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ROS and NO production in compatible and incompatible tomato-Meloidogyne incognita interactions

Academic Article
Publication Date:
2011
abstract:
Nitric oxide (NO) has been shown to be an essential regulatory molecule in plant response to pathogen infection in synergy with reactive oxygen species (ROS). At the present, nothing is known about the role of NO in disease resistance to nematode infection. We used a resistant tomato cultivar with different sensitivity to avirulent and virulent populations of the root-knot nematode Meloidogyne incognita to investigate the key components involved in oxidative and nitrosative metabolism. We analyzed the superoxide radical production, hydrogen peroxide content, and nitric oxide synthase (NOS)-like and nitrate reductase activities, as potential sources of NO. A rapid NO accumulation and ROS production were found at 12 h after infection in compatible and incompatible tomatonematode interactions, whereas the amount of NO and ROS gave different results 24 and 48 h after infection amongst compatible and incompatible interactions. NOS-like arginine-dependent enzyme rather than nitrate reductase was the main source of NO production, and NOS-like activity increased substantially in the incompatibleinteraction.We can envisage a functional overlap of both NO and ROS in tomato defence response to nematode invasion, NO and H2O2 cooperating in triggering hypersensitive cell death. Therefore, NO and ROS are key molecules which may help to orchestrate events following nematode challenge, and which may influence the host cellular metabolism.
Iris type:
01.01 Articolo in rivista
Keywords:
Defence response; H2O2; NO; ROS; Root-knot nematodes
List of contributors:
Bleve, Teresa; Leone, Antonella; Veronico, Pasqua; Leonetti, Paola; Melillo, MARIA TERESA
Authors of the University:
LEONE ANTONELLA
LEONETTI PAOLA
VERONICO PASQUA
Handle:
https://iris.cnr.it/handle/20.500.14243/144391
Published in:
EUROPEAN JOURNAL OF PLANT PATHOLOGY
Journal
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URL

http://link.springer.com/article/10.1007%2Fs10658-011-9768-4
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