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Characterization of human bocavirus-like particles generated by recombinant baculoviruses.
Fang, Ling; Wang, Zejun; Song, Shili; Kataoka, Michiyo; Ke, Changwen; Suzuki, Tetsuro; Wakita, Takaji; Takeda, Naokazu; Li, Tian-Cheng.
Afiliação
  • Fang L; Institute of Pathogenic Microbiology, Center for Disease Control and Prevention of Guangdong Province, 160 Qunxian Road, Dashi Street, Panyu District, Guangzhou 511430, China.
  • Wang Z; Department of Genetic Engineering, Wuhan Institute of Biological Products (WIBP) , Linjiang Avenue, Wuchang, Wuhan, 430060, China.
  • Song S; Institute of Microbiology, Yuhang Center for Disease Control and Prevention, 930 Shijidadao Avenue, Hangzhou 311100, China.
  • Kataoka M; Department of Pathology, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-murayama 208-0011, Tokyo, Japan.
  • Ke C; Institute of Pathogenic Microbiology, Center for Disease Control and Prevention of Guangdong Province, 160 Qunxian Road, Dashi Street, Panyu District, Guangzhou 511430, China.
  • Suzuki T; Department of Infectious Diseases, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu 431-3192, Japan.
  • Wakita T; Department of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-murayama 208-0011, Tokyo, Japan.
  • Takeda N; Research Institute for Microbial Diseases, Osaka University, Suita 565-0781, Osaka, Japan.
  • Li TC; Department of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-murayama 208-0011, Tokyo, Japan. Electronic address: litc@nih.go.jp.
J Virol Methods ; 207: 38-44, 2014 Oct.
Article em En | MEDLINE | ID: mdl-24992668
Human bocavirus (HBoV) is a nonenveloped, single-stranded DNA virus, classified recently into the genus Bocavirus in the family Parvoviridae. A recombinant baculovirus expression system was used to express the major capsid protein VP2 of HBoV1, HBoV2, HBoV3 and HBoV4 in insect cells. A large amount of the 61-kDa VP2 capsid protein (p61) of HBoVs was generated and efficiently released into the supernatant. The capsid protein was self-assembled into 22-nm-dia. virus-like particles (VLPs) with a buoyant density of 1.30g/cm(3). The morphology of HBoVs-LPs was similar to that of the native HBoV particles, and immunogenic studies demonstrated the cross-reactivity among HBoV1, HBoV2, HBoV3 and HBoV4. When VP1 and VP2 protein of HBoV1 were co-expressed in insect cells, both proteins were detected in the same fraction after CsCl gradient centrifugation, suggesting that the VP1 protein is a minor structural protein of HBoVs. We developed an ELISA using purified VLPs as the antigen and used it to detect antibodies against HBoV1, HBoV2, HBoV3 and HBoV4. A high prevalence of antibodies against HBoVs was found in a general population of healthy Japanese, indicating that HBoVs have spread throughout Japan.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Baculoviridae / Infecções por Parvoviridae / Virossomos / Proteínas do Capsídeo / Bocavirus Humano / Vetores Genéticos / Anticorpos Antivirais Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Baculoviridae / Infecções por Parvoviridae / Virossomos / Proteínas do Capsídeo / Bocavirus Humano / Vetores Genéticos / Anticorpos Antivirais Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2014 Tipo de documento: Article