Novel PCR Assays for the Detection of Biological Agents Responsible for Wheat Rust Diseases: Puccinia triticina and Puccinia striiformis f. sp tritici

被引:5
|
作者
Kuzdralinski, Adam [1 ]
Kot, Anna [1 ]
Szczerba, Hubert [1 ]
Ostrowska, Agnieszka [1 ]
Nowak, Michal [2 ]
Muszynska, Marta [1 ]
Lechowski, Michal [1 ]
Muzyka, Pawel [1 ]
机构
[1] Univ Life Sci, Dept Biotechnol Human Nutr & Sci Food Commod, 8 Skromna St, PL-20704 Lublin, Poland
[2] Univ Life Sci, Inst Plant Genet Breeding & Biotechnol, Lublin, Poland
关键词
Wheat leaf rust; Wheat stripe rust; PCR; Phytopathology; Multiplex PCR; Molecular detection; SEPTORIA-TRITICI; STRIPE RUST; STAGONOSPORA-NODORUM; LEAF RUST; DIAGNOSIS;
D O I
10.1159/000481799
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The species Puccinia triticina (Pt) and Puccinia striiformis f. sp. tritici (Pst) are devastating cereal pathogens that cause leaf and stripe rust diseases. We developed PCR assays for the species-specific detection of Pt and Pst, 2 biological agents that cause wheat rust disease. For each pathogen, we validated 3 primer sets that target the second largest subunits of the RNA polymerase II (rpb2) and beta-tubulin 1 (tub1) genes. The specificities of the primers were verified using naturally infected plant materials with visual symptoms of disease. All primer sets amplified a single DNA fragment of the expected length. The primer sets LidPr15/16, LidPr1/2, and LidPs13/14 were able to detect small amounts of pure fungal DNA with sensitivities of 0.1, 1, and 10 pg/mu L, respectively. A sufficient detection limit (1 pg/mu L to 5 ng/mu L) was observed for all assays when the sensitivity test was performed with host plant DNA. The study also evaluated the simultaneous detection of both rust pathogens, and the multiplex PCR assay generated amplicons of 240 and 144 bp in length for Pts (LidPs9/10) and Pt (LidPr1/2), respectively. (c) 2017 S. Karger AG, Basel
引用
收藏
页码:299 / 305
页数:7
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