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Heterologous Protein Expression Favors the Formation of Protein Aggregates in Persister and Viable but Nonculturable Bacteria

Authors :
Jeremy Metz
Olivia Goode
Stefano Pagliara
Zehra Kahveci
Georgina Glover
Rosemary A. Bamford
Alice L. J. Carr
Ashley Smith
Erin Attrill
Urszula Łapińska
Source :
ACS Infectious Diseases. 7:1848-1858
Publication Year :
2021
Publisher :
American Chemical Society (ACS), 2021.

Abstract

Environmental and intracellular stresses can perturb protein homeostasis and trigger the formation and accumulation of protein aggregates. It has been recently suggested that the level of protein aggregates accumulated in bacteria correlates with the frequency of persister and viable but nonculturable cells that transiently survive treatment with multiple antibiotics. However, these findings have often been obtained employing fluorescent reporter strains. This enforced heterologous protein expression facilitates the visualization of protein aggregates but could also trigger the formation and accumulation of protein aggregates. Using microfluidics-based single-cell microscopy and a library of green fluorescent protein reporter strains, we show that heterologous protein expression favors the formation of protein aggregates. We found that persister and viable but nonculturable bacteria surviving treatment with antibiotics are more likely to contain protein aggregates and downregulate the expression of heterologous proteins. Our data also suggest that such aggregates are more basic with respect to the rest of the cell. These findings provide evidence for a strong link between heterologous protein expression, protein aggregation, intracellular pH, and phenotypic survival to antibiotics, suggesting that antibiotic treatments against persister and viable but nonculturable cells could be developed by modulating protein aggregation and pH regulation.

Details

ISSN :
23738227
Volume :
7
Database :
OpenAIRE
Journal :
ACS Infectious Diseases
Accession number :
edsair.doi.dedup.....de93ff6247156ffa151b847cc124cd92
Full Text :
https://doi.org/10.1021/acsinfecdis.1c00154