Table 5.4.
Species | Family | Location | Disease/Pathogen | Social aspect | Analysis | Ref |
---|---|---|---|---|---|---|
Myotis lucifugus, M. septentrionalis, M. sodalis, M. leibii, Perimyotis subflavus, Eptesicus fuscus | Vespertilionidae | North America | White-Nose Syndrome (WNS) | Effect of hibernation cluster size on WNS detection | Population surveys, statistical models | 1 |
M. lucifugus, M. septentrionalis, M. sodalis, M. leibii, P. subflavus, E. fuscus | Vespertilionidae | North America | WNS | Variation in sociality between species | Population surveys, statistical models | 2 |
M. lucifugus | Vespertilionidae | North America | WNS | Female philopatry and colony connectivity | Population Genetic Structure (FST) | 3 |
M. lucifugus | Vespertilionidae | North America | WNS | Effect of colony size on WNS risk | Population surveys, statistical models | 4 |
M. lucifugus, M. septentrionalis, M. sodalis, M. leibii, P. subflavus, E. fuscus, M. emarginatus, M. myotis, M dasycneme, M. brandtii, M. mystacinus, M. daubentonii, M. nattereri, Pipistrellus pipistrellus, E. nilssonii, E. serotinus | Vespertilionidae |
North America & Europe |
WNS | Variation in pre- and post-WNS colony size of North American and European bat species | Population surveys and statistical models | 5 |
E. fuscus | Vespertilionidae | USA | Rabies | Effect of colony size on rabies acquisition | Field data, statistical models | 6 |
E. fuscus | Vespertilionidae | Canada & USA | Hypothetical | Variation in fission–fusion dynamics between pregnant and lactating bats influences hypothetical pathogen dynamics | Social network analysis, epidemiological models | 7 |
Nyctalus lasiopterus | Vespertilionidae | Spain | Hypothetical | Variation in roosting behavior and fission–fusion dynamics influences hypothetical pathogen dynamics | Social network analysis, epidemiological models | 8 |
Desmodus rotundus | Phyllostomidae | Peru | Rabies | Effect of migration and group size on rabies prevalence | Field data, epidemiological models | 9 |
D. rotundus | Phyllostomidae | Peru | Rabies | Effect of colony size on rabies seroprevalence | Field data, statistical models | 10 |
M. myotis | Vespertilionidae | Germany | Coronaviruses, Astroviruses, and Adenoviruses | Effect of colony size on viral amplification | PCR to identify viruses, field data, and statistical models | 11 |
Pteropus giganteus | Pteropodidae | Bangladesh | Nipah virus | Effect of roost selection and colony size on predicted Nipah outbreaks | Field data, epidemiological models | 12 |
P. alecto, P. poliocephalus | Pteropodidae | Australia | Hendra virus | Colony size and absence of migratory behavior of urban populations | Field data, epidemiological models | 13 |
Eptesicus serotinus, Hypsugo savii, M. blythii, M.capaccinii, M. daubentonii, M. emarginatus, M. escalerai, M. myotis, Nyctalus leisleri, Plecotus auritus, P.austriacus, P. kuhlii, P. nathusii, P. pipistrellus, P. pygmaeus, Miniopterus schreibersii, Rhinolophus euryale, R. ferrumequinum, R. hipposideros, Tadarida teniotis |
Vespertilionidae Miniopteridae Rhinolophidae Molossidae |
Spain |
European bat Lyssavirus |
Effect of colony size on Lyssavirus seroprevalence | Field data, seroprevalence, and statistical models | 14 |
Hypothetical | – | – | Hypothetical | Effects of fission–fusion dynamics, group size, and information exchange on predicted pathogen dynamics | Social network analysis, epidemiological models | 15 |
[1] Langwig et al. (2012), [2] Langwig et al. (2015), [3] Miller-Butterworth et al. (2014), [4] Wilder et al. (2011), [5] Frick et al. (2015), [6] Pearce et al. (2007), [7] Webber et al. (2016), [8] Fortuna et al. (2009), [9] Blackwood et al. (2013), [10] Streicker et al. (2012), [11] Drexler et al. (2011), [12] Hahn et al. (2014), [13] Plowright et al. (2011), [14] Serra Cabo et al. (2013), [15] Kashima et al. (2013)