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一种新的基于荧光的方法,用于直接可视化芽孢杆菌在孢子形成过程中的外壳形成。

A new fluorescence-based approach for direct visualization of coat formation during sporulation in Bacillus cereus.

机构信息

INRAE, Avignon Université, UMR SQPOV, 84000, Avignon, France.

MICALIS Institute, INRAE, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.

出版信息

Sci Rep. 2023 Sep 13;13(1):15136. doi: 10.1038/s41598-023-42143-9.

DOI:10.1038/s41598-023-42143-9
PMID:37704668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10499802/
Abstract

The human pathogenic bacteria Bacillus cereus, Bacillus anthracis and the entomopathogenic Bacillus thuringiensis form spores encased in a protein coat surrounded by a balloon-like exosporium. These structures mediate spore interactions with its environment, including the host immune system, control the transit of molecules that trigger germination and thus are essential for the spore life cycle. Formation of the coat and exosporium has been traditionally visualized by transmission electronic microscopy on fixed cells. Recently, we showed that assembly of the exosporium can be directly observed in live B. cereus cells by super resolution-structured illumination microscopy (SR-SIM) using the membrane MitoTrackerGreen (MTG) dye. Here, we demonstrate that the different steps of coat formation can also be visualized by SR-SIM using MTG and SNAP-cell TMR-star dyes during B. cereus sporulation. We used these markers to characterize a subpopulation of engulfment-defective B. cereus cells that develops at a suboptimal sporulation temperature. Importantly, we predicted and confirmed that synthesis and accumulation of coat material, as well as synthesis of the σ-dependent protein BxpB, occur in cells arrested during engulfment. These results suggest that, unlike the well-studied model organism Bacillus subtilis, the activity of σ is not strictly linked to the state of forespore development in B. cereus.

摘要

人类病原体细菌蜡状芽孢杆菌、炭疽芽孢杆菌和昆虫病原芽孢杆菌形成的孢子被包裹在一层蛋白质外壳中,外壳周围是一个气球状的外孢囊。这些结构介导孢子与环境的相互作用,包括宿主免疫系统,控制触发发芽的分子的转运,因此对孢子的生命周期至关重要。传统上,通过固定细胞的透射电子显微镜观察外壳和外孢囊的形成。最近,我们通过使用膜 MitoTrackerGreen(MTG)染料的超分辨率结构照明显微镜(SR-SIM),在活的蜡状芽孢杆菌细胞中直接观察到了外孢囊的组装。在这里,我们证明了使用 MTG 和 SNAP-cell TMR-star 染料在蜡状芽孢杆菌的孢子形成过程中也可以通过 SR-SIM 观察到外壳形成的不同步骤。我们使用这些标记物来表征在非最佳孢子形成温度下发育的吞噬缺陷蜡状芽孢杆菌细胞的亚群。重要的是,我们预测并证实了外壳物质的合成和积累,以及 σ 依赖性蛋白 BxpB 的合成,发生在吞噬过程中被阻断的细胞中。这些结果表明,与研究充分的模式生物枯草芽孢杆菌不同,σ 的活性与蜡状芽孢杆菌中前孢子发育的状态并不严格相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/ca2d4dee3812/41598_2023_42143_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/32823aca99e9/41598_2023_42143_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/6d23d6e6c568/41598_2023_42143_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/7b9c2c4d42f6/41598_2023_42143_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/2d6cdde8147c/41598_2023_42143_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/9d048f2f268b/41598_2023_42143_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/ca2d4dee3812/41598_2023_42143_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/32823aca99e9/41598_2023_42143_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/6d23d6e6c568/41598_2023_42143_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/7b9c2c4d42f6/41598_2023_42143_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/2d6cdde8147c/41598_2023_42143_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/9d048f2f268b/41598_2023_42143_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/10499802/ca2d4dee3812/41598_2023_42143_Fig6_HTML.jpg

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CotG Mediates Spore Surface Permeability in Bacillus subtilis.
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