Abstract

Simple SummaryCultivated chrysanthemums are one of the most economically important ornamental greenhouse crops worldwide. Classical breeding programs have mainly focused on improving aesthetic characteristics to meet the continuous increasing customer demands for new flower varieties. Consequently, commercial cultivars often lack insect resistance traits. Among the most important production constraints are biotic foes, in particular thrips and leaf miner infestations form a prominent hazard during its vegetative state. To maintain the desired aesthetic characteristics, clonal commercial propagation is aided by the use of auxin hormones for root promotion. This study aims to evaluate the potential of root promoting auxins in antiherbivore defenses. We demonstrate that water dipping of unrooted basal cut ends, coated with the commercial rooting hormone indole-3-butyric acid (IBA), conferred protection in chrysanthemum against thrips and leaf miner. Our findings add an interesting twist to the traditional role of auxins. We advocate a new twist of auxins beyond its traditional role in rooting in order to maximize plant yield by reducing herbivory through feasible, cost-effective water dipping treatments.Auxins are commonly used for commercial propagation of chrysanthemums by stem cuttings. Recent studies imply that these root-promoting hormones also affect plant defense responses. The underlying motive of this study stems from the serendipitous observation that water dipping of auxin-coated cuttings beneficially affected thrips herbivory. Therefore, the primary objective of this investigation was to explore the role of indole-3-butyric acid (IBA) in relation to herbivore susceptibility in chrysanthemum. We observed contrasting findings concerning the physical presence of IBA and it’s role in promoting susceptibility of cuttings to thrips, which may in part be explained by the phenotypical variations of cuttings generated from mother plants. Nonetheless, we repeatedly demonstrated considerable protection, in some experiments up to 37%, against thrips and leaf miner upon water dipping of IBA-coated cuttings. Assessment of polyphenol oxidase activity (PPO), 14 days after dipping treatment, suggests that neither direct induction nor priming of plant defenses are involved. Future experiments aimed at understanding the early signaling events may help to explain the underlying mechanisms involved in conferring herbivore protection. We propose a dual role for auxins in early integrated pest management strategies to maximize plant development and minimize herbivory through feasible, cost-effective water dipping treatments.

Highlights

  • Chrysanthemum morifolium (Ramat) is a semi hardy herbaceous, perennial flowering plant and belongs to the family of Asteraceae

  • In preliminary experiments we observed that when the basal portion of chrysanthemum cuttings were dipped in a solution with β-alanine were more resistant to thrips, i.e., displayed less silver damage, than untreated cuttings of cuttings (Figure S1; t(7) = 2.149, p = 0.069)

  • The observations of reduced silver damage upon water dipping gave rise to the hypothesis that of auxin on thrips susceptibility, unrooted cuttings with and without indole-3-butyric acid (IBA) were infested with adult auxins may exert an antagonistic the jasmonic acid (JA) signaling pathway, increase thrips after a rooting periodinteraction of two weeks. on we evaluated the effect ofand water dipping at three different time points namely; 0–30–45 and 60 min

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Summary

Introduction

Chrysanthemum morifolium (Ramat) is a semi hardy herbaceous, perennial flowering plant and belongs to the family of Asteraceae (formerly known as Compositeae). Chrysanthemums are among the most important commercially grown greenhouse ornamentals worldwide and are extensively used as cut flowers and as pot plants [1,2,3]. Classical breeding programs have mainly focused on improving various characteristics to enhance ornamental values, including flower color, size and shape. Driven by such consumer needs, breeders are often under pressure to supply novel varieties within a restricted timeframe and with very specific choices, leaving few options for altering other agronomic traits. In addition to the limited gene pool, chrysanthemums are hexaploids and genetically highly heterozygous, complicating the development of resistant varieties and plant novelties at the same time [4]. Many commercial varieties often lack resistance traits to biotic and abiotic stresses

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