Cargando…

Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)

Habitat-mediated global change is driving shifts in species’ distributions which can alter the spatial risks associated with emerging zoonotic pathogens. Many emerging infectious pathogens are transmitted by highly mobile species, including bats, which can act as spill-over hosts for pathogenic viru...

Descripción completa

Detalles Bibliográficos
Autores principales: Boardman, Wayne S. J., Baker, Michelle L., Boyd, Victoria, Crameri, Gary, Peck, Grantley R., Reardon, Terry, Smith, Ian G., Caraguel, Charles G. B., Prowse, Thomas A. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202650/
https://www.ncbi.nlm.nih.gov/pubmed/32374743
http://dx.doi.org/10.1371/journal.pone.0232339
_version_ 1783529741838450688
author Boardman, Wayne S. J.
Baker, Michelle L.
Boyd, Victoria
Crameri, Gary
Peck, Grantley R.
Reardon, Terry
Smith, Ian G.
Caraguel, Charles G. B.
Prowse, Thomas A. A.
author_facet Boardman, Wayne S. J.
Baker, Michelle L.
Boyd, Victoria
Crameri, Gary
Peck, Grantley R.
Reardon, Terry
Smith, Ian G.
Caraguel, Charles G. B.
Prowse, Thomas A. A.
author_sort Boardman, Wayne S. J.
collection PubMed
description Habitat-mediated global change is driving shifts in species’ distributions which can alter the spatial risks associated with emerging zoonotic pathogens. Many emerging infectious pathogens are transmitted by highly mobile species, including bats, which can act as spill-over hosts for pathogenic viruses. Over three years, we investigated the seroepidemiology of paramyxoviruses and Australian bat lyssavirus in a range-expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus), in a new camp in Adelaide, South Australia. Over six, biannual, sampling sessions, we quantified median florescent intensity (MFI) antibody levels for four viruses for a total of 297 individual bats using a multiplex Luminex binding assay. Where appropriate, florescence thresholds were determined using finite mixture modelling to classify bats’ serological status. Overall, apparent seroprevalence of antibodies directed at Hendra, Cedar and Tioman virus antigens was 43.2%, 26.6% and 95.7%, respectively. We used hurdle models to explore correlates of seropositivity and antibody levels when seropositive. Increased body condition was significantly associated with Hendra seropositivity (Odds ratio = 3.67; p = 0.002) and Hendra virus levels were significantly higher in pregnant females (p = 0.002). While most bats were seropositive for Tioman virus, antibody levels for this virus were significantly higher in adults (p < 0.001). Unexpectedly, all sera were negative for Australian bat lyssavirus. Temporal variation in antibody levels suggests that antibodies to Hendra virus and Tioman virus may wax and wane on a seasonal basis. These findings suggest a common exposure to Hendra virus and other paramyxoviruses in this flying fox camp in South Australia.
format Online
Article
Text
id pubmed-7202650
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-72026502020-05-12 Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus) Boardman, Wayne S. J. Baker, Michelle L. Boyd, Victoria Crameri, Gary Peck, Grantley R. Reardon, Terry Smith, Ian G. Caraguel, Charles G. B. Prowse, Thomas A. A. PLoS One Research Article Habitat-mediated global change is driving shifts in species’ distributions which can alter the spatial risks associated with emerging zoonotic pathogens. Many emerging infectious pathogens are transmitted by highly mobile species, including bats, which can act as spill-over hosts for pathogenic viruses. Over three years, we investigated the seroepidemiology of paramyxoviruses and Australian bat lyssavirus in a range-expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus), in a new camp in Adelaide, South Australia. Over six, biannual, sampling sessions, we quantified median florescent intensity (MFI) antibody levels for four viruses for a total of 297 individual bats using a multiplex Luminex binding assay. Where appropriate, florescence thresholds were determined using finite mixture modelling to classify bats’ serological status. Overall, apparent seroprevalence of antibodies directed at Hendra, Cedar and Tioman virus antigens was 43.2%, 26.6% and 95.7%, respectively. We used hurdle models to explore correlates of seropositivity and antibody levels when seropositive. Increased body condition was significantly associated with Hendra seropositivity (Odds ratio = 3.67; p = 0.002) and Hendra virus levels were significantly higher in pregnant females (p = 0.002). While most bats were seropositive for Tioman virus, antibody levels for this virus were significantly higher in adults (p < 0.001). Unexpectedly, all sera were negative for Australian bat lyssavirus. Temporal variation in antibody levels suggests that antibodies to Hendra virus and Tioman virus may wax and wane on a seasonal basis. These findings suggest a common exposure to Hendra virus and other paramyxoviruses in this flying fox camp in South Australia. Public Library of Science 2020-05-06 /pmc/articles/PMC7202650/ /pubmed/32374743 http://dx.doi.org/10.1371/journal.pone.0232339 Text en © 2020 Boardman et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Boardman, Wayne S. J.
Baker, Michelle L.
Boyd, Victoria
Crameri, Gary
Peck, Grantley R.
Reardon, Terry
Smith, Ian G.
Caraguel, Charles G. B.
Prowse, Thomas A. A.
Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title_full Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title_fullStr Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title_full_unstemmed Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title_short Seroprevalence of three paramyxoviruses; Hendra virus, Tioman virus, Cedar virus and a rhabdovirus, Australian bat lyssavirus, in a range expanding fruit bat, the Grey-headed flying fox (Pteropus poliocephalus)
title_sort seroprevalence of three paramyxoviruses; hendra virus, tioman virus, cedar virus and a rhabdovirus, australian bat lyssavirus, in a range expanding fruit bat, the grey-headed flying fox (pteropus poliocephalus)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202650/
https://www.ncbi.nlm.nih.gov/pubmed/32374743
http://dx.doi.org/10.1371/journal.pone.0232339
work_keys_str_mv AT boardmanwaynesj seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT bakermichellel seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT boydvictoria seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT cramerigary seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT peckgrantleyr seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT reardonterry seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT smithiang seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT caraguelcharlesgb seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus
AT prowsethomasaa seroprevalenceofthreeparamyxoviruseshendravirustiomanviruscedarvirusandarhabdovirusaustralianbatlyssavirusinarangeexpandingfruitbatthegreyheadedflyingfoxpteropuspoliocephalus