Development of a DNA-Based Real-Time PCR Assay To Quantify Allorhizobium vitis Over Time in Grapevine (Vitis vinifera L.) Plantlets

Author:

Nguyen-Huu Trong1ORCID,Doré Jeanne2,Aït Barka Essaïd1,Lavire Céline2ORCID,Clément Christophe1,Vial Ludovic2,Sanchez Lisa1ORCID

Affiliation:

1. Unité EA 4707 Résistance Induite et Bioprotection des Plantes, SFR Condorcet FR Centre National de la Recherche Scientifique (CNRS) 3417, Université de Reims Champagne-Ardenne, Reims, France

2. UMR Ecologie Microbienne, CNRS, National Research Institute for Agriculture, Food and Environment, VetAgro Sup, Université Claude-Bernard Lyon, Université de Lyon, F-69622 Villeurbanne, Lyon, France

Abstract

Allorhizobium vitis is the primary causal pathogen of grapevine crown gall disease. Because this endophytic bacterium can survive as a systemic latent (symptomless) infection in grapevine, detecting and monitoring its development in planta is of great importance. In plant bacteria studies, plate counting is routinely used as a simple and reliable method to evaluate the bacterial population level in planta. However, isolation techniques are time-consuming and present some disadvantages such as the risk of contamination and the need for fresh samples for research. In this study, we developed a DNA-based real-time PCR assay that can replace the classical method to monitor the development of Allorhizobium vitis in grapevine plantlets. Primers targeting Allorhizobium vitis chromosomic genes and the virulent tumor-inducing plasmid were validated. The proposed quantitative real-time PCR technique is highly reliable and reproducible to assess Allorhizobium vitis numeration at the earliest stage of infection until tumor development in grapevine plantlets. Moreover, this low-cost technique provides rapid and robust in planta quantification of the pathogen and is suitable for fundamental research to monitor bacterial development over time.

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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