Synergistic, collaterally sensitive β-lactam combinations suppress resistance in MRSA
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Brent A. Biddy | G. Dantas | M. Suckow | C. Burnham | S. Mobashery | R. Bouley | Valerie A. Schroeder | W. Wolter | Mayland Chang | M. Pesesky | Patrick R Gonzales | Anna Ballard
[1] M. Suckow,et al. Discovery of antibiotic (E)-3-(3-carboxyphenyl)-2-(4-cyanostyryl)quinazolin-4(3H)-one. , 2015, Journal of the American Chemical Society.
[2] Christian Munck,et al. Prediction of resistance development against drug combinations by collateral responses to component drugs , 2014, Science Translational Medicine.
[3] S. W. Long,et al. PBP2a Mutations Causing High-Level Ceftaroline Resistance in Clinical Methicillin-Resistant Staphylococcus aureus Isolates , 2014, Antimicrobial Agents and Chemotherapy.
[4] J. Hermoso,et al. Disruption of Allosteric Response as an Unprecedented Mechanism of Resistance to Antibiotics , 2014, Journal of the American Chemical Society.
[5] S. Mobashery,et al. Regulation of the Expression of the β-Lactam Antibiotic-Resistance Determinants in Methicillin-Resistant Staphylococcus aureus (MRSA) , 2014, Biochemistry.
[6] Ellsworth M. Campbell,et al. A Population Model Evaluating the Consequences of the Evolution of Double-Resistance and Tradeoffs on the Benefits of Two-Drug Antibiotic Treatments , 2014, PloS one.
[7] J. Hermoso,et al. How allosteric control of Staphylococcus aureus penicillin binding protein 2a enables methicillin resistance and physiological function , 2013, Proceedings of the National Academy of Sciences.
[8] M. Sommer,et al. Use of Collateral Sensitivity Networks to Design Drug Cycling Protocols That Avoid Resistance Development , 2013, Science Translational Medicine.
[9] P. Arede,et al. Redefining the Role of the β-Lactamase Locus in Methicillin-Resistant Staphylococcus aureus: β-Lactamase Regulators Disrupt the MecI-Mediated Strong Repression on mecA and Optimize the Phenotypic Expression of Resistance in Strains with Constitutive mecA Expression , 2013, Antimicrobial Agents and Chemotherapy.
[10] B. Levin,et al. The Pharmaco –, Population and Evolutionary Dynamics of Multi-drug Therapy: Experiments with S. aureus and E. coli and Computer Simulations , 2013, PLoS pathogens.
[11] Stefan Niemann,et al. Whole-genome sequencing of rifampicin-resistant M. tuberculosis strains identifies compensatory mutations in RNA polymerase , 2011, Nature Genetics.
[12] Terry Roemer,et al. Antagonism of chemical genetic interaction networks resensitize MRSA to β-lactam antibiotics. , 2011, Chemistry & biology.
[13] D. Livermore,et al. Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study. , 2011, The Lancet. Infectious diseases.
[14] D. Paterson,et al. Emergence of daptomycin resistance following vancomycin-unresponsive Staphylococcus aureus bacteraemia in a daptomycin-naïve patient—a review of the literature , 2011, European Journal of Clinical Microbiology & Infectious Diseases.
[15] K. Brodolin,et al. Resistance to rifampicin: at the crossroads between ecological, genomic and medical concerns. , 2010, International journal of antimicrobial agents.
[16] B. Murray,et al. Antibiotic-resistant bugs in the 21st century--a clinical super-challenge. , 2009, The New England journal of medicine.
[17] Henry F. Chambers,et al. Waves of resistance: Staphylococcus aureus in the antibiotic era , 2009, Nature Reviews Microbiology.
[18] Christopher T. Walsh,et al. Antibiotics for Emerging Pathogens , 2009, Science.
[19] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[20] N. Masuda,et al. Affinity of Tomopenem (CS-023) for Penicillin-Binding Proteins in Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa , 2008, Antimicrobial Agents and Chemotherapy.
[21] D. Hartl,et al. Accelerated evolution of resistance in multidrug environments , 2008, Proceedings of the National Academy of Sciences.
[22] S. Mobashery,et al. Co-opting the cell wall in fighting methicillin-resistant Staphylococcus aureus: potent inhibition of PBP 2a by two anti-MRSA beta-lactam antibiotics. , 2008, Journal of the American Chemical Society.
[23] L. Saiman. Clinical utility of synergy testing for multidrug-resistant Pseudomonas aeruginosa isolated from patients with cystic fibrosis: 'the motion for'. , 2007, Paediatric respiratory reviews.
[24] Rui Wang,et al. Antibacterial Activity of Allicin Alone and in Combination with β-Lactams against Staphylococcus spp. and Pseudomonas aeruginosa , 2007, The Journal of Antibiotics.
[25] G. Archer,et al. Identification and Phenotypic Characterization of a β-Lactam-Dependent, Methicillin-Resistant Staphylococcus aureus Strain , 2007, Antimicrobial Agents and Chemotherapy.
[26] D. Nicolau,et al. Bactericidal Activities of Meropenem and Ertapenem against Extended-Spectrum-β-Lactamase-Producing Escherichia coli and Klebsiella pneumoniae in a Neutropenic Mouse Thigh Model , 2007, Antimicrobial Agents and Chemotherapy.
[27] L. Rice,et al. Antimicrobial resistance in gram-positive bacteria. , 2006, The American journal of medicine.
[28] Y. Bhusal,et al. Determination of in vitro synergy when three antimicrobial agents are combined against Mycobacterium tuberculosis. , 2005, International journal of antimicrobial agents.
[29] S. Mobashery,et al. β-Lactam resistance in Staphylococcus aureus: the adaptive resistance of a plastic genome , 2005, Cellular and Molecular Life Sciences.
[30] S. Mobashery,et al. Activation for catalysis of penicillin-binding protein 2a from methicillin-resistant Staphylococcus aureus by bacterial cell wall. , 2005, Journal of the American Chemical Society.
[31] S. Mobashery,et al. The Basis for Resistance to β-Lactam Antibiotics by Penicillin-binding Protein 2a of Methicillin-resistant Staphylococcus aureus* , 2004, Journal of Biological Chemistry.
[32] M. Blaser,et al. Long-Term Persistence of Resistant Enterococcus Species after Antibiotics To Eradicate Helicobacter pylori , 2003, Annals of Internal Medicine.
[33] F. Lowy. Antimicrobial resistance: the example of Staphylococcus aureus. , 2003, The Journal of clinical investigation.
[34] M. Kanehisa,et al. Whole genome sequencing of meticillin-resistant Staphylococcus aureus , 2001, The Lancet.
[35] W. Craig,et al. The pharmacology of meropenem, a new carbapenem antibiotic. , 1997, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[36] D. Wilson,et al. In vivo activities of U-100592 and U-100766, novel oxazolidinone antimicrobial agents, against experimental bacterial infections , 1996, Antimicrobial agents and chemotherapy.
[37] J. Davies,et al. Origins and Evolution of Antibiotic Resistance , 1996, Microbiology and Molecular Biology Reviews.
[38] C. Hackbarth,et al. blaI and blaR1 regulate beta-lactamase and PBP 2a production in methicillin-resistant Staphylococcus aureus , 1993, Antimicrobial Agents and Chemotherapy.
[39] M. Kinzig,et al. Pharmacokinetics and tissue penetration of tazobactam and piperacillin in patients undergoing colorectal surgery , 1992, Antimicrobial Agents and Chemotherapy.
[40] Berenbaum Mc. What is synergy? , 1989, Pharmacological reviews.
[41] P. Somani,et al. Pharmacokinetics of imipenem-cilastatin in patients with renal insufficiency undergoing continuous ambulatory peritoneal dialysis , 1988, Antimicrobial Agents and Chemotherapy.
[42] F. Malouin,et al. Modification of penicillin-binding proteins as mechanisms of beta-lactam resistance , 1986, Antimicrobial Agents and Chemotherapy.
[43] M. Marks,et al. In vitro antimicrobial activity of aztreonam alone and in combination against bacterial isolates from pediatric patients , 1984, Antimicrobial Agents and Chemotherapy.
[44] M. Berenbaum,et al. A method for testing for synergy with any number of agents. , 1978, The Journal of infectious diseases.
[45] S. Sonstein,et al. Loss of the Penicillinase Plasmid After Treatment of Staphylococcus aureus with Sodium Dodecyl Sulfate , 1972, Journal of bacteriology.
[46] R. Humphries,et al. The emerging problem of linezolid-resistant Staphylococcus. , 2013, The Journal of antimicrobial chemotherapy.
[47] B. Kégl,et al. Bacterial evolution of antibiotic hypersensitivity , 2013, Molecular systems biology.
[48] J. Bartlett,et al. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[49] J. Lehár,et al. Multi-target therapeutics: when the whole is greater than the sum of the parts. , 2007, Drug discovery today.
[50] Mary Jane Ferraro,et al. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically : approved standard , 2000 .
[51] K. Bush,et al. Biochemical comparison of imipenem, meropenem and biapenem: permeability, binding to penicillin-binding proteins, and stability to hydrolysis by beta-lactamases. , 1995, The Journal of antimicrobial chemotherapy.
[52] J. Strominger,et al. Penicillin-binding proteins and the mechanism of action of beta-lactam antibiotics. , 1983, Annual review of biochemistry.