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Novel Fungal Pathogenicity and Leaf Defense Strategies Are Revealed by Simultaneous Transcriptome Analysis of Colletotrichum fructicola and Strawberry Infected by This Fungus

79

Citations

83

References

2018

Year

Abstract

<i>Colletotrichum fructicola</i>, which is part of the <i>C. gloeosporioides</i> species complex, can cause anthracnose diseases in strawberries worldwide. However, the molecular interactions between <i>C. fructicola</i> and strawberry are largely unknown. A deep RNA-sequencing approach was applied to gain insights into the pathogenicity mechanisms of <i>C. fructicola</i> and the defense response of strawberry plants at different stages of infection. The transcriptome data showed stage-specific transcription accompanied by a step-by-step strawberry defense response and the evasion of this defense system by fungus. Fungal genes involved in plant cell wall degradation, secondary metabolism, and detoxification were up-regulated at different stage of infection. Most importantly, <i>C. fructicola</i> infection was accompanied by a large number of highly expressed effectors. Four new identified effectors function in the suppression of Bax-mediated programmed cell death. Strawberry utilizes pathogen-associated molecular patterns (PAMP)-triggered immunity and effector-triggered immunity to prevent <i>C. fructicola</i> invasion, followed by the initiation of downstream innate immunity. The up-regulation of genes related to salicylic acid provided evidence that salicylic acid signaling may serve as the core defense signaling mechanism, while jasmonic acid and ethylene pathways were largely inhibited by <i>C. fructicola</i>. The necrotrophic stage displayed a significant up-regulation of genes involved in reactive oxygen species activation. Collectively, the transcriptomic data of both <i>C. fructicola</i> and strawberry shows that even though plants build a multilayered defense against infection, <i>C. fructicola</i> employs a series of escape or antagonizing mechanisms to successfully infect host cells.

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