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Impact of spores on the comparative efficacies of five antibiotics for treatment of Bacillus anthracis in an in vitro hollow fiber pharmacodynamic model

机译:在体外中空纤维药效学模型中,孢子对五种抗生素治疗炭疽芽孢杆菌的比较功效的影响

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摘要

Bacillus anthracis, the bacterium that causes anthrax, is an agent of bioterrorism. The most effective antimicrobial therapy for B. anthracis infections is unknown. An in vitro pharmacodynamic model of B. anthracis was used to compare the efficacies of simulated clinically prescribed regimens of moxifloxacin, linezolid, and meropenem with the "gold standards," doxycycline and ciprofloxacin. Treatment outcomes for isogenic spore-forming and non-spore-forming strains of B. anthracis were compared. Against spore-forming B. anthracis, ciprofloxacin, moxifloxacin, linezolid, and meropenem reduced the B. anthracis population by 4 log 10 CFU/ml over 10 days. Doxycycline reduced the population of this B. anthracis strain by 5 log 10 CFU/ml (analysis of variance [ANOVA] P=0.01 versus other drugs). Against an isogenic non-spore-forming strain, meropenem killed the vegetative B. anthracis the fastest, followed by moxifloxacin and ciprofloxacin and then doxycycline. Linezolid offered the lowest bacterial kill rate. Heat shock studies using the spore-producing B. anthracis strain showed that with moxifloxacin, ciprofloxacin, and meropenem therapies the total population was mostly spores, while the population was primarily vegetative bacteria with linezolid and doxycycline therapies. Spores have a profound impact on the rate and extent of killing of B. anthracis. Against sporeforming B. anthracis, the five antibiotics killed the total (spore and vegetative) bacterial population at similar rates (within 1 log 10 CFU/ml of each other). However, bactericidal antibiotics killed vegetative B. anthracis faster than bacteriostatic drugs. Since only vegetative-phase B. anthracis produces the toxins that may kill the infected host, the rate and mechanism of killing of an antibiotic may determine its overall in vivo efficacy. Further studies are needed to examine this important observation.
机译:炭疽杆菌是引起炭疽的细菌,是生物恐怖活动的媒介。炭疽芽孢杆菌感染最有效的抗菌疗法尚不清楚。用炭疽芽孢杆菌的体外药效学模型比较了莫西沙星,利奈唑胺和美罗培南的临床模拟处方方案与“黄金标准”,强力霉素和环丙沙星的疗效。比较了炭疽芽孢杆菌等基因芽孢形成菌株和非芽孢形成菌株的治疗效果。针对形成孢子的炭疽芽孢杆菌,环丙沙星,莫西沙星,利奈唑胺和美洛培南在10天内使炭疽芽孢杆菌种群减少了4 log 10 CFU / ml。强力霉素使该炭疽芽孢杆菌菌株的种群减少了5 log 10 CFU / ml(与其他药物相比,方差分析[ANOVA] P = 0.01)。针对同基因的非孢子形成菌株,美洛培南以最快的速度杀死植物性炭疽芽孢杆菌,其次是莫西沙星和环丙沙星,然后是强力霉素。利奈唑胺的细菌杀灭率最低。使用产芽孢炭疽芽孢杆菌菌株进行的热休克研究表明,采用莫西沙星,环丙沙星和美罗培南疗法的总菌群多数为孢子,而主要种群为营养菌,并使用利奈唑胺和强力霉素治疗。孢子对炭疽芽孢杆菌的杀灭速度和程度有深远的影响。针对形成孢子的炭疽芽孢杆菌,这五种抗生素以相似的速率杀死了总的(孢子和营养性)细菌种群(彼此之间的相互关系为1 log 10 CFU / ml)。但是,杀菌性抗生素杀死植物性炭疽芽孢杆菌的速度要快于抑菌药。由于仅营养期炭疽芽孢杆菌会产生可杀死感染宿主的毒素,因此抗生素的杀灭速率和杀伤机制可能决定其总体体内功效。需要进一步研究以检查这一重要观察结果。

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