An Assay Based on the Polymerase Chain Reaction for the Detection of N‐ and L‐types of Pseudocercosporella herpotrichoides in Wheat
M. L. Gac, F. Montfort, N. Cavelier
Abstract
M. L. Gac, F. Montfort, N. Cavelier
Abstract
Abstract A polymerase chain reaction (PCR) test combined with restriction enzyme digestion of an amplified ribosomal DNA fragment is currently available for the identification of N‐ and L‐type isolates of Pseudocercosporella herpotrichoides from purified fungal DNA. This study shows that both types of the fungus can be differentiated in the plant using the PCR assay and that the test is extremely sensitive. The PCR assay is used to compare the development of one isolate of each the N‐ and L‐type in wheat under glasshouse conditions. The results indicate that for an identical infection date, the N‐type tends to penetrate the tissues faster than the L‐type.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract A polymerase chain reaction (PCR) test combined with restriction enzyme digestion of an amplified ribosomal DNA fragment is currently available for the identification of N‐ and L‐type isolates of Pseudocercosporella herpotrichoides from purified fungal DNA. This study shows that both types of the fungus can be differentiated in the plant using the PCR assay and that the test is extremely sensitive. The PCR assay is used to compare the development of one isolate of each the N‐ and L‐type in wheat under glasshouse conditions. The results indicate that for an identical infection date, the N‐type tends to penetrate the tissues faster than the L‐type.
Key concepts: Biology, Polymerase chain reaction, Ribosomal DNA, Fungi imperfecti, Restriction enzyme, Fungus, DNA, Ribosomal RNA