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

被引:24
|
作者
Goode, Olivia [1 ]
Smith, Ashley [1 ]
Lapinska, Urszula [1 ]
Bamford, Rosemary [1 ]
Kahveci, Zehra [1 ]
Glover, Georgina [1 ]
Attrill, Erin [1 ]
Carr, Alice [1 ]
Metz, Jeremy [1 ]
Pagliara, Stefano [1 ]
机构
[1] Univ Exeter, Living Syst Inst & Biosci, Exeter EX4 4QD, Devon, England
来源
ACS INFECTIOUS DISEASES | 2021年 / 7卷 / 06期
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会; 欧盟地平线“2020”;
关键词
persisters; viable but nonculturable cells; protein aggregation; antimicrobial resistance; microfluidics; heterologous expression; ESCHERICHIA-COLI; MICROFLUIDICS; HETEROGENEITY; REPORTERS; INCREASES; SECRETION; CELLS; PH;
D O I
10.1021/acsinfecdis.1c00154
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:1848 / 1858
页数:11
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