Spatiotemporal Aspects of Hendra Virus Infection in Pteropid Bats (Flying-Foxes) in Eastern Australia.

Hume Field1,2 David Jordan3 Daniel Edson1,4 Stephen Morris3 Debra Melville1 Kerryn Parry-Jones5 Alice Broos1 Anja Divljan5,6 Lee McMichael1,7 Rodney Davis8 Nina Kung1,9 Peter Kirkland8 Craig Smith1
Affiliations 9 institutions
  1. Queensland Centre for Emerging Infectious Diseases, Biosecurity Queensland, Department of Agriculture and Fisheries, Brisbane, Queensland, Australia.
  2. EcoHealth Alliance, New York, New York, United States of America.
  3. Wollongbar Primary Industries Institute, Department of Primary Industries, Wollongbar, New South Wales, Australia.
  4. Department of Agriculture, Canberra, Australian Capital Territory, Australia.
  5. Institute of Wildlife Research, School of Biological Sciences, University of Sydney, Sydney, New South Wales, Australia.
  6. Australian Museum, Sydney, New South Wales, Australia.
  7. School of Veterinary Science, University of Queensland, Gatton, Queensland, Australia.
  8. Elizabeth Macarthur Agricultural Institute, Department of Primary Industries, Menangle, New South Wales, Australia.
  9. Biosecurity Queensland, Department of Agriculture and Fisheries, Brisbane, Queensland, Australia.

Abstract

Hendra virus (HeV) causes highly lethal disease in horses and humans in the eastern Australian states of Queensland (QLD) and New South Wales (NSW), with multiple equine cases now reported on an annual basis. Infection and excretion dynamics in pteropid bats (flying-foxes), the recognised natural reservoir, are incompletely understood. We sought to identify key spatial and temporal factors associated with excretion in flying-foxes over a 2300 km latitudinal gradient from northern QLD to southern NSW which encompassed all known equine case locations. The aim was to strengthen knowledge of Hendra virus ecology in flying-foxes to improve spillover risk prediction and exposure risk mitigation strategies, and thus better protect horses and humans. Monthly pooled urine samples were collected from under roosting flying-foxes over a three-year period and screened for HeV RNA by quantitative RT-PCR. A generalised linear model was employed to investigate spatiotemporal associations with HeV detection in 13,968 samples from 27 roosts. There was a non-linear relationship between mean HeV excretion prevalence and five latitudinal regions, with excretion moderate in northern and central QLD, highest in southern QLD/northern NSW, moderate in central NSW, and negligible in southern NSW. Highest HeV positivity occurred where black or spectacled flying-foxes were present; nil or very low positivity rates occurred in exclusive grey-headed flying-fox roosts. Similarly, little red flying-foxes are evidently not a significant source of virus, as their periodic extreme increase in numbers at some roosts was not associated with any concurrent increase in HeV detection. There was a consistent, strong winter seasonality to excretion in the southern QLD/northern NSW and central NSW regions. This new information allows risk management strategies to be refined and targeted, mindful of the potential for spatial risk profiles to shift over time with changes in flying-fox species distribution.

Supporting text Virus Host Location
Animals 1948 Chiroptera 371 Hendra Virus 39 Henipavirus Infections 65 New South Wales 3 Queensland 6 RNA, Viral 193 Seasons 47

Evidence records

3 total
Zoonotic Surveillance
3 records · 2 evidence types
Evidence type
1 records
OVE2245
Key finding

Hendra virus RNA was detected in pooled urine samples from roosting flying-foxes across Queensland and New South Wales using quantitative RT-PCR.

Virus
Host
Location
Supporting text

Monthly pooled urine samples were collected from under roosting flying-foxes over a three-year period and screened for HeV RNA by quantitative RT-PCR. There was a non-linear relationship between mean HeV excretion prevalence and five latitudinal regions, with excretion moderate in northern and central QLD, highest in southern QLD/northern NSW, moderate in central NSW, and negligible in southern NSW.

Method
quantitative RT-PCR
Sample type
pooled urine samples
Geographic raw
Queensland | New South Wales
Country inferred
AUS
Evidence type
2 records
OVE2246
Key finding

Hendra virus excretion prevalence differed among flying-fox species, being highest where black or spectacled flying-foxes roosted and lowest in grey-headed and little red flying-fox colonies, indicating species-specific maintenance patterns.

Virus
Host
Location
Supporting text

Highest HeV positivity occurred where black or spectacled flying-foxes were present; nil or very low positivity rates occurred in exclusive grey-headed flying-fox roosts. Similarly, little red flying-foxes are evidently not a significant source of virus, as their periodic extreme increase in numbers at some roosts was not associated with any concurrent increase in HeV detection.

Method
quantitative RT-PCR | generalised linear model analysis
Sample type
pooled urine samples
Geographic raw
Queensland | New South Wales
Country inferred
AUS
OVE2247
Key finding

Hendra virus excretion in flying-foxes showed consistent winter seasonality in southern Queensland, northern New South Wales, and central New South Wales, reflecting temporal ecological patterns of viral circulation.

Virus
Host
Location
Supporting text

There was a consistent, strong winter seasonality to excretion in the southern QLD/northern NSW and central NSW regions.

Method
quantitative RT-PCR | generalised linear model analysis | temporal pattern analysis
Sample type
pooled urine samples
Geographic raw
southern Queensland | northern New South Wales | central New South Wales
Country inferred
AUS