Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas
Antibiotic resistance often evolves by mutations at conserved sites in essential genes, resulting in parallel molecular evolution between divergent bacterial strains and species. Whether these resistance mutations are having parallel effects on fitness across bacterial taxa, however, is unclear. Thi...
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| Format: | Journal article |
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Royal Society
2016
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| _version_ | 1797088839684063232 |
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| author | Maclean, R Vogwill, T Kojadinovic, M |
| author_facet | Maclean, R Vogwill, T Kojadinovic, M |
| author_sort | Maclean, R |
| collection | OXFORD |
| description | Antibiotic resistance often evolves by mutations at conserved sites in essential genes, resulting in parallel molecular evolution between divergent bacterial strains and species. Whether these resistance mutations are having parallel effects on fitness across bacterial taxa, however, is unclear. This is an important point to address, because the fitness effects of resistance mutations play a key role in the spread and maintenance of resistance in pathogen populations. We address this idea by measuring the fitness effect of a collection of rifampicin resistance mutations in the β subunit of RNA polymerase (rpoB) across 8 strains that span the diversity of the genus Pseudomonas. We find that almost 50% of rpoB mutations have background-dependent fitness costs, demonstrating that epistatic interactions between rpoB and the rest of the genome are common. Moreover, epistasis is typically strong, and it is the dominant genetic determinant of the cost of resistance mutations. To investigate the functional basis of epistasis, we measured the effects of common rpoB mutations on transcriptional efficiency across 3 strains of Pseudomonas. Transcriptional efficiency correlates strongly to fitness across strains, and epistasis arises because individual rpoB mutations have differential effects on transcriptional efficiency in different genetic backgrounds. |
| first_indexed | 2024-03-07T02:55:51Z |
| format | Journal article |
| id | oxford-uuid:af4413a5-ed99-445e-8651-cfb25539255e |
| institution | University of Oxford |
| last_indexed | 2024-03-07T02:55:51Z |
| publishDate | 2016 |
| publisher | Royal Society |
| record_format | dspace |
| spelling | oxford-uuid:af4413a5-ed99-445e-8651-cfb25539255e2022-03-27T03:48:20ZEpistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of PseudomonasJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:af4413a5-ed99-445e-8651-cfb25539255eSymplectic Elements at OxfordRoyal Society2016Maclean, RVogwill, TKojadinovic, MAntibiotic resistance often evolves by mutations at conserved sites in essential genes, resulting in parallel molecular evolution between divergent bacterial strains and species. Whether these resistance mutations are having parallel effects on fitness across bacterial taxa, however, is unclear. This is an important point to address, because the fitness effects of resistance mutations play a key role in the spread and maintenance of resistance in pathogen populations. We address this idea by measuring the fitness effect of a collection of rifampicin resistance mutations in the β subunit of RNA polymerase (rpoB) across 8 strains that span the diversity of the genus Pseudomonas. We find that almost 50% of rpoB mutations have background-dependent fitness costs, demonstrating that epistatic interactions between rpoB and the rest of the genome are common. Moreover, epistasis is typically strong, and it is the dominant genetic determinant of the cost of resistance mutations. To investigate the functional basis of epistasis, we measured the effects of common rpoB mutations on transcriptional efficiency across 3 strains of Pseudomonas. Transcriptional efficiency correlates strongly to fitness across strains, and epistasis arises because individual rpoB mutations have differential effects on transcriptional efficiency in different genetic backgrounds. |
| spellingShingle | Maclean, R Vogwill, T Kojadinovic, M Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title | Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title_full | Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title_fullStr | Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title_full_unstemmed | Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title_short | Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas |
| title_sort | epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of pseudomonas |
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