4.8 Article

Evolution of antibiotic resistance is linked to any genetic mechanism affecting bacterial duration of carriage

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1617849114

Keywords

antibiotic resistance; coexistence; Streptococcus pneumoniae; epistasis; multistrain model

Funding

  1. Models of Infectious Disease Agent Study [NIH National Institute of General Medical Sciences (NIGMS) Grant] [U01GM110721]
  2. Marie Sklodowska-Curie Individual Fellowship [657768]
  3. Sir Henry Dale Fellowship (Wellcome Trust) [104169/Z/14/Z]
  4. Wellcome Trust Training Fellowship [083735/Z/07/Z]
  5. NIH [R01AI048935, U54GM088558]
  6. Sir Henry Dale Fellowship (Royal Society) [104169/Z/14/Z]
  7. Medical Research Council [MR/L016265/1, MR/K010174/1B] Funding Source: researchfish
  8. Wellcome Trust [104169/Z/14/Z] Funding Source: researchfish
  9. Marie Curie Actions (MSCA) [657768] Funding Source: Marie Curie Actions (MSCA)
  10. Wellcome Trust [083735/Z/07/Z, 104169/Z/14/Z] Funding Source: Wellcome Trust
  11. MRC [MR/L016265/1] Funding Source: UKRI

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Understanding how changes in antibiotic consumption affect the prevalence of antibiotic resistance in bacterial pathogens is important for public health. In a number of bacterial species, including Streptococcus pneumoniae, the prevalence of resistance has remained relatively stable despite prolonged selection pressure from antibiotics. The evolutionary processes allowing the robust coexistence of antibiotic sensitive and resistant strains are not fully understood. While allelic diversity can be maintained at a locus by direct balancing selection, there is no evidence for such selection acting in the case of resistance. In this work, we propose a mechanism for maintaining coexistence at the resistance locus: linkage to a second locus that is under balancing selection and that modulates the fitness effect of resistance. We show that duration of carriage plays such a role, with long duration of carriage increasing the fitness advantage gained from resistance. We therefore predict that resistance will be more common in strains with a long duration of carriage and that mechanisms maintaining diversity in duration of carriage will also maintain diversity in antibiotic resistance. We test these predictions in S. pneumoniae and find that the duration of carriage of a serotype is indeed positively correlated with the prevalence of resistance in that serotype. These findings suggest heterogeneity in duration of carriage is a partial explanation for the coexistence of sensitive and resistant strains and that factors determining bacterial duration of carriage will also affect the prevalence of resistance.

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