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d-Pinitol as a key oviposition stimulant for sulfur butterfly, Colias erate: chemical basis for female acceptance of host- and non-host plants

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Abstract

The sulfur butterfly, Colias erate, utilizes various legumes as host plants. We examined the chemical constituents of its primary host plant, Trifolium repens (white clover), to identify phytochemicals inducing oviposition by C. erate females. Since one of the four aqueous subfractions prepared from a methanolic extract of the plant has previously been shown to be the most responsible for the oviposition-stimulatory activity exerted by the plant, chemical analyses were conducted of the fraction concerned. Activity-directed fractionation of the subfraction by ion-exchange chromatography revealed that the key substance(s) resided in the neutral fraction. Preparative TLC of the neutral fraction and subsequent spectral analyses identified d-(+)-pinitol, glycerin, methyl β-d-glucoside, and myo-inositol as characteristic components together with ubiquitous sugars (e.g., sucrose and glucose). Of these, only pinitol singly evoked significant oviposition responses at concentrations over 0.05%. In dual-choice bioassays, however, females laid significantly more eggs on pinitol solutions admixed with glycerin or methyl β-d-glucoside than on pinitol alone. Two cyanoglucosides, linamarin, and lotaustralin, occurring in the other aqueous subfractions, also synergistically increased the oviposition response in combination with pinitol. The results clearly indicated that pinitol is a crucial oviposition stimulant involved in host recognition, while glycerin, methyl β-d-glucoside, linamarin, and lotaustralin function as synergists. We further examined the oviposition responses of C. erate females to aqueous fractions, along with their chemical compositions, that had been prepared from five other host plants and a non-host plant, Aristolochia debilis (Aristolochiaceae), on which oviposition occasionally took place in an outdoor cage during the experiments. The plant species accepted by ovipositing females were all found to contain pinitol in amounts enough to induce egg laying by the butterfly, thus leading to the conclusion that pinitol serves as the essential mediator in recognizing and accepting potential host plants.

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References

  • Berenbaum MR, Feeny PP (2008) Chemical mediation of host-plant specialization: the papilionid paradigm. In: Tilmon K (ed) Specialization, speciation, and radiation: the evolutionary biology of herbivorous insects. University of California Press, California, pp 3–19

    Google Scholar 

  • Chew FS, Renwick JAA (1995) Host-plant choice in Pieris butterflies. In: Cardé RT, Bell WJ (eds) Chemical ecology of insects 2. Chapman and Hall, New York, pp 214–238

    Chapter  Google Scholar 

  • Chew FS, Robbins RK (1984) Egg-laying in butterflies. In: Vane-Wright IR, Ackery PR (eds) The biology of butterflies. Academic Press, London, pp 65–79

    Google Scholar 

  • Dreyer DL, Binder RG, Chan BG, Waiss AC Jr, Hartwig EE, Beland GL (1979) Pinitol, a larval growth inhibitor for Heliothis zea in soybeans. Experientia 35:1182–1183

    Article  PubMed  CAS  Google Scholar 

  • Endo S, Nihira I (1990) Larval food of Japanese butterflies. Group Tamamushi, Tokyo (in Japanese)

  • Feeny P, Sachdev K, Rosenberry L, Cater M (1988) Luteolin 7-O-(6′′-O-malonyl)-β-d-glucoside and trans-chlorogenic acid: Oviposition stimulants for the black swallowtail butterfly. Phytochemistry 27:3439–3448

    Article  CAS  Google Scholar 

  • Ford CW (1984) Accumulation of low molecular weight solutes in water-stressed tropical legumes. Phytochemistry 23:1007–1015

    Article  CAS  Google Scholar 

  • Honda K (1990) Identification of host-plant chemicals stimulating oviposition by swallowtail butterfly, Papilio protenor. J Chem Ecol 16:325–337

    Article  CAS  Google Scholar 

  • Honda K (1995) Chemical basis of differential oviposition by lepidopterous insects. Arch Insect Biochem Physiol 30:1–23

    Article  CAS  Google Scholar 

  • Honda K (2005) Larval feeding habit and host selection. In: Honda K, Kato Y (eds) Biology of butterflies. University of Tokyo Press, Tokyo, pp 255–301 (in Japanese)

    Google Scholar 

  • Honda K, Nishii W, Hayashi N (1997) Oviposition stimulants for sulfur butterfly, Colias erate poliographus: cyanoglucosides as synergists involved in host preference. J Chem Ecol 23:323–331

    Article  CAS  Google Scholar 

  • Honda K, Ômura H, Hayashi N, Abe F, Yamauchi T (2001) Oviposition-stimulatory activity of phenanthroindolizidine alkaloids of host-plant origin to a danaid butterfly, Ideopsis similis. Physiol Entomol 26:6–10

    Article  CAS  Google Scholar 

  • Honda K, Ômura H, Hayashi N, Abe F, Yamauchi T (2004) Conduritols as oviposition stimulants for the danaid butterfly, Parantica sita, identified from a host plant, Marsdenia tomentosa. J Chem Ecol 30:2285–2296

    Article  PubMed  CAS  Google Scholar 

  • Honda K, Ômura H, Hori M, Kainoh Y (2010) Allelochemicals in plant-insect interactions. In: Mander L, Lui H-W (eds) Comprehensive natural products II. Chemistry and biology. Elsevier, Oxford, pp 563–594

    Chapter  Google Scholar 

  • Huang X, Renwick JAA, Sachdev-Gupta K (1994) Oviposition stimulants in Barbarea vulgaris for Pieris rapae and P. napi oleracea: isolation, identification and differential activity. J Chem Ecol 20:423–438

    Article  CAS  Google Scholar 

  • Hudlicky T, Cebulak M (1993) Cyclitols and their derivatives: a handbook of physical, spectral, and synthetic data. VCH Publishers Inc, New York

    Google Scholar 

  • McManus MT, Bieleski RL, Caradus JR, Barker DJ (2000) Pinitol accumulation in mature leaves of white clover in response to a water deficit. Environ Exp Bot 43:11–18

    Article  CAS  Google Scholar 

  • Miller JS, Feeny PP (1989) Interspecific differences among swallowtail larvae (Lepidoptera: Papilionidae) in susceptibility to aristolochic acids and berberine. Ecol Entomol 14:287–296

    Article  Google Scholar 

  • Nakayama T, Honda K, Ômura H, Hayashi N (2003) Oviposition stimulants for the tropical swallowtail butterfly, Papilio polytes, feeding on a rutaceous plant, Toddalia asiatica. J Chem Ecol 29:1621–1634

    Article  PubMed  CAS  Google Scholar 

  • Nishida R, Fukami H (1989) Oviposition stimulants of an Aristolochiaceae-feeding swallowtail butterfly, Atrophaneura alcinous. J Chem Ecol 15:2565–2575

    Article  CAS  Google Scholar 

  • Nishida R, Ohsugi T, Kokubo S, Fumaki H (1987) Oviposition stimulants of a Citrus-feeding swallowtail butterfly, Papilio xuthus L. Experientia 43:342–344

    Article  CAS  Google Scholar 

  • Numata A, Hokimoto K, Shimada A, Yamaguchi H, Takaishi K (1979) Plant constituents biologically active to insects. I. Feeding stimulants for the larvae of the yellow butterfly. Eurema hecabe mandarina. Chem Pharm Bull 27:602–608

    Article  CAS  Google Scholar 

  • Numata A, Yamaguchi H, Hokimoto K, Ohtani M, Takaishi K (1985) Host-plant selection by the yellow butterfly larvae, Eurema hecabe mandarina (Lepidoptera: Pieridae): attractants and arrestants. Appl Entomol Zool 20:314–321

    Google Scholar 

  • Orthen B, Popp M (2000) Cyclitols as cryoprotectants for spinach and chickpea thylakoids. Environ Exp Bot 44:125–132

    Article  PubMed  CAS  Google Scholar 

  • Papaj DR, Feeny P, Sachdev-Gupta K, Rosenberry L (1992) D-(+)-pinitol, an oviposition stimulant for the pipevine swallowtail butterfly, Battus philenor. J Chem Ecol 18:799–815

    Article  CAS  Google Scholar 

  • Reese JC, Chan BG, Waiss AC Jr (1982) Effects of cotton condensed tannin, maysin (corn) and pinitol (soybeans) on Heliothis zea growth and development. J Chem Ecol 8:1429–1436

    Article  CAS  Google Scholar 

  • Renwick JAA, Chew FS (1994) Oviposition behavior in Lepidoptera. Annu Rev Entomol 39:377–400

    Article  Google Scholar 

  • Sachdev-Gupta K, Feeny PP, Carter M (1993) Oviposition stimulants for the pipevine swallowtail butterfly, Battus philenor (Papilionidae), from an Aristolochia host plant: synergism between inositols, aristolochic acids and a monogalactosyl diglyceride. Chemoecology 4:19–28

    Article  CAS  Google Scholar 

  • Stefanescu C, Jubany J, Dantart J (2006) Egg–laying by the butterfly Iphiclides podalirius (Lepidoptera, Papilionidae) on alien plants: a broadening of host range or oviposition mistake? Anim Biodiv Conserv 29:83–90

    Google Scholar 

  • Traynier RMM, Truscott RJW (1991) Potent natural egg-laying stimulant for cabbage butterfly Pieris rapae. J Chem Ecol 17:1371–1380

    Article  CAS  Google Scholar 

  • van Loon JJA, Blaakmeer A, Griepink FC, van Beek TA, Schoonhoven LM, de Groot A (1992) Leaf surface compound from Brassica oleracea (Cruciferae) induces oviposition by Pieris brassicae (Lepidoptera: Pieridae). Chemoecology 3:39–44

    Article  Google Scholar 

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Correspondence to Keiichi Honda.

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Honda, K., Minematsu, H., Muta, K. et al. d-Pinitol as a key oviposition stimulant for sulfur butterfly, Colias erate: chemical basis for female acceptance of host- and non-host plants. Chemoecology 22, 55–63 (2012). https://doi.org/10.1007/s00049-011-0098-y

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