Title
R/Avr gene expression study of Rpi-vnt1.1 transgenic potato resistant to the Phytophthora infestans clonal lineage EC-1
Date Issued
01 November 2017
Access level
open access
Resource Type
journal article
Author(s)
Publisher(s)
Springer Netherlands
Abstract
The Avr avirulence gene of Phytophthora infestans and R gene of the potato are the genetic components of the gene-for-gene interaction resulting in host plant resistance. This effector-triggered immunity has been recently exploited to generate extreme resistance to late blight in potato by genetic engineering. The choice of the R genes, their number forming a R gene stack, and the pathogen Avr gene diversity will likely determine how long this extreme resistance will last. Here, we report on a comparative study on the Rpi-vnt1.1 gene which originated from Solanum venturii, and was introduced in the potato variety ‘Desiree’ by genetic transformation, and the Avr-vnt1 gene from two isolates of the EC-1 lineage of P. infestans. EC-1 was reported previously as not expressing the Avr-vnt1 gene and, therefore, being virulent on Rpi-vnt1.1 transgenic plants. Unexpectedly, whole-plant resistance assays identified 5 out of 52 transgenic events as resistant to two isolates of P. infestans, POX067 and POX109, belonging to the EC-1 lineage. We demonstrated that in both isolates, the Avr-vnt1.1 gene was expressed at a low level. Expression of the Rpi-vnt1.1 gene was shown to be rapidly increased by two-fold and subsequently to have steady state expression for at least 5 days after the inoculation. The Rpi-vnt1.1 gene in addition to other R genes as a stack in farmers’ preferred varieties will confer extreme resistance to late blight disease and rotations of plants with different R-gene-stack in time is likely to last longer than plants with single R gene.
Start page
259
End page
268
Volume
131
Issue
2
Language
English
OCDE Knowledge area
Ciencias de las plantas, Botánica
Protección y nutrición de las plantas
Subjects
Scopus EID
2-s2.0-85024482830
Source
Plant Cell, Tissue and Organ Culture
ISSN of the container
01676857
Sponsor(s)
Acknowledgements This research was supported by the United States Agency for International Development (USAID) and recently by the 2Blades foundation.
Sources of information:
Directorio de Producción Científica
Scopus