4.6 Article

Henipavirus Neutralising Antibodies in an Isolated Island Population of African Fruit Bats

Journal

PLOS ONE
Volume 7, Issue 1, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0030346

Keywords

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Funding

  1. Institute of Zoology, Zoological Society of London
  2. Cambridge Infectious Diseases Consortium, University of Cambridge
  3. Charles Slater Trust
  4. Zebra Foundation for Veterinary Zoological Education
  5. Wellcome Trust
  6. Science and Technology Directorate, Department of Homeland Security, USA
  7. Department for Environment, Food and Rural Affairs (Defra) [SEV3500]
  8. Royal Society
  9. UK Medical Research Council [G0801176]
  10. Medical Research Council [G0801176] Funding Source: researchfish
  11. MRC [G0801176] Funding Source: UKRI

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Isolated islands provide valuable opportunities to study the persistence of viruses in wildlife populations, including population size thresholds such as the critical community size. The straw-coloured fruit bat, Eidolon helvum, has been identified as a reservoir for henipaviruses (serological evidence) and Lagos bat virus (LBV; virus isolation and serological evidence) in continental Africa. Here, we sampled from a remote population of E. helvum annobonensis fruit bats on Annobon island in the Gulf of Guinea to investigate whether antibodies to these viruses also exist in this isolated subspecies. Henipavirus serological analyses (Luminex multiplexed binding and inhibition assays, virus neutralisation tests and western blots) and lyssavirus serological analyses (LBV: modified Fluorescent Antibody Virus Neutralisation test, LBV and Mokola virus: lentivirus pseudovirus neutralisation assay) were undertaken on 73 and 70 samples respectively. Given the isolation of fruit bats on Annobon and their lack of connectivity with other populations, it was expected that the population size on the island would be too small to allow persistence of viruses that are thought to cause acute and immunising infections. However, the presence of antibodies against henipaviruses was detected using the Luminex binding assay and confirmed using alternative assays. Neutralising antibodies to LBV were detected in one bat using both assays. We demonstrate clear evidence for exposure of multiple individuals to henipaviruses in this remote population of E. helvum annobonensis fruit bats on Annobon island. The situation is less clear for LBV. Seroprevalences to henipaviruses and LBV in Annobon are notably different to those in E. helvum in continental locations studied using the same sampling techniques and assays. Whilst cross-sectional serological studies in wildlife populations cannot provide details on viral dynamics within populations, valuable information on the presence or absence of viruses may be obtained and utilised for informing future studies.

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