• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.3389/fcimb.2017.00370
PMID:28861399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5562752/
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/5562752/695ec27e37cb/fcimb-07-00370-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/4799d7f5ad7c/fcimb-07-00370-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/db48cba24f02/fcimb-07-00370-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/0de7976fb94c/fcimb-07-00370-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/3895bee249ba/fcimb-07-00370-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/98e1a07ec82b/fcimb-07-00370-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/695ec27e37cb/fcimb-07-00370-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/4799d7f5ad7c/fcimb-07-00370-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/db48cba24f02/fcimb-07-00370-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/0de7976fb94c/fcimb-07-00370-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/3895bee249ba/fcimb-07-00370-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/98e1a07ec82b/fcimb-07-00370-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e69c/5562752/695ec27e37cb/fcimb-07-00370-g0006.jpg

相似文献

1
Overexpression of Adenylyl Cyclase Encoded by the Rv2212 Gene Confers Improved Fitness, Accelerated Recovery from Dormancy and Enhanced Virulence in Mice.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。
Front Cell Infect Microbiol. 2017 Aug 17;7:370. doi: 10.3389/fcimb.2017.00370. eCollection 2017.
2
Interaction of Erp Protein of Mycobacterium tuberculosis with Rv2212 Enhances Intracellular Survival of Mycobacterium smegmatis.结核分枝杆菌的Erp蛋白与Rv2212的相互作用增强耻垢分枝杆菌的细胞内存活能力。
J Bacteriol. 2016 Sep 22;198(20):2841-52. doi: 10.1128/JB.00120-16. Print 2016 Oct 15.
3
Cyclic AMP-dependent resuscitation of dormant Mycobacteria by exogenous free fatty acids.外源性游离脂肪酸通过环 AMP 依赖性复苏休眠分枝杆菌。
PLoS One. 2013 Dec 23;8(12):e82914. doi: 10.1371/journal.pone.0082914. eCollection 2013.
4
BCG constitutively expressing the adenylyl cyclase encoded by Rv2212 increases its immunogenicity and reduces replication of M. tuberculosis in lungs of BALB/c mice.持续表达由Rv2212编码的腺苷酸环化酶的卡介苗可增强其免疫原性,并减少结核分枝杆菌在BALB/c小鼠肺部的复制。
Tuberculosis (Edinb). 2018 Dec;113:19-25. doi: 10.1016/j.tube.2018.08.012. Epub 2018 Aug 24.
5
The adenylyl cyclase Rv2212 modifies the proteome and infectivity of Mycobacterium bovis BCG.腺苷酸环化酶Rv2212可改变卡介苗的蛋白质组和感染性。
Folia Microbiol (Praha). 2015 Jan;60(1):21-31. doi: 10.1007/s12223-014-0335-1. Epub 2014 Jul 21.
6
Chemical activation of adenylyl cyclase Rv1625c inhibits growth of Mycobacterium tuberculosis on cholesterol and modulates intramacrophage signaling.腺苷酸环化酶Rv1625c的化学激活抑制结核分枝杆菌在胆固醇上的生长并调节巨噬细胞内信号传导。
Mol Microbiol. 2017 Jul;105(2):294-308. doi: 10.1111/mmi.13701. Epub 2017 May 23.
7
Cyclic AMP in mycobacteria: characterization and functional role of the Rv1647 ortholog in Mycobacterium smegmatis.分枝杆菌中的环磷酸腺苷:耻垢分枝杆菌中Rv1647直系同源物的特性及功能作用
J Bacteriol. 2008 Jun;190(11):3824-34. doi: 10.1128/JB.00138-08. Epub 2008 Apr 4.
8
Cholesterol plays a larger role during Mycobacterium tuberculosis in vitro dormancy and reactivation than previously suspected.胆固醇在结核分枝杆菌体外休眠和再激活过程中所起的作用比之前认为的更大。
Tuberculosis (Edinb). 2017 Mar;103:1-9. doi: 10.1016/j.tube.2016.12.004. Epub 2016 Dec 18.
9
PE17 protein from Mycobacterium tuberculosis enhances Mycobacterium smegmatis survival in macrophages and pathogenicity in mice.结核分枝杆菌 PE17 蛋白增强耻垢分枝杆菌在巨噬细胞中的存活能力并提高其在小鼠中的致病性。
Microb Pathog. 2019 Jan;126:63-73. doi: 10.1016/j.micpath.2018.10.030. Epub 2018 Oct 23.
10
Cyclic AMP intoxication of macrophages by a Mycobacterium tuberculosis adenylate cyclase.结核分枝杆菌腺苷酸环化酶对巨噬细胞的环磷酸腺苷中毒作用
Nature. 2009 Jul 2;460(7251):98-102. doi: 10.1038/nature08123. Epub 2009 Jun 10.

引用本文的文献

1
Exploiting cAMP signaling in Mycobacterium tuberculosis for drug discovery.利用结核分枝杆菌中的环磷酸腺苷信号进行药物研发。
Trends Microbiol. 2024 Sep;32(9):874-883. doi: 10.1016/j.tim.2024.01.008. Epub 2024 Feb 14.
2
Cyclic AMP-Mediated Inhibition of Cholesterol Catabolism in by the Novel Drug Candidate GSK2556286.新型药物候选物 GSK2556286 通过环磷酸腺苷抑制 中的胆固醇分解代谢。
Antimicrob Agents Chemother. 2023 Jan 24;67(1):e0129422. doi: 10.1128/aac.01294-22. Epub 2023 Jan 5.
3
CRISPR Interference of Adenylate Cyclases from .

本文引用的文献

1
Interaction of Erp Protein of Mycobacterium tuberculosis with Rv2212 Enhances Intracellular Survival of Mycobacterium smegmatis.结核分枝杆菌的Erp蛋白与Rv2212的相互作用增强耻垢分枝杆菌的细胞内存活能力。
J Bacteriol. 2016 Sep 22;198(20):2841-52. doi: 10.1128/JB.00120-16. Print 2016 Oct 15.
2
Characterization of a cAMP responsive transcription factor, Cmr (Rv1675c), in TB complex mycobacteria reveals overlap with the DosR (DevR) dormancy regulon.结核分枝杆菌复合群中一种环磷酸腺苷(cAMP)反应性转录因子Cmr(Rv1675c)的特性揭示其与DosR(DevR)休眠调节子存在重叠。
Nucleic Acids Res. 2016 Jan 8;44(1):134-51. doi: 10.1093/nar/gkv889. Epub 2015 Sep 10.
3
来自……的腺苷酸环化酶的CRISPR干扰
Appl Biochem Microbiol. 2021;57(4):421-425. doi: 10.1134/S0003683821040128. Epub 2021 Jul 27.
4
Dormant Cell Formation and Photodynamic Inactivation.休眠细胞形成与光动力灭活
Front Microbiol. 2020 Dec 18;11:605899. doi: 10.3389/fmicb.2020.605899. eCollection 2020.
5
Mycobacterial Control of Host Mitochondria: Bioenergetic and Metabolic Changes Shaping Cell Fate and Infection Outcome.分枝杆菌对宿主线粒体的控制:生物能量和代谢变化塑造细胞命运和感染结局。
Front Cell Infect Microbiol. 2020 Sep 30;10:457. doi: 10.3389/fcimb.2020.00457. eCollection 2020.
6
Prolonged infection triggered by dormant Mycobacterium tuberculosis: Immune and inflammatory responses in lungs of genetically susceptible and resistant mice.潜伏结核分枝杆菌引发的长期感染:易感和抗性基因小鼠肺部的免疫和炎症反应。
PLoS One. 2020 Sep 24;15(9):e0239668. doi: 10.1371/journal.pone.0239668. eCollection 2020.
7
One-Year Old Dormant, "Non-culturable" Preserves Significantly Diverse Protein Profile.一年休眠“不可培养”状态保存了显著不同的蛋白质谱。
Front Cell Infect Microbiol. 2020 Jan 31;10:26. doi: 10.3389/fcimb.2020.00026. eCollection 2020.
8
What bacteria want.细菌的欲望
Environ Microbiol. 2018 Dec;20(12):4221-4229. doi: 10.1111/1462-2920.14398. Epub 2018 Oct 25.
Cyclic AMP Signaling in Mycobacteria.
分枝杆菌中的环 AMP 信号转导
Microbiol Spectr. 2014 Apr;2(2). doi: 10.1128/microbiolspec.MGM2-0011-2013.
4
Role of intragenic binding of cAMP responsive protein (CRP) in regulation of the succinate dehydrogenase genes Rv0249c-Rv0247c in TB complex mycobacteria.环磷酸腺苷反应蛋白(CRP)基因内结合在结核分枝杆菌复合群中琥珀酸脱氢酶基因Rv0249c - Rv0247c调控中的作用
Nucleic Acids Res. 2015 Jun 23;43(11):5377-93. doi: 10.1093/nar/gkv420. Epub 2015 May 4.
5
The adenylyl cyclase Rv2212 modifies the proteome and infectivity of Mycobacterium bovis BCG.腺苷酸环化酶Rv2212可改变卡介苗的蛋白质组和感染性。
Folia Microbiol (Praha). 2015 Jan;60(1):21-31. doi: 10.1007/s12223-014-0335-1. Epub 2014 Jul 21.
6
Mycobacterium tuberculosis subverts the TLR-2-MyD88 pathway to facilitate its translocation into the cytosol.结核分枝杆菌破坏Toll样受体2-髓样分化因子88信号通路,以促进其向胞质溶胶的转运。
PLoS One. 2014 Jan 27;9(1):e86886. doi: 10.1371/journal.pone.0086886. eCollection 2014.
7
Cyclic AMP-dependent resuscitation of dormant Mycobacteria by exogenous free fatty acids.外源性游离脂肪酸通过环 AMP 依赖性复苏休眠分枝杆菌。
PLoS One. 2013 Dec 23;8(12):e82914. doi: 10.1371/journal.pone.0082914. eCollection 2013.
8
Dysregulation of serine biosynthesis contributes to the growth defect of a Mycobacterium tuberculosis crp mutant.丝氨酸生物合成的失调导致结核分枝杆菌 crp 突变体的生长缺陷。
Mol Microbiol. 2011 Oct;82(1):180-98. doi: 10.1111/j.1365-2958.2011.07806.x. Epub 2011 Sep 8.
9
Reversible acetylation and inactivation of Mycobacterium tuberculosis acetyl-CoA synthetase is dependent on cAMP.结核分枝杆菌乙酰辅酶 A 合成酶的可逆乙酰化和失活依赖于 cAMP。
Biochemistry. 2011 Jul 5;50(26):5883-92. doi: 10.1021/bi200156t. Epub 2011 Jun 10.
10
Dormant ovoid cells of Mycobacterium tuberculosis are formed in response to gradual external acidification.结核分枝杆菌的休眠卵圆细胞是对外界逐渐酸化的反应而形成的。
Tuberculosis (Edinb). 2011 Mar;91(2):146-54. doi: 10.1016/j.tube.2010.12.006. Epub 2011 Jan 22.