Screening of bird sera for pre-S (A) and e-antigens (B) and viral DNA (C) by immunoblotting and PCR, respectively. (A) Serum samples loaded were from manschurian cranes (lanes 1 and 2), a black stork (lane 3), demoiselle cranes (lanes 4 to 7), and crowned cranes (lanes 8 to 10). HHBV-positive and -negative heron sera used as controls were loaded in lanes 11 and 12, respectively. The pre-S antigens were detected with an HHBV pre-S antiserum. The full-length HHBV pre-S-specific band is indicated by an arrow. (B) e-protein in crowned (lanes 1 to 5 [lanes 4 and 5 correspond to different serum aliquots from the same cranes as in lanes 1 and 2, respectively]) and demoiselle (lanes 6 to 9) cranes as well as in HHBV-negative (lane 10) and -positive (lane 11) heron sera as detected by a DHBV-core- and e-antigen-specific antiserum. (C) Agarose gel analysis of PCR products amplified from crane sera. Serial dilutions (1/20 [lanes a], 1/200 [lanes b], and 1/2,000 [lanes c]) of four crane sera (lanes 2 to 13), one STHBV-positive stork serum (lanes 14 to 16), and one DHBV-negative serum (lanes 17 to 19) were subjected to PCR using STHBV full-length primers PS1 and PS2. A standard DNA size marker was loaded in lane 1.