Agents that increase the permeability of the outer membrane

Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor.

Zasloff, M. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.15.5449 · Cited by 2,305 · see citing works

Structure and Function of Lipopolysaccharide Binding Protein

Schumann, R. R., Leong, S. R., Flaggs, G., Gray, P. W., Wright, S. D., Mathison, J. C., Tobias, P. S., & Ulevitch, R. J. (1990) · Science · doi:10.1126/science.2402637 · Cited by 1,672 · see citing works

The Release of Enzymes from Escherichia coli by Osmotic Shock and during the Formation of Spheroplasts

Neu, H. C., & HEPPEL, L. A. (1965) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)97200-5 · Cited by 1,490 · see citing works

Defensins. Natural peptide antibiotics of human neutrophils.

Ganz, T., Selsted, M. E., Szklarek, D., Harwig, S. S. L., Daher, K. A., Bainton, D. F., & Lehrer, R. I. (1985) · Journal of Clinical Investigation · doi:10.1172/jci112120 · Cited by 1,416 · see citing works

Insect Immunity. Purification and Properties of Three Inducible Bactericidal Proteins from Hemolymph of Immunized Pupae of Hyalophora cecropia

Hultmark, D., Steiner, H., Rasmuson, T., & Boman, H. G. (1980) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1980.tb05991.x · Cited by 1,007 · see citing works

Polymyxin and Related Peptide Antibiotics

Storm, D. R., Rosenthal, K. S., & Swanson, P. E. (1977) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.46.070177.003451 · Cited by 759 · see citing works

Molecular architecture and functioning of the outer membrane of Escherichia coli and other gram-negative bacteria

Lugtenberg, B. J. J., & van Alphen, L. (1983) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(83)90014-x · Cited by 742 · see citing works

Interaction of human defensins with Escherichia coli. Mechanism of bactericidal activity.

Lehrer, R. I., Barton, A. P., Daher, K. A., Harwig, S. S. L., Ganz, T., & Selsted, M. E. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114198 · Cited by 712 · see citing works

All-D amino acid-containing channel-forming antibiotic peptides.

Wade, D. C., Boman, A., Wåhlin, B., Drain, C. M., Andreu, D., Boman, H. G., & Merrifield, R. B. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4761 · Cited by 677 · see citing works

The Outer Membrane of Gram-negative Bacteria

Nikaido, H., & Nakae, T. (1980) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/s0065-2911(08)60208-8 · Cited by 588 · see citing works

PEPTIDES FROM FROG SKIN

Bevins, C. L., & ZASLOFF, M. A. (1990) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.59.070190.002143 · Cited by 584 · see citing works

Antibacterial peptides: Key components needed in immunity

Boman, H. G. (1991) · Cell · doi:10.1016/0092-8674(91)90154-q · Cited by 569 · see citing works

ALTERATIONS IN OUTER MEMBRANE PERMEABILITY

Hancock, R. E. W. (1984) · Annual Review of Microbiology · doi:10.1146/annurev.mi.38.100184.001321 · Cited by 567 · see citing works

Molecular basis of bacterial outer membrane permeability

Nikaido, H., & Vaara, M. (1985) · Microbiological Reviews · doi:10.1128/mr.49.1.1-32.1985 · Cited by 553 · see citing works

Damage of the outer membrane of enteric gram-negative bacteria by lactoferrin and transferrin

Ellison, R. T., Giehl, T. J., & LaForce, F. M. (1988) · Infection and Immunity · doi:10.1128/iai.56.11.2774-2781.1988 · Cited by 540 · see citing works

Antimicrobial defensin peptides form voltage-dependent ion-permeable channels in planar lipid bilayer membranes.

Kagan, B. L., Selsted, M. E., Ganz, T., & Lehrer, R. I. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.1.210 · Cited by 532 · see citing works

Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab (Tachypleus tridentatus). Isolation and chemical structure.

Nakamura, T., Furunaka, H., Miyata, T., Tokunaga, F., Muta, T., Iwanaga, S., Niwa, M., Takao, T., & Shimonishi, Y. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)37448-9 · Cited by 531 · see citing works

THE BARRIER FUNCTION OF THE GRAM‐NEGATIVE ENVELOPE

Leive, L. (1974) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1974.tb43261.x · Cited by 514 · see citing works

Channel-forming properties of cecropins and related model compounds incorporated into planar lipid membranes.

Christensen, B., Fink, J., Merrifield, R. B., & Mauzerall, D. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.14.5072 · Cited by 514 · see citing works

Use of the fluorescent probe 1-N-phenylnaphthylamine to study the interactions of aminoglycoside antibiotics with the outer membrane of Pseudomonas aeruginosa

Loh, B. A., Grant, C. W. M., & Hancock, R. E. W. (1984) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.26.4.546 · Cited by 494 · see citing works

Release of lipopolysaccharide by EDTA treatment of E., coli

Leive, L. (1965) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(65)90191-9 · Cited by 470 · see citing works

Apidaecins: antibacterial peptides from honeybees.

Casteels, P., Ampè, C., Jacobs, F. H. H., Vaeck, M., & Tempst, P. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08368.x · Cited by 469 · see citing works

Outer membrane barrier as a mechanism of antimicrobial resistance

Nikaido, H. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.11.1831 · Cited by 464 · see citing works

Antimicrobial action of .EPSILON.-poly-L-lysine.

Shima, S., Matsuoka, H., IWAMOTO, T., & Sakai, H. (1984) · The Journal of Antibiotics · doi:10.7164/antibiotics.37.1449 · Cited by 463 · see citing works

Purification and characterization of a potent bactericidal and membrane active protein from the granules of human polymorphonuclear leukocytes.

Weiss, J. P., Elsbach, P., Olsson, I., & Odeberg, H. (1978) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)40872-6 · Cited by 451 · see citing works

Insect immunity. Attacins, a family of antibacterial proteins from Hyalophora cecropia.

Hultmark, D., Engström, Å., Andersson, K., Steiner, H., Bennich, H., & Boman, H. G. (1983) · The EMBO Journal · doi:10.1002/j.1460-2075.1983.tb01465.x · Cited by 442 · see citing works

Antibacterial peptides from pig intestine: isolation of a mammalian cecropin.

Lee, J. Y., Boman, A., Sun, C., Andersson, M., Jörnvall, H., Mutt, V., & Boman, H. G. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.23.9159 · Cited by 436 · see citing works

Outer membrane of Salmonella typhimurium

Nikaido, H. (1976) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(76)90182-6 · Cited by 378 · see citing works

Antimicrobial activity of synthetic magainin peptides and several analogues.

Zasloff, M., Martin, B., & Chen, H. C. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.3.910 · Cited by 373 · see citing works

Outer membrane of Salmonella typhimurium: accessibility of phospholipid head groups to phospholipase C and cyanogen bromide activated dextran in the external medium

Kamio, Y., & Nikaido, H. (1976) · Biochemistry · doi:10.1021/bi00657a012 · Cited by 371 · see citing works

Electrodialysis of Lipopolysaccharides and Their Conversion to Uniform Salt Forms

Galanos, C., & Luderitz, O. (1975) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1975.tb04172.x · Cited by 362 · see citing works

Antibiotic magainins exert cytolytic activity against transformed cell lines through channel formation.

Cruciani, R. A., Barker, J. L., ZASLOFF, M. A., Chen, H. C., & Colamonici, O. R. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.9.3792 · Cited by 362 · see citing works

Identification of a Lipid A Binding Site in the Acute Phase Reactant Lipopolysaccharide Binding Protein

Tobias, P. S., Soldau, K., & Ulevitch, R. J. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)81700-8 · Cited by 352 · see citing works

Defensins: Endogenous antibiotic peptides of animal cells

Lehrer, R. I., Ganz, T., & Selsted, M. E. (1991) · Cell · doi:10.1016/0092-8674(91)90632-9 · Cited by 345 · see citing works

Interaction of divalent cations and polymyxin B with lipopolysaccharide

Schindler, M., & Osborn, M. (1979) · Biochemistry · doi:10.1021/bi00587a024 · Cited by 336 · see citing works

Insect immunity: isolation from immune blood of the dipteran Phormia terranovae of two insect antibacterial peptides with sequence homology to rabbit lung macrophage bactericidal peptides.

Lambert, J., Keppi, E., Dimarcq, J. L., Wicker, C., Reichhart, J., Dunbar, B., Lepage, P., DORSSELAER, A. V., Hoffmann, J. A., & Fothergill, J. E. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.1.262 · Cited by 324 · see citing works

Antibacterial and antimalarial properties of peptides that are cecropin‐melittin hybrids

Boman, H. G., Wade, D. C., Boman, I. A., Wåhlin, B., & Merrifield, R. B. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)81505-4 · Cited by 314 · see citing works

Purification and antibacterial activity of antimicrobial peptides of rabbit granulocytes

Selsted, M. E., Szklarek, D., & Lehrer, R. I. (1984) · Infection and Immunity · doi:10.1128/iai.45.1.150-154.1984 · Cited by 306 · see citing works

Isolation and characterization of abaecin, a major antibacterial response peptide in the honeybee (Apis mellifera)

Casteels, P., Ampè, C., Riviere, L. R., van Damme, J., Elicone, C., Fleming, M. D., JACOBS, F., & Tempst, P. (1990) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1990.tb15315.x · Cited by 305 · see citing works

Purification, composition, and activity of two bactenecins, antibacterial peptides of bovine neutrophils

Gennaro, R., Skerlavaj, B., & Romeo, D. (1989) · Infection and Immunity · doi:10.1128/iai.57.10.3142-3146.1989 · Cited by 300 · see citing works

Antimicrobial Peptides, Isolated from Horseshoe Crab Hemocytes, Tachyplesin II, and Polyphemusins I and II: Chemical Structures and Biological Activity1

Miyata, T., Tokunaga, F., Yoneya, T., Yoshikawa, K., Iwanaga, S., Niwa, M., Takao, T., & Shimonishi, Y. (1989) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a122913 · Cited by 294 · see citing works

All‐D‐magainin: chirality, antimicrobial activity and proteolytic resistance

Bessalle, R., Kapitkovsky, A., Gorea, A., Shalit, I., & Fridkin, M. (1990) · FEBS Letters · doi:10.1016/0014-5793(90)81351-n · Cited by 294 · see citing works

Antibacterial properties of eosinophil major basic protein and eosinophil cationic protein.

Lehrer, R., Szklarek, D., Barton, A. P., Ganz, T., Hamann, K. J., & Gleich, G. J. (1989) · The Journal of Immunology · doi:10.4049/jimmunol.142.12.4428 · Cited by 292 · see citing works

Compounds which increase the permeability of the Pseudomonas aeruginosa outer membrane

Hancock, R. E. W., & Wong, P. G. (1984) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.26.1.48 · Cited by 286 · see citing works

Lysis of gram-negative organisms and the role of versene

Repaske, R. (1958) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(58)90044-1 · Cited by 279 · see citing works

Antibiotic proteins of human polymorphonuclear leukocytes.

Gabay, J. E., Scott, R., Campanelli, D., Griffith, J. E., Wilde, C., Marra, M. N., Seeger, M., & Nathan, C. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.14.5610 · Cited by 271 · see citing works

Bactericidal/permeability-increasing protein has endotoxin-neutralizing activity.

MARRA, M. N., WILDE, C. G., Griffith, J. E., Snable, J. L., & Scott, R. W. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.144.2.662 · Cited by 270 · see citing works

Cell‐free immunity in Cecropia

Boman, H. G., Faye, I., Gudmundsson, G. H., Jong‐Youn, L. E. E., & Lidholm, D.-A. (1991) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1991.tb16252.x · Cited by 263 · see citing works

Routes of quinolone permeation in Escherichia coli

Chapman, J., & Georgopapadakou, N. H. (1988) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.32.4.438 · Cited by 254 · see citing works

Polycations as outer membrane-disorganizing agents

Vaara, M., & Vaara, T. (1983) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.24.1.114 · Cited by 252 · see citing works

Separation and purification of a potent bactericidal/permeability-increasing protein and a closely associated phospholipase A2 from rabbit polymorphonuclear leukocytes. Observations on their relationship.

Elsbach, P., Weiss, J. P., Franson, R. C., Beckerdite-Quagliata, S., Schneider, A., & Harris, L. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)86622-x · Cited by 235 · see citing works

Interaction of polycationic antibiotics with Pseudomonas aeruginosa lipopolysaccharide and lipid A studied by using dansyl-polymyxin

Moore, R. A., Bates, N. C., & Hancock, R. E. W. (1986) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.29.3.496 · Cited by 235 · see citing works

Sensitization of Gram-negative bacteria to antibiotics and complement by a nontoxic oligopeptide

Vaara, M., & Vaara, T. (1983) · Nature · doi:10.1038/303526a0 · Cited by 232 · see citing works

Role of Lipopolysaccharides in Antibiotic Resistance and Bacteriophage Adsorption of Escherichia coli K-12

Tamaki, S., Sato, T., & Matsuhashi, M. (1971) · Journal of Bacteriology · doi:10.1128/jb.105.3.968-975.1971 · Cited by 230 · see citing works

Antimicrobial peptide magainin I from Xenopus skin forms anion-permeable channels in planar lipid bilayers

Duclohier, H., Molle, G., & Spach, G. (1989) · Biophysical Journal · doi:10.1016/s0006-3495(89)82746-8 · Cited by 222 · see citing works

Outer membrane protein H1 of Pseudomonas aeruginosa: involvement in adaptive and mutational resistance to ethylenediaminetetraacetate, polymyxin B, and gentamicin

Nicas, T. I., & Hancock, R. E. W. (1980) · Journal of Bacteriology · doi:10.1128/jb.143.2.872-878.1980 · Cited by 221 · see citing works

Involvement of the outer membrane in gentamicin and streptomycin uptake and killing in Pseudomonas aeruginosa

Hancock, R. E. W., Raffle, V. J., & Nicas, T. I. (1981) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.19.5.777 · Cited by 221 · see citing works

Azurocidin and a homologous serine protease from neutrophils. Differential antimicrobial and proteolytic properties.

Campanelli, D., Detmers, P., Nathan, C., & Gabay, J. E. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114518 · Cited by 216 · see citing works

Polycations sensitize enteric bacteria to antibiotics

Vaara, M., & Vaara, T. (1983) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.24.1.107 · Cited by 215 · see citing works

A family of lipopolysaccharide binding proteins involved in responses to gram-negative sepsis.

Tobias, P. S., Mathison, J. C., & Ulevitch, R. J. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)68262-6 · Cited by 212 · see citing works

Concurrent assessment of inner and outer membrane permeabilization and bacteriolysis in E. coli by multiple-wavelength spectrophotometry

Lehrer, R. I., Barton, A. P., & Ganz, T. (1988) · Journal of Immunological Methods · doi:10.1016/0022-1759(88)90414-0 · Cited by 211 · see citing works

Cationic antimicrobial proteins isolated from human neutrophil granulocytes in the presence of diisopropyl fluorophosphate

Shafer, W. M., Martin, L., & Spitznagel, J. (1984) · Infection and Immunity · doi:10.1128/iai.45.1.29-35.1984 · Cited by 210 · see citing works

Actinomycin sensitivity in Escherichiacoli produced by EDTA

Leive, L. (1965) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(65)90874-0 · Cited by 207 · see citing works

Antimicrobial polypeptides of human neutrophils

Lehrer, R., & Ganz, T. (1990) · Blood · doi:10.1182/blood.v76.11.2169.bloodjournal76112169 · Cited by 206 · see citing works

Antibiotic uptake into gram-negative bacteria

Hancock, R. E. W., & Bell, A. (1988) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf01975036 · Cited by 205 · see citing works

Rapid membrane permeabilization and inhibition of vital functions of gram-negative bacteria by bactenecins

Skerlavaj, B., Romeo, D., & Gennaro, R. (1990) · Infection and Immunity · doi:10.1128/iai.58.11.3724-3730.1990 · Cited by 202 · see citing works

Amino acid sequences of two proline-rich bactenecins. Antimicrobial peptides of bovine neutrophils.

Frank, R. W., Gennaro, R., Schneider, K., Przybylski, M., & Romeo, D. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)30595-1 · Cited by 199 · see citing works

Cloning of the cDNA of a Human Neutrophil Bactericidal Protein

Gray, P. W., Flaggs, G., Leong, S. R., Gumina, R. J., Weiss, J. P., Ooi, C. E., & Elsbach, P. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)60560-5 · Cited by 199 · see citing works

High state of order of isolated bacterial lipopolysaccharide and its possible contribution to the permeation barrier property of the outer membrane

Labischinski, H., Barnickel, G., Bradaczek, H., Naumann, D., Rietschel, E., & Giesbrecht, P. (1985) · Journal of Bacteriology · doi:10.1128/jb.162.1.9-20.1985 · Cited by 197 · see citing works

Characterization of the lipopolysaccharide from the polymyxin‐resistant pmrA mutants of Salmonella typhimurium

Vaara, M., Vaara, T., Jensen, M., Helander, I. M., Nurminen, M., Rietschel, E., & Mäkelä, P. H. (1981) · FEBS Letters · doi:10.1016/0014-5793(81)80777-6 · Cited by 195 · see citing works

Outer membranes of Gram‐negative bacteria are permeable to steroid probes

Plésiat, P., & Nikaido, H. (1992) · Molecular Microbiology · doi:10.1111/j.1365-2958.1992.tb00853.x · Cited by 191 · see citing works

Manipulation of intracellular magnesium content in polymyxin B nonapeptide-sensitized Escherichia coli by ionophore A23187

Alatossava, T., Jütte, H., Kühn, A., & Kellenberger, E. (1985) · Journal of Bacteriology · doi:10.1128/jb.162.1.413-419.1985 · Cited by 185 · see citing works

Endotoxin-neutralizing properties of the 25 kD N-terminal fragment and a newly isolated 30 kD C-terminal fragment of the 55-60 kD bactericidal/permeability-increasing protein of human neutrophils.

Ooi, C. E., Weiss, J. P., Doerfler, M. E., & Elsbach, P. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.174.3.649 · Cited by 181 · see citing works

Interaction of aminoglycosides with the outer membranes and purified lipopolysaccharide and OmpF porin of Escherichia coli

Hancock, R. E. W., Farmer, S. W., Li, Z. S., & Poole, K. (1991) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.35.7.1309 · Cited by 180 · see citing works

Isolation and Biological Activities of Limulus Anticoagulant (Anti-LPS Factor) which Interacts with Lipopolysaccharide (LPS)1

Morita, T., Ohtsubo, S., Nakamura, T., Tanaka, S., Iwanaga, S., Ohashi, K., & Niwa, M. (1985) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a135218 · Cited by 168 · see citing works

Lipopolysaccharide interaction with lysozyme

Ohno, N., & Morrison, D. C. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)83761-9 · Cited by 165 · see citing works

Structural characterization of the lipid A component of Bacteroides fragilis strain NCTC 9343 lipopolysaccharide

Weintraub, A., Zähringer, U., Wollenweber, H. W., Seydel, U., & Rietschel, E. T. (1989) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1989.tb14945.x · Cited by 164 · see citing works

Purification, toxicity, and antiendotoxin activity of polymyxin B nonapeptide

Danner, R. L., Joiner, K. A., Rubin, M., Patterson, W. H., Johnson, N., AYERS, K. M., & Parrillo, J. E. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.9.1428 · Cited by 159 · see citing works

Binding of polycationic antibiotics and polyamines to lipopolysaccharides of Pseudomonas aeruginosa

Peterson, A. A., Hancock, R. E. W., & McGroarty, E. J. (1985) · Journal of Bacteriology · doi:10.1128/jb.164.3.1256-1261.1985 · Cited by 158 · see citing works

Antibiotic proteins of human neutrophils.

Spitznagel, J. K. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114851 · Cited by 158 · see citing works

Attacin, an antibacterial protein from Hyalophora cecropia, inhibits synthesis of outer membrane proteins in Escherichia coli by interfering with omp gene transcription

Carlsson, A., Engström, P., Palva, E. T., & Bennich, H. (1991) · Infection and Immunity · doi:10.1128/iai.59.9.3040-3045.1991 · Cited by 154 · see citing works

A 25-kDa NH2-terminal fragment carries all the antibacterial activities of the human neutrophil 60-kDa bactericidal/permeability-increasing protein.

Ooi, C. E., Weiss, J. P., Elsbach, P., Frangione, B., & Mannion, B. A. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48110-0 · Cited by 151 · see citing works

Primary structure of limulus anticoagulant anti-lipopolysaccharide factor.

Aketagawa, J., Miyata, T., Ohtsubo, S., Nakamura, T., Morita, T., Hayashida, H., Miyata, T., Iwanaga, S., Takao, T., & Shimonishi, Y. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)38399-0 · Cited by 151 · see citing works

Interaction of macrophage cationic proteins with the outer membrane of Pseudomonas aeruginosa

Sawyer, J. G., Martin, N., & Hancock, R. E. W. (1988) · Infection and Immunity · doi:10.1128/iai.56.3.693-698.1988 · Cited by 151 · see citing works

Antibacterial agents specifically inhibiting lipopolysaccharide synthesis

Goldman, R. C., Kohlbrenner, W. E., Lartey, P. A., & Pernet, A. G. (1987) · Nature · doi:10.1038/329162a0 · Cited by 143 · see citing works

Chemical structure of the lipid A component of the lipopolysaccharide from a Proteus mirabilis Re‐mutant

Sidorczyk, Z., Zähringer, U., & Rietschel, E. (1983) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1983.tb07789.x · Cited by 141 · see citing works

The Effect of Defined Lipopolysaccharide Core Defects upon Antibiotic Resistances of Salmonella typhimurium

Roantree, R. J., Kuo, T. T., & MacPhee, D. G. (1977) · Journal of General Microbiology · doi:10.1099/00221287-103-2-223 · Cited by 138 · see citing works

Two mutations which affect the barrier function of the Escherichia coli K-12 outer membrane

Coleman, W. G., & Leive, L. (1979) · Journal of Bacteriology · doi:10.1128/jb.139.3.899-910.1979 · Cited by 137 · see citing works

Involvement of outer membrane of Pseudomonas cepacia in aminoglycoside and polymyxin resistance

Moore, R. A., & Hancock, R. E. W. (1986) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.30.6.923 · Cited by 133 · see citing works

Outer-Membrane Permeability of Bacteria

Nakae, T. (1986) · CRC Critical Reviews in Microbiology · doi:10.3109/10408418609108734 · Cited by 132 · see citing works

Role of permeability barriers in resistance to β-lactam antibiotics

Nikaido, H. (1985) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(85)90069-5 · Cited by 131 · see citing works

Lactoferrin and transferrin damage of the Gram-negative outer membrane is modulated by Ca2+ and Mg2+

Ellison, R. T., LaForce, F. M., Giehl, T. J., Boose, D., & Dunn, B. E. (1990) · Journal of General Microbiology · doi:10.1099/00221287-136-7-1437 · Cited by 131 · see citing works

Mode of action of gramicidin S on Escherichia coli membrane

Katsu, T., Kobayashi, H., & Fujita, Y. (1986) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(86)90560-2 · Cited by 128 · see citing works

Antibacterial activity of microbicidal cationic proteins 1 and 2, natural peptide antibiotics of rabbit lung macrophages

Lehrer, R. I., Selsted, M. E., Szklarek, D., & Fleischmann, J. (1983) · Infection and Immunity · doi:10.1128/iai.42.1.10-14.1983 · Cited by 126 · see citing works

The antibacterial effect of attacins from the silk moth Hyalophora cecropia is directed against the outer membrane of Escherichia coli.

Engström, P., Carlsson, A., Engström, Å., Tao, Z., & Bennich, H. (1984) · The EMBO Journal · doi:10.1002/j.1460-2075.1984.tb02302.x · Cited by 122 · see citing works

Partial characterization and purification of a rabbit granulocyte factor that increases permeability of Escherichia coli.

Weiss, J. P., Franson, R. C., Beckerdite-Quagliata, S., Schmeidler, K., & Elsbach, P. (1975) · Journal of Clinical Investigation · doi:10.1172/jci107915 · Cited by 121 · see citing works

Mechanism of action of DuP 721: inhibition of an early event during initiation of protein synthesis

Eustice, D. C., Feldman, P., Zajac, I., & Slee, A. (1988) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.32.8.1218 · Cited by 118 · see citing works

Separation of sublethal and lethal effects of the bactericidal/permeability increasing protein on Escherichia coli.

Mannion, B. A., Weiss, J. P., & Elsbach, P. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114512 · Cited by 116 · see citing works

Identification of the primary antimicrobial domains in human neutrophil cathepsin G.

Bangalore, N., Travis, J. W., Onunka, V. C., Pohl, J., & Shafer, W. M. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)77388-2 · Cited by 115 · see citing works

Release of Surface Enzymes in Enterobacteriaceae by Osmotic Shock

Neu, H. C., & Chou, J. (1967) · Journal of Bacteriology · doi:10.1128/jb.94.6.1934-1945.1967 · Cited by 114 · see citing works

Outer Membrane Permeability Barrier Disruption by Polymyxin in Polymyxin-Susceptible and -Resistant Salmonella typhimurium

Vaara, M., & Vaara, T. (1981) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.19.4.578 · Cited by 113 · see citing works

Susceptibility of gram-negative bacteria to polymyxin B nonapeptide

Viljanen, P., & Vaara, M. (1984) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.25.6.701 · Cited by 112 · see citing works

Leakage of periplasmic proteins from Escherichia coli mediated by polymyxin B nonapeptide

DIXON, R. A., & Chopra, I. (1986) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.29.5.781 · Cited by 112 · see citing works

Investigation into the fluidity of lipopolysaccharide and free lipid A membrane systems by Fourier‐transform infrared spectroscopy and differential scanning calorimetry

Brandenburg, K., & Seydel, U. (1990) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1990.tb19114.x · Cited by 106 · see citing works

Mechanisms for the microbicidal activity of cationic proteins of human granulocytes

Odeberg, H., & Olsson, I. (1976) · Infection and Immunity · doi:10.1128/iai.14.6.1269-1275.1976 · Cited by 105 · see citing works

The lipid A biosynthesis mutation lpxA2 of Escherichia coli results in drastic antibiotic supersusceptibility

Vuorio, R., & Vaara, M. (1992) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.36.4.826 · Cited by 103 · see citing works

Permeability of lipopolysaccharide-deficient (rough) mutants of Salmonella typhimurium to antibiotics, lysozyme, and other agents

Sanderson, K. E., MacAlister, T. J., Costerton, J. W., & Cheng, K.-J. (1974) · Canadian Journal of Microbiology · doi:10.1139/m74-176 · Cited by 102 · see citing works

Primary Structure of Anti-Lipopolysaccharide Factor from American Horseshoe Crab, Limulus polyphemus1

Muta, T., Miyata, T., Tokunaga, F., Nakamura, T., & Iwanaga, S. (1987) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a121999 · Cited by 99 · see citing works

Ionizing groups in lipopolysaccharides of Pseudomonas cepacia in relation to antibiotic resistance

Cox, A. D., & Wilkinson, S. G. (1991) · Molecular Microbiology · doi:10.1111/j.1365-2958.1991.tb00735.x · Cited by 96 · see citing works

Binding of polymyxin B nonapeptide to gram-negative bacteria

Vaara, M., & Viljanen, P. (1985) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.27.4.548 · Cited by 96 · see citing works

Increased outer membrane resistance to ethylenediaminetetraacetate and cations in novel lipid A mutants

Vaara, M. (1981) · Journal of Bacteriology · doi:10.1128/jb.148.2.426-434.1981 · Cited by 94 · see citing works

Microbicidal mechanisms of human granulocytes: synergistic effects of granulocyte elastase and myeloperoxidase or chymotrypsin-like cationic protein

Odeberg, H., & Olsson, I. (1976) · Infection and Immunity · doi:10.1128/iai.14.6.1276-1283.1976 · Cited by 94 · see citing works

Polymyxin B and polymyxin B nonapeptide alter cytoplasmic membrane permeability in Escherichia coli

DIXON, R. A., & Chopra, I. (1986) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/18.5.557 · Cited by 94 · see citing works

Late intraphagosomal hydrogen ion concentration favors the in vitro antimicrobial capacity of a 37-kilodalton cationic granule protein of human neutrophil granulocytes

Shafer, W. M., Martin, L. E., & Spitznagel, J. K. (1986) · Infection and Immunity · doi:10.1128/iai.53.3.651-655.1986 · Cited by 93 · see citing works

Delta pH-dependent accumulation of tetracycline in Escherichia coli

Yamaguchi, A., Ohmori, H., Kaneko-Ohdera, M., Nomura, T., & Sawai, T. (1991) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.35.1.53 · Cited by 92 · see citing works

The role of lipopolysaccharides in the action of the bactericidal/permeability-increasing neutrophil protein on the bacterial envelope.

Weiss, J. P., Muello, K., Victor, M., & Elsbach, P. (1984) · The Journal of Immunology · doi:10.4049/jimmunol.132.6.3109 · Cited by 90 · see citing works

envM genes of Salmonella typhimurium and Escherichia coli

Turnowsky, F., Fuchs, K. P., Jeschek, C., & Högenauer, G. (1989) · Journal of Bacteriology · doi:10.1128/jb.171.12.6555-6565.1989 · Cited by 89 · see citing works

Decreased binding of antibiotics to lipopolysaccharides from polymyxin-resistant strains of Escherichia coli and Salmonella typhimurium

Peterson, A. A., Fesik, S. W., & McGroarty, E. J. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.2.230 · Cited by 89 · see citing works

Interactions between magainin 2 and Salmonella typhimurium outer membranes: effect of lipopolysaccharide structure

Rana, F. R., Macias, E. A., Sultany, C. M., Modzrakowski, M. C., & Blazyk, J. (1991) · Biochemistry · doi:10.1021/bi00238a008 · Cited by 86 · see citing works

The Chemical Structure of the Lipid A Component of Lipopolysaccharides from Chromobacterium violaceum NCTC 9694

Hase, S., & Rietschel, E. (1977) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1977.tb11500.x · Cited by 85 · see citing works

Role of Charge and Hydrophobic Interactions in the Action of Bactericidal/Permeability-increasing Protein of Neutrophils on Gram-negative Bacteria

Weiss, J. P., Victor, M., & Elsbach, P. (1983) · Journal of Clinical Investigation · doi:10.1172/jci110798 · Cited by 84 · see citing works

Outer Membrane Permeability of Pseudomonas aeruginosa

Nikaido, H., & HANCOCK, R. E. W. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-307210-8.50009-9 · Cited by 84 · see citing works

Correlation between renal membrane binding and nephrotoxicity of aminoglycosides

Williams, P. D., Bennett, D. B., Gleason, C. R., & Hottendorf, G. H. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.4.570 · Cited by 81 · see citing works

Purification, primary structure, and biological activity of guinea pig neutrophil cationic peptides

Yamashita, T., & Saito, K. (1989) · Infection and Immunity · doi:10.1128/iai.57.8.2405-2409.1989 · Cited by 81 · see citing works

Human lysosomal cathepsin G and granzyme B share a functionally conserved broad spectrum antibacterial peptide.

Shafer, W. M., Pohl, J., Onunka, V. C., Bangalore, N., & Travis, J. W. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)52409-1 · Cited by 79 · see citing works

Decreased binding of polymyxin by polymyxin-resistant mutants of Salmonella typhimurium

Vaara, M., Vaara, T., & Sarvas, M. (1979) · Journal of Bacteriology · doi:10.1128/jb.139.2.664-667.1979 · Cited by 78 · see citing works

Antigonococcal activity of human neutrophil cathepsin G

Shafer, W. M., Onunka, V. C., & Martin, L. E. (1986) · Infection and Immunity · doi:10.1128/iai.54.1.184-188.1986 · Cited by 71 · see citing works

Amino acid sequence of CAP37, a human neutrophil granule‐derived antibacterial and monocyte‐specific chemotactic glycoprotein structurally similar to neutrophil elastase

Pohl, J., Pereira, H. A., Martin, N. M., & Spitznagel, J. K. (1990) · FEBS Letters · doi:10.1016/0014-5793(90)80484-z · Cited by 71 · see citing works

EARLY AND DISCRETE CHANGES IN PERMEABILITY OF ESCHERICHIA COLI AND CERTAIN OTHER GRAM-NEGATIVE BACTERIA DURING KILLING BY GRANULOCYTES

Beckerdite-Quagliata, S., Mooney, C. L., Weiss, J. P., Franson, R., & Elsbach, P. (1974) · The Journal of Experimental Medicine · doi:10.1084/jem.140.2.396 · Cited by 71 · see citing works

Binding and neutralization of bacterial lipopolysaccharide by colistin nonapeptide

Warren, H. S., Kania, S. A., & Siber, G. R. (1985) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.28.1.107 · Cited by 67 · see citing works

Molecular cloning, sequencing, and characterization of cDNA for sarcotoxin IIA, an inducible antibacterial protein of Sarcophaga peregrina (flesh fly)

Ando, K., & Natori, S. (1988) · Biochemistry · doi:10.1021/bi00405a050 · Cited by 66 · see citing works

Preferential binding of the neutrophil cytoplasmic granule-derived bactericidal/permeability increasing protein to target bacteria. Implications and use as a means of purification.

Mannion, B. A., Kalatzis, E. S., Weiss, J. P., & Elsbach, P. (1989) · The Journal of Immunology · doi:10.4049/jimmunol.142.8.2807 · Cited by 63 · see citing works

Interaction of polymyxin B nonapeptide with anionic phospholipids

Kubesch, P., Boggs, J. M., Luciano, L., Maass, G., & Tuemmler, B. (1987) · Biochemistry · doi:10.1021/bi00382a012 · Cited by 62 · see citing works

Effects of Organic Cations on the Gram-negative Cell Wall and Their Bactericidal Activity with Ethylenediaminetetra-acetate and Surface Active Agents

Voss, J. G. (1967) · Journal of General Microbiology · doi:10.1099/00221287-48-3-391 · Cited by 61 · see citing works

Alteration Of Susceptibility To Edta, Polymyxin B And Gentamicin In Pseudomonas Aeruginosa By Divalent Cation Regulation Of Outer Membrane Protein H1

Nicas, T. I., & Hancock, R. E. W. (1983) · Microbiology · doi:10.1099/00221287-129-2-509 · Cited by 60 · see citing works

Fatty acid alterations and polymyxin B binding by lipopolysaccharides from Pseudomonas aeruginosa adapted to polymyxin B resistance

Conrad, R. S., & Galanos, C. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.10.1724 · Cited by 60 · see citing works

Influence of outer membrane mutations on susceptibility of Escherichia coli to the dibasic macrolide azithromycin

Farmer, S., Li, Z., & Hancock, R. E. W. (1992) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/29.1.27 · Cited by 60 · see citing works

Leakage of periplasmic enzymes from envA1 strains of Escherichia coli

Young, K., & Silver, L. L. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.12.3609-3614.1991 · Cited by 59 · see citing works

Partitioning of hydrophobic probes into lipopolysaccharide bilayers

Vaara, M., Plachy, W. Z., & Nikaido, H. (1990) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(90)90218-d · Cited by 56 · see citing works

Pseudomonas aeruginosa outer membrane protein OprH: expression from the cloned gene and function in EDTA and gentamicin resistance

Bell, A., Bains, M., & Hancock, R. E. W. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.21.6657-6664.1991 · Cited by 55 · see citing works

[Amino acid metabolism in larvae of the silkworm Bombyx mori].

Filippovich, I. B., & Bungova, V. G. (1968) · PubMed · Cited by 54 · see citing works

Salmonella typhimurium and Escherichia coli mutants with increased outer membrane permeability to hydrophobic compounds

Sukupolvi, S., & Vaara, M. (1989) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(89)90011-7 · Cited by 54 · see citing works

EFFECT OF POLYMYXIN ON THE LYSIS OF NEISSERIA CATARRHALIS BY LYSOZYME

Warren, G. H., Gray, J., & Yurchenco, J. A. (1957) · Journal of Bacteriology · doi:10.1128/jb.74.6.788-793.1957 · Cited by 53 · see citing works

Complementary DNA sequence of human neutrophil azurocidin, an antibiotic with extensive homology to serine proteases

de Almeida, R. P., Melchior, M., Campanelli, D., Nathan, C., & Gabay, J. E. (1991) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(91)91843-2 · Cited by 53 · see citing works

Polymyxin B octapeptide and polymyxin B heptapeptide are potent outer membrane permeability-increasing agents.

Kimura, Y., Matsunaga, H., & Vaara, M. (1992) · The Journal of Antibiotics · doi:10.7164/antibiotics.45.742 · Cited by 53 · see citing works

Sodium hexametaphosphate sensitizes Pseudomonas aeruginosa, several other species of Pseudomonas, and Escherichia coli to hydrophobic drugs

Vaara, M., & Jaakkola, J. J. K. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.10.1741 · Cited by 53 · see citing works

An outer membrane-disorganizing peptide PMBN sensitizes E. coli strains to serum bactericidal action.

Vaara, M., Viljanen, P., Vaara, T., & Mäkelä, P. H. (1984) · The Journal of Immunology · doi:10.4049/jimmunol.132.5.2582 · Cited by 52 · see citing works

Interaction of the Fluorescent Dye l-N-Phenylnaphthylamine with Escherichia coli Cells during Heat Stress and Recovery from Heat Stress

Tsuchido, T., Aoki, I., & Takano, M. (1989) · Microbiology · doi:10.1099/00221287-135-7-1941 · Cited by 52 · see citing works

Isolation and genetic characterization of polymyxin-resistant mutants of Salmonella

HELENAMAKELA, P., Sarvas, M., Calcagno, S., & Lounatmaa, K. (1978) · FEMS Microbiology Letters · doi:10.1016/0378-1097(78)90018-6 · Cited by 52 · see citing works

Isolation and genetic characterization of polymyxin-resistant mutants of Salmonella

Mäkelä, P. H., Sarvas, M., Calcagno, S., et al. (1978) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1978.tb01963.x · Cited by 51 · see citing works

In vitro cytotoxicity and antibiotic activity of polymyxin B nonapeptide

Duwe, A. K., Rupar, C. A., Horsman, G. B., & Vas, S. I. (1986) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.30.2.340 · Cited by 51 · see citing works

O antigen and lipid A phosphoryl groups in resistance of Salmonella typhimurium LT-2 to nonoxidative killing in human polymorphonuclear neutrophils

Stinavage, P., Martin, L. E., & Spitznagel, J. K. (1989) · Infection and Immunity · doi:10.1128/iai.57.12.3894-3900.1989 · Cited by 51 · see citing works

Novel antibiotic hypersensitive mutants ofEscherichia coligenetic mapping and chemical characterization

Clark, D. P. (1984) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1984.tb00209.x · Cited by 50 · see citing works

Defensins mediate the microbicidal activity of human neutrophil granule extract against Acinetobacter calcoaceticus

Greenwald, G. I., & Ganz, T. (1987) · Infection and Immunity · doi:10.1128/iai.55.6.1365-1368.1987 · Cited by 49 · see citing works

Chemical Synthesis, Isolation and Characterization of α-N-Fattyacyl Colistin Nonapeptide with Special Reference to the Correlation between Antimicrobial Activity and Carbon Number of Fattyacyl Moiety

Chihara, S., Ito, A., Yahata, M., Tobita, T., & Koyama, Y. (1974) · Agricultural and Biological Chemistry · doi:10.1271/bbb1961.38.521 · Cited by 49 · see citing works

The outer membrane permeability-increasing action of deacylpolymyxins.

Viljanen, P., Matsunaga, H., Kimura, Y., & Vaara, M. (1991) · The Journal of Antibiotics · doi:10.7164/antibiotics.44.517 · Cited by 49 · see citing works

Anti‐LPS factor in the horseshoe crab, Tachypleus tridentatus

Ohashi, K., Niwa, M., Nakamura, T., Morita, T., & Iwanaga, S. (1984) · FEBS Letters · doi:10.1016/0014-5793(84)80942-4 · Cited by 48 · see citing works

Secretion of alkaline phosphatase and phsopholipase C in Pseudomonas aeruginosa is specific and does not involve an increase in outer membrane permeability

Poole, K., & Hancock, R. E. W. (1983) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1983.tb00252.x · Cited by 48 · see citing works

Outer-Membrane Penetration Barriers as Components of Intrinsic Resistance to Beta-Lactam and Other Antibiotics in Escherichia coli K-12

Scudamore, R. A., Beveridge, T. J., & Goldner, M. (1979) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.15.2.182 · Cited by 48 · see citing works

Effect of small cationic leukocyte peptides (defensins) on the permeability barrier of the outer membrane

Viljanen, P., Koski, P., & Vaara, M. (1988) · Infection and Immunity · doi:10.1128/iai.56.9.2324-2329.1988 · Cited by 47 · see citing works

Disruption of the Escherichia coli outer membrane permeability barrier by immobilized polymyxin B.

Rosenthal, K. S., & Storm, D. R. (1977) · The Journal of Antibiotics · doi:10.7164/antibiotics.30.1087 · Cited by 47 · see citing works

Polymyxin B nonapeptide complexes with lipopolysaccharide

Vaara, M. (1983) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1983.tb00461.x · Cited by 45 · see citing works

Bactericidal cationic peptides involved in bacterial antagonism and host defence.

Hg, S. (1985) · PubMed · Cited by 45 · see citing works

Activation and Inactivation of Melittin Channels

Tosteson, M. T., & Tosteson, D. C. (1984) · Biophysical Journal · doi:10.1016/s0006-3495(84)84130-2 · Cited by 44 · see citing works

Escherichia coli susceptible to glycopeptide antibiotics

Shlaes, D. M., Shlaes, J. H., DAVIES, J. E., & Williamson, R. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.2.192 · Cited by 42 · see citing works

A synthetic 13-residue peptide corresponding to the hydrophobic region of bovine seminalplasmin has antibacterial activity and also causes lysis of red blood cells.

Sitaram, N., & Nagaraj, R. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)86965-4 · Cited by 41 · see citing works

Lipopolysaccharide structure determines ionic and hydrophobic binding of a cationic antimicrobial neutrophil granule protein

Farley, M. M., Shafer, W. M., & Spitznagel, J. K. (1988) · Infection and Immunity · doi:10.1128/iai.56.6.1589-1592.1988 · Cited by 41 · see citing works

Effects of lipopolysaccharide chemotype structure on binding and inactivation of hen egg lysozyme

Ohno, N., & Morrison, D. C. (1989) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1989.tb15252.x · Cited by 41 · see citing works

Sensitization by heat treatment of Escherichia coli K-12 cells to hydrophobic antibacterial compounds

Tsuchido, T., & Takano, M. (1988) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.32.11.1680 · Cited by 40 · see citing works

Detection of Agents That Alter the Bacterial Cell Surface

Sud, I. J., & FEINGOLD, D. S. (1975) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.8.1.34 · Cited by 39 · see citing works

Reconstitution of the lipid matrix of the outer membrane of Gram-negative bacteria as asymmetric planar bilayer

Seydel, U., Schröder, G., & Brandenburg, K. (1989) · The Journal of Membrane Biology · doi:10.1007/bf01870848 · Cited by 39 · see citing works

Repair of Injury in Freeze-Dried Salmonella anatum

Ray, B., Jezeski, J. J., & Busta, F. F. (1971) · Applied Microbiology · doi:10.1128/am.22.3.401-407.1971 · Cited by 38 · see citing works

Effect of ethylenediaminetetraacetate on phospholipids and outer membrane function in Escherichia coli

Hardaway, K. L., & Buller, C. S. (1979) · Journal of Bacteriology · doi:10.1128/jb.137.1.62-68.1979 · Cited by 37 · see citing works

EM49: A NEW POLYPEPTIDE ANTIBIOTIC ACTIVE AGAINST CELL MEMBRANES

Meyers, E., Parker, W. L., Brown, W. E., Linnett, P. E., & Strominger, J. L. (1974) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1974.tb43286.x · Cited by 37 · see citing works

Identification and sequence analysis of the gene mutated in the conditionally lethal outer membrane permeability mutant SS‐C of Salmonella typhimurium.

Hirvas, L., Koski, P., & Vaara, M. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb08036.x · Cited by 37 · see citing works

The Cell Envelope of Gram-Negative Bacteria: New Aspects of Its Function in Transport and Chemotaxis

Brass, J. M. (1986) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-71399-6_1 · Cited by 35 · see citing works

Effect of polymyxins on the lipopolysaccharide-defective mutants of Proteus mirabilis.

Kaca, W., Radziejewska‐Lebrecht, J., & Ur, B. (1990) · PubMed · Cited by 35 · see citing works

The ontogeny of a 57-Kd cationic antimicrobial protein of human polymorphonuclear leukocytes: localization to a novel granule population

Pereira, H., Spitznagel, J. K., Winton, E., Shafer, W. M., Martin, L., Guzman, G. S., Pohl, J., Scott, R., Marra, M. N., & Kinkade, J. J. (1990) · Blood · doi:10.1182/blood.v76.4.825.825 · Cited by 34 · see citing works

Inhibitory Effect of Sarcotoxin IIA, an Antibacterial Protein of Sarcophaga peregrina, on Growth of Escherichia coli1

Ando, K., & Natori, S. (1988) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a122337 · Cited by 34 · see citing works

The outer membrane permeability-increasing action of linear analogues of polymyxin B nonapeptide.

Vaara, M. (1991) · PubMed · Cited by 34 · see citing works

Comparison of granule proteins from human polymorphonuclear leukocytes which are bactericidal toward Pseudomonas aeruginosa

Wasiluk, K. R., Skubitz, K. M., & Gray, B. H. (1991) · Infection and Immunity · doi:10.1128/iai.59.11.4193-4200.1991 · Cited by 33 · see citing works

Comparative X‐ray and Fourier‐transform‐infrared investigations of conformational properties of bacterial and synthetic lipid A of Escherichia coli and Salmonella minnesota as well as partial structures and analogues thereof

Labischinski, H., Naumann, D., SCHULTZ, C., Kusumoto, S., Shiba, T., Rietschel, E., & Giesbrecht, P. (1989) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1989.tb14598.x · Cited by 32 · see citing works

The Pseudomonas aeruginosa Outer Membrane Permeability Barrier and How to Overcome It

Hancock, R. E. W. (2015) · Antibiotics and chemotherapy/Antibiotica et chemotherapia · doi:10.1159/000410475 · Cited by 31 · see citing works

Physiological effects of a bactericidal protein from human polymorphonuclear leukocytes on Pseudomonas aeruginosa

Hovde, C. J., & Gray, B. H. (1986) · Infection and Immunity · doi:10.1128/iai.52.1.90-95.1986 · Cited by 30 · see citing works

Increased outer membrane ornithine-containing lipid and lysozyme penetrability of Paracoccus denitrificans grown in a complex medium deficient in divalent cations

Wee, S., & Wilkinson, B. J. (1988) · Journal of Bacteriology · doi:10.1128/jb.170.7.3283-3286.1988 · Cited by 29 · see citing works

Ultrastructural Study of Salmonella typhimurium Treated with Membrane-Active Agents: Specific Reaction of Dansylchloride with Cell Envelope Components

Schindler, P. R. G., & Teuber, M. (1978) · Journal of Bacteriology · doi:10.1128/jb.135.1.198-206.1978 · Cited by 28 · see citing works

A highly efficient procedure for the quantitative formation of intact and viable lysozyme spheroplasts from escherichia coli

Marvin, H. J. P., & Witholt, B. (1987) · Analytical Biochemistry · doi:10.1016/0003-2697(87)90500-8 · Cited by 27 · see citing works

Dissipation of membrane potential of Escherichia coli cells induced by macromolecular polylysine

Katsu, T., Tsuchiya, T., & Fujita, Y. (1984) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(84)90489-3 · Cited by 27 · see citing works

The outer membrane as the penetration barrier against mupirocin in Gram-negative enteric bacteria

Vaara, M. (1992) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/29.2.221 · Cited by 27 · see citing works

Membrane-disorganizing property of polymyxin B nonapeptide

Lam, C., Hildebrandt, J., Schütze, E., & Wenzel, A. F. (1986) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/18.1.9 · Cited by 25 · see citing works

Expression of H1 outer-membrane protein of Pseudomonas aeruginosa in relation to sensitivity to EDTA and polymyxin B

Said, A. A., Livermore, D. M., & Williams, R. J. (1987) · Journal of Medical Microbiology · doi:10.1099/00222615-24-3-267 · Cited by 24 · see citing works

Role of the Outer Membrane of Gram-Negative Bacteria in Antimicrobial Resistance

Nikaido, H. (1989) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-74095-4_1 · Cited by 23 · see citing works

Chain length heterogeneity of lipopolysaccharide released from Salmonella typhimurium by ethylenediaminetetraacetic acid or polycations

Hukari, R., Helander, I. M., & Vaara, M. (1986) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1986.tb09450.x · Cited by 23 · see citing works

Magainin-2 Releases Histamine from Rat Mast Cells

Hook, W. A., Tsuji, S., & Siraganian, R. P. (1990) · Experimental Biology and Medicine · doi:10.3181/00379727-193-42989 · Cited by 22 · see citing works

Mechanism of polymyxin B-mediated lysis of lipopolysaccharide-treated erythrocytes

Carr, C., & Morrison, D. C. (1985) · Infection and Immunity · doi:10.1128/iai.49.1.84-89.1985 · Cited by 21 · see citing works

Effect of defined lipopolysaccharide core defects on resistance of Salmonella typhimurium to freezing and thawing and other stresses

Bennett, G. M., Seaver, A., & Calcott, P. H. (1981) · Applied and Environmental Microbiology · doi:10.1128/aem.42.5.843-849.1981 · Cited by 20 · see citing works

Bacteriolytic Activity of Seminalplasmin

Chitnis, S. N., Prasad, K. N., & Bhargava, P. (1987) · Microbiology · doi:10.1099/00221287-133-5-1265 · Cited by 20 · see citing works

Effect of a diazaborine derivative (Sa 84.474) on the virulence of Escherichia coli

Lam, C., Turnowsky, F., Högenauer, G., & Schütze, E. (1987) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/20.1.37 · Cited by 20 · see citing works

Antimicrobial susceptibility of Salmonella typhimurium carrying the outer membrane permeability mutation SS-B

Vaara, M. (1990) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.34.5.853 · Cited by 19 · see citing works

Does polymyxin B nonapeptide increase outer membrane permeability in antibiotic supersensitive enterobacterial mutants?

Vaara, M., Viljanen, P., Sukupolvi, S., & Vaara, T. (1985) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1985.tb01613.x · Cited by 19 · see citing works

Essential oils: Their antibacterial properties and potential applications in foods—A review

Burt, S. (2004) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2004.03.022 · Cited by 10,488 · see citing works

Antiseptics and Disinfectants: Activity, Action, and Resistance

McDonnell, G. E., & Russell, A. D. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.1.147 · Cited by 4,795 · see citing works

Molecular Basis of Bacterial Outer Membrane Permeability Revisited

Nikaido, H. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.4.593-656.2003 · Cited by 4,316 · see citing works

Effect of essential oils on pathogenic bacteria

Nazzaro, F., Fratianni, F., De Martino, L., Coppola, R., & De Feo, V. (2013) · Pharmaceuticals · doi:10.3390/ph6121451 · Cited by 2,186 · see citing works

Outer membrane permeability and antibiotic resistance

Delcour, A. H. (2008) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2008.11.005 · Cited by 1,756 · see citing works

Characterization of the action of selected essential oil components on Gram-negative bacteria

Helander, I. M., Alakomi, H.-L., Latva-Kala, K., Mattila-Sandholm, T., Pol, I., Smid, E. J., Gorris, L. G. M., & von Wright, A. (1998) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf980154m · Cited by 1,664 · see citing works

The Challenge of Efflux-Mediated Antibiotic Resistance in Gram-Negative Bacteria

Li, X.-Z., Plésiat, P., & Nikaido, H. (2015) · Clinical Microbiology Reviews · doi:10.1128/cmr.00117-14 · Cited by 1,648 · see citing works

Proteomic Analysis of the Mode of Antibacterial Action of Silver Nanoparticles

Lok, C., Ho, C., Chen, R., He, Q., Yu, W., Sun, H., Tam, P. K. H., Chiu, J., & Che, C. (2006) · Journal of Proteome Research · doi:10.1021/pr0504079 · Cited by 1,577 · see citing works

Chitosan disrupts the barrier properties of the outer membrane of Gram-negative bacteria

Helander, I. M., Nurmiaho‐Lassila, E., Ahvenainen, R. T., Rhoades, J., & Roller, S. D. (2001) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(01)00609-2 · Cited by 1,368 · see citing works

Diversity of antimicrobial peptides and their mechanisms of action

Epand, R. M., & Vogel, H. J. (1999) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00198-4 · Cited by 1,354 · see citing works

Antibacterial Activity and Mode of Action of Ferulic and Gallic Acids Against Pathogenic Bacteria

Borges, A. D. S., Ferreira, C., Saavedra, M. J., & Simões, M. V. (2013) · Microbial Drug Resistance · doi:10.1089/mdr.2012.0244 · Cited by 1,275 · see citing works

Amphipathic, α-helical antimicrobial peptides

Tossi, A., Sandri, L., & Giangaspero, A. (2000) · Biopolymers · doi:10.1002/1097-0282(2000)55:1 · Cited by 1,245 · see citing works

Bacteriocin-based strategies for food biopreservation

Gálvez, A., Abriouel, H., López, R. L., & Benomar, N. (2007) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2007.06.001 · Cited by 1,224 · see citing works

Designing surfaces that kill bacteria on contact

Tiller, J. C., Liao, C.-J., Lewis, K., & Klibanov, A. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111143098 · Cited by 1,196 · see citing works

Bacterial lipopolysaccharides and innate immunity

Alexander, C., & Rietschel, E. T. (2001) · Journal of Endotoxin Research · doi:10.1179/096805101101532675 · Cited by 1,173 · see citing works

Aminoglycosides: Activity and Resistance

Mingeot‐Leclercq, M., Glupczynski, Y., & Tulkens, P. M. (1999) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.43.4.727 · Cited by 1,105 · see citing works

Lactic Acid Permeabilizes Gram-Negative Bacteria by Disrupting the Outer Membrane

Alakomi, H.-L., Skyttä, E., Saarela, M., Mattila-Sandholm, T., Latva-Kala, K., & Helander, I. M. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.5.2001-2005.2000 · Cited by 1,093 · see citing works

Preservative Agents in Foods: Mode of Action and Microbial Resistance Mechanisms

Brul, S. (1999) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(99)00072-0 · Cited by 1,041 · see citing works

Efflux-Mediated Drug Resistance in Bacteria

Li, X.-Z., & Nikaido, H. (2009) · Drugs · doi:10.2165/11317030-000000000-00000 · Cited by 976 · see citing works

Synergism between natural products and antibiotics against infectious diseases

Hemaiswarya, S., Kruthiventi, A. K., & Doble, M. (2008) · Phytomedicine · doi:10.1016/j.phymed.2008.06.008 · Cited by 937 · see citing works

Adaptive and Mutational Resistance: Role of Porins and Efflux Pumps in Drug Resistance

Fernández, L., & Hancock, R. E. W. (2012) · Clinical Microbiology Reviews · doi:10.1128/cmr.00043-12 · Cited by 905 · see citing works

Identification and Characterization of Inhibitors of Multidrug Resistance Efflux Pumps in Pseudomonas aeruginosa : Novel Agents for Combination Therapy

Lomovskaya, O., Warren, M. S., Lee, A. Y., Galazzo, J. L., Fronko, R. M., Lee, M., Blais, J., Cho, D., Chamberland, S., Renau, T., et al. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.1.105-116.2001 · Cited by 903 · see citing works

Predictive compound accumulation rules yield a broad-spectrum antibiotic

Richter, M. F., Drown, B., Riley, A. P., Garcia, A., Shirai, T., Svec, R. L., & Hergenrother, P. J. (2017) · Nature · doi:10.1038/nature22308 · Cited by 901 · see citing works

Noble metal nanoparticles for water purification: A critical review

Pradeep, T., & Anshup (2009) · Thin Solid Films · doi:10.1016/j.tsf.2009.03.195 · Cited by 810 · see citing works

Efflux-Mediated Drug Resistance in Bacteria

Li, X.-Z., & Nikaido, H. (2004) · Drugs · doi:10.2165/00003495-200464020-00004 · Cited by 803 · see citing works

Bacteriophage Endolysins as Novel Antimicrobials

Schmelcher, M., Donovan, D. M., & Loessner, M. J. (2012) · Future Microbiology · doi:10.2217/fmb.12.97 · Cited by 786 · see citing works

Broad-specificity efflux pumps and their role in multidrug resistance of Gram-negative bacteria

Nikaido, H., & Pagès, J. (2011) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00290.x · Cited by 770 · see citing works

Antimicrobial Peptides: Mechanisms of Action and Resistance

Bechinger, B., & Gorr, S. (2016) · Journal of Dental Research · doi:10.1177/0022034516679973 · Cited by 734 · see citing works

Intrinsic antibiotic resistance: Mechanisms, origins, challenges and solutions

Cox, G., & Wright, G. D. (2013) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2013.02.009 · Cited by 721 · see citing works

Plant extracts for the control of bacterial growth: Efficacy, stability and safety issues for food application

Negi, P. S. (2012) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2012.03.006 · Cited by 687 · see citing works

Evaluation of diffusion and dilution methods to determine the antibacterial activity of plant extracts

Klančnik, A., Piskernik, S., Jeršek, B., & Možina, S. S. (2010) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2010.02.004 · Cited by 676 · see citing works

Virulence factors are released from Pseudomonas aeruginosa in association with membrane vesicles during normal growth and exposure to gentamicin: a novel mechanism of enzyme secretion

Kadurugamuwa, J. L., & Beveridge, T. J. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.14.3998-4008.1995 · Cited by 673 · see citing works

Amphipathic alpha helical antimicrobial peptides. . A systematic study of the effects of structural and physical properties on biological activity

Giangaspero, A., Sandri, L., & Tossi, A. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2001.02494.x · Cited by 650 · see citing works

PmrA–PmrB‐regulated genes necessary for 4‐aminoarabinose lipid A modification and polymyxin resistance

Gunn, J. S., Lim, K. B., Krueger, J., Kim, K., Guo, L., Hackett, M., & Miller, S. I. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.00757.x · Cited by 648 · see citing works

Plant defense peptides

García‐Olmedo, F., Molina, A., Alamillo, J. M., & Rodríguez‐Palenzuela, P. (1998) · Biopolymers · doi:10.1002/(sici)1097-0282(1998)47:6 · Cited by 521 · see citing works

In vitro antimicrobial effects and mechanism of action of selected plant essential oil combinations against four food-related microorganisms

Lv, F., Liang, H., Yuan, Q., & Li, C. (2011) · Food Research International · doi:10.1016/j.foodres.2011.07.030 · Cited by 609 · see citing works

Use of natural aroma compounds to improve shelf-life and safety of minimally processed fruits

Lanciotti, R., Gianotti, A., Patrignani, F., Belletti, N., Guerzoni, M. E., & Gardini, F. (2003) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2003.10.004 · Cited by 594 · see citing works

Small Molecule-Capped Gold Nanoparticles as Potent Antibacterial Agents That Target Gram-Negative Bacteria

Zhao, Y., Tian, Y., Cui, Y. C., Liu, W., Ma, W., & Jiang, X. (2010) · Journal of the American Chemical Society · doi:10.1021/ja1028843 · Cited by 593 · see citing works

Antimicrobial Photodynamic Therapy to Kill Gram-negative Bacteria

Sperandio, F. F., Huang, Y., & Hamblin, M. R. (2013) · Recent Patents on Anti-Infective Drug Discovery · doi:10.2174/1574891x113089990012 · Cited by 590 · see citing works

A comprehensive review on surface modified polymer membranes for biofouling mitigation

Kochkodan, V., & Hilal, N. (2014) · Desalination · doi:10.1016/j.desal.2014.09.015 · Cited by 586 · see citing works

Antimicrobial Polymeric Materials with Quaternary Ammonium and Phosphonium Salts

Xue, Y., Xiao, H., & Zhang, Y. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16023626 · Cited by 580 · see citing works

Human CAP18: a novel antimicrobial lipopolysaccharide-binding protein

Larrick, J. W., Hirata, M., Balint, R. F., Lee, J. H., Zhong, J., & Wright, S. C. (1995) · Infection and Immunity · doi:10.1128/iai.63.4.1291-1297.1995 · Cited by 570 · see citing works

Structure of bacterial lipopolysaccharides

Caroff, M., & Karibian, D. (2003) · Carbohydrate Research · doi:10.1016/j.carres.2003.07.010 · Cited by 562 · see citing works

Peptidomimetic Antibiotics Target Outer-Membrane Biogenesis in Pseudomonas aeruginosa

Srinivas, N., Jetter, P., Ueberbacher, B. J., Werneburg, M., Zerbe, K., Steinmann, J., van der Meijden, B., Bernardini, F., Lederer, A., Dias, R. L. A., et al. (2010) · Science · doi:10.1126/science.1182749 · Cited by 550 · see citing works

Permanent, nonleaching antibacterial surfaces: 1. Synthesis by atom transfer radical polymerization

Lee, S. B., Koepsel, R. R., Morley, S. W., Matyjaszewski, K., Sun, Y., & Russell, A. J. (2004) · Biomacromolecules · doi:10.1021/bm034352k · Cited by 545 · see citing works

Berry Phenolics: Antimicrobial Properties and Mechanisms of Action Against Severe Human Pathogens

Nohynek, L. J., Alakomi, H., Kähkönen, M. P., Heinonen, M., Helander, I. M., Oksman‐Caldentey, K., & Puupponen‐Pimiä, R. (2006) · Nutrition and Cancer · doi:10.1207/s15327914nc5401_4 · Cited by 541 · see citing works

Bacterial resistance to antibiotics: Active efflux and reduced uptake

Kumar, A., & Schweizer, H. P. (2005) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2005.04.004 · Cited by 537 · see citing works

Fluorometric assessment of Gram-negative bacterial permeabilization

Helander, I. M., & Mattila, T. (2000) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2000.00971.x · Cited by 532 · see citing works

Plants as sources of new antimicrobials and resistance-modifying agents

Abreu, A. C., McBain, A. J., & Simões, M. V. (2012) · Natural Product Reports · doi:10.1039/c2np20035j · Cited by 531 · see citing works

Schrödinger’s microbes: Tools for distinguishing the living from the dead in microbial ecosystems

Emerson, J., Adams, R. I., Betancourt‐Román, C. M., Brooks, B., Coil, D. A., Dahlhausen, K. E., Ganz, H. H., Hartmann, E. M., Hsu, T. Y., Justice, N. B., et al. (2017) · Microbiome · doi:10.1186/s40168-017-0285-3 · Cited by 523 · see citing works

Food applications of natural antimicrobial compounds

Lucera, A., Costa, C. S., Conte, A., & Nobile, M. A. D. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00287 · Cited by 521 · see citing works

Methods of downstream processing for the production of biodiesel from microalgae

Kim, J., Yoo, G., Lee, H., Lim, J., Kim, K., Kim, C. W., Park, M. S., & Yang, J.-W. (2013) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.04.006 · Cited by 519 · see citing works

Capsule Polysaccharide Mediates Bacterial Resistance to Antimicrobial Peptides

Campos, M. A. L., Vargas, M. A., Regueiro, V., Llompart, C. M., Albertí, S., & Bengoechea, J. A. (2004) · Infection and Immunity · doi:10.1128/iai.72.12.7107-7114.2004 · Cited by 515 · see citing works

Interactions among Strategies Associated with Bacterial Infection: Pathogenicity, Epidemicity, and Antibiotic Resistance

Martínez, J. L., & Baquero, F. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.4.647-679.2002 · Cited by 512 · see citing works

Mechanisms of bacterial biocide and antibiotic resistance

Poole, K. (2002) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.92.5s1.8.x · Cited by 508 · see citing works

Plant antimicrobial polyphenols as potential natural food preservatives

Bouarab-Chibane, L., Degraeve, P., Ferhout, H., Bouajila, J., & Oulahal, N. (2018) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.9357 · Cited by 478 · see citing works

Chelator-Induced Dispersal and Killing of Pseudomonas aeruginosa Cells in a Biofilm

Banin, E., Brady, K. M., & Greenberg, E. P. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.3.2064-2069.2006 · Cited by 473 · see citing works

Bacterial target sites for biocide action

Maillard, J. (2002) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.92.5s1.3.x · Cited by 469 · see citing works

Process-scale disruption of microorganisms

Middelberg, A. P. J. (1995) · Biotechnology Advances · doi:10.1016/0734-9750(95)02007-p · Cited by 466 · see citing works

High-Resolution Atomic Force Microscopy Studies of the Escherichia coli Outer Membrane: Structural Basis for Permeability

Amro, N. A., Kotra, L. P., Wadumesthrige, K., Bulychev, A., Mobashery, S., & Liu, G.-Y. (2000) · Langmuir · doi:10.1021/la991013x · Cited by 445 · see citing works

Genetically Engineered Phages: a Review of Advances over the Last Decade

Pires, D. P., Cleto, S., Sillankorva, S., Azeredo, J., & Lu, T. K. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00069-15 · Cited by 441 · see citing works

Engineered Endolysin-Based “Artilysins” To Combat Multidrug-Resistant Gram-Negative Pathogens

Briers, Y., Walmagh, M., Puyenbroeck, V. V., Cornelissen, A., Cenens, W., Aertsen, A., Oliveira, H., Azeredo, J., Verween, G., Pirnay, J., et al. (2014) · mBio · doi:10.1128/mbio.01379-14 · Cited by 432 · see citing works

The antimicrobial activity of microencapsulated thymol and carvacrol

Guarda, A., Rubilar, J. F., Miltz, J. W., & Galotto, M. J. (2011) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2011.02.011 · Cited by 419 · see citing works

Essential oils as potential antimicrobial agents in meat and meat products: A review

Jayasena, D. D., & Jo, C. (2013) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2013.09.002 · Cited by 402 · see citing works

PhoP-PhoQ activates transcription of pmrAB, encoding a two-component regulatory system involved in Salmonella typhimurium antimicrobial peptide resistance

Gunn, J. S., & Miller, S. I. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.23.6857-6864.1996 · Cited by 401 · see citing works

Chitosan antimicrobial and eliciting properties for pest control in agriculture: a review

Xing, K., Zhu, X. F., Peng, X., & Qin, S. (2014) · Agronomy for Sustainable Development · doi:10.1007/s13593-014-0252-3 · Cited by 400 · see citing works

Antimicrobial peptide resistance mediates resilience of prominent gut commensals during inflammation

Cullen, T. W., Schofield, W. B., Barry, N. A., Putnam, E. E., Rundell, E. A., Trent, M. S., Degnan, P. H., Booth, C. J., Yu, H., & Goodman, A. L. (2015) · Science · doi:10.1126/science.1260580 · Cited by 395 · see citing works

Bacterial resistance to disinfectants: present knowledge and future problems

Russell, A. D. (1999) · Journal of Hospital Infection · doi:10.1016/s0195-6701(99)90066-x · Cited by 393 · see citing works

Effect of Divalent Cation Removal on the Structure of Gram-Negative Bacterial Outer Membrane Models

Clifton, L. A., Skoda, M. W. A., Brun, A. P. L., Ciesielski, F., Kuzmenko, I., Holt, S. A., & Lakey, J. H. (2014) · Langmuir · doi:10.1021/la504407v · Cited by 391 · see citing works

Endolysins as Antimicrobials

Nelson, D. C., Schmelcher, M., Rodríguez‐Rubio, L., Klumpp, J., Pritchard, D. G., Dong, S., & Donovan, D. M. (2012) · Advances in virus research · doi:10.1016/b978-0-12-394438-2.00007-4 · Cited by 375 · see citing works

Microbial fuel cell (MFC) power performance improvement through enhanced microbial electrogenicity

Li, M., Zhou, M., Tian, X., Tan, C., McDaniel, C. T., Hassett, D. J., & Gu, T. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.04.010 · Cited by 368 · see citing works

Reassessing the Host Defense Peptide Landscape

Haney, E. F., Straus, S. K., & Hancock, R. E. W. (2019) · Frontiers in Chemistry · doi:10.3389/fchem.2019.00043 · Cited by 362 · see citing works

The Antimicrobial Mechanism of Action of Epsilon-Poly- l -Lysine

Hyldgaard, M., Mygind, T., Vad, B. S., Stenvang, M., Otzen, D. E., & Meyer, R. L. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.02204-14 · Cited by 361 · see citing works

Antibiotic resistance breakers: current approaches and future directions

Laws, M., Shaaban, A., & Rahman, K. M. (2019) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuz014 · Cited by 358 · see citing works

Photodynamic Therapy Targeted to Pathogens

Demidova, T. N., & Hamblin, M. R. (2004) · International Journal of Immunopathology and Pharmacology · doi:10.1177/039463200401700304 · Cited by 357 · see citing works

Interaction of antimicrobial peptides with biological and model membranes: structural and charge requirements for activity

Sitaram, N., & Nagaraj, R. (1999) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00199-6 · Cited by 353 · see citing works

A two‐component regulatory system playing a critical role in plant pathogens and endosymbionts is present in Brucella abortus and controls cell invasion and virulence

Sola‐Landa, A., Pizarro‐Cerdá, J., Grilló, M. J., Moreno, E., Moriyón, I., Blasco, J. M., Gorvel, J., & López‐Goñi, I. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.00913.x · Cited by 348 · see citing works

Transition metal catalyzed sulfite auto-oxidation systems for oxidative decontamination in waters: A state-of-the-art minireview

Zhou, D., Chen, L., Li, J., & Wu, F. (2018) · Chemical Engineering Journal · doi:10.1016/j.cej.2018.04.016 · Cited by 348 · see citing works

Bacteriophage Endolysins as a Novel Class of Antibacterial Agents

Borysowski, J., Weber‐Dąbrowska, B., & Górski, A. (2006) · Experimental Biology and Medicine · doi:10.1177/153537020623100402 · Cited by 339 · see citing works

Natural Polymer-Based Antimicrobial Hydrogels without Synthetic Antibiotics as Wound Dressings

Zhong, Y., Xiao, H., Seidi, F., & Jin, Y. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c00760 · Cited by 338 · see citing works

Defensins

Ganz, T., & Lehrer, R. I. (1994) · Current Opinion in Immunology · doi:10.1016/0952-7915(94)90145-7 · Cited by 337 · see citing works

Pentamidine sensitizes Gram-negative pathogens to antibiotics and overcomes acquired colistin resistance

Stokes, J. M., MacNair, C. R., Ilyas, B., French, S., Côté, J., Bouwman, C., Farha, M. A., Sieron, A. O., Whitfield, C., Coombes, B. K., et al. (2017) · Nature Microbiology · doi:10.1038/nmicrobiol.2017.28 · Cited by 335 · see citing works

Membrane Damage and Microbial Inactivation by Chlorine in the Absence and Presence of a Chlorine-Demanding Substrate

Virto, R., Mañas, P., Álvarez, I., Condón, S., & Raso, J. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.9.5022-5028.2005 · Cited by 332 · see citing works

Metallo-β-Lactamases: Structure, Function, Epidemiology, Treatment Options, and the Development Pipeline

Boyd, S. E., Livermore, D. M., Hooper, D. C., & Hope, W. W. (2020) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00397-20 · Cited by 332 · see citing works

Potential virulence factors of Proteus bacilli

Różalski, A., Sidorczyk, Z., & KOTELKO, K. (1997) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.61.1.65-89.1997 · Cited by 331 · see citing works

An Inner Membrane Enzyme in Salmonellaand Escherichia coli That Transfers 4-Amino-4-deoxy-l-arabinose to Lipid A

Trent, M. S., Ribeiro, A. A., Lin, S., Cotter, R. J., & Raetz, C. R. H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m106961200 · Cited by 328 · see citing works

Mechanisms of action of antibacterial biocides

Denyer, S. P. (1995) · International Biodeterioration & Biodegradation · doi:10.1016/0964-8305(96)00015-7 · Cited by 327 · see citing works

Predicting the Bioavailability of Metals and Metal Complexes: Critical Review of the Biotic Ligand Model

Slaveykova, V. I., & Wilkinson, K. J. (2005) · Environmental Chemistry · doi:10.1071/en04076 · Cited by 326 · see citing works

Antibiotic Adjuvants: Diverse Strategies for Controlling Drug‐Resistant Pathogens

Gill, E. E., Franco, O. L., & Hancock, R. E. W. (2014) · Chemical Biology & Drug Design · doi:10.1111/cbdd.12478 · Cited by 322 · see citing works

Antibacterial mechanism of chitosan microspheres in a solid dispersing system against E. coli

Kong, M., Chen, X. G., Liu, C., Liu, C., Meng, X., & Yu, L. (2008) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2008.04.003 · Cited by 321 · see citing works

Preventing drug access to targets: cell surface permeability barriers and active efflux in bacteria

Nikaido, H. (2001) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.2000.0247 · Cited by 319 · see citing works

Insect defensin, an inducible antibacterial peptide, forms voltage-dependent channels in Micrococcus luteus.

Cociancich, S., Ghazi, A., Hétru, C., Hoffmann, J. A., & Letellìer, L. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)36505-6 · Cited by 318 · see citing works

The Structure of Human β-Defensin-2 Shows Evidence of Higher Order Oligomerization

Hoover, D. M., Rajashankar, K. R., Blumenthal, R., Puri, A., Oppenheim, J. J., Chertov, O., & Lubkowski, J. T. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006098200 · Cited by 318 · see citing works

Immobilized N‐alkylated polyethylenimine avidly kills bacteria by rupturing cell membranes with no resistance developed

Milović, N. M., Wang, J., Lewis, K., & Klibanov, A. M. (2005) · Biotechnology and Bioengineering · doi:10.1002/bit.20454 · Cited by 316 · see citing works

The antimicrobial effect of oregano essential oil, nisin and their combination against Salmonella Enteritidis in minced sheep meat during refrigerated storage

Govaris, A., Σολωμάκος, Ν., Pexara, A., & Chatzopoulou, P. S. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.12.017 · Cited by 314 · see citing works

Essential oils as alternatives to antibiotics in swine production

Omonijo, F. A., Ni, L., Gong, J., Wang, Q., Lahaye, L., & Yang, C. (2017) · Animal nutrition · doi:10.1016/j.aninu.2017.09.001 · Cited by 313 · see citing works

Capsule polysaccharide is a bacterial decoy for antimicrobial peptides

Llobet, E., Tomás, J. M., & Bengoechea, J. A. (2008) · Microbiology · doi:10.1099/mic.0.2008/022301-0 · Cited by 311 · see citing works

Potential of lactic acid bacteria and novel antimicrobials against Gram-negative bacteria

Helander, I. M., von Wright, A., & Mattila-Sandholm, T. (1997) · Trends in Food Science & Technology · doi:10.1016/s0924-2244(97)01030-3 · Cited by 306 · see citing works

The Antiviral Activity of Chitosan (Review)

Chirkov, S. N. (2002) · Applied Biochemistry and Microbiology · doi:10.1023/a:1013206517442 · Cited by 302 · see citing works

Antibacterial peptides isolated from insects

Ötvös, L. (2000) · Journal of Peptide Science · doi:10.1002/1099-1387(200010)6:10 · Cited by 296 · see citing works

Polymyxin B octapeptide and polymyxin B heptapeptide are potent outer membrane permeability-increasing agents.

Kimura, Y., Matsunaga, H., & Vaara, M. (1992) · The Journal of Antibiotics · doi:10.7164/antibiotics.45.742 · Cited by 53 · see citing works

Polycations as outer membrane-disorganizing agents

Vaara, M., & Vaara, T. (1983) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.24.1.114 · Cited by 252 · see citing works

Outer membrane phospholipase is not the mediator in the bactericidal or outer membrane permeability-in-creasing actions of polycations

(1983) · FEMS Microbiology Letters · doi:10.1016/0378-1097(83)90213-6

Increases in permeability of Escherichia coli outer membrane induced by polycations

Katsu, T., Yoshimura, S., & Fujita, Y. (1984) · FEBS Letters · doi:10.1016/0014-5793(84)80067-8 · Cited by 17 · see citing works

Interaction of Aminoglycosides and Ciprofloxacin with Bacterial Membranes

Dalhoff, A. (1985) · Springer eBooks · doi:10.1007/978-3-642-70748-3_2 · Cited by 11 · see citing works