Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista da Sociedade Brasileira de Medicina Tropical |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822015000600731 |
Resumo: | Abstract: INTRODUCTION : Molecular analyses are auxiliary tools for detecting Koch's bacilli in clinical specimens from patients with suspected tuberculosis (TB). However, there are still no efficient diagnostic tests that combine high sensitivity and specificity and yield rapid results in the detection of TB. This study evaluated single-tube nested polymerase chain reaction (STNPCR) as a molecular diagnostic test with low risk of cross contamination for detecting Mycobacterium tuberculosis in clinical samples. METHODS: Mycobacterium tuberculosis deoxyribonucleic acid (DNA) was detected in blood and urine samples by STNPCR followed by agarose gel electrophoresis. In this system, reaction tubes were not opened between the two stages of PCR (simple and nested). RESULTS: STNPCR demonstrated good accuracy in clinical samples with no cross contamination between microtubes. Sensitivity in blood and urine, analyzed in parallel, was 35%-62% for pulmonary and 41%-72% for extrapulmonary TB. The specificity of STNPCR was 100% in most analyses, depending on the type of clinical sample (blood or urine) and clinical form of disease (pulmonary or extrapulmonary). CONCLUSIONS: STNPCR was effective in detecting TB, especially the extrapulmonary form for which sensitivity was higher, and had the advantage of less invasive sample collection from patients for whom a spontaneous sputum sample was unavailable. With low risk of cross contamination, the STNPCR can be used as an adjunct to conventional methods for diagnosing TB. |
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Revista da Sociedade Brasileira de Medicina Tropical |
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Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urineMycobacterium tuberculosisMolecular diagnostic testNested polymerase chain reactionBloodUrineAbstract: INTRODUCTION : Molecular analyses are auxiliary tools for detecting Koch's bacilli in clinical specimens from patients with suspected tuberculosis (TB). However, there are still no efficient diagnostic tests that combine high sensitivity and specificity and yield rapid results in the detection of TB. This study evaluated single-tube nested polymerase chain reaction (STNPCR) as a molecular diagnostic test with low risk of cross contamination for detecting Mycobacterium tuberculosis in clinical samples. METHODS: Mycobacterium tuberculosis deoxyribonucleic acid (DNA) was detected in blood and urine samples by STNPCR followed by agarose gel electrophoresis. In this system, reaction tubes were not opened between the two stages of PCR (simple and nested). RESULTS: STNPCR demonstrated good accuracy in clinical samples with no cross contamination between microtubes. Sensitivity in blood and urine, analyzed in parallel, was 35%-62% for pulmonary and 41%-72% for extrapulmonary TB. The specificity of STNPCR was 100% in most analyses, depending on the type of clinical sample (blood or urine) and clinical form of disease (pulmonary or extrapulmonary). CONCLUSIONS: STNPCR was effective in detecting TB, especially the extrapulmonary form for which sensitivity was higher, and had the advantage of less invasive sample collection from patients for whom a spontaneous sputum sample was unavailable. With low risk of cross contamination, the STNPCR can be used as an adjunct to conventional methods for diagnosing TB.Sociedade Brasileira de Medicina Tropical - SBMT2015-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822015000600731Revista da Sociedade Brasileira de Medicina Tropical v.48 n.6 2015reponame:Revista da Sociedade Brasileira de Medicina Tropicalinstname:Sociedade Brasileira de Medicina Tropical (SBMT)instacron:SBMT10.1590/0037-8682-0210-2015info:eu-repo/semantics/openAccessLima,Juliana Figueirêdo da CostaGuedes,Gabriela de Moraes RêgoLima,Juliana Falcão de AraújoLira,Laís Ariane de SiqueiraSantos,Fabiana Cristina FulcoArruda,Mercia Eliane deMontenegro,Lílian Maria LapaSchindler,Haiana Charifkereng2015-12-08T00:00:00Zoai:scielo:S0037-86822015000600731Revistahttps://www.sbmt.org.br/portal/revista/ONGhttps://old.scielo.br/oai/scielo-oai.php||dalmo@rsbmt.uftm.edu.br|| rsbmt@rsbmt.uftm.edu.br1678-98490037-8682opendoar:2015-12-08T00:00Revista da Sociedade Brasileira de Medicina Tropical - Sociedade Brasileira de Medicina Tropical (SBMT)false |
dc.title.none.fl_str_mv |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
title |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
spellingShingle |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine Lima,Juliana Figueirêdo da Costa Mycobacterium tuberculosis Molecular diagnostic test Nested polymerase chain reaction Blood Urine |
title_short |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
title_full |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
title_fullStr |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
title_full_unstemmed |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
title_sort |
Single-tube nested PCR assay with in-house DNA extraction for Mycobacterium tuberculosis detection in blood and urine |
author |
Lima,Juliana Figueirêdo da Costa |
author_facet |
Lima,Juliana Figueirêdo da Costa Guedes,Gabriela de Moraes Rêgo Lima,Juliana Falcão de Araújo Lira,Laís Ariane de Siqueira Santos,Fabiana Cristina Fulco Arruda,Mercia Eliane de Montenegro,Lílian Maria Lapa Schindler,Haiana Charifker |
author_role |
author |
author2 |
Guedes,Gabriela de Moraes Rêgo Lima,Juliana Falcão de Araújo Lira,Laís Ariane de Siqueira Santos,Fabiana Cristina Fulco Arruda,Mercia Eliane de Montenegro,Lílian Maria Lapa Schindler,Haiana Charifker |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Lima,Juliana Figueirêdo da Costa Guedes,Gabriela de Moraes Rêgo Lima,Juliana Falcão de Araújo Lira,Laís Ariane de Siqueira Santos,Fabiana Cristina Fulco Arruda,Mercia Eliane de Montenegro,Lílian Maria Lapa Schindler,Haiana Charifker |
dc.subject.por.fl_str_mv |
Mycobacterium tuberculosis Molecular diagnostic test Nested polymerase chain reaction Blood Urine |
topic |
Mycobacterium tuberculosis Molecular diagnostic test Nested polymerase chain reaction Blood Urine |
description |
Abstract: INTRODUCTION : Molecular analyses are auxiliary tools for detecting Koch's bacilli in clinical specimens from patients with suspected tuberculosis (TB). However, there are still no efficient diagnostic tests that combine high sensitivity and specificity and yield rapid results in the detection of TB. This study evaluated single-tube nested polymerase chain reaction (STNPCR) as a molecular diagnostic test with low risk of cross contamination for detecting Mycobacterium tuberculosis in clinical samples. METHODS: Mycobacterium tuberculosis deoxyribonucleic acid (DNA) was detected in blood and urine samples by STNPCR followed by agarose gel electrophoresis. In this system, reaction tubes were not opened between the two stages of PCR (simple and nested). RESULTS: STNPCR demonstrated good accuracy in clinical samples with no cross contamination between microtubes. Sensitivity in blood and urine, analyzed in parallel, was 35%-62% for pulmonary and 41%-72% for extrapulmonary TB. The specificity of STNPCR was 100% in most analyses, depending on the type of clinical sample (blood or urine) and clinical form of disease (pulmonary or extrapulmonary). CONCLUSIONS: STNPCR was effective in detecting TB, especially the extrapulmonary form for which sensitivity was higher, and had the advantage of less invasive sample collection from patients for whom a spontaneous sputum sample was unavailable. With low risk of cross contamination, the STNPCR can be used as an adjunct to conventional methods for diagnosing TB. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822015000600731 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822015000600731 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0037-8682-0210-2015 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Medicina Tropical - SBMT |
publisher.none.fl_str_mv |
Sociedade Brasileira de Medicina Tropical - SBMT |
dc.source.none.fl_str_mv |
Revista da Sociedade Brasileira de Medicina Tropical v.48 n.6 2015 reponame:Revista da Sociedade Brasileira de Medicina Tropical instname:Sociedade Brasileira de Medicina Tropical (SBMT) instacron:SBMT |
instname_str |
Sociedade Brasileira de Medicina Tropical (SBMT) |
instacron_str |
SBMT |
institution |
SBMT |
reponame_str |
Revista da Sociedade Brasileira de Medicina Tropical |
collection |
Revista da Sociedade Brasileira de Medicina Tropical |
repository.name.fl_str_mv |
Revista da Sociedade Brasileira de Medicina Tropical - Sociedade Brasileira de Medicina Tropical (SBMT) |
repository.mail.fl_str_mv |
||dalmo@rsbmt.uftm.edu.br|| rsbmt@rsbmt.uftm.edu.br |
_version_ |
1752122160097263616 |