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A new PCR-based approach for the specific amplification of DNA from different Schistosoma species applicable to human urine samples
Currently available methods for the diagnosis of human schistosomiasis often lack enough sensitivity and specificity. Recently, several authors have developed more specific and sensitive diagnostic methods, mainly based on the polymerase chain reaction (PCR) technique. Nevertheless, these have been...
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Published in: | Parasitology 2006-11, Vol.133 (5), p.581-587 |
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description | Currently available methods for the diagnosis of human schistosomiasis often lack enough sensitivity and specificity. Recently, several authors have developed more specific and sensitive diagnostic methods, mainly based on the polymerase chain reaction (PCR) technique. Nevertheless, these have been only applied for the diagnosis of 1 out of 4 Schistosoma species affecting man (S. mansoni). Additionally, application of specific PCR has been exclusively used for blood or faecal patients' samples. Here, we develop a new, high sensitive PCR approach that allows the genus- and species-specific amplification of the main 4 Schistosoma species causing disease in man plus S. bovis. We further successfully apply this technique for the detection of parasite DNA in easy-to-handle urine samples from patients with schistosomiasis. With these samples, we have found 94·4% sensitivity and 99·9% specificity when applying a genus-specific (Schistosoma spp.) primer pair, and 100% sensitivity and 98·9% specificity in a species-specific (S. mansoni) PCR. |
doi_str_mv | 10.1017/S0031182006000898 |
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We further successfully apply this technique for the detection of parasite DNA in easy-to-handle urine samples from patients with schistosomiasis. With these samples, we have found 94·4% sensitivity and 99·9% specificity when applying a genus-specific (Schistosoma spp.) primer pair, and 100% sensitivity and 98·9% specificity in a species-specific (S. mansoni) PCR.</description><identifier>ISSN: 0031-1820</identifier><identifier>EISSN: 1469-8161</identifier><identifier>DOI: 10.1017/S0031182006000898</identifier><identifier>PMID: 16834820</identifier><identifier>CODEN: PARAAE</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Animals ; Biological and medical sciences ; Deoxyribonucleic acid ; Design ; diagnosis ; DNA ; DNA Primers ; DNA, Helminth - urine ; Fundamental and applied biological sciences. Psychology ; General aspects ; General aspects and techniques. Study of several systematic groups. 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Plathelmintha ; Parasites ; Parasitology ; Patients ; PCR ; Polymerase Chain Reaction - methods ; Ribosomal DNA ; Schistosoma - genetics ; Schistosoma - isolation & purification ; Schistosoma spp ; Schistosomiasis ; Schistosomiasis - diagnosis ; Sensitivity and Specificity ; Spain ; Species Specificity ; Tropical diseases ; Urine</subject><ispartof>Parasitology, 2006-11, Vol.133 (5), p.581-587</ispartof><rights>2006 Cambridge University Press</rights><rights>2006 INIST-CNRS</rights><rights>Copyright Cambridge University Press Nov 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-42170821c84ef77e8ad0970ed637ff6e269061cd501f043661a9e2462e23f1223</citedby><cites>FETCH-LOGICAL-c504t-42170821c84ef77e8ad0970ed637ff6e269061cd501f043661a9e2462e23f1223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0031182006000898/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,72730</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18251050$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16834820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SANDOVAL, N.</creatorcontrib><creatorcontrib>SILES-LUCAS, M.</creatorcontrib><creatorcontrib>PÉREZ-ARELLANO, J. L.</creatorcontrib><creatorcontrib>CARRANZA, C.</creatorcontrib><creatorcontrib>PUENTE, S.</creatorcontrib><creatorcontrib>LÓPEZ-ABÁN, J.</creatorcontrib><creatorcontrib>MURO, A.</creatorcontrib><title>A new PCR-based approach for the specific amplification of DNA from different Schistosoma species applicable to human urine samples</title><title>Parasitology</title><addtitle>Parasitology</addtitle><description>Currently available methods for the diagnosis of human schistosomiasis often lack enough sensitivity and specificity. Recently, several authors have developed more specific and sensitive diagnostic methods, mainly based on the polymerase chain reaction (PCR) technique. Nevertheless, these have been only applied for the diagnosis of 1 out of 4 Schistosoma species affecting man (S. mansoni). Additionally, application of specific PCR has been exclusively used for blood or faecal patients' samples. Here, we develop a new, high sensitive PCR approach that allows the genus- and species-specific amplification of the main 4 Schistosoma species causing disease in man plus S. bovis. We further successfully apply this technique for the detection of parasite DNA in easy-to-handle urine samples from patients with schistosomiasis. With these samples, we have found 94·4% sensitivity and 99·9% specificity when applying a genus-specific (Schistosoma spp.) primer pair, and 100% sensitivity and 98·9% specificity in a species-specific (S. mansoni) PCR.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Deoxyribonucleic acid</subject><subject>Design</subject><subject>diagnosis</subject><subject>DNA</subject><subject>DNA Primers</subject><subject>DNA, Helminth - urine</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>General aspects and techniques. Study of several systematic groups. Models</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Invertebrates</subject><subject>Male</subject><subject>Nemathelminthia. Plathelmintha</subject><subject>Parasites</subject><subject>Parasitology</subject><subject>Patients</subject><subject>PCR</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Ribosomal DNA</subject><subject>Schistosoma - genetics</subject><subject>Schistosoma - isolation & purification</subject><subject>Schistosoma spp</subject><subject>Schistosomiasis</subject><subject>Schistosomiasis - diagnosis</subject><subject>Sensitivity and Specificity</subject><subject>Spain</subject><subject>Species Specificity</subject><subject>Tropical diseases</subject><subject>Urine</subject><issn>0031-1820</issn><issn>1469-8161</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kU9v1DAQxS0EokvhA3BBFhLcAh47cZzjaqEFqfxpCxy4WF5nzLokcbATAWe-OI52xUogTh55fu_pzQwhD4E9Awb182vGBIDijEnGmGrULbKCUjaFAgm3yWppF0v_hNxL6SYzUkh-l5yAVKLM_yvya00H_E7fb66KrUnYUjOOMRi7oy5EOu2QphGtd95S04_dUpjJh4EGR1-8XVMXQ09b7xxGHCZ6bXc-TSGF3uyFmBbHLqu2HdIp0N3cm4HO0Q_ZerHEdJ_ccaZL-ODwnpKPZy8_bF4VF-_OX2_WF4WtWDkVJYeaKQ5WlejqGpVpWVMzbKWonZPIZcMk2LZi4FgppATTIC8lRy4ccC5OydO9b57w24xp0r1PFrvODBjmpGXeoBK8yuDjv8CbMMchZ9M875dD0yxusIdsDClFdHqMvjfxpwaml_Pof86TNY8OxvO2x_aoONwjA08OgEnWdC6awfp05BSvgFULV-y5vG388adv4lcta1FXWp5f6s9ls7k8e_NJX2VeHMKafht9-wWPI_0_7m8d6rSd</recordid><startdate>20061101</startdate><enddate>20061101</enddate><creator>SANDOVAL, N.</creator><creator>SILES-LUCAS, M.</creator><creator>PÉREZ-ARELLANO, J. L.</creator><creator>CARRANZA, C.</creator><creator>PUENTE, S.</creator><creator>LÓPEZ-ABÁN, J.</creator><creator>MURO, A.</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20061101</creationdate><title>A new PCR-based approach for the specific amplification of DNA from different Schistosoma species applicable to human urine samples</title><author>SANDOVAL, N. ; SILES-LUCAS, M. ; PÉREZ-ARELLANO, J. 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Additionally, application of specific PCR has been exclusively used for blood or faecal patients' samples. Here, we develop a new, high sensitive PCR approach that allows the genus- and species-specific amplification of the main 4 Schistosoma species causing disease in man plus S. bovis. We further successfully apply this technique for the detection of parasite DNA in easy-to-handle urine samples from patients with schistosomiasis. With these samples, we have found 94·4% sensitivity and 99·9% specificity when applying a genus-specific (Schistosoma spp.) primer pair, and 100% sensitivity and 98·9% specificity in a species-specific (S. mansoni) PCR.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>16834820</pmid><doi>10.1017/S0031182006000898</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Deoxyribonucleic acid Design diagnosis DNA DNA Primers DNA, Helminth - urine Fundamental and applied biological sciences. Psychology General aspects General aspects and techniques. Study of several systematic groups. Models Hospitals Humans Invertebrates Male Nemathelminthia. Plathelmintha Parasites Parasitology Patients PCR Polymerase Chain Reaction - methods Ribosomal DNA Schistosoma - genetics Schistosoma - isolation & purification Schistosoma spp Schistosomiasis Schistosomiasis - diagnosis Sensitivity and Specificity Spain Species Specificity Tropical diseases Urine |
title | A new PCR-based approach for the specific amplification of DNA from different Schistosoma species applicable to human urine samples |
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