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1.
Virology ; 278(2): 456-66, 2000 Dec 20.
Article in English | MEDLINE | ID: mdl-11118368

ABSTRACT

For the cytopathogenic (cp) bovine viral diarrhea virus (BVDV) strain CP 821, a duplication of the genomic region encoding part of NS2, NS3, NS4A, and part of NS4B together with a nonviral insertion was detected. Further analyses including molecular cloning and sequencing of the putative cellular recombination partner showed that the insertion in CP 821 originated from a bovine mRNA encoding the cellular protein NEDD8, which is 58% identical to ubiquitin. To our knowledge the genome of CP 821 represents the first viral RNA with a NEDD8 coding insertion. Remarkably, the insertion site differs from that described for insertions of ubiquitin. The NEDD8 sequence allows an additional cleavage of the viral polyprotein, whereby an NS3 with an unusual N-terminus is generated. Furthermore, the CP 821-specific genomic alterations were introduced into an infectious noncytopathogenic (noncp) BVDV cDNA clone. After transfection of bovine cells with the respective RNA, a cp virus was recovered. This showed that the NEDD8 coding insertion together with the duplicated viral sequences represents the genetic basis for cytopathogenicity of CP 821. In addition to the recovered cp virus, noncp BVDV rapidly evolved after transfection. This is the first time that a change from the cp to the noncp phenotype was demonstrated in the course of replication in tissue culture cells.


Subject(s)
Diarrhea Viruses, Bovine Viral/genetics , Diarrhea Viruses, Bovine Viral/pathogenicity , Ubiquitins/genetics , Amino Acid Sequence , Animals , Base Sequence , Cattle , Cell Line , Cricetinae , Diarrhea Viruses, Bovine Viral/physiology , Gene Duplication , Genes, Viral , Molecular Sequence Data , Mutagenesis, Insertional , RNA, Messenger/genetics , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment , Sequence Homology, Amino Acid , Transfection , Ubiquitins/chemistry , Viral Structural Proteins/genetics
2.
Virology ; 262(1): 64-71, 1999 Sep 15.
Article in English | MEDLINE | ID: mdl-10489341

ABSTRACT

The complete Npro coding sequences were determined for 16 pestiviruses isolated from cattle, pig, and several wild ruminant species including reindeer, bison, deer, and bongo. Phylogenetic analysis enabled the segregation of pestiviruses into the established species bovine viral diarrhea virus-1 (BVDV-1), BVDV-2, border disease virus (BDV), and classical swine fever virus (CSFV). For BVDV-1 five distinct subgroups were identified, while BVDV-2, BDV, and CSFV were each subdivided into two subgroups. The virus isolates from bongo and deer as well as one porcine virus isolate belong to BVDV-1. Interestingly, the isolates from reindeer and bison are distinct from the established pestivirus species. The Npro sequences from these two viruses are more similar to BDV than to the other pestivirus species. Calculation of the pairwise evolutionary distances allowed a clear separation of the categories species, subgroup, and isolate only when the reindeer/bison viruses were considered as members of an additional pestivirus species. Furthermore, the entire E2 coding sequences of a representative set of virus isolates covering all recognized species and subgroups were studied. Segregation of pestiviruses based on the E2 region was identical with that obtained with the N(pro) sequences.


Subject(s)
Genetic Variation/genetics , Pestivirus/classification , Pestivirus/genetics , Amino Acid Sequence , Animals , Bison , Cattle , Deer , Glycoproteins/analysis , Glycoproteins/genetics , Molecular Sequence Data , Pestivirus/isolation & purification , Pestivirus Infections/classification , Pestivirus Infections/diagnosis , Phylogeny , Reindeer , Sequence Homology, Amino Acid , Swine , Viral Envelope Proteins/genetics
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