Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine

Autores
Lodh, Nilanjan; Caro, Reynaldo; Sofer, Shterna; Scott, Alan; Krolewiecki, Alejandro Javier; Shiff, Clive
Año de publicación
2016
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Detecting infections of Strongyloides stercoralis is arduous and has low sensitivity. Clinically this is a major problem because chronic infections may disseminate in the host and lead to a life threatening condition.Epidemiologically, S. stercoralis is often missed in surveys as it is difficult to identify by standard stool examination procedures. We present, for the first time, evidence that the infection can be detected in filtered urine samples collected and processed in the field and subsequently assayed for the presence of parasite DNA. Urine specimens (∼40 mL) were collected from 125 test and control individuals living in rural and peri-urban regions of Northern Argentina. From the same individuals, fresh stool specimens were processed using three different copropological methods. Urine specimens were filtered in the field through a 12.5 cm Whatman No. 3 filter. The filters were dried and packed individually in sealable plastic bags with desiccant and shipped to a laboratory where DNA was recovered from the filter and PCRamplified with primers specific to a dispersed repetitive sequence. Prevalence of S. stercoralis infectionby stool culture and direct examination was 35/125 (28%), In contrast, PCR-based detection of parasitespecific trans-renal DNA in urine indicated that 56/125 (44.8%) carried the parasite. Of the patients that tested positive for urine-based parasite DNA, approximately half also tested positive in their stool specimens. There were 6.4% of cases where parasite larvae were seen in the stool but no DNA was amplified from the urine. As proof of principle, DNA amplification from urine residue reveals significantly more cases of S. stercoralis infection than the current standard stool examination techniques. Additional work is required to establish the relative utility, sensitivity and specificity of urine-based analysis compared to parasitological and nucleic acid detection from stool for clinical and epidemiological detection for S.stercoralis infection.
Fil: Lodh, Nilanjan. Marquette University; Estados Unidos
Fil: Caro, Reynaldo. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; Argentina
Fil: Sofer, Shterna. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
Fil: Scott, Alan. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
Fil: Krolewiecki, Alejandro Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; Argentina
Fil: Shiff, Clive. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
Materia
STRONGYLOIDES STERCORALIS
DIAGNOSTICS TEST
DNA DETECTION
URINE SPECIMEN
GASTRO-INTESTINAL PARASITE
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/29934

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urineLodh, NilanjanCaro, ReynaldoSofer, ShternaScott, AlanKrolewiecki, Alejandro JavierShiff, CliveSTRONGYLOIDES STERCORALISDIAGNOSTICS TESTDNA DETECTIONURINE SPECIMENGASTRO-INTESTINAL PARASITEhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Detecting infections of Strongyloides stercoralis is arduous and has low sensitivity. Clinically this is a major problem because chronic infections may disseminate in the host and lead to a life threatening condition.Epidemiologically, S. stercoralis is often missed in surveys as it is difficult to identify by standard stool examination procedures. We present, for the first time, evidence that the infection can be detected in filtered urine samples collected and processed in the field and subsequently assayed for the presence of parasite DNA. Urine specimens (∼40 mL) were collected from 125 test and control individuals living in rural and peri-urban regions of Northern Argentina. From the same individuals, fresh stool specimens were processed using three different copropological methods. Urine specimens were filtered in the field through a 12.5 cm Whatman No. 3 filter. The filters were dried and packed individually in sealable plastic bags with desiccant and shipped to a laboratory where DNA was recovered from the filter and PCRamplified with primers specific to a dispersed repetitive sequence. Prevalence of S. stercoralis infectionby stool culture and direct examination was 35/125 (28%), In contrast, PCR-based detection of parasitespecific trans-renal DNA in urine indicated that 56/125 (44.8%) carried the parasite. Of the patients that tested positive for urine-based parasite DNA, approximately half also tested positive in their stool specimens. There were 6.4% of cases where parasite larvae were seen in the stool but no DNA was amplified from the urine. As proof of principle, DNA amplification from urine residue reveals significantly more cases of S. stercoralis infection than the current standard stool examination techniques. Additional work is required to establish the relative utility, sensitivity and specificity of urine-based analysis compared to parasitological and nucleic acid detection from stool for clinical and epidemiological detection for S.stercoralis infection.Fil: Lodh, Nilanjan. Marquette University; Estados UnidosFil: Caro, Reynaldo. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; ArgentinaFil: Sofer, Shterna. Johns Hopkins Bloomberg School of Public Health; Estados UnidosFil: Scott, Alan. Johns Hopkins Bloomberg School of Public Health; Estados UnidosFil: Krolewiecki, Alejandro Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; ArgentinaFil: Shiff, Clive. Johns Hopkins Bloomberg School of Public Health; Estados UnidosElsevier Science2016-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/29934Lodh, Nilanjan; Caro, Reynaldo; Sofer, Shterna; Scott, Alan; Krolewiecki, Alejandro Javier; et al.; Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine; Elsevier Science; Acta Tropica; 163; 7-2016; 9-130001-706XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.actatropica.2016.07.014info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0020751912001701info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117362/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:47:15Zoai:ri.conicet.gov.ar:11336/29934instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:47:15.453CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
title Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
spellingShingle Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
Lodh, Nilanjan
STRONGYLOIDES STERCORALIS
DIAGNOSTICS TEST
DNA DETECTION
URINE SPECIMEN
GASTRO-INTESTINAL PARASITE
title_short Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
title_full Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
title_fullStr Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
title_full_unstemmed Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
title_sort Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine
dc.creator.none.fl_str_mv Lodh, Nilanjan
Caro, Reynaldo
Sofer, Shterna
Scott, Alan
Krolewiecki, Alejandro Javier
Shiff, Clive
author Lodh, Nilanjan
author_facet Lodh, Nilanjan
Caro, Reynaldo
Sofer, Shterna
Scott, Alan
Krolewiecki, Alejandro Javier
Shiff, Clive
author_role author
author2 Caro, Reynaldo
Sofer, Shterna
Scott, Alan
Krolewiecki, Alejandro Javier
Shiff, Clive
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv STRONGYLOIDES STERCORALIS
DIAGNOSTICS TEST
DNA DETECTION
URINE SPECIMEN
GASTRO-INTESTINAL PARASITE
topic STRONGYLOIDES STERCORALIS
DIAGNOSTICS TEST
DNA DETECTION
URINE SPECIMEN
GASTRO-INTESTINAL PARASITE
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Detecting infections of Strongyloides stercoralis is arduous and has low sensitivity. Clinically this is a major problem because chronic infections may disseminate in the host and lead to a life threatening condition.Epidemiologically, S. stercoralis is often missed in surveys as it is difficult to identify by standard stool examination procedures. We present, for the first time, evidence that the infection can be detected in filtered urine samples collected and processed in the field and subsequently assayed for the presence of parasite DNA. Urine specimens (∼40 mL) were collected from 125 test and control individuals living in rural and peri-urban regions of Northern Argentina. From the same individuals, fresh stool specimens were processed using three different copropological methods. Urine specimens were filtered in the field through a 12.5 cm Whatman No. 3 filter. The filters were dried and packed individually in sealable plastic bags with desiccant and shipped to a laboratory where DNA was recovered from the filter and PCRamplified with primers specific to a dispersed repetitive sequence. Prevalence of S. stercoralis infectionby stool culture and direct examination was 35/125 (28%), In contrast, PCR-based detection of parasitespecific trans-renal DNA in urine indicated that 56/125 (44.8%) carried the parasite. Of the patients that tested positive for urine-based parasite DNA, approximately half also tested positive in their stool specimens. There were 6.4% of cases where parasite larvae were seen in the stool but no DNA was amplified from the urine. As proof of principle, DNA amplification from urine residue reveals significantly more cases of S. stercoralis infection than the current standard stool examination techniques. Additional work is required to establish the relative utility, sensitivity and specificity of urine-based analysis compared to parasitological and nucleic acid detection from stool for clinical and epidemiological detection for S.stercoralis infection.
Fil: Lodh, Nilanjan. Marquette University; Estados Unidos
Fil: Caro, Reynaldo. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; Argentina
Fil: Sofer, Shterna. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
Fil: Scott, Alan. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
Fil: Krolewiecki, Alejandro Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina. Universidad Nacional de Salta. Sede Regional Orán. Instituto de Investigación de Enfermedades Tropicales; Argentina
Fil: Shiff, Clive. Johns Hopkins Bloomberg School of Public Health; Estados Unidos
description Detecting infections of Strongyloides stercoralis is arduous and has low sensitivity. Clinically this is a major problem because chronic infections may disseminate in the host and lead to a life threatening condition.Epidemiologically, S. stercoralis is often missed in surveys as it is difficult to identify by standard stool examination procedures. We present, for the first time, evidence that the infection can be detected in filtered urine samples collected and processed in the field and subsequently assayed for the presence of parasite DNA. Urine specimens (∼40 mL) were collected from 125 test and control individuals living in rural and peri-urban regions of Northern Argentina. From the same individuals, fresh stool specimens were processed using three different copropological methods. Urine specimens were filtered in the field through a 12.5 cm Whatman No. 3 filter. The filters were dried and packed individually in sealable plastic bags with desiccant and shipped to a laboratory where DNA was recovered from the filter and PCRamplified with primers specific to a dispersed repetitive sequence. Prevalence of S. stercoralis infectionby stool culture and direct examination was 35/125 (28%), In contrast, PCR-based detection of parasitespecific trans-renal DNA in urine indicated that 56/125 (44.8%) carried the parasite. Of the patients that tested positive for urine-based parasite DNA, approximately half also tested positive in their stool specimens. There were 6.4% of cases where parasite larvae were seen in the stool but no DNA was amplified from the urine. As proof of principle, DNA amplification from urine residue reveals significantly more cases of S. stercoralis infection than the current standard stool examination techniques. Additional work is required to establish the relative utility, sensitivity and specificity of urine-based analysis compared to parasitological and nucleic acid detection from stool for clinical and epidemiological detection for S.stercoralis infection.
publishDate 2016
dc.date.none.fl_str_mv 2016-07
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/29934
Lodh, Nilanjan; Caro, Reynaldo; Sofer, Shterna; Scott, Alan; Krolewiecki, Alejandro Javier; et al.; Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine; Elsevier Science; Acta Tropica; 163; 7-2016; 9-13
0001-706X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/29934
identifier_str_mv Lodh, Nilanjan; Caro, Reynaldo; Sofer, Shterna; Scott, Alan; Krolewiecki, Alejandro Javier; et al.; Diagnosis of Strongyloides stercoralis: Detection of parasite-derived DNA in urine; Elsevier Science; Acta Tropica; 163; 7-2016; 9-13
0001-706X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.actatropica.2016.07.014
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0020751912001701
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117362/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
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dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
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