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某些铜绿假单胞菌菌株的体外和体内抗生素敏感性测试结果之间的差异。

Dissociation between results of in vitro and in vivo antibiotic susceptibility tests for some strains of Pseudomonas aeruginosa.

作者信息

Davis S D

出版信息

Antimicrob Agents Chemother. 1974 Mar;5(3):281-8. doi: 10.1128/AAC.5.3.281.

Abstract

The relative efficacy in vivo of the polymyxin and aminoglycoside antibiotics in experimental Pseudomonas infection has apparently never been established. This study was designed to determine such efficacy in experimental infection of mice. Eleven strains of Pseudomonas aeruginosa were selected for the study, representing six of the seven recognized immunotypes. All strains were susceptible to colistin, gentamicin, and tobramycin in vitro, and all were virulent for mice. None was lethal because of preformed toxins. Infections were established in mice by intraperitoneal (i.p.) injection of 100 ID(50) of bacteria (infectious doses that would kill 50% of the mice). Graduated doses of antibiotics or saline were given subcutaneously 1 h later. Infections by three strains of P. aeruginosa were cured by low doses of all three antibiotics. Infections by two strains were relatively resistant in vivo to all three antibiotics. Infections by seven strains were relatively resistant in vivo to colistimethate. For most strains, colistimethate was less effective in vivo than gentamicin or tobramycin. To determine the influence of the size of the bacterial inoculum upon the results of chemotherapy, groups of mice were infected with serial dilutions of bacterial suspensions and treated with antibiotics. The antibiotics were more effective when a lighter bacterial inoculum was used. However, colistimethate at 30 mg/kg failed to cure some infections established with an inoculum of only 10 ID(50). To examine the possibility that death despite apparently adequate chemotherapy might be due to bacterial lysis and delayed release of toxins, numbers of viable bacteria in the peritoneal cavity of treated animals were determined by colony count. Antibiotic failure by colistimethate was associated with a steady rise in the number of i.p. bacteria. The findings support the conclusion that i.p. infections in mice with some strains of P. aeruginosa that are fully susceptible in vitro are relatively resistant to chemotherapy in vivo. The dissociation between in vitro and in vivo results was greatest for colistimethate.

摘要

多粘菌素和氨基糖苷类抗生素在实验性铜绿假单胞菌感染中的体内相对疗效显然从未得到确定。本研究旨在确定这些抗生素在小鼠实验性感染中的疗效。选择了11株铜绿假单胞菌进行研究,代表了7种公认免疫型中的6种。所有菌株在体外对多粘菌素、庆大霉素和妥布霉素均敏感,且对小鼠均有致病性。无一株因预形成毒素而致死。通过腹腔注射100个半数感染量(ID50)的细菌(能杀死50%小鼠的感染剂量)在小鼠中建立感染。1小时后皮下给予不同剂量的抗生素或生理盐水。三种铜绿假单胞菌菌株的感染可被低剂量的所有三种抗生素治愈。两种菌株的感染在体内对所有三种抗生素相对耐药。七种菌株的感染在体内对多粘菌素甲磺酸钠相对耐药。对于大多数菌株,多粘菌素甲磺酸钠在体内的效果不如庆大霉素或妥布霉素。为了确定细菌接种量大小对化疗结果的影响,将小鼠分组用系列稀释的细菌悬液感染并给予抗生素治疗。使用较轻的细菌接种量时,抗生素效果更佳。然而,30mg/kg的多粘菌素甲磺酸钠未能治愈一些仅用10个ID50接种量建立的感染。为了研究尽管化疗看似充分但仍死亡可能是由于细菌裂解和毒素延迟释放的可能性,通过菌落计数确定治疗动物腹腔内活菌数量。多粘菌素甲磺酸钠治疗失败与腹腔内细菌数量稳步增加有关。这些发现支持以下结论:体外完全敏感的某些铜绿假单胞菌菌株在小鼠中的腹腔感染在体内对化疗相对耐药。体外和体内结果之间的差异对多粘菌素甲磺酸钠最为明显。

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