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黄色黏球菌中群体流动和聚集的遗传及环境决定因素。

Genetic and environmental determinants of streaming and aggregation in Myxococcus xanthus.

作者信息

Khan Trosporsha T, Murphy Patrick, Zhang Jiangguo, Igoshin Oleg A, Welch Roy D

机构信息

Department of Biology, Syracuse University, Syracuse, NY, USA.

Department of Bioengineering, Rice University, Houston, TX, USA.

出版信息

Sci Rep. 2025 Aug 21;15(1):30673. doi: 10.1038/s41598-025-15915-8.

DOI:10.1038/s41598-025-15915-8
PMID:40835634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12368150/
Abstract

Under starvation conditions, a spot of a few million Myxococcus xanthus cells on agar will migrate inward to form aggregates that mature into dome-shaped fruiting bodies. This migration is thought to occur within structures called 'streams,' which are considered crucial for initiating aggregation. The prevailing traffic jam model hypothesizes that intersections of streams cause cell crowding and 'jamming,' thereby initiating the process of aggregate formation. However, this hypothesis has not been rigorously tested, in part due to the lack of a standardized, quantifiable definition of streams. To address this gap, we captured time-lapse movies and conducted fluorescent cell tracking experiments using wild-type and two motility-deficient mutant M. xanthus strains. By quantitatively defining streams and developing a novel stream detection mask, we show that streams are not essential for nascent aggregate formation, though they may accelerate the process. Moreover, our results indicate that streaming has a genetic component: disrupting only one of the two M. xanthus motility systems hinders stream formation. Together, these findings challenge the idea that stream intersections are required to drive aggregate formation and suggest that M. xanthus aggregation may be driven by mechanisms independent of streaming, highlighting the need for alternative models to fully explain aggregation dynamics.

摘要

在饥饿条件下,琼脂上数百万个黄色粘球菌细胞的斑点会向内迁移形成聚集体,这些聚集体会成熟为圆顶形子实体。这种迁移被认为发生在称为“流”的结构内,“流”被认为对启动聚集至关重要。流行的交通堵塞模型假设,流的交叉点会导致细胞拥挤和“堵塞”,从而启动聚集体形成过程。然而,这一假设尚未得到严格验证,部分原因是缺乏对流的标准化、可量化定义。为了填补这一空白,我们拍摄了延时电影,并使用野生型和两种运动缺陷型突变黄色粘球菌菌株进行了荧光细胞追踪实验。通过对流进行定量定义并开发一种新颖的流检测掩码,我们发现流对于新生聚集体的形成并非必不可少,尽管它们可能会加速这一过程。此外,我们的结果表明流具有遗传成分:仅破坏黄色粘球菌两种运动系统中的一种就会阻碍流的形成。这些发现共同挑战了流交叉点是驱动聚集体形成所必需的这一观点,并表明黄色粘球菌的聚集可能由独立于流的机制驱动,凸显了需要替代模型来充分解释聚集动态的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/d39a771ffb38/41598_2025_15915_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/f1715d58a5e2/41598_2025_15915_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/16f37e65a68a/41598_2025_15915_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/9c3439650f05/41598_2025_15915_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/d39a771ffb38/41598_2025_15915_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/f1715d58a5e2/41598_2025_15915_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/16f37e65a68a/41598_2025_15915_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/9c3439650f05/41598_2025_15915_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/739b/12368150/d39a771ffb38/41598_2025_15915_Fig4_HTML.jpg

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