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Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models

BACKGROUND: Breeding livestock for improved resistance to disease is an increasingly important selection goal. However, the risk of pathogens adapting to livestock bred for improved disease resistance is difficult to quantify. Here, we explore the possibility of gastrointestinal worms adapting to sh...

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Autores principales: Kemper, Kathryn E, Goddard, Michael E, Bishop, Stephen C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704967/
https://www.ncbi.nlm.nih.gov/pubmed/23714384
http://dx.doi.org/10.1186/1297-9686-45-14
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author Kemper, Kathryn E
Goddard, Michael E
Bishop, Stephen C
author_facet Kemper, Kathryn E
Goddard, Michael E
Bishop, Stephen C
author_sort Kemper, Kathryn E
collection PubMed
description BACKGROUND: Breeding livestock for improved resistance to disease is an increasingly important selection goal. However, the risk of pathogens adapting to livestock bred for improved disease resistance is difficult to quantify. Here, we explore the possibility of gastrointestinal worms adapting to sheep bred for low faecal worm egg count using computer simulation. Our model assumes sheep and worm genotypes interact at a single locus, such that the effect of an A allele in sheep is dependent on worm genotype, and the B allele in worms is favourable for parasitizing the A allele sheep but may increase mortality on pasture. We describe the requirements for adaptation and test if worm adaptation (1) is slowed by non-genetic features of worm infections and (2) can occur with little observable change in faecal worm egg count. RESULTS: Adaptation in worms was found to be primarily influenced by overall worm fitness, viz. the balance between the advantage of the B allele during the parasitic stage in sheep and its disadvantage on pasture. Genetic variation at the interacting locus in worms could be from de novo or segregating mutations, but de novo mutations are rare and segregating mutations are likely constrained to have (near) neutral effects on worm fitness. Most other aspects of the worm infection we modelled did not affect the outcomes. However, the host-controlled mechanism to reduce faecal worm egg count by lowering worm fecundity reduced the selection pressure on worms to adapt compared to other mechanisms, such as increasing worm mortality. Temporal changes in worm egg count were unreliable for detecting adaptation, despite the steady environment assumed in the simulations. CONCLUSIONS: Adaptation of worms to sheep selected for low faecal worm egg count requires an allele segregating in worms that is favourable in animals with improved resistance but less favourable in other animals. Obtaining alleles with this specific property seems unlikely. With support from experimental data, we conclude that selection for low faecal worm egg count should be stable over a short time frame (e.g. 20 years). We are further exploring model outcomes with multiple loci and comparing outcomes to other control strategies.
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spelling pubmed-37049672013-07-12 Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models Kemper, Kathryn E Goddard, Michael E Bishop, Stephen C Genet Sel Evol Research BACKGROUND: Breeding livestock for improved resistance to disease is an increasingly important selection goal. However, the risk of pathogens adapting to livestock bred for improved disease resistance is difficult to quantify. Here, we explore the possibility of gastrointestinal worms adapting to sheep bred for low faecal worm egg count using computer simulation. Our model assumes sheep and worm genotypes interact at a single locus, such that the effect of an A allele in sheep is dependent on worm genotype, and the B allele in worms is favourable for parasitizing the A allele sheep but may increase mortality on pasture. We describe the requirements for adaptation and test if worm adaptation (1) is slowed by non-genetic features of worm infections and (2) can occur with little observable change in faecal worm egg count. RESULTS: Adaptation in worms was found to be primarily influenced by overall worm fitness, viz. the balance between the advantage of the B allele during the parasitic stage in sheep and its disadvantage on pasture. Genetic variation at the interacting locus in worms could be from de novo or segregating mutations, but de novo mutations are rare and segregating mutations are likely constrained to have (near) neutral effects on worm fitness. Most other aspects of the worm infection we modelled did not affect the outcomes. However, the host-controlled mechanism to reduce faecal worm egg count by lowering worm fecundity reduced the selection pressure on worms to adapt compared to other mechanisms, such as increasing worm mortality. Temporal changes in worm egg count were unreliable for detecting adaptation, despite the steady environment assumed in the simulations. CONCLUSIONS: Adaptation of worms to sheep selected for low faecal worm egg count requires an allele segregating in worms that is favourable in animals with improved resistance but less favourable in other animals. Obtaining alleles with this specific property seems unlikely. With support from experimental data, we conclude that selection for low faecal worm egg count should be stable over a short time frame (e.g. 20 years). We are further exploring model outcomes with multiple loci and comparing outcomes to other control strategies. BioMed Central 2013-05-28 /pmc/articles/PMC3704967/ /pubmed/23714384 http://dx.doi.org/10.1186/1297-9686-45-14 Text en Copyright © 2013 Kemper et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kemper, Kathryn E
Goddard, Michael E
Bishop, Stephen C
Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title_full Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title_fullStr Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title_full_unstemmed Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title_short Adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
title_sort adaptation of gastrointestinal nematode parasites to host genotype: single locus simulation models
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704967/
https://www.ncbi.nlm.nih.gov/pubmed/23714384
http://dx.doi.org/10.1186/1297-9686-45-14
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