Polymerase Chain Reaction Assays for the Detection and Discrimination of the Soybean Rust PathogensPhakopsora pachyrhiziandP. meibomiae
Author(s) -
Reid D. Frederick,
Christine L. Snyder,
Gary L. Peterson,
M. R. Bonde
Publication year - 2002
Publication title -
phytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.264
H-Index - 131
eISSN - 1943-7684
pISSN - 0031-949X
DOI - 10.1094/phyto.2002.92.2.217
Subject(s) - phakopsora pachyrhizi , biology , soybean rust , polymerase chain reaction , nucleic acid sequence , genetics , virology , botany , gene , fungicide
ABSTRACT Soybean rust occurs in Australia and many countries throughout Africa, Asia, and South America. The causal agents of soybean rust are two closely related fungi, Phakopsora pachyrhizi and P. meibomiae, which are differentiated based upon morphological characteristics of the telia. Determination of the nucleotide sequence of the internal transcribed spacer (ITS) region revealed greater than 99% nucleotide sequence similarity among isolates of either P. pachyrhizi or P. meibomiae, but only 80% sequence similarity between the two species. Utilizing differences within the ITS region, four sets of polymerase chain reaction (PCR) primers were designed specifically for P. pachyrhizi and two sets for P. meibomiae. Classical and real-time fluorescent PCR assays were developed to identify and differentiate between P. pachyrhizi and P. meibomiae. Identification of P. pachyrhizi from infected soybean leaves using the real-time PCR assay will allow for more rapid diagnoses.
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