author_facet Araki, Koichi
Yoshimatsu, Kumiko
Ogino, Michiko
Ebihara, Hideki
Lundkvist, Åke
Kariwa, Hiroaki
Takashima, Ikuo
Arikawa, Jiro
Araki, Koichi
Yoshimatsu, Kumiko
Ogino, Michiko
Ebihara, Hideki
Lundkvist, Åke
Kariwa, Hiroaki
Takashima, Ikuo
Arikawa, Jiro
author Araki, Koichi
Yoshimatsu, Kumiko
Ogino, Michiko
Ebihara, Hideki
Lundkvist, Åke
Kariwa, Hiroaki
Takashima, Ikuo
Arikawa, Jiro
spellingShingle Araki, Koichi
Yoshimatsu, Kumiko
Ogino, Michiko
Ebihara, Hideki
Lundkvist, Åke
Kariwa, Hiroaki
Takashima, Ikuo
Arikawa, Jiro
Journal of Clinical Microbiology
Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
Microbiology (medical)
author_sort araki, koichi
spelling Araki, Koichi Yoshimatsu, Kumiko Ogino, Michiko Ebihara, Hideki Lundkvist, Åke Kariwa, Hiroaki Takashima, Ikuo Arikawa, Jiro 0095-1137 1098-660X American Society for Microbiology Microbiology (medical) http://dx.doi.org/10.1128/jcm.39.7.2397-2404.2001 <jats:title>ABSTRACT</jats:title> <jats:p>Truncated recombinant nucleocapsid proteins (rNPs) of Hantaan virus (HTNV), Seoul virus (SEOV), and Dobrava virus (DOBV) were expressed by a baculovirus system. The truncated rNPs, which lacked 49 (rNP50) or 154 (rNP155) N-terminal amino acids of the NPs of HTNV, SEOV, and DOBV, were able to differentiate HTNV-, SEOV-, and DOBV-specific immune sera. Recombinant NP50s retained higher reactivities than rNP155s and were proven useful for enzyme-linked immunosorbent assay (ELISA). The ELISAs based on the rNP50s of HTNV, SEOV, and DOBV successfully differentiated three groups of patient sera, previously defined by neutralization tests: 17 with HTNV infection, 12 with SEOV infection, and 20 with DOBV infection. The entire rNP of Puumala virus (PUUV) distinguished PUUV infection from the other types of hantavirus infection. Serotyping with these rNP50s can be recommended as a rapid and efficient system for hantavirus diagnosis.</jats:p> Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections Journal of Clinical Microbiology
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title Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_unstemmed Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_full Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_fullStr Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_full_unstemmed Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_short Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_sort truncated hantavirus nucleocapsid proteins for serotyping hantaan, seoul, and dobrava hantavirus infections
topic Microbiology (medical)
url http://dx.doi.org/10.1128/jcm.39.7.2397-2404.2001
publishDate 2001
physical 2397-2404
description <jats:title>ABSTRACT</jats:title> <jats:p>Truncated recombinant nucleocapsid proteins (rNPs) of Hantaan virus (HTNV), Seoul virus (SEOV), and Dobrava virus (DOBV) were expressed by a baculovirus system. The truncated rNPs, which lacked 49 (rNP50) or 154 (rNP155) N-terminal amino acids of the NPs of HTNV, SEOV, and DOBV, were able to differentiate HTNV-, SEOV-, and DOBV-specific immune sera. Recombinant NP50s retained higher reactivities than rNP155s and were proven useful for enzyme-linked immunosorbent assay (ELISA). The ELISAs based on the rNP50s of HTNV, SEOV, and DOBV successfully differentiated three groups of patient sera, previously defined by neutralization tests: 17 with HTNV infection, 12 with SEOV infection, and 20 with DOBV infection. The entire rNP of Puumala virus (PUUV) distinguished PUUV infection from the other types of hantavirus infection. Serotyping with these rNP50s can be recommended as a rapid and efficient system for hantavirus diagnosis.</jats:p>
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author Araki, Koichi, Yoshimatsu, Kumiko, Ogino, Michiko, Ebihara, Hideki, Lundkvist, Åke, Kariwa, Hiroaki, Takashima, Ikuo, Arikawa, Jiro
author_facet Araki, Koichi, Yoshimatsu, Kumiko, Ogino, Michiko, Ebihara, Hideki, Lundkvist, Åke, Kariwa, Hiroaki, Takashima, Ikuo, Arikawa, Jiro, Araki, Koichi, Yoshimatsu, Kumiko, Ogino, Michiko, Ebihara, Hideki, Lundkvist, Åke, Kariwa, Hiroaki, Takashima, Ikuo, Arikawa, Jiro
author_sort araki, koichi
container_issue 7
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container_title Journal of Clinical Microbiology
container_volume 39
description <jats:title>ABSTRACT</jats:title> <jats:p>Truncated recombinant nucleocapsid proteins (rNPs) of Hantaan virus (HTNV), Seoul virus (SEOV), and Dobrava virus (DOBV) were expressed by a baculovirus system. The truncated rNPs, which lacked 49 (rNP50) or 154 (rNP155) N-terminal amino acids of the NPs of HTNV, SEOV, and DOBV, were able to differentiate HTNV-, SEOV-, and DOBV-specific immune sera. Recombinant NP50s retained higher reactivities than rNP155s and were proven useful for enzyme-linked immunosorbent assay (ELISA). The ELISAs based on the rNP50s of HTNV, SEOV, and DOBV successfully differentiated three groups of patient sera, previously defined by neutralization tests: 17 with HTNV infection, 12 with SEOV infection, and 20 with DOBV infection. The entire rNP of Puumala virus (PUUV) distinguished PUUV infection from the other types of hantavirus infection. Serotyping with these rNP50s can be recommended as a rapid and efficient system for hantavirus diagnosis.</jats:p>
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spelling Araki, Koichi Yoshimatsu, Kumiko Ogino, Michiko Ebihara, Hideki Lundkvist, Åke Kariwa, Hiroaki Takashima, Ikuo Arikawa, Jiro 0095-1137 1098-660X American Society for Microbiology Microbiology (medical) http://dx.doi.org/10.1128/jcm.39.7.2397-2404.2001 <jats:title>ABSTRACT</jats:title> <jats:p>Truncated recombinant nucleocapsid proteins (rNPs) of Hantaan virus (HTNV), Seoul virus (SEOV), and Dobrava virus (DOBV) were expressed by a baculovirus system. The truncated rNPs, which lacked 49 (rNP50) or 154 (rNP155) N-terminal amino acids of the NPs of HTNV, SEOV, and DOBV, were able to differentiate HTNV-, SEOV-, and DOBV-specific immune sera. Recombinant NP50s retained higher reactivities than rNP155s and were proven useful for enzyme-linked immunosorbent assay (ELISA). The ELISAs based on the rNP50s of HTNV, SEOV, and DOBV successfully differentiated three groups of patient sera, previously defined by neutralization tests: 17 with HTNV infection, 12 with SEOV infection, and 20 with DOBV infection. The entire rNP of Puumala virus (PUUV) distinguished PUUV infection from the other types of hantavirus infection. Serotyping with these rNP50s can be recommended as a rapid and efficient system for hantavirus diagnosis.</jats:p> Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections Journal of Clinical Microbiology
spellingShingle Araki, Koichi, Yoshimatsu, Kumiko, Ogino, Michiko, Ebihara, Hideki, Lundkvist, Åke, Kariwa, Hiroaki, Takashima, Ikuo, Arikawa, Jiro, Journal of Clinical Microbiology, Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections, Microbiology (medical)
title Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_full Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_fullStr Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_full_unstemmed Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_short Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
title_sort truncated hantavirus nucleocapsid proteins for serotyping hantaan, seoul, and dobrava hantavirus infections
title_unstemmed Truncated Hantavirus Nucleocapsid Proteins for Serotyping Hantaan, Seoul, and Dobrava Hantavirus Infections
topic Microbiology (medical)
url http://dx.doi.org/10.1128/jcm.39.7.2397-2404.2001