Literature DB >> 20120807

Transmission dynamics of Tasmanian devil facial tumor disease may lead to disease-induced extinction.

Hamish McCallum1, Menna Jones, Clare Hawkins, Rodrigo Hamede, Shelly Lachish, David L Sinn, Nick Beeton, Billie Lazenby.   

Abstract

Most pathogens threatening to cause extinction of a host species are maintained on one or more reservoir hosts, in addition to the species that is threatened by disease. Further, most conventional host-pathogen theory assumes that transmission is related to host density, and therefore a pathogen should become extinct before its sole host. Tasmanian devil facial tumor disease is a recently emerged infectious cancer that has led to massive population declines and grave concerns for the future persistence of this largest surviving marsupial carnivore. Here we report the results of mark-recapture studies at six sites and use these data to estimate epidemiological parameters critical to both accurately assessing the risk of extinction from this disease and effectively managing this disease threat. Three sites were monitored from before or close to the time of disease arrival, and at three others disease was well established when trapping began, in one site for at least 10 years. We found no evidence for sex-specific differences in disease prevalence and little evidence of consistent seasonal variation in the force of infection. At all sites, the disease was maintained at high levels of prevalence (>50% in 2-3-year-old animals), despite causing major population declines. We also provide the first estimates of the basic reproductive rate R0 for this disease. Using a simple age-structured deterministic model, we show that our results are not consistent with transmission being proportional to the density of infected hosts but are consistent with frequency-dependent transmission. This conclusion is further supported by the observation that local disease prevalence in 2-3-year-olds still exceeds 50% at a site where population density has been reduced by up to 90% in the past 12 years. These findings lend considerable weight to concerns that this host-specific pathogen will cause the extinction of the Tasmanian devil. Our study highlights the importance of rapidly implementing monitoring programs to determine how transmission depends on host density and emphasizes the need for ongoing management strategies involving a disease-free "insurance population," along with ongoing field monitoring programs to confirm whether local population extinction occurs.

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Year:  2009        PMID: 20120807     DOI: 10.1890/08-1763.1

Source DB:  PubMed          Journal:  Ecology        ISSN: 0012-9658            Impact factor:   5.499


  71 in total

1.  Competing pressures on populations: long-term dynamics of food availability, food quality, disease, stress and animal abundance.

Authors:  Colin A Chapman; Valérie A M Schoof; Tyler R Bonnell; Jan F Gogarten; Sophie Calmé
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-05-26       Impact factor: 6.237

2.  Host persistence or extinction from emerging infectious disease: insights from white-nose syndrome in endemic and invading regions.

Authors:  Joseph R Hoyt; Kate E Langwig; Keping Sun; Guanjun Lu; Katy L Parise; Tinglei Jiang; Winifred F Frick; Jeffrey T Foster; Jiang Feng; A Marm Kilpatrick
Journal:  Proc Biol Sci       Date:  2016-03-16       Impact factor: 5.349

3.  Enemies and turncoats: bovine tuberculosis exposes pathogenic potential of Rift Valley fever virus in a common host, African buffalo (Syncerus caffer).

Authors:  B R Beechler; C A Manore; B Reininghaus; D O'Neal; E E Gorsich; V O Ezenwa; A E Jolles
Journal:  Proc Biol Sci       Date:  2015-04-22       Impact factor: 5.349

4.  Disease introduction is associated with a phase transition in bighorn sheep demographics.

Authors:  Kezia Manlove; E Frances Cassirer; Paul C Cross; Raina K Plowright; Peter J Hudson
Journal:  Ecology       Date:  2016-09-19       Impact factor: 5.499

5.  Evidence that disease-induced population decline changes genetic structure and alters dispersal patterns in the Tasmanian devil.

Authors:  S Lachish; K J Miller; A Storfer; A W Goldizen; M E Jones
Journal:  Heredity (Edinb)       Date:  2010-03-10       Impact factor: 3.821

6.  Disease swamps molecular signatures of genetic-environmental associations to abiotic factors in Tasmanian devil (Sarcophilus harrisii) populations.

Authors:  Alexandra K Fraik; Mark J Margres; Brendan Epstein; Soraia Barbosa; Menna Jones; Sarah Hendricks; Barbara Schönfeld; Amanda R Stahlke; Anne Veillet; Rodrigo Hamede; Hamish McCallum; Elisa Lopez-Contreras; Samantha J Kallinen; Paul A Hohenlohe; Joanna L Kelley; Andrew Storfer
Journal:  Evolution       Date:  2020-06-03       Impact factor: 3.694

7.  Emerging Frontiers in the Study of Molecular Evolution.

Authors:  David A Liberles; Belinda Chang; Kerry Geiler-Samerotte; Aaron Goldman; Jody Hey; Betül Kaçar; Michelle Meyer; William Murphy; David Posada; Andrew Storfer
Journal:  J Mol Evol       Date:  2020-04       Impact factor: 2.395

8.  Telomere Length is a Susceptibility Marker for Tasmanian Devil Facial Tumor Disease.

Authors:  Lane E Smith; Menna E Jones; Rodrigo Hamede; Rosana Risques; Austin H Patton; Patrick A Carter; Andrew Storfer
Journal:  Ecohealth       Date:  2020-10-30       Impact factor: 3.184

9.  Changes in physiological stress and behaviour in semi-free-ranging red-capped mangabeys (Cercocebus torquatus) following antiparasitic treatment.

Authors:  Sagan Friant; Toni E Ziegler; Tony L Goldberg
Journal:  Proc Biol Sci       Date:  2016-07-27       Impact factor: 5.349

10.  Disease and the dynamics of extinction.

Authors:  Hamish McCallum
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-10-19       Impact factor: 6.237

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