Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/61017 |
Resumo: | This study was funded by AMED program of the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID; JP18fm0108008) and Research Program on Emerging and Re-emerging Infectious Diseases (JP18fk0108108) and Japan Society for the Promotion of Science (JSPS) KAKENHI (16H05805). This study was also supported by Grants-in-Aid for Scientific Research on Innovative Areas from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (16H06429, 16H06431, 16K21723) and OSIMO foundation. The Flavivirus Laboratory was funded by Faperj (Fundac¸ão Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro) under the grant no. E-26/2002.930/2016, by European Union’s Horizon 2020 program under grant agreements ZIKACTION no. 734857 and ZIKAPLAN no. 734548. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |
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Hayashida, KyokoOrba, YasukoSequeira, Patricia C.Sugimoto, ChihiroHall, William W.Eshita, YukiSuzuki, YutakaRuntuwene, LuckyBrasil, PatriciaCalvet, GuilhermeRodrigues, Cintia D. S.Santos, Carolina C. dosMares-Guia, Maria A. M.Yamagishi, JunyaFilippis, Ana M. B. deSawa, Hirofumi2023-11-02T14:50:32Z2023-11-02T14:50:32Z2019HAYASHIDA, Kyoko et al. Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing. PLoS Neglected Tropical Diseases, v. 13, n. 6, p. 1-15, Jun. 2019.1935-2727https://www.arca.fiocruz.br/handle/icict/6101710.1371/journal.pntd.00074801935-2735This study was funded by AMED program of the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID; JP18fm0108008) and Research Program on Emerging and Re-emerging Infectious Diseases (JP18fk0108108) and Japan Society for the Promotion of Science (JSPS) KAKENHI (16H05805). This study was also supported by Grants-in-Aid for Scientific Research on Innovative Areas from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (16H06429, 16H06431, 16K21723) and OSIMO foundation. The Flavivirus Laboratory was funded by Faperj (Fundac¸ão Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro) under the grant no. E-26/2002.930/2016, by European Union’s Horizon 2020 program under grant agreements ZIKACTION no. 734857 and ZIKAPLAN no. 734548. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan.Oswaldo Cruz Foundation. Oswaldo Cruz Institute. Flavivirus Laboratory. Rio de Janeiro, RJ, Brazil.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan / Global Station for Zoonosis Control. Global Institution for Collaborative Research and Education (GI-CoRE). Hokkaido University. Sapporo, Japan.Global Station for Zoonosis Control. Global Institution for Collaborative Research and Education (GI-CoRE). Hokkaido University. Sapporo, Japan / Centre for Research in Infectious Diseases. School of Medicine and Medical Science. University College Dublin. Dublin, Ireland / Global Virus Network. Baltimore, Maryland, USA.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan.Global Virus Network. Baltimore, Maryland, USA.Global Virus Network. Baltimore, Maryland, USA.Oswaldo Cruz Foundation. Evandro Chagas National Institute of Infectious Diseases. Acute Febrile Illnesses Laboratory. Rio de Janeiro, RJ, Brazil / Global Virus Network. Baltimore, Maryland, USA.Oswaldo Cruz Foundation. Evandro Chagas National Institute of Infectious Diseases. Acute Febrile Illnesses Laboratory. Rio de Janeiro, RJ, Brazil / Global Virus Network. Baltimore, Maryland, USA.Oswaldo Cruz Foundation. Oswaldo Cruz Institute. Flavivirus Laboratory. Rio de Janeiro, RJ, Brazil.Oswaldo Cruz Foundation. Oswaldo Cruz Institute. Flavivirus Laboratory. Rio de Janeiro, RJ, Brazil.Oswaldo Cruz Foundation. Oswaldo Cruz Institute. Flavivirus Laboratory. Rio de Janeiro, RJ, Brazil.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan / Global Station for Zoonosis Control. Global Institution for Collaborative Research and Education (GI-CoRE). Hokkaido University. Sapporo, Japan.Oswaldo Cruz Foundation. Oswaldo Cruz Institute. Flavivirus Laboratory. Rio de Janeiro, RJ, Brazil.Research Center for Zoonosis Control. Hokkaido University. Sapporo, Japan / Global Station for Zoonosis Control. Global Institution for Collaborative Research and Education (GI-CoRE). Hokkaido University. Sapporo, Japan / Global Virus Network. Baltimore, Maryland, USA.Detection and sequencing of chikungunya virus (CHIKV) genome was performed using a combination of a modified reverse transcription loop-mediated isothermal amplification (RT-LAMP) method and a MinION sequencer. We developed the protocol for drying all the reagents for the RT-LAMP in a single reaction tube. Using this system, the CHIKV genome was effectively amplified under isothermal conditions, and used as a template for MinION sequencing with a laptop computer. Our in-house RT-LAMP method and MinION sequencing system were also validated with RNAs and serum samples from recent outbreaks of CHIKV patients in Brazil. The obtained sequence data confirmed the CHIKV outbreaks and identified the genotype. In summary, our established inexpensive on-site genome detection and sequencing system is applicable for both diagnosis of CHIKV infected patients and genotyping of the CHIKV virus in future outbreak in remote areas.engPublic Library of ScienceField diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencinginfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleChikungunya virus (CHIKV)GenomeMinION sequencingTranscription loop-mediated isothermal amplification (RT-LAMP)info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; 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dc.title.en_US.fl_str_mv |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
title |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
spellingShingle |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing Hayashida, Kyoko Chikungunya virus (CHIKV) Genome MinION sequencing Transcription loop-mediated isothermal amplification (RT-LAMP) |
title_short |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
title_full |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
title_fullStr |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
title_full_unstemmed |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
title_sort |
Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing |
author |
Hayashida, Kyoko |
author_facet |
Hayashida, Kyoko Orba, Yasuko Sequeira, Patricia C. Sugimoto, Chihiro Hall, William W. Eshita, Yuki Suzuki, Yutaka Runtuwene, Lucky Brasil, Patricia Calvet, Guilherme Rodrigues, Cintia D. S. Santos, Carolina C. dos Mares-Guia, Maria A. M. Yamagishi, Junya Filippis, Ana M. B. de Sawa, Hirofumi |
author_role |
author |
author2 |
Orba, Yasuko Sequeira, Patricia C. Sugimoto, Chihiro Hall, William W. Eshita, Yuki Suzuki, Yutaka Runtuwene, Lucky Brasil, Patricia Calvet, Guilherme Rodrigues, Cintia D. S. Santos, Carolina C. dos Mares-Guia, Maria A. M. Yamagishi, Junya Filippis, Ana M. B. de Sawa, Hirofumi |
author2_role |
author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Hayashida, Kyoko Orba, Yasuko Sequeira, Patricia C. Sugimoto, Chihiro Hall, William W. Eshita, Yuki Suzuki, Yutaka Runtuwene, Lucky Brasil, Patricia Calvet, Guilherme Rodrigues, Cintia D. S. Santos, Carolina C. dos Mares-Guia, Maria A. M. Yamagishi, Junya Filippis, Ana M. B. de Sawa, Hirofumi |
dc.subject.en.en_US.fl_str_mv |
Chikungunya virus (CHIKV) Genome MinION sequencing Transcription loop-mediated isothermal amplification (RT-LAMP) |
topic |
Chikungunya virus (CHIKV) Genome MinION sequencing Transcription loop-mediated isothermal amplification (RT-LAMP) |
description |
This study was funded by AMED program of the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID; JP18fm0108008) and Research Program on Emerging and Re-emerging Infectious Diseases (JP18fk0108108) and Japan Society for the Promotion of Science (JSPS) KAKENHI (16H05805). This study was also supported by Grants-in-Aid for Scientific Research on Innovative Areas from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (16H06429, 16H06431, 16K21723) and OSIMO foundation. The Flavivirus Laboratory was funded by Faperj (Fundac¸ão Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro) under the grant no. E-26/2002.930/2016, by European Union’s Horizon 2020 program under grant agreements ZIKACTION no. 734857 and ZIKAPLAN no. 734548. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |
publishDate |
2019 |
dc.date.issued.fl_str_mv |
2019 |
dc.date.accessioned.fl_str_mv |
2023-11-02T14:50:32Z |
dc.date.available.fl_str_mv |
2023-11-02T14:50:32Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
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article |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
HAYASHIDA, Kyoko et al. Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing. PLoS Neglected Tropical Diseases, v. 13, n. 6, p. 1-15, Jun. 2019. |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/61017 |
dc.identifier.issn.en_US.fl_str_mv |
1935-2727 |
dc.identifier.doi.none.fl_str_mv |
10.1371/journal.pntd.0007480 |
dc.identifier.eissn.none.fl_str_mv |
1935-2735 |
identifier_str_mv |
HAYASHIDA, Kyoko et al. Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing. PLoS Neglected Tropical Diseases, v. 13, n. 6, p. 1-15, Jun. 2019. 1935-2727 10.1371/journal.pntd.0007480 1935-2735 |
url |
https://www.arca.fiocruz.br/handle/icict/61017 |
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eng |
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eng |
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Public Library of Science |
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Public Library of Science |
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