Zika detection: comparison of methodologies
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.bjm.2017.04.011 http://hdl.handle.net/11449/160125 |
Resumo: | Many countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan (R) RT-qPCR assay. We used a SYBR (R) Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan (R) RT-qPCR assay, 100% (Kappa = 0.670) were also found to be negative by SYBR (R) Green RT-qPCR based on Tm comparison; however, 14% (Kappa = 0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus. (C) 2017 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. |
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Zika detection: comparison of methodologiesZika virusDetectionSensitivitySpecificityMany countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan (R) RT-qPCR assay. We used a SYBR (R) Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan (R) RT-qPCR assay, 100% (Kappa = 0.670) were also found to be negative by SYBR (R) Green RT-qPCR based on Tm comparison; however, 14% (Kappa = 0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus. (C) 2017 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fac Med Sao Jose do Rio Preto FAMERP, Sao Jose Do Rio Preto, SP, BrazilUniv Estadual Paulista, Inst Biociencias Botucatu, Lab Virol, Botucatu, SP, BrazilUniv Nova Lisboa, GHTM, Lisbon, PortugalPrefeitura Sao Jose do Rio Preto, Dept Vigilancia Saude, Sao Jose Do Rio Preto, SP, BrazilUniv Estadual Paulista, Inst Biociencias Botucatu, Lab Virol, Botucatu, SP, BrazilFAPESP: 2013/21719-3Soc Brasileira MicrobiologiaUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Univ Nova LisboaPrefeitura Sao Jose do Rio PretoColombo, Tatiana EliasBernardes Terzian, Ana CarolinaAraujo Junior, Joao Pessoa [UNESP]Parreira, RicardoSotello Cabrer, Eliana MarciaPenha dos Santos, Izalco NurembergNegri Reis, Andreia FrancesliCosta, Fabiana RodriguesArao Antonio Cruz, Lilian ElisaRombola, Patricia LopesNogueira, Mauricio Lacerda2018-11-26T15:47:34Z2018-11-26T15:47:34Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article144-147application/pdfhttp://dx.doi.org/10.1016/j.bjm.2017.04.011Brazilian Journal Of Microbiology. Sao Paulo: Soc Brasileira Microbiologia, v. 49, n. 1, p. 144-147, 2018.1517-8382http://hdl.handle.net/11449/16012510.1016/j.bjm.2017.04.011S1517-83822018000100144WOS:000426369900023S1517-83822018000100144.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrazilian Journal Of Microbiology0,630info:eu-repo/semantics/openAccess2023-10-08T06:07:28Zoai:repositorio.unesp.br:11449/160125Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:21:18.244554Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Zika detection: comparison of methodologies |
title |
Zika detection: comparison of methodologies |
spellingShingle |
Zika detection: comparison of methodologies Colombo, Tatiana Elias Zika virus Detection Sensitivity Specificity |
title_short |
Zika detection: comparison of methodologies |
title_full |
Zika detection: comparison of methodologies |
title_fullStr |
Zika detection: comparison of methodologies |
title_full_unstemmed |
Zika detection: comparison of methodologies |
title_sort |
Zika detection: comparison of methodologies |
author |
Colombo, Tatiana Elias |
author_facet |
Colombo, Tatiana Elias Bernardes Terzian, Ana Carolina Araujo Junior, Joao Pessoa [UNESP] Parreira, Ricardo Sotello Cabrer, Eliana Marcia Penha dos Santos, Izalco Nuremberg Negri Reis, Andreia Francesli Costa, Fabiana Rodrigues Arao Antonio Cruz, Lilian Elisa Rombola, Patricia Lopes Nogueira, Mauricio Lacerda |
author_role |
author |
author2 |
Bernardes Terzian, Ana Carolina Araujo Junior, Joao Pessoa [UNESP] Parreira, Ricardo Sotello Cabrer, Eliana Marcia Penha dos Santos, Izalco Nuremberg Negri Reis, Andreia Francesli Costa, Fabiana Rodrigues Arao Antonio Cruz, Lilian Elisa Rombola, Patricia Lopes Nogueira, Mauricio Lacerda |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) Univ Nova Lisboa Prefeitura Sao Jose do Rio Preto |
dc.contributor.author.fl_str_mv |
Colombo, Tatiana Elias Bernardes Terzian, Ana Carolina Araujo Junior, Joao Pessoa [UNESP] Parreira, Ricardo Sotello Cabrer, Eliana Marcia Penha dos Santos, Izalco Nuremberg Negri Reis, Andreia Francesli Costa, Fabiana Rodrigues Arao Antonio Cruz, Lilian Elisa Rombola, Patricia Lopes Nogueira, Mauricio Lacerda |
dc.subject.por.fl_str_mv |
Zika virus Detection Sensitivity Specificity |
topic |
Zika virus Detection Sensitivity Specificity |
description |
Many countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan (R) RT-qPCR assay. We used a SYBR (R) Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan (R) RT-qPCR assay, 100% (Kappa = 0.670) were also found to be negative by SYBR (R) Green RT-qPCR based on Tm comparison; however, 14% (Kappa = 0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus. (C) 2017 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-11-26T15:47:34Z 2018-11-26T15:47:34Z 2018-01-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.bjm.2017.04.011 Brazilian Journal Of Microbiology. Sao Paulo: Soc Brasileira Microbiologia, v. 49, n. 1, p. 144-147, 2018. 1517-8382 http://hdl.handle.net/11449/160125 10.1016/j.bjm.2017.04.011 S1517-83822018000100144 WOS:000426369900023 S1517-83822018000100144.pdf |
url |
http://dx.doi.org/10.1016/j.bjm.2017.04.011 http://hdl.handle.net/11449/160125 |
identifier_str_mv |
Brazilian Journal Of Microbiology. Sao Paulo: Soc Brasileira Microbiologia, v. 49, n. 1, p. 144-147, 2018. 1517-8382 10.1016/j.bjm.2017.04.011 S1517-83822018000100144 WOS:000426369900023 S1517-83822018000100144.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal Of Microbiology 0,630 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
144-147 application/pdf |
dc.publisher.none.fl_str_mv |
Soc Brasileira Microbiologia |
publisher.none.fl_str_mv |
Soc Brasileira Microbiologia |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128350887084032 |