Rotavirus is associated with decompensated diarrhea among young rhesus macaques (Macaca mulatta).
ICD
colony management
enterocolitis
gastroenteritis
idiopathich chronic diarrhea
Journal
American journal of primatology
ISSN: 1098-2345
Titre abrégé: Am J Primatol
Pays: United States
ID NLM: 8108949
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
11
04
2018
revised:
08
10
2018
accepted:
30
11
2018
pubmed:
9
1
2019
medline:
10
1
2020
entrez:
9
1
2019
Statut:
ppublish
Résumé
Diarrhea with secondary decompensation is the main cause of morbidity and mortality in captive young rhesus macaque (Macaca mulatta) colonies. Approximately 25% of diarrhea cases with secondary decompensation are considered to be idiopathic chronic diarrhea. The purpose of this study was to investigate the suspected but not systematically examined association between rotavirus infection and diarrhea with secondary decompensation among young rhesus macaques at the California National Primate Research Center (CNPRC). Blood and stool samples were collected from 89 randomly selected young animals (age range: 6 months to 1.5 years) and were tested for the presence of rotavirus antibody, and rotavirus antigen, respectively, using enzyme-linked immunosorbent assays (ELISA's). Test and clinical data were analyzed using Fisher's exact tests and multivariate logistic regression model. Our analysis indicates that rotavirus is endemic among young outdoor-housed rhesus macaques at the CNPRC. Although the relationship between detectable rotavirus antigen in stool and symptomatic diarrhea with secondary decompensation was not significant, there was a significant association between rotavirus seropositivity and a history of diarrhea with secondary decompensation within the past 6 months. While our cross-sectional and case-control study suggests an association between rotavirus infection and diarrhea with secondary decompensation among captive rhesus macaques, more extensive longitudinal studies on larger cohorts and with more intensive sample collection are needed to confirm these findings.
Identifiants
pubmed: 30620103
doi: 10.1002/ajp.22948
pmc: PMC8729819
mid: NIHMS1764472
doi:
Substances chimiques
Antibodies, Viral
0
Antigens, Viral
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e22948Subventions
Organisme : NIH HHS
ID : P51 OD011107
Pays : United States
Organisme : NCRR NIH HHS
ID : P51 RR000169
Pays : United States
Organisme : NIH HHS
ID : U42 OD010990
Pays : United States
Informations de copyright
© 2019 Wiley Periodicals, Inc.
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