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The development of the host-response in juvenileLymnaea palustris to invasion byFasciola hepatica

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Abstract

Laboratory studies indicate that miracidia ofFasciola hepatica can penetrate several species of lymnaeids in Europe, other than the natural hostLymnaea truncatula. However, the production of cercariae from infections in abnormal hosts is limited to a small percentage of juvenile snails infected before a species-specific age.

JuvenileLymnaea palustris, of known ages, were exposed individually toF. hepatica miracidia and killed at 24 h intervals up to 14 days post exposure, and then processed for histological examination to ascertain reasons for the failure ofF. hepatica infections to develop successfully in this abnormal host.

The results indicate that the course of infection is rapidly halted by a cellular encapsulation response against the sporocyst. The response may be divided into two stages: first, the development of a cellular capsule and the concomitant degeneration of the sporocyst; second, the removal of the remains of the parasite and dispersal of the capsule. The efficiency of the response appears to increase with increasing age of the snail; statistical manipulation of the data obtained from histological investigations suggest that the defence mechanisms develop quickly in the first 6 days post hatching with little subsequent development during the experimental period. However, as sporocysts were encapsulated and killed regardless of age of the snail at exposure to infection, it is unlikely that in the host-parasite system used any of the infections would have survived.

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References

  • Boray JC (1966) Studies on the relative susceptibility of some lymnaeids to infection withFasciola hepatica andF. gigantica and on the adaptation ofFasciola spp. Ann Trop Med Parasitol 60:114–124

    Google Scholar 

  • Carter OS, Bogitsch BJ (1975) Histological and cytological observations on the effects ofSchistosoma mansoni onBiomphalaria glabrata. Ann NY Acad Sci 266:380–393

    Google Scholar 

  • Cheng TC, Garrabrant TA (1977) Acid phosphatase in granulocytic encapsulation formed in strains ofBiomphalaria glabrata totally and partially resistant toSchistosoma mansoni. Int J Parasitol 7:467–472

    Google Scholar 

  • Harris KR, Cheng TC (1975) The encapsulation process inBiomphalaria glabrata experimentally infected with the metastrongylidAngiostrongylus cantonensis: enzyme histochemistry. J Invertebr Pathol 26:367–374

    Google Scholar 

  • Kendall SB (1950) Snail hosts ofFasciola hepatica in Great Britain. J Helminthol 24:63–74

    Google Scholar 

  • Lie KS, Heyneman D (1976) Studies on resistance on snails 5: Tissue reaction ofEchinostoma lindoense in naturally resistantBiomphalaria glabrata. J Parasitol 62:292–297

    Google Scholar 

  • Loverde PT (1979) Defence reactions in snails against the intramolluscan stages of schistosomes. Zentralbl Bakteriol, I. Abt Ref Bd 263:207–208

    Google Scholar 

  • Meuleman EA, Holzmann PJ, Peet RC (1980) The development of daughter sporocysts inside the mother sporocyst ofSchistosoma mansoni with special reference to the ultrastructure of the body wall. Z Parasitenkd 61:201–212

    Google Scholar 

  • Nansen P, Frandsen F, Christensen NO (1976) A study on snail location byFasciola hepatica using radioactively labelled miracidia. Parasitology 72:163–171

    Google Scholar 

  • Newton WL (1952) The comparative tissue reaction of two strains ofAustralorbis glabratus to infection withSchistosoma mansoni. J Parasitol 38:362–365

    Google Scholar 

  • Pan CT (1965) Studies on the host-parasite relationship betweenSchistosoma mansoni and the snailAustralorbis glabratus. Am J Trop Med Hyg 14:931–976

    Google Scholar 

  • Rondelaud D, Barthe D (1980) Etude descriptive d'une réaction amibocytaire chezLymnaea truncatula Müller infestée parFasciola hepatica L. Z Parasitenkd 61:187–196

    Google Scholar 

  • Sazanov AM (1972) A protective response of lymnaeid molluscs to the penetration ofFasciola hepatica miracidia. Trudy usesoyuznogo Instituta Gel'minthologii un KI Skrjabina 19:163–170

    Google Scholar 

  • Sudds RH (1960) Observations of schistosome miracidia behaviour in the presence of normal and abnormal snail hosts and subsequent tissue studies of these hosts. J Elisha Mitchell Scient Soc 76:121–133

    Google Scholar 

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McReath, A.M., Reader, T.A.J. & Southgate, V.R. The development of the host-response in juvenileLymnaea palustris to invasion byFasciola hepatica . Z. Parasitenkd. 67, 175–184 (1982). https://doi.org/10.1007/BF00928113

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