Schlosser-Silverman E, Elgrably-Weiss M, Rosenshine I, Kohen R, Altuvia S
Department of Molecular Genetics and Biotechnology, The Hebrew University-Hadassah Medical School, The Hebrew University, Jerusalem, Israel.
J Bacteriol. 2000 Sep;182(18):5225-30. doi: 10.1128/JB.182.18.5225-5230.2000.
Macrophages are armed with multiple oxygen-dependent and -independent bactericidal properties. However, the respiratory burst, generating reactive oxygen species, is believed to be a major cause of bacterial killing. We exploited the susceptibility of Escherichia coli in macrophages to characterize the effects of the respiratory burst on intracellular bacteria. We show that E. coli strains recovered from J774 macrophages exhibit high rates of mutations. We report that the DNA damage generated inside macrophages includes DNA strand breaks and the modification 8-oxo-2'-deoxyguanosine, which are typical oxidative lesions. Interestingly, we found that under these conditions, early in the infection the majority of E. coli cells are viable but gene expression is inhibited. Our findings demonstrate that macrophages can cause severe DNA damage to intracellular bacteria. Our results also suggest that protection against the macrophage-induced DNA damage is an important component of the bacterial defense mechanism within macrophages.
巨噬细胞具备多种依赖氧和不依赖氧的杀菌特性。然而,产生活性氧的呼吸爆发被认为是细菌杀伤的主要原因。我们利用大肠杆菌在巨噬细胞中的易感性来表征呼吸爆发对细胞内细菌的影响。我们发现从J774巨噬细胞中回收的大肠杆菌菌株表现出高突变率。我们报告称,巨噬细胞内产生的DNA损伤包括DNA链断裂和8-氧代-2'-脱氧鸟苷修饰,这些都是典型的氧化损伤。有趣的是,我们发现在这些条件下,在感染早期大多数大肠杆菌细胞是存活的,但基因表达受到抑制。我们的研究结果表明,巨噬细胞可对细胞内细菌造成严重的DNA损伤。我们的结果还表明,抵御巨噬细胞诱导的DNA损伤是巨噬细胞内细菌防御机制的重要组成部分。