Diversity of the cassiicolin gene in Corynespora cassiicola and relation with the pathogenicity in Hevea brasiliensis.

Corynespora cassiicola is an important plant pathogenic Ascomycete causing the damaging Corynespora Leaf Fall (CLF) disease in rubber tree (Hevea brasiliensis). A small secreted glycoprotein named cassiicolin was previously described as an important effector of C. cassiicola. In this study, the diversity of the cassiicolin-encoding gene was analysed in C. cassiicola isolates sampled from various hosts and geographical origins. A cassiicolin gene was detected in 47 % of the isolates, encoding up to six distinct protein isoforms. In three isolates, two gene variants encoding cassiicolin isoforms Cas2 and Cas6 were found in the same isolate. A phylogenetic tree based on four combined loci and elucidating the diversity of the whole collection was strongly structured by the toxin class, as defined by the cassiicolin isoform. The isolates carrying the Cas1 gene (toxin class Cas1), all grouped in the same highly supported clade, were found the most aggressive on two rubber tree cultivars. Some isolates in which no Cas gene was detected could nevertheless generate moderate symptoms, suggesting the existence of other yet uncharacterized effectors. This study provides a useful base for future studies of C. cassiicola population biology and epidemiological surveys in various host plants.

Characterization of a cassiicolin-encoding gene from Corynespora cassiicola, pathogen of rubber tree (Hevea brasiliensis).

Corynespora Leaf Fall (CLF) is a major disease of rubber tree (Hevea brasiliensis) caused by the Ascomycota Corynespora cassiicola. Here we describe the cloning and characterization of a gene encoding cassiicolin (Cas), a glycosylated cystein-rich small secreted protein (SSP) identified as a potential CLF disease effector in rubber tree. Three isolates with contrasted levels of aggressiveness were analyzed comparatively. The cassiicolin gene was detected - and the toxin successfully purified - from the isolates with high and medium aggressiveness (CCP and CCAM3 respectively) but not from the isolate with the lowest aggressiveness (CCAM1), suggesting the existence of a different disease effector in the later. CCP and CCAM3 carried strictly identical cassiicolin genes and produced toxins of identical mass, as evidence by mass spectrometry analysis, thus suggesting conserved post-translational modifications in addition to sequence identity. The differences in aggressiveness between CCP and CCAM3 may be attributed to differences in cassiicolin transcript levels rather than qualitative variations in cassiicolin structure. Cassiicolin may play an important role in the early phase of infection since a peak of cassiicolin transcripts occurred in 1 or 2 days after inoculation (before the occurrence of the first symptoms), in both the tolerant and the susceptible cultivars.

Contrasting strategies to cope with chilling stress among clones of a tropical tree, Hevea brasiliensis.

Eight Hevea brasiliensis Muell. Arg. clones (GT1, YUNYAN77-4, IRCA707, IRCA317, PB217, PB260, PR107 and RRIM600) were compared for their tolerance towards chilling stress. Net photosynthesis (Pn), stomatal conductance (Gs), optimal and effective photochemical efficiencies (F(v)/F(m) and ), non-photochemical quenching, cellular lysis and leaf necrosis were measured on trees chilled at 10 °C for 96 h, as well as upon recovery at 28 °C. In addition, ascorbate peroxidase, catalase, dehydroascorbate reductase, glutathione reductase, monodehydroascorbate reductase and superoxide dismutase activities were monitored. Clone RRIM600 appeared to be the most tolerant, because it showed no cellular lysis or leaf necrosis and the best recovery as revealed by Pn, Gs, F(v)/F(m) and . Its ability to sustain chilling stress seemed related in part to the fast closure of stomata, suggesting an 'avoidance strategy' for this clone. IRCA707, GT1 and YUNYAN77-4 were also tolerant to the cold treatment as only a few leaf injuries were observed. However, YUNYAN77-4 showed a particular behaviour with a large stomata opening during the first hour of chilling, some photosynthetic activity after 96 h at 10 °C, but the slowest recovery in Pn. The greatest cell or leaf damage was observed on PB260, IRCA317, PR107 and PB217 clones, thus classified as sensitive to chilling. These clones showed the strongest decrease in Pn, F(v)/F(m) and and the slowest recovery for F(v)/F(m) and , indicating a high sensitivity of photosystem II to cold temperatures. Punctual increases of various enzymatic activities were observed for all clones during chilling kinetics. During recovery, the strongest increases in enzymatic activity were observed for the most tolerant clones, suggesting that efficient reactive oxygen species elimination is a crucial step for determining chilling tolerance in Hevea although the enzymes implicated varied from one tolerant clone to another. This study points out contrasted strategies of the Hevea clones in copping with chilling stress and recovery.