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.
机构:
Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USAPenn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
Kwan, Brian W.
Valenta, John A.
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机构:
Texas A&M Univ, Dept Biol, College Stn, TX 77843 USAPenn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
Valenta, John A.
Benedik, Michael J.
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机构:
Texas A&M Univ, Dept Biol, College Stn, TX 77843 USAPenn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
Benedik, Michael J.
Wood, Thomas K.
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机构:
Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USAPenn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
机构:
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Moscow Institute of Physics and Technology, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Vasilenko E.O.
Kozin S.A.
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机构:
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Kozin S.A.
Mitkevich V.A.
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机构:
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, MoscowEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Mitkevich V.A.
Buchelnikov A.S.
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机构:
Sevastopol State University, SevastopolEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Buchelnikov A.S.
Nechipurenko Y.D.
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机构:
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow
Sevastopol State University, SevastopolEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow