Cell death-mediated antiviral effect of chitosan in tobacco

The antiviral activity induced by chitosan (CHT), and the mechanisms underlying it, were studied in a tobacco–tobacco necrosis necrovirus (TNV) pathosystem. Treatments with 0.1% CHT enhanced tobacco inducible defenses against TNV, reducing significantly the virus-induced necrotic lesions (in a range...

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Veröffentlicht in:Plant physiology and biochemistry 2006-11, Vol.44 (11), p.893-900
Hauptverfasser: Iriti, M., Sironi, M., Gomarasca, S., Casazza, A.P., Soave, C., Faoro, F.
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Sprache:eng
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Zusammenfassung:The antiviral activity induced by chitosan (CHT), and the mechanisms underlying it, were studied in a tobacco–tobacco necrosis necrovirus (TNV) pathosystem. Treatments with 0.1% CHT enhanced tobacco inducible defenses against TNV, reducing significantly the virus-induced necrotic lesions (in a range from 32% to 83%). In planta, this resistance was associated with a network of callose deposits, micro-oxidative bursts and micro-hypersensitive responses (micro-HRs), as assessed, respectively, by aniline blue, 3,3′-diaminobenzidine (DAB) and Evans blue staining. In order to verify if CHT-elicited cell death could be regarded as an apoptotic process, tobacco bright yellow 2 (BY2) cell cultures were treated with different CHT concentrations, ranging from 0.01% to 0.1%. After 6 h about half of the cultured cells incubated in 0.05% CHT were Evans blue positive, showing some typical morphological features of apoptosis, such as cytoplasm shrinkage and nuclear chromatin condensation. The latter was checked by 4′,6-diamino-2-phenylindole (DAPI) and ethidium bromide nuclear staining and was visible already at 2 h after treatment. Moreover, the cell death kinetic induced by CHT was delayed by Verapamil®, a calcium channel blocker. Finally, electrophoresis of genomic DNA extracted from cultured cell after 48 h treatment showed internucleosomal fragmentation, visualized as a distinct ladder of DNA bands corresponding to oligonucleosomal units.
ISSN:0981-9428
1873-2690
DOI:10.1016/j.plaphy.2006.10.009