Plants have limited resources to allocate to defences against infection and herbivory. While interactions between plant responses to microbial and herbivore attack are complex, it is often the case that the induction of one response will act antagonistically to the other. Recent studies have shown that plant growth promoting rhizobacteria, which improves overall plant health and general stress resistance, can enhance both anti-microbial and anti-herbivore defences. We investigated how soil application of the biofungicide Serenade ASO (Bacillus subtilis strain QST 713), which primes plant defences against fungal and bacterial infection and promotes plant growth, affects anti-herbivore defences by measuring both constitutive and induced defences. We applied Serenade one or two times to the soil of tomato plants and measured the numbers of type IV glandular trichomes on leaves, the weight gain of a generalist caterpillar (beet armyworms; BAW), and the activity of two enzymes associated with defence against insects (polyphenoloxidase and peroxidase). Serenade treated plants grew faster and foliage from treated plants had significantly higher numbers of glandular trichomes and higher polyphenoloxidase and peroxidase activities than untreated plants. However, Serenade treatment did not affect the degree of induction of plant defences when damaged by BAW feeding and did not slow the growth rate of BAW relative to plants not treated with Serenade. Therefore, the biofungicide Serenade increased plant growth and altered the densities of trichomes and the activities of two defensive enzymes in plants, but it did not affect overall susceptibility of the plants to a generalist herbivore.

Microorganisms associated with plant roots significantly impact the quality and quantity of plant defences. However, the bottom-up effects of soil microbes on the aboveground multitrophic interactions remain largely under studied. To address this gap, we investigated the chemicallymediated effects of nitrogen-fixing rhizobia on legume-herbivore-parasitoid multitrophic interactions. To address this, we initially examined the cascading effects of the rhizobia bean association on herbivore caterpillars, their parasitoids, and subsequently investigated how rhizobia influence on plant volatiles and extrafloral nectar. Our goal was to understand how these plantmediated effects can affect parasitoids. Lima bean plants (Phaseoulus lunatus) inoculated with rhizobia exhibited better growth, and the number of root nodules positively correlated with defensive cyanogenic compounds. Despite increase of these chemical defences, Spodoptera latifascia caterpillars preferred to feed and grew faster on rhizobia-inoculated plants. Moreover, the emission of plant volatiles after leaf damage showed distinct patterns between inoculation treatments, with inoculated plants producing more sesquiterpenes and benzyl nitrile than noninoculated plants. Despite these differences, Euplectrus platyhypenae parasitoid wasps were similarly attracted to rhizobia- or no rhizobia-treated plants. Yet, the oviposition and offspring development of E. platyhypenae was better on caterpillars fed with rhizobia-inoculated plants. We additionally show that rhizobia-inoculated common bean plants (Phaseolus vulgaris) produced more extrafloral nectar, with higher hydrocarbon concentration, than non-inoculated plants. Consequently, parasitoids performed better when fed with extrafloral nectar from rhizobiainoculated plants. While the overall effects of bean-rhizobia symbiosis on caterpillars were positive, rhizobia also indirectly benefited parasitoids through the caterpillar host, and directly through the improved production of high quality extrafloral nectar. This study underscores the importance of exploring diverse facets and chemical mechanisms that influence the dynamics between herbivores and predators. This knowledge is crucial for gaining a comprehensive understanding of the ecological implications of rhizobia symbiosis on these interactions.