Luchi N, Capretti P, Pinzani P, Orlando C, Pazzagli M
Dipartimento di Biotecnologie Agrarie, Sezione di Patologia vegetale, Università degli Studi di Firenze, Piazzale delle Cascine, Florence, Italy.
Lett Appl Microbiol. 2005;41(1):61-8. doi: 10.1111/j.1472-765X.2005.01701.x.
Real-time PCR, based on TaqMan chemistry, was used to detect Biscogniauxia mediterranea, a fungal pathogen that after a long endophytic phase may cause charcoal disease in oak trees.
Specific primers and probe were designed and tested on axenic cultures of B. mediterranea and other fungi commonly colonizing oaks. Twig samples were collected in Tuscany from apparently healthy oaks (Quercus cerris, Quercus ilex and Quercus pubescens) growing near trees infected with the fungus. Twigs were divided into two groups: one for isolation in agar plates, and one for real-time PCR after DNA extraction. The detection limit of the assay was 0.01 pg/DNA, whereas the amounts of fungal DNA detected in asymptomatic tissue were >0.5 pg microg(-1) total DNA extracted. In the apparently healthy twigs the frequency of isolation found on agar was 25.0%, much lower than that with real-time PCR (96.4%).
Real-time PCR is a sensitive and fast technique able to specifically detect and quantify the DNA of B. mediterranea in oak tissue.
This diagnostic method is a precise tool to localize fungi in symptomless plant tissues and promises to advance our understanding of fungal infection during their latent phase.
基于TaqMan化学原理的实时荧光定量PCR技术用于检测地中海盘菌,这种真菌病原体在经历较长的内生阶段后可能会导致橡树发生炭腐病。
设计了特异性引物和探针,并在地中海盘菌及其他常见于橡树的真菌的无菌培养物上进行了测试。在托斯卡纳地区,从生长在感染该真菌树木附近的看似健康的橡树(栓皮栎、冬青栎和柔毛栎)上采集嫩枝样本。嫩枝分为两组:一组用于在琼脂平板上分离培养,另一组用于DNA提取后进行实时荧光定量PCR检测。该检测方法的检测限为0.01 pg/DNA,而在无症状组织中检测到的真菌DNA量为>0.5 pg/μg总DNA提取物。在看似健康的嫩枝中,琼脂平板上的分离频率为25.0%,远低于实时荧光定量PCR检测的频率(96.4%)。
实时荧光定量PCR是一种灵敏且快速的技术,能够特异性地检测和定量橡树组织中地中海盘菌的DNA。
这种诊断方法是在无症状植物组织中定位真菌的精确工具,有望推动我们对真菌感染潜伏期的理解。