Literature DB >> 2839709

Nucleotide sequence and genomic organization of Aleutian mink disease parvovirus (ADV): sequence comparisons between a nonpathogenic and a pathogenic strain of ADV.

M E Bloom, S Alexandersen, S Perryman, D Lechner, J B Wolfinbarger.   

Abstract

A DNA sequence of 4,592 nucleotides (nt) was derived for the nonpathogenic ADV-G strain of Aleutian mink disease parvovirus (ADV). The 3'(left) end of the virion strand contained a 117-nt palindrome that could assume a Y-shaped configuration similar to, but less stable than, that of other parvoviruses. The sequence obtained for the 5' end was incomplete and did not contain the 5' (right) hairpin structure but ended just after a 25-nt A + T-rich direct repeat. Features of ADV genomic organization are (i) major left (622 amino acids) and right (702 amino acids) open reading frames (ORFs) in different translational frames of the plus-sense strand, (ii) two short mid-ORFs, (iii) eight potential promoter motifs (TATA boxes), including ones at 3 and 36 map units, and (iv) six potential polyadenylation sites, including three clustered near the termination of the right ORF. Although the overall homology to other parvoviruses is less than 50%, there are short conserved amino acid regions in both major ORFs. However, two regions in the right ORF allegedly conserved among the parvoviruses were not present in ADV. At the DNA level, ADV-G is 97.5% related to the pathogenic ADV-Utah 1. A total of 22 amino acid changes were found in the right ORF; changes were found in both hydrophilic and hydrophobic regions and generally did not affect the theoretical hydropathy. However, there is a short heterogeneous region at 64 to 65 map units in which 8 out of 11 residues have diverged; this hypervariable segment may be analogous to short amino acid regions in other parvoviruses that determine host range and pathogenicity. These findings suggested that this region may harbor some of the determinants responsible for the differences in pathogenicity of ADV-G and ADV-Utah 1.

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Year:  1988        PMID: 2839709      PMCID: PMC253728          DOI: 10.1128/JVI.62.8.2903-2915.1988

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  69 in total

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Authors:  K I Berns; M A Labow
Journal:  J Gen Virol       Date:  1987-03       Impact factor: 3.891

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Authors:  L W Mayer; B Aasted; C F Garon; M E Bloom
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4.  Rapid transfer of DNA from agarose gels to nylon membranes.

Authors:  K C Reed; D A Mann
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5.  A nonstructural protein of feline panleukopenia virus: expression in Escherichia coli and detection of multiple forms in infected cells.

Authors:  J O Carlson; M K Lynde-Maas; Z D Shen
Journal:  J Virol       Date:  1987-02       Impact factor: 5.103

6.  Monoclonal antibodies against Aleutian disease virus distinguish virus strains and differentiate sites of virus replication from sites of viral antigen sequestration.

Authors:  R E Race; B Chesebro; M E Bloom; B Aasted; J Wolfinbarger
Journal:  J Virol       Date:  1986-01       Impact factor: 5.103

7.  An Escherichia coli recBCsbcBrecF host permits the deletion-resistant propagation of plasmid clones containing the 5'-terminal palindrome of minute virus of mice.

Authors:  R Boissy; C R Astell
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8.  Hemagglutinin of swine influenza virus: a single amino acid change pleiotropically affects viral antigenicity and replication.

Authors:  G W Both; C H Shi; E D Kilbourne
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9.  Characterization and recombination mapping of an antigenic and host range mutation of canine parvovirus.

Authors:  C R Parrish; L E Carmichael
Journal:  Virology       Date:  1986-01-15       Impact factor: 3.616

10.  Antigenic variation and resistance to neutralization in poliovirus type 1.

Authors:  D C Diamond; B A Jameson; J Bonin; M Kohara; S Abe; H Itoh; T Komatsu; M Arita; S Kuge; A Nomoto
Journal:  Science       Date:  1985-09-13       Impact factor: 47.728

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  52 in total

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Authors:  K I Berns
Journal:  Microbiol Rev       Date:  1990-09

2.  SAT: a late NS protein of porcine parvovirus.

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3.  Nucleotide sequence analysis of Aleutian mink disease parvovirus shows that multiple virus types are present in infected mink.

Authors:  E Gottschalck; S Alexandersen; A Cohn; L A Poulsen; M E Bloom; B Aasted
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

4.  Characterization of variable regions in the envelope and S3 open reading frame of equine infectious anemia virus.

Authors:  S Alexandersen; S Carpenter
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

5.  The transcription profile of Aleutian mink disease virus in CRFK cells is generated by alternative processing of pre-mRNAs produced from a single promoter.

Authors:  Jianming Qiu; Fang Cheng; Lisa R Burger; David Pintel
Journal:  J Virol       Date:  2006-01       Impact factor: 5.103

6.  Identification of a hypervariable region in the long terminal repeat of equine infectious anemia virus.

Authors:  S Carpenter; S Alexandersen; M J Long; S Perryman; B Chesebro
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

7.  Aleutian disease parvovirus infection of mink and ferrets elicits an antibody response to a second nonstructural viral protein.

Authors:  D D Porter; H G Porter; A E Larsen
Journal:  J Virol       Date:  1990-04       Impact factor: 5.103

8.  Mutational analysis of the adeno-associated virus type 2 Rep68 protein helicase motifs.

Authors:  S L Walker; R S Wonderling; R A Owens
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9.  Regulated expression of the feline panleukopenia virus P38 promoter on extrachromosomal FPV/EBV chimeric plasmids.

Authors:  D L Clemens; J O Carlson
Journal:  J Virol       Date:  1989-06       Impact factor: 5.103

Review 10.  Viral proteins containing the purine NTP-binding sequence pattern.

Authors:  A E Gorbalenya; E V Koonin
Journal:  Nucleic Acids Res       Date:  1989-11-11       Impact factor: 16.971

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