Trichoderma atroviride P1 Colonization of Tomato Plants Enhances Both Direct and Indirect Defense Barriers Against Insects

• Published in: Frontiers in physiology Vol. 10; p. 813
• Main Authors: Coppola, Mariangela, Cascone, Pasquale, Lelio, Ilaria Di, Woo, Sheridan Lois, Lorito, Matteo, Rao, Rosa, Pennacchio, Francesco, Guerrieri, Emilio, Digilio, Maria Cristina
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 05.07.2019
• Subjects: Aphidius ervi; Macrosiphum euphorbiae; Physiology; plant induced defence; root symbionts; Spodoptera littoralis; VOCs; plant induced defence; VOCs; Aphidius ervi; Macrosiphum euphorbiae; root symbionts; Spodoptera littoralis
• ISSN: 1664-042X; 1664-042X
• DOI: 10.3389/fphys.2019.00813

Numerous microbial root symbionts are known to induce different levels of enhanced plant protection against a variety of pathogens. However, more recent studies have demonstrated that beneficial microbes are able to induce plant systemic resistance that confers some degree of protection against insects. Here, we report how treatments with the fungal biocontrol agent strain P1 in tomato plants induce responses that affect pest insects with different feeding habits: the noctuid moth (Boisduval) and the aphid (Thomas). We observed that the tomato plant- P1 interaction had a negative impact on the development of moth larvae and on aphid longevity. These effects were attributed to a plant response induced by that was associated with transcriptional changes of a wide array of defense-related genes. While the impact on aphids could be related to the up-regulation of genes involved in the oxidative burst reaction, which occur early in the defense reaction, the negative performance of moth larvae was associated with the enhanced expression of genes encoding for protective enzymes (i.e., Proteinase inhibitor I (PI), Threonine deaminase, Leucine aminopeptidase A1, Arginase 2, and Polyphenol oxidase) that are activated downstream in the defense cascade. In addition, P1 produced alterations in plant metabolic pathways leading to the production and release of volatile organic compounds (VOCs) that are involved in the attraction of the aphid parasitoid , thus reinforcing the indirect plant defense barriers. Our findings, along with the evidence available in the literature, indicate that the outcome of the tripartite interaction among plant, , and pests is highly specific and only a comprehensive approach, integrating both insect phenotypic changes and plant transcriptomic alterations, can allow a reliable prediction of its potential for plant protection.