采后
生物
代谢组学
蓝色模具
计算生物学
病菌
毒力
蛋白质组学
质谱法
抗菌剂
生物技术
化学
信号通路
生物化学
代谢途径
作者
Evandro Silva,Aline Midori Kanashiro,José Rodrigo Ferreira Maciel,Rodolfo Dantas Lima,Maria Antonia Fraga Botelho,Alana Kelyene Pereira,Stephanie Nemesio da Silva,Jonas Henrique Costa,João Guilherme de Moraes Pontes,Amanda Ferreira da Silva,Igor D. Jurberg,Roberto G. S. Berlinck,Taícia Pacheco Fill
标识
DOI:10.1021/acs.jafc.5c07618
摘要
High Resolution Image Download MS PowerPoint Slide Penicillium italicum, the causal agent of citrus blue mold, is a major postharvest pathogen that reduces fruit quality and global citrus productivity. Understanding the molecular basis of infection is crucial to reveal virulence mechanisms, host defense responses, and potential targets for disease control. Here, we investigated the metabolic profile of the Citrus sinensis – P. italicum interaction using mass spectrometry-based metabolomics and desorption electrospray ionization mass spectrometry imaging. Key differential P. italicum -derived metabolites were identified, including 12,13-dehydroprolyltryptophanyldiketopiperazine, deoxybrevianamide E, dehydrodeoxybrevianamide E, deoxyisoaustamide, and brevianamide F. To assess its biological role, brevianamide F was chemically synthesized and tested against citrus-associated endophytes. It selectively inhibited Diaporthe sp., suggesting that P. italicum may utilize this compound as an antimicrobial strategy to modulate the endophytic community during infection. These results provide the first insights into the natural products involved in P. italicum association with citrus and point to potential alternative strategies for controlling blue mold disease.
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