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通过定量PCR、半乳甘露聚糖酶免疫测定和定量培养评估豚鼠肺组织中烟曲霉负荷量。

Assessment of Aspergillus fumigatus burden in pulmonary tissue of guinea pigs by quantitative PCR, galactomannan enzyme immunoassay, and quantitative culture.

作者信息

Vallor Ana C, Kirkpatrick William R, Najvar Laura K, Bocanegra Rosie, Kinney Marsha C, Fothergill Annette W, Herrera Monica L, Wickes Brian L, Graybill John R, Patterson Thomas F

机构信息

The University of Texas Health Science Center at San Antonio, Department of Medicine, Division of Infectious Diseases, 7703 Floyd Curl Drive, Mail Code 7881, San Antonio, TX 78229-3900, USA.

出版信息

Antimicrob Agents Chemother. 2008 Jul;52(7):2593-8. doi: 10.1128/AAC.00276-08. Epub 2008 May 12.

Abstract

Early diagnosis of invasive pulmonary aspergillosis is problematic in some patient groups due to the lack of rapid, sensitive, specific, and reliable diagnostic tests. Fungal burden and therapeutic efficacy were assessed by survival, quantitative culture (CFU counts), galactomannan enzyme immunoassay (GM-EIA), and quantitative PCR (qPCR) in a new guinea pig model of invasive pulmonary aspergillosis using an aerosol challenge. At 1 day postinfection, qPCR determined that the pulmonary fungal burden was 2 log(10) higher than that determined by CFU counting and increased significantly (P < 0.03) over time. In contrast, the tissue burden assessed by CFU counting did not rise over the course of the study. Therapy with the antifungal drug voriconazole produced statistically significant decreases in pulmonary fungal burden, as detected by CFU counting (P < 0.02), qPCR, and GM-EIA (both P < 0.0002). Daily assessment of the progression of fungal infection in serum was performed by qPCR and GM-EIA. GM-EIA demonstrated a statistically significant reduction in the fungal load on days 6 and 7 in voriconazole-treated animals compared to time-matched controls (P < 0.02). Confirmation of fungal tissue burden by two or more methods should provide a more precise account of the burden, allowing improved assessment of diagnostic and therapeutic strategies in invasive pulmonary aspergillosis.

摘要

由于缺乏快速、灵敏、特异且可靠的诊断检测方法,侵袭性肺曲霉病的早期诊断在某些患者群体中存在问题。在一种新的经气溶胶攻击建立的侵袭性肺曲霉病豚鼠模型中,通过存活情况、定量培养(菌落形成单位计数)、半乳甘露聚糖酶免疫测定(GM-EIA)和定量聚合酶链反应(qPCR)评估真菌负荷和治疗效果。感染后1天,qPCR测定的肺部真菌负荷比通过菌落形成单位计数测定的结果高2个对数(10),并且随时间显著增加(P < 0.03)。相比之下,通过菌落形成单位计数评估的组织负荷在研究过程中并未增加。抗真菌药物伏立康唑治疗后,通过菌落形成单位计数(P < 0.02)、qPCR和GM-EIA(均为P < 0.0002)检测发现肺部真菌负荷有统计学意义的下降。通过qPCR和GM-EIA对血清中真菌感染进展进行每日评估。与时间匹配的对照组相比,GM-EIA显示伏立康唑治疗的动物在第6天和第7天真菌载量有统计学意义的降低(P < 0.02)。通过两种或更多方法确认真菌组织负荷应能更精确地描述负荷情况,从而改进对侵袭性肺曲霉病诊断和治疗策略的评估。

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