Evolutionary rescue of spherical mreB deletion mutants of the rod-shape bacterium Pseudomonas fluorescens SBW25.

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-03-31 DOI:10.7554/eLife.98218
Paul Richard J Yulo, Nicolas Desprat, Monica L Gerth, Barbara Ritzl-Rinkenberger, Andrew D Farr, Yunhao Liu, Xue-Xian Zhang, Michael Miller, Felipe Cava, Paul B Rainey, Heather L Hendrickson
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引用次数: 0

Abstract

Maintenance of rod-shape in bacterial cells depends on the actin-like protein MreB. Deletion of mreB from Pseudomonas fluorescens SBW25 results in viable spherical cells of variable volume and reduced fitness. Using a combination of time-resolved microscopy and biochemical assay of peptidoglycan synthesis, we show that reduced fitness is a consequence of perturbed cell size homeostasis that arises primarily from differential growth of daughter cells. A 1000-generation selection experiment resulted in rapid restoration of fitness with derived cells retaining spherical shape. Mutations in the peptidoglycan synthesis protein Pbp1A were identified as the main route for evolutionary rescue with genetic reconstructions demonstrating causality. Compensatory pbp1A mutations that targeted transpeptidase activity enhanced homogeneity of cell wall synthesis on lateral surfaces and restored cell size homeostasis. Mechanistic explanations require enhanced understanding of why deletion of mreB causes heterogeneity in cell wall synthesis. We conclude by presenting two testable hypotheses, one of which posits that heterogeneity stems from non-functional cell wall synthesis machinery, while the second posits that the machinery is functional, albeit stalled. Overall, our data provide support for the second hypothesis and draw attention to the importance of balance between transpeptidase and glycosyltransferase functions of peptidoglycan building enzymes for cell shape determination.

棒状荧光假单胞菌SBW25球形mreB缺失突变体的进化拯救
细菌细胞的棒状维持依赖于肌动蛋白样蛋白MreB。从荧光假单胞菌SBW25中删除mreB导致活的球形细胞变体积和适应性降低。结合时间分辨显微镜和肽聚糖合成的生化分析,我们发现适应度降低是由于子细胞的差异生长引起的细胞大小稳态紊乱的结果。经过1000代的选择实验,获得的细胞保持球形,适应度迅速恢复。肽聚糖合成蛋白Pbp1A的突变被确定为进化拯救的主要途径,基因重建证明了因果关系。靶向转肽酶活性的代偿性pbp1A突变增强了细胞壁侧面合成的均匀性,恢复了细胞大小的稳态。机制解释需要加强理解为什么mreB的缺失导致细胞壁合成的异质性。最后,我们提出了两个可测试的假设,其中一个假设异质性源于无功能的细胞壁合成机制,而第二个假设该机制是功能性的,尽管停滞不前。总的来说,我们的数据支持第二种假设,并引起人们对肽聚糖构建酶的转肽酶和糖基转移酶功能平衡对细胞形状决定的重要性的关注。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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