An Inter-Laboratory Comparative Study on the Influence of Reagents to Perform the Identification of the <i>Xylella fastidiosa</i> Subspecies Using Tetraplex Real Time PCR
Nicoletta Pucci,
Valeria Scala,
Erica Cesari,
Valeria Crosara,
Riccardo Fiorani,
Alessia L’Aurora,
Simone Lucchesi,
Giuseppe Tatulli,
Eleonora Barra,
Serena Ciarroni,
Francesca De Amicis,
Salvatore Fascella,
Francesca Giacobbi,
Francesca Gaffuri,
Valeria Gualandri,
Lucia Landi,
Giuliana Loconsole,
Giulia Molinatto,
Stefania Pollastro,
Maria Luisa Raimondo,
Domenico Rizzo,
Chiara Roggia,
Maria Rosaria Silletti,
Simona Talevi,
Marco Testa,
Stefania Loreti
Affiliations
Nicoletta Pucci
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Valeria Scala
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Erica Cesari
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Valeria Crosara
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Riccardo Fiorani
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Alessia L’Aurora
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Simone Lucchesi
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
Giuseppe Tatulli
Council for Agricultural Research and Economics, Research Centre for Plant Protection and Certification (CREA-DC), 00156 Rome, Italy
In 2022, a test performance study (TPS) assessing the influence of different master mixes on the performance of the tetraplex real-time PCR (TqPCR) assay was organized. TqPCR allows for the specific detection and identification of Xylella fastidiosa (Xf) subspecies in a single reaction. Eighteen official laboratories of the Italian National Plant Protection Organization received a panel of 12 blind samples, controls, primers, probes, and different master mixes to participate in the TPS. Furthermore, the Research Centre for Plant Protection and Certification of the Council for Agricultural Research and Economics performed an intra-laboratory study (ITS) on spiked plant matrices to evaluate the analytical sensitivity of TqPCR employing the selected master mixes with the best performance. Naturally infected samples were analyzed for subspecies identification via TqPCR compared with the official multilocus-sequence-typing (MLST) method. The best results in this comparative study were obtained using Fast Universal PCR Master Mix (Applied Biosystems) and Brilliant multiplex QPCR Master Mix (Agilent), and they confirmed that the TqPCR test is reliable, offering the advantage of identifying this subspecies at the same time, thus saving time and resources. The TqPCR assay is suggested among the tests to be used by laboratories performing the official diagnosis of Xf to support the activities of official monitoring.