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The Capacity of Mycobacterium tuberculosis To Survive Iron Starvation Might Enable It To Persist in Iron-Deprived Microenvironments of Human Granulomas

机译:结核分枝杆菌维持铁饥饿的能力可能使其持续存在于人类肉芽肿缺铁的微环境中

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摘要

This study was conducted to investigate the role of iron deprivation in the persistence of Mycobacterium tuberculosis. We present evidence of iron restriction in human necrotic granulomas and demonstrate that under iron starvation M. tuberculosis persists, refractive to antibiotics and capable of restarting replication when iron is made available. Transcriptomics and metabolomic analyses indicated that the persistence of M. tuberculosis under iron starvation is dependent on strict control of endogenous Fe utilization and is associated with upregulation of pathogenicity and intrinsic antibiotic resistance determinants. M. tuberculosis mutants compromised in their ability to survive Fe starvation were identified. The findings of this study advance the understanding of the physiological settings that may underpin the chronicity of human tuberculosis (TB) and are relevant to the design of effective antitubercular therapies. IMPORTANCE One-third of the world population may harbor persistent M. tuberculosis, causing an asymptomatic infection that is refractory to treatment and can reactivate to become potentially lethal tuberculosis disease. However, little is known about the factors that trigger and maintain M. tuberculosis persistence in infected individuals. Iron is an essential nutrient for M. tuberculosis growth. In this study, we show, first, that in human granulomas the immune defense creates microenvironments in which M. tuberculosis likely experiences drastic Fe deprivation and, second, that Fe-starved M. tuberculosis is capable of long-term persistence without growth. Together, these observations suggest that Fe deprivation in the lung might trigger a state of persistence in M. tuberculosis and promote chronic TB. We also identified vulnerabilities of iron-restricted persistent M. tuberculosis, which can be exploited for the design of new antitubercular therapies.
机译:进行这项研究以调查铁缺乏在结核分枝杆菌持续存在中的作用。我们目前在人类坏死肉芽肿中铁限制的证据,并证明在铁饥饿的情况下,结核分枝杆菌持续存在,对抗生素具有屈光性,并在铁可用时能够重新开始复制​​。转录组学和代谢组学分析表明,铁饥饿状态下结核分枝杆菌的持续存在取决于严格控制内源铁的利用,并与致病性和内在抗生素耐药性决定因素的上调有关。鉴定了在铁饥饿中存活能力受损的结核分枝杆菌突变体。这项研究的发现提高了对可能支持人类结核病(TB)慢性病的生理环境的理解,并且与有效的抗结核疗法的设计有关。重要性世界上三分之一的人口可能患有持久性结核分枝杆菌,导致无症状的感染,这种症状难以治疗,并且可以重新活化成潜在的致命性结核病。但是,关于触发和维持感染个体中结核分枝杆菌持久性的因素知之甚少。铁是结核分枝杆菌生长的必需营养素。在这项研究中,我们表明,首先,在人类肉芽肿中,免疫防御产生了微环境,其中结核分枝杆菌可能会经历铁的急剧剥夺;其次,缺铁的结核分枝杆菌能够长期坚持而没有生长。总之,这些观察结果表明,肺中铁的缺乏可能触发结核分枝杆菌的持续状态并促进慢性结核病。我们还确定了铁限制的持久性结核分枝杆菌的弱点,可以利用该弱点来设计新的抗结核疗法。

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