Genomic analysis for virulence determinants in feline herpesvirus type-1 isolates.
Cat
Disease severity
Feline herpesvirus
Herpes
Host response
Virulence
Journal
Virus genes
ISSN: 1572-994X
Titre abrégé: Virus Genes
Pays: United States
ID NLM: 8803967
Informations de publication
Date de publication:
Feb 2020
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
49-57Subventions
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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