Riera L, Gariglio M, Pagano M, Gaiola O, Simon M M, Landolfo S
Department of Public Health and Microbiology, Medical School, Torino, Italy.
New Microbiol. 2001 Jul;24(3):231-8.
The course of mouse cytomegalovirus (MCMV) infection was compared between mutant C57BL/6 (B6) mice deficient in either perforin (perf-/-), or perforin, granzyme A and B (perfxgzmAxB-/-), and B6 gld mice lacking functionally active Fas ligand to elucidate the contribution of the two main cytolytic pathways in the early control of MCMV infection. At 15 and 30 days post infection (p.i.) virus titers were elevated in salivary glands of perf-/- and perfxgzmAxB-/-, but almost undetectable in those of mutant gld and C57BL/6 wild-type mice. No virus was detectable in lung and spleen tissues of the mutant or B6 mice at the time points tested. At 15 days p.i., scanty lymphocytic periductal infiltration was seen in salivary glands of perf-/- and perfxgzmAxB-/; these pathological alterations were minimal at 30 days p.i.. In contrast, no pathological alterations were seen in the respective organs of infected B6 and gld mice at the two time points p.i.. At 15 days p.i., reactive follicles were observed in the white pulp of spleen tissues from both mutant and B6 mice, but at 30 days p.i. only in those of mutant mice. No inflammatory responses were seen in the lung tissues of any of the four mouse strains tested. Together with previous observations (Riera et al.. 2000), the results demonstrate that both perforin and granzymes A/B, but not the FasL/Fas system are critical for viral elimination in salivary glands during the acute phase of infection. However, for the long-term control of MCMV infection, neither of the two cytolytic pathways seem to be necessary.
比较了穿孔素缺陷型(perf-/-)、穿孔素、颗粒酶A和B缺陷型(perfxgzmAxB-/-)的突变C57BL/6(B6)小鼠以及缺乏功能性活性Fas配体的B6 gld小鼠的小鼠巨细胞病毒(MCMV)感染过程,以阐明两种主要细胞溶解途径在MCMV感染早期控制中的作用。感染后15天和30天(p.i.),perf-/-和perfxgzmAxB-/-小鼠唾液腺中的病毒滴度升高,但在突变gld小鼠和C57BL/6野生型小鼠的唾液腺中几乎检测不到。在测试的时间点,突变小鼠或B6小鼠的肺和脾组织中均未检测到病毒。感染后15天,在perf-/-和perfxgzmAxB-/-小鼠的唾液腺中可见少量淋巴细胞导管周围浸润;这些病理改变在感染后30天时最小。相比之下,在感染后两个时间点,感染的B6和gld小鼠的相应器官中均未观察到病理改变。感染后15天,在突变小鼠和B6小鼠脾脏组织的白髓中均观察到反应性滤泡,但在感染后30天,仅在突变小鼠中观察到。在所测试的四种小鼠品系的肺组织中均未观察到炎症反应。与先前的观察结果(Riera等人,2000年)一起,结果表明,在感染急性期,穿孔素和颗粒酶A/B对唾液腺中的病毒清除至关重要,但FasL/Fas系统并非如此。然而,对于MCMV感染的长期控制,这两种细胞溶解途径似乎都不是必需的。