Bialek R, Ibricevic A, Aepinus C, Najvar L K, Fothergill A W, Knobloch J, Graybill J R
Institute for Tropical Medicine, University Hospital Tübingen, D-72074 Tübingen, Germany.
J Clin Microbiol. 2000 Aug;38(8):2940-2. doi: 10.1128/JCM.38.8.2940-2942.2000.
A nested PCR assay for the detection of Paracoccidioides brasiliensis DNA was evaluated, using a sequence of the immunogenic gp43 gene as a target. This gene encodes an outer membrane protein unique to this dimorphic fungus. DNA from six clinical isolates and the ATCC strain 60885 of P. brasiliensis, as well as DNA from closely related fungi, was examined to determine detection limits and cross-reactions. PCR was done on DNA extracts of lung homogenates from 23 experimentally P. brasiliensis-infected and two uninfected BALB/c mice and from 20 Histoplasma capsulatum-infected ICR mice. The results were compared to quantitative cultures. A detection limit of 0.5 fg of specific DNA was determined using cloned plasmid DNA. In all seven P. brasiliensis isolates, the expected 196-bp nested PCR product was found. Their sequences were 100% identical to the gp43 gene sequence in GenBank. DNA extracts of all other, related fungi were negative. The PCR assay was positive in 21 out of 23 culture-positive lung homogenates with concentrations of 1 x 10(3) to 1.3 x 10(7) CFU of P. brasiliensis per g of lung. Uninfected BALB/c mice and H. capsulatum-infected mice samples gave negative results. The high sensitivity and specificity of this new nested PCR assay for the detection of P. brasiliensis in tissue samples were demonstrated. The assay may be useful for diagnosis in human tissue samples.
评估了一种用于检测巴西副球孢子菌DNA的巢式PCR检测方法,该方法以免疫原性gp43基因序列为靶标。该基因编码这种双态真菌特有的一种外膜蛋白。检测了来自6株临床分离株和巴西副球孢子菌ATCC菌株60885的DNA,以及来自密切相关真菌的DNA,以确定检测限和交叉反应。对23只经实验感染巴西副球孢子菌的BALB/c小鼠和2只未感染的BALB/c小鼠的肺匀浆DNA提取物,以及20只感染荚膜组织胞浆菌的ICR小鼠的肺匀浆DNA提取物进行了PCR检测。将结果与定量培养结果进行比较。使用克隆质粒DNA确定特异性DNA的检测限为0.5 fg。在所有7株巴西副球孢子菌分离株中,均发现了预期的196 bp巢式PCR产物。它们的序列与GenBank中的gp43基因序列100%相同。所有其他相关真菌的DNA提取物均为阴性。在每克肺中巴西副球孢子菌浓度为1×10(3)至1.3×10(7) CFU的23份培养阳性肺匀浆中,有21份PCR检测呈阳性。未感染的BALB/c小鼠和感染荚膜组织胞浆菌的小鼠样本结果均为阴性。证明了这种新的巢式PCR检测方法在检测组织样本中巴西副球孢子菌时具有高灵敏度和特异性。该检测方法可能对人体组织样本的诊断有用。