Genetic diversity of human Parvovirus B19 VP1 unique region

OBJECTIVE: Human Parvovirus B19 (HPV B19) is a small (23 nm), non-enveloped DNA virus found in 1974. It has been proved that HPV B19 is associated with a variety of childhood diseases, such as erythema infectious, transient aplastic crisis, aplastic anemia, idiopathic thrombocytopenic purpura and ar...

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Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 41(2003), 2 vom: 15. Feb., Seite 128-30
Auteur principal: Qian, Xin-hong (Auteur)
Autres auteurs: Zhang, Guo-cheng, Jiao, Xi-ying, Zhang, Ping, Sun, Xin, Cao, Yu-hong, Xu, Dong-liang, Fei, Lin-lin, Huang, Wen-jin
Format: Article
Langue:Chinese
Publié: 2003
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:English Abstract Journal Article Research Support, Non-U.S. Gov't Capsid Proteins DNA, Viral capsid protein VP1, parvovirus B19
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245 1 0 |a Genetic diversity of human Parvovirus B19 VP1 unique region 
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520 |a OBJECTIVE: Human Parvovirus B19 (HPV B19) is a small (23 nm), non-enveloped DNA virus found in 1974. It has been proved that HPV B19 is associated with a variety of childhood diseases, such as erythema infectious, transient aplastic crisis, aplastic anemia, idiopathic thrombocytopenic purpura and arthropathy, etc. There have been no any effective vaccines to prevent HPV B19 infection so far. The HPV B19 genome is composed of 5.6 kb single strand DNA. This genome encodes a nonstructural protein NS1, two structural proteins VP1 and VP2. Most neutralizing linear epitopes of HPV B19 cluster in the VP1 unique and VP1-VP2 junction regions. Only proteins encoded by genes of the VP1 unique and VP1-VP2 junction regions can stimulate bodies to produce protective antibodies. Aim of the present study was to get the VP1 unique region gene of HPV B19 and to analyze the genetic diversity so as to further study its function and application 
520 |a METHODS: The VP1 unique region gene of HPV B19 was amplified from the serum of a child with idiopathic thrombocytopenic purpura by PCR. The purified PCR product was cloned into pGEM-T easy vector and transfected into the host strain E. coli (DH5 alpha). Positive clones were chosen and then the target gene was sequenced 
520 |a RESULTS: The target gene sequence of HPV B19 VP1 unique region was amplified and cloned successfully. It had 705 nucleotides. Compared with the relevant sequences published in Genbank, the sequencing results were revealed with two nucleotides changes in the HPV B19 VP1 unique region, but their coding amino acid were not changed 
520 |a CONCLUSION: It is suggested that genetic diversity exists in the VP1 unique region of HPV B19. Construction of the recombinant plasmid of HPV B19 VP1 unique region gene might benefit to further study 
650 4 |a English Abstract 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Capsid Proteins  |2 NLM 
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650 7 |a capsid protein VP1, parvovirus B19  |2 NLM 
700 1 |a Zhang, Guo-cheng  |e verfasserin  |4 aut 
700 1 |a Jiao, Xi-ying  |e verfasserin  |4 aut 
700 1 |a Zhang, Ping  |e verfasserin  |4 aut 
700 1 |a Sun, Xin  |e verfasserin  |4 aut 
700 1 |a Cao, Yu-hong  |e verfasserin  |4 aut 
700 1 |a Xu, Dong-liang  |e verfasserin  |4 aut 
700 1 |a Fei, Lin-lin  |e verfasserin  |4 aut 
700 1 |a Huang, Wen-jin  |e verfasserin  |4 aut 
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