“…The second reason is because the absence of BDV RNA in samples does not exclude the possibility of BDV infection, since RNA detection is less reliable than the detection of other virus particles (Ag or CIC) because of the low replication rate of this virus and the small amount of RNA in PBMCs. Also, the presence of BDV RNA in the brain does not necessarily reflect an active state of BDV infection (Bode et al, 2001, Sauder & de la Torre, 1998Thakur et al, 2009;Wolff et al, 2006). Currently, the detection of BDV CIC by ELISA and viral isolation from PBMCs are recommended as the best screening methods of active BDV infection because of their relative stability and frequency.…”