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本文引用的文献

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In vitro activity of BAL30072 against Burkholderia pseudomallei.BAL30072 对伯克霍尔德氏菌的体外活性。
Int J Antimicrob Agents. 2011 Aug;38(2):157-9. doi: 10.1016/j.ijantimicag.2011.03.019. Epub 2011 May 18.
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Immunotherapy markedly increases the effectiveness of antimicrobial therapy for treatment of Burkholderia pseudomallei infection.免疫疗法显著提高了抗菌治疗治疗伯克霍尔德氏菌感染的效果。
Antimicrob Agents Chemother. 2010 May;54(5):1785-92. doi: 10.1128/AAC.01513-09. Epub 2010 Feb 22.
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Synthesis and in vitro Efficacy Studies of Silver Carbene Complexes on Biosafety Level 3 Bacteria.卡宾银配合物对生物安全3级细菌的合成及体外疗效研究
Eur J Inorg Chem. 2009 May 1;2009(13):1739-1745. doi: 10.1002/ejic.200801159.
4
Burkholderia pseudomallei isocitrate lyase is a persistence factor in pulmonary melioidosis: implications for the development of isocitrate lyase inhibitors as novel antimicrobials.伯克霍尔德菌属类鼻疽杆菌异柠檬酸裂解酶是肺类鼻疽病中的一个持续存在因素:对开发异柠檬酸裂解酶抑制剂作为新型抗菌药物的启示。
Infect Immun. 2009 Oct;77(10):4275-83. doi: 10.1128/IAI.00609-09. Epub 2009 Jul 20.
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Comparative antimicrobial activity of granulysin against bacterial biothreat agents.颗粒溶素对细菌生物威胁因子的抗菌活性比较
Open Microbiol J. 2009 Jun 5;3:92-6. doi: 10.2174/1874285800903010092.
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The medicinal applications of imidazolium carbene-metal complexes.咪唑鎓卡宾-金属配合物的医学应用。
Chem Rev. 2009 Aug;109(8):3859-84. doi: 10.1021/cr800500u.
7
In vitro and murine efficacy and toxicity studies of nebulized SCC1, a methylated caffeine-silver(I) complex, for treatment of pulmonary infections.雾化吸入SCC1(一种甲基化咖啡因 - 银(I)络合物)治疗肺部感染的体外及小鼠有效性和毒性研究
Antimicrob Agents Chemother. 2009 Aug;53(8):3285-93. doi: 10.1128/AAC.00314-09. Epub 2009 May 18.
8
Comparison of the in vitro and in vivo susceptibilities of Burkholderia mallei to Ceftazidime and Levofloxacin.鼻疽伯克霍尔德菌对头孢他啶和左氧氟沙星的体外及体内药敏性比较。
BMC Microbiol. 2009 May 9;9:88. doi: 10.1186/1471-2180-9-88.
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The antimicrobial efficacy of sustained release silver-carbene complex-loaded L-tyrosine polyphosphate nanoparticles: characterization, in vitro and in vivo studies.负载缓释卡宾银配合物的L-酪氨酸多磷酸盐纳米颗粒的抗菌效果:表征、体外和体内研究
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Variations in ceftazidime and amoxicillin-clavulanate susceptibilities within a clonal infection of Burkholderia pseudomallei.在一株克隆性感染的类鼻疽伯克霍尔德菌中头孢他啶和阿莫西林-克拉维酸敏感性的差异
J Clin Microbiol. 2009 May;47(5):1556-8. doi: 10.1128/JCM.01657-08. Epub 2009 Mar 18.

类鼻疽和鼻疽的当前和未来治疗策略。

Present and future therapeutic strategies for melioidosis and glanders.

机构信息

Department of Microbiology and Immunology, Department of Pathology and The Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-1070, USA.

出版信息

Expert Rev Anti Infect Ther. 2010 Mar;8(3):325-38. doi: 10.1586/eri.10.4.

DOI:10.1586/eri.10.4
PMID:20192686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2856610/
Abstract

Burkholderia pseudomallei and Burkholderia mallei are the causative agents of melioidosis and glanders, respectively. Both Gram-negative pathogens are endemic in many parts of the world. Although natural acquisition of these pathogens is rare in the majority of countries, these bacteria have recently gained much interest because of their potential as bioterrorism agents. In modern times, their potential destructive impact on public health has escalated owing to the ability of these pathogens to cause opportunistic infections in diabetic and perhaps otherwise immunocompromised people, two growing populations worldwide. For both pathogens, severe infection in humans carries a high mortality rate, both species are recalcitrant to antibiotic therapy - B. pseudomallei more so than B. mallei - and no licensed vaccine exists for either prophylactic or therapeutic use. The potential malicious use of these organisms has accelerated the investigation of new ways to prevent and to treat the diseases. The availability of several B. pseudomallei and B. mallei genome sequences has greatly facilitated target identification and development of new therapeutics. This review provides a compilation of literature covering studies in antimelioidosis and antiglanders antimicrobial drug discovery, with a particular focus on potential novel therapeutic approaches to combat these diseases.

摘要

类鼻疽伯克霍尔德菌和鼻疽伯克霍尔德菌分别是类鼻疽和鼻疽的病原体。这两种革兰氏阴性病原体在世界上许多地区都有地方性流行。尽管在大多数国家,这些病原体的自然感染很少见,但由于它们可能被用作生物恐怖主义制剂,这些细菌最近引起了广泛关注。在现代,由于这些病原体能够在糖尿病患者和可能免疫功能低下的人中引起机会性感染,而糖尿病患者和可能免疫功能低下的人群在全球范围内不断增加,这些病原体对公众健康的潜在破坏性影响加剧了。对于这两种病原体,人类的严重感染都有很高的死亡率,这两种病原体对抗生素治疗都有耐药性——类鼻疽伯克霍尔德菌比鼻疽伯克霍尔德菌更耐药——而且都没有针对预防或治疗用途的许可疫苗。这些生物体的恶意使用加速了对预防和治疗这些疾病的新方法的研究。几个类鼻疽伯克霍尔德菌和鼻疽伯克霍尔德菌基因组序列的可用性极大地促进了靶标鉴定和新疗法的开发。这篇综述提供了一份涵盖抗类鼻疽和抗鼻疽抗菌药物发现研究的文献汇编,特别关注了对抗这些疾病的潜在新治疗方法。