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Natural Selection on Individual Variation in Tolerance of Gastrointestinal Nematode Infection

Author

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  • Adam D Hayward
  • Daniel H Nussey
  • Alastair J Wilson
  • Camillo Berenos
  • Jill G Pilkington
  • Kathryn A Watt
  • Josephine M Pemberton
  • Andrea L Graham

Abstract

A 25-year study of wild sheep shows that individuals vary in how quickly they lose weight as parasite infections increase, and that those who lose the least weight when heavily infected produce more offspring.Hosts may mitigate the impact of parasites by two broad strategies: resistance, which limits parasite burden, and tolerance, which limits the fitness or health cost of increasing parasite burden. The degree and causes of variation in both resistance and tolerance are expected to influence host–parasite evolutionary and epidemiological dynamics and inform disease management, yet very little empirical work has addressed tolerance in wild vertebrates. Here, we applied random regression models to longitudinal data from an unmanaged population of Soay sheep to estimate individual tolerance, defined as the rate of decline in body weight with increasing burden of highly prevalent gastrointestinal nematode parasites. On average, individuals lost weight as parasite burden increased, but whereas some lost weight slowly as burden increased (exhibiting high tolerance), other individuals lost weight significantly more rapidly (exhibiting low tolerance). We then investigated associations between tolerance and fitness using selection gradients that accounted for selection on correlated traits, including body weight. We found evidence for positive phenotypic selection on tolerance: on average, individuals who lost weight more slowly with increasing parasite burden had higher lifetime breeding success. This variation did not have an additive genetic basis. These results reveal that selection on tolerance operates under natural conditions. They also support theoretical predictions for the erosion of additive genetic variance of traits under strong directional selection and fixation of genes conferring tolerance. Our findings provide the first evidence of selection on individual tolerance of infection in animals and suggest practical applications in animal and human disease management in the face of highly prevalent parasites.Author Summary: Animals can defend themselves against parasites through either resistance (reducing parasite numbers, for example, by killing them) or tolerance (maintaining health as infections levels increase, for example, by repairing damage). Resistance has been well-studied in wild animals, but tolerance has been less so. We analysed data on body weight collected over 25 years on a natural population of Soay sheep, infected with parasitic gut worms. As parasite burden increased, sheep lost weight. Crucially, there was variation among individuals: some lost weight rapidly with increasing infections (i.e., showed “low tolerance”), whereas others lost weight slowly (i.e., showed “high tolerance”). The least tolerant individuals lost 4.5 kg of body weight across the range of parasite burdens that we saw, whereas the most tolerant lost only around 0.36 kg. However, variation in tolerance did not have a heritable genetic basis, so that although tolerance varied between individuals, this was not due to genetic differences. Further analysis revealed that there was natural selection on tolerance. Individuals who were more tolerant of infection produced more offspring over the course of their lives. This study shows that natural selection can act upon resistance and tolerance simultaneously in nature, a result that has implications for both human health and livestock management.

Suggested Citation

  • Adam D Hayward & Daniel H Nussey & Alastair J Wilson & Camillo Berenos & Jill G Pilkington & Kathryn A Watt & Josephine M Pemberton & Andrea L Graham, 2014. "Natural Selection on Individual Variation in Tolerance of Gastrointestinal Nematode Infection," PLOS Biology, Public Library of Science, vol. 12(7), pages 1-13, July.
  • Handle: RePEc:plo:pbio00:1001917
    DOI: 10.1371/journal.pbio.1001917
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    References listed on IDEAS

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    1. Hadfield, Jarrod D., 2010. "MCMC Methods for Multi-Response Generalized Linear Mixed Models: The MCMCglmm R Package," Journal of Statistical Software, Foundation for Open Access Statistics, vol. 33(i02).
    2. Joanne Lello & Brian Boag & Andrew Fenton & Ian R. Stevenson & Peter J. Hudson, 2004. "Competition and mutualism among the gut helminths of a mammalian host," Nature, Nature, vol. 428(6985), pages 840-844, April.
    3. Mark D. Rausher, 2001. "Co-evolution and plant resistance to natural enemies," Nature, Nature, vol. 411(6839), pages 857-864, June.
    4. Susan E. Johnston & Jacob Gratten & Camillo Berenos & Jill G. Pilkington & Tim H. Clutton-Brock & Josephine M. Pemberton & Jon Slate, 2013. "Life history trade-offs at a single locus maintain sexually selected genetic variation," Nature, Nature, vol. 502(7469), pages 93-95, October.
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    Cited by:

    1. Iliana Medina & Naomi E Langmore, 2018. "Tolerance in hosts of brood parasites: a comment on Avilés," Behavioral Ecology, International Society for Behavioral Ecology, vol. 29(3), pages 523-524.
    2. Juan J Soler, 2018. "Tolerance to brood parasitism: a comment on Avilés," Behavioral Ecology, International Society for Behavioral Ecology, vol. 29(3), pages 521-521.
    3. Jesús M Avilés, 2018. "Can hosts tolerate avian brood parasites? An appraisal of mechanisms," Behavioral Ecology, International Society for Behavioral Ecology, vol. 29(3), pages 509-519.

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