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  Segregational drift hinders the evolution of antibiotic resistance on polyploid replicons

Garoña, A., Santer, M., Hülter, N. F., Uecker, H., & Dagan, T. (2023). Segregational drift hinders the evolution of antibiotic resistance on polyploid replicons. PLoS Genetics, 19(8): e1010829. doi:10.1371/journal.pgen.1010829.

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 Creators:
Garoña, Ana, Author
Santer, Mario1, 2, Author           
Hülter, Nils F., Author
Uecker, Hildegard1, Author           
Dagan, Tal, Author
Affiliations:
1Research Group Stochastic Evolutionary Dynamics (Uecker), Department Theoretical Biology (Traulsen), Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_2640692              
2IMPRS for Evolutionary Biology, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445639              

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 Abstract: The emergence of antibiotic resistance under treatment depends on the availability of resistance alleles and their establishment in the population. Novel resistance alleles are encoded either in chromosomal or extrachromosomal genetic elements; both types may be present in multiple copies within the cell. However, the effect of polyploidy on the emergence of antibiotic resistance remains understudied. Here we show that the establishment of resistance alleles in microbial populations depends on the ploidy level. Evolving bacterial populations under selection for antibiotic resistance, we demonstrate that resistance alleles in polyploid elements are lost frequently in comparison to alleles in monoploid elements due to segregational drift. Integrating the experiments with a mathematical model, we find an agreement between the theoretical and empirical allele dynamics, confirming our understanding of the allele segregation process. Using the mathematical model, we further show that the effect of polyploidy on the establishment probability of beneficial alleles is strongest for low replicon copy numbers and plateaus for high replicon copy numbers. Our results suggest that the distribution of fitness effects for mutations that get fixed in a population depends on the replicon ploidy level. Our study indicates that strategies for drug treatment of bacterial infections should take into consideration the pathogen ploidy level.

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Language(s): eng - English
 Dates: 2023-02-012023-02-022023-06-142023-08-03
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1371/journal.pgen.1010829
 Degree: -

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Project name : The role of plasmids in bacterial adaptation
Grant ID : 418432175
Funding program : -
Funding organization : Deutsche Forschungsgemeinschaft (DFG)

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Title: PLoS Genetics
  Other : PLoS Genet.
Source Genre: Journal
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Publ. Info: San Francisco, CA : Public Library of Science
Pages: - Volume / Issue: 19 (8) Sequence Number: e1010829 Start / End Page: - Identifier: ISSN: 1553-7390
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000017180