Predicting Ebola virus disease risk and the role of African bat birthing.

C Reed Hranac1 Jonathan C Marshall2 Ara Monadjem3,4 David T S Hayman5
Affiliations 5 institutions
  1. Molecular Epidemiology and Public Health Laboratory, Hopkirk Research Institute, Massey University, Private Bag, 11 222, Palmerston North 4442, New Zealand. Electronic address: [email protected].
  2. Institute of Fundamental Sciences, Massey University, Private Bag 11 222, Palmerston North 4442, New Zealand.
  3. Department of Biological Sciences, University of Eswatini, Private Bag 4, Kwaluseni, Eswatini
  4. Mammal Research Institute, Department of Zoology and Entomology, University of Pretoria, Pretoria, Republic of South Africa.
  5. Molecular Epidemiology and Public Health Laboratory, Hopkirk Research Institute, Massey University, Private Bag, 11 222, Palmerston North 4442, New Zealand. Electronic address: [email protected].

Abstract

Ebola virus disease (EVD) presents a threat to public health throughout equatorial Africa. Despite numerous 'spillover' events into humans and apes, the maintenance reservoirs and mechanism of spillover are poorly understood. Evidence suggests fruit bats play a role in both instances, yet data remain sparse and bats exhibit a wide range of life history traits. Here we pool sparse data and use a mechanistic approach to examine how birthing cycles of African fruit bats, molossid bats, and non-molossid microbats inform the spatio-temporal occurrence of EVD spillover. We create ensemble niche models to predict spatio-temporally varying bat birthing and model outbreaks as spatio-temporal Poisson point processes. We predict three distinct annual birthing patterns among African bats along a latitudinal gradient. Of the EVD spillover models tested, the best by quasi-Akaike information criterion (qAIC) and by out of sample prediction included significant African bat birth-related terms. Temporal bat birthing terms fit in the best models for both human and animal outbreaks were consistent with hypothesized viral dynamics in bat populations, but purely spatial models also performed well. Our best model predicted risk of EVD spillover at locations of the two 2018 EVD outbreaks in the Democratic Republic of the Congo was within the top 12-35% and 0.1% of all 25 × 25 km spatial cells analyzed in sub-Saharan Africa. Results suggest that sparse data can be leveraged to help understand complex systems.

Supporting text Virus Host Location
Chiroptera 376 Ebolavirus 35 Ecological niche model 3 Pteropodidae 4 Spatio-temporal Poisson point process 1 Spillover 105 Viral ecology 4 Ebolavirus 31 Animals 1948 Chiroptera 371 Democratic Republic of the Congo 13 Disease Outbreaks 170 Disease Reservoirs 149 Hemorrhagic Fever, Ebola 27 Humans 1440

Evidence records

3 total
Zoonotic Surveillance
2 records · 1 evidence types
Evidence type
2 records
OVE3507
Key finding

Ebola virus disease spillover into humans in Africa was modeled as being associated with African bat birthing cycles, suggesting bat-related temporal patterns in animal-to-human transmission.

Virus
Host
Location
Supporting text

Of the EVD spillover models tested, the best by quasi-Akaike information criterion and by out of sample prediction included significant African bat birth-related terms.

Method
ensemble niche models | spatio-temporal Poisson point process modeling
Geographic raw
Africa
OVE3506
Key finding

Mechanistic modeling linked African bat birthing cycles to spatio-temporal patterns of Ebola virus disease spillover, suggesting that reproductive timing in bats may influence viral maintenance and transmission.

Virus
Host
Location
Supporting text

Ebola virus disease (EVD) presents a threat to public health throughout equatorial Africa. Here we pool sparse data and use a mechanistic approach to examine how birthing cycles of African fruit bats, molossid bats, and non-molossid microbats inform the spatio-temporal occurrence of EVD spillover.

Method
mechanistic modeling | ensemble niche models | spatio-temporal Poisson point process models
Geographic raw
Africa
Transmission Evidence
1 records · 1 evidence types
Evidence type
1 records
OVE3508
Key finding

Model analysis evaluated Ebola virus disease outbreak locations in the Democratic Republic of the Congo during 2018, showing they occurred within regions of high predicted spillover risk.

Virus
Host
Location
Supporting text

Our best model predicted risk of EVD spillover at locations of the two 2018 EVD outbreaks in the Democratic Republic of the Congo was within the top 12–35% and 0.1% of all spatial cells analyzed.

Method
spatio-temporal Poisson point process modeling | ensemble niche modeling
Transmission direction
animal-to-human
Geographic raw
Democratic Republic of the Congo
Country inferred
COD
Outbreak setting
community outbreaks
Outbreak time
2018
Outbreak scale
two outbreaks