Search

Considering that the mechanisms for phosphite-afforded disease control remain elusive, this study investigated whether zinc (Zn) and copper (Cu) phosphites could possible potentiate common bean resistance to white mold, caused by Sclerotinia sclerotiorum, through the stimulation of biochemical defence responses. Lesion area and disease severity were decreased by phosphites spray, but Zn phosphite outcompeted Cu phosphite. Histopathological observations revealed fewer fungal hyphae and less collapse of the mesophyll cells in the Zn and Cu phosphite-sprayed plants compared to water-sprayed ones. The S. sclerotiorum-triggered accumulation of reactive oxygen species, oxalic acid (a fungal secreted toxin) and malondialdehyde (an indicator of cellular damage) were constrained as a result of Zn and Cu phosphites spray. Activities of antioxidant enzymes (superoxide dismutase, peroxidase, ascorbate peroxidase and glutathione-S-transferase at 12 h after inoculation (hai) and catalase at 60 and 84 hai) were higher for Zn and Cu phosphites-sprayed plants than for water-sprayed ones. Activities of defence-related enzymes chitinase (CHI) at 12 hai, β-1,3-glucanase (GLU) and polyphenoloxidase (PPO) were higher at 12-84 hai for Zn, and Cu phosphites sprayed plants, phenylalanine ammonia-lyase at 36-84 hai for the Zn phosphite sprayed ones, CHI at 12-36 hai, GLU at 12-60 hai, PPO at 36 hai and PAL and lipoxygenase at 12 hai for the Cu phosphite sprayed ones upon inoculation with S. sclerotiorum relative to their water-sprayed counterparts. Concentrations of total soluble phenols and lignin-thioglycolic acid derivatives were not affected by Cu phosphite spray on infected plants but were higher and lower, respectively, for Zn phosphite sprayed plants at 60 hai compared to water-sprayed ones. Taken together, the findings from the present study shed light on the biochemical defence mechanisms involved in the Zn and Cu phosphites-mediated suppression of white mold in common bean., (Copyright © 2018 Elsevier Masson SAS. All rights reserved.)

The success of Sclerotinia sclerotiorum infection relies mainly on the production of the non-host selective toxin named oxalic acid (OA). This toxin is known to play multiple roles in a host infected by the fungus, but its effect on photosynthesis and the antioxidant system of common bean plants remain elusive. Therefore, we performed detailed analysis of leaf gas exchange, chlorophyll a fluorescence, activities of antioxidant enzymes, concentrations of reactive oxygen species and photosynthetic pigments to investigate the OA's role during the S. sclerotiorum pathogenesis. To achieve this goal, common bean plants were sprayed with water or with oxalic acid (referred to as -OA and +OA plants, respectively) and either non-challenged or challenged with a wild-type (WT) or an OA-defective mutant (A4) of S. sclerotiorum. Irrespective of OA spray, the WT isolate was more aggressive than the A4 isolate and spraying OA increased OA concentration in the leaflets as well as the aggressiveness of both isolates. Biochemical limitations were behind S. sclerotiorum-induced photosynthetic impairments notably for the +OA plants inoculated with the WT isolate. Inoculated plants were not able to fully capture and exploit the collected energy due to the degradation of photosynthetic pigments. Photoinhibition of photosynthesis and photochemical dysfunctions were potentiated by OA. Higher activities of superoxide dismutase, peroxidase and ascorbate peroxidase besides reductions on catalase activity were noticed for plants inoculated with the WT isolate. OA was able to counteract most of the increases in the activities of antioxidant enzymes thereby increasing the generation of superoxide and hydrogen peroxide and the concurrent damage to the membranes of host cells as evidenced by the high malondialdehyde concentration. In conclusion, OA was found to enhance biochemical limitations to photosynthesis, photochemical dysfunctions and oxidative stress in the leaflets of common bean plants infected by S. sclerotiorum., (Copyright © 2018 Elsevier Masson SAS. All rights reserved.)