Johnson Suzanne M, Carlson Erin L, Pappagianis Demosthenes
Department of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, 1 Shields Avenue, Davis, CA, 95616, USA,
Mycopathologia. 2015 Feb;179(1-2):45-51. doi: 10.1007/s11046-014-9820-y. Epub 2014 Oct 17.
The use of PCR-based assays to detect fungi and diagnose fungal infections as well as to monitor fungal organ burden with diseases such as coccidioidomycosis is becoming more common. The target of these assays is frequently one or more of the ribosomal DNA (rDNA) gene subunits. The multicopy nature of this gene affords greater sensitivity over single-copy genes. However, there are few studies reporting the precise number of copies of the rDNA gene per genome in pathogenic fungi. Quantitative PCR was used to determine the number of copies of rDNA as well as CTS1, a single-copy gene, in samples of Coccidioides genomic DNA by the absolute quantification method. Variability of rDNA genome copy number was determined using 13 different Coccidioides isolates and was found to vary between 20 and 146 copies per genome. This suggests that detection of rDNA will likely afford an increased sensitivity of at least 20-fold over single-copy genes. However, estimation of the number of organisms present by quantification of the rDNA cannot be made prior to knowledge of each isolate's rDNA copy number because of the strain variation.
使用基于聚合酶链反应(PCR)的检测方法来检测真菌、诊断真菌感染以及监测如球孢子菌病等疾病中的真菌器官负荷正变得越来越普遍。这些检测方法的靶标通常是核糖体DNA(rDNA)基因亚基中的一个或多个。该基因的多拷贝性质比单拷贝基因具有更高的灵敏度。然而,很少有研究报道致病真菌中每个基因组rDNA基因的确切拷贝数。采用绝对定量法,运用定量PCR来测定球孢子菌基因组DNA样本中rDNA以及单拷贝基因CTS1的拷贝数。使用13种不同的球孢子菌分离株测定rDNA基因组拷贝数的变异性,发现每个基因组的拷贝数在20至146之间变化。这表明检测rDNA可能比单拷贝基因的灵敏度至少提高20倍。然而,由于菌株变异,在了解每个分离株的rDNA拷贝数之前,无法通过rDNA定量来估计存在的生物体数量。