Literature DB >> 31285232

Spheroplast-Mediated Carbapenem Tolerance in Gram-Negative Pathogens.

Trevor Cross1,2, Brett Ransegnola1,2, Jung-Ho Shin1,2, Anna Weaver1,2, Kathy Fauntleroy3, Michael S VanNieuwenhze4,5, Lars F Westblade6,7, Tobias Dörr8,2,9.   

Abstract

Antibiotic tolerance, the ability to temporarily sustain viability in the presence of bactericidal antibiotics, constitutes an understudied and yet potentially widespread cause of antibiotic treatment failure. We have previously shown that the Gram-negative pathogen Vibrio cholerae can tolerate exposure to the typically bactericidal β-lactam antibiotics by assuming a spherical morphotype devoid of detectable cell wall material. However, it is unclear how widespread β-lactam tolerance is. Here, we tested a panel of clinically significant Gram-negative pathogens for their response to the potent, broad-spectrum carbapenem antibiotic meropenem. We show that clinical isolates of Enterobacter cloacae, Klebsiella aerogenes, and Klebsiella pneumoniae, but not Escherichia coli, exhibited moderate to high levels of tolerance of meropenem, both in laboratory growth medium and in human serum. Importantly, tolerance was mediated by cell wall-deficient spheroplasts, which readily recovered wild-type morphology and growth upon removal of antibiotic. Our results suggest that carbapenem tolerance is prevalent in clinically significant bacterial species, and we suggest that this could contribute to treatment failure associated with these organisms.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  L-form; antibiotic; carbapenem; carbapenemase; meropenem; tolerance

Mesh:

Substances:

Year:  2019        PMID: 31285232      PMCID: PMC6709500          DOI: 10.1128/AAC.00756-19

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  46 in total

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Authors:  Asher Brauner; Ofer Fridman; Orit Gefen; Nathalie Q Balaban
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5.  Crystal structure of New Delhi metallo-β-lactamase reveals molecular basis for antibiotic resistance.

Authors:  Dustin King; Natalie Strynadka
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6.  Persisters: a distinct physiological state of E. coli.

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9.  An Experimental Framework for Quantifying Bacterial Tolerance.

Authors:  Asher Brauner; Noam Shoresh; Ofer Fridman; Nathalie Q Balaban
Journal:  Biophys J       Date:  2017-06-20       Impact factor: 4.033

Review 10.  Cell wall-deficient, L-form bacteria in the 21st century: a personal perspective.

Authors:  Jeff Errington
Journal:  Biochem Soc Trans       Date:  2017-04-15       Impact factor: 5.407

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  14 in total

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Authors:  Elena Espinosa; Sandra Daniel; Sara B Hernández; Anthony Goudin; Felipe Cava; François-Xavier Barre; Elisa Galli
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2.  Structural basis of peptidoglycan endopeptidase regulation.

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4.  Lysin LysMK34 of Acinetobacter baumannii Bacteriophage PMK34 Has a Turgor Pressure-Dependent Intrinsic Antibacterial Activity and Reverts Colistin Resistance.

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5.  Peptidoglycan Recycling Promotes Outer Membrane Integrity and Carbapenem Tolerance in Acinetobacter baumannii.

Authors:  Nowrosh Islam; Misha I Kazi; Katie N Kang; Jacob Biboy; Joe Gray; Feroz Ahmed; Richard D Schargel; Cara C Boutte; Tobias Dörr; Waldemar Vollmer; Joseph M Boll
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6.  Engineering a Lysin with Intrinsic Antibacterial Activity (LysMK34) by Cecropin A Fusion Enhances Its Antibacterial Properties against Acinetobacter baumannii.

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7.  A multifaceted cellular damage repair and prevention pathway promotes high-level tolerance to β-lactam antibiotics.

Authors:  Jung-Ho Shin; Donghui Choe; Brett Ransegnola; Hye-Rim Hong; Ikenna Onyekwere; Trevor Cross; Qiaojuan Shi; Byung-Kwan Cho; Lars F Westblade; Ilana L Brito; Tobias Dörr
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Review 9.  The evolution of spherical cell shape; progress and perspective.

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10.  Antibiotic tolerance.

Authors:  Lars F Westblade; Jeff Errington; Tobias Dörr
Journal:  PLoS Pathog       Date:  2020-10-15       Impact factor: 6.823

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