| Literature DB >> 11701842 |
Robert R Martin1, Delano James2, C André Lévesque3.
Abstract
Detection and diagnosis of plant viruses has included serological laboratory tests since the 1960s. Relatively little work was done on serological detection of plant pathogenic bacteria and fungi prior to the development of ELISA and monoclonal antibody technologies. Most applications for laboratory-based tests were directed at virus detection with relatively little emphasis on fungal and bacterial pathogens, though there was some good work done with other groups of plant pathogens. With the advent of molecular biology and the ability to compare regions of genomic DNA representing conserved sequences, the development of laboratory tests increased at an amazing rate for all groups of plant pathogens. Comparison of ITS regions of bacteria, fungi, and nematodes has proven useful for taxonomic purposes. Sequencing of conserved genes has been used to develop PCR-based detection with varying levels of specificity for viruses, fungi, and bacteria. Combinations of ELISA and PCR technologies are used to improve sensitivity of detection and to avoid problems with inhibitors or PCR often found in plants. The application of these technologies in plant pathology has greatly improved our ability to detect plant pathogens and is increasing our understanding of, their ecology and epidemiology.Keywords: ELISA; PCR; disease diagnosis; disease management; microarrays; pathogen detection; plant quarantine; polymerase chain reaction
Year: 2000 PMID: 11701842 DOI: 10.1146/annurev.phyto.38.1.207
Source DB: PubMed Journal: Annu Rev Phytopathol ISSN: 0066-4286 Impact factor: 13.078