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Journal of General Virology (2001), 82, 1233-1238.
© 2001 Society for General Microbiology


Animal: DNA Viruses

Identification of a genetic determinant of pathogenicity in chicken anaemia virus

S. Yamaguchi1, T. Imada1, N. Kajib,1, M. Mase1, K. Tsukamoto1, N. Tanimura1 and N. Yuasa1

National Institute of Animal Health, 3-1-1 Kannondai, Tsukuba, Ibaraki 305-0856, Japan1

Author for correspondence: Shigeo Yamaguchi. Fax +81 298 38 7760. e-mail syama{at}niah.affrc.go.jp

The molecular basis of pathogenicity of the chicken anaemia virus (CAV) needs to be clarified in order to develop a safe, live virus vaccine. In this study, several high- and low-pathogenic infectious DNA clones were obtained from field virus samples after 12 or 38 passages in MDCC-MSB1 cells. The high-pathogenic clones induced a low haematocrit, low weight gain and high mortality. Nucleotide sequence analyses identified one amino acid, at residue 394 of the VP1 capsid protein, as a major determinant of pathogenicity. To determine the role of this amino acid in pathogenicity, chimeric infectious DNA clones and point-mutated clones were used for chicken pathogenicity tests. These analyses clearly demonstrated that residue 394 of VP1 was crucial for the pathogenicity of CAV; all of the cloned viruses with glutamine at this position were highly pathogenic, whereas those with histidine had low pathogenicity. Low-pathogenic CAV, based on an infectious DNA clone, is a candidate for a genetically homogeneous and stable CAV live vaccine.




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