Serological Evidence of Multiple Zoonotic Viral Infections among Wild Rodents in Barbados.

Kirk Osmond Douglas, Claire Cayol, Kristian Michael Forbes, Thelma Alafia Samuels, Olli Vapalahti, Tarja Sironen, Marquita Gittens-St Hilaire
Author Information
  1. Kirk Osmond Douglas: Centre for Biosecurity Studies, University of the West Indies, Cave Hill, St. Michael BB11000, Barbados.
  2. Claire Cayol: Department of Wildlife, Fish, and Environmental Studies, Swedish University of Agricultural Sciences, Skogsmarksgränd 17, 901 83 Umeå, Sweden. ORCID
  3. Kristian Michael Forbes: Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, USA.
  4. Thelma Alafia Samuels: Epidemiology Research Unit, Caribbean Institute for Health Research (CAIHR), The University of the West Indies, Mona, Kingston 7, Jamaica.
  5. Olli Vapalahti: Department of Virology, Faculty of Medicine, University of Helsinki, Medicum, Haartmaninkatu 3, 0290 Helsinki, Finland.
  6. Tarja Sironen: Department of Virology, Faculty of Medicine, University of Helsinki, Medicum, Haartmaninkatu 3, 0290 Helsinki, Finland. ORCID
  7. Marquita Gittens-St Hilaire: Faculty of Medical Sciences, University of the West Indies, Cave Hill, St. Michael BB11000, Barbados.

Abstract

BACKGROUND: Rodents are reservoirs for several zoonotic pathogens that can cause human infectious diseases, including orthohantaviruses, mammarenaviruses and orthopoxviruses. Evidence exists for these viruses circulating among rodents and causing human infections in the Americas, but much less evidence exists for their presence in wild rodents in the Caribbean.
METHODS: Here, we conducted serological and molecular investigations of wild rodents in Barbados to determine the prevalence of orthohantavirus, mammarenavirus and orthopoxvirus infections, and the possible role of these rodent species as reservoirs of zoonotic pathogens. Using immunofluorescent assays (IFA), rodent sera were screened for the presence of antibodies to orthohantavirus, mammarenavirus (Lymphocytic choriomeningitis virus-LCMV) and orthopoxvirus (Cowpox virus-CPXV) infections. RT-PCR was then conducted on orthohantavirus and mammarenavirus-seropositive rodent sera and tissues, to detect the presence of viral RNA.
RESULTS: We identified antibodies against orthohantavirus, mammarenavirus, and orthopoxvirus among wild mice and rats (3.8%, 2.5% and 7.5% seropositivity rates respectively) in Barbados. No orthohantavirus or mammarenavirus viral RNA was detected from seropositive rodent sera or tissues using RT-PCR.
CONCLUSIONS: Key findings of this study are the first serological evidence of orthohantavirus infections in and the first serological evidence of mammarenavirus and orthopoxvirus infections in and in the English-speaking Caribbean. Rodents may present a potential zoonotic and biosecurity risk for transmission of three human pathogens, namely orthohantaviruses, mammarenaviruses and orthopoxviruses in Barbados.

Keywords

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