Biao He1, Quanshui Fan1, Fanli Yang, Tingsong Hu, Wei Qiu, Ye Feng, Zuosheng Li, Yingying Li, Fuqiang Zhang, Huancheng Guo, Xiaohuan Zou, and Changchun Tu
Author affiliations: Academy of Military Medical Sciences, Changchun, People’s Republic of China (B. He, F. Yang, Y. Feng, Y. Li, H. Guo, X. Zou, C. Tu); Center for Disease Control and Prevention of Chengdu Military Region, Kunming, People’s Republic of China (Q. Fan, T. Hu, W. Qiu, Z. Li, F. Zhang)
Figure 1. . Predicted schematic representation of the bat hepatitis virus (BtHV) genome and its phylogenetic relationship with other hepadnaviruses. A) Genomic structural map of BtHV. Boxes and arrows represent the open reading frames encoding the main proteins: pol gene (2,305–1,636), preS1/S2 and S gene (2,864–833), preC/C gene (1,815–2,468) and X gene (1,378–1,812). Two 12-nt direct repeat sequences (DR1 from 1,825 to 1,836 and DR2 from 1,594 to 1,605), the encapsidation signal ε (1,848–1,903), and YMDD domain (734–745) are also depicted in the map. B) Phylogenetic analysis of BtHVs and other hepadnaviruses based on amino acid sequences of pol genes. Representatives of hepadnavirus species belonging to Orthohepadnavirus and Avihepadnavirus genera were used; their GenBank accession nos. are shown in the trees. The different genotypes of human hepatitis B virus are also included. The 3 BtHV isolates are identified by black triangles. Scale bar indicates nucleotide substitutions per site.
The opinions expressed by authors contributing to this journal do not necessarily reflect the opinions of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.