Cargando…

Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations

BACKGROUND: High prevalence of Fasciola hepatica infection (>70%) was noted during several outbreaks before the 2000s in several French farms where Galba truncatula is lacking. Other lymnaeids such as Lymnaea fuscus, L. glabra and/or Radix balthica are living in meadows around these farms but onl...

Descripción completa

Detalles Bibliográficos
Autores principales: Rondelaud, Daniel, Titi, Amal, Vignoles, Philippe, Mekroud, Abdeslam, Dreyfuss, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090179/
https://www.ncbi.nlm.nih.gov/pubmed/24986589
http://dx.doi.org/10.1186/1756-3305-7-296
_version_ 1782480597929689088
author Rondelaud, Daniel
Titi, Amal
Vignoles, Philippe
Mekroud, Abdeslam
Dreyfuss, Gilles
author_facet Rondelaud, Daniel
Titi, Amal
Vignoles, Philippe
Mekroud, Abdeslam
Dreyfuss, Gilles
author_sort Rondelaud, Daniel
collection PubMed
description BACKGROUND: High prevalence of Fasciola hepatica infection (>70%) was noted during several outbreaks before the 2000s in several French farms where Galba truncatula is lacking. Other lymnaeids such as Lymnaea fuscus, L. glabra and/or Radix balthica are living in meadows around these farms but only juvenile snails can sustain complete larval development of F. hepatica while older snails were resistant. The low prevalence of infection (<20%) and limited cercarial production (<50 cercariae per infected snail) noted with these juveniles could not explain the high values noted in these cattle herds. As paramphistomosis due to Calicophoron daubneyi was not still noted in these farms, the existence of another mode of infection was hypothesized. Experimental infection of several successive generations of L. glabra, originating from eggs laid by their parents already infected with this parasite resulted in a progressive increase in prevalence of snail infection and the number of shed cercariae. The aim of this paper was to determine if this mode of snail infection was specific to L. glabra, or it might occur in other lymnaeid species such as L. fuscus and R. balthica. METHODS: Five successive generations of L. fuscus and R. balthica were subjected to individual bimiracidial infections in the laboratory. Resulting rediae and cercariae in the first four generations were counted after snail dissection at day 50 p.e. (20°C), while the dynamics of cercarial shedding was followed in the F5 generation. RESULTS: In the first experiment, prevalence and intensity of F. hepatica infection in snails progressively increased from the F1 (R. balthica) or F2 (L. fuscus) generation. In the second experiment, the prevalence of F. hepatica infection and the number of shed cercariae were significantly lower in L. fuscus and R. balthica (without significant differences between both lymnaeids) than in G. truncatula. CONCLUSION: The F. hepatica infection of several successive snail generations, coming from parents infected with this parasite, resulted in a progressive increase in prevalence and intensity of snail infection. This may explain high prevalence of fasciolosis noted in several cattle-breeding farms when the common snail host of this digenean, G. truncatula, is lacking.
format Online
Article
Text
id pubmed-4090179
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40901792014-07-10 Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations Rondelaud, Daniel Titi, Amal Vignoles, Philippe Mekroud, Abdeslam Dreyfuss, Gilles Parasit Vectors Research BACKGROUND: High prevalence of Fasciola hepatica infection (>70%) was noted during several outbreaks before the 2000s in several French farms where Galba truncatula is lacking. Other lymnaeids such as Lymnaea fuscus, L. glabra and/or Radix balthica are living in meadows around these farms but only juvenile snails can sustain complete larval development of F. hepatica while older snails were resistant. The low prevalence of infection (<20%) and limited cercarial production (<50 cercariae per infected snail) noted with these juveniles could not explain the high values noted in these cattle herds. As paramphistomosis due to Calicophoron daubneyi was not still noted in these farms, the existence of another mode of infection was hypothesized. Experimental infection of several successive generations of L. glabra, originating from eggs laid by their parents already infected with this parasite resulted in a progressive increase in prevalence of snail infection and the number of shed cercariae. The aim of this paper was to determine if this mode of snail infection was specific to L. glabra, or it might occur in other lymnaeid species such as L. fuscus and R. balthica. METHODS: Five successive generations of L. fuscus and R. balthica were subjected to individual bimiracidial infections in the laboratory. Resulting rediae and cercariae in the first four generations were counted after snail dissection at day 50 p.e. (20°C), while the dynamics of cercarial shedding was followed in the F5 generation. RESULTS: In the first experiment, prevalence and intensity of F. hepatica infection in snails progressively increased from the F1 (R. balthica) or F2 (L. fuscus) generation. In the second experiment, the prevalence of F. hepatica infection and the number of shed cercariae were significantly lower in L. fuscus and R. balthica (without significant differences between both lymnaeids) than in G. truncatula. CONCLUSION: The F. hepatica infection of several successive snail generations, coming from parents infected with this parasite, resulted in a progressive increase in prevalence and intensity of snail infection. This may explain high prevalence of fasciolosis noted in several cattle-breeding farms when the common snail host of this digenean, G. truncatula, is lacking. BioMed Central 2014-07-01 /pmc/articles/PMC4090179/ /pubmed/24986589 http://dx.doi.org/10.1186/1756-3305-7-296 Text en Copyright © 2014 Rondelaud et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rondelaud, Daniel
Titi, Amal
Vignoles, Philippe
Mekroud, Abdeslam
Dreyfuss, Gilles
Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title_full Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title_fullStr Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title_full_unstemmed Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title_short Adaptation of Lymnaea fuscus and Radix balthica to Fasciola hepatica through the experimental infection of several successive snail generations
title_sort adaptation of lymnaea fuscus and radix balthica to fasciola hepatica through the experimental infection of several successive snail generations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090179/
https://www.ncbi.nlm.nih.gov/pubmed/24986589
http://dx.doi.org/10.1186/1756-3305-7-296
work_keys_str_mv AT rondelauddaniel adaptationoflymnaeafuscusandradixbalthicatofasciolahepaticathroughtheexperimentalinfectionofseveralsuccessivesnailgenerations
AT titiamal adaptationoflymnaeafuscusandradixbalthicatofasciolahepaticathroughtheexperimentalinfectionofseveralsuccessivesnailgenerations
AT vignolesphilippe adaptationoflymnaeafuscusandradixbalthicatofasciolahepaticathroughtheexperimentalinfectionofseveralsuccessivesnailgenerations
AT mekroudabdeslam adaptationoflymnaeafuscusandradixbalthicatofasciolahepaticathroughtheexperimentalinfectionofseveralsuccessivesnailgenerations
AT dreyfussgilles adaptationoflymnaeafuscusandradixbalthicatofasciolahepaticathroughtheexperimentalinfectionofseveralsuccessivesnailgenerations