메뉴 건너뛰기




Volumn 3, Issue 12, 2017, Pages 941-954

Polymyxin B3-Tobramycin Hybrids with Pseudomonas aeruginosa-Selective Antibacterial Activity and Strong Potentiation of Rifampicin, Minocycline, and Vancomycin

Author keywords

adjuvant; antimicrobial hybrid; polymyxin; Pseudomonas aeruginosa; rifampicin; tobramycin

Indexed keywords

CARBAPENEM; CHLORAMPHENICOL; CLINDAMYCIN; DOXYCYCLINE; IMIPENEM; LINEZOLID; MEROPENEM; MINOCYCLINE; NOVOBIOCIN; POLYMYXIN B3; POLYPEPTIDE ANTIBIOTIC AGENT; RIFAMPICIN; TIGECYCLINE; TOBRAMYCIN; TRIMETHOPRIM; UNCLASSIFIED DRUG; VANCOMYCIN; ANTIINFECTIVE AGENT; POLYMYXIN;

EID: 85033796462     PISSN: None     EISSN: 23738227     Source Type: Journal    
DOI: 10.1021/acsinfecdis.7b00145     Document Type: Article
Times cited : (25)

References (48)
  • 2
    • 85019237541 scopus 로고    scopus 로고
    • The threat of antimicrobial resistance in developing countries: Causes and control strategies
    • Ayukekbong, J. A., Ntemgwa, M., and Atabe, A. N. (2017) The threat of antimicrobial resistance in developing countries: Causes and control strategies Antimicrob. Resist. Infect. Control 6, 47 10.1186/s13756-017-0208-x
    • (2017) Antimicrob. Resist. Infect. Control , vol.6 , pp. 47
    • Ayukekbong, J.A.1    Ntemgwa, M.2    Atabe, A.N.3
  • 3
    • 84955461306 scopus 로고    scopus 로고
    • Antibacterial drug discovery in the resistance era
    • Brown, E. D. and Wright, G. D. (2016) Antibacterial drug discovery in the resistance era Nature 529 (7586) 336-343 10.1038/nature17042
    • (2016) Nature , vol.529 , Issue.7586 , pp. 336-343
    • Brown, E.D.1    Wright, G.D.2
  • 4
    • 85002873168 scopus 로고    scopus 로고
    • Potential economic burden of carbapenem-resistant Enterobacteriaceae (CRE) in the United States
    • Bartsch, S. M., McKinnell, J. A., Mueller, L. E., Miller, L. G., Gohil, S. K., Huang, S. S., and Lee, B. Y. (2017) Potential economic burden of carbapenem-resistant Enterobacteriaceae (CRE) in the United States Clin. Microbiol. Infect. 23 (1) 48.e9-48.e16 10.1016/j.cmi.2016.09.003
    • (2017) Clin. Microbiol. Infect. , vol.23 , Issue.1 , pp. 48e9-48e16
    • Bartsch, S.M.1    McKinnell, J.A.2    Mueller, L.E.3    Miller, L.G.4    Gohil, S.K.5    Huang, S.S.6    Lee, B.Y.7
  • 5
    • 79953740494 scopus 로고    scopus 로고
    • Fix the antibiotics pipeline
    • Cooper, M. A. and Shlaes, D. (2011) Fix the antibiotics pipeline Nature 472 (7341) 32 10.1038/472032a
    • (2011) Nature , vol.472 , Issue.7341 , pp. 32
    • Cooper, M.A.1    Shlaes, D.2
  • 7
    • 85002213837 scopus 로고    scopus 로고
    • Gestalt approach to Gram-negative entry
    • Silver, L. L. A. (2016) Gestalt approach to Gram-negative entry Bioorg. Med. Chem. 24 (24) 6379-6389 10.1016/j.bmc.2016.06.044
    • (2016) Bioorg. Med. Chem. , vol.24 , Issue.24 , pp. 6379-6389
    • Silver, L.L.A.1
  • 8
    • 77955967899 scopus 로고    scopus 로고
    • Dual-acting hybrid antibiotics: A promising strategy to combat bacterial resistance
    • Pokrovskaya, V. and Baasov, T. (2010) Dual-acting hybrid antibiotics: A promising strategy to combat bacterial resistance Expert Opin. Drug Discovery 5 (9) 883-902 10.1517/17460441.2010.508069
    • (2010) Expert Opin. Drug Discovery , vol.5 , Issue.9 , pp. 883-902
    • Pokrovskaya, V.1    Baasov, T.2
  • 9
    • 84975217786 scopus 로고    scopus 로고
    • Hybrid antibiotics-clinical progress and novel designs
    • Parkes, A. L. and Yule, I. A. (2016) Hybrid antibiotics-clinical progress and novel designs Expert Opin. Drug Discovery 11 (7) 665-680 10.1080/17460441.2016.1187597
    • (2016) Expert Opin. Drug Discovery , vol.11 , Issue.7 , pp. 665-680
    • Parkes, A.L.1    Yule, I.A.2
  • 10
    • 85022194756 scopus 로고    scopus 로고
    • Bifunctional antimicrobial conjugates and hybrid antimicrobials
    • Klahn, P. and Bronstrup, M. (2017) Bifunctional antimicrobial conjugates and hybrid antimicrobials Nat. Prod. Rep. 34 (7) 832-885 10.1039/C7NP00006E
    • (2017) Nat. Prod. Rep. , vol.34 , Issue.7 , pp. 832-885
    • Klahn, P.1    Bronstrup, M.2
  • 11
    • 84943635689 scopus 로고    scopus 로고
    • The PEW Charitable Trust. (), (accessed Jun 1, 2017).
    • The PEW Charitable Trust. (2014) Antibiotics Currently in Clinical Development, http://www.pewtrusts.org/en/multimedia/data-visualizations/2014/antibiotics-currently-in-clinical-development (accessed Jun 1, 2017).
    • (2014) Antibiotics Currently in Clinical Development
  • 12
    • 85005784390 scopus 로고    scopus 로고
    • Cefiderocol, a siderophore cephalosporin for Gram-negative bacterial infections: Pharmacokinetics and safety in subjects with renal impairment
    • Katsube, T., Echols, R., Arjona Ferreira, J. C., Krenz, H. K., Berg, J. K., and Galloway, C. (2017) Cefiderocol, a siderophore cephalosporin for Gram-negative bacterial infections: Pharmacokinetics and safety in subjects with renal impairment J. Clin. Pharmacol. 57 (5) 584-591 10.1002/jcph.841
    • (2017) J. Clin. Pharmacol. , vol.57 , Issue.5 , pp. 584-591
    • Katsube, T.1    Echols, R.2    Arjona Ferreira, J.C.3    Krenz, H.K.4    Berg, J.K.5    Galloway, C.6
  • 13
    • 85016146767 scopus 로고    scopus 로고
    • Cadazolid for the treatment of Clostridium difficile
    • Endres, B. T., Basseres, E., Alam, M. J., and Garey, K. W. (2017) Cadazolid for the treatment of Clostridium difficile Expert Opin. Invest. Drugs 26 (4) 509-514 10.1080/13543784.2017.1304538
    • (2017) Expert Opin. Invest. Drugs , vol.26 , Issue.4 , pp. 509-514
    • Endres, B.T.1    Basseres, E.2    Alam, M.J.3    Garey, K.W.4
  • 14
    • 84958760300 scopus 로고    scopus 로고
    • Adjuvants based on hybrid antibiotics overcome resistance in Pseudomonas aeruginosa and enhance fluoroquinolone efficacy
    • Gorityala, B. K., Guchhait, G., Fernando, D. M., Deo, S., McKenna, S. A., Zhanel, G. G., Kumar, A., and Schweizer, F. (2016) Adjuvants based on hybrid antibiotics overcome resistance in Pseudomonas aeruginosa and enhance fluoroquinolone efficacy Angew. Chem., Int. Ed. 55 (2) 555-559 10.1002/anie.201508330
    • (2016) Angew. Chem., Int. Ed. , vol.55 , Issue.2 , pp. 555-559
    • Gorityala, B.K.1    Guchhait, G.2    Fernando, D.M.3    Deo, S.4    McKenna, S.A.5    Zhanel, G.G.6    Kumar, A.7    Schweizer, F.8
  • 15
    • 84988701271 scopus 로고    scopus 로고
    • Hybrid antibiotic overcomes resistance in P. Aeruginosa by enhancing outer membrane penetration and reducing efflux
    • Gorityala, B. K., Guchhait, G., Goswami, S., Fernando, D. M., Kumar, A., Zhanel, G. G., and Schweizer, F. (2016) Hybrid antibiotic overcomes resistance in P. aeruginosa by enhancing outer membrane penetration and reducing efflux J. Med. Chem. 59 (18) 8441-8455 10.1021/acs.jmedchem.6b00867
    • (2016) J. Med. Chem. , vol.59 , Issue.18 , pp. 8441-8455
    • Gorityala, B.K.1    Guchhait, G.2    Goswami, S.3    Fernando, D.M.4    Kumar, A.5    Zhanel, G.G.6    Schweizer, F.7
  • 16
    • 85019215287 scopus 로고    scopus 로고
    • A tobramycin vector enhances synergy and efficacy of efflux pump inhibitors against multidrug-resistant Gram-negative bacteria
    • Yang, X., Goswami, S., Gorityala, B. K., Domalaon, R., Lyu, Y., Kumar, A., Zhanel, G. G., and Schweizer, F. (2017) A tobramycin vector enhances synergy and efficacy of efflux pump inhibitors against multidrug-resistant Gram-negative bacteria J. Med. Chem. 60 (9) 3913-3932 10.1021/acs.jmedchem.7b00156
    • (2017) J. Med. Chem. , vol.60 , Issue.9 , pp. 3913-3932
    • Yang, X.1    Goswami, S.2    Gorityala, B.K.3    Domalaon, R.4    Lyu, Y.5    Kumar, A.6    Zhanel, G.G.7    Schweizer, F.8
  • 17
    • 85019177780 scopus 로고    scopus 로고
    • Amphiphilic tobramycin-lysine conjugates sensitize multidrug resistant Gram-negative bacteria to rifampicin and minocycline
    • Lyu, Y., Yang, X., Goswami, S., Gorityala, B. K., Idowu, T., Domalaon, R., Zhanel, G. G., Shan, A., and Schweizer, F. (2017) Amphiphilic tobramycin-lysine conjugates sensitize multidrug resistant Gram-negative bacteria to rifampicin and minocycline J. Med. Chem. 60 (9) 3684-3702 10.1021/acs.jmedchem.6b01742
    • (2017) J. Med. Chem. , vol.60 , Issue.9 , pp. 3684-3702
    • Lyu, Y.1    Yang, X.2    Goswami, S.3    Gorityala, B.K.4    Idowu, T.5    Domalaon, R.6    Zhanel, G.G.7    Shan, A.8    Schweizer, F.9
  • 18
    • 0019802634 scopus 로고
    • Aminoglycoside uptake and mode of action-with special reference to streptomycin and gentamicin. II. Effects of aminoglycosides on cells
    • Hancock, R. E. (1981) Aminoglycoside uptake and mode of action-with special reference to streptomycin and gentamicin. II. Effects of aminoglycosides on cells J. Antimicrob. Chemother. 8 (6) 429-445 10.1093/jac/8.6.429
    • (1981) J. Antimicrob. Chemother. , vol.8 , Issue.6 , pp. 429-445
    • Hancock, R.E.1
  • 19
    • 84923646618 scopus 로고    scopus 로고
    • Tobramycin and nebramine as pseudo-oligosaccharide scaffolds for the development of antimicrobial cationic amphiphiles
    • Berkov-Zrihen, Y., Herzog, I. M., Benhamou, R. I., Feldman, M., Steinbuch, K. B., Shaul, P., Lerer, S., Eldar, A., and Fridman, M. (2015) Tobramycin and nebramine as pseudo-oligosaccharide scaffolds for the development of antimicrobial cationic amphiphiles Chem.-Eur. J. 21 (11) 4340-4349 10.1002/chem.201406404
    • (2015) Chem.-Eur. J. , vol.21 , Issue.11 , pp. 4340-4349
    • Berkov-Zrihen, Y.1    Herzog, I.M.2    Benhamou, R.I.3    Feldman, M.4    Steinbuch, K.B.5    Shaul, P.6    Lerer, S.7    Eldar, A.8    Fridman, M.9
  • 20
    • 84960455257 scopus 로고    scopus 로고
    • Synthesis and evaluation of membrane permeabilizing properties of cationic amphiphiles derived from the disaccharide trehalose
    • Shaul, P., Benhamou, R. I., Herzog, I. M., Louzoun Zada, S., Ebenstein, Y., and Fridman, M. (2016) Synthesis and evaluation of membrane permeabilizing properties of cationic amphiphiles derived from the disaccharide trehalose Org. Biomol. Chem. 14 (11) 3012-3015 10.1039/C6OB00031B
    • (2016) Org. Biomol. Chem. , vol.14 , Issue.11 , pp. 3012-3015
    • Shaul, P.1    Benhamou, R.I.2    Herzog, I.M.3    Louzoun Zada, S.4    Ebenstein, Y.5    Fridman, M.6
  • 22
    • 84976421894 scopus 로고    scopus 로고
    • Negatively Charged Lipids as a Potential Target for New Amphiphilic Aminoglycoside Antibiotics: A Biophysical Study
    • Sautrey, G., El Khoury, M., Dos Santos, A. G., Zimmermann, L., Deleu, M., Lins, L., Decout, J.-L., and Mingeot-Leclercq, M.-P. (2016) Negatively Charged Lipids as a Potential Target for New Amphiphilic Aminoglycoside Antibiotics: A BIOPHYSICAL STUDY J. Biol. Chem. 291 (26) 13864-13874 10.1074/jbc.M115.665364
    • (2016) J. Biol. Chem. , vol.291 , Issue.26 , pp. 13864-13874
    • Sautrey, G.1    El Khoury, M.2    Dos Santos, A.G.3    Zimmermann, L.4    Deleu, M.5    Lins, L.6    Decout, J.-L.7    Mingeot-Leclercq, M.-P.8
  • 23
    • 84868131679 scopus 로고    scopus 로고
    • Antibacterial activity of amphiphilic tobramycin
    • Dhondikubeer, R., Bera, S., Zhanel, G. G., and Schweizer, F. (2012) Antibacterial activity of amphiphilic tobramycin J. Antibiot. 65 (10) 495-498 10.1038/ja.2012.59
    • (2012) J. Antibiot. , vol.65 , Issue.10 , pp. 495-498
    • Dhondikubeer, R.1    Bera, S.2    Zhanel, G.G.3    Schweizer, F.4
  • 24
    • 84994030706 scopus 로고    scopus 로고
    • New broad-spectrum antibacterial amphiphilic aminoglycosides active against resistant bacteria: From neamine derivatives to smaller neosamine analogues
    • Zimmermann, L., Das, I., Desire, J., Sautrey, G., Barros R S, V., El Khoury, M., Mingeot-Leclercq, M.-P., and Decout, J.-L. (2016) New broad-spectrum antibacterial amphiphilic aminoglycosides active against resistant bacteria: From neamine derivatives to smaller neosamine analogues J. Med. Chem. 59 (20) 9350-9369 10.1021/acs.jmedchem.6b00818
    • (2016) J. Med. Chem. , vol.59 , Issue.20 , pp. 9350-9369
    • Zimmermann, L.1    Das, I.2    Desire, J.3    Sautrey, G.4    Barros, R.S.V.5    El Khoury, M.6    Mingeot-Leclercq, M.-P.7    Decout, J.-L.8
  • 25
    • 84865506551 scopus 로고    scopus 로고
    • Synthesis and antibacterial activities of amphiphilic neomycin B-based bilipid conjugates and fluorinated neomycin B-based lipids
    • Bera, S., Dhondikubeer, R., Findlay, B., Zhanel, G. G., and Schweizer, F. (2012) Synthesis and antibacterial activities of amphiphilic neomycin B-based bilipid conjugates and fluorinated neomycin B-based lipids Molecules 17 (8) 9129-9141 10.3390/molecules17089129
    • (2012) Molecules , vol.17 , Issue.8 , pp. 9129-9141
    • Bera, S.1    Dhondikubeer, R.2    Findlay, B.3    Zhanel, G.G.4    Schweizer, F.5
  • 26
    • 77952069162 scopus 로고    scopus 로고
    • Antibacterial activities of aminoglycoside antibiotics-derived cationic amphiphiles. Polyol-modified neomycin B-, kanamycin A-, amikacin-, and neamine-based amphiphiles with potent broad spectrum antibacterial activity
    • Bera, S., Zhanel, G. G., and Schweizer, F. (2010) Antibacterial activities of aminoglycoside antibiotics-derived cationic amphiphiles. Polyol-modified neomycin B-, kanamycin A-, amikacin-, and neamine-based amphiphiles with potent broad spectrum antibacterial activity J. Med. Chem. 53 (9) 3626-3631 10.1021/jm1000437
    • (2010) J. Med. Chem. , vol.53 , Issue.9 , pp. 3626-3631
    • Bera, S.1    Zhanel, G.G.2    Schweizer, F.3
  • 27
    • 77953507637 scopus 로고    scopus 로고
    • Antibacterial activity of guanidinylated neomycin B- A nd kanamycin A-derived amphiphilic lipid conjugates
    • Bera, S., Zhanel, G. G., and Schweizer, F. (2010) Antibacterial activity of guanidinylated neomycin B- A nd kanamycin A-derived amphiphilic lipid conjugates J. Antimicrob. Chemother. 65 (6) 1224-1227 10.1093/jac/dkq083
    • (2010) J. Antimicrob. Chemother. , vol.65 , Issue.6 , pp. 1224-1227
    • Bera, S.1    Zhanel, G.G.2    Schweizer, F.3
  • 28
    • 53549117489 scopus 로고    scopus 로고
    • Design, synthesis, and antibacterial activities of neomycin-lipid conjugates: Polycationic lipids with potent Gram-positive activity
    • Bera, S., Zhanel, G. G., and Schweizer, F. (2008) Design, synthesis, and antibacterial activities of neomycin-lipid conjugates: Polycationic lipids with potent Gram-positive activity J. Med. Chem. 51 (19) 6160-6164 10.1021/jm800345u
    • (2008) J. Med. Chem. , vol.51 , Issue.19 , pp. 6160-6164
    • Bera, S.1    Zhanel, G.G.2    Schweizer, F.3
  • 29
    • 84874655977 scopus 로고    scopus 로고
    • Investigation of antibacterial mode of action for traditional and amphiphilic aminoglycosides
    • Udumula, V., Ham, Y. W., Fosso, M. Y., Chan, K. Y., Rai, R., Zhang, J., Li, J., and Chang, C.-W. T. (2013) Investigation of antibacterial mode of action for traditional and amphiphilic aminoglycosides Bioorg. Med. Chem. Lett. 23 (6) 1671-1675 10.1016/j.bmcl.2013.01.073
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , Issue.6 , pp. 1671-1675
    • Udumula, V.1    Ham, Y.W.2    Fosso, M.Y.3    Chan, K.Y.4    Rai, R.5    Zhang, J.6    Li, J.7    Chang, C.-W.T.8
  • 31
    • 85001079028 scopus 로고    scopus 로고
    • Synergistic combinations of polymyxins
    • Lenhard, J. R., Nation, R. L., and Tsuji, B. T. (2016) Synergistic combinations of polymyxins Int. J. Antimicrob. Agents 48 (6) 607-613 10.1016/j.ijantimicag.2016.09.014
    • (2016) Int. J. Antimicrob. Agents , vol.48 , Issue.6 , pp. 607-613
    • Lenhard, J.R.1    Nation, R.L.2    Tsuji, B.T.3
  • 32
    • 0034426126 scopus 로고    scopus 로고
    • Substrate specificities of MexAB-OprM, MexCD-OprJ, and MexXY-oprM efflux pumps in Pseudomonas aeruginosa
    • Masuda, N., Sakagawa, E., Ohya, S., Gotoh, N., Tsujimoto, H., and Nishino, T. (2000) Substrate specificities of MexAB-OprM, MexCD-OprJ, and MexXY-oprM efflux pumps in Pseudomonas aeruginosa Antimicrob. Agents Chemother. 44 (12) 3322-3327 10.1128/AAC.44.12.3322-3327.2000
    • (2000) Antimicrob. Agents Chemother. , vol.44 , Issue.12 , pp. 3322-3327
    • Masuda, N.1    Sakagawa, E.2    Ohya, S.3    Gotoh, N.4    Tsujimoto, H.5    Nishino, T.6
  • 33
    • 77949346087 scopus 로고    scopus 로고
    • Structure-activity relationships of polymyxin antibiotics
    • Velkov, T., Thompson, P. E., Nation, R. L., and Li, J. (2010) Structure-activity relationships of polymyxin antibiotics J. Med. Chem. 53 (5) 1898-1916 10.1021/jm900999h
    • (2010) J. Med. Chem. , vol.53 , Issue.5 , pp. 1898-1916
    • Velkov, T.1    Thompson, P.E.2    Nation, R.L.3    Li, J.4
  • 34
    • 84878293341 scopus 로고    scopus 로고
    • Pharmacology of polymyxins: New insights into an "old" class of antibiotics
    • Velkov, T., Roberts, K. D., Nation, R. L., Thompson, P. E., and Li, J. (2013) Pharmacology of polymyxins: New insights into an "old" class of antibiotics Future Microbiol. 8 (6) 711-724 10.2217/fmb.13.39
    • (2013) Future Microbiol , vol.8 , Issue.6 , pp. 711-724
    • Velkov, T.1    Roberts, K.D.2    Nation, R.L.3    Thompson, P.E.4    Li, J.5
  • 35
    • 0037429028 scopus 로고    scopus 로고
    • Tobramycin analogues with C-5 aminoalkyl ether chains intended to mimic rings III and IV of paromomycin
    • Hanessian, S., Tremblay, M., and Swayze, E. E. (2003) Tobramycin analogues with C-5 aminoalkyl ether chains intended to mimic rings III and IV of paromomycin Tetrahedron 59 (7) 983-993 10.1016/S0040-4020(02)01624-1
    • (2003) Tetrahedron , vol.59 , Issue.7 , pp. 983-993
    • Hanessian, S.1    Tremblay, M.2    Swayze, E.E.3
  • 36
    • 62549141514 scopus 로고    scopus 로고
    • Contribution of each amino acid residue in polymyxin B(3) to antimicrobial and lipopolysaccharide binding activity
    • Kanazawa, K., Sato, Y., Ohki, K., Okimura, K., Uchida, Y., Shindo, M., and Sakura, N. (2009) Contribution of each amino acid residue in polymyxin B(3) to antimicrobial and lipopolysaccharide binding activity Chem. Pharm. Bull. 57 (3) 240-244 10.1248/cpb.57.240
    • (2009) Chem. Pharm. Bull. , vol.57 , Issue.3 , pp. 240-244
    • Kanazawa, K.1    Sato, Y.2    Ohki, K.3    Okimura, K.4    Uchida, Y.5    Shindo, M.6    Sakura, N.7
  • 37
  • 39
    • 0034632833 scopus 로고    scopus 로고
    • Structure-function studies of polymyxin B nonapeptide: Implications to sensitization of gram-negative bacteria
    • Tsubery, H., Ofek, I., Cohen, S., and Fridkin, M. (2000) Structure-function studies of polymyxin B nonapeptide: Implications to sensitization of gram-negative bacteria J. Med. Chem. 43 (16) 3085-3092 10.1021/jm0000057
    • (2000) J. Med. Chem. , vol.43 , Issue.16 , pp. 3085-3092
    • Tsubery, H.1    Ofek, I.2    Cohen, S.3    Fridkin, M.4
  • 41
    • 79951870210 scopus 로고    scopus 로고
    • Introduction to the CANWARD Study (2007-2009)
    • Hoban, D. J. and Zhanel, G. G. (2011) Introduction to the CANWARD Study (2007-2009) Diagn. Microbiol. Infect. Dis. 69, 289-290 10.1016/j.diagmicrobio.2010.10.024
    • (2011) Diagn. Microbiol. Infect. Dis. , vol.69 , pp. 289-290
    • Hoban, D.J.1    Zhanel, G.G.2
  • 42
    • 78650293305 scopus 로고    scopus 로고
    • Targeting bacterial membrane function: An underexploited mechanism for treating persistent infections
    • Hurdle, J. G., O'Neill, A. J., Chopra, I., and Lee, R. E. (2011) Targeting bacterial membrane function: An underexploited mechanism for treating persistent infections Nat. Rev. Microbiol. 9 (1) 62-75 10.1038/nrmicro2474
    • (2011) Nat. Rev. Microbiol. , vol.9 , Issue.1 , pp. 62-75
    • Hurdle, J.G.1    O'Neill, A.J.2    Chopra, I.3    Lee, R.E.4
  • 43
    • 84964945443 scopus 로고    scopus 로고
    • The Clinical and Laboratory Standards Institute. ((), 26 th ed. Clinical and Laboratory Standards Institute, Wayne, PA.
    • The Clinical and Laboratory Standards Institute. ((2016) Performance Standards for Antimicrobial Susceptibility Testing CLSI supplement M100S, 26 th ed., Clinical and Laboratory Standards Institute, Wayne, PA.
    • (2016) Performance Standards for Antimicrobial Susceptibility Testing CLSI Supplement M100S
  • 45
    • 84875392510 scopus 로고    scopus 로고
    • Bacterial resistance to cationic antimicrobial peptides
    • Anaya-Lopez, J. L., Lopez-Meza, J. E., and Ochoa-Zarzosa, A. (2013) Bacterial resistance to cationic antimicrobial peptides Crit. Rev. Microbiol. 39 (2) 180-195 10.3109/1040841X.2012.699025
    • (2013) Crit. Rev. Microbiol. , vol.39 , Issue.2 , pp. 180-195
    • Anaya-Lopez, J.L.1    Lopez-Meza, J.E.2    Ochoa-Zarzosa, A.3
  • 46
    • 85016616771 scopus 로고    scopus 로고
    • Polymyxins: Antibacterial activity, susceptibility testing, and resistance mechanisms encoded by plasmids or chromosomes
    • Poirel, L., Jayol, A., and Nordmann, P. (2017) Polymyxins: Antibacterial activity, susceptibility testing, and resistance mechanisms encoded by plasmids or chromosomes Clin. Microbiol. Rev. 30 (2) 557-596 10.1128/CMR.00064-16
    • (2017) Clin. Microbiol. Rev. , vol.30 , Issue.2 , pp. 557-596
    • Poirel, L.1    Jayol, A.2    Nordmann, P.3
  • 47
    • 75749101383 scopus 로고    scopus 로고
    • Defining fractional inhibitory concentration index cutoffs for additive interactions based on self-drug additive combinations, Monte Carlo simulation analysis, and in vitro-in vivo correlation data for antifungal drug combinations against Aspergillus fumi
    • Meletiadis, J., Pournaras, S., Roilides, E., and Walsh, T. J. (2010) Defining fractional inhibitory concentration index cutoffs for additive interactions based on self-drug additive combinations, Monte Carlo simulation analysis, and in vitro-in vivo correlation data for antifungal drug combinations against Aspergillus fumi Antimicrob. Agents Chemother. 54 (2) 602-609 10.1128/AAC.00999-09
    • (2010) Antimicrob. Agents Chemother. , vol.54 , Issue.2 , pp. 602-609
    • Meletiadis, J.1    Pournaras, S.2    Roilides, E.3    Walsh, T.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.