<i>Alternaria alternata</i> AT Toxin Induces Programmed Cell Death in Tobacco

Abstract

Abstract Detached tobacco leaves were infiltrated with an AT toxin preparation from the foliar pathogen Alternaria alternata tobacco pathotype. The AT toxin preparation caused formation of necrotic lesions within 5 days post‐infiltration in a concentration‐dependent manner. Cell death was accompanied by increased levels of the stress metabolites hydrogen peroxide, malondialdehyde, free proline and by enhanced total protease activity. Lesion development and the production of stress metabolites were suppressed if the infiltration site was pre‐infiltrated with caspase‐specific peptide inhibitors (irreversible caspase‐1 inhibitor acyl‐Tyr‐Val‐Ala‐Asp‐chloromethylketone (Ac‐YVAD‐CMK) and the broad range caspase inhibitor benzyoxycarbonyl‐Asp‐2,6‐dichlorobenzoyloxymethylketone (Z‐Asp‐CH2‐DCB)), the serine protease inhibitor Nα‐p‐tosyl‐ l ‐lysine chloromethylketone and the polyamine spermine. Extensive accumulation of reactive oxygen species (ROS), as determined by staining with 3‐3′‐diaminobenzidine and 2′,7′‐dichlorofluorescein diacetate, was found in the AT toxin‐challenged lesions. The data show that AT toxin‐induced cell death in tobacco is a type of programmed cell death in which caspase‐like proteases and ROS signalling play a prominent role.