Abstract
Vector-borne plant pathogens often change host traits to manipulate vector behavior in a way that favors their spread. By contrast, infection by opportunistic fungi does not depend on vectors, although damage caused by an herbivore may facilitate infection. Manipulation of hosts and vectors, such as insect herbivores, has not been demonstrated in interactions with fungal pathogens. Herein, we establish a new paradigm for the plant-insect-fungus association in sugarcane. It has long been assumed that Fusarium verticillioides is an opportunistic fungus, where it takes advantage of the openings left by Diatraea saccharalis caterpillar attack to infect the plant. In this work, we show that volatile emissions from F. verticillioides attract D. saccharalis caterpillars. Once they become adults, the fungus is transmitted vertically to their offspring, which continues the cycle by inoculating the fungus into healthy plants. Females not carrying the fungus prefer to lay their eggs on fungus-infected plants than mock plants, while females carrying the fungus prefer to lay their eggs on mock plants than fungus-infected plants. Even though the fungus impacts D. saccharalis sex behavior, larval weight and reproduction rate, most individuals complete their development. Our data demonstrate that the fungus manipulates both the host plant and insect herbivore across life cycle to promote its infection and dissemination.
Highlights
Our study indicates that F. verticillioides is not just an opportunistic fungus, and a fungus more intimately associated with an insect herbivore, manipulating the plant and the insect to increase its potential for dissemination
The A. nidulans fungus is not related to sugarcane diseases, and caterpillars challenged by A. nidulans volatile organic compounds (VOCs) preferred the control over the fungus-colonized diet, indicating either no preference or a repellent effect (Fig. 1b)
The same type of assay was performed with D. saccharalis fifth-instar caterpillars, which were attracted to F. verticillioides VOCs (Supplementary Fig. S2), indicating that the attraction was consistent across different larval stages
Summary
These proteins affect F. verticillioides morphology, causing fungal death, but are not able to affect Aspergillus nidulans, a non-sugarcane pathogenic fungus, indicating a close and specific interaction between D. saccharalis and F. verticillioides [21, 22] This close association between an opportunistic fungus and the sugarcane borer led us to investigate the role of D. saccharalis as a dissemination vector for F. verticillioides, possibly corroborating the “host manipulation hypothesis”. D. saccharalis vertically transmits the fungus F. verticillioides to its offspring In this scenario, our study indicates that F. verticillioides is not just an opportunistic fungus, and a fungus more intimately associated with an insect herbivore, manipulating the plant and the insect to increase its potential for dissemination
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