A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax

ABSTRACT: As the global burden of malaria decreases and countries strive towards disease elimination, there is a greater demand for sensitive diagnostics to target the submicroscopic reservoir of infection. We describe here a sensitive species-specific RT-qPCR method to differentiate between Plasmod...

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Autores:
Gavina, Kenneth
Arango Flórez, Eliana María
Álvarez Larrotta, Catalina
Maestre Buitrago, Amanda Elena
Kim Yanow, Stephanie
Tipo de recurso:
Article of investigation
Fecha de publicación:
2017
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/21416
Acceso en línea:
http://hdl.handle.net/10495/21416
Palabra clave:
Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Malaria
Plasmodium falciparum
Plasmodium vivax
Diagnóstico
Diagnosis
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
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network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
title A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
spellingShingle A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Malaria
Plasmodium falciparum
Plasmodium vivax
Diagnóstico
Diagnosis
title_short A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
title_full A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
title_fullStr A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
title_full_unstemmed A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
title_sort A sensitive species-specific reverse transcription real-time PCR method for detection of Plasmodium falciparum and Plasmodium vivax
dc.creator.fl_str_mv Gavina, Kenneth
Arango Flórez, Eliana María
Álvarez Larrotta, Catalina
Maestre Buitrago, Amanda Elena
Kim Yanow, Stephanie
dc.contributor.author.none.fl_str_mv Gavina, Kenneth
Arango Flórez, Eliana María
Álvarez Larrotta, Catalina
Maestre Buitrago, Amanda Elena
Kim Yanow, Stephanie
dc.contributor.researchgroup.spa.fl_str_mv Salud y Comunidad
dc.subject.decs.none.fl_str_mv Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Malaria
Plasmodium falciparum
Plasmodium vivax
Diagnóstico
Diagnosis
topic Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Malaria
Plasmodium falciparum
Plasmodium vivax
Diagnóstico
Diagnosis
description ABSTRACT: As the global burden of malaria decreases and countries strive towards disease elimination, there is a greater demand for sensitive diagnostics to target the submicroscopic reservoir of infection. We describe here a sensitive species-specific RT-qPCR method to differentiate between Plasmodium falciparum and P. vivax infections at the submicroscopic level. With amplification of the 18S rRNA genes from total nucleic acids (both DNA and RNA), we discern P. falciparum and P. vivax with a limit of detection of 10 parasites/mL and 18 copies/μL, respectively. This assay was validated with 519 blood samples, negative by thick-smear, from febrile and asymptomatic cohorts from Colombia. These results were directly compared to a qPCR-based method (DNA only) as the gold standard. Of the samples from patients who presented with fever (n = 274), 34 infections were identified by RT-qPCR (16 P. falciparum, 15 P. vivax, and 3 mixed), of which only 10 infections were identified at the species level by qPCR. Within the asymptomatic cohort (n = 245), 13 infections were identified by RT-qPCR (3 P. falciparum, 3 P. vivax, and 7 mixed), whereas the species for only one infection was determined by qPCR. We conclude that this species-specific RT-qPCR method provides a more sensitive tool for species identification compared to DNA based qPCR methods.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2021-08-02T13:23:46Z
dc.date.available.none.fl_str_mv 2021-08-02T13:23:46Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.issn.none.fl_str_mv 2405-6731
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/21416
dc.identifier.doi.none.fl_str_mv 10.1016/j.parepi.2017.04.001
identifier_str_mv 2405-6731
10.1016/j.parepi.2017.04.001
url http://hdl.handle.net/10495/21416
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Parasite Epidemiol Control
dc.relation.citationendpage.spa.fl_str_mv 76
dc.relation.citationissue.spa.fl_str_mv 2
dc.relation.citationstartpage.spa.fl_str_mv 70
dc.relation.citationvolume.spa.fl_str_mv 2
dc.relation.ispartofjournal.spa.fl_str_mv Parasite Epidemiology and Control
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dc.publisher.spa.fl_str_mv Elsevier
dc.publisher.place.spa.fl_str_mv Amsterdam, Países Bajos
institution Universidad de Antioquia
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spelling Gavina, KennethArango Flórez, Eliana MaríaÁlvarez Larrotta, CatalinaMaestre Buitrago, Amanda ElenaKim Yanow, StephanieSalud y Comunidad2021-08-02T13:23:46Z2021-08-02T13:23:46Z20172405-6731http://hdl.handle.net/10495/2141610.1016/j.parepi.2017.04.001ABSTRACT: As the global burden of malaria decreases and countries strive towards disease elimination, there is a greater demand for sensitive diagnostics to target the submicroscopic reservoir of infection. We describe here a sensitive species-specific RT-qPCR method to differentiate between Plasmodium falciparum and P. vivax infections at the submicroscopic level. With amplification of the 18S rRNA genes from total nucleic acids (both DNA and RNA), we discern P. falciparum and P. vivax with a limit of detection of 10 parasites/mL and 18 copies/μL, respectively. This assay was validated with 519 blood samples, negative by thick-smear, from febrile and asymptomatic cohorts from Colombia. These results were directly compared to a qPCR-based method (DNA only) as the gold standard. Of the samples from patients who presented with fever (n = 274), 34 infections were identified by RT-qPCR (16 P. falciparum, 15 P. vivax, and 3 mixed), of which only 10 infections were identified at the species level by qPCR. Within the asymptomatic cohort (n = 245), 13 infections were identified by RT-qPCR (3 P. falciparum, 3 P. vivax, and 7 mixed), whereas the species for only one infection was determined by qPCR. 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