Synchronous shedding of multiple bat paramyxoviruses coincides with peak periods of Hendra virus spillover.

Alison J Peel1 Konstans Wells2 John Giles3 Victoria Boyd4 Amy Burroughs4 Daniel Edson5 Gary Crameri4 Michelle L Baker4 Hume Field6,7 Lin-Fa Wang8 Hamish McCallum1 Raina K Plowright9 Nicholas Clark10
Affiliations 10 institutions
  1. Environmental Futures Research Institute, Griffith University , Nathan , Queensland , Australia.
  2. Department of Biosciences, Swansea University , Swansea , Wales , UK.
  3. Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health , Baltimore , MD , USA.
  4. CSIRO, Health and Biosecurity Business Unit, Australian Animal Health Laboratory , Geelong , Vic , Australia.
  5. Department of Agriculture, Animal Health Policy Branch , Canberra , ACT , Australia.
  6. EcoHealth Alliance , New York , NY , USA.
  7. School of Veterinary Science, The University of Queensland , Gatton , Queensland , Australia.
  8. Programme in Emerging Infectious Diseases, Duke-National University of Singapore Medical School , Singapore.
  9. Department of Microbiology and Immunology, Montana State University , Bozeman , Montana , USA.
  10. UQ Spatial Epidemiology Laboratory, School of Veterinary Science, the University of Queensland , Gatton , Queensland , Australia.

Abstract

Within host-parasite communities, viral co-circulation and co-infections of hosts are the norm, yet studies of significant emerging zoonoses tend to focus on a single parasite species within the host. Using a multiplexed paramyxovirus bead-based PCR on urine samples from Australian flying foxes, we show that multi-viral shedding from flying fox populations is common. We detected up to nine bat paramyxoviruses shed synchronously. Multi-viral shedding infrequently coalesced into an extreme, brief and spatially restricted shedding pulse, coinciding with peak spillover of Hendra virus, an emerging fatal zoonotic pathogen of high interest. Such extreme pulses of multi-viral shedding could easily be missed during routine surveillance yet have potentially serious consequences for spillover of novel pathogens to humans and domestic animal hosts. We also detected co-occurrence patterns suggestive of the presence of interactions among viruses, such as facilitation and cross-immunity. We propose that multiple viruses may be interacting, influencing the shedding and spillover of zoonotic pathogens. Understanding these interactions in the context of broader scale drivers, such as habitat loss, may help predict shedding pulses of Hendra virus and other fatal zoonoses.

Supporting text Virus Host Location
co-occurrence analyses 1 disease ecology 7 emerging infectious diseases 11 Markov Random Fields 1 multi-viral 1 Pteropus 7 viral communities 2 zoonoses 477 Disease Transmission, Infectious 22 Virus Shedding 51 Animals 1948 Chiroptera 371 Coinfection 15 Paramyxoviridae Infections 16 Paramyxovirinae 14 Urine 9 Zoonoses 397

Evidence records

1 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE3433
Key finding

Multiplexed PCR detected up to nine bat paramyxoviruses shed synchronously in Australian flying fox urine samples.

Virus
Host
Location
Supporting text

Using a multiplexed paramyxovirus bead-based PCR on urine samples from Australian flying foxes, we show that multi-viral shedding from flying fox populations is common. We detected up to nine bat paramyxoviruses shed synchronously.

Method
multiplexed paramyxovirus bead-based PCR
Sample type
urine samples
Geographic raw
Australia
Country inferred
AUS