The detection of BFV (bovine foamy virus) in Vietnamese cattle was performed using conventional PCR targeting pol and gag genes. Out of 243 tested samples, ten (4.1%) and eight (3.3%) samples were positive for BFV gag and pol DNA, respectively. The prevalence of BLV (bovine leukemia virus) estimated by detection of proviral DNA using nested PCR targeting env gene was 26.7% (65/243). The results of nucleotide sequence alignment and the phylogenetic analysis suggested that Vietnamese BFV strains showed high homology to isolates belonging to either European or non-European clades. There was no significant correlation between BLV and BFV. This study provides information regarding BFV infection and confirms the existence of two BFV clades among Vietnamese cattle for the first time.
KEY WORDS: bovine foamy virus (BFV), bovine leukemia virus (BLV), cattle, VietnamFoamy viruses (FVs) belong to the subfamily Spumaretrovirinae within the family Retroviridae. FVs are ubiquitous in a wide range of mammals, including nonhuman primates (Simian FV, or SFV), chimpanzees (Prototype FV, or PFV), bats (Chiropteran FV, or CFV), cats (feline FV, or FFV), horses (equine FV, or EFV), and cattle (bovine FV, or BFV). In their natural hosts, they establish a lifelong, persistent infection [21,28]. Although FVs have been known to cause a pronounced cytopathic effect in many tissue culture cells in vitro [21,31], these viruses have not been shown to be associated to a defined disease with obvious clinical signs. However, the pathogenic potential of FVs was suggested. A previous study demonstrated the transient depression of the cell-mediated immune response occurred in rabbits infected by SFV [10].Another study showed that chronic progressive polyarthritis of cats has been associated with FFV [24]. In humans, among patients with subacute granulomatous thyroiditis (de Quervain) and autoimmune hyperthyroidism (Grave's disease), PFV was commonly found [17,32]. Besides, mice transgenic expressing the partial or complete genome of PFV were shown to develop progressive encephalopathy and myopathy [1,4].BFV was first isolated from lymphosarcomatous and apparently healthy cattle in 1969 [19]. Subsequently, BFV infection was confirmed in livestock cattle in different parts of the world [2,3,5,11,12,14,20,23,27,33]. Moreover, the previous studies showed the concomitant infection of BFV with either bovine leukemia virus (BLV) or bovine immunodeficiency virus, and suggested the presence of BFV in the host may contribute to diseases caused by other pathogens [2,12,13].The BFV genome is composed of gag, pol, and env structural genes flanked by the long terminal repeats (LTRs) and additional accessory genes designated as tas and bet [26]. The previous results of phylogenetic analysis suggested that BFV could be classified into two distinct clades, the European clade and the non-European clade [7,9,23]. The European clade comprised the two