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由Rv2212基因编码的腺苷酸环化酶过表达赋予小鼠更好的适应性、加速从休眠状态恢复以及增强毒力。

Overexpression of Adenylyl Cyclase Encoded by the Rv2212 Gene Confers Improved Fitness, Accelerated Recovery from Dormancy and Enhanced Virulence in Mice.

作者信息

Shleeva Margarita O, Kondratieva Tatyana K, Demina Galina R, Rubakova Elvira I, Goncharenko Anna V, Apt Alexander S, Kaprelyants Arseny S

机构信息

Federal Research Centre 'Fundamentals of Biotechnology' of the Russian Academy of Sciences, A. N. Bach Institute of BiochemistryMoscow, Russia.

Department of Immunology, Laboratory for Immunogenetics, Central Institute for TuberculosisMoscow, Russia.

出版信息

Front Cell Infect Microbiol. 2017 Aug 17;7:370. doi: 10.3389/fcimb.2017.00370. eCollection 2017.

Abstract

Earlier we demonstrated that the adenylyl cyclase (AC) encoded by the gene plays a key role in the resuscitation and growth of dormant and that overexpression of this gene leads to an increase in intracellular cAMP concentration and prevents the transition of from active growth to dormancy in an extended stationary phase accompanied by medium acidification. We surmised that the homologous gene of (), the main cAMP producer, plays similar physiological roles by supporting, under these conditions, the active state and reactivation of dormant bacteria. To test this hypothesis, we established strain overexpressing and compared its and growth characteristics with a control strain. , the AC-overexpressing pMind strain demonstrated faster growth in a liquid medium, prolonged capacity to form CFUs and a significant delay or even prevention of transition toward dormancy. AC-overexpressing cells exhibited easier recovery from dormancy. , AC-overexpressing bacteria demonstrated significantly higher growth rates (virulence) in the lungs and spleens of infected mice compared to the control strain, and, unlike the latter, killed mice in the TB-resistant strain before month 8 of infection. Even in the absence of selecting hygromycin B, all pMind CFUs retained the insert during growth, strongly suggesting that AC overexpression is beneficial for bacteria. Taken together, our results indicate that cAMP supports the maintenance of cells vitality under unfavorable conditions and their virulence .

摘要

我们之前证明,由该基因编码的腺苷酸环化酶(AC)在休眠菌的复苏和生长中起关键作用,并且该基因的过表达会导致细胞内cAMP浓度升高,并在伴随着培养基酸化的延长稳定期阻止菌从活跃生长转变为休眠。我们推测,主要的cAMP产生菌的同源基因()在这些条件下通过支持休眠细菌的活跃状态和重新激活发挥类似的生理作用。为了验证这一假设,我们构建了过表达的菌株,并将其生长和存活特性与对照菌株进行比较。过表达AC的pMind菌株在液体培养基中生长更快,形成菌落形成单位(CFU)的能力延长,并且向休眠转变显著延迟甚至被阻止。过表达AC的细胞从休眠中恢复更容易。此外,与对照菌株相比,过表达AC的细菌在感染小鼠的肺和脾中表现出显著更高的生长速率(毒力),并且与对照菌株不同,在感染8个月前就在耐结核菌株中杀死了小鼠。即使在没有选择潮霉素B的情况下,所有pMind CFU在生长期间都保留了插入片段,强烈表明AC过表达对细菌有益。综上所述,我们的结果表明,cAMP在不利条件下支持细胞活力的维持及其毒力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/4799d7f5ad7c/fcimb-07-00370-g0001.jpg

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