Hentges D J, Stein A J, Casey S W, Que J U
Infect Immun. 1985 Jan;47(1):118-22. doi: 10.1128/iai.47.1.118-122.1985.
Swiss white mice were given ampicillin, clindamycin, kanamycin, metronidazole, or streptomycin in drinking water for a period of 3 weeks. One week after the initiation of antibiotic administration, the treated mice and untreated control mice were challenged orally with approximately 10(8) viable, streptomycin-resistant (SR) Pseudomonas aeruginosa isolates. All five of the antibiotics decreased the resistance of the mice to intestinal colonization with SR P. aeruginosa, as reflected by an increased fecal carriage of the organism and an increase in population levels of SR P. aeruginosa in feces as compared with untreated controls. Metronidazole was least effective in this regard. The antibiotics lowered the dose of SR P. aeruginosa that resulted in implantation in 50% of the mice ID50 to various degrees. Administration of streptomycin, the most effective antibiotic, caused a 10,000-fold decrease in ID50 as compared with untreated controls. Oral inoculation of approximately 10(8) organisms of SR P. aeruginosa resulted in translocation of the organism to the mesenteric lymph nodes, spleens, or livers of 13 or 17 streptomycin-treated mice, 1 of 20 clindamycin-treated mice, and 1 of 14 metronidazole-treated mice. Translocation was not observed, however, in ampicillin- or kanamycin-treated animals. Antibiotic activity was detected in the cecal contents of streptomycin-, kanamycin, and clindamycin-treated mice but not in the cecal contents of ampicillin- or metronidazole-treated animals.
给瑞士小白鼠饮用含氨苄青霉素、克林霉素、卡那霉素、甲硝唑或链霉素的水,持续3周。在开始给予抗生素1周后,给经处理的小鼠和未处理的对照小鼠经口接种约10⁸ 株有活力的、耐链霉素的铜绿假单胞菌分离株。所有这五种抗生素均降低了小鼠对耐链霉素铜绿假单胞菌肠道定植的抵抗力,这表现为该菌的粪便携带量增加,且与未处理的对照相比,粪便中耐链霉素铜绿假单胞菌的种群水平升高。在这方面,甲硝唑效果最差。这些抗生素不同程度地降低了导致50%小鼠定植的耐链霉素铜绿假单胞菌的剂量(ID50)。最有效的抗生素链霉素的使用使ID50与未处理的对照相比降低了10000倍。经口接种约10⁸ 株耐链霉素铜绿假单胞菌导致该菌转移至13只或17只经链霉素处理的小鼠、20只经克林霉素处理的小鼠中的1只以及14只经甲硝唑处理的小鼠中的1只的肠系膜淋巴结、脾脏或肝脏。然而,在经氨苄青霉素或卡那霉素处理的动物中未观察到转移现象。在经链霉素、卡那霉素和克林霉素处理的小鼠盲肠内容物中检测到了抗生素活性,但在经氨苄青霉素或甲硝唑处理的动物盲肠内容物中未检测到。