Skip to main content
Log in

Bacteria associated with four species of Dacus (Diptera: Tephritidae) and their role in the nutrition of the larvae

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

The bacteria associated with Dacus tryoni (Froggatt), Dacus jarvisi (Tryon), Dacus neohumeralis (Hardy) and Dacus cacuminatus (Hering) were examined. Bacteria were isolated from the surface of freshly-laid eggs, from within surface sterilised pupae, from heads and abdomens of wild and laboratory-maintained flies, and from decomposed fruits in which the wild larvae were feeding. A more diverse flora was associated with D. tryoni and D. jarvisi (15 and 14 species, respectively) than with D. neohumeralis and D. cacuminatus (9 and 6 species, respectively). Most of the bacteria belonged to the family Enterobacteriaceae and while there were similarities of bacterial associations between fly species there was no evidence of a strict symbiotic association of a particular bacterium or bacteria with each species of fly. The larvae of D. jarvisi were unable to develop normally in an artificial medium containing unhydrolysed protein and free of bacteria and on a medium containing casein and Serratia liquefaciens (isolated from the flies and shown to secrete protease) the larvae died. On the same casein medium containing Enterobacter cloacae (isolated from the flies and shown to be protease negative) the larvae developed normally. Larvae of D. tryoni and D. jarvisi were devoid of protease and cellulase activity, but contained some amylase activity. The significance of these results in terms of current hypotheses concerning symbioses between tephritids and bacteria is discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Allen TC, Riker AJ (1932) A rot of apple fruit caused by Phytomonas melophthora sp. nov. following invasion by the apple maggot. Phytopathol 22:557–571

    Google Scholar 

  • Allen TC, Pinckard JA, Riker AJ (1934) Frequent association of Phytomonas melophthora with various stages of the life cycle of the apple maggot, Rhagoletis pomonella. Phytopathol 24:228–238

    Google Scholar 

  • Bateman MA (1967) Adaptations to temperature in geographic races of the Queensland fruit fly, Dacus (Strumeta) tryoni. Aust J Zool 15:1141–1161

    Google Scholar 

  • Bateman MA (1972) The ecology of fruit flies. A Rev Ent 17:493–518

    Article  Google Scholar 

  • Boush GM, Matsumara F (1967) Insecticidal degradation by Pseudomonas melophthora, the bacterial symbiote of the apple maggot. J econ Ent 60:918–920

    Google Scholar 

  • Brooks MA (1963) The microorganisms of healthy insects. In: Insect pathology: An advanced treatise, Vol 1, EA Steinhaus (ed), pp 215–250. Academic Press, New York

    Google Scholar 

  • Bucher GE (1963) Nonsporulating bacterial pathogens. In: Insect pathology: An advanced treatise, Vol 2, EA Steinhaus (ed), pp 117–148. Academic Press, New York

    Google Scholar 

  • Buchner P (1965) Endosymbiosis of animals with plant microorganisms. Wiley, New York

    Google Scholar 

  • Charpentier R, Charpentier B, Zethner O (1978) The bacterial flora of the midgut of two Danish populations of healthy fifth instar larvae of the turnip moth, Scotia segetum. J Inv Pathol 32:59–63

    PubMed  Google Scholar 

  • Dean RW (1933) Morphology of the digestive tract of the apple maggot fly, Rhagoletis pomonella. NY State Agr Exp Sta Bull No 215, 17 pp

  • Dean RW (1935) Anatomy and postpupal development of the female reproductive system in the apple maggot fly, Rhagoletis pomonella. NY State Agr Exp Sta Bull No 229. 18 pp

  • Doetsch RN (1981) Determinative methods of light microscopy. In: Manual of methods for general bacteriology, P Gerhardt (ed), pp 21–33. Amer Soc Micro, Washington

    Google Scholar 

  • Drew RAI, Courtice AC, Teakle DS (1983) Bacteria as a natural source of food for adult fruit flies (Diptera: Tephritidae). Oecologia (Berlin) 60:279–284

    Google Scholar 

  • Falcon LA (1971) Use of bacteria for microbial control of insects. In: Microbial control of insects and mites, HD Burgess, NW Hussey (eds), pp 67–90. Academic Press, New York

    Google Scholar 

  • Fytizas E, Tzanakakis ME (1966) Some effects of streptomycin when added to the adult food, on the adults of Dacus oleae and their progeny. Ann Ent Soc Amer 59:269–273

    Google Scholar 

  • Girolami V (1973) Morpho-histological findings on the bacterial symbiosis of Dacus oleae Gmel. and other trypetid Diptera, in nature and in rearings on artificial substrates. Redia 54:269–294

    Google Scholar 

  • Girolami V (1983) Fruit fly symbiosis and adult survival: general aspects. In: Fruit flies of economic importance, R Cavolloro (ed), pp 74–75. Balkema, Rotterdam

    Google Scholar 

  • Grimont PAD, Grimont F (1978) The genus Serratia. A Rev Micro 32:221–248

    Article  Google Scholar 

  • Hagen KS (1966) The dependence of the Olive fly, Dacus oleae, larvae on symbiosis with Pseudomonas savastanoi for the utilization of olive. Nature 209:423–424

    Google Scholar 

  • Hagen KS, Tassan RI (1972) Exploring nutritional roles of extracellular symbiotes on the reproduction of honeydew feeding adult chrysopids and tephritids. In: Insect and mite nutrition, JG Rodriguez (ed), pp 323–351. North-Holland, Amsterdam

    Google Scholar 

  • Hansen E (1970) Proteins. In: The biochemistry of fruits and their products, AC Hulme (ed), pp 147–158. Academic Press, London

    Google Scholar 

  • Hellmuth H (1956) Untersuchungen zur Bakteriensymbiose der Trypetiden (Diptera). Z Morphol Okol Tiere 44:483–517

    Google Scholar 

  • Iverson KL, Bromel NC, Anderson AW, Freeman TP (1984) Bacterial symbionts in the sugar beet root maggot, Tetanops myopaeformis (von Roder). App environ Microbiol 47:22–27

    Google Scholar 

  • Linderova Z (1977) Symbionts of larvae and imagoes of R. cerasi L. Pol'nohospodarstro 23:918–924

    Google Scholar 

  • Luthy P, Studer D, Jaquet F, Yamvrias C (1983) Morphology and in vitro cultivation of the bacterial symbiote of Dacus oleae. Mitt Schweiz Entomol Gesellschaft 56:67–72

    Google Scholar 

  • Lynch RE, Lewis LC, Brindley TA (1976) Bacteria associated with eggs and first instar larvae of the European corn borer; identification and frequency of occurrence. J inv Pathol 27:229–237

    Google Scholar 

  • Mattson WL (1980) Herbivory in relation to plant nitrogen content. A Rev ecol Syst 11:119–161

    Article  Google Scholar 

  • Miyazaki S, Boush GM, Baerwald RJ (1968) Amino acid synthesis by Pseudomonas melophthora, bacterial symbiote of Rhagoletis pomonella. J Insect Physiol 14:513–518

    Article  PubMed  Google Scholar 

  • Petri L (1910) Untersuchungen über die Darmbakterien der Olivenfliege. Zentralbl Bakteriol Parasitenkd Infektionskr II 26:357–367

    Google Scholar 

  • Ratner SS, Stoffolano JG (1982) Development of the oesophageal bulb of the apple maggot, Rhagoletis pomonella (Diptera: Tephritidae): morphological, histological and histochemical study. A Ent Soc Amer 75:555–562

    Google Scholar 

  • Rossiter MC, Howard DJ, Bush GL (1983) Symbiotic bacteria of Rhagoletis pomonella. In: Fruit flies of economic importance, R Cavolloro (ed), pp 77–84. Balkema, Rotterdam

    Google Scholar 

  • Stammer HJ (1929) Die Bakteriensymbiose der Trypetiden (Diptera). Z Morphol Oekol Tiere 15:481–523

    Google Scholar 

  • Steinhaus EA (1946) Insect microbiology, 763 pp. Comstock, New York

    Google Scholar 

  • Steinhaus EA (1949) Principles of insect pathology, 757 pp. McGraw Hill, New York

    Google Scholar 

  • Steinhaus EA (1959) Serratia marcesens Bizio as an insect pathogen. Hilgardia 28:351–380

    Google Scholar 

  • Tsiropoulos GJ (1976) Bacteria associated with the Walnut Husk Fly, Rhagoletis completa. Environ Ent 5:83–86

    Google Scholar 

  • Tsiropoulos GJ (1980a) Quality problems associated with the mass-production of Dacus oleae (Gmel.) (Dipt., Trypetidae). Z ang Ent 90:413–420

    Google Scholar 

  • Tsiropoulos GJ (1980b) The importance of vitamins in adult Dacus oleae (Diptera: Tephritidae) nutrition. A ent Soc Amer 75:705–707

    Google Scholar 

  • Tsiropoulos GJ (1981) Effect of antibiotics incorporated into defined adult diets on survival and reproduction of the walnut husk fly, Rhagoletis completa Cress. (Dipt., Trypetidae). Z ang Ent 91:100–106

    Google Scholar 

  • Waterhouse DF, Day M (1953) Function of the gut in absorption, excretion and metabolism. In: Insect physiology, KD Roeder (ed), pp 331–349. Wiley, New York

    Google Scholar 

  • Yamvrias C, Panagopoulos C, Psallidus PG (1970) Preliminary study of the intestinal bacteria flora of the olive fruit fly, Dacus oleae Gmel. Ann Inst phytopathol Benaki NS 9:201–206

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fitt, G.P., O'Brien, R.W. Bacteria associated with four species of Dacus (Diptera: Tephritidae) and their role in the nutrition of the larvae. Oecologia 67, 447–454 (1985). https://doi.org/10.1007/BF00384954

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00384954

Keywords

Navigation