Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 20, Number 9—September 2014
Letter

Schistosomiasis Haematobium, Corsica, France

On This Page
Figures
Article Metrics
75
citations of this article
EID Journal Metrics on Scopus

Cite This Article

To the Editor: In Europe, urinary schistosomiasis (1) has previously been detected only in Portugal, where this focus disappeared during the 1950s (2). However, freshwater snails of the species Bulinus contortus, B. truncatus, and Planorbarius metidjensis, which are recognized intermediate hosts for Schistosoma haematobium trematodes, have been found in Portugal (3), Spain (4), and Corsica (5,6). This finding suggested that autochthonous schistosomiasis could re-emerge in southern Europe if these mollusks become infected. We report a probable focus for transmission of schistosomiasis haematobium in Corsica, France.

In March 2014, a 4-year-old girl (index case-patient) from France was referred to the Toulouse University Hospital (Toulouse, France), with gross hematuria. Ultrasonography and cystoscopic examination of the bladder detected a polyp. Examination of the polyp for parasites identified bodies that were consistent with schistosome eggs. Parasitologic examination of urine confirmed schistosomiasis by detecting viable S. haematobium eggs.

The parents of the girl (family A) did not report any stay or travel in an area to which urinary schistosomiasis was endemic; they reported summer holidays only in Mallorca in the Balearic Islands (Spain) and Corsica. However, her father reported that since 2012, he had experienced gross hematuria that had been evaluated by standard urologic investigations but not by cystoscopy; no etiology was determined. Parasitologic urinalysis in our hospital department showed numerous viable S. haematobium eggs in the father’s urine.

The parents of the index case-patient also reported that an 8-year-old boy in a friend’s family (family B), who shared summer vacations with them had exhibited gross hematuria since February 2013. A third family (family C) was also investigated because they also spent holidays in Corsica with families A and B. Families B and C had also spent a summer in Mallorca, but they denied any contact with freshwater. Of 11 French native-born members of the 3 families, 6 had positive results for S. haematobium by urine examination. All case-patients had specific positive immunodiagnostic results by an ELISA that used S. mansoni extracts and by indirect hemagglutination. In addition, 2 family members who had a negative result by urine examination had a positive serologic result.

Spending summer vacations in the same village in Corsica (Sainte-Lucie de Porto-Vecchio), where members of the 3 families had bathed at least once per holiday period in the Cavu River, was the epidemiologically prominent feature that linked these persons. Families A and C were in Sainte-Lucie de Porto-Vecchio in August 2011, and families A, B, and C were in the same location in August 2013.

During these investigations, we were contacted by the Department of Tropical Medicine, Dusseldorf University Hospital (Dusseldorf, Germany), because a 10-year-old boy and his father had been given diagnoses of schistosomiasis haematobium on the basis of positive urinalysis results for S. haematobium eggs. Two other members of this family (5 persons) had a positive immunodiagnostic result. Locations of previous vacations for this family outside Germany included Spain (not the Balearic Islands) and Corsica, where they bathed frequently in the Cavu River. These epidemiologic findings provide strong circumstantial evidence supporting the presence of a previously unrecognized focus of urinary schistosomiasis in Corsica.

We performed molecular analysis of schistosomal miracidia DNA. The second internal transcribed spacer region of the ribosomal gene complex (7,8) was amplified and sequenced. Viable eggs obtained from the patients in France were those of S. haematobium. Additional molecular investigations are being conducted to assess genetic diversity of this isolate from Corsica and the geographic origin of the introduced parasite.

Figure

Thumbnail of Corsica, France, showing malacologic survey sampling sites (oval) in 3 rivers (Tarcu, Cavu, and Osu). Bulinus truncatus snails were found at sites 1, 2, 3, 5, and 6.

Figure. Corsica, France, showing malacologic survey sampling sites (oval) in 3 rivers (Tarcu, Cavu, and Osu). Bulinus truncatus snails were found at sites 1, 2, 3, 5, and 6.

The malacologic situation in Sainte Lucie de Porto-Vecchio was investigated during May 12–19, 2014; three rivers (Figure) were included in the survey. Four sites were sampled in the Cavu River, and B. truncatus snails were found in 3 sites that corresponded to bathing areas (site 1: 41°43′53.57″N, 9°17′36.70″E; site 2: 41°43′22.13″N, 9°17′59.87″E; site 3: 41°42′8.40″N, 9°21′5.82″E). Snails were also found in the nearby Tarcu River (site 5) and Osu River (site 6). These findings confirmed previous data for the presence of B. truncatus snails in Corsica (5,6). Water temperature was recorded at 11:00 am at these 3 sites (range 15°C–16°C). This temperature range is not optimal for the snail intermediate host stage of the parasite life cycle (9,10). Of 148 live snails that were obtained in the Cavu River, none were infected with schistosome cercariae.

Data from the field survey and epidemiologic information for the cases in France and Germany, indicated transmission of schistosomiasis haematobium in the Cavu River in southeastern Corsica in 2011 and 2013. Additional supportive evidence is the fact that the father of the index case-patient had gross hematuria in 2012 and 2013.

Two hypotheses are proposed to account for this situation. The first hypothesis is that the parasite (i.e., schistosome eggs) was transmitted by an infected person into the Cavu River in June or July 2011, when environmental conditions were favorable for snail infection. However, questions arise about survival of infected snails during the winter and their ability to reinfect the area during the following summers in 2012 and 2013. The second hypothesis is that schistosome eggs were spread by infected persons at the beginning of summer and caused a permanent transmission cycle in this focus. This situation would be difficult to control. Additional information should be obtained by a long-term malacologic survey to detect infected mollusks in this region.

Top

Antoine BerryComments to Author , Hélène Moné, Xavier Iriart, Gabriel Mouahid, Olivier Aboo, Jérôme Boissier, Judith Fillaux, Sophie Cassaing, Cécile Debuisson, Alexis Valentin, Guillaume Mitta, André Théron, and Jean-François Magnaval
Author affiliations: Centre Hospitalier Universitaire, Toulouse, France (A. Berry, X. Iriart, O. Aboo, J. Fillaux, S. Cassaing, C. Debuisson, A. Valentin); Institut National de la Santé et de la Recherche Médicale, Toulouse (A. Berry, X. Iriart); Centre National de la Recherche Scientifique, Perpignan, France (H. Moné, J. Boissier, G. Mouahid, G. Mitta, A. Théron); Centre National de la Recherche Scientifique, Toulouse (J.-F. Magnaval)

Top

References

  1. Schistosomiasis  GB. Infect Dis Clin North Am. 2012;26:38397 . DOIPubMedGoogle Scholar
  2. Fraga de Azevedo  J, da Silva  JB, Coito  AM, Coelho  MF, Colaco  AT. Portuguese focus of schistosomiasis [in Portuguese]. An Inst Med Trop (Lisb). 1948;5:175222.
  3. de Azevedo  JF. Biological relationships among the different geographical strains of the Schistosoma haematobium complex [in French]. Bull Soc Pathol Exot. 1969;62:34875.
  4. Perez-Quintero  JC, Bech Taberner  M, Huertsa Dionisio  L. Molluscs of the inland waters of the province of Huleva (SO Spain) [in Spanish]. Iberus. 2004;22:1931.
  5. Gretillat  S. Epidemiology of certain trematode diseases of domestic animals in Corsica (bovine bilharzosis and bovine and ovine distomiasis). Observations conducted during a mission accomplished during the autumn of 1962 [in French]. Ann Parasitol Hum Comp. 1963;38:47181 .PubMedGoogle Scholar
  6. Doby  JM, Rault  B, Deblock  S, Chabaud  A. Snails and bilharziasis in Corsica. Distribution, frequency and biology of Bulinus truncatus [in French]. Ann Parasitol Hum Comp. 1966;41:33749 .PubMedGoogle Scholar
  7. Webster  BL, Emery  AM, Webster  JP, Gouvras  A, Garba  A, Diaw  O, Genetic diversity within Schistosoma haematobium: DNA barcoding reveals two distinct groups. PLoS Negl Trop Dis. 2012;6:e1882. . Epub 2012 Oct 25.DOIGoogle Scholar
  8. Glenn  TC, Lance  SL, McKee  AM, Webster  BL, Emery  AM, Zerlotini  A, Significant variance in genetic diversity among populations of Schistosoma haematobium detected using microsatellite DNA loci from a genome-wide database. Parasit Vectors. 2013;6:300.
  9. Capron  A, Deblock  S, Biguet  J, Clay  A, Adenis  L, Vernes  A. Contribution to the experimental study of bilharziasis caused by Schistosoma haematobium [in French]. Bull World Health Organ. 1965;32:75578 .PubMedGoogle Scholar
  10. Pflüger  W, Roushdy  MZ, El Emam  M. The prepatent period and cercarial production of Schistosoma haematobium in Bulinus truncatus (Egyptian field strains) at different constant temperatures. Z Parasitenkd. 1984;70:95103. DOIPubMedGoogle Scholar

Top

Figure

Top

Cite This Article

DOI: 10.3201/eid2009.140928

Related Links

Top

Table of Contents – Volume 20, Number 9—September 2014

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Antoine Berry, Service de Parasitologie-Mycologie, Institut Fédératif de Biologie, Hôpital Purpan, Centre Hospitalier Universitaire de Toulouse, TSA 40031, 31059 Toulouse CEDEX 9, France

Send To

10000 character(s) remaining.

Top

Page created: August 18, 2014
Page updated: August 18, 2014
Page reviewed: August 18, 2014
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external