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All issues Volume 19 / No 4 (November 2012) Parasite, 19 4 (2012) 445-449 Full HTML
Open Access
Issue
Parasite
Volume 19, Number 4, November 2012
Page(s) 445 - 449
DOI https://doi.org/10.1051/parasite/2012194445
Published online 15 November 2012

© PRINCEPS Editions, Paris, 2012, transferred to Société Française de Parasitologie

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Parasitosis due to Paramphistomum daubneyi (rumen fluke) affects ruminants in numerous countries of Europe (see the review by Sey, 1980), Middle East (Ozdal et al., 2010), Africa (Dinnik, 1962; Pacenowsky et al., 1987; Seck et al., 2008), India and New Zealand (Sey, 1980). Even though this digenean is mainly found in cattle (Dorchies et al., 1998, Dorchies et al., 2000), natural and experimental infections can develop in other ruminants such as sheep (Vignoles et al., 2008) and goats (Silvestre et al., 2000). In Africa and Europe, the main snail host is Galba truncatula (Sey, 1979; Brown, 1994). However, other European lymnaeids such as Omphiscola glabra, Stagnicola fuscus and S. palustris (Abrous et al., 1998; Degueurce et al., 1999) may support larval development of P. daubneyi if they have been co-infected with another digenean, Fasciola hepatica. Under these conditions, snails may harbour larval forms of the first parasite, the second, or both (Rondelaud et al., 2009).

The aim of the present paper was to identify lymnaeids other than European species, which may act as intermediate hosts in the life cycle of P. daubneyi. Due to the global distribution of this digenean (see above), we chose amphibious lymnaeids from South America for the following two reasons: i) numerous cattle and other animals were introduced to this continent in the 16th century by Spanish and Portuguese (Mas-Coma et al., 2009); and ii) the paramphistomid currently present in cattle from Spain and Portugal is P. daubneyi (Diaz et al., 2007; Arias et al., 2011). Experimental infections of two South American lymnaeids: Lymnaea neotropica and L. viatrix var. ventricosa with a French isolate of P. daubneyi miracidia were thus carried out to determine their capacity to sustain the development of larval forms and to specify the quantity of P. daubneyi cercariae these snail species might produce when the method proposed by Rondelaud et al. (2007) for amphibious snails was used for their breeding. Controls came from a French population of G. truncatula infected and raised according to the same protocol.

Material and Methods

The two South American lymnaeids have been raised under laboratory conditions at CEDIVE (Faculty of Veterinary Sciences, National University of La Plata, Buenos Aires, Argentina) since 2008 (L. neotropica) and 1996 (L. v. ventricosa). The first species came from a population living in San Pedro, Buenos Aires, Argentina (33° 40’ S, 59° 39’ W), while L. v. ventricosa originated from Paysandú, Uruguay (36° 00’ S, 57° 30’ W). As the systematics of South American lymnaeids is controversial and cannot be done with the use of single morphological criteria (Duffy et al., 2009; Mera y Sierra et al., 2009), the identification of these two species was performed using PCR-RFLP and sequencing of the ITS-1 segment of their nuclear rDNA (Sanabria et al., 2012). The French population of G. truncatula was collected from a road ditch (45° 55’ 33’’ N, 2° 2’ 33’’ E) in the commune of Saint-Michel-de-Veisse, department of Creuse. The habitat of this last population was located on siliceous soil so that the upper shell height of adults (8–9 mm) was the same as that of South American adults. To obtain P. daubneyi eggs, adult worms were collected from the rumen of infected cattle at the slaughterhouse of Limoges (France) and dipped in a physiological saline (ClNa, 0.9 %; glucose, 0.45 %) solution before being placed at 37 °C for three hours. Eggs were washed several times with spring water and incubated at 20 °C in the dark according to the report by Ollerenshaw (1971) for F. hepatica.

Two experiments were carried out in the present study. The aptitude of each snail species as an intermediate host of P. daubneyi was studied in experiment (A). One hundred snails, each measuring 4 mm in height, were randomly chosen from each population and subjected to individual quadrimiracidial exposures for four hours at 20 °C. The choice of four miracidia per snail came from the results of a preliminary experiment with these three populations and routine bimiracidial infections. Under these conditions, 3.2 % and 6.1 % of L. neotropica and L. v. ventricosa, respectively, were infected (instead of 91.8 % of G. truncatula) but most snails died without cercarial shedding (unpublished data). Snails were then raised in groups of ten individuals in 14 cm Petri dishes during the first 30 days according to the method of Rondelaud et al. (2007). They were maintained on dried lettuce leaves and dead grass leaves (Molinia caerulea), while several stems of live Fontinalis sp. ensured oxygenation of the water layer. Petri dishes were placed at a constant temperature of 20 °C (± 1 °C), with a natural photoperiod of ten hours light. At day 30 post exposure (p.e.), each surviving snail was placed in a 35 mm Petri dish with pieces of dead grass, lettuce and spring moss, and also kept at 20 °C. Snails were observed daily to change spring water and food if necessary, and to count metacercariae before their removal from dishes. When the first cercarial shedding occurred, the surviving snails were subjected to a thermal shock every three days by placing their Petri dishes at 10–13 °C for three hours (outdoors) to stimulate cercariae exit. Experiment (B) was carried out on order to determine cercarial production of P. daubneyi in snails dissected at day 65 p.e. at 20 °C (the first cercarial shedding generally occurred at the end of week 9 p.e.). Each experimental group contained 50 snails. Snail exposure to miracidia and their breeding were similar to those of experiment (A). At day 65, each snail was dissected under a stereomicroscope to count free white procercariae and yellowish brown cercariae of P. daubneyi. Free rediae were also taken into account.

The first two parameters were snail survival at day 30 p.e. and prevalence of P. daubneyi infection (calculated in relation to the number of surviving snails at day 30 p.e.). Prevalence took into account the number of cercariae-shedding snails (CS snails) and infected individuals, which died without cercariae exit (NCS snails) in experiment (A), and all snails carrying larval forms of P. daubneyi in experiment (B). For each parameter, the difference between the values noted for the three snail groups was analyzed using a χ2 test. In experiment (A), the growth of CS snails during the experiment, length of the prepatent period, length of the patent period, and total number of metacercariae were also taken into account. In experiment (B), the number of free rediae, quantity of procercariae and that of free cercariae were considered. Individual values recorded for these last seven parameters were averaged and their standard deviations calculated considering snail groups. One-way analysis of variance was used to establish levels of significance. All statistics were made using Statview 5.0 software.

Results and Discussion

Compared to the survival of control G. truncatula at day 30 p.e. (Table I), the rate of L. neotropica was significantly greater while that of L. v. ventricosa was lower (χ2 = 11.50, P < 0.01). The differences between prevalence of infection, growth of CS snails, lengths of prepatent periods, and those of patent periods were insignificant. In contrast, the number of metacercariae shed by L. neotropica was significantly lower (F = 4.70, P < 0.05) than those released by the other two lymnaeids. Contrary to G. truncatula, which shed its cercariae during several waves, most L. neotropica and L. v. ventricosa released these larvae during a single shedding wave and died after (data not shown).

Table I.

Main characteristics of P. daubneyi infection in three species of lymnaeid snails (experiment A).

Table II gives the results of experiment (B). Significant differences (χ2 = 18.05, P < 0.001) were noted between the survival of G. truncatula at day 30 p.e. and the rates of the other two lymnaeids. As for experiment (A), prevalence of P. daubneyi infection in the three snail groups did not differ significantly from each other. Significantly lower numbers of free rediae (F = 4.26, P < 0.05) and free cercariae (F = 3.58, P < 0.05) were seen for L. neotropica, whereas the differences existing between the other two lymnaeids were insignificant. In all three snail groups, the numbers of free procercariae were similar and no significant difference was noted.

Table II.

Counts of P. daubneyi rediae and cercariae in three species of lymnaeids at day 65 p.e. at 20 °C (experiment B).

If the number of shed cercariae (Table I) was compared to total cercarial production within the snail body (Table II), the percentage of larvae which exited from the snail was 75.6 % for G. truncatula and 91.4 % for L. v. ventricosa, while it was only 21.6 % for L. neotropica.

As the intermediate hosts of P. daubneyi in Africa and Europe are G. truncatula and Lymnaea peregra (Sey, 1979), the findings reported in the present study demonstrated that L. neotropica and L. v. ventricosa also were potential snail hosts for this digenean. Two perhaps complementary hypotheses may be proposed to explain these results. First, P. daubneyi is apparently present in South America, at least in Argentina and Uruguay, even though other paramphistomids such as Paramphistomum cervi (Nascimento et al., 2006) and Paramphistomum leydeni (Sanabria et al., 2011a, b) have already been reported on this continent. Secondly, larval development of P. daubneyi might occur in several species of the genus Galba/Fossaria. An argument supporting this last approach was the report by Castro-Trejo et al. (1990) with P. cervi larvae developing in three lymnaeids (Lymnaea cubensis, L. humilis and L. palustris).

In the two South American lymnaeids, there was a strong disparity in snail response to larval development of P. daubneyi. Compared to control G. truncatula, the mean redial and cercarial burdens in L. v. ventricosa (Table II) were slightly higher and this snail population shed 91.4 % of its cercariae. In contrast, in L. neotropica, redial and cercarial burdens were significantly lower (Table II) and only 21.6 % of cercariae were shed. These findings may be interpreted as consequences of a still incomplete adaptation between both partners and this incomplete adaptation would be greater for L. neotropica than for L. v. ventricosa. This hypothesis is supported by the fact that numerous South American lymnaeids shed their cercariae during a single wave. According to Rondelaud et al. (2009), the exit of F. hepatica cercariae during a single wave of one or several days, followed by snail death, indicated an incomplete adaptation between snail population and the parasite.

Low lengths of patent periods were noted for infected L. neotropica and L. v. ventricosa in the present study. In contrast, longer patent periods up to a mean of 96.3 days for L. v. ventricosa, for example, infected by Fascioloides magna (Sanabria et al., 2012) were reported. As control G. truncatula also showed low lengths of patent periods (Table I), these findings can be explained by the use of four miracidia per snail.

Conclusion

Even if the miracidial burden of P. daubneyi used in the present study seemed to clearly reduce life expectation of infected L. v. ventricosa, this species is a good candidate for metacercarial production of this digenean. As breeding of this snail in the laboratory using the method by Rondelaud et al. (2007) was easier than for G. truncatula, this lymnaeid might replace G. truncatula as a snail host for P. daubneyi. However, a study on the viability of metacercariae produced by L. v. ventricosa and their development into adults in the definitive host is still necessary to optimize the characterization of this snail species.

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All Tables

Table I.

Main characteristics of P. daubneyi infection in three species of lymnaeid snails (experiment A).

In the text
Table II.

Counts of P. daubneyi rediae and cercariae in three species of lymnaeids at day 65 p.e. at 20 °C (experiment B).

In the text

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