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      Ecology of Zoonotic Infectious Diseases in Bats: Current Knowledge and Future Directions

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          Abstract

          Bats are hosts to a range of zoonotic and potentially zoonotic pathogens. Human activities that increase exposure to bats will likely increase the opportunity for infections to spill over in the future. Ecological drivers of pathogen spillover and emergence in novel hosts, including humans, involve a complex mixture of processes, and understanding these complexities may aid in predicting spillover. In particular, only once the pathogen and host ecologies are known can the impacts of anthropogenic changes be fully appreciated. Cross-disciplinary approaches are required to understand how host and pathogen ecology interact. Bats differ from other sylvatic disease reservoirs because of their unique and diverse lifestyles, including their ability to fly, often highly gregarious social structures, long lifespans and low fecundity rates. We highlight how these traits may affect infection dynamics and how both host and pathogen traits may interact to affect infection dynamics. We identify key questions relating to the ecology of infectious diseases in bats and propose that a combination of field and laboratory studies are needed to create data-driven mechanistic models to elucidate those aspects of bat ecology that are most critical to the dynamics of emerging bat viruses. If commonalities can be found, then predicting the dynamics of newly emerging diseases may be possible. This modelling approach will be particularly important in scenarios when population surveillance data are unavailable and when it is unclear which aspects of host ecology are driving infection dynamics.

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          Most cited references193

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          Population biology of infectious diseases: Part I.

          If the host population is taken to be a dynamic variable (rather than constant, as conventionally assumed), a wider understanding of the population biology of infectious diseases emerges. In this first part of a two-part article, mathematical models are developed, shown to fit data from laboratory experiments, and used to explore the evolutionary relations among transmission parameters. In the second part of the article, to be published in next week's issue, the models are extended to include indirectly transmitted infections, and the general implications for infectious diseases are considered.
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            Species interactions in a parasite community drive infection risk in a wildlife population.

            Most hosts, including humans, are simultaneously or sequentially infected with several parasites. A key question is whether patterns of coinfection arise because infection by one parasite species affects susceptibility to others or because of inherent differences between hosts. We used time-series data from individual hosts in natural populations to analyze patterns of infection risk for a microparasite community, detecting large positive and negative effects of other infections. Patterns remain once variations in host susceptibility and exposure are accounted for. Indeed, effects are typically of greater magnitude, and explain more variation in infection risk, than the effects associated with host and environmental factors more commonly considered in disease studies. We highlight the danger of mistaken inference when considering parasite species in isolation rather than parasite communities.
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              Isolation of Hendra virus from pteropid bats: a natural reservoir of Hendra virus.

              Since it was first described in Australia in 1994, Hendra virus (HeV) has caused two outbreaks of fatal disease in horses and humans, and an isolated fatal horse case. Our preliminary studies revealed a high prevalence of neutralizing antibodies to HeV in bats of the genus PTEROPUS:, but it was unclear whether this was due to infection with HeV or a related virus. We developed the hypothesis that HeV excretion from bats might be related to the birthing process and we targeted the reproductive tract for virus isolation. Three virus isolates were obtained from the uterine fluid and a pool of foetal lung and liver from one grey-headed flying-fox (Pteropus poliocephalus), and from the foetal lung of one black flying-fox (P. alecto). Antigenically, these isolates appeared to be closely related to HeV, returning positive results on immunofluorescent antibody staining and constant-serum varying-virus neutralization tests. Using an HeV-specific oligonucleotide primer pair, genomic sequences of the isolates were amplified. Sequencing of 200 nucleotides in the matrix gene identified that these three isolates were identical to HeV. Isolations were confirmed after RNA extracted from original material was positive for HeV RNA when screened on an HeV Taqman assay. The isolation of HeV from pteropid bats corroborates our earlier serological and epidemiological evidence that they are a natural reservoir host of the virus.
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                Author and article information

                Journal
                Zoonoses Public Health
                Zoonoses Public Health
                zph
                Zoonoses and Public Health
                Blackwell Publishing Ltd (Oxford, UK )
                1863-1959
                1863-2378
                February 2013
                : 60
                : 1
                : 2-21
                Affiliations
                [1 ]Disease Dynamics Unit, Department of Veterinary Medicine, University of Cambridge Cambridge, UK
                [2 ]Department of Biology, Colorado State University Fort Collins, CO, USA
                [3 ]Institute of Zoology, Zoological Society of London London, UK
                [4 ]Animal Health and Veterinary Laboratories Agency Weybridge, UK
                [5 ]Department of Biomedical Sciences, Colorado State University Fort Collins, CO, USA
                [6 ]U.S. Geological Survey, Fort Collins Science Center Fort Collins, CO, USA
                [7 ]Department of Ecology and Evolutionary Biology, University of Tennessee Knoxville, TN, USA
                [8 ]National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention Atlanta, GA, USA
                Author notes
                D. T. S. Hayman. Department of Biology, Colorado State University, Fort Collins, CO-80523, USA. Tel.: 970 491 0423; Fax: 970 491 0649: E-mail: davidtshayman@ 123456gmail.com
                Article
                10.1111/zph.12000
                3600532
                22958281
                3650f727-e17f-4d8c-b09f-ba72173e7d8e
                © 2012 Blackwell Verlag GmbH

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 10 November 2011
                Categories
                Special Issue – Bats

                epidemiology,zoonoses,mathematical modeling,nipah virus,public health,rabies,filovirus,coronavirus

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