Ultrastructural Changes in Apple Leaves Inoculated with a Virulent or an Avirulent Strain of Erwinia amylovora

1970 ◽  
Vol 68 (3) ◽  
pp. 258-268 ◽  
Author(s):  
R. N. Goodman ◽  
A. Burkowicz
2011 ◽  
pp. 489-494 ◽  
Author(s):  
M. Sklodowska ◽  
E. Gajewska ◽  
E. Kuzniak ◽  
M. Wielanek ◽  
A. Mikiciński ◽  
...  

Author(s):  
Maria Skłodowska ◽  
Artur Mikiciński ◽  
Marzena Wielanek ◽  
Elżbieta Kuźniak ◽  
Piotr Sobiczewski

2011 ◽  
Vol 24 (5) ◽  
pp. 577-584 ◽  
Author(s):  
Tristan Boureau ◽  
Sabrina Siamer ◽  
Claude Perino ◽  
Stéphane Gaubert ◽  
Oriane Patrit ◽  
...  

Erwinia amylovora is responsible for fire blight of apple and pear trees. Its pathogenicity depends on a type III secretion system (T3SS) mediating the translocation of effectors into the plant cell. The DspA/E effector suppresses callose deposition on apple leaves. We found that E. amylovora and Pseudomonas syringae DC3000 tts mutants or peptide flg22 do not trigger callose deposition as strongly as the dspA/E mutant on apple leaves. This suggests that, on apple leaves, callose deposition is poorly elicited by pathogen-associated molecular patterns (PAMPs) such as flg22 or other PAMPs harbored by tts mutants and is mainly elicited by injected effectors or by the T3SS itself. Callose elicitation partly depends on HrpW because an hrpW-dspA/E mutant elicits lower callose deposition than a dspA/E mutant. Furthermore, an hrpN-dspA/E mutant does not trigger callose deposition, indicating that HrpN is required to trigger this plant defense reaction. We showed that HrpN plays a general role in the translocation process. Thus, the HrpN requirement for callose deposition may be explained by its role in translocation: HrpN could be involved in the translocation of other effectors inducing callose deposition. Furthermore, HrpN may also directly contribute to the elicitation process because we showed that purified HrpN induces callose deposition.


2009 ◽  
Vol 99 (2) ◽  
pp. 128-138 ◽  
Author(s):  
K. B. Johnson ◽  
T. L. Sawyer ◽  
V. O. Stockwell ◽  
T. N. Temple

As a prerequisite to infection of flowers, Erwinia amylovora grows epiphytically on stigmas, which provide a conducive habitat for bacterial growth. Stigmas also support growth of several other bacterial genera, which allows for biological control of fire blight; although, in practice, it is very difficult to exclude E. amylovora completely from this habitat. We investigated the dynamics of growth suppression of E. amylovora by comparing the ability of virulent and avirulent strains of E. amylovora to compete with each other on stigmas of pear, apple, and blackberry, and to compete with a co-inoculated mixture of effective bacterial antagonists. When strains were inoculated individually, virulent E. amylovora strain Ea153N attained the highest population size on stigmas, with population sizes that were approximately double those of an avirulent hrpL mutant of Ea153 or the bacterial antagonists. In competition experiments, growth of the avirulent derivative was suppressed by the antagonist mixture to a greater extent than the virulent strain. Unexpectedly, the virulent strain enhanced the population size of the antagonist mixture. Similarly, a small dose of virulent Ea153N added to inoculum of an avirulent hrpL mutant of Ea153 significantly increased the population size of the avirulent strain. A pathogenesis-gene reporter strain, Ea153 dspE::gfp, was applied to flowers and a subset of the population expressed the green fluorescent protein while growing epiphytically on stigmas of apple. These results are consistent with the hypothesis that virulent E. amylovora modifies the epiphytic habitat presented by the stigma through a pathogenesis-related process, which increases host resources available to itself and, coincidentally, to nonpathogenic competitors. Over nine orchard trials, avirulent Ea153 hrpL significantly suppressed the incidence of fire blight four times compared with six for the antagonist mixture. The degree of biological control achievable with an avirulent strain of E. amylovora likely is limited by its inability to utilize the stigmatic habitat to the same degree as a virulent strain.


2011 ◽  
Vol 159 (7-8) ◽  
pp. 495-504 ◽  
Author(s):  
Maria Skłodowska ◽  
Ewa Gajewska ◽  
Elżbieta Kuźniak ◽  
Marzena Wielanek ◽  
Artur Mikiciński ◽  
...  

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