Becker Y, Hadar J, Tabor E, Ben-Hur T, Raibstein I, Rösen A, Darai G
Virology. 1986 Mar;149(2):255-9. doi: 10.1016/0042-6822(86)90128-5.
The virulence of herpes simplex virus-1 (HSV-1) strains by the intraperitoneal (ip) route of injection in mice depends on the presence of an intact sequence in the HpaI DNA fragment P within coordinates 0.762 to 0.787. Deletion of the HpaI-P region (e.g., strain HFEM) abrogates the ability of the virus to infect mice by the ip route without affecting pathogenicity by the intracerebral (ic) route. A recombinant virus (M1C1) derived from DNA of the HSV-1 HFEM strain and the MLUIDNA fragment (coordinates 0.761 to 0.796) spanning the HpaI-P sequence of the pathogenic strain F regained pathogenicity for mice by the ip route.
单纯疱疹病毒1型(HSV-1)毒株经腹腔(ip)注射途径对小鼠的毒力取决于位于坐标0.762至0.787之间的HpaI DNA片段P中完整序列的存在。缺失HpaI-P区域(如HFEM毒株)会消除病毒经腹腔途径感染小鼠的能力,而不影响其经脑内(ic)途径的致病性。源自HSV-1 HFEM毒株DNA以及跨越致病毒株F的HpaI-P序列的MLU DNA片段(坐标0.761至0.796)的重组病毒(M1C1)恢复了经腹腔途径对小鼠的致病性。