The Rate of Osmotic Downshock Determines the Survival Probability of Bacterial Mechanosensitive Channel Mutants
Abstract
Mechanosensitive (MS) channels allow cells to sense and respond to environmental changes. In bacteria, these channels are believed to protect against an osmotic shock. The physiological function of these channels has been characterized primarily by a standardized assay, where aliquots of batch-cultured cells are rapidly pipetted into a hypotonic medium. Under this method, it has been inferred many types of MS channels (MscS homologs in Escherichia coli) demonstrate limited effectiveness against shock, typically rescuing less than 10% of the cells when expressed at native levels. We introduce a single-cell-based assay which allows us to control how fast the osmolarity changes, over time scales ranging from a fraction of a second to several minutes. We find that the protection provided by MS channels depends strongly on the rate of osmotic change, revealing that, under a slow enough osmotic drop, MscS homologs can lead to survival rates comparable to those found in wild-type strains. Further, after the osmotic downshift, we observe multiple death phenotypes, which are inconsistent with the prevailing paradigm of how cells lyse. Both of these findings require a reevaluation of our basic understanding of the physiology of MS channels.
Additional Information
© 2015 American Society for Microbiology. Received 4 August 2014; Accepted 20 October 2014; Accepted manuscript posted online 27 October 2014. We thank Ian Booth, Doug Rees, Bill Klug, Pierre Sens, and Liz Haswell for many helpful comments and discussions, and Samantha Miller, Susan Black, and the CGSC at Yale University for valuable materials. R.P., M.B.-F., and H.J.L. were supported by NIH grant R01 GM084211 and National Institutes of Health Director's Pioneer Award grant DP1 OD000217. M.B.-F. was supported by a Caltech Provost's office fellowship.Attached Files
Published - J._Bacteriol.-2015-Bialecka-Fornal-231-7.pdf
Accepted Version - J._Bacteriol.-2014-Bialecka-Fornal-JB.02175-14.pdf
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Supplemental Material - zjb999093438so7.pdf
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Additional details
- PMCID
- PMC4288683
- Eprint ID
- 53398
- Resolver ID
- CaltechAUTHORS:20150108-145321538
- NIH
- R01 GM084211
- NIH
- DP1 OD000217A
- Caltech Provost's Office Fellowship
- Created
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2015-01-08Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field