INVESTIGADORES
CASTAGNARO Atilio Pedro
artículos
Título:
Induction of a defense response in strawberry mediated by an avirulent strain
Autor/es:
S. M. SALAZAR, A. P. CASTAGNARO, M. E. ARIAS, N. CHALFOUN, U. TONELLO, AND J. C. DÝAZ RICCI
Revista:
EUROPEAN JOURNAL OF PLANT PATHOLOGY
Referencias:
Año: 2006 vol. 117 p. 109 - 112
ISSN:
0929-1873
Resumen:
In the strawberry crop area of Tucuma´ n (north-west Argentina) the three species of Colletotrichum causing
anthracnose disease (C. acutatum, C. fragariae and C. gloeosporioides) were detected. Among all isolates
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
anthracnose disease (C. acutatum, C. fragariae and C. gloeosporioides) were detected. Among all isolates
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
Colletotrichum causing
anthracnose disease (C. acutatum, C. fragariae and C. gloeosporioides) were detected. Among all isolates
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
C. acutatum, C. fragariae and C. gloeosporioides) were detected. Among all isolates
characterized, one of them identified as C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitro
C. acutatum (M11) and another as C. fragariae (F7) were selected
due to their conspicuous interaction with the strawberry cultivar Pa´ jaro. Whereas isolate M11 produced a
strong compatible interaction in cv. Pa´ jaro with clear disease symptoms (DSR = 5.0), the isolate F7
brought about a typical incompatible interaction (DSR = 1.0). When plants of cv. Pa´ jaro were inoculated
with F7 prior to the inoculation with M11, the former avirulent strain prevented the growth of the latter
virulent pathogen. Experimental evidence indicated that the time elapsed between the first inoculation with
the avirulent pathogen and the second inoculation with the virulent one was crucial to inhibit the growth of
the latter. The growth of F7 on the plant without provoking damage and the fact that there was no in vitroin vitro
antagonistic effect between the pathogens, suggests that the avirulent strain triggers a plant defensive
response against M11. The defense response was further confirmed by the detection of an early oxidative
burst occurring within 4 h after the first inoculation and by the observation of anatomical changes associated
with defense mechanisms that lasted 50 days after the inoculation with F7. Results obtained support
the hypothesis that the plant resistance against the virulent strain M11 is elicited by one or more diffusible(
s) compound(s) produced by the avirulent strain F7.