High-throughput laboratory evolution and evolutionary constraints in Escherichia coli
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Chikara Furusawa | Takaaki Horinouchi | Junichiro Iwasawa | C. Furusawa | Takaaki Horinouchi | Hazuki Kotani | Kumi Tanabe | Natsue Sakata | Aki Sakai | Hazuki Kotani | Kumi Tanabe | Tomoya Maeda | Natsue Sakata | Masako Kawada | Tomoya Maeda | Akio Sakai | Masako Kawada | J. Iwasawa
[1] C. Furusawa,et al. Toward prediction and control of antibiotic-resistance evolution. , 2018, Current opinion in biotechnology.
[2] Robert A. Edwards,et al. Quality control and preprocessing of metagenomic datasets , 2011, Bioinform..
[3] Jeffrey E. Barrick,et al. Identification of mutations in laboratory-evolved microbes from next-generation sequencing data using breseq. , 2014, Methods in molecular biology.
[4] J. Hearst,et al. Molecular cloning and characterization of acrA and acrE genes of Escherichia coli , 1993, Journal of bacteriology.
[5] Chikara Furusawa,et al. Development of an Automated Culture System for Laboratory Evolution , 2014, Journal of laboratory automation.
[6] Daisuke Motooka,et al. Mutation accumulation under UV radiation in Escherichia coli , 2017, Scientific Reports.
[7] T. Silhavy,et al. The LysR Homolog LrhA Promotes RpoS Degradation by Modulating Activity of the Response Regulator SprE , 1999, Journal of bacteriology.
[8] H. Shimizu,et al. Prediction of Cross-resistance and Collateral Sensitivity by Gene Expression profiles and Genomic Mutations , 2017, Scientific Reports.
[9] E. Groisman,et al. The antibacterial action of protamine: evidence for disruption of cytoplasmic membrane energization in Salmonella typhimurium. , 1996, Microbiology.
[10] S. Molin,et al. Drug-Driven Phenotypic Convergence Supports Rational Treatment Strategies of Chronic Infections , 2018, Cell.
[11] R. Kishony,et al. Opposing effects of target overexpression reveal drug mechanisms , 2014, Nature Communications.
[12] Yunxin J. Jiao,et al. Population diversity jeopardizes the efficacy of antibiotic cycling , 2016, bioRxiv.
[13] Tim N. Enke,et al. Metabolic constraints on the evolution of antibiotic resistance , 2017, Molecular systems biology.
[14] A. F. Bennett,et al. The Molecular Diversity of Adaptive Convergence , 2012, Science.
[15] A. Lupas,et al. prlF and yhaV encode a new toxin-antitoxin system in Escherichia coli. , 2007, Journal of molecular biology.
[16] Roy Kishony,et al. Understanding, predicting and manipulating the genotypic evolution of antibiotic resistance , 2013, Nature Reviews Genetics.
[17] Hengjin Dong,et al. Economic burden of antibiotic resistance in ESKAPE organisms: a systematic review , 2019, Antimicrobial Resistance & Infection Control.
[18] T. Ferenci,et al. Maintaining a healthy SPANC balance through regulatory and mutational adaptation , 2005, Molecular microbiology.
[19] Ashkan Golshani,et al. Systematic Genetic Screens Reveal the Dynamic Global Functional Organization of the Bacterial Translation Machinery. , 2016, Cell reports.
[20] H. Shimizu,et al. Evaluating 13C enrichment data of free amino acids for precise metabolic flux analysis , 2011, Biotechnology journal.
[21] Joel Nothman,et al. SciPy 1.0-Fundamental Algorithms for Scientific Computing in Python , 2019, ArXiv.
[22] B. Kégl,et al. Genome-wide analysis captures the determinants of the antibiotic cross-resistance interaction network , 2014, Nature Communications.
[23] Remy Chait,et al. Evolutionary paths to antibiotic resistance under dynamically sustained drug selection , 2011, Nature Genetics.
[24] H. Nikaido,et al. Mutants of Escherichia coli That Are Resistant to Certain Beta-Lactam Compounds Lack the ompF Porin , 1981, Antimicrobial Agents and Chemotherapy.
[25] Terence P. Speed,et al. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias , 2003, Bioinform..
[26] Matthias Heinemann,et al. Molecular Systems Biology Peer Review Process File Bacterial Persistence Is an Active Σ S Stress Response to Metabolic Flux Limitation Transaction Report , 2022 .
[27] E. Véscovi,et al. Activation of Multiple Antibiotic Resistance in Uropathogenic Escherichia coli Strains by Aryloxoalcanoic Acid Compounds , 2001, Antimicrobial Agents and Chemotherapy.
[28] M. Inouye,et al. Interaction of a transcriptional activator, OmpR, with reciprocally osmoregulated genes, ompF and ompC, of Escherichia coli. , 1986, The Journal of biological chemistry.
[29] High-throughput identification of the sensitivities of an Escherichia coli ΔrecA mutant strain to various chemical compounds , 2019, The Journal of Antibiotics.
[30] R. Kishony,et al. Antibiotic Resistance , 2018, Cell.
[31] Nathan E Lewis,et al. Microbial laboratory evolution in the era of genome-scale science , 2011, Molecular systems biology.
[32] J. Collins,et al. Bacterial charity work leads to population-wide resistance , 2010, Nature.
[33] A. Matin,et al. EmrR is a negative regulator of the Escherichia coli multidrug resistance pump EmrAB , 1995, Journal of bacteriology.
[34] Ville Mustonen,et al. Predicting evolution , 2017, Nature Ecology &Evolution.
[35] M. May. Drug development: Time for teamwork , 2014, Nature.
[36] Alison K. Hottes,et al. Genetic Architecture of Intrinsic Antibiotic Susceptibility , 2009, PloS one.
[37] J. O'Neill,et al. Tackling drug-resistant infections globally: final report and recommendations , 2016 .
[38] Christian Munck,et al. Prediction of resistance development against drug combinations by collateral responses to component drugs , 2014, Science Translational Medicine.
[39] Jacob G. Scott,et al. Antibiotic collateral sensitivity is contingent on the repeatability of evolution , 2019, Nature Communications.
[40] Sabrina Galiñanes Reyes,et al. Time-programmable drug dosing allows the manipulation, suppression and reversal of antibiotic drug resistance in vitro , 2017, Nature Communications.
[41] István Nagy,et al. A highly precise and portable genome engineering method allows comparison of mutational effects across bacterial species , 2016, Proceedings of the National Academy of Sciences.
[42] H. Nikaido,et al. Efflux-Mediated Drug Resistance in Bacteria , 2009, Drugs.
[43] H. Nikaido,et al. Contributions of the AmpC β-Lactamase and the AcrAB Multidrug Efflux System in Intrinsic Resistance of Escherichia coli K-12 to β-Lactams , 2000, Antimicrobial Agents and Chemotherapy.
[44] Saloni R. Jain,et al. Bactericidal Antibiotics Induce Toxic Metabolic Perturbations that Lead to Cellular Damage. , 2015, Cell reports.
[45] Dilay Hazal Ayhan,et al. Quantifying the Determinants of Evolutionary Dynamics Leading to Drug Resistance , 2015, PLoS biology.
[46] Jonathan E. Suk,et al. Natural disasters and infectious disease in Europe: a literature review to identify cascading risk pathways , 2020, European journal of public health.
[47] S. Linn,et al. Mutagenesis and stress responses induced in Escherichia coli by hydrogen peroxide , 1987, Journal of bacteriology.
[48] P. Rosenstiel,et al. Alternative Evolutionary Paths to Bacterial Antibiotic Resistance Cause Distinct Collateral Effects , 2017, Molecular biology and evolution.
[49] A. Delcour,et al. Outer membrane permeability and antibiotic resistance. , 2009, Biochimica et biophysica acta.
[50] C. Furusawa,et al. Prediction of antibiotic resistance by gene expression profiles , 2014, Nature Communications.
[51] F. Blattner,et al. Emergent Properties of Reduced-Genome Escherichia coli , 2006, Science.
[52] H. Nikaido,et al. AcrAB efflux pump plays a major role in the antibiotic resistance phenotype of Escherichia coli multiple-antibiotic-resistance (Mar) mutants , 1996, Journal of bacteriology.