Steinbach William J, Benjamin Daniel K, Trasi Scott A, Miller Jackie L, Schell Wiley A, Zaas Aimee K, Foster W Michael, Perfect John R
Division of Pediatric Infectious Diseases, Box 3499, Duke University Medical Center, Durham, NC 27710, USA.
Med Mycol. 2004 Oct;42(5):417-25. doi: 10.1080/13693780410001712034.
Animal models of invasive aspergillosis have been used for virulence studies and antifungal efficacy evaluations but results have been inconsistent. In an attempt to reproduce human infection, many Aspergillus animal models have utilized a 'pulmonary route' for delivery of conidia, largely through intranasal instillation. However, several radiolabeled particle studies have shown that aerosol delivery is preferable to intranasal instillation to create a more homogenous delivery to the lungs. We hypothesized that an inhalational model would be more robust for studies of invasive aspergillosis pathogenesis and antifungal therapy. We developed an inhalational model of Aspergillus fumigatus infection using a Hinners inhalation chamber and demonstrated by quantitative polymerase chain reaction that this new inhalational model creates a more homogenous murine pneumonia, facilitating analysis of mutant strains and treatment regimens.
侵袭性曲霉病的动物模型已用于毒力研究和抗真菌疗效评估,但结果并不一致。为了重现人类感染情况,许多曲霉动物模型采用“肺部途径”来接种分生孢子,主要是通过滴鼻法。然而,多项放射性标记颗粒研究表明,气溶胶给药比滴鼻法更适合在肺部实现更均匀的给药。我们推测,吸入模型对于侵袭性曲霉病发病机制和抗真菌治疗的研究将更加强有力。我们使用辛纳斯吸入室开发了烟曲霉感染的吸入模型,并通过定量聚合酶链反应证明,这种新的吸入模型可造成更均匀的小鼠肺炎,便于对突变菌株和治疗方案进行分析。