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dc.contributor.authorDaigle, Laurence
dc.contributor.authorKhalid, Hattaw
dc.contributor.authorGagnon, Carl A.
dc.contributor.authorArsenault, Julie
dc.contributor.authorBienzle, Dorothee
dc.contributor.authorBisson, Sarah-Kim
dc.contributor.authorBlais, Marie-Claude
dc.contributor.authorDenis-Robichaud, José
dc.contributor.authorForest, Caroline
dc.contributor.authorGrenier St-Sauveur, Valérie
dc.contributor.authorKöszegi, Marika
dc.contributor.authorMacNicol, Jennifer
dc.contributor.authorNantel-Fortier, Nicolas
dc.contributor.authorNury, Charlotte
dc.contributor.authorPrystajecky, Natalie
dc.contributor.authorFraser, Erin
dc.contributor.authorCarabin, Hélène
dc.contributor.authorAenishaenslin, Cécile
dc.date.accessioned2024-07-12T11:48:51Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2024-07-12T11:48:51Z
dc.date.issued2024-07-09
dc.identifier.urihttp://hdl.handle.net/1866/33549
dc.publisherBMCfr
dc.rightsATTRIBUTION 4.0 INTERNATIONAL CC BY 4.0 Deed
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/deed.fr
dc.subjectCatsfr
dc.subjectCOVID-19fr
dc.subjectExposurefr
dc.subjectOne Healthfr
dc.subjectPrevalencefr
dc.subjectSARS-CoV-2fr
dc.subjectHouseholdsfr
dc.titleHigh prevalence of SARS-CoV-2 antibodies and low prevalence of SARS-CoV-2 RNA in cats recently exposed to human casesfr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté de médecine vétérinairefr
dc.identifier.doi10.1186/s12917-024-04150-4
dcterms.abstractBackground The primary objective of this cross-sectional study, conducted in Québec and Bristish Columbia (Canada) between February 2021 and January 2022, was to measure the prevalence of viral RNA in oronasal and rectal swabs and serum antibodies to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) amongst cats living in households with at least one confirmed human case. Secondary objectives included a description of potential risk factors for the presence of SARS-CoV-2 antibodies and an estimation of the association between the presence of viral RNA in swabs as well as SARS-CoV-2 antibodies and clinical signs. Oronasal and rectal swabs and sera were collected from 55 cats from 40 households at most 15 days after a human case confirmation, and at up to two follow-up visits. A RT-qPCR assay and an ELISA were used to detect SARS-CoV-2 RNA in swabs and serum SARS-CoV-2 IgG antibodies, respectively. Prevalence and 95% Bayesian credibility intervals (BCI) were calculated, and associations were evaluated using prevalence ratio and 95% BCI obtained from Bayesian mixed log-binomial models. Results Nine (0.16; 95% BCI = 0.08–0.28) and 38 (0.69; 95% BCI = 0.56–0.80) cats had at least one positive RT-qPCR and at least one positive serological test result, respectively. No risk factor was associated with the prevalence of SARS-CoV-2 serum antibodies. The prevalence of clinical signs suggestive of COVID-19 in cats, mainly sneezing, was 2.12 (95% BCI = 1.03–3.98) times higher amongst cats with detectable viral RNA compared to those without. Conclusions We showed that cats develop antibodies to SARS-CoV-2 when exposed to recent human cases, but detection of viral RNA on swabs is rare, even when sampling occurs soon after confirmation of a human case. Moreover, cats with detectable levels of virus showed clinical signs more often than cats without signs, which can be useful for the management of such cases.fr
dcterms.isPartOfurn:ISSN:1746-6148fr
dcterms.languageengfr
UdeM.ReferenceFournieParDeposantDaigle L, Khalid H, Gagnon CA, Arsenault J, Bienzle D, Bisson SK, Blais MC, Denis-Robichaud J, Forest C, Grenier St-Sauveur V, Koszegi M, MacNicol J, Nantel-Fortier N, Nury C, Prystajecky N, Fraser E, Carabin H, Aenishaenslin C. High prevalence of SARS-CoV-2 antibodies and low prevalence of SARS-CoV-2 RNA in cats recently exposed to human cases. BMC Vet Res. 2024 Jul 9;20(1):304. doi: 10.1186/s12917-024-04150-4. PMID: 38982461.fr
UdeM.VersionRioxxVersion publiée / Version of Recordfr
oaire.citationTitleBMC Veterinary researchfr
oaire.citationVolume20fr
oaire.citationIssue1fr


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  CC BY 4.0
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