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J Gen Virol 87 (2006), 1189-1195; DOI 10.1099/vir.0.81561-0

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© 2006 Society for General Microbiology

Genome of a novel circovirus of starlings, amplified by multiply primed rolling-circle amplification

Reimar Johne1, Daniel Fernández-de-Luco2, Ursula Höfle3 and Hermann Müller1

1 Institute for Virology, Faculty of Veterinary Medicine, University of Leipzig, An den Tierkliniken 29, D-04103 Leipzig, Germany
2 Department of Animal Pathology, Veterinary Faculty, University of Zaragoza, Spain
3 Centro de Investigación Agropecuaria, El Deheson del Encinar, Oropesa, Spain

Correspondence
Reimar Johne
johne{at}vetmed.uni-leipzig.de

The genus Circovirus comprises small non-enveloped viruses with a circular single-stranded DNA genome. By using PCR with degenerate primers, a novel circovirus (starling circovirus, StCV) was detected in spleen samples of wild starlings (Sturnus vulgaris and Sturnus unicolor) found dead during an epidemic outbreak of septicaemic salmonellosis in northeastern Spain. Using a specific PCR, StCV was also detected in apparently healthy birds from the same population. The genome was amplified using multiply primed rolling-circle amplification and cloned. Open reading frames (ORFs) with similarities to the replication-associated protein and the capsid protein of circoviruses as well as an additional ORF encoding a protein of 106 aa were evident from the sequence. Phylogenetic analysis of circovirus genomes revealed the highest degree of similarity (67·1 %) between StCV and canary circovirus. A similar analysis of the evolutionarily conserved cytochrome b gene of the circovirus host species revealed a strict co-evolution of circoviruses with their hosts; however, the circoviruses showed about a threefold higher genetic divergence than their hosts.

The GenBank/EMBL/DDBJ accession number of the sequence reported in this paper is DQ172906 [GenBank] .




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P. Biagini, R. Uch, M. Belhouchet, H. Attoui, J.-F. Cantaloube, N. Brisbarre, and P. de Micco
Circular genomes related to anelloviruses identified in human and animal samples by using a combined rolling-circle amplification/sequence-independent single primer amplification approach
J. Gen. Virol., October 1, 2007; 88(10): 2696 - 2701.
[Abstract] [Full Text] [PDF]




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