z-logo
open-access-imgOpen Access
DspA/E, a Type III Effector Essential for Erwinia amylovora Pathogenicity and Growth In Planta, Induces Cell Death in Host Apple and Nonhost Tobacco Plants
Author(s) -
Tristan Boureau,
Hayat ElMaarouf-Bouteau,
Amélie Garnier,
Marie-Noëlle Brisset,
C. Perino,
Igor Pucheu,
MarieAnne Barny
Publication year - 2006
Publication title -
molecular plant-microbe interactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.565
H-Index - 153
eISSN - 1943-7706
pISSN - 0894-0282
DOI - 10.1094/mpmi-19-0016
Subject(s) - erwinia , biology , hypersensitive response , fire blight , microbiology and biotechnology , virulence , effector , type three secretion system , secretion , callose , necrosis , programmed cell death , cell wall , bacteria , botany , gene , genetics , immunology , apoptosis , biochemistry
Erwinia amylovora is responsible for fire blight, a necrotic disease of apples and pears. E. amylovora relies on a type III secretion system (TTSS) to induce disease on hosts and hypersensitive response (HR) on nonhost plants. The DspA/E protein is essential for E. amylovora pathogenicity and is secreted via the TTSS in vitro. DspA/E belongs to a type III effector family that is conserved in several phytopathogenic bacteria. In E. amylovora, DspA/E has been implicated in the generation of an oxidative stress during disease and the suppression of callose deposition. We investigated the fate of DspA/E in planta. DspA/E delivered artificially to apple or tobacco cells by agroinfection induced necrotic symptoms, indicating that DspA/E was probably injected via the TTSS. We confirmed that DspA/E acts as a major cell-death inducer during disease and HR, because the dspA/E mutant is severely impaired in its ability to induce electrolyte leakage in apple and tobacco leaves. Expression of the defense marker gene PR1 was delayed when dspA/E was transiently expressed in tobacco, suggesting that DspA/E-mediated necrosis may be associated with an alteration of defense responses.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here