Live-cell and super-resolution imaging reveal that the distribution of wall-associated protein A is correlated with the cell chain integrity of Streptococcus mutans

被引:6
|
作者
Li, Y. [1 ]
Liu, Z. [2 ]
Zhang, Y. [3 ]
Su, Q. P. [2 ]
Xue, B. [2 ]
Shao, S. [2 ]
Zhu, Y. [2 ]
Xu, X. [1 ]
Wei, S. [1 ]
Sun, Y. [2 ]
机构
[1] Peking Univ, Sch & Hosp Stomatol, Lab Interdisciplinary Studies, Dept Oral & Maxillofacial Surg, Beijing 100081, Peoples R China
[2] Peking Univ, Sch Life Sci, Biodynam Optic Imaging Ctr BIOPIC, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100081, Peoples R China
[3] Peking Univ, Sch & Hosp Stomatol, Cent Lab, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
biofilm; cell wall anchored proteins; dynamic distribution; live cell imaging; Streptococcus mutans; super-resolution imaging; wall-associated protein A; ARCHITECTURE; SEQUENCE; DYNAMICS; BIOFILMS; WAPA;
D O I
10.1111/omi.12100
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Streptococcus mutans is a primary pathogen responsible for dental caries. It has an outstanding ability to form biofilm, which is vital for virulence. Previous studies have shown that knockout of Wall-associated protein A (WapA) affects cell chain and biofilm formation of S.mutans. As a surface protein, the distribution of WapA remains unknown, but it is important to understand the mechanism underlying the function of WapA. This study applied the fluorescence protein mCherry as a reporter gene to characterize the dynamic distribution of WapA in S.mutans via time-lapse and super-resolution fluorescence imaging. The results revealed interesting subcellular distribution patterns of WapA in single, dividing and long chains of S.mutans cells. It appears at the middle of the cell and moves to the poles as the cell grows and divides. In a cell chain, after each round of cell division, such dynamic relocation results in WapA distribution at the previous cell division sites, resulting in a pattern where WapA is located at the boundary of two adjacent cell pairs. This WapA distribution pattern corresponds to the breaking segmentation of wapA deletion cell chains. The dynamic relocation of WapA through the cell cycle increases our understanding of the mechanism of WapA in maintaining cell chain integrity and biofilm formation.
引用
收藏
页码:376 / 383
页数:8
相关论文
共 35 条
  • [21] Live Cell and In vivo Super-resolution Imaging Based on STED
    Zhou Han-Qiu
    Zhu Yin-Ru
    Han Hong-Yi
    Wang Lu-Wei
    Yang Zhi-Gang
    Yan Wei
    Qu Jun-Le
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2023, 50 (03) : 513 - 528
  • [22] Live-cell super-resolution imaging of actin using LifeAct-14 with a PAINT-based approach
    Bhaskar, Haresh
    Kleinjan, Dirk-Jan
    Oi, Curran
    Gidden, Zoe
    Rosser, Susan J. J.
    Horrocks, Mathew H. H.
    Regan, Lynne
    PROTEIN SCIENCE, 2023, 32 (02)
  • [23] Descriptor ΔGC-OEnables the Quantitative Design of Spontaneously Blinking Rhodamines for Live-Cell Super-Resolution Imaging
    Chi, Weijie
    Qiao, Qinglong
    Wang, Chao
    Zheng, Jiazhu
    Zhou, Wei
    Xu, Ning
    Wu, Xia
    Jiang, Xiao
    Tan, Davin
    Xu, Zhaochao
    Liu, Xiaogang
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (45) : 20215 - 20223
  • [24] A millisecond structured illumination microscope for super-resolution live cell imaging
    Suzuki, Tomu
    Kajimoto, Shinji
    Kitamura, Narufumi
    Takano-Kasuya, Mayumi
    Furusawa, Naoko
    Nakano, Yasushi
    Fukumura, Hiroshi
    Gonda, Kohsuke
    Nakabayashi, Takakazu
    APPLIED PHYSICS EXPRESS, 2020, 13 (04)
  • [25] Correlative Live-Cell and Super-Resolution Imaging to Link Presynaptic Molecular Organisation With Function (vol 14, 830583, 2022)
    Jackson, Rachel E.
    Compans, Benjamin
    Burrone, Juan
    FRONTIERS IN SYNAPTIC NEUROSCIENCE, 2022, 14
  • [26] Fast live-cell conventional fluorophore nanoscopy with ImageJ through super-resolution radial fluctuations
    Gustafsson, Nils
    Culley, Sian
    Ashdown, George
    Owen, Dylan M.
    Pereira, Pedro Matos
    Henriques, Ricardo
    NATURE COMMUNICATIONS, 2016, 7
  • [27] Surface-Functionalized Halo-Tag Gold Nanoprobes for Live-Cell Long-Term Super-Resolution Imaging of Endoplasmic Reticulum Dynamics
    Xu, Peng
    Zhong, Simei
    Wei, Yunfei
    Duan, Xinxin
    Zhang, Meng
    Shen, Wei
    Ma, Yan
    Zhang, Yu-Hui
    ACS NANO, 2024, 18 (32) : 21433 - 21446
  • [28] Self-supervised denoising for multimodal structured illumination microscopy enables long-term super-resolution live-cell imaging
    Xingye Chen
    Chang Qiao
    Tao Jiang
    Jiahao Liu
    Quan Meng
    Yunmin Zeng
    Haoyu Chen
    Hui Qiao
    Dong Li
    Jiamin Wu
    PhotoniX, 5
  • [29] Self-supervised denoising for multimodal structured illumination microscopy enables long-term super-resolution live-cell imaging
    Chen, Xingye
    Qiao, Chang
    Jiang, Tao
    Liu, Jiahao
    Meng, Quan
    Zeng, Yunmin
    Chen, Haoyu
    Qiao, Hui
    Li, Dong
    Wu, Jiamin
    PHOTONIX, 2024, 5 (01)
  • [30] Dual-color live-cell super-resolution fluorescence lifetime imaging via polarization modulation-based fluorescence emission difference
    Dong, Wanjie
    Huang, Yuran
    Tao, Wenli
    Xu, Liang
    Han, Yubing
    Hao, Xiang
    Kuang, Cuifang
    Liu, Xu
    OPTICS AND LASERS IN ENGINEERING, 2025, 184