Literature DB >> 16995636

The fitting of general force-of-infection models to wildlife disease prevalence data.

Dennis M Heisey1, Damien O Joly, François Messier.   

Abstract

Researchers and wildlife managers increasingly find themselves in situations where they must deal with infectious wildlife diseases such as chronic wasting disease, brucellosis, tuberculosis, and West Nile virus. Managers are often charged with designing and implementing control strategies, and researchers often seek to determine factors that influence and control the disease process. All of these activities require the ability to measure some indication of a disease's foothold in a population and evaluate factors affecting that foothold. The most common type of data available to managers and researchers is apparent prevalence data. Apparent disease prevalence, the proportion of animals in a sample that are positive for the disease, might seem like a natural measure of disease's foothold, but several properties, in particular, its dependency on age structure and the biasing effects of disease-associated mortality, make it less than ideal. In quantitative epidemiology, the "force of infection," or infection hazard, is generally the preferred parameter for measuring a disease's foothold, and it can be viewed as the most appropriate way to "adjust" apparent prevalence for age structure. The typical ecology curriculum includes little exposure to quantitative epidemiological concepts such as cumulative incidence, apparent prevalence, and the force of infection. The goal of this paper is to present these basic epidemiological concepts and resulting models in an ecological context and to illustrate how they can be applied to understand and address basic epidemiological questions. We demonstrate a practical approach to solving the heretofore intractable problem of fitting general force-of-infection models to wildlife prevalence data using a generalized regression approach. We apply the procedures to Mycobacterium bovis (bovine tuberculosis) prevalence in bison (Bison bison) in Wood Buffalo National Park, Canada, and demonstrate strong age dependency in the force of infection as well as an increased mortality hazard in positive animals.

Entities:  

Mesh:

Year:  2006        PMID: 16995636     DOI: 10.1890/0012-9658(2006)87[2356:tfogfm]2.0.co;2

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


  17 in total

1.  Revisiting Rayong: shifting seroprofiles of dengue in Thailand and their implications for transmission and control.

Authors:  Isabel Rodríguez-Barraquer; Rome Buathong; Sopon Iamsirithaworn; Ananda Nisalak; Justin Lessler; Richard G Jarman; Robert V Gibbons; Derek A T Cummings
Journal:  Am J Epidemiol       Date:  2013-11-05       Impact factor: 4.897

Review 2.  Deciphering serology to understand the ecology of infectious diseases in wildlife.

Authors:  Amy T Gilbert; A R Fooks; D T S Hayman; D L Horton; T Müller; R Plowright; A J Peel; R Bowen; J L N Wood; J Mills; A A Cunningham; C E Rupprecht
Journal:  Ecohealth       Date:  2013-08-06       Impact factor: 3.184

3.  Inferring seasonal infection risk at population and regional scales from serology samples.

Authors:  Mark Q Wilber; Colleen T Webb; Fred L Cunningham; Kerri Pedersen; Xiu-Feng Wan; Kim M Pepin
Journal:  Ecology       Date:  2019-11-19       Impact factor: 5.499

4.  Identifying the age cohort responsible for transmission in a natural outbreak of Bordetella bronchiseptica.

Authors:  Gráinne H Long; Divya Sinha; Andrew F Read; Stacy Pritt; Barry Kline; Eric T Harvill; Peter J Hudson; Ottar N Bjørnstad
Journal:  PLoS Pathog       Date:  2010-12-16       Impact factor: 6.823

5.  Integrated survival analysis using an event-time approach in a Bayesian framework.

Authors:  Daniel P Walsh; Victoria J Dreitz; Dennis M Heisey
Journal:  Ecol Evol       Date:  2015-01-17       Impact factor: 2.912

6.  Intensive Circulation of Japanese Encephalitis Virus in Peri-urban Sentinel Pigs near Phnom Penh, Cambodia.

Authors:  Julien Cappelle; Veasna Duong; Long Pring; Lida Kong; Maud Yakovleff; Didot Budi Prasetyo; Borin Peng; Rithy Choeung; Raphaël Duboz; Sivuth Ong; San Sorn; Philippe Dussart; Arnaud Tarantola; Philippe Buchy; Véronique Chevalier
Journal:  PLoS Negl Trop Dis       Date:  2016-12-07

7.  Estimating Loss of Brucella Abortus Antibodies from Age-Specific Serological Data In Elk.

Authors:  J A Benavides; D Caillaud; B M Scurlock; E J Maichak; W H Edwards; P C Cross
Journal:  Ecohealth       Date:  2017-05-15       Impact factor: 3.184

8.  Reconstruction of Rift Valley fever transmission dynamics in Madagascar: estimation of force of infection from seroprevalence surveys using Bayesian modelling.

Authors:  Marie-Marie Olive; Vladimir Grosbois; Annelise Tran; Lalaina Arivony Nomenjanahary; Mihaja Rakotoarinoro; Soa-Fy Andriamandimby; Christophe Rogier; Jean-Michel Heraud; Veronique Chevalier
Journal:  Sci Rep       Date:  2017-01-04       Impact factor: 4.379

9.  Elucidating transmission dynamics and host-parasite-vector relationships for rodent-borne Bartonella spp. in Madagascar.

Authors:  Cara E Brook; Ying Bai; Emily O Yu; Hafaliana C Ranaivoson; Haewon Shin; Andrew P Dobson; C Jessica E Metcalf; Michael Y Kosoy; Katharina Dittmar
Journal:  Epidemics       Date:  2017-03-16       Impact factor: 4.396

10.  Interacting Effects of Newcastle Disease Transmission and Illegal Trade on a Wild Population of White-Winged Parakeets in Peru: A Modeling Approach.

Authors:  Elizabeth F Daut; Glenn Lahodny; Markus J Peterson; Renata Ivanek
Journal:  PLoS One       Date:  2016-01-27       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.