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Variation in Mutant Prevention Concentrations
Objectives:Understanding how phenotypic traits vary has been a longstanding goal of evolutionary biologists. When examining antibiotic-resistance in bacteria, it is generally understood that the minimum inhibitory concentration (MIC) has minimal variation specific to each bacterial strain-antibiotic...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365975/ https://www.ncbi.nlm.nih.gov/pubmed/30766517 http://dx.doi.org/10.3389/fmicb.2019.00042 |
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author | Gianvecchio, Crystal Lozano, Natalie Ann Henderson, Claire Kalhori, Pooneh Bullivant, Austin Valencia, Alondra Su, Lauren Bello, Gladys Wong, Michele Cook, Emoni Fuller, Lakhia Neal, Jerome B. Yeh, Pamela J. |
author_facet | Gianvecchio, Crystal Lozano, Natalie Ann Henderson, Claire Kalhori, Pooneh Bullivant, Austin Valencia, Alondra Su, Lauren Bello, Gladys Wong, Michele Cook, Emoni Fuller, Lakhia Neal, Jerome B. Yeh, Pamela J. |
author_sort | Gianvecchio, Crystal |
collection | PubMed |
description | Objectives:Understanding how phenotypic traits vary has been a longstanding goal of evolutionary biologists. When examining antibiotic-resistance in bacteria, it is generally understood that the minimum inhibitory concentration (MIC) has minimal variation specific to each bacterial strain-antibiotic combination. However, there is a less studied resistance trait, the mutant prevention concentration (MPC), which measures the MIC of the most resistant sub-population. Whether and how MPC varies has been poorly understood. Here, we ask a simple, yet important question: How much does the MPC vary, within a single strain-antibiotic association? Using a Staphylococcus species and five antibiotics from five different antibiotic classes—ciprofloxacin, doxycycline, gentamicin, nitrofurantoin, and oxacillin—we examined the frequency of resistance for a wide range of concentrations per antibiotic, and measured the repeatability of the MPC, the lowest amount of antibiotic that would ensure no surviving cells in a 10(10) population of bacteria. Results: We found a wide variation within the MPC and distributions that were rarely normal. When antibiotic resistance evolved, the distribution of the MPC changed, with all distributions becoming wider and some multi-modal. Conclusion: Unlike the MIC, there is high variability in the MPC for a given bacterial strain-antibiotic combination. |
format | Online Article Text |
id | pubmed-6365975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63659752019-02-14 Variation in Mutant Prevention Concentrations Gianvecchio, Crystal Lozano, Natalie Ann Henderson, Claire Kalhori, Pooneh Bullivant, Austin Valencia, Alondra Su, Lauren Bello, Gladys Wong, Michele Cook, Emoni Fuller, Lakhia Neal, Jerome B. Yeh, Pamela J. Front Microbiol Microbiology Objectives:Understanding how phenotypic traits vary has been a longstanding goal of evolutionary biologists. When examining antibiotic-resistance in bacteria, it is generally understood that the minimum inhibitory concentration (MIC) has minimal variation specific to each bacterial strain-antibiotic combination. However, there is a less studied resistance trait, the mutant prevention concentration (MPC), which measures the MIC of the most resistant sub-population. Whether and how MPC varies has been poorly understood. Here, we ask a simple, yet important question: How much does the MPC vary, within a single strain-antibiotic association? Using a Staphylococcus species and five antibiotics from five different antibiotic classes—ciprofloxacin, doxycycline, gentamicin, nitrofurantoin, and oxacillin—we examined the frequency of resistance for a wide range of concentrations per antibiotic, and measured the repeatability of the MPC, the lowest amount of antibiotic that would ensure no surviving cells in a 10(10) population of bacteria. Results: We found a wide variation within the MPC and distributions that were rarely normal. When antibiotic resistance evolved, the distribution of the MPC changed, with all distributions becoming wider and some multi-modal. Conclusion: Unlike the MIC, there is high variability in the MPC for a given bacterial strain-antibiotic combination. Frontiers Media S.A. 2019-01-31 /pmc/articles/PMC6365975/ /pubmed/30766517 http://dx.doi.org/10.3389/fmicb.2019.00042 Text en Copyright © 2019 Gianvecchio, Lozano, Henderson, Kalhori, Bullivant, Valencia, Su, Bello, Wong, Cook, Fuller, Neal and Yeh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Gianvecchio, Crystal Lozano, Natalie Ann Henderson, Claire Kalhori, Pooneh Bullivant, Austin Valencia, Alondra Su, Lauren Bello, Gladys Wong, Michele Cook, Emoni Fuller, Lakhia Neal, Jerome B. Yeh, Pamela J. Variation in Mutant Prevention Concentrations |
title | Variation in Mutant Prevention Concentrations |
title_full | Variation in Mutant Prevention Concentrations |
title_fullStr | Variation in Mutant Prevention Concentrations |
title_full_unstemmed | Variation in Mutant Prevention Concentrations |
title_short | Variation in Mutant Prevention Concentrations |
title_sort | variation in mutant prevention concentrations |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365975/ https://www.ncbi.nlm.nih.gov/pubmed/30766517 http://dx.doi.org/10.3389/fmicb.2019.00042 |
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