Gago Sara, Buitrago María José, Clemons Karl V, Cuenca-Estrella Manuel, Mirels Laurence F, Stevens David A
Servicio de Micología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
California Institute for Medical Research, San Jose, CA, USA; Department of Medicine, Santa Clara Valley Medical Center, San Jose, CA, USA; Department of Medicine, Stanford University, Stanford, CA, USA.
Diagn Microbiol Infect Dis. 2014 Jun;79(2):214-21. doi: 10.1016/j.diagmicrobio.2014.01.029. Epub 2014 Feb 20.
A new real-time polymerase chain reaction (RT-PCR) assay based on a Coccidioides genus-specific molecular beacon probe was developed for the detection of coccidioidomycosis and validated with tissues from animal models and clinical samples. The assay showed high analytic reproducibility (r(2) > 0.99) and specificity for cultured strains (100%); the lower limit of detection was 1 fg of genomic DNA/μL of reaction. Fungal burdens in the organs of mice infected with Coccidioides posadasii strain Silveira were more accurately quantified by RT-PCR compared to colony-forming unit for all tissues. The RT-PCR assay was positive for 97.7% of spleen and 100% of liver or lung. Progression of infection in all organs was similar by both methods (P > 0.05). The sensitivity of the assay also was 100% for paraffin-embedded samples and samples from patients with positive cultures. Our RT-PCR assay is effective for the diagnosis and monitoring of Coccidioides infection, and its use also avoids the biohazard and time delay of identifying cultures in the clinical setting.
开发了一种基于球孢子菌属特异性分子信标探针的新型实时聚合酶链反应(RT-PCR)检测方法,用于检测球孢子菌病,并在动物模型组织和临床样本中进行了验证。该检测方法具有很高的分析重现性(r(2)>0.99)和对培养菌株的特异性(100%);检测下限为1 fg基因组DNA/μL反应液。与所有组织的菌落形成单位相比,通过RT-PCR更准确地定量了感染波萨达斯球孢子菌菌株Silveira的小鼠器官中的真菌负荷。RT-PCR检测对97.7%的脾脏样本以及100%的肝脏或肺样本呈阳性。两种方法检测所有器官的感染进展情况相似(P>0.05)。该检测方法对石蜡包埋样本和培养阳性患者的样本的敏感性也为100%。我们的RT-PCR检测方法对球孢子菌感染的诊断和监测有效,并且其应用还避免了临床环境中鉴定培养物的生物危害和时间延迟。