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dc.contributor.authorCnops, L.
dc.contributor.authorHuyse, T.
dc.contributor.authorManiewski , U.
dc.contributor.authorSoentjens , P.
dc.contributor.authorBottieau , E.
dc.contributor.authorVan Esbroeck, M.
dc.contributor.authorClerinx , J.
dc.date2020
dc.date.accessioned2024-03-14T13:22:49Z
dc.date.available2024-03-14T13:22:49Z
dc.identifier.issn1058-4838
dc.identifier.urihttps://orfeo.belnet.be/handle/internal/12628
dc.descriptionBACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers simultaneously exposed to freshwater in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PCR assays were performed at week 4-5 (w4-5, early symptomatic phase), week 7-8 (w7-8, praziquantel treatment), and week 12-14 (w12-14, post-treatment). Sequencing was done on serum of 3 patients to identify the species. RESULTS: Of the 34 travelers (16 adults, 18 children), 32 developed symptoms 2 to 6 weeks after exposure. A raised eosinophil count (>750/µL) count was seen in 12/33 at w4-5, and in 22/34 at w7-8. Schistosoma antibodies were detected in 3/33 at w4-5, in 12/34 at w7-8 and w12-14. The Dra1 PCR was positive in 24/33 travelers at w4-5, in 31/34 at w7-8, in 25/34 at w12-14, and at least once in all. Ova were absent in all urine and fecal samples obtained. Sequencing identified S. mattheei nuclear and S. haematobium mitochondrial DNA, indicative of a hybrid species. CONCLUSION: The Dra-1 PCR confirmed diagnosis in all exposed travelers at a much earlier stage than conventional tests. The causative species is probably a S. mattheei x S. haematobium hybrid.
dc.languageeng
dc.titleAcute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa.
dc.typeArticle
dc.subject.frascatiClinical medicine
dc.audienceScientific
dc.subject.freeInvertebrates
dc.source.titleClinical Infectious Diseases
Orfeo.peerreviewedYes
dc.identifier.doihttps://doi.org/10.1093/cid/ciaa312
dc.identifier.rmca5952


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