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Fast detection by loop-mediated isothermal amplification (LAMP) of the three begomovirus species infecting tomato in Panama
Authors:J A Herrera-Vásquez  A V Puchades  L Elvira-González  J N Jaén-Sanjur  C Carpino  L Rubio  L Galipienso
Institution:1.Grupo de Investigación de Protección Vegetal (GIPV), Centro de Investigación Agropecuaria Central (CIAC), Instituto de Investigación Agropecuaria de Panamá (IDIAP),Herrera,Panama;2.Instituto Valenciano de Investigaciones Agrarias (IVIA),Valencia,Spain;3.Escuela de Biología, Facultad de Ciencias Naturales, Exactas y Tecnología,Ciudad Universitaria Dr. Octavio Méndez Pereira, Universidad de Panamá (UP), Estafeta Universitaria,Panama 4,Panama;4.Department of Agricultural and Forestry Science,University of Palermo,Palermo,Italy;5.Departamento de Biotecnología, Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural,Universitat Politècnica de València (UPV),València,Spain
Abstract:Potato yellow mosaic Panama virus (PYMPV), Tomato leaf curl Sinaloa virus (ToLCSiV) and Tomato yellow mottle virus (TYMoV) of genus Begomovirus (family Geminiviridae) are the only three begomovirus species detected infecting tomato (Solanum lycopersicum L.) in Panama. PYMPV, ToLCSiV and TYMoV induce symptoms of stunting, yellowing, curling, distortion of leaves and reduction of fruit size and cause important economic loses. A loop-mediated amplification under isothermal conditions (LAMP) assay was developed for the individual detection of these three begomovirus species by using a set of three primer pairs specific per each one of them. Amplification products were visualized by gel electrophoresis or direct Gel-Red staining of DNA into the reaction tube. PYMPV, ToLCSiV and TYMoV were detected in total DNA extracts obtained from different plant tissues such as leaves, stems, flowers, fruits and roots of infected tomato plants collected in different production regions of Panama. LAMP sensitivity was similar to that of conventional PCR but, the first procedure was faster and cheaper than the last one. Moreover, all three viruses were successfully detected by LAMP and not by conventional PCR from sap extracts obtained from leaf tissues of infected tomato plants which were embedded into 3MM Whatman paper and stored several days, facilitating the samples processing as well as the material movement among different laboratories. Therefore, LAMP is a specific, rapid and cheap procedure to detect all three begomoviruses infecting tomato in Panama and it is suitable for field surveys and sanitation programs.
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