Yang Yong, Richards Jacob P, Gundrum Jennifer, Ojha Anil K
Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, NY, United States.
Department of Infectious Diseases and Microbiology, University of Pittsburgh, Pittsburgh, PA, United States.
Front Microbiol. 2018 Jul 4;9:1428. doi: 10.3389/fmicb.2018.01428. eCollection 2018.
Mycobacteria spontaneously form surface-associated multicellular communities, called biofilms, which display resistance to a wide range of exogenous stresses. A causal relationship between biofilm formation and emergence of stress resistance is not known. Here, we report that activation of a nitrogen starvation response regulator, GlnR, during the development of biofilms leads to peroxide resistance. The resistance arises from induction of a GlnR-dependent peroxide resistance () gene cluster comprising of 8 ORFs (MSMEG_0565-0572). Expression of increases the NADPH to NADP ratio, suggesting that a reduced cytosolic environment of nitrogen-starved cells in biofilms contributes to peroxide resistance. Increased NADPH levels from activity likely support the activity of enzymes involved in nitrogen assimilation, as suggested by a higher threshold of nitrogen supplement required by a mutant to form biofilms. Together, our study uniquely interlinks a nutrient sensing mechanism with emergence of stress resistance during mycobacterial biofilm development. The gene cluster is conserved in several mycobacteria that can cause nosocomial infections, offering a possible explanation for their resistance to peroxide-based sterilization of medical equipment.
分枝杆菌能自发形成与表面相关的多细胞群落,即生物膜,这些生物膜对多种外源应激具有抗性。生物膜形成与应激抗性出现之间的因果关系尚不清楚。在此,我们报告在生物膜形成过程中,氮饥饿反应调节因子GlnR的激活导致了对过氧化物的抗性。这种抗性源于诱导一个由8个开放阅读框(MSMEG_0565 - 0572)组成的依赖GlnR的过氧化物抗性()基因簇。的表达增加了NADPH与NADP的比率,这表明生物膜中氮饥饿细胞的胞质环境还原有助于过氧化物抗性。来自活性的NADPH水平升高可能支持参与氮同化的酶的活性,这一点由突变体形成生物膜所需的更高氮补充阈值所表明。总之,我们的研究独特地将一种营养感知机制与分枝杆菌生物膜形成过程中应激抗性的出现联系起来。该基因簇在几种可引起医院感染的分枝杆菌中是保守的,这为它们对基于过氧化物的医疗设备消毒的抗性提供了一种可能的解释。