Abstract:
:Three full-length genomic clones (pB19-M20, pB19-FL and pB19-HG1) of parvovirus B19 were produced in different laboratories. pB19-M20 was shown to produce infectious virus. To determine the differences in infectivity, all three plasmids were tested by transfection and infection assays. All three clones were similar in viral DNA replication, RNA transcription, and viral capsid protein production. However, only pB19-M20 and pB19-HG1 produced infectious virus. Comparison of viral sequences showed no significant differences in ITR or NS regions. In the capsid region, there was a nucleotide sequence difference conferring an amino acid substitution (E176K) in the phospholipase A2-like motif of the VP1-unique (VP1u) region. The recombinant VP1u with the E176K mutation had no catalytic activity as compared with the wild-type. When this mutation was introduced into pB19-M20, infectivity was significantly attenuated, confirming the critical role of this motif. Investigation of the original serum from which pB19-FL was cloned confirmed that the phospholipase mutation was present in the native B19 virus.
journal_name
Virologyjournal_title
Virologyauthors
Filippone C,Zhi N,Wong S,Lu J,Kajigaya S,Gallinella G,Kakkola L,Söderlund-Venermo M,Young NS,Brown KEdoi
10.1016/j.virol.2008.01.002subject
Has Abstractpub_date
2008-05-10 00:00:00pages
444-52issue
2eissn
0042-6822issn
1096-0341pii
S0042-6822(08)00011-1journal_volume
374pub_type
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