Ehrt S, Shiloh M U, Ruan J, Choi M, Gunzburg S, Nathan C, Xie Q, Riley L W
Division of International Medicine and Infectious Disease, Department of Medicine, Cornell University Medical College, New York 10021, USA.
J Exp Med. 1997 Dec 1;186(11):1885-96. doi: 10.1084/jem.186.11.1885.
Among the major antimicrobial products of macrophages are reactive intermediates of the oxidation of nitrogen (RNI) and the reduction of oxygen (ROI). Selection of recombinants in acidified nitrite led to the cloning of a novel gene, noxR1, from a pathogenic clinical isolate of Mycobacterium tuberculosis. Expression of noxR1 conferred upon Escherichia coli and Mycobacterium smegmatis enhanced ability to resist RNI and ROI, whether the bacteria were exposed to exogenous compounds in medium or to endogenous products in macrophages. These studies provide the first identification of an RNI resistance mechanism in mycobacteria, point to a new mechanism for resistance to ROI, and raise the possibility that inhibition of the noxR1 pathway might enhance the ability of macrophages to control tuberculosis.
巨噬细胞的主要抗菌产物包括氮氧化反应中间体(RNI)和氧还原反应中间体(ROI)。在酸化亚硝酸盐中筛选重组体,导致从结核分枝杆菌的致病性临床分离株中克隆出一个新基因noxR1。noxR1的表达使大肠杆菌和耻垢分枝杆菌抵抗RNI和ROI的能力增强,无论细菌是暴露于培养基中的外源性化合物还是巨噬细胞中的内源性产物。这些研究首次鉴定了分枝杆菌中的RNI抗性机制,指出了一种新的ROI抗性机制,并增加了抑制noxR1途径可能增强巨噬细胞控制结核病能力的可能性。