Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil

Detalhes bibliográficos
Autor(a) principal: Camilo,Lilian Muniz
Data de Publicação: 2017
Outros Autores: Pereira-Chioccola,Vera Lucia, Gava,Ricardo, Meira-Strejevitch,Cristina da Silva, Vidal,Jose Ernesto, Mattos,Cinara Cássia Brandão de, Frederico,Fábio Batista, De Mattos,Luiz Carlos, Spegiorin,Lígia Cosentino Junqueira Franco, Murata,Fernando Henrique Antunes, Ferreira,Marina Neves, Barbosa,Deusenia Machado Ulisses, Gonçalves,Fausto da Silva, Dias,Cristiane Moraes, Catelan,Marcia Wakai, Siqueira,Rubens Camargo, Previato,Mariana, Barbosa,Amanda Pires, Cavallini,Danilo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Infectious Diseases
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702017000600638
Resumo: ABSTRACT Symptomatic forms of toxoplasmosis are a serious public health problem and occur in around 10-20% of the infected people. Aiming to improve the molecular diagnosis of symptomatic toxoplasmosis in Brazilian patients, this study evaluated the performance of real time PCR testing two primer sets (B1 and REP-529) in detecting Toxoplasma gondii DNA. The methodology was assayed in 807 clinical samples with known clinical diagnosis, ELISA, and conventional PCR results in a 9-year period. All samples were from patients with clinical suspicion of several features of toxoplasmosis. According to the minimum detection limit curve (in CT), REP-529 had greater sensitivity to detect T. gondii DNA than B1. Both primer sets were retrospectively evaluated using 515 DNA from different clinical samples. The 122 patients without toxoplasmosis provided high specificity (REP-529, 99.2% and B1, 100%). From the 393 samples with positive ELISA, 146 had clinical diagnosis of toxoplasmosis and positive conventional PCR. REP-529 and B1 sensitivities were 95.9% and 83.6%, respectively. Comparison of REP-529 and B1 performances was further analyzed prospectively in 292 samples. Thus, from a total of 807 DNA analyzed, 217 (26.89%) had positive PCR with, at least one primer set and symptomatic toxoplasmosis confirmed by clinical diagnosis. REP-529 was positive in 97.23%, whereas B1 amplified only 78.80%. After comparing several samples in a Brazilian referral laboratory, this study concluded that REP-529 primer set had better performance than B1 one. These observations were based after using cases with defined clinical diagnosis, ELISA, and conventional PCR.
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spelling Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, BrazilToxoplasma gondiiSymptomatic toxoplasmosisDiagnosisReal-time polymerase chain reactionABSTRACT Symptomatic forms of toxoplasmosis are a serious public health problem and occur in around 10-20% of the infected people. Aiming to improve the molecular diagnosis of symptomatic toxoplasmosis in Brazilian patients, this study evaluated the performance of real time PCR testing two primer sets (B1 and REP-529) in detecting Toxoplasma gondii DNA. The methodology was assayed in 807 clinical samples with known clinical diagnosis, ELISA, and conventional PCR results in a 9-year period. All samples were from patients with clinical suspicion of several features of toxoplasmosis. According to the minimum detection limit curve (in CT), REP-529 had greater sensitivity to detect T. gondii DNA than B1. Both primer sets were retrospectively evaluated using 515 DNA from different clinical samples. The 122 patients without toxoplasmosis provided high specificity (REP-529, 99.2% and B1, 100%). From the 393 samples with positive ELISA, 146 had clinical diagnosis of toxoplasmosis and positive conventional PCR. REP-529 and B1 sensitivities were 95.9% and 83.6%, respectively. Comparison of REP-529 and B1 performances was further analyzed prospectively in 292 samples. Thus, from a total of 807 DNA analyzed, 217 (26.89%) had positive PCR with, at least one primer set and symptomatic toxoplasmosis confirmed by clinical diagnosis. REP-529 was positive in 97.23%, whereas B1 amplified only 78.80%. After comparing several samples in a Brazilian referral laboratory, this study concluded that REP-529 primer set had better performance than B1 one. These observations were based after using cases with defined clinical diagnosis, ELISA, and conventional PCR.Brazilian Society of Infectious Diseases2017-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702017000600638Brazilian Journal of Infectious Diseases v.21 n.6 2017reponame:Brazilian Journal of Infectious Diseasesinstname:Brazilian Society of Infectious Diseases (BSID)instacron:BSID10.1016/j.bjid.2017.07.003info:eu-repo/semantics/openAccessCamilo,Lilian MunizPereira-Chioccola,Vera LuciaGava,RicardoMeira-Strejevitch,Cristina da SilvaVidal,Jose ErnestoMattos,Cinara Cássia Brandão deFrederico,Fábio BatistaDe Mattos,Luiz CarlosSpegiorin,Lígia Cosentino Junqueira FrancoMurata,Fernando Henrique AntunesFerreira,Marina NevesBarbosa,Deusenia Machado UlissesGonçalves,Fausto da SilvaDias,Cristiane MoraesCatelan,Marcia WakaiSiqueira,Rubens CamargoPreviato,MarianaBarbosa,Amanda PiresCavallini,Daniloeng2017-12-11T00:00:00Zoai:scielo:S1413-86702017000600638Revistahttps://www.bjid.org.br/https://old.scielo.br/oai/scielo-oai.phpbjid@bjid.org.br||lgoldani@ufrgs.br1678-43911413-8670opendoar:2017-12-11T00:00Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)false
dc.title.none.fl_str_mv Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
title Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
spellingShingle Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
Camilo,Lilian Muniz
Toxoplasma gondii
Symptomatic toxoplasmosis
Diagnosis
Real-time polymerase chain reaction
title_short Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
title_full Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
title_fullStr Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
title_full_unstemmed Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
title_sort Molecular diagnosis of symptomatic toxoplasmosis: a 9-year retrospective and prospective study in a referral laboratory in São Paulo, Brazil
author Camilo,Lilian Muniz
author_facet Camilo,Lilian Muniz
Pereira-Chioccola,Vera Lucia
Gava,Ricardo
Meira-Strejevitch,Cristina da Silva
Vidal,Jose Ernesto
Mattos,Cinara Cássia Brandão de
Frederico,Fábio Batista
De Mattos,Luiz Carlos
Spegiorin,Lígia Cosentino Junqueira Franco
Murata,Fernando Henrique Antunes
Ferreira,Marina Neves
Barbosa,Deusenia Machado Ulisses
Gonçalves,Fausto da Silva
Dias,Cristiane Moraes
Catelan,Marcia Wakai
Siqueira,Rubens Camargo
Previato,Mariana
Barbosa,Amanda Pires
Cavallini,Danilo
author_role author
author2 Pereira-Chioccola,Vera Lucia
Gava,Ricardo
Meira-Strejevitch,Cristina da Silva
Vidal,Jose Ernesto
Mattos,Cinara Cássia Brandão de
Frederico,Fábio Batista
De Mattos,Luiz Carlos
Spegiorin,Lígia Cosentino Junqueira Franco
Murata,Fernando Henrique Antunes
Ferreira,Marina Neves
Barbosa,Deusenia Machado Ulisses
Gonçalves,Fausto da Silva
Dias,Cristiane Moraes
Catelan,Marcia Wakai
Siqueira,Rubens Camargo
Previato,Mariana
Barbosa,Amanda Pires
Cavallini,Danilo
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Camilo,Lilian Muniz
Pereira-Chioccola,Vera Lucia
Gava,Ricardo
Meira-Strejevitch,Cristina da Silva
Vidal,Jose Ernesto
Mattos,Cinara Cássia Brandão de
Frederico,Fábio Batista
De Mattos,Luiz Carlos
Spegiorin,Lígia Cosentino Junqueira Franco
Murata,Fernando Henrique Antunes
Ferreira,Marina Neves
Barbosa,Deusenia Machado Ulisses
Gonçalves,Fausto da Silva
Dias,Cristiane Moraes
Catelan,Marcia Wakai
Siqueira,Rubens Camargo
Previato,Mariana
Barbosa,Amanda Pires
Cavallini,Danilo
dc.subject.por.fl_str_mv Toxoplasma gondii
Symptomatic toxoplasmosis
Diagnosis
Real-time polymerase chain reaction
topic Toxoplasma gondii
Symptomatic toxoplasmosis
Diagnosis
Real-time polymerase chain reaction
description ABSTRACT Symptomatic forms of toxoplasmosis are a serious public health problem and occur in around 10-20% of the infected people. Aiming to improve the molecular diagnosis of symptomatic toxoplasmosis in Brazilian patients, this study evaluated the performance of real time PCR testing two primer sets (B1 and REP-529) in detecting Toxoplasma gondii DNA. The methodology was assayed in 807 clinical samples with known clinical diagnosis, ELISA, and conventional PCR results in a 9-year period. All samples were from patients with clinical suspicion of several features of toxoplasmosis. According to the minimum detection limit curve (in CT), REP-529 had greater sensitivity to detect T. gondii DNA than B1. Both primer sets were retrospectively evaluated using 515 DNA from different clinical samples. The 122 patients without toxoplasmosis provided high specificity (REP-529, 99.2% and B1, 100%). From the 393 samples with positive ELISA, 146 had clinical diagnosis of toxoplasmosis and positive conventional PCR. REP-529 and B1 sensitivities were 95.9% and 83.6%, respectively. Comparison of REP-529 and B1 performances was further analyzed prospectively in 292 samples. Thus, from a total of 807 DNA analyzed, 217 (26.89%) had positive PCR with, at least one primer set and symptomatic toxoplasmosis confirmed by clinical diagnosis. REP-529 was positive in 97.23%, whereas B1 amplified only 78.80%. After comparing several samples in a Brazilian referral laboratory, this study concluded that REP-529 primer set had better performance than B1 one. These observations were based after using cases with defined clinical diagnosis, ELISA, and conventional PCR.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702017000600638
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjid.2017.07.003
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv Brazilian Journal of Infectious Diseases v.21 n.6 2017
reponame:Brazilian Journal of Infectious Diseases
instname:Brazilian Society of Infectious Diseases (BSID)
instacron:BSID
instname_str Brazilian Society of Infectious Diseases (BSID)
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reponame_str Brazilian Journal of Infectious Diseases
collection Brazilian Journal of Infectious Diseases
repository.name.fl_str_mv Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)
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