• 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

相似文献

1
Sequential adaptation in latent tuberculosis bacilli: observation by atomic force microscopy (AFM).潜伏性结核杆菌的序贯适应性:通过原子力显微镜(AFM)观察
Int J Clin Exp Med. 2011;4(3):193-9. Epub 2011 Sep 15.
2
Populations of latent Mycobacterium tuberculosis lack a cell wall: Isolation, visualization, and whole-genome characterization.潜伏性结核分枝杆菌群体缺乏细胞壁:分离、可视化及全基因组特征分析
Int J Mycobacteriol. 2016 Mar;5(1):66-73. doi: 10.1016/j.ijmyco.2015.12.001. Epub 2015 Dec 28.
3
Growth and cell-division in extensive (XDR) and extremely drug resistant (XXDR) tuberculosis strains: transmission and atomic force observation.广泛耐药(XDR)和极度耐药(XXDR)结核菌株的生长与细胞分裂:传播与原子力观察
Int J Clin Exp Med. 2010 Sep 30;3(4):308-14.
4
Identification of seven types of pili in : Using atomic force microscopy.利用原子力显微镜鉴定 7 种菌毛。
Int J Mycobacteriol. 2023 Oct-Dec;12(4):478-485. doi: 10.4103/ijmy.ijmy_190_23.
5
Mycobacterial stationary phase induced by low oxygen tension: cell wall thickening and localization of the 16-kilodalton alpha-crystallin homolog.低氧张力诱导的分枝杆菌稳定期:细胞壁增厚及16千道尔顿α-晶状体蛋白同源物的定位
J Bacteriol. 1998 Feb;180(4):801-8. doi: 10.1128/JB.180.4.801-808.1998.
6
THE CORRELATION BETWEEN THE HISTOLOGICAL CHANGES AND THE FATE OF LIVING TUBERCLE BACILLI IN THE ORGANS OF TUBERCULOUS RABBITS.结核兔器官内组织学变化与活菌命运的相关性。
J Exp Med. 1932 Jan 1;55(1):31-54. doi: 10.1084/jem.55.1.31.
7
Anaerobic Mycobacterium tuberculosis Cell Death Stems from Intracellular Acidification Mitigated by the DosR Regulon.厌氧结核分枝杆菌的细胞死亡源于DosR调控子减轻的细胞内酸化。
J Bacteriol. 2017 Oct 31;199(23). doi: 10.1128/JB.00320-17. Print 2017 Dec 1.
8
A mathematical representation of the development of Mycobacterium tuberculosis active, latent and dormant stages.结核分枝杆菌活动期、潜伏期和休眠期发展的数学模型。
J Theor Biol. 2012 Jan 7;292:44-59. doi: 10.1016/j.jtbi.2011.09.025. Epub 2011 Sep 29.
9
Dormancy: How to Fight a Hidden Danger.休眠:如何应对隐藏的危险。
Microorganisms. 2022 Nov 25;10(12):2334. doi: 10.3390/microorganisms10122334.
10
THE FATE OF THE GIANT CELLS IN HEALING TUBERCULOUS TISSUE, AS OBSERVED IN A CASE OF HEALING TUBERCULOUS MENINGITIS.结核组织愈合过程中巨细胞的命运:结核性脑膜炎愈合病例观察。
J Exp Med. 1898 Jan 1;3(1):21-52.

引用本文的文献

1
Nanotechnology meets medicine: applications of atomic force microscopy in disease.纳米技术与医学相遇:原子力显微镜在疾病中的应用
Biophys Rev. 2025 Apr 3;17(2):359-384. doi: 10.1007/s12551-025-01306-w. eCollection 2025 Apr.
2
Age-Dependent Pleomorphism in Cultures.培养物中的年龄依赖性多形性。
Microorganisms. 2025 Feb 20;13(3):475. doi: 10.3390/microorganisms13030475.
3
Drug resistant Mycobacterium tuberculosis strains have altered cell envelope hydrophobicity that influences infection outcomes in human macrophages.耐药结核分枝杆菌菌株改变了细胞包膜疏水性,这会影响人类巨噬细胞中的感染结果。
Sci Rep. 2024 Dec 28;14(1):30840. doi: 10.1038/s41598-024-81457-0.
4
Drug resistant strains have altered cell envelope hydrophobicity that influences infection outcomes in human macrophages.耐药菌株改变了细胞包膜疏水性,这会影响人类巨噬细胞中的感染结果。
bioRxiv. 2024 Apr 11:2024.04.10.588986. doi: 10.1101/2024.04.10.588986.
5
Drug-resistant strains of : cell envelope profiles and interactions with the host.耐药菌株:细胞包膜特征及其与宿主的相互作用。
Front Cell Infect Microbiol. 2023 Oct 27;13:1274175. doi: 10.3389/fcimb.2023.1274175. eCollection 2023.
6
The Biological and Clinical Aspects of a Latent Tuberculosis Infection.潜伏性结核感染的生物学及临床特征
Trop Med Infect Dis. 2022 Mar 8;7(3):48. doi: 10.3390/tropicalmed7030048.
7
Drug Susceptibility Screening Using In Vitro Models of Hypoxic Non-Replicating Persistent Mycobacteria.利用缺氧非复制持久分枝杆菌的体外模型进行药物敏感性筛查。
Methods Mol Biol. 2021;2314:247-260. doi: 10.1007/978-1-0716-1460-0_10.
8
HflX is a GTPase that controls hypoxia-induced replication arrest in slow-growing mycobacteria.HflX 是一种 GTPase,可控制低氧诱导的缓慢生长分枝杆菌的复制停滞。
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12). doi: 10.1073/pnas.2006717118.
9
Cells Surviving in the Continued Presence of Bactericidal Concentrations of Rifampicin Develop Negatively Charged Thickened Capsular Outer Layer That Restricts Permeability to the Antibiotic.在杀菌浓度的利福平持续存在的情况下存活的细胞会形成带负电荷的增厚荚膜外层,这会限制抗生素的通透性。
Front Microbiol. 2020 Dec 17;11:554795. doi: 10.3389/fmicb.2020.554795. eCollection 2020.
10
Mechanisms of Drug-Induced Tolerance in Mycobacterium tuberculosis.药物诱导的结核分枝杆菌耐药机制。
Clin Microbiol Rev. 2020 Oct 14;34(1). doi: 10.1128/CMR.00141-20. Print 2020 Dec 16.

本文引用的文献

1
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.
2
New insight into extremely drug-resistant tuberculosis: using atomic force microscopy.对极端耐药结核病的新见解:使用原子力显微镜。
Eur Respir J. 2010 Dec;36(6):1490-3. doi: 10.1183/09031936.00064510.
3
Growth and cell-division in extensive (XDR) and extremely drug resistant (XXDR) tuberculosis strains: transmission and atomic force observation.广泛耐药(XDR)和极度耐药(XXDR)结核菌株的生长与细胞分裂:传播与原子力观察
Int J Clin Exp Med. 2010 Sep 30;3(4):308-14.
4
Do mycobacteria produce endospores?分枝杆菌会产生芽孢吗?
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):878-81. doi: 10.1073/pnas.0911299107. Epub 2009 Dec 22.
5
Sporulation in mycobacteria.分枝杆菌中的孢子形成
Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10781-6. doi: 10.1073/pnas.0904104106. Epub 2009 Jun 16.
6
On the nature of Mycobacterium tuberculosis-latent bacilli.论结核分枝杆菌潜伏菌的本质
Eur Respir J. 2004 Dec;24(6):1044-51. doi: 10.1183/09031936.04.00072604.
7
Electron microscopy analysis of Mycobacterium tuberculosis cell division.结核分枝杆菌细胞分裂的电子显微镜分析。
FEMS Microbiol Lett. 2004 Nov 1;240(1):15-20. doi: 10.1016/j.femsle.2004.09.004.
8
Fate of Mycobacterium tuberculosis in mouse tissues as determined by the microbial enumeration technique. I. The persistence of drug-susceptible tubercle bacilli in the tissues despite prolonged antimicrobial therapy.通过微生物计数技术测定小鼠组织中结核分枝杆菌的命运。I. 尽管进行了长时间的抗菌治疗,组织中仍存在对药物敏感的结核杆菌。
J Exp Med. 1956 Nov 1;104(5):737-62. doi: 10.1084/jem.104.5.737.
9
[Tuberculosis etiology].[结核病病因学]
Dtsch Gesundheitsw. 1952 Apr 10;7(15):457-65.
10
Mycobacterial persistence and immunity.分枝杆菌的持续性与免疫。
Front Biosci. 2002 Feb 1;7:d458-69. doi: 10.2741/A788.

潜伏性结核杆菌的序贯适应性:通过原子力显微镜(AFM)观察

Sequential adaptation in latent tuberculosis bacilli: observation by atomic force microscopy (AFM).

作者信息

Velayati Ali Akbar, Farnia Parissa, Masjedi Mohammad Reza, Zhavnerko Gennady Konstantinovich, Merza Muayad Aghali, Ghanavi Jalladein, Tabarsi Payam, Farnia Poopak, Poleschuyk Nikolai Nikolaevich, Ignatyev George

出版信息

Int J Clin Exp Med. 2011;4(3):193-9. Epub 2011 Sep 15.

PMID:21977232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3182511/
Abstract

Mycobacterium tuberculosis (MTB) can persist within the human host for years without causing disease, in a syndrome known as latent tuberculosis. The mechanisms by which M. tuberculosis establishes a latent metabolic state is unknown, but it is hypothesized that reduced oxygen tension may trigger the bacillus to enter a state of latency. Therefore, we are studying anaerobic culture of M. tuberculosis (H37RV) as a model of latency. For the first time, the sequential adaptation of latent bacilli (every 90 days for 48 months) viewed under Atomic Force Microscopy (AFM). Two types of adaptation were observed and are described here. First, cells are undergoing temporary adaptation (from 1 to 18 months of latency) that includes; thickening of cell wall (20.5±1.8 nm versus 15.2±1.8 nm, P<0.05), formation of ovoid cells by "folding phenomena"(65-70%), size reduction (0.8±0.1 μm versus 2.5±0.5 μm), and budding type of cell division (20-25%).A second feature include changes that accompany development of specialized cells i.e., production of spore like cells (0.5±0.2 μm) and their progeny (filterable non -acid fast forms; 150 to 300 μm in size). Although, these cells were not real spore because they fail to form a heat resistant colony forming units, after incubation for 35-40 min at 65°C. The filterable non-acid fast forms of bacilli are metabolically active and increased their number by symmetrical type of cell-division. Therefore, survival strategies that developed by M. tuberculosis under oxygen limited condition are linked to its shape, size and conspicuous loss of acid fastness.

摘要

结核分枝杆菌(MTB)可在人类宿主体内潜伏数年而不引发疾病,这种综合征被称为潜伏性结核病。结核分枝杆菌建立潜伏代谢状态的机制尚不清楚,但据推测,氧张力降低可能促使该杆菌进入潜伏状态。因此,我们正在研究结核分枝杆菌(H37RV)的厌氧培养,以此作为潜伏模型。首次在原子力显微镜(AFM)下观察到潜伏杆菌的顺序适应性变化(每90天观察一次,共48个月)。观察到两种类型的适应性变化并在此进行描述。首先,细胞经历暂时适应性变化(潜伏1至18个月),包括:细胞壁增厚(20.5±1.8纳米对15.2±1.8纳米,P<0.05),通过“折叠现象”形成卵形细胞(65 - 70%),尺寸减小(0.8±0.1微米对2.5±0.5微米),以及出芽型细胞分裂(20 - 25%)。第二个特征包括伴随特殊细胞发育的变化,即产生类孢子细胞(0.5±0.2微米)及其后代(可过滤的非抗酸形式;大小为150至300微米)。尽管这些细胞并非真正的孢子,因为它们在65°C孵育35 - 40分钟后无法形成耐热菌落形成单位。杆菌的可过滤非抗酸形式具有代谢活性,并通过对称型细胞分裂增加其数量。因此,结核分枝杆菌在氧气受限条件下形成的生存策略与其形状、大小以及显著的抗酸性丧失有关。