DELAYED ANTIBIOTIC-INDUCED LYSIS OF ESCHERICHIA-COLI INVITRO IS CORRELATED WITH ENHANCEMENT OF LPS RELEASE

被引:49
作者
VANDENBERG, C
DENEELING, AJ
SCHOT, CS
HUSTINX, WNM
WEMER, J
DEWILDT, DJ
机构
[1] NATL INST PUBL HLTH & ENVIRONM PROTECT,CHEMOTHERAPY LAB,3720 BA BILTHOVEN,NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT,NATL POISON CTR,BILTHOVEN,NETHERLANDS
[3] UNIV UTRECHT,RUDOLF MAGNUS INST,UTRECHT,NETHERLANDS
关键词
D O I
10.3109/00365549209054648
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A kinetic turbidimetric Limulus amebocyte lysate (LAL) assay was used to study the effects of gentamicin, amoxycillin and ciprofloxacin (16 X MIC) upon release of lipopolysaccharide at different stages of a growing Escherichia coli 055:B5:H culture in vitro. In this model a linear correlation was present between the logarithms of colony counts and free LAL activities. Untreated E. coli grew from log values of 4.9 +/- 0.15 (low inoculum) and 6.8 +/- 0.08 cfu/ml (high inoculum) at t = 0 to 8.9 +/- 0.05 and 9.1 +/- 0.13 cfu/ml at t = 6 h, respectively. The log values of basal free LAL activities at low and high inoculum sizes were 1.9 +/- 0.07 and 3.3 +/- 0.14 endotoxin units/ml, increasing 2100- and 69-fold, respectively during a 6-h growth. Amoxycillin-induced lysis was not significantly associated with an increase in tree LAL activity. Efficacy of bacterial killing by gentamicin was high, but free LAL activity increased only 3.2- and 7.7-fold at the low and high inoculum experiments, respectively. Ciprofloxacin induced cell filamentation during the experiments. At low and high inoculum conditions exposure to ciprofloxacin induced a 43- and 68-fold increase in free LAL activities, respectively. Our data indicate that (a) LPS is released as long as E. coli remain structurally intact; (b) LPS release is enhanced when bacterial biomass increases; and (c) are taken as evidence against the concept of lysis-correlated LPS release.
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页码:619 / 627
页数:9
相关论文
共 30 条
[11]   ENDOTOXEMIA ASSOCIATED WITH JARISCH-HERXHEIMER REACTION [J].
GELFAND, JA ;
ELIN, RJ ;
BERRY, FW ;
FRANK, MM .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (04) :211-213
[12]  
GOTO H, 1980, JPN J EXP MED, V50, P35
[13]  
HOPKIN D A B, 1978, Lancet, V2, P1193
[14]  
JOHNSTON CA, 1984, T ASSOC AM PHYSICIAN, V97, P172
[15]  
LEVIN J, 1968, THROMB DIATH HAEMOST, V19, P186
[16]  
Luderitz O., 1982, PHARMACOL THERAPEUT, V15, P383
[17]  
NOVITSKY TJ, 1989, PHARMEUROPA, V1, P9
[18]   THE BENEFICIAL-EFFECTS OF EARLY DEXAMETHASONE ADMINISTRATION IN INFANTS AND CHILDREN WITH BACTERIAL-MENINGITIS [J].
ODIO, CM ;
FAINGEZICHT, I ;
PARIS, M ;
NASSAR, M ;
BALTODANO, A ;
ROGERS, J ;
SAEZLLORENS, X ;
OLSEN, KD ;
MCCRACKEN, GH .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (22) :1525-1531
[19]   PHYSICAL-PROPERTIES OF SHORT-O-ANTIGEN-CONTAINING AND LONG-O-ANTIGEN-CONTAINING FRACTIONS OF LIPOPOLYSACCHARIDE FROM ESCHERICHIA-COLI 0111-B4 [J].
PETERSON, AA ;
HAUG, A ;
MCGROARTY, EJ .
JOURNAL OF BACTERIOLOGY, 1986, 165 (01) :116-122
[20]   KINETICS OF ENDOTOXIN RELEASE DURING ANTIBIOTIC-THERAPY FOR EXPERIMENTAL GRAM-NEGATIVE BACTERIAL SEPSIS [J].
SHENEP, JL ;
MOGAN, KA .
JOURNAL OF INFECTIOUS DISEASES, 1984, 150 (03) :380-388