Zink Steven D, Burns Drusilla L
CBER, FDA HFM-434, 8800 Rockville Pike, Bethesda, MD 20892, USA.
Infect Immun. 2005 Aug;73(8):5222-8. doi: 10.1128/IAI.73.8.5222-5228.2005.
We examined the effect of mutation of two sortase genes of Bacillus anthracis, srtA and srtB, on the ability of the bacterium to grow in J774A.1 cells, a mouse macrophage-like cell line. While disruption of either srtA or srtB had no effect on the ability of the bacteria to grow in rich culture media, mutations in each of these genes dramatically attenuated growth of the bacterium in J774A.1 cells. Complementation of the mutation restored the ability of bacteria to grow in the cells. Since the initial events in inhalation anthrax are believed to be uptake of B. anthracis spores by alveolar macrophages followed by germination of the spores and growth of the bacteria within the macrophages, these results suggest that two sortases of B. anthracis may be critical in the early stages of inhalation anthrax.
我们研究了炭疽芽孢杆菌的两种分选酶基因srtA和srtB的突变对该细菌在J774A.1细胞(一种小鼠巨噬细胞样细胞系)中生长能力的影响。虽然srtA或srtB的破坏对细菌在丰富培养基中的生长能力没有影响,但这些基因中的每一个发生突变都会显著减弱细菌在J774A.1细胞中的生长。突变的互补恢复了细菌在细胞中生长的能力。由于吸入性炭疽的初始事件被认为是肺泡巨噬细胞摄取炭疽芽孢杆菌孢子,随后孢子萌发并在巨噬细胞内生长,这些结果表明炭疽芽孢杆菌的两种分选酶可能在吸入性炭疽的早期阶段至关重要。