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Changes in taste receptor cell sensitivity in a polyphagous caterpillar reflect carbohydrate but not protein imbalance

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Abstract

Caterpillars of the polyphagous arctiid, Grammia geneura, have a single cell in the medial galeal sensillum that responds to some sugars and to some amino acids. After conditioning on artificial diet containing unbalanced amounts of carbohydrate and protein, the responses of this cell alter. After protein-biased food it increases slightly, but after carbohydrate-biased food it decreases. Responses to both sucrose and amino acids change in the same direction and the changes would not provide the information necessary to redress a shortage of protein. The lateral galeal sensillum contains one cell that responds to fructose and another responding to some amino acids. The responses of each of these cells in the lateral sensillum are not consistently affected by conditioning diets. After conditioning for 20 h on a protein- or carbohydrate-biased diet, the insects started to feed without delay if offered carbohydrate-biased diet, but only after a pause if given protein-biased diet. This occurred irrespective of the conditioning diet. The duration of the first feeding bout was also longer on carbohydrate-biased diet and the longest bouts followed protein-biased conditioning.

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References

  • Abisgold JD, Simpson SJ (1987) The physiology of compensation by locusts for changes in dietary protein. J Exp Biol 129:329–346

    Google Scholar 

  • Abisgold JD, Simpson SJ (1988) The effect of dietary protein levels and haemolymph composition on the sensitivity of the maxillary palp chemoreceptors of locusts. J Ex. Biol 135:215–229

    CAS  Google Scholar 

  • Ahmad I, Waldbauer GP, Friedman S (1993) Maxillectomy does not disrupt self-selection by larvae of Manduca sexta (Lepidoptera: Sphingidae). Ann Entomol Soc Am 86:459–463

    Google Scholar 

  • Bernays EA, Chapman RF (2001a) Electrophysiological responses to nutrient mixtures by a polyphagous caterpillar. J Comp Physiol A 187:205–213

    Google Scholar 

  • Bernays EA, Chapman RF (2001b) Taste cell responses in the polyphagous arctiid, Grammia geneura: towards a general pattern for caterpillars. J Insect Physiol 47:1029–1043

    Article  CAS  PubMed  Google Scholar 

  • Bernays EA, Chapman RF, Singer MS (2000) Sensitivity to chemically diverse phagostimulants in a single gustatory neuron of a polyphagous caterpillar. J Comp Physiol A 186:13–19

    CAS  PubMed  Google Scholar 

  • Blaney WM, Simmonds MSJ (1988) Food selection in adults and larvae of three species of Lepidoptera: a behavioral and electrophysiological study. Entomol Exp Appl 49:111–121

    CAS  Google Scholar 

  • Blaney WM, Simmonds MSJ, Simpson SJ (1990) Dietary selection behaviour: comparisons between locusts and caterpillars. Symp Biol Hung 39:47–52

    Google Scholar 

  • Blom F (1978) Sensory activity and food intake: a study of input-output relationships in two phytophagous insects. Neth J Zool 28:277–340

    Google Scholar 

  • Crawley MJ (1983) Herbivory. Blackwells, Oxford

  • Frazier JL, Hanson FE (1986) Electrophysiological recording and analysis of insect chemosensory responses. In: Miller TA, Miller J (eds) Insect-plant interactions. Springer, Berlin Heidelberg New York, pp 285–330

  • Friedman S, WaldbauerGP, Eertmoed JE, Naeem M, Ghent AW (1991) Blood trehalose levels have a role in the control of dietary self-selection by Heliothis zea larvae. J Insect Physiol 37:919–928

    Article  CAS  Google Scholar 

  • Glendinning JI, Valcic S, Timmermann BN (1998) Maxillary palps can mediate taste rejection of plant allelochemicals by caterpillars. J Comp Physiol A 183:35–43

    Google Scholar 

  • Glendinning JI, Domdom S, Long E (2001) Selective adaptation to noxious foods by a herbivorous insect. J Exp Biol 204: 3355–3367

    CAS  PubMed  Google Scholar 

  • Gothilf S, Hanson FE (1994) A technique for electrophysiologically recording from chemosensory organs of intact caterpillars. Entomol Exp Appl 72:305–310

    Google Scholar 

  • Hodgson ES, Lettvin JY, Roeder KD (1955) Physiology of a primary chemoreceptor unit. Science 122:417–418

    CAS  Google Scholar 

  • Ma WC (1972) Dynamics of feeding responses in Pieris brassicae Linn. as a function of chemosensory input: a behavioural, ultrastructural and electrophysiological study. Meded Landbouwhog Wageningen 72:162 pp

    Google Scholar 

  • Noldus LPJJ (1991) The observer: a software system for collection and analysis of observational data. Behav Res Methods Instrum Comput 23:415–429

    Google Scholar 

  • Schiff NM, Waldbauer GP, Friedman S (1989a) Response of last instar Heliothis zea larvae to carbohydrates: stimulation of biting, nutritional value. Entomol Exp Appl 52:29-38

    CAS  Google Scholar 

  • Schiff NM, Waldbauer GP, Friedman S (1989b) Dietary self-selection by Heliothis zea larvae: roles of metabolic feedback and chemosensory stimuli. Entomol Exp Appl 52:261–270

    CAS  Google Scholar 

  • Schoonhoven LM, Loon JJA van (2002) An inventory of taste in caterpillars: each species its own key. Symp Biol Hung 48 [Suppl 1]:215–263

    Google Scholar 

  • Simmonds MSJ, Simpson SJ, Blaney WM (1992) Dietary selection behaviour in Spodoptera littoralis: the effects of conditioning diet and conditioning period on neural responsiveness and selection behaviour. J Exp Biol 162:73–90

    Google Scholar 

  • Simpson SJ, Raubenheimer D (1993) A multi-level analysis of feeding behaviour: the geometry of nutritional decisions. Philos Trans R Soc Lond Ser B 342:381–402

    Google Scholar 

  • Simpson SJ, Raubenheimer D (1997) Geometric analysis of macronutrient selection in the rat. Appetite 28:201–213

    Article  CAS  PubMed  Google Scholar 

  • Simpson SJ, Simmonds MSJ, Blaney WM (1988) A comparison of dietary selection behaviour in larval Locusta migratoria and Spodoptera littoralis. Physiol Entomol 13:225–238

    Google Scholar 

  • Simpson CL, Chyb S, Simpson SJ (1990) Changes in chemoreceptor sensitivity in relation to dietary selection by adult Locusta migratoria. Entomol Exp Appl 56:259–268

    CAS  Google Scholar 

  • Simpson SJ, Raubenheimer D, Chambers PG (1995) The mechanisms of nutritional homeostasis. In: Chapman RF, Boer G de (eds) Regulatory mechanisms in insect feeding. Chapman and Hall, New York, pp 251–278

  • Singer MS, Bernays EA, Carrière Y (2002) The interplay between nutrient balancing and toxin dilution in foraging by a generalist herbivore. Anim Behav 64:629–645

    Article  Google Scholar 

  • Smith JJB, Mitchell BK, Rolseth BM, Whitehead AT, Albert PJ (1990) SAPID Tools: microcomputer programs for analysis of multi-unit nerve recordings. Chem Senses 15:253–270

    Google Scholar 

  • Stockhoff BA (1993) Protein intake by gypsy moth larvae on homogeneous and heterogeneous diets. Physiol Entomol 18:409–419

    Google Scholar 

  • Telang A, Booton V, Chapman RF, Wheeler DE (2001) How female caterpillars accumulate their nutrient reserves. J Insect Physiol 47:1055–1064

    Article  CAS  PubMed  Google Scholar 

  • Thompson SN, Redak RA (2000) Interaction of dietary protein and carbohydrate determine blood sugar level and regulate nutrient selection in the insect Manduca sexta L. Biochim Biophys Acta 1523:91–102

    Article  CAS  PubMed  Google Scholar 

  • Waldbauer GP, Friedman S (1991) Self-selection of optimal diets by insects. Annu Rev Entomol 36:43–63

    Google Scholar 

  • Waldbauer GP, Cohen RW, Friedman S (1984) Self-selection of an optimal nutrient mix from defined diets by larvae of the corn-earworm, Heliothis zea (Boddie). Physiol Zool 57:590–597

    Google Scholar 

  • Yamamoto RT (1969) Mass rearing of the tobacco hornworm. II. Larval rearing and pupation. J Econ Entomol 62:1427–1431

    Google Scholar 

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Correspondence to E. A. Bernays.

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Bernays, E.A., Chapman, R.F. & Singer, M.S. Changes in taste receptor cell sensitivity in a polyphagous caterpillar reflect carbohydrate but not protein imbalance. J Comp Physiol A 190, 39–48 (2004). https://doi.org/10.1007/s00359-003-0472-5

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  • DOI: https://doi.org/10.1007/s00359-003-0472-5

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