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西他霉素介导的抗鼠疫病原菌鼠疫耶尔森氏菌感染的保护作用及其与左氧氟沙星的比较

Cethromycin-mediated protection against the plague pathogen Yersinia pestis in a rat model of infection and comparison with levofloxacin.

机构信息

Department of Biology, Center for Bionanotechnology and Environmental Research, Texas Southern University, 3100 Cleburne Street, Houston, Texas 77555-1070, USA.

出版信息

Antimicrob Agents Chemother. 2011 Nov;55(11):5034-42. doi: 10.1128/AAC.00632-11. Epub 2011 Aug 22.

Abstract

The Gram-negative plague bacterium, Yersinia pestis, has historically been regarded as one of the deadliest pathogens known to mankind, having caused three major pandemics. After being transmitted by the bite of an infected flea arthropod vector, Y. pestis can cause three forms of human plague: bubonic, septicemic, and pneumonic, with the latter two having very high mortality rates. With increased threats of bioterrorism, it is likely that a multidrug-resistant Y. pestis strain would be employed, and, as such, conventional antibiotics typically used to treat Y. pestis (e.g., streptomycin, tetracycline, and gentamicin) would be ineffective. In this study, cethromycin (a ketolide antibiotic which inhibits bacterial protein synthesis and is currently in clinical trials for respiratory tract infections) was evaluated for antiplague activity in a rat model of pneumonic infection and compared with levofloxacin, which operates via inhibition of bacterial topoisomerase and DNA gyrase. Following a respiratory challenge of 24 to 30 times the 50% lethal dose of the highly virulent Y. pestis CO92 strain, 70 mg of cethromycin per kg of body weight (orally administered twice daily 24 h postinfection for a period of 7 days) provided complete protection to animals against mortality without any toxic effects. Further, no detectable plague bacilli were cultured from infected animals' blood and spleens following cethromycin treatment. The antibiotic was most effective when administered to rats 24 h postinfection, as the animals succumbed to infection if treatment was further delayed. All cethromycin-treated survivors tolerated 2 subsequent exposures to even higher lethal Y. pestis doses without further antibiotic treatment, which was related, in part, to the development of specific antibodies to the capsular and low-calcium-response V antigens of Y. pestis. These data demonstrate that cethromycin is a potent antiplague drug that can be used to treat pneumonic plague.

摘要

革兰氏阴性鼠疫杆菌,即鼠疫耶尔森菌,曾被认为是人类已知的最致命病原体之一,它曾引发过三次大流行。鼠疫耶尔森菌通过受感染的跳蚤等节肢动物媒介的叮咬传播,可引起三种人类鼠疫:腺鼠疫、败血型鼠疫和肺鼠疫,后两者的死亡率非常高。随着生物恐怖主义威胁的增加,很可能会使用多药耐药的鼠疫耶尔森菌菌株,而传统的抗生素通常用于治疗鼠疫耶尔森菌(例如链霉素、四环素和庆大霉素)将无效。在这项研究中,西他霉素(一种酮内酯抗生素,可抑制细菌蛋白质合成,目前正在进行呼吸道感染的临床试验)在肺鼠疫感染的大鼠模型中被评估了抗鼠疫活性,并与左氧氟沙星进行了比较,左氧氟沙星通过抑制细菌拓扑异构酶和 DNA 回旋酶发挥作用。在高毒力的鼠疫耶尔森菌 CO92 菌株的 50%致死剂量的 24 至 30 倍的呼吸道挑战后,70 毫克/千克体重的西他霉素(每天口服两次,感染后 24 小时开始,持续 7 天)可完全保护动物免受死亡,且无任何毒性作用。此外,在用西他霉素治疗后,从感染动物的血液和脾脏中均未培养出鼠疫杆菌。抗生素在感染后 24 小时给予大鼠时最有效,因为如果进一步延迟治疗,动物将死于感染。所有接受西他霉素治疗的幸存者在没有进一步抗生素治疗的情况下耐受了 2 次甚至更高致命的鼠疫耶尔森菌剂量的再次暴露,这部分与针对鼠疫耶尔森菌荚膜和低钙反应 V 抗原的特异性抗体的发展有关。这些数据表明,西他霉素是一种有效的抗鼠疫药物,可用于治疗肺鼠疫。

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