ANTIBIOTIC-INDUCED RELEASE OF ENDOTOXIN IN CHRONICALLY BACTERIURIC PATIENTS

被引:39
作者
HURLEY, JC
LOUIS, WJ
TOSOLINI, FA
CARLIN, JB
机构
[1] AUSTIN HOSP,DEPT CLIN PHARMACOL & THERAPEUT,HEIDELBERG,VIC 3084,AUSTRALIA
[2] AUSTIN HOSP,DEPT MED MICROBIOL,HEIDELBERG,VIC 3084,AUSTRALIA
[3] ROYAL CHILDRENS HOSP,DEPT CLIN EPIDEMIOL & BIOSTAT,PARKVILLE,VIC 3052,AUSTRALIA
关键词
D O I
10.1128/AAC.35.11.2388
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A novel in vivo model for the study of antibiotic-induced release of endotoxin from gram-negative bacteria is described. The model uses the chronically colonized urinary tracts of patients whose spinal cords have been injured. At baseline, the organisms were present in the range of 1 x 10(3) to 2 x 10(7) CFU/ml, and the concentration of endotoxin ranged from 2 x 10(-1) to 1 x 10(3) ng/ml in 44 studies. In 10 control studies, the concentration of endotoxin and the numbers of viable gram-negative bacteria over time changed by an average of less than 0.15 log10 units from the baseline values. At 2 h after antibiotic administration, the average decrease in CFU was 0.93 log10 units, and because antibiotics cause the release of endotoxin, an average increase in endotoxin concentration of 0.59 log10 units was noted in 21 studies with susceptible bacteria. Similar changes in response to antibiotic exposure were seen in studies with susceptible Pseudomonas bacteria in comparison with those seen in studies with susceptible members of the family Enterobacteriaceae. These results provide evidence that this novel model may be useful for comparing the effects of antibiotics with different modes of action, both as single agents and in combination, on the concentration of endotoxin in relation to changes in the numbers of bacteria, under conditions of bacterial replication and antibiotic exposure more closely resembling those found in vivo than is possible in other models.
引用
收藏
页码:2388 / 2394
页数:7
相关论文
共 42 条
[1]  
ANDERSEN BM, 1980, ACTA PATH MICRO IM B, V88, P231
[2]  
CATTELL W R, 1970, British Journal of Urology, V42, P290
[3]   RELEASE OF ENDOTOXIN FROM BACTERIA EXPOSED TO CIPROFLOXACIN AND ITS PREVENTION WITH POLYMYXIN-B [J].
COHEN, J ;
MCCONNELL, JS .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1986, 5 (01) :13-17
[4]   EFFECT OF GROWTH RATE ON COMPOSITION OF S ENTERITIDIS CELL WALLS [J].
COLLINS, FM .
AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1964, 42 (02) :255-&
[5]   COMBINED NEPHROTOXIC EFFECTS OF CYCLOSPORINE AND ENDOTOXIN [J].
COSIO, FG ;
INNES, JT ;
NAHMAN, NS ;
MAHAN, JD ;
FERGUSON, RM .
TRANSPLANTATION, 1987, 44 (03) :425-428
[6]   EVALUATION OF THE BACTERICIDAL ACTIVITY OF BETA-LACTAM ANTIBIOTICS ON SLOWLY GROWING BACTERIA CULTURED IN THE CHEMOSTAT [J].
COZENS, RM ;
TUOMANEN, E ;
TOSCH, W ;
ZAK, O ;
SUTER, J ;
TOMASZ, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (05) :797-802
[7]   THE LETHAL ACTION OF AMINOGLYCOSIDES [J].
DAVIS, BD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 22 (01) :1-3
[8]   RELEASE OF ENDOTOXIC LIPOPOLYSACCHARIDE BY SENSITIVE STRAINS OF ESCHERICHIA-COLI SUBMITTED TO THE BACTERICIDAL ACTION OF HUMAN-SERUM [J].
DEMONTY, J ;
DEGRAEVE, J .
MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 1982, 170 (04) :265-277
[9]   IMMUNOLABELING OF LIPOPOLYSACCHARIDE LIBERATED FROM ANTIBIOTIC-TREATED ESCHERICHIA-COLI [J].
FLYNN, PM ;
SHENEP, JL ;
GIGLIOTTI, F ;
DAVIS, DS ;
HILDNER, WK .
INFECTION AND IMMUNITY, 1988, 56 (10) :2760-2762
[10]  
FRIERER J, 1974, J IMMUNOL, V112, P2184