Mechanisms of antibiotic resistance

Molecular Basis of Bacterial Outer Membrane Permeability Revisited

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Extended-Spectrum β-Lactamases: a Clinical Update

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Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study

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Antibiotic resistance is ancient

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Waves of resistance: Staphylococcus aureus in the antibiotic era

Chambers, H. F., & DeLeo, F. R. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2200 · Cited by 2,718 · see citing works

Carbapenemases: the Versatile β-Lactamases

Queenan, A. M., & Bush, K. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00001-07 · Cited by 2,504 · see citing works

Updated Functional Classification of β-Lactamases

Bush, K., & Jacoby, G. A. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01009-09 · Cited by 2,367 · see citing works

Mechanisms of, and Barriers to, Horizontal Gene Transfer between Bacteria

Thomas, C. M., & Nielsen, K. M. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1234 · Cited by 2,194 · see citing works

AmpC β-Lactamases

Jacoby, G. A. (2009) · Clinical Microbiology Reviews · doi:10.1128/cmr.00036-08 · Cited by 2,171 · see citing works

Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility

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The rise of the Enterococcus: beyond vancomycin resistance

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Novel Carbapenem-Hydrolyzing β-Lactamase, KPC-1, from a Carbapenem-Resistant Strain of <i>Klebsiella pneumoniae</i>

Yigit, H., Queenan, A. M., Anderson, G. J., Domenech-Sanchez, A., Biddle, J. W., Steward, C. D., Alberti, S., Bush, K., & Tenover, F. C. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.4.1151-1161.2001 · Cited by 1,639 · see citing works

The real threat of Klebsiella pneumoniae carbapenemase-producing bacteria

Nordmann, P., Cuzon, G., & Naas, T. (2009) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(09)70054-4 · Cited by 1,583 · see citing works

Structural Mechanism for Rifampicin Inhibition of Bacterial RNA Polymerase

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Multidrug-resistance efflux pumps ? not just for resistance

Piddock, L. J. V. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1464 · Cited by 1,523 · see citing works

Aminoglycoside modifying enzymes

Ramirez, M. S., & Tolmasky, M. E. (2010) · Drug Resistance Updates · doi:10.1016/j.drup.2010.08.003 · Cited by 1,504 · see citing works

Growing Group of Extended-Spectrum β-Lactamases: the CTX-M Enzymes

Bonnet, R. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.1.1-14.2004 · Cited by 1,494 · see citing works

An Enzyme from Bacteria able to Destroy Penicillin

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Mechanism of Quinolone Action and Resistance

Aldred, K. J., Kerns, R. J., & Osheroff, N. (2014) · Biochemistry · doi:10.1021/bi5000564 · Cited by 1,282 · see citing works

The Relationship between Antimicrobial Resistance and Patient Outcomes: Mortality, Length of Hospital Stay, and Health Care Costs

Cosgrove, S. E. (2006) · Clinical Infectious Diseases · doi:10.1086/499406 · Cited by 1,271 · see citing works

Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study

Walsh, T. R., Weeks, J. L., Livermore, D. M., & Toleman, M. A. (2011) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(11)70059-7 · Cited by 1,255 · see citing works

Clinically Relevant Chromosomally Encoded Multidrug Resistance Efflux Pumps in Bacteria

Piddock, L. J. V. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.19.2.382-402.2006 · Cited by 1,231 · see citing works

Methicillin resistance in staphylococci: molecular and biochemical basis and clinical implications

Chambers, H. F. “. (1997) · Clinical Microbiology Reviews · doi:10.1128/cmr.10.4.781 · Cited by 1,128 · see citing works

Quinolone resistance from a transferable plasmid

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Mechanisms of Resistance to Macrolides and Lincosamides: Nature of the Resistance Elements and Their Clinical Implications

Leclercq, R. (2002) · Clinical Infectious Diseases · doi:10.1086/324626 · Cited by 1,102 · see citing works

Efflux-mediated antimicrobial resistance

Poole, K. (2005) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dki171 · Cited by 1,082 · see citing works

Ribosome-targeting antibiotics and mechanisms of bacterial resistance

Wilson, D. N. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3155 · Cited by 1,054 · see citing works

Vancomycin Resistance in Gram-Positive Cocci

Courvalin, P. (2006) · Clinical Infectious Diseases · doi:10.1086/491711 · Cited by 1,028 · see citing works

Update on acquired tetracycline resistance genes

Roberts, M. C. (2005) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2005.02.034 · Cited by 1,010 · see citing works

Erythromycin resistance by ribosome modification

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Reduced Vancomycin Susceptibility in <i>Staphylococcus aureus</i> , Including Vancomycin-Intermediate and Heterogeneous Vancomycin-Intermediate Strains: Resistance Mechanisms, Laboratory Detection, and Clinical Implications

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The porin and the permeating antibiotic: a selective diffusion barrier in Gram-negative bacteria

Pagès, J.-M., James, C. E., & Winterhalter, M. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1994 · Cited by 939 · see citing works

OXA β-Lactamases

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Molecular basis of bacterial resistance to chloramphenicol and florfenicol

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Intrinsic and acquired resistance mechanisms in enterococcus

Hollenbeck, B. L., & Rice, L. B. (2012) · Virulence · doi:10.4161/viru.21282 · Cited by 795 · see citing works

Mechanisms of antibiotic resistance in enterococci

Miller, W. R., Munita, J. M., & Arias, C. A. (2014) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.2014.956092 · Cited by 772 · see citing works

Structure, biochemistry and mechanism of action of glycopeptide antibiotics

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The emerging NDM carbapenemases

Nordmann, P., Poirel, L., Walsh, T. R., & Livermore, D. M. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.09.005 · Cited by 666 · see citing works

Structure of the AcrAB–TolC multidrug efflux pump

Du, D., Wang, Z., James, N. R., Voss, J. E., Klimont, E., Ohene‐Agyei, T., Venter, H., Chiu, W., & Luisi, B. F. (2014) · Nature · doi:10.1038/nature13205 · Cited by 664 · see citing works

Hospital Epidemiology and Infection Control in Acute-Care Settings

Sydnor, E. R. M., & Perl, T. M. (2011) · Clinical Microbiology Reviews · doi:10.1128/cmr.00027-10 · Cited by 652 · see citing works

Metallo-β-lactamases: a last frontier for β-lactams?

Cornaglia, G., Giamarellou, H., & Rossolini, G. M. (2011) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(11)70056-1 · Cited by 614 · see citing works

Active efflux of tetracycline encoded by four genetically different tetracycline resistance determinants in Escherichia coli.

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Mechanisms of vancomycin resistance in Staphylococcus aureus

Gardete, S., & Tomasz, A. (2014) · Journal of Clinical Investigation · doi:10.1172/jci68834 · Cited by 565 · see citing works

RifamycinMode of Action, Resistance, and Biosynthesis

Floss, H. G., & Yu, T.-W. (2005) · Chemical Reviews · doi:10.1021/cr030112j · Cited by 547 · see citing works

Resistance to Trimethoprim-Sulfamethoxazole

Eliopoulos, G. M., & Huovinen, P. (2001) · Clinical Infectious Diseases · doi:10.1086/320532 · Cited by 500 · see citing works

Vancomycin-Resistant Staphylococcus aureus in the United States, 2002-2006

Sievert, D. M., Rudrik, J. T., Patel, J. B., McDonald, L. C., Wilkins, M. J., & Hageman, J. C. (2008) · Clinical Infectious Diseases · doi:10.1086/527392 · Cited by 483 · see citing works

Comparison of Mortality Associated with Vancomycin-Resistant and Vancomycin-Susceptible Enterococcal Bloodstream Infections: A Meta-analysis

DiazGranados, C. A., Zimmer, S. M., Mitchel, K., & Jernigan, J. A. (2005) · Clinical Infectious Diseases · doi:10.1086/430909 · Cited by 459 · see citing works

Ribosomal Protection Proteins and Their Mechanism ofTetracyclineResistance

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Update on macrolide-lincosamide-streptogramin, ketolide, and oxazolidinone resistance genes: MLSKO genes

Roberts, M. C. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01145.x · Cited by 392 · see citing works

Genetic Basis for In Vivo Daptomycin Resistance in Enterococci

Arias, C. A., Panesso, D., McGrath, D. M., Qin, X., Mojica, M. F., Miller, C., Diaz, L., Tran, T. T., Rincon, S., Barbu, E. M., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1011138 · Cited by 377 · see citing works

Inducible erythromycin resistance in staphlyococci is encoded by a member of the ATP‐binding transport super‐gene family

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Transferable resistance to third-generation cephalosporins in clinical isolates of Klebsiella pneumoniae: identification of CTX-1, a novel β-lactamase

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Proliferation and significance of clinically relevant β‐lactamases

Bush, K. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12023 · Cited by 338 · see citing works

The VanS-VanR two-component regulatory system controls synthesis of depsipeptide peptidoglycan precursors in Enterococcus faecium BM4147

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Acquisition of a natural resistance gene renders a clinical strain of methicillin‐resistant<i>Staphylococcus aureus</i>resistant to the synthetic antibiotic linezolid

Toh, S., Xiong, L., Arias, C. A., Villegas, M. V., Lolans, K., Quinn, J., & Mankin, A. S. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05744.x · Cited by 338 · see citing works

Molecular understanding of aminoglycoside action and resistance

Jana, S., & Deb, J. K. (2006) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-005-0279-0 · Cited by 335 · see citing works

Methicillin-Resistant Staphylococcus aureus: An Evolving Pathogen

Stryjewski, M. E., & Corey, G. R. (2014) · Clinical Infectious Diseases · doi:10.1093/cid/cit613 · Cited by 334 · see citing works

Cytosolic Intermediates for Cell Wall Biosynthesis and Degradation Control Inducible β-Lactam Resistance in Gram-Negative Bacteria

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Fluoroquinolone resistance among Gram-positive cocci

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Daptomycin-Mediated Reorganization of Membrane Architecture Causes Mislocalization of Essential Cell Division Proteins

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Function of <i>Pseudomonas</i> Porins in Uptake and Efflux

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Mechanisms of daptomycin resistance in <i>Staphylococcus aureus</i>: role of the cell membrane and cell wall

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Carbapenemases: Molecular Diversity and Clinical Consequences

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Plasmid-mediated quinolone resistance: an update

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Bacterial cell‐wall recycling

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Efflux-Mediated Resistance to Tigecycline (GAR-936) in <i>Pseudomonas aeruginosa</i> PAO1

Dean, C. R., Visalli, M. A., Projan, S. J., Sum, P.-E., & Bradford, P. A. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.3.972-978.2003 · Cited by 286 · see citing works

Emergence of Resistance to Imipenem During Therapy for Pseudomonas aeruginosa Infections

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An <i>Enterococcus faecalis</i> ABC Homologue (Lsa) Is Required for the Resistance of This Species to Clindamycin and Quinupristin-Dalfopristin

Singh, K. V., Weinstock, G. M., & Murray, B. E. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.6.1845-1850.2002 · Cited by 263 · see citing works

Gene Dosage and Linezolid Resistance in <i>Enterococcus faecium</i> and <i>Enterococcus faecalis</i>

Marshall, S. H., Donskey, C. J., Hutton-Thomas, R., Salata, R. A., & Rice, L. B. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.10.3334-3336.2002 · Cited by 263 · see citing works

The ABCD’s of β-lactamase nomenclature

Bush, K. (2013) · Journal of Infection and Chemotherapy · doi:10.1007/s10156-013-0640-7 · Cited by 239 · see citing works

MRSA: the first half century

Moellering, R. C. (2012) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkr437 · Cited by 236 · see citing works

IS Ecp1B -Mediated Transposition of bla CTX-M in Escherichia coli

Poirel, L., Lartigue, M.-F., Decousser, J., & Nordmann, P. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.1.447-450.2005 · Cited by 228 · see citing works

Linezolid update: Stable in vitro activity following more than a decade of clinical use and summary of associated resistance mechanisms

Mendes, R. E., Deshpande, L. M., & Jones, R. N. (2014) · Drug Resistance Updates · doi:10.1016/j.drup.2014.04.002 · Cited by 221 · see citing works

Conserved small protein associates with the multidrug efflux pump AcrB and differentially affects antibiotic resistance

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Structural basis for TetM-mediated tetracycline resistance

Dönhöfer, A., Franckenberg, S., Wickles, S., Berninghausen, O., Beckmann, R., & Wilson, D. N. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208037109 · Cited by 217 · see citing works

Mechanism of chromosomal transfer of <i>Enterococcus faecalis</i> pathogenicity island, capsule, antimicrobial resistance, and other traits

Manson, J. M., Hancock, L. E., & Gilmore, M. S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000139107 · Cited by 192 · see citing works

Daptomycin-Resistant Enterococcus faecalis Diverts the Antibiotic Molecule from the Division Septum and Remodels Cell Membrane Phospholipids

Tran, T. T., Panesso, D., Mishra, N. N., Mileykovskaya, E., Guan, Z., Munita, J. M., Reyes, J., Diaz, L., Weinstock, G. M., Murray, B. E., et al. (2013) · mBio · doi:10.1128/mbio.00281-13 · Cited by 192 · see citing works

Genomic Basis for Methicillin Resistance in<i>Staphylococcus aureus</i>

Hiramatsu, K., Ito, T., Tsubakishita, S., Sasaki, T., Takeuchi, F., Morimoto, Y., Katayama, Y., Matsuo, M., Kuwahara-Arai, K., Hishinuma, T., et al. (2013) · Infection &amp; Chemotherapy · doi:10.3947/ic.2013.45.2.117 · Cited by 189 · see citing works

Transferable Vancomycin Resistance in a Community-Associated MRSA Lineage

Rossi, F., Diaz, L., Wollam, A., Panesso, D., Zhou, Y., Rincon, S., Narechania, A., Xing, G., Di Gioia, T. S. R., Doi, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1303359 · Cited by 182 · see citing works

Translation and Protein Synthesis:  Macrolides

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AcrAB Multidrug Efflux Pump Is Associated with Reduced Levels of Susceptibility to Tigecycline (GAR-936) in <i>Proteus mirabilis</i>

Visalli, M. A., Murphy, E., Projan, S. J., & Bradford, P. A. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.2.665-669.2003 · Cited by 165 · see citing works

Cardiolipin Prevents Membrane Translocation and Permeabilization by Daptomycin

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Role of <i>Klebsiella pneumoniae</i> OmpK35 Porin in Antimicrobial Resistance

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Mechanism of tetracycline resistance by ribosomal protection protein Tet(O)

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Whole-Genome Analyses of Enterococcus faecium Isolates with Diverse Daptomycin MICs

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Detection and Prevalence of Active Drug Efflux Mechanism in Various Multidrug-Resistant <i>Klebsiella pneumoniae</i> Strains from Turkey

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Impact of rpoB Mutations on Reduced Vancomycin Susceptibility in Staphylococcus aureus

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Whole-Genome Analysis of a Daptomycin-Susceptible Enterococcus faecium Strain and Its Daptomycin-Resistant Variant Arising during Therapy

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Correlation between Mutations in <i>liaFSR</i> of Enterococcus faecium and MIC of Daptomycin: Revisiting Daptomycin Breakpoints

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In-Depth Profiling of the LiaR Response of<i>Bacillus subtilis</i>

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Massive overproduction of dihydrofolate reductase in bacteria as a response to the use of trimethoprim

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Tedizolid for the Management of Human Infections: In Vitro Characteristics

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A liaR Deletion Restores Susceptibility to Daptomycin and Antimicrobial Peptides in Multidrug-Resistant Enterococcus faecalis

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