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dc.contributor.author
Besuschio, Susana Alicia
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Llano Murcia, Mónica
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Benatar, Alejandro Francisco
dc.contributor.author
Curto, Maria de Los Angeles
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Cruz, Israel
dc.contributor.author
Monnerat, Séverine
dc.contributor.author
Picado, Albert
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Puerta, Concepción
dc.contributor.author
Ndungu, Joseph
dc.contributor.author
Schijman, Alejandro Gabriel
dc.date.available
2023-10-17T12:06:20Z
dc.date.issued
2016
dc.identifier.citation
A loop-mediated is othermal amplification (LAMP) kit for molecular detection of Trypanosoma cruzi dna: A feasibility study; The 65th American Society of Tropical Medicine and Hygiene Annual Meeting; Atlanta; Estados Unidos; 2016; 163-164
dc.identifier.issn
0002-9637
dc.identifier.uri
http://hdl.handle.net/11336/215107
dc.description.abstract
Loop-mediated isothermal amplification (LAMP) tests have been developedas molecular tests for neglected parasitic diseases such as leishmaniasisor sleeping sickness. A LAMP test for Trypanosoma cruzi, the etiologicalagent of Chagas Disease (ChD), would allow a rapid and reliable diagnosis,in particular in cases of acute and congenital ChD (CChD). We evaluatedthe performance a Trypanosoma cruzi LAMP kit using purified DNA, spikedblood and clinical specimens. Quantitative PCR (qPCR) was used as areference. Different extraction methods for LAMP were also evaluated. TheLAMP reaction was performed at 62.5°C for 45 min. Analytical sensitivitywas measured in ten-fold dilutions of CL Brener (TcVI) and Silvio X10(TcI) DNA. Analytical specificity was measured using ten-fold dilutions ofdifferent Leishmania species and Trypanosoma rangeli DNAs as well asnon-infected human DNA. Seronegative blood in EDTA (EB) or heparin (HB)was spiked with ten-fold dilutions of CL Brener. EB spiked blood was alsoused as dried blood spot (DBS). Stored DNA from EB clinical samples wastested, including 4 Congenital ChD cases, 5 Chronic ChD cases with lowparasite loads, 10 immunosuppressed ChD patients and 5 seronegativecontrols. DNA extraction was done with a commercial kit (EB, HB and DBSsamples) and using the boil & spin (B&S) method (HB samples only). TheT. cruzi LAMP kit showed better analytical sensitivity than qPCR in purifiedDNA specimens, especially for TcI DNA. Analytical sensitivity was 10-2 and10-1 par.eq/mL from spiked EB and HB extracted by columns, respectively,and 10-2 par.eq/mL from HB using B&S. The analytical sensitivity in DBSsamples was 10-2 par.eq/mL. T. cruzi LAMP was positive in congenital andimmunosuppressed ChD samples spanning from 4.8 to 3,684 par.eq/ml,in agreement with qPCR. Chronic ChD samples were only detectable byqPCR, with Ct values below the limit of quantification. The kit was specificfor T. cruzi DNA and samples from seropositive patients.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
The American Society of Tropical Medicine and Hygiene
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
LAMP
dc.subject
Trypanosoma Cruzi
dc.subject
molecular diagnosis
dc.subject
Congenital Chagas disease
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Bioquímica y Biología Molecular
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Ciencias Biológicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
A loop-mediated is othermal amplification (LAMP) kit for molecular detection of Trypanosoma cruzi dna: A feasibility study
dc.type
info:eu-repo/semantics/publishedVersion
dc.type
info:eu-repo/semantics/conferenceObject
dc.type
info:ar-repo/semantics/documento de conferencia
dc.date.updated
2023-09-15T12:51:19Z
dc.identifier.eissn
1476-1645
dc.journal.volume
95
dc.journal.number
5 Suppl.
dc.journal.pagination
163-164
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Arlington
dc.description.fil
Fil: Besuschio, Susana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
dc.description.fil
Fil: Llano Murcia, Mónica. Pontificia Universidad Javeriana; Colombia
dc.description.fil
Fil: Benatar, Alejandro Francisco. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
dc.description.fil
Fil: Curto, Maria de Los Angeles. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
dc.description.fil
Fil: Cruz, Israel. Foundation For Innovative Diagnostics; Suiza
dc.description.fil
Fil: Monnerat, Séverine. Foundation For Innovative Diagnostics; Suiza
dc.description.fil
Fil: Picado, Albert. Foundation For Innovative Diagnostics; Suiza
dc.description.fil
Fil: Puerta, Concepción. Pontificia Universidad Javeriana; Colombia
dc.description.fil
Fil: Ndungu, Joseph. Foundation For Innovative Diagnostics; Suiza
dc.description.fil
Fil: Schijman, Alejandro Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ajtmh.org/view/journals/tpmd/95/5_Suppl/tpmd.95.issue-5_Suppl.xml
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dc.coverage
Internacional
dc.type.subtype
Reunión
dc.description.nombreEvento
The 65th American Society of Tropical Medicine and Hygiene Annual Meeting
dc.date.evento
2016-11-13
dc.description.ciudadEvento
Atlanta
dc.description.paisEvento
Estados Unidos
dc.type.publicacion
Journal
dc.description.institucionOrganizadora
American Society of Tropical Medicine and Hygiene
dc.source.revista
The American Journal of Tropical Medicine and Hygiene
dc.date.eventoHasta
2016-11-17
dc.type
Reunión
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