Agriculture Reference
In-Depth Information
or an undistinguished morphology, including many viruses, bacteria and some fungi
(particularly fungi imperfecti and mycelia sterilia), can now be detected and
identified in host tissue and hence be eradicated at such early stages that losses can
be minimized. At the same time, such techniques allow the complete progress of an
epidemic to be observed. These methods are both sensitive and specific. An extreme
example of this is the use of PCR to detect strains of fungi that are resistant to
fungicides because of a single base-pair mutation (Martin et al., 1992b). This
technique also allows other minor changes in the genome of intraspecific strains,
races and genets of a pathogen to be monitored quickly, and even the origin and
period of mutation and its subsequent evolution may be identified (Smith et al.,
1992).
The majority of nucleic acid hybridization dot-blot tests may escape from the
confines of the laboratory in the future if immunocapture allows the handicap of
non-mobility to be overcome. Portability will increase the usefulness of this valuable
technique to plant disease epidemiologists, who have generally rejected any method
that is more restricted than immunological techniques and involves the services of
professional operators. In time, both immunological and nucleic acid identification
techniques are increasingly likely to be used in plant disease epidemiological studies
as they become automated to make them more rapid and affordable.
REFERENCES
Akagi, H., Yokozeki, Y., Inagaki, A. et al . (1996) A codominant DNA marker closely linked to the rice
nuclear restorer gene, Rf-1, identified with inter-SSR fingerprinting. Genome, 39 , 1205-1209.
Albani, M.C. and Wilkinson, M.J. (1998) Inter simple sequence repeat polymerase chain reaction for the
detection of somaclonal variation. Plant Breeding, 117 , 573-575.
Alizadeh, A.A., Eisen, M.B., Davis, R.E. et al . (2000) Distinct types of diffuse large B-cell lymphoma
identified by gene expression profiling. Nature , 286 , 503-511.
Alvarez, A.M. (2004) Integrated approaches for detection of plant pathogenic bacteria and diagnosis of
bacterial diseases. Annual Review of Phytopathology , 42 , 339-366.
Alwine, J.C., Kemp, D.J. and Stark, G.R. (1977) Method for detection of specific RNAs in agarose gels
by transfer to diazobenzyloxy-methyl paper and hybridization with DNA probes. Proceedings of the
National Academy of Sciences USA, 74 , 5350-5354.
Anderson, J.B., Petsche, D.M. and Smith, M.L. (1987) Restriction fragment polymorphisms in biological
species of Armillaria mellea in North America. Mycologia , 79 , 69-76.
Arcade, A., Anselin, F., Rampant, P.F. et al . (2000) Application of AFLP, RAPD and ISSR markers to
genetic mapping of European and Japanese larch. Theoretical and Applied Genetics , 100 , 299-307.
Assefa, K., Merker, A. and Tefera, H. (2003) Inter simple sequence repeat (ISSR) analysis of genetic
diversity in tef Eragrostis tef (Zucc.) Trotter. Hereditas, 139 , 174-183.
Audy, P., Laroche, A., Saindon, G. et al . (1994) Detection of the bean common blight bacteria,
Xanthomonas campestris pv. phaseoli and X. c. phaseoli var. fuscans , using the polymerase chain
reaction. Phytopathology , 84 , 1185-1192.
Avery, R.J., Norton, J.D., Jones, J.S. et al. (1980) Interferon inhibits transformation by murine sarcoma
viruses before integration of provirus. Nature, 289 , 93-95.
Barker, I. and Pitt, D. (1988) Detection of the leaf curl pathogen of anemones in corms by enzyme-
immunosorbent assay (ELISA). Plant Pathology, 37 , 417-422.
Barnes, L.W. (1986) The future of phytopathological diagnostics. Plant Disease, 70 , 180.
Barton, R.J. (1985) The development of sensitive mushroom virus detection methods. Mushroom
Journal, 151 , 223-228.
Search WWH ::




Custom Search