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

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posted on 2025-08-01, 12:23 authored by O Goode, A Smith, U Łapińska, R Bamford, Z Kahveci, G Glover, E Attrill, A Carr, J Metz, S Pagliara
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.

Funding

BB/M009122/1

Biotechnology and Biological Sciences Research Council (BBSRC)

DSTL

EP/M506527/1

Engineering and Physical Sciences Research Council (EPSRC)

GBMF5514

H2020-MSCA-ITN-2015–675752

MCPC17189

MR/P016162/1

Marie Skłodowska‐Curie

Medical Research Council (MRC)

RG180007

The Gordon and Betty Moore Foundation

The Royal Society

University of Exeter

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© 2021 The Authors. Published by American Chemical Society

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This is the final version. Available from the American Chemical Society via the DOI in this record.

Journal

ACS Infectious Diseases

Publisher

American Chemical Society

Place published

United States

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  • Version of Record

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en

FCD date

2021-05-28T08:17:32Z

FOA date

2021-05-28T08:28:32Z

Citation

Published online 17 May 2021

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