Silverman J, Paturzo F, Smith A L
Lab Anim Sci. 1982 Jun;32(3):273-4.
Three deer mice (Peromyscus maniculatus) given 10(4) TCID50 of mouse hepatitis virus -S intranasally all had significant serum neutralization titers to mouse hepatitis virus -S 3 weeks later. Ten other deer mice were given 10(3) TCID50 of mouse hepatitis virus -3 intranasally and placed with sentinel laboratory mice (CF1, C3H/Rv, and nu/nu) and uninoculated deer mice. One inoculated deer mouse died, but mouse hepatitis virus was not isolated. No other inoculated or uninoculated animals exhibited signs of disease. No sentinel animals exhibited serum neutralization titers for mouse hepatitis virus -3. Three of the remaining nine inoculated deer mice had positive antibody titers. It was concluded that deer mice do not develop clinical manifestations of mouse hepatitis virus or transmit the virus to potentially susceptible laboratory mice.
三只经鼻接种10⁴半数组织培养感染剂量(TCID₅₀)小鼠肝炎病毒-S的鹿鼠,3周后对小鼠肝炎病毒-S均具有显著的血清中和效价。另外十只鹿鼠经鼻接种10³ TCID₅₀小鼠肝炎病毒-3,并与哨兵实验小鼠(CF1、C3H/Rv和裸鼠)以及未接种的鹿鼠放在一起。一只接种的鹿鼠死亡,但未分离到小鼠肝炎病毒。其他接种或未接种的动物均未表现出疾病迹象。没有哨兵动物表现出针对小鼠肝炎病毒-3的血清中和效价。其余九只接种的鹿鼠中有三只抗体效价呈阳性。得出的结论是,鹿鼠不会出现小鼠肝炎病毒的临床表现,也不会将该病毒传播给潜在易感的实验小鼠。