Yager J A, Prescott C A, Kramar D P, Hannah H, Balson G A, Croy B A
Department of Pathology, Ontario Veterinary College, University of Guelph, Ontario, Canada.
Vet Microbiol. 1991 Aug 30;28(4):363-76. doi: 10.1016/0378-1135(91)90071-m.
To investigate the pathogenesis of respiratory lesions caused by the facultative intracellular pathogen, Rhodococcus equi, pulmonary clearance was compared in four groups of genetically defined mice, chosen for their specific deficits in immune and inflammatory responses. Complement-deficient A/J, immunodeficient nu/nu (nude), scid/scid.bg/bg (SCID/beige), C57BI/6J.bg/bg (beige) and normal Swiss mice (SW) received approximately 10(7) R. equi intranasally on day 0. Bacterial clearance was assessed in lung, liver and spleen on days 1, 4, 7 and 14. Pulmonary clearance was not significantly different between SW and A/J mice. Beige mice cleared R. equi more rapidly and completely than A/J and SW, indicating that deficits in phagocytic and NK cell function associated with the bg/bg gene did not compromise clearance. Pulmonary clearance in immunodeficient SCID/beige mice paralleled that of the SW and A/J mice initially but bacterial proliferation produced significant differences from SW mice at day 14. Nude mice were unable to clear R. equi from day 1, resulting in the death of two nude mice at day 11. Both SCID/beige and nude mice developed severe pyogranulomatous bronchopneumonia, whereas A/J and SW mice developed transient pulmonary lesions. Beige mice developed minimal lung lesions. Significant systemic bacterial proliferation occurred only in nude and SCID/beige mice. We conclude that deficiencies in complement components, phagocytic and NK cells do not impair the pulmonary clearance of R. equi but that a competent cellular immune system is required to prevent pneumonia and death. The difference in early phase pulmonary clearance in nude and SCID/beige mice indicates two phases are important for clearance. An acapsular mutant of R. equi was completely cleared from the lungs of SCID/beige mice suggesting an important role for the capsule in virulence for mice.
为了研究兼性胞内病原体马红球菌引起呼吸道病变的发病机制,我们比较了四组基因明确的小鼠的肺清除情况,这些小鼠因其在免疫和炎症反应方面的特定缺陷而被选用。补体缺陷的A/J小鼠、免疫缺陷的裸鼠(nu/nu)、重症联合免疫缺陷/米色小鼠(scid/scid.bg/bg,SCID/米色)、C57BI/6J.bg/bg(米色)小鼠和正常的瑞士小鼠(SW)在第0天经鼻接种约10⁷个马红球菌。在第1、4、7和14天评估肺、肝和脾中的细菌清除情况。SW小鼠和A/J小鼠的肺清除情况没有显著差异。米色小鼠比A/J和SW小鼠更快速、更彻底地清除马红球菌,这表明与bg/bg基因相关的吞噬细胞和自然杀伤(NK)细胞功能缺陷并未损害清除能力。免疫缺陷的SCID/米色小鼠的肺清除情况最初与SW和A/J小鼠相似,但在第14天细菌增殖导致与SW小鼠出现显著差异。裸鼠从第1天起就无法清除马红球菌,导致两只裸鼠在第11天死亡。SCID/米色小鼠和裸鼠均发生了严重的脓性肉芽肿性支气管肺炎,而A/J和SW小鼠出现了短暂的肺部病变。米色小鼠的肺部病变最小。仅在裸鼠和SCID/米色小鼠中发生了显著的全身细菌增殖。我们得出结论,补体成分、吞噬细胞和NK细胞的缺陷不会损害马红球菌的肺清除能力,但需要有功能的细胞免疫系统来预防肺炎和死亡。裸鼠和SCID/米色小鼠早期肺清除情况的差异表明两个阶段对清除都很重要。马红球菌的无荚膜突变体从SCID/米色小鼠的肺部被完全清除,这表明荚膜在对小鼠的毒力方面起重要作用。