In vitro activity of PR-39, a proline-arginine-rich peptide, against susceptible and multi-drug-resistant Mycobacterium tuberculosis.
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S. Hoffner | M. Andersson | C. Linde | M. Andersson | C M Linde | S E Hoffner | E Refai | M Andersson | E. Refai
[1] T. Ganz,et al. Monocyte-chemotactic activity of defensins from human neutrophils. , 1989, The Journal of clinical investigation.
[2] R. Gallo,et al. PR-39, a Syndecan-inducing Antimicrobial Peptide, Binds and Affects p130Cas * , 1998, The Journal of Biological Chemistry.
[3] H. Kalbacher,et al. Inactivation of the dlt Operon inStaphylococcus aureus Confers Sensitivity to Defensins, Protegrins, and Other Antimicrobial Peptides* , 1999, The Journal of Biological Chemistry.
[4] W. Shafer,et al. Modulation of Neisseria gonorrhoeae susceptibility to vertebrate antibacterial peptides due to a member of the resistance/nodulation/division efflux pump family. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[5] D. S. McVey,et al. Antibacterial activity of a synthetic peptide (PR-26) derived from PR-39, a proline-arginine-rich neutrophil antimicrobial peptide , 1996, Antimicrobial agents and chemotherapy.
[6] M. Denis. Human neutrophils, activated with cytokines or not, do not kill virulent Mycobacterium tuberculosis. , 1991, The Journal of infectious diseases.
[7] P. Spagnuolo,et al. Evidence for activation of a respiratory burst in the interaction of human neutrophils with Mycobacterium tuberculosis , 1987, Infection and immunity.
[8] C. Ross,et al. Chemoattractant properties of PR‐39, a neutrophil antibacterial peptide , 1997, Journal of leukocyte biology.
[9] G Middlebrook,et al. Automatable radiometric detection of growth of Mycobacterium tuberculosis in selective media. , 1977, The American review of respiratory disease.
[10] B. Andersen,et al. Killing of Mycobacterium tuberculosis by neutrophils: a nonoxidative process. , 1990, The Journal of infectious diseases.
[11] T. Ganz. Extracellular release of antimicrobial defensins by human polymorphonuclear leukocytes , 1987, Infection and immunity.
[12] M. Iseman,et al. Determination of ansamycin MICs for Mycobacterium avium complex in liquid medium by radiometric and conventional methods , 1985, Antimicrobial Agents and Chemotherapy.
[13] T. Ganz,et al. Activity of defensins from human neutrophilic granulocytes against Mycobacterium avium-Mycobacterium intracellulare , 1992, Infection and immunity.
[14] M. Iseman,et al. Ethambutol MICs and MBCs for Mycobacterium avium complex and Mycobacterium tuberculosis , 1986, Antimicrobial Agents and Chemotherapy.
[15] V. Mutt,et al. Amino acid sequence of PR-39. Isolation from pig intestine of a new member of the family of proline-arginine-rich antibacterial peptides. , 1991, European journal of biochemistry.
[16] R. B. Merrifield,et al. Synthesis and antibacterial action of cecropin and proline-arginine-rich peptides from pig intestine. , 2009, The journal of peptide research : official journal of the American Peptide Society.
[17] Samuel I. Miller,et al. Lipid A Acylation and Bacterial Resistance against Vertebrate Antimicrobial Peptides , 1998, Cell.
[18] J. Johansson,et al. Secondary structure and membrane interaction of PR-39, a Pro+Arg-rich antibacterial peptide. , 1994, European journal of biochemistry.
[19] R. Appelberg,et al. Neutrophils Play a Protective Nonphagocytic Role in Systemic Mycobacterium tuberculosis Infection of Mice , 2000, Infection and Immunity.
[20] C. Ross,et al. PR-39, a proline-rich antibacterial peptide that inhibits phagocyte NADPH oxidase activity by binding to Src homology 3 domains of p47 phox. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[21] D. Snider,et al. Rapid drug-susceptibility testing of Mycobacterium tuberculosis. , 1981, The American review of respiratory disease.
[22] E. Böttger,et al. Correlation of molecular resistance mechanisms and phenotypic resistance levels in streptomycin-resistant Mycobacterium tuberculosis , 1996, Antimicrobial agents and chemotherapy.
[23] A. Rao,et al. In vitro activity of the antimicrobial peptides human and rabbit defensins and porcine leukocyte protegrin against Mycobacterium tuberculosis , 1996, Infection and immunity.
[24] J. Ernst,et al. Roles of calcium and annexins in phagocytosis and elimination of an attenuated strain of Mycobacterium tuberculosis in human neutrophils. , 1998, Microbial pathogenesis.
[25] C. Ross,et al. Salmonella infection increases porcine antibacterial peptide concentrations in serum , 1997, Clinical and diagnostic laboratory immunology.
[26] H. Jörnvall,et al. Antibacterial components in bronchoalveolar lavage fluid from healthy individuals and sarcoidosis patients. , 1999, American journal of respiratory and critical care medicine.
[27] V. Mutt,et al. Spleen antibacterial peptides: high levels of PR-39 and presence of two forms of NK-lysin , 1999, Cellular and Molecular Life Sciences CMLS.
[28] B. Andersen,et al. Capacity of human neutrophils to kill Mycobacterium tuberculosis. , 1987, The Journal of infectious diseases.
[29] G. Khuller,et al. Biochemical interaction of human neutrophil peptide-1 with Mycobacterium tuberculosis H37Ra , 1999, Archives of Microbiology.
[30] H. G. Boman,et al. Mechanisms of action on Escherichia coli of cecropin P1 and PR-39, two antibacterial peptides from pig intestine , 1993, Infection and immunity.
[31] M. Klagsbrun,et al. Syndecans, cell surface heparan sulfate proteoglycans, are induced by a proline-rich antimicrobial peptide from wounds. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[32] D. Andreu,et al. Animal antimicrobial peptides: an overview. , 1998, Biopolymers.
[33] S. Hoffner,et al. In-vitro activity of fluorinated quinolones and macrolides against drug-resistant Mycobacterium tuberculosis. , 1997, The Journal of antimicrobial chemotherapy.
[34] H. G. Boman,et al. Peptide antibiotics and their role in innate immunity. , 1995, Annual review of immunology.