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Review
. 2013 Jul 23;5(7):1867-84.
doi: 10.3390/v5071867.

Small ruminant lentiviruses (SRLVs) break the species barrier to acquire new host range

Affiliations
Review

Small ruminant lentiviruses (SRLVs) break the species barrier to acquire new host range

Juliano Cezar Minardi da Cruz et al. Viruses. .

Abstract

Zoonotic events of simian immunodeficiency virus (SIV) from non-human primates to humans have generated the acquired immunodeficiency syndrome (AIDS), one of the most devastating infectious disease of the last century with more than 30 million people dead and about 40.3 million people currently infected worldwide. Human immunodeficiency virus (HIV-1 and HIV-2), the two major viruses that cause AIDS in humans are retroviruses of the lentivirus genus. The genus includes arthritis-encephalitis virus (CAEV) and Maedi-Visna virus (MVV), and a heterogeneous group of viruses known as small ruminant lentiviruses (SRLVs), affecting goat and sheep. Lentivirus genome integrates into the host DNA, causing persistent infection associated with a remarkable diversity during viral replication. Direct evidence of mixed infections with these two closely related SRLVs was found in both sheep and goats. The evidence of a genetic continuum with caprine and ovine field isolates demonstrates the absence of an efficient species barrier preventing cross-species transmission. In dual-infected animals, persistent infections with both CAEV and MVV have been described, and viral chimeras have been detected. This not only complicates animal trade between countries but favors the risk that highly pathogenic variants may emerge as has already been observed in the past in Iceland and, more recently, in outbreaks with virulent strains in Spain. SRLVs affecting wildlife have already been identified, demonstrating the existence of emergent viruses adapted to new hosts. Viruses adapted to wildlife ruminants may acquire novel biopathological properties which may endanger not only the new host species but also domestic ruminants and humans. SRLVs infecting sheep and goats follow a genomic evolution similar to that observed in HIV or in other lentiviruses. Lentivirus genetic diversity and host factors leading to the establishment of naturally occurring virulent versus avirulent infections, in addition to the emergence of new strains, challenge every aspect of SRLV control measures for providing efficient tools to prevent the transmission of diseases between wild ungulates and livestock.

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Figures

Figure 1
Figure 1
Organization of HIV-1 and CAEV/MVV lentivirus genomes. Both genomes have a 5' LTR and 3' LTR at each of their extremities and the structural and enzyme gag, pol, and env genes common to all retroviruses. In addition, HIV-1 genome carries six open reading frames (vif, vpr, vpu, tat, rev and nef) that encode regulatory and accessory proteins. Both CAEV and MVV genomes have only three additional open reading frames (vif, vpr and rev).
Figure 2
Figure 2
Cross-species transmission of SRLVs in domestic and wild ruminants. CAEV and MVV cause natural infection, adaptation and induced pathogenesis in both domestic sheep and goats (left). Experimental and natural cross-species infections were recently documented in wild small ruminants (right).
Figure 3
Figure 3
Example of phylogenetic analysis of CAEV sequences in goats and following spill over in goat/ibex hybrids and in wild ibex. Sequence analyses in gag gene from naturally infected goats (G), hybrids (H) and wild ibex (I) were used for alignment and phylogenetic analysis. The prototypic molecular clone CAEV-co was used as reference.

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