POTENTIATION OF AMINOGLYCOSIDE INHIBITION AND REDUCTION OF CAPSULAR POLYSACCHARIDE PRODUCTION IN KLEBSIELLA-PNEUMONIAE BY SODIUM-SALICYLATE

被引:15
作者
DOMENICO, P [1 ]
HOPKINS, T [1 ]
SCHOCH, PE [1 ]
CUNHA, BA [1 ]
机构
[1] SUNY STONY BROOK, SCH MED, STONY BROOK, NY 11794 USA
关键词
D O I
10.1093/jac/25.6.903
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
This study determined the effects of sodium salicylate combined with several aminoglycoside antibiotics on the growth and capsular polysaccharide (CPS) production of Klebsiella pneumoniae. Salicylate significantly enhanced the inhibitory effect of all aminoglycoside antibiotics against all bacterial strains tested. The production of CPS was decreased by 62-86% when 2.5 mw salicylate was used. Amikacin combined with salicylate reduced CPS only slightly more than salicylate alone. The chelating agents, ethylenediamine tetra-acetic acid and ethylene bis tetraacetic acid, which have similar CPS-reducing properties, did not enhance the inhibitory effect of amikacin. Noncapsular variants of strains of K. pneumoniae were as susceptible to amikacin as the fully encapsulated strains, with or without salicylate present. Therefore, the combination of salicylate and the aminoglycosides acted synergistically to inhibit K. pneumoniae growth, but the increase in antibiotic sensitivity with salicylate was not a result of a reduction in CPS production. The use of salicylate in maximum therapeutic doses may enhance the activity of aminoglycosides sufficiently to allow the dose of aminoglycoside to be reduced when infections due to K. pneumoniae are treated. © 1990 The British Society for Antimicrobial Chemotherapy.
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收藏
页码:903 / 914
页数:12
相关论文
共 27 条
[1]  
ANAND N, 1960, NATURE, V185, P22, DOI [10.1038/185022a0, 10.1038/185023a0]
[2]   NEW METHOD FOR QUANTITATIVE-DETERMINATION OF URONIC ACIDS [J].
BLUMENKR.N ;
ASBOEHAN.G .
ANALYTICAL BIOCHEMISTRY, 1973, 54 (02) :484-489
[3]   THE ETIOLOGY AND PERSISTENCE OF CRYPTIC BACTERIAL-INFECTIONS - A HYPOTHESIS [J].
COSTERTON, JW .
REVIEWS OF INFECTIOUS DISEASES, 1984, 6 :S608-S616
[4]   R-FACTOR RESPONSIBLE FOR AN OUTBREAK OF MULTIPLY ANTIBIOTIC-RESISTANT KLEBSIELLA-PNEUMONIAE [J].
COURTNEY, MA ;
MILLER, JR ;
SUMMERSGILL, J ;
MELO, J ;
RAFF, MJ ;
STREIPS, UN .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1980, 18 (06) :926-929
[6]   ROLE OF THE MEMBRANE-POTENTIAL IN BACTERIAL-RESISTANCE TO AMINOGLYCOSIDE ANTIBIOTICS [J].
DAMPER, PD ;
EPSTEIN, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 20 (06) :803-808
[7]   LOBAR PNEUMONIA IN RATS PRODUCED BY CLINICAL ISOLATES OF KLEBSIELLA-PNEUMONIAE [J].
DOMENICO, P ;
JOHANSON, WG ;
STRAUS, DC .
INFECTION AND IMMUNITY, 1982, 37 (01) :327-335
[8]   REDUCTION OF CAPSULAR POLYSACCHARIDE PRODUCTION IN KLEBSIELLA-PNEUMONIAE BY SODIUM-SALICYLATE [J].
DOMENICO, P ;
SCHWARTZ, S ;
CUNHA, BA .
INFECTION AND IMMUNITY, 1989, 57 (12) :3778-3782
[9]   EXTRACELLULAR POLYSACCHARIDE PRODUCTION BY KLEBSIELLA-PNEUMONIAE AND ITS RELATIONSHIP TO VIRULENCE [J].
DOMENICO, P ;
DIEDRICH, DL ;
STRAUS, DC .
CANADIAN JOURNAL OF MICROBIOLOGY, 1985, 31 (05) :472-478
[10]   QUANTITATIVE EXTRACTION AND PURIFICATION OF EXOPOLYSACCHARIDES FROM KLEBSIELLA-PNEUMONIAE [J].
DOMENICO, P ;
DIEDRICH, DL ;
CUNHA, BA .
JOURNAL OF MICROBIOLOGICAL METHODS, 1989, 9 (03) :211-219