin, Germany.
Veterinary Centre for Resistance Research (TZR), Freie Universität Berlin, Berlin, Germany.

Classifications MeSH