Identification to the species level of the plant pathogens Phytophthora and Pythium by using unique sequences of the ITS1 region of ribosomal DNA as capture probes for PCR ELISA

被引:42
作者
Bailey, AM [1 ]
Mitchell, DJ
Manjunath, KL
Nolasco, G
Niblett, CL
机构
[1] IPN, CINVESTAV, Dept Ingn Genet Plantas, Unidad Irapuato, Irapuato, Mexico
[2] Univ Florida, Dept Plant Pathol, Gainesville, FL 32611 USA
[3] Univ Florida, Dept Hort Sci, Gainesville, FL 32611 USA
[4] Univ Algarve, FERN, Faro, Portugal
关键词
internal transcribed spacer 1 region; ribosomal DNA; PCR ELISA; Pythium; Phytophthora;
D O I
10.1111/j.1574-6968.2002.tb11044.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ribosomal internal transcribed spacer 1 region was sequenced for 10 species of Phythium and eight species of Phytophthora. Alignment of the sequences revealed considerable sequence microheterogeneity, which was utilized to prepare a capture probe of unique sequence for each species. The capture probes were tested by PCR ELISA, combining the sensitivity and specificity of the polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay (ELISA). The probes were entirely species specific, enabling the detection and identification of the amplified DNA of species from individual Cultures or front mixed samples of the DNAs of two different species. This approach to species identification, which provides a molecular technology to process large numbers of samples and still identify the fungi with a high level of confidence, may greatly reduce the resources and the time of highly trained specialists currently needed to identify these important species of plant pathogenic fungi. (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 158
页数:6
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