LaeA regulation of secondary metabolism modulates virulence in Penicillium expansum and is mediated by sucrose
Kumar, D; Barad, S; Chen, Y; Luo, X; Tannous, J; Dubey, A; Glam Matana, N; Tian, S; Li, B; Keller, N; Prusky, D
| HERO ID | 4943342 |
|---|---|
| In Press | No |
| Year | 2017 |
| Title | LaeA regulation of secondary metabolism modulates virulence in Penicillium expansum and is mediated by sucrose |
| Authors | Kumar, D; Barad, S; Chen, Y; Luo, X; Tannous, J; Dubey, A; Glam Matana, N; Tian, S; Li, B; Keller, N; Prusky, D |
| Journal | Molecular Plant Pathology |
| Volume | 18 |
| Issue | 8 |
| Page Numbers | 1150-1163 |
| Abstract | Penicillium expansum, the causal agent of blue mould rot, is a critical health concern because of the production of the mycotoxin patulin in colonized apple fruit tissue. Although patulin is produced by many Penicillium species, the factor(s) activating its biosynthesis are not clear. Sucrose, a key sugar component of apple fruit, was found to modulate patulin accumulation in a dose-responsive pattern. An increase in sucrose culture amendment from 15 to 175 mm decreased both patulin accumulation and expression of the global regulator laeA by 175- and five-fold, respectively, whilst increasing expression of the carbon catabolite repressor creA. LaeA was found to regulate several secondary metabolite genes, including the patulin gene cluster and concomitant patulin synthesis in vitro. Virulence studies of ΔlaeA mutants of two geographically distant P. expansum isolates (Pe-21 from Israel and Pe-T01 from China) showed differential reduction in disease severity in freshly harvested fruit, ranging from no reduction for Ch-Pe-T01 strains to 15%-25% reduction for both strains in mature fruit, with the ΔlaeA strains of Is-Pe-21 always showing a greater loss in virulence. The results suggest the importance of abiotic factors in LaeA regulation of patulin and other secondary metabolites that contribute to pathogenicity. |
| Doi | 10.1111/mpp.12469 |
| Pmid | 27528575 |
| Wosid | WOS:000410743300010 |
| Is Certified Translation | No |
| Dupe Override | No |
| Is Public | Yes |
| Language Text | English |