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Real-time monitoring of bacterial infection in vivo: development of bioluminescent staphylococcal foreign-body and deep-thigh-wound mouse infection models.体内细菌感染的实时监测:生物发光葡萄球菌异物和大腿深部伤口小鼠感染模型的建立
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本文引用的文献

1
Methicillin resistant Staphylococcus aureus (MRSA) in the intensive care unit.重症监护病房中的耐甲氧西林金黄色葡萄球菌(MRSA)
Postgrad Med J. 2002 Jul;78(921):385-92. doi: 10.1136/pmj.78.921.385.
2
In vitro activity of linezolid, quinupristin-dalfopristin, vancomycin, teicoplanin, moxifloxacin and mupirocin against methicillin-resistant Staphylococcus aureus: comparative evaluation by the E test and a broth microdilution method.利奈唑胺、奎奴普丁-达福普汀、万古霉素、替考拉宁、莫西沙星和莫匹罗星对耐甲氧西林金黄色葡萄球菌的体外活性:采用E试验和肉汤微量稀释法进行比较评价。
Diagn Microbiol Infect Dis. 2002 Aug;43(4):319-21. doi: 10.1016/s0732-8893(02)00407-8.
3
In vitro activity of linezolid, synercid and telithromycin against genetically defined high level fluoroquinolone-resistant methicillin-resistant Staphylococcus aureus.利奈唑胺、奎奴普丁/达福普汀和泰利霉素对基因明确的高水平氟喹诺酮耐药耐甲氧西林金黄色葡萄球菌的体外活性。
Int J Antimicrob Agents. 2002 Jul;20(1):61-4. doi: 10.1016/s0924-8579(02)00107-3.
4
In vitro evaluation of AZD2563, a novel oxazolidinone, against 603 recent staphylococcal isolates.新型恶唑烷酮类药物AZD2563对603株近期葡萄球菌分离株的体外评估
Antimicrob Agents Chemother. 2002 Aug;46(8):2662-4. doi: 10.1128/AAC.46.8.2662-2664.2002.
5
In vitro activities of quinupristin-dalfopristin and cefepime, alone and in combination with various antimicrobials, against multidrug-resistant staphylococci and enterococci in an in vitro pharmacodynamic model.在体外药效学模型中,单独及与多种抗菌药物联合使用时,奎奴普丁-达福普汀和头孢吡肟对耐多药葡萄球菌和肠球菌的体外活性。
Antimicrob Agents Chemother. 2002 Aug;46(8):2606-12. doi: 10.1128/AAC.46.8.2606-2612.2002.
6
Effects of 2 different anti-tumor necrosis factor-alpha agents in a primate model of subcutaneous abscess formation.两种不同的抗肿瘤坏死因子-α制剂在灵长类动物皮下脓肿形成模型中的作用
J Infect Dis. 2002 Jan 15;185(2):204-13. doi: 10.1086/338451. Epub 2002 Jan 3.
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Revealing the spatiotemporal patterns of bacterial infectious diseases using bioluminescent pathogens and whole body imaging.
Contrib Microbiol. 2001;9:71-88. doi: 10.1159/000060392.
8
The changing epidemiology of Staphylococcus aureus?金黄色葡萄球菌流行病学的变化?
Emerg Infect Dis. 2001 Mar-Apr;7(2):178-82. doi: 10.3201/eid0702.010204.
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The impact of hospital-acquired bloodstream infections.医院获得性血流感染的影响。
Emerg Infect Dis. 2001 Mar-Apr;7(2):174-7. doi: 10.3201/eid0702.010203.
10
Visualizing pneumococcal infections in the lungs of live mice using bioluminescent Streptococcus pneumoniae transformed with a novel gram-positive lux transposon.利用经新型革兰氏阳性lux转座子转化的生物发光肺炎链球菌,在活小鼠肺部可视化肺炎球菌感染。
Infect Immun. 2001 May;69(5):3350-8. doi: 10.1128/IAI.69.5.3350-3358.2001.

体内细菌感染的实时监测:生物发光葡萄球菌异物和大腿深部伤口小鼠感染模型的建立

Real-time monitoring of bacterial infection in vivo: development of bioluminescent staphylococcal foreign-body and deep-thigh-wound mouse infection models.

作者信息

Kuklin Nelly A, Pancari Gregory D, Tobery Timothy W, Cope Leslie, Jackson Jesse, Gill Charles, Overbye Karen, Francis Kevin P, Yu Jun, Montgomery Donna, Anderson Annaliesa S, McClements William, Jansen Kathrin U

机构信息

Merck and Co, Inc, West Point, Pennsylvania 19486, USA.

出版信息

Antimicrob Agents Chemother. 2003 Sep;47(9):2740-8. doi: 10.1128/AAC.47.9.2740-2748.2003.

DOI:10.1128/AAC.47.9.2740-2748.2003
PMID:12936968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC182637/
Abstract

Staphylococcal infections associated with catheter and prosthetic implants are difficult to eradicate and often lead to chronic infections. Development of novel antibacterial therapies requires simple, reliable, and relevant models for infection. Using bioluminescent Staphylococcus aureus, we have adapted the existing foreign-body and deep-wound mouse models of staphylococcal infection to allow real-time monitoring of the bacterial colonization of catheters or tissues. This approach also enables kinetic measurements of bacterial growth and clearance in each infected animal. Persistence of infection was observed throughout the course of the study until termination of the experiment at day 16 in a deep-wound model and day 21 in the foreign-body model, providing sufficient time to test the effects of antibacterial compounds. The usefulness of both animal models was assessed by using linezolid as a test compound and comparing bioluminescent measurements to bacterial counts. In the foreign-body model, a three-dose antibiotic regimen (2, 5, and 24 h after infection) resulted in a decrease in both luminescence and bacterial counts recovered from the implant compared to those of the mock-treated infected mice. In addition, linezolid treatment prevented the formation of subcutaneous abscesses, although it did not completely resolve the infection. In the thigh model, the same treatment regimen resulted in complete resolution of the luminescent signal, which correlated with clearance of the bacteria from the thighs.

摘要

与导管和人工植入物相关的葡萄球菌感染难以根除,且常常导致慢性感染。新型抗菌疗法的开发需要简单、可靠且相关的感染模型。利用生物发光金黄色葡萄球菌,我们对现有的葡萄球菌感染的异物和深部伤口小鼠模型进行了改进,以实现对导管或组织细菌定植的实时监测。这种方法还能够对每只感染动物体内细菌的生长和清除进行动力学测量。在整个研究过程中均观察到感染持续存在,直至在深部伤口模型中于第16天、在异物模型中于第21天实验终止,这为测试抗菌化合物的效果提供了足够的时间。通过使用利奈唑胺作为测试化合物,并将生物发光测量结果与细菌计数进行比较,对这两种动物模型的实用性进行了评估。在异物模型中,与未治疗的感染小鼠相比,三剂量抗生素方案(感染后2、5和24小时)导致从植入物中回收的发光和细菌计数均下降。此外,利奈唑胺治疗可预防皮下脓肿的形成,尽管它并未完全消除感染。在大腿模型中,相同的治疗方案导致发光信号完全消失,这与大腿中细菌的清除相关。