Innovative tools for detection of plant pathogenic viruses and bacteria Autors/ores María M. López Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Edson Bertolini Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Antonio Olmos Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Paola Caruso Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain María Teresa Gorris Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Pablo Llop Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Ramón Penyalve Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Mariano Cambra Instituto Valenciano de Investigaciones Agrarias, Moncada, Valencia, Spain Paraules clau: antibodies, co-operational PCR, DNA microarrays, elisa, enrichment, fish, multiplex PCR, nested-multiplex PCR, real time PCR Resum Detection of harmful viruses and bacteria in plant material, vectors or natural reservoirs is essential to ensure safe and sustainable agriculture. The techniques available have evolved significantly in the last few years to achieve rapid and reliable detection of pathogens, extraction of the target from the sample being important for optimising detection. For viruses, sample preparation has been simplified by imprinting or squashing plant material or insect vectors onto membranes. To improve the sensitivity of techniques for bacterial detection, a prior enrichment step in liquid or solid medium is advised. Serological and molecular techniques are currently the most appropriate when high numbers of samples need to be analysed. Specific monoclonal and/or recombinant antibodies are available for many plant pathogens and have contributed to the specificity of serological detection. Molecular detection can be optimised through the automatic purification of nucleic acids from pathogens by columns or robotics. New variants of PCR, such as simple or multiplex nested PCR in a single closed tube, co-operative- PCR and real-time monitoring of amplicons or quantitative PCR, allow high sensitivity in the detection of one or several pathogens in a single assay. The latest development in the analysis of nucleic acids is microarray technology, but it requires generic DNA/RNA extraction and pre-amplification methods to increase detection sensitivity. The advances in research that will result from the sequencing of many plant pathogen genomes, especially now in the era of proteomics, represent a new source of information for the future development of sensitive and specific detection techniques for these microorganisms. Descàrregues PDF (English) Publicat 2010-03-03 Número Vol. 6 Núm. 4 (2003) Secció Review Articles Llicència Submission of a manuscript to International Microbiology implies: that the work described has not been published before, including publication in the World Wide Web (except in the form of an Abstract or as part of a published lecture, review, or thesis); that it is not under consideration for publication elsewhere; that all the coauthors have agreed to its publication. The corresponding author signs for and accepts responsability for releasing this material and will act on behalf of any and all coauthors regarding the editorial review and publication process.If an article is accepted for publication in International Microbiology, the authors (or other copyright holder) must transfer to the journal the right–not exclusive–to reproduce and distribute the article including reprints, translations, photographic reproductions, microform, electronic form (offline, online) or any other reproductions of similar nature. Nevertheless, all article in International Microbiology will be available on the Internet to any reader at no cost. The journal allows users to freely download, copy, print, distribute, search, and link to the full text of any article, provided the authorship and source of the published article is cited. The copyright owner's consent does not include copying for new works, or resale. In these cases, the specific written permission of International Microbiology must first be obtained.Authors are requested to create a link to the published article on the journal's website. The link must be accompanied by the following text: "The original publication is available on LINK at <http://www.im.microbios.org>. Please use the appropiate URL for the article in LINK. Articles disseminated via LINK are indexed, abstracted, and referenced by many abstracting and information services, bibliographic networks, subscription agencies, library networks, and consortia.