Lu Sha, Li Xiqing, Calderone Richard, Zhang Jing, Ma Jianchi, Cai Wenying, Xi Liyan
Department of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University.
Department of Dermatology and Venereology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Med Mycol. 2016 Feb;54(2):162-8. doi: 10.1093/mmy/myv068. Epub 2015 Oct 13.
Talaromyces marneffei is a dimorphic pathogenic fungus, which is a life-threatening invasive mycosis in the immunocompromised host. Prompt diagnosis of T. marneffei infection remains difficult although there has been progress in attempts to expedite the diagnosis of this infection. We previously demonstrated the value of nested polymerase chain reaction (PCR) to detect T. marneffei in paraffin embedded tissue samples with high sensitivity and specificity. In this study, this assay was used to detect the DNA of T. marneffei in whole blood samples. Real-time PCR assay was also evaluated to identify T. marneffei in the same samples. Twenty out of 30 whole blood samples (67%) collected from 23 patients were found positive by using the nested PCR assay, while 23/30 (77%) samples were found positive by using the real-time PCR assay. In order to express accurately the fungal loads, we used a normalized linearized plasmid as an internal control for real-time PCR. The assay results were correlated as the initial quantity (copies/μl) with fungal burden. These data indicate that combination of nested PCR and real-time PCR assay provides an attractive alternative for identification of T. marneffei DNA in whole blood samples of HIV-infected patients.
马尔尼菲篮状菌是一种双相致病性真菌,在免疫功能低下的宿主中会引发危及生命的侵袭性真菌病。尽管在加快该感染的诊断方面已有进展,但马尔尼菲篮状菌感染的快速诊断仍然困难。我们之前证明了巢式聚合酶链反应(PCR)在检测石蜡包埋组织样本中的马尔尼菲篮状菌时具有高灵敏度和特异性。在本研究中,该检测方法用于检测全血样本中马尔尼菲篮状菌的DNA。还评估了实时PCR检测方法以鉴定相同样本中的马尔尼菲篮状菌。使用巢式PCR检测方法时,从23名患者采集的30份全血样本中有20份(67%)呈阳性,而使用实时PCR检测方法时,30份样本中有23份(77%)呈阳性。为了准确表达真菌载量,我们使用标准化的线性化质粒作为实时PCR的内部对照。检测结果以初始量(拷贝数/微升)与真菌负荷相关联。这些数据表明,巢式PCR和实时PCR检测方法相结合为鉴定HIV感染患者全血样本中的马尔尼菲篮状菌DNA提供了一种有吸引力的替代方法。