Furthermore, it was found that the attenuated strain spread less

Furthermore, it was found that the attenuated strain spread less efficiently in the brain than did GSK3235025 cell line the virulent strain. These findings indicate that amino acid substitution at position 333 in the G protein affects the efficiency of cell-to-cell spread and induction of apoptosis. It is known that other amino acid substitutions in the G protein also contribute to determination of pathogenicity. The fixed rabies virus Nishigahara strain kills adult mice after IC inoculation, whereas the RC-HL strain, which was established by serial passages of Nishigahara strain in chicken embryos and cultured cells, causes non-lethal infection in mice (15). The fact that both strains have

an Arg residue at position 333 in the G protein (16, 17) indicates that another gene region determines the different pathogenicities of the two strains. We previously reported that an RC-HL mutant, R(G 242/255/268) strain, in which three amino acids at positions 242, 255 and 268 (Ser, Asn and Leu, respectively) in the RC-HL G protein have been replaced with the ones in the Nishigahara Gemcitabine nmr strain (Ala,

Asp and Ile, respectively), kills adult mice after IC inoculation (18). This result indicates that the three amino acids in the G protein are responsible for differences between the pathogenicities of RC-HL and Nishigahara strains. However, the mechanism by which these amino acid substitutions affect the pathogenicity remains to be elucidated. Also, it remains unclear whether cell-to-cell spread and apoptosis-inducing ability differ between the RC-HL and R(G 242/255/268) strains. In this study, in order to obtain insights into the mechanism of the different pathogenicities of R(G 242/255/268) and Dapagliflozin RC-HL strains, the

efficiency of spread of viral infection and the apoptosis-inducing ability of the attenuated RC-HL strain and the virulent R(G 242/255/268) strain were compared. Mouse NA cells were maintained in E-MEM supplemented with 10% FCS. The RC-HL strain, a recombinant virus that had previously been generated by a reverse genetic system (8) was used in this study. The R(G 242/255/268) strain, in which the three amino acids at positions 242, 255 and 268 in the G protein are derived from the virulent Nishigahara strain in the genetic background of the attenuated RC-HL strain, and which demonstrates a pathogenic phenotype (Fig. 1a and b), had previously been recovered from full-length genome plasmids (18). Stocks of all strains were prepared in NA cells. Four-week-old female ddY mice (Japan SLC, Hamamatsu, Japan) were inoculated intracerebrally with 0.03 ml of 104 FFU of each strain. Mock-infected mice were inoculated with 0.03 ml diluent (E-MEM supplemented with 5% FCS) alone. To examine the spread of infection of each strain in the mouse brain, the infected mice were anesthetized by intraperitoneal injection of pentobarbital (0.125 mg/g body weight) and then perfused with PBS followed by 4% paraformaldehyde in PBS.

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