Acute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa
BACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers with simultaneous freshwater exposure in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PC...
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Veröffentlicht in: | Clinical Infectious Diseases 2020-05, Vol.72 (10), p.1693-1698 |
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description | BACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers with simultaneous freshwater exposure in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PCR assays were performed at weeks 4-5 (early symptomatic phase), 7-8 (praziquantel treatment), and 13-14 (after treatment). Sequencing was done on serum samples from 3 patients to identify the species. RESULTS: Of the 34 travelers (16 adults and 18 children), 32 developed symptoms 2-6 weeks after exposure. A raised eosinophil count (>750/µL) was seen in 12 of 33 at weeks 4-5, and in 22 of 34 at weeks 7-8. Schistosoma antibodies were detected in 3 of 33 at weeks 4-5 and in 12 of 34 at weeks 7-8 and weeks 13-14. The Dra1 PCR result was positive in 24 of 33 travelers at weeks 4-5, in 31 of 34 at weeks 7-8, in 25 of 34 at weeks 13-14, and at least once in all. Ova were absent in all urine and stool samples obtained. Sequencing identified Schistosoma mattheei nuclear and Schistosoma haematobium mitochondrial DNA, indicative of a hybrid species. CONCLUSIONS: The Dra1 PCR confirmed the diagnosis in all exposed travelers at a much earlier stage than conventional tests. The causative species is probably an S. mattheei × S. haematobium hybrid. |
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Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>Lirias (KU Leuven Association)</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Cnops, L ; Huyse, T ; Maniewski, U ; Soentjens, P ; Bottieau, E ; Van Esbroeck, M ; Clerinx, J</creator><creatorcontrib>Cnops, L ; Huyse, T ; Maniewski, U ; Soentjens, P ; Bottieau, E ; Van Esbroeck, M ; Clerinx, J</creatorcontrib><description>BACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers with simultaneous freshwater exposure in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PCR assays were performed at weeks 4-5 (early symptomatic phase), 7-8 (praziquantel treatment), and 13-14 (after treatment). Sequencing was done on serum samples from 3 patients to identify the species. RESULTS: Of the 34 travelers (16 adults and 18 children), 32 developed symptoms 2-6 weeks after exposure. A raised eosinophil count (>750/µL) was seen in 12 of 33 at weeks 4-5, and in 22 of 34 at weeks 7-8. Schistosoma antibodies were detected in 3 of 33 at weeks 4-5 and in 12 of 34 at weeks 7-8 and weeks 13-14. The Dra1 PCR result was positive in 24 of 33 travelers at weeks 4-5, in 31 of 34 at weeks 7-8, in 25 of 34 at weeks 13-14, and at least once in all. Ova were absent in all urine and stool samples obtained. Sequencing identified Schistosoma mattheei nuclear and Schistosoma haematobium mitochondrial DNA, indicative of a hybrid species. CONCLUSIONS: The Dra1 PCR confirmed the diagnosis in all exposed travelers at a much earlier stage than conventional tests. The causative species is probably an S. mattheei × S. haematobium hybrid.</description><identifier>ISSN: 1058-4838</identifier><language>eng</language><publisher>Oxford University Press (OUP)</publisher><ispartof>Clinical Infectious Diseases, 2020-05, Vol.72 (10), p.1693-1698</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,776,780,27837</link.rule.ids></links><search><creatorcontrib>Cnops, L</creatorcontrib><creatorcontrib>Huyse, T</creatorcontrib><creatorcontrib>Maniewski, U</creatorcontrib><creatorcontrib>Soentjens, P</creatorcontrib><creatorcontrib>Bottieau, E</creatorcontrib><creatorcontrib>Van Esbroeck, M</creatorcontrib><creatorcontrib>Clerinx, J</creatorcontrib><title>Acute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa</title><title>Clinical Infectious Diseases</title><description>BACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers with simultaneous freshwater exposure in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PCR assays were performed at weeks 4-5 (early symptomatic phase), 7-8 (praziquantel treatment), and 13-14 (after treatment). Sequencing was done on serum samples from 3 patients to identify the species. RESULTS: Of the 34 travelers (16 adults and 18 children), 32 developed symptoms 2-6 weeks after exposure. A raised eosinophil count (>750/µL) was seen in 12 of 33 at weeks 4-5, and in 22 of 34 at weeks 7-8. Schistosoma antibodies were detected in 3 of 33 at weeks 4-5 and in 12 of 34 at weeks 7-8 and weeks 13-14. The Dra1 PCR result was positive in 24 of 33 travelers at weeks 4-5, in 31 of 34 at weeks 7-8, in 25 of 34 at weeks 13-14, and at least once in all. Ova were absent in all urine and stool samples obtained. Sequencing identified Schistosoma mattheei nuclear and Schistosoma haematobium mitochondrial DNA, indicative of a hybrid species. CONCLUSIONS: The Dra1 PCR confirmed the diagnosis in all exposed travelers at a much earlier stage than conventional tests. The causative species is probably an S. mattheei × S. haematobium hybrid.</description><issn>1058-4838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>FZOIL</sourceid><recordid>eNqNjLFOwzAQQD2ARCn8w20MqCiuk8YdqwoUBqZ0j1znohwkceU7l7Lw7SgSH9Dp6UlP70YtdFbYVW6NvVP3zJ9ZprXNioX63fkkCLXviSVwGMkxMXyT9LCD-gU-nEiPSHCZrXI4OglHSiNUP8dILdQn9IQMNIGD_ZBYMELowORwiO6MA0aG96lDL9jOVR3SPO8iefegbjs3MD7-c6me3l4P-2r1lQZMZ5yalk_OY6PXJi82pd02m7LcamOW6vm6spGLmOu_fyMjW78</recordid><startdate>20200515</startdate><enddate>20200515</enddate><creator>Cnops, L</creator><creator>Huyse, T</creator><creator>Maniewski, U</creator><creator>Soentjens, P</creator><creator>Bottieau, E</creator><creator>Van Esbroeck, M</creator><creator>Clerinx, J</creator><general>Oxford University Press (OUP)</general><scope>FZOIL</scope></search><sort><creationdate>20200515</creationdate><title>Acute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa</title><author>Cnops, L ; Huyse, T ; Maniewski, U ; Soentjens, P ; Bottieau, E ; Van Esbroeck, M ; Clerinx, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kuleuven_dspace_123456789_6779133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cnops, L</creatorcontrib><creatorcontrib>Huyse, T</creatorcontrib><creatorcontrib>Maniewski, U</creatorcontrib><creatorcontrib>Soentjens, P</creatorcontrib><creatorcontrib>Bottieau, E</creatorcontrib><creatorcontrib>Van Esbroeck, M</creatorcontrib><creatorcontrib>Clerinx, J</creatorcontrib><collection>Lirias (KU Leuven Association)</collection><jtitle>Clinical Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cnops, L</au><au>Huyse, T</au><au>Maniewski, U</au><au>Soentjens, P</au><au>Bottieau, E</au><au>Van Esbroeck, M</au><au>Clerinx, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa</atitle><jtitle>Clinical Infectious Diseases</jtitle><date>2020-05-15</date><risdate>2020</risdate><volume>72</volume><issue>10</issue><spage>1693</spage><epage>1698</epage><pages>1693-1698</pages><issn>1058-4838</issn><abstract>BACKGROUND: Diagnosis of schistosomiasis remains elusive soon after infection. We evaluated several diagnostic methods in a cluster of travelers with simultaneous freshwater exposure in South Africa. METHODS: Eosinophil count, schistosome antibody tests, stool and urine microscopy, and serum Dra1 PCR assays were performed at weeks 4-5 (early symptomatic phase), 7-8 (praziquantel treatment), and 13-14 (after treatment). Sequencing was done on serum samples from 3 patients to identify the species. RESULTS: Of the 34 travelers (16 adults and 18 children), 32 developed symptoms 2-6 weeks after exposure. A raised eosinophil count (>750/µL) was seen in 12 of 33 at weeks 4-5, and in 22 of 34 at weeks 7-8. Schistosoma antibodies were detected in 3 of 33 at weeks 4-5 and in 12 of 34 at weeks 7-8 and weeks 13-14. The Dra1 PCR result was positive in 24 of 33 travelers at weeks 4-5, in 31 of 34 at weeks 7-8, in 25 of 34 at weeks 13-14, and at least once in all. Ova were absent in all urine and stool samples obtained. Sequencing identified Schistosoma mattheei nuclear and Schistosoma haematobium mitochondrial DNA, indicative of a hybrid species. CONCLUSIONS: The Dra1 PCR confirmed the diagnosis in all exposed travelers at a much earlier stage than conventional tests. The causative species is probably an S. mattheei × S. haematobium hybrid.</abstract><pub>Oxford University Press (OUP)</pub></addata></record> |
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title | Acute Schistosomiasis with A S. Mattheei x S. Haematobium Hybrid Species in a Cluster of 34 Travelers Infected in South Africa |
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