首页> 外文期刊>Antimicrobial agents and chemotherapy. >Emergence of resistant Klebsiella pneumoniae in the intestinal tract during successful treatment of Klebsiella pneumoniae lung infection in rats.
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Emergence of resistant Klebsiella pneumoniae in the intestinal tract during successful treatment of Klebsiella pneumoniae lung infection in rats.

机译:成功治疗大鼠肺炎克雷伯菌肺部感染过程中,肠道抗性肺炎克雷伯菌的出现。

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Antibiotic treatment of lung infections may lead to the emergence of resistance in the gut flora. Appropriate dosing regimens could mitigate this adverse effect. In gnotobiotic rats harboring intestinal Escherichia coli and Enterococcus faecium populations, a lung infection by Klebsiella pneumoniae was instigated with two different sizes of inoculum to represent an early or a late initiation of antibiotic treatment. The rats were treated with marbofloxacin, an expanded-spectrum fluoroquinolone, by a single-shot administration or a fractionated regimen over 4 days. Intestinal bacterial populations were monitored during and after treatment. At the infection site, bacterial cure without any selection of resistance was observed. Whatever the dosage regimen, fluoroquinolone treatment had a transient negative impact on the E. coli gut population but not on that of E. faecium. The intestinal flora was colonized by the pathogenic lung bacteria, and there was the emergence of intestine-resistant K. pneumoniae, occurring more often in animals treated with a single marbofloxacin dose than with the fractionated dose. Bacterial cure without resistance selection at the infection site with fluoroquinolone treatment can be linked to colonization of the digestive tract by targeted pulmonary bacteria, followed by the emergence of resistance.
机译:肺部感染的抗生素治疗可能会导致肠道菌群出现耐药性。适当的给药方案可以减轻这种不良影响。在具有肠道大肠埃希菌和粪肠球菌种群的gnotobiotic大鼠中,用两种不同大小的接种物激发了肺炎克雷伯菌的肺部感染,代表了抗生素治疗的早期或晚期。通过单次给药或在4天内分次给药方案,用扩大剂量的氟喹诺酮马波沙星治疗大鼠。在治疗期间和之后监测肠道细菌种群。在感染部位,观察到细菌治愈,没有任何抗性选择。无论采用哪种剂量方案,氟喹诺酮治疗对大肠杆菌肠道菌群都有短暂的负面影响,但对粪肠球菌却没有。肠道菌群被病原性肺细菌定殖,出现了肠道抗药性肺炎克雷伯菌,这种现象在单剂量马波沙星治疗的动物中比分剂量给药的动物更常见。氟喹诺酮治疗在感染部位未选择耐药性的细菌治愈可能与靶向肺细菌在消化道的定殖有关,随后出现耐药性。

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