Quinolone antibiotics induce shiga toxin-encoding bacteriophages, toxin production, and death in mice

被引:390
作者
Zhang, XP [1 ]
McDaniel, AD [1 ]
Wolf, LE [1 ]
Keusch, GT [1 ]
Waldor, MK [1 ]
Acheson, DWK [1 ]
机构
[1] New England Med Ctr, Tupper Res Inst, Div Geog Med & Infect Dis, Boston, MA 02111 USA
关键词
D O I
10.1086/315239
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Shiga toxin-producing Escherichia coli (STEC) cause significant disease; treatment is supportive and antibiotic use is controversial. Ciprofloxacin but not fosfomycin causes Shiga toxin-encoding bacteriophage induction and enhanced Shiga toxin (Stx) production from E. coli O157:H7 in vitro. The potential clinical relevance of this was examined in mice colonized with E. coli O157:H7 and given either ciprofloxacin or fosfomycin, Both antibiotics caused a reduction in fecal STEC, However, animals treated with ciprofloxacin had a marked increase in free fecal Stx, associated with death in two-thirds of the mice, whereas fosfomycin did not. Experiments that used a kanamycin-marked Stx2 prophage demonstrated that ciprofloxacin, but not fosfomycin, caused enhanced intraintestinal transfer of Stx2 prophage from one E. coli to another. These observations suggest that treatment of human STEC infection with bacteriophage-inducing antibiotics, such as fluoroquinolones, may have significant adverse clinical consequences and that fluoroquinolone antibiotics may enhance the movement of virulence factors in vivo.
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收藏
页码:664 / 670
页数:7
相关论文
共 33 条
  • [31] MOUSE MODEL FOR COLONIZATION AND DISEASE CAUSED BY ENTEROHEMORRHAGIC ESCHERICHIA-COLI O157-H7
    WADOLKOWSKI, EA
    BURRIS, JA
    OBRIEN, AD
    [J]. INFECTION AND IMMUNITY, 1990, 58 (08) : 2438 - 2445
  • [32] Bacteriophage biology and bacterial virulence
    Waldor, MK
    [J]. TRENDS IN MICROBIOLOGY, 1998, 6 (08) : 295 - 297
  • [33] EFFECT OF SUBINHIBITORY CONCENTRATIONS OF ANTIBIOTICS ON EXTRACELLULAR SHIGA-LIKE TOXIN-I
    WALTERSPIEL, JN
    ASHKENAZI, S
    MORROW, AL
    CLEARY, TG
    [J]. INFECTION, 1992, 20 (01) : 25 - 29