Gene expression and in vitro replication of bovine gammaherpesvirus type 4.


Journal

Archives of virology
ISSN: 1432-8798
Titre abrégé: Arch Virol
Pays: Austria
ID NLM: 7506870

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 20 07 2020
accepted: 11 10 2020
pubmed: 7 1 2021
medline: 5 2 2021
entrez: 6 1 2021
Statut: ppublish

Résumé

In vitro cell cultures are widely used models for dissecting cellular and molecular mechanisms that lead to certain physiological conditions and diseases. The pathogenesis of BoHV-4 in the bovine reproductive tract has been studied by conducting tests on primary cultures. However, many questions remain to be answered about the role of BoHV-4 in endometrial cells. The aim of this study was to compare the replication and gene expression of BoHV-4 in cell lines and bovine reproductive tract primary cells as an in vitro model for the study of this virus. We demonstrated that BoHV-4 strains differ in their in vitro growth kinetics and gene expression but have the same cell type preference. Our results demonstrate that BoHV-4 replicates preferentially in bovine endometrial cells (BEC). However, its replication capacity extends to various cell types, since all cells that were tested were permissive to BoHV-4 infection. The highest virus titers were obtained in BEC cells. Nevertheless, virus replication efficiency could not be fully predicted from the mRNA expression profiles. This implies that there are multiple cell-type-dependent factors and strain properties that determine the level of BoHV-4 replication. The results of this study provide relevant information about the in vitro behavior of two field isolates of BoHV-4 in different cell cultures. These findings may be useful for the design of future in vitro experiments to obtain reliable results not only about the pathogenic role of BoHV-4 in the bovine female reproductive tract but also in the development of efficient antiviral strategies.

Identifiants

pubmed: 33403475
doi: 10.1007/s00705-020-04898-8
pii: 10.1007/s00705-020-04898-8
doi:

Substances chimiques

RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

535-544

Subventions

Organisme : Fondo para la Investigación Científica y Tecnológica
ID : PICT 2015-2263

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Auteurs

F Romeo (F)

Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT), Godoy Cruz 2370, C1425FQD, Buenos Aires, Argentina.
Facultad de Ciencias Agrarias, Universidad Nacional de Mar del Plata, 7600, Mar del Plata, Argentina.

E Louge-Uriarte (E)

Grupo de Sanidad Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), 7620, Balcarce, Argentina.

E Gonzalez-Altamiranda (E)

Grupo de Sanidad Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), 7620, Balcarce, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, C1033AAJ, Buenos Aires, Argentina.

S Delgado (S)

Facultad de Ciencias Agrarias, Universidad Nacional de Mar del Plata, 7600, Mar del Plata, Argentina.

S Pereyra (S)

Grupo de Sanidad Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), 7620, Balcarce, Argentina.

P Morán (P)

Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires (UNCPBA), Sede Tandil, Buenos Aires, Argentina.

A Odeón (A)

Facultad de Ciencias Agrarias, Universidad Nacional de Mar del Plata, 7600, Mar del Plata, Argentina.

S Pérez (S)

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, C1033AAJ, Buenos Aires, Argentina.
Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires (UNCPBA), Sede Tandil, Buenos Aires, Argentina.

Andrea E Verna (AE)

Grupo de Sanidad Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), 7620, Balcarce, Argentina. verna.andrea@inta.gob.ar.
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rivadavia 1917, C1033AAJ, Buenos Aires, Argentina. verna.andrea@inta.gob.ar.

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