Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing

Detalhes bibliográficos
Autor(a) principal: Hayashida, Kyoko
Data de Publicação: 2019
Outros Autores: 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
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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spelling 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
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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
dc.language.iso.fl_str_mv eng
language eng
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https://www.arca.fiocruz.br/bitstream/icict/61017/2/Hayashida_Kyoko_etal_INI_2019.pdf
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