Genomic analysis for virulence determinants in feline herpesvirus type-1 isolates.


Journal

Virus genes
ISSN: 1572-994X
Titre abrégé: Virus Genes
Pays: United States
ID NLM: 8803967

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 06 08 2019
accepted: 21 11 2019
pubmed: 30 11 2019
medline: 2 6 2020
entrez: 29 11 2019
Statut: ppublish

Résumé

Feline herpesvirus type 1 (FHV-1) is a widespread cause of respiratory and ocular disease in domestic cats. A spectrum of disease severity is observed in host animals, but there has been limited prior investigation into viral genome factors which could be responsible. Stocks of FHV-1 were established from oropharyngeal swabs obtained from twenty-five cats with signs of infection housed in eight animal shelters around the USA. A standardized numerical host clinical disease severity scoring scheme was used for each cat from which an isolate was obtained. Illumina MiSeq was used to sequence the genome of each isolate. Genomic homogeneity among isolates was relatively high. A general linear model for fixed effects determined that only two synonymous single nucleotide polymorphisms across two genes (UL37/39) in the same isolate (from one host animal with a low disease severity score) were significantly associated (p ≤ 0.05) with assigned host respiratory and total disease severity score. No variants in any isolate were found to be significantly associated with assigned host ocular disease severity score. A concurrent analysis of missense mutations among the viral isolates identified three genes as being primarily involved in the observed genomic variation, but none were significantly associated with host disease severity scores. An ancestral state likelihood reconstruction was performed and determined that there was no evidence of a connection between host disease severity score and viral evolutionary state. We conclude from our results that the spectrum of host disease severity observed with FHV-1 is unlikely to be primarily related to viral genomic variations, and is instead due to host response and/or other factors.

Identifiants

pubmed: 31776852
doi: 10.1007/s11262-019-01718-3
pii: 10.1007/s11262-019-01718-3
pmc: PMC7027352
mid: NIHMS1064010
doi:

Substances chimiques

Viral Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

49-57

Subventions

Organisme : NIH HHS
ID : UL1TR000427
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002373
Pays : United States
Organisme : NIH HHS
ID : P30EY016665
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY016665
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000427
Pays : United States

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Auteurs

Andrew C Lewin (AC)

Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Skip Bertman Drive, Baton Rouge, LA, 70803, USA. alewin1@lsu.edu.

Lyndon M Coghill (LM)

Center for Computation and Technology, Louisiana State University, 340 E Parker Boulevard, Baton Rouge, LA, 70808, USA.
Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Skip Bertman Drive, Baton Rouge, LA, 70803, USA.

Gillian J McLellan (GJ)

Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Drive, Madison, WI, 53706, USA.
Department of Ophthalmology and Visual Sciences, School of Medicine and Public Health, University of Wisconsin-Madison, 1300 University Avenue, Madison, WI, 53706, USA.

Ellison Bentley (E)

Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Drive, Madison, WI, 53706, USA.

Konstantin G Kousoulas (KG)

Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Skip Bertman Drive, Baton Rouge, LA, 70803, USA.

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Classifications MeSH