摘要

A real-time quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) was employed to investigate the transcriptional levels of putative defence genes expressed during postharvest storage of Actinidia chinensis'Hort16A' kiwifruit. Significant decreases (80% reduction) in normalized gene expression over time relative to the basal levels of gene expression at harvest in control fruit were observed for thaumatin-like protein (TLP), class IV acidic chitinase, chalcone-flavonone isomerase (CHI) and glucan endo-1,3-beta-glucosidase (beta-1,3-glucosidase). Reduction in transcript abundance for these genes paralleled the significant increase in postharvest ripe rot disease incidence over time (P = 0.0008). Gene expression levels were approximately the same in control vs. inoculated fruit for all the four genes described above, except for beta-1,3-glucosidase where expression was significantly greater (P = 0.007) in inoculated than in control fruit. For one of the genes of interest that we had studied by qRT-PCR, TLP, a small amount of protein was purified and assayed in vitro for activity against Cryptosporiopsis actinidiae and Phomopsis spp., the causal agents of ripe rots of 'Hort16A' kiwifruit. TLP from kiwifruit did not appear to be directly toxic to either pathogen. TLP does not prevent ripe rots, but it may be useful as a marker of resistance given the temporal correlation between decreased TLP and increased ripe rots that was demonstrated by qRT-PCR.

  • 出版日期2011-6