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Hastings, A. P.

Publications and source records attributed to Hastings, A. P..

3 recordsLinked to original sources

Cardenolide toxin diversity impacts monarch butterfly growth and sequestration

In classic coevolutionary interactions, host plants are thought to accrue novel chemical defenses which are later countered by detoxification strategies and sometimes sequestration in specialist herbivores. We recently discovered that unusual nitrogen- and sulfur-containing (N,S-) cardenolides in some milkweed species are highly toxic, and broken down to less toxic forms which are sequestered by monarch butterflies (Danaus plexippus). Here we isolated and purified five dominant cardenolide toxins from the tropical milkweed, Asclepias curassavica, a globally abundant host plant of monarchs, and fed them to caterpillars individually or in mixture. We hypothesized that the two N,S-cardenolides in A. curassavica (uscharin and voruscharin) would reduce caterpillar growth and sequestration more than other abundant related cardenolides (15-Hydroxy calotropin, frugoside, calactin). Overall, cardenolide treatments caused monarchs to feed more and grow more compared to controls; nonetheless, one N,S-cardenolide (voruscharin) was not stimulatory and caused substantial reductions in growth efficiency. Consuming N,S-cardenolides caused caterpillars to sequester the lowest total amounts of cardenolides, and also reduced their efficiency of sequestration. We next tested the phytochemical diversity hypothesis, that toxin mixtures pose a substantial burden for caterpillars compared to individual compounds provided in equimolar concentrations. We prepared two types of mixtures, one containing equal concentrations of the five compounds and another "realistic mixture" where toxin concentrations reflect their natural proportions in leaves. Mixtures had a negative impact on caterpillar feeding, growth, sequestration, and sequestration efficiency compared to the average of single compounds. The equal and realistic mixtures had similar impacts on feeding and growth, but feeding on the realistic mixture resulted in the lowest sequestration. We conclude that as a result of coevolutionary interactions, even sequestering herbivores may be thwarted by highly specialized plant metabolites such as N,S-cardenolides, and that phytochemical mixtures strengthen plant defense. Toxin mixtures likely challenge detoxification and transport of plant defenses, reducing the herbivores growth and sequestration.

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Reversing the escape from herbivory: Knockout of cardiac glycoside biosynthesis in wormseed wallflower (Erysimum cheiranthoides L., Brassicaceae)

O_LIThe chemical arms race between plants and insects is foundational to the generation and maintenance of biological diversity. We asked how the evolution of a novel defensive compound in an already well-defended plant lineage impacts interactions with diverse herbivores. Erysimum cheiranthoides (Brassicaceae), which produces both ancestral glucosinolates and novel cardiac glycosides, served as a model. C_LIO_LIWe analyzed gene expression to identify cardiac glycoside biosynthetic enzymes in E. cheiranthoides and characterized these enzymes via heterologous expression and CRISPR/Cas9 knockout. Using E. cheiranthoides cardiac glycoside-deficient lines, we conducted insect experiments in both the laboratory and field. C_LIO_LIEcCYP87A126 initiates cardiac glycoside biosynthesis via sterol side chain cleavage, and EcCYP716A418 has a role in cardiac glycoside hydroxylation. In EcCYP87A126 knockout lines, cardiac glycoside production was eliminated. Laboratory experiments with these lines revealed that cardiac glycosides were highly effective defenses against two species of glucosinolate-tolerant specialist herbivores but did not protect against all crucifer-feeding specialist herbivores in the field. Cardiac glycosides had lesser to no effect on two broad generalist herbivores. C_LIO_LIThese results begin elucidation of the E. cheiranthoides cardiac glycoside biosynthetic pathway and demonstrate in vivo that cardiac glycoside production allows Erysimum to escape from some, but not all, specialist herbivores. C_LI

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Less Is More: A Mutation in the Chemical Defense Pathway of Erysimum cheiranthoides (Brassicaceae) Reduces Total Cardenolide Abundance but Increases Resistance to Insect Herbivores

Many plants produce structurally related defensive metabolites with the same target sites in insect herbivores. Two possible drivers of this chemical diversity are: (i) interacting effects of structurally related compounds increase resistance against individual herbivores, and (ii) variants of the same chemical structures differentially affect diverse herbivore species or feeding guilds. Erysimum cheiranthoides L (Brassicaceae; wormseed wallflower) produces abundant and diverse cardenolide toxins, which are derived from digitoxigenin, cannogenol, and strophanthidin, all of which inhibit Na+/K+-ATPases in animal cells. Here we describe an E. cheiranthoides mutant with 66% lower cardenolide content, resulting from greatly decreased cannogenol- and strophanthidin-derived cardenolides, partially compensated for by increases in digitoxigenin-derived cardenolides. This compositional change created a more even cardenolide distribution, decreased the average cardenolide polarity, but did not impact glucosinolates, a different class of chemical defenses. Growth of generalist herbivores from two feeding guilds, Myzus persicae Sulzer (Hemiptera: Aphididae; green peach aphid) and Trichoplusia ni Hubner (Lepidoptera: Noctuidae; cabbage looper), was decreased on the mutant line compared to wildtype. Both herbivores accumulated cardenolides in proportion to plant content, with T. ni accumulating higher total concentrations than M. persicae. Helveticoside, an abundant cardenolide in E. cheiranthoides, was absent in M. persicae, suggesting that this compound is not present in the phloem. Our results support the hypothesis that cardenolide diversity protects plants against different herbivores, with digitoxigenin-derived compounds providing better protection against insects like M. persicae and T. ni, whereas cannogenol and strophanthidin provide better protection against other herbivores of E. cheiranthoides. FundingThis research was funded by US National Science Foundation awards 1907491 to AAA and 1645256 to GJ and AAA, Swiss National Science Foundation grant PZ00P3-161472 to TZ, and a Triad Foundation grant to GJ.

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