The Nucleocapsid Protein Of Newcastle Disease Virus As A Carrier For The Vp1 Polypeptides Of Enterovirus 71
Human enterovirus 71 (EV71) is an important human enterovirus which belongs to the Enterovirus genus of the Picornaviridae family. Large outbreaks of EV71 have been associated with severe central nervous disease (CNS) manifestations including the hand, foot and mouth disease (HFMD). To date, ther...
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| 格式: | Thesis |
| 语言: | English |
| 出版: |
2005
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| 主题: | |
| 在线阅读: | http://psasir.upm.edu.my/id/eprint/5910/1/FBSB_2005_10%20IR.pdf |
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| 总结: | Human enterovirus 71 (EV71) is an important human enterovirus which belongs
to the Enterovirus genus of the Picornaviridae family. Large outbreaks of EV71
have been associated with severe central nervous disease (CNS) manifestations
including the hand, foot and mouth disease (HFMD). To date, there is no
effective antiviral drug available to treat the infections. Therefore, the
development of an effective vaccine is considered as one of the best choice to
prevent the diseases caused by EV71.
The VP1 protein which is the most immunogenic capsid protein of EV71, can be
used in the development of subunit EV71 vaccines. The complete VP1 protein of
EV71 was truncated into six regions and fused to the full length nucleocapsid
protein (NPfl) and truncated NP (NPt; which lacks 20% amino acids from its Cterminal
end). Western blot analysis using rabbit anti-VP1 serum showed that the
N-terminal region of the VP1 protein contained a major antigenic region. Of all
the recombinant NP proteins, the ones carrying truncated VP1 protein, VP11-100
were efficiently expressed in Escherichia coli system. Electron microscopic
analysis of the purified NPt-VPl-loo revealed that this protein predominantly selfassembled
into intact ring-like structure whereas NPfl-VPl-loo showed disrupted
ring-like formations. Rabbits immunized with these purified recombinant proteins
exhibited a strong immune response against the complete VP1 protein. The
antisera of these recombinant proteins also reacted positively with the authentic
EV71 when analyzed by an immuno flourescence assay thus suggesting their
potential as subunit vaccine candidates against EV71 infections and also as
immunological reagents for the detection of anti-EV71 antibodies in serum
samples. |
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