2001
DOI: 10.2527/2001.7982057x
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Utilizing stochastic genetic epidemiological models to quantify the impact of selection for resistance to infectious diseases in domestic livestock.

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2001
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Cited by 18 publications
(13 citation statements)
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“…The concept that infectious disease may have a genetic component is, of course, not new. Many agricultural geneticists make their livings by breeding disease resistance into both plants and animals [82,83]. One of the founders of behavioral genetics, Franz Kallmann [84], showed genetic factors influenced acquiring tuberculosis (DZ concordance = 26%, MZ concordance = 87%), an observation that was confirmed in modern times [85,86].…”
Section: Discussionmentioning
confidence: 99%
“…The concept that infectious disease may have a genetic component is, of course, not new. Many agricultural geneticists make their livings by breeding disease resistance into both plants and animals [82,83]. One of the founders of behavioral genetics, Franz Kallmann [84], showed genetic factors influenced acquiring tuberculosis (DZ concordance = 26%, MZ concordance = 87%), an observation that was confirmed in modern times [85,86].…”
Section: Discussionmentioning
confidence: 99%
“…Innocent, Morrison, Brownlie & Gettingby (1997) tested effects of different management practices on disease incidence in a closed dairy herd, and Stärk, Pfeiffer & Morris (2000) determined disease spread between farms stochastically. MacKenzie & Bishop (2001b)) developed a stochastic model of hypothetical epidemics caused by microparasites in a pig farm and later applied the same model to quantify the impact of selection for disease resistance by adapting host genotype in the model (MacKenzie & Bishop 2001b). However, the weakness of many of these models is that they do not have robust data against which to parameterise or test their model.…”
Section: Discussionmentioning
confidence: 99%
“…The stochastic setting of the compartmental model is described below for the SLIR model. There are two components in the stochastic models: the event type (Table 1) and the inter‐event time (Renshaw 1991; MacKenzie & Bishop 2001a,b). The time periods between events may be considered random, with probability of specific events defined by the components of the model as described by Renshaw (1991).…”
Section: Methodsmentioning
confidence: 99%
“…The models used are simple insofar as the only epidemiological parameters included are transmission coefficient and recovery rate. However, other parameters can easily be incorporated, as demonstrated by MacKenzie and Bishop (2001). Similarly, the farm parameters, such as contact rate, can be modified to inves- tigate the effect of farm structure on disease epidemiology.…”
Section: Discussionmentioning
confidence: 99%