Laboratorio GeMBio, Centro de Investigación Científica de Yucatán A.C, Calle 43 # 130, Col. Chuburná de Hidalgo, Mérida, Yucatán, 97200, México.
Mol Biotechnol. 2011 Sep;49(1):48-55. doi: 10.1007/s12033-011-9377-7.
Colletotrichum capsici is an important fungal species that causes anthracnose in many genera of plants causing severe economic losses worldwide. A primer set was designed based on the sequences of the ribosomal internal transcribed spacer (ITS1 and ITS2) regions for use in a conventional PCR assay. The primer set (CcapF/CcapR) amplified a single product of 394 bp with DNA extracted from 20 Mexican isolates of C. capsici. The specificity of primers was confirmed by the absence of amplified product with DNA of four other Colletotrichum species and eleven different fungal genera. This primer set is capable of amplifying only C. capsici from different contaminated tissues or fungal structures, thereby facilitating rapid diagnoses as there is no need to isolate and cultivate the fungus in order to identify it. The sensitivity of detection with this PCR method was 10 pg of genomic DNA from the pathogen. This is the first report of a C. capsici-specific primer set. It allows rapid pathogen detection and provides growers with a powerful tool for a rational selection of fungicides to control anthracnose in different crops and in the post-harvest stage.
辣椒炭疽菌是一种重要的真菌物种,可引起许多属植物的炭疽病,在全球范围内造成严重的经济损失。本研究基于核糖体内部转录间隔区(ITS1 和 ITS2)序列设计了一套引物,用于常规 PCR 检测。该引物对(CcapF/CcapR)可从 20 个墨西哥辣椒炭疽菌分离株的 DNA 中扩增出 394 bp 的单一产物。通过对 4 种其他炭疽菌和 11 种不同真菌属的 DNA 进行检测,证实了引物的特异性。该引物对仅能从不同污染组织或真菌结构中扩增出辣椒炭疽菌,从而促进了快速诊断,因为无需分离和培养真菌即可对其进行鉴定。该 PCR 方法的检测灵敏度为 10 pg 病原体基因组 DNA。这是首次报道辣椒炭疽菌特异性引物。它可以快速检测病原体,并为种植者提供了一种强有力的工具,用于在不同作物和收获后阶段合理选择杀菌剂来控制炭疽病。