Keyword search (4,163 papers available)

"Findlay BL" Authored Publications:

Title Authors PubMed ID
1 Sequential antibiotic exposure restores antibiotic susceptibility Chowdhury FR; Findlay BL; 41060280
BIOLOGY
2 Luminescent Electro-Spun Nanofibers Crosslinked with Boronic Esters Exhibiting Controlled Release of Carbon Dots for Detection of Wound pHs and Enhanced Antimicrobial Lokuge ND; Casillas-Popova SN; Singh P; Clermont-Paquette A; Skinner CD; Findlay BL; Naccache R; Oh JK; 40920389
BIOLOGY
3 Large scale laboratory evolution uncovers clinically relevant collateral antibiotic sensitivity Chowdhury FR; Banari V; Lesnic V; Zhanel GG; Findlay BL; 40615056
BIOLOGY
4 Multi-stimuli-responsive degradable boronic ester-crosslinked e-spun nanofiber wound dressings Casillas-Popova SN; Lokuge ND; Singh P; Cirillo A; Thinphang-Nga A; Skinner CD; Vuckovic D; Findlay BL; Oh JK; 40557709
BIOLOGY
5 Tripartite loops reverse antibiotic resistance Chowdhury FR; Findlay BL; 40478208
BIOLOGY
6 De novo evolution of antibiotic resistance to Oct-TriA1 Chowdhury FR; Mercado LD; Kharitonov K; Findlay BL; 39832423
BIOLOGY
7 pH-Responsive Degradable Electro-Spun Nanofibers Crosslinked via Boronic Ester Chemistry for Smart Wound Dressings Casillas-Popova SN; Lokuge ND; Andrade-Gagnon B; Chowdhury FR; Skinner CD; Findlay BL; Oh JK; 38989606
BIOLOGY
8 Discovery of an adjuvant that resensitizes polymyxin B-resistant bacteria Mahdavi M; Findlay BL; 38096681
BIOLOGY
9 Fitness Costs of Antibiotic Resistance Impede the Evolution of Resistance to Other Antibiotics Chowdhury FR; Findlay BL; 37726252
BIOLOGY
10 Roles of inter- and intramolecular tryptophan interactions in membrane-active proteins revealed by racemic protein crystallography Lander AJ; Mercado LD; Li X; Taily IM; Findlay BL; Jin Y; Luk LYP; 37464011
CHEMBIOCHEM
11 Opposites Attract: Electrostatically Driven Loading of Antimicrobial Peptides into Phytoglycogen Nanocarriers Ali DA; Domínguez Mercado L; Findlay BL; Badia A; DeWolf C; 36525622
CHEMBIOCHEM
12 Electrospun Upconverting Nanofibrous Hybrids with Smart NIR-Light-Controlled Drug Release for Wound Dressing Huang HY; Skripka A; Zaroubi L; Findlay BL; Vetrone F; Skinner C; Oh JK; Cuccia LA; 35019380
CHEMBIOCHEM
13 The Chemical Ecology of Predatory Soil Bacteria. Findlay BL 27035738
CHEMISTRY
14 Access to high-impact mutations constrains the evolution of antibiotic resistance in soft agar. Ghaddar N, Hashemidahaj M, Findlay BL 30451932
CHEMBIOCHEM

 

Title:Access to high-impact mutations constrains the evolution of antibiotic resistance in soft agar.
Authors:Ghaddar NHashemidahaj MFindlay BL
Link:https://www.ncbi.nlm.nih.gov/pubmed/30451932?dopt=Abstract
Publication:
Keywords:
PMID:30451932 Category:Sci Rep Date Added:2019-05-31
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Concordia University, Montreal, Québec, Canada.
2 Lady Davis Institute for Medical Research, McGill University, Montreal, Québec, Canada.
3 Department of Chemistry and Biochemistry, Concordia University, Montreal, Québec, Canada. brandon.findlay@concordia.ca.

Description:

Access to high-impact mutations constrains the evolution of antibiotic resistance in soft agar.

Sci Rep. 2018 Nov 19;8(1):17023

Authors: Ghaddar N, Hashemidahaj M, Findlay BL

Abstract

Despite widespread resistance to many important antibiotics, the factors that govern the emergence and prevalence of antibiotic-resistant bacteria are still unclear. When exposed to antibiotic gradients in soft agar plates measuring as little as 1.25?×?11?cm we found that Escherichia coli rapidly became resistant to representatives from every class of antibiotics active against Gram-negative bacteria. Evolution kinetics were independent of the frequency of spontaneous mutations that confer antibiotic resistance or antibiotic dose-response curves, and were only loosely correlated to maximal antibiotic concentrations. Instead, rapid evolution required unrealized mutations that could markedly decrease antibiotic susceptibility. When bacteria could not evolve through these "high-impact" mutations, populations frequently bottlenecked, reducing the number of cells from which mutants could arise and prolonging evolution times. This effect was independent of the antibiotic's mechanism of action, and may affect the evolution of antibiotic resistance in clinical settings.

PMID: 30451932 [PubMed - in process]





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