Sun Jiufeng, Li Xiqing, Zeng Hanxiang, Xie Zhi, Lu Changming, Xi Liyan, de Hoog Gert S
Department of Dermatology, The Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
FEMS Immunol Med Microbiol. 2010 Apr;58(3):381-8. doi: 10.1111/j.1574-695X.2010.00647.x. Epub 2010 Jan 26.
Penicillium marneffei is the etiologic agent of a severe systemic disease in immunocompromised hosts in Southeast Asia. In the present study, a novel method, known as loop-mediated isothermal amplification (LAMP), is described for the rapid and specific detection of the species, using a primer set derived from the internal transcribed spacer (ITS) region of the rRNA gene. Amplification products can be detected macroscopically by visual inspection in vials using SYBR Green I as well as by electrophoresis on agarose gel. The LAMP assay resulted in specific amplification of P. marneffei ITS using pure cultures after a 1-h reaction at 65 degrees C in a water bath; no cross-reactivity with other fungi including other biverticillate penicillia was observed. The detectable DNA limit was two copies. In addition, specific amplification was achieved using paraffin wax-embedded tissue samples from patients with penicilliosis marneffei and tissue samples from bamboo rats. The method provides a powerful tool for rapid diagnostics in the clinical lab, and has potential for use in ecological studies.
马尔尼菲青霉是东南亚免疫功能低下宿主中一种严重系统性疾病的病原体。在本研究中,描述了一种名为环介导等温扩增(LAMP)的新方法,用于快速、特异性检测该菌种,使用的引物组源自rRNA基因的内转录间隔区(ITS)。扩增产物可通过在小瓶中使用SYBR Green I肉眼观察以及在琼脂糖凝胶上进行电泳进行宏观检测。在65℃水浴中反应1小时后,LAMP分析使用纯培养物对马尔尼菲青霉ITS进行了特异性扩增;未观察到与包括其他双轮青霉在内的其他真菌有交叉反应。可检测的DNA极限为两个拷贝。此外,使用来自马尔尼菲青霉病患者的石蜡包埋组织样本和来自竹鼠的组织样本实现了特异性扩增。该方法为临床实验室的快速诊断提供了有力工具,并且在生态学研究中具有应用潜力。