Vranes J
Medical School, University of Zagreb, Croatia.
Chemotherapy. 1996 May-Jun;42(3):177-85. doi: 10.1159/000239439.
The effect of subinhibitory concentrations (sub-MICs) of ceftazidime, ciprofloxacin, and azithromycin on the hemagglutination (HA) and adherence ability of 29 P-fimbriated Escherichia coli strains to the buffalo green monkey kidney (BGMK) cell line was investigated. Comparisons were made between the values of HA titer before and those after exposure of strains to 1/2, 1/4, 1/8, 1/16 and 1/32 MIC of antibiotics, as well as between the number of bacteria attached to the BGMK cells before and the number after their exposure to the same concentrations of antibiotics. Azithromycin at concentrations of 1/2 and 1/4 MIC damaged the HA capacity of the studied strains, while ceftazidime at concentrations of 1/2, 1/4, 1/8 and 1/16 MIC and ciprofloxacin at concentrations of 1/2 and 1/4 MIC increased the HA capacity of P-fimbriated E. coli. All three antibiotics decreased the adhesive capacity of E. coli to the BGMK cells. Comparing the number of adhered bacteria before and after exposure to sub-MICs of antibiotics, statistically significant differences were determined (p < 0.01) after exposure of the strains to all the concentrations of ceftazidime used after exposure to 1/2, 1/4, 1/8 and 1/16 MIC of ciprofloxacin, and after exposure to 1/2, 1/4 and 1/8 MIC of azithromycin. Filaments formed by sub-MICs of ceftazidime and ciprofloxacin in a static experimental system caused HA, but in an experimental system imitating in vivo conditions, the strains adhered poorly to the cells.
研究了头孢他啶、环丙沙星和阿奇霉素的亚抑菌浓度(亚最小抑菌浓度,sub-MICs)对29株产P菌毛大肠杆菌血凝(HA)及黏附于水牛绿猴肾(BGMK)细胞系能力的影响。比较了菌株暴露于抗生素1/2、1/4、1/8、1/16和1/32 MIC前后的HA效价,以及菌株暴露于相同浓度抗生素前后黏附于BGMK细胞的细菌数量。浓度为1/2和1/4 MIC的阿奇霉素破坏了所研究菌株的HA能力,而浓度为1/2、1/4、1/8和1/16 MIC的头孢他啶以及浓度为1/2和1/4 MIC的环丙沙星提高了产P菌毛大肠杆菌的HA能力。这三种抗生素均降低了大肠杆菌对BGMK细胞的黏附能力。比较暴露于抗生素亚MIC前后黏附细菌的数量,在菌株暴露于所用的所有浓度的头孢他啶后、暴露于1/2、1/4、1/8和1/16 MIC的环丙沙星后以及暴露于1/2、1/4和1/8 MIC的阿奇霉素后,均确定有统计学显著差异(p < 0.01)。在静态实验系统中,头孢他啶和环丙沙星的亚MIC形成的丝状物引起HA,但在模拟体内条件的实验系统中,菌株对细胞的黏附性较差。