Molecular Diagnostics in Tomato: Chip Digital PCR Assays Targeted to Identify and Quantify <i>Clavibacter michiganensis</i> subsp. <i>michiganensis</i> and <i>Ralstonia solanacearum in planta</i>
Caterina Morcia,
Isabella Piazza,
Roberta Ghizzoni,
Valeria Terzi,
Ilaria Carrara,
Giovanni Bolli,
Giorgio Chiusa
Affiliations
Caterina Morcia
Council for Agricultural Research and Economics (CREA), Research Centre for Genomics and Bioinformatics (GB), Via S. Protaso 302, 29017 Fiorenzuola d’Arda, PC, Italy
Isabella Piazza
Council for Agricultural Research and Economics (CREA), Research Centre for Genomics and Bioinformatics (GB), Via S. Protaso 302, 29017 Fiorenzuola d’Arda, PC, Italy
Roberta Ghizzoni
Council for Agricultural Research and Economics (CREA), Research Centre for Genomics and Bioinformatics (GB), Via S. Protaso 302, 29017 Fiorenzuola d’Arda, PC, Italy
Valeria Terzi
Council for Agricultural Research and Economics (CREA), Research Centre for Genomics and Bioinformatics (GB), Via S. Protaso 302, 29017 Fiorenzuola d’Arda, PC, Italy
Ilaria Carrara
Council for Agricultural Research and Economics (CREA), Research Centre for Genomics and Bioinformatics (GB), Via S. Protaso 302, 29017 Fiorenzuola d’Arda, PC, Italy
Giovanni Bolli
DIPROVES, Dipartimento di Scienze delle Produzioni Vegetali Sostenibili—Università Cattolica del Sacro Cuore, Via Emilia Parmense 84, 29122 Piacenza, PC, Italy
Giorgio Chiusa
DIPROVES, Dipartimento di Scienze delle Produzioni Vegetali Sostenibili—Università Cattolica del Sacro Cuore, Via Emilia Parmense 84, 29122 Piacenza, PC, Italy
Clavibacter michiganensis subsp. michiganensis (Cmm) and Ralstonia solanacearum (Rs) are important bacterial pathogens of tomatoes (Solanum lycopersicum), are included in A2 list in the EPPO (European and Mediterranean Plant Protection Organization) region and are recommended for regulation as quarantine pests. The control of quarantine pathogens requires accurate and rapid detection tools. In this study, a method based on chip digital PCR (cdPCR) was developed to identify and quantify Cmm and Rs. The assays were tested on pure bacteria samples and on tomato samples naturally contaminated or spiked with bacteria DNA. For a better estimation of infection level in host plants, duplex assays that are able to simultaneously amplify plant and bacteria DNA were developed. The two cdPCR assays proposed can be used for the rapid and timely detection of this group of high-risk quarantine bacteria to prevent the spread of pathogens and the occurrence of disease in other areas.