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Microbial lag phase can be indicative of, or independent from, cellular stress

Measures of microbial growth, used as indicators of cellular stress, are sometimes quantified at a single time-point. In reality, these measurements are compound representations of length of lag, exponential growth-rate, and other factors. Here, we investigate whether length of lag phase can act as...

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Autores principales: Hamill, Philip G., Stevenson, Andrew, McMullan, Phillip E., Williams, James P., Lewis, Abiann D. R., S, Sudharsan, Stevenson, Kath E., Farnsworth, Keith D., Khroustalyova, Galina, Takemoto, Jon Y., Quinn, John P., Rapoport, Alexander, Hallsworth, John E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125082/
https://www.ncbi.nlm.nih.gov/pubmed/32246056
http://dx.doi.org/10.1038/s41598-020-62552-4
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author Hamill, Philip G.
Stevenson, Andrew
McMullan, Phillip E.
Williams, James P.
Lewis, Abiann D. R.
S, Sudharsan
Stevenson, Kath E.
Farnsworth, Keith D.
Khroustalyova, Galina
Takemoto, Jon Y.
Quinn, John P.
Rapoport, Alexander
Hallsworth, John E.
author_facet Hamill, Philip G.
Stevenson, Andrew
McMullan, Phillip E.
Williams, James P.
Lewis, Abiann D. R.
S, Sudharsan
Stevenson, Kath E.
Farnsworth, Keith D.
Khroustalyova, Galina
Takemoto, Jon Y.
Quinn, John P.
Rapoport, Alexander
Hallsworth, John E.
author_sort Hamill, Philip G.
collection PubMed
description Measures of microbial growth, used as indicators of cellular stress, are sometimes quantified at a single time-point. In reality, these measurements are compound representations of length of lag, exponential growth-rate, and other factors. Here, we investigate whether length of lag phase can act as a proxy for stress, using  a number of model systems (Aspergillus penicillioides; Bacillus subtilis; Escherichia coli; Eurotium amstelodami, E. echinulatum, E. halophilicum, and E. repens; Mrakia frigida; Saccharomyces cerevisiae; Xerochrysium xerophilum; Xeromyces bisporus) exposed to mechanistically distinct types of cellular stress including low water activity, other solute-induced stresses, and dehydration-rehydration cycles. Lag phase was neither proportional to germination rate for X. bisporus (FRR3443) in glycerol-supplemented media (r(2) = 0.012), nor to exponential growth-rates for other microbes. In some cases, growth-rates varied greatly with stressor concentration even when lag remained constant. By contrast, there were strong correlations for B. subtilis in media supplemented with polyethylene-glycol 6000 or 600 (r(2) = 0.925 and 0.961), and for other microbial species. We also  analysed data from independent studies of food-spoilage fungi under glycerol stress (Aspergillus aculeatinus and A. sclerotiicarbonarius); mesophilic/psychrotolerant bacteria under diverse, solute-induced stresses (Brochothrix thermosphacta, Enterococcus faecalis, Pseudomonas fluorescens, Salmonella typhimurium, Staphylococcus aureus); and fungal enzymes under acid-stress (Terfezia claveryi lipoxygenase and Agaricus bisporus tyrosinase). These datasets also exhibited diversity, with some strong- and moderate correlations between length of lag and exponential growth-rates; and sometimes none. In conclusion, lag phase is not  a reliable measure of stress because length of lag and growth-rate inhibition are sometimes highly correlated, and sometimes not at all.
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spelling pubmed-71250822020-04-08 Microbial lag phase can be indicative of, or independent from, cellular stress Hamill, Philip G. Stevenson, Andrew McMullan, Phillip E. Williams, James P. Lewis, Abiann D. R. S, Sudharsan Stevenson, Kath E. Farnsworth, Keith D. Khroustalyova, Galina Takemoto, Jon Y. Quinn, John P. Rapoport, Alexander Hallsworth, John E. Sci Rep Article Measures of microbial growth, used as indicators of cellular stress, are sometimes quantified at a single time-point. In reality, these measurements are compound representations of length of lag, exponential growth-rate, and other factors. Here, we investigate whether length of lag phase can act as a proxy for stress, using  a number of model systems (Aspergillus penicillioides; Bacillus subtilis; Escherichia coli; Eurotium amstelodami, E. echinulatum, E. halophilicum, and E. repens; Mrakia frigida; Saccharomyces cerevisiae; Xerochrysium xerophilum; Xeromyces bisporus) exposed to mechanistically distinct types of cellular stress including low water activity, other solute-induced stresses, and dehydration-rehydration cycles. Lag phase was neither proportional to germination rate for X. bisporus (FRR3443) in glycerol-supplemented media (r(2) = 0.012), nor to exponential growth-rates for other microbes. In some cases, growth-rates varied greatly with stressor concentration even when lag remained constant. By contrast, there were strong correlations for B. subtilis in media supplemented with polyethylene-glycol 6000 or 600 (r(2) = 0.925 and 0.961), and for other microbial species. We also  analysed data from independent studies of food-spoilage fungi under glycerol stress (Aspergillus aculeatinus and A. sclerotiicarbonarius); mesophilic/psychrotolerant bacteria under diverse, solute-induced stresses (Brochothrix thermosphacta, Enterococcus faecalis, Pseudomonas fluorescens, Salmonella typhimurium, Staphylococcus aureus); and fungal enzymes under acid-stress (Terfezia claveryi lipoxygenase and Agaricus bisporus tyrosinase). These datasets also exhibited diversity, with some strong- and moderate correlations between length of lag and exponential growth-rates; and sometimes none. In conclusion, lag phase is not  a reliable measure of stress because length of lag and growth-rate inhibition are sometimes highly correlated, and sometimes not at all. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125082/ /pubmed/32246056 http://dx.doi.org/10.1038/s41598-020-62552-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hamill, Philip G.
Stevenson, Andrew
McMullan, Phillip E.
Williams, James P.
Lewis, Abiann D. R.
S, Sudharsan
Stevenson, Kath E.
Farnsworth, Keith D.
Khroustalyova, Galina
Takemoto, Jon Y.
Quinn, John P.
Rapoport, Alexander
Hallsworth, John E.
Microbial lag phase can be indicative of, or independent from, cellular stress
title Microbial lag phase can be indicative of, or independent from, cellular stress
title_full Microbial lag phase can be indicative of, or independent from, cellular stress
title_fullStr Microbial lag phase can be indicative of, or independent from, cellular stress
title_full_unstemmed Microbial lag phase can be indicative of, or independent from, cellular stress
title_short Microbial lag phase can be indicative of, or independent from, cellular stress
title_sort microbial lag phase can be indicative of, or independent from, cellular stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125082/
https://www.ncbi.nlm.nih.gov/pubmed/32246056
http://dx.doi.org/10.1038/s41598-020-62552-4
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