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Xanthomonas citri MinC Oscillates from Pole to Pole to Ensure Proper Cell Division and Shape
André S G Lorenzoni1, Giordanni C Dantas2, Tessa Bergsma1
1Department of Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of GroningenGroningen, Netherlands.
Abstract:
Xanthomonas citri (Xac) is the causal agent of citrus canker, a disease that affects citrus crops and causes economic impact worldwide. To further characterize cell division in this plant pathogen, we investigated the role of the protein MinC in cell division, chromosome segregation, and peptidoglycan incorporation by deleting the gene minC using allele exchange. Xac with minC deleted exhibited the classic Δmin phenotype observed in other bacteria deleted for min components: minicells and short filamentation. In addition we noticed the formation of branches, which is similar to what was previously described for Escherichia coli deleted for either min or for several low molecular weight penicillin-binding proteins (PBPs). The branching phenotype was medium dependent and probably linked to gluconeogenic growth. We complemented the minC gene by integrating gfp-minC into the amy locus. Xac complemented strains displayed a wild-type phenotype. In addition, GFP-MinC oscillated from pole to pole, similar to MinCD oscillations observed in E. coli and more recently in Synechococcus elongatus. Further investigation of the branching phenotype revealed that in branching cells nucleoid organization, divisome formation and peptidoglycan incorporation were disrupted.
Insights
The MinC protein is crucial for cell division in Xanthomonas citri, the citrus canker pathogen. Deleting its gene causes abnormal cell shapes and division, impacting bacterial growth.
Area of Science:
- Bacteriology
- Molecular Biology
- Plant Pathology
Background:
- Citrus canker, caused by Xanthomonas citri (Xac), poses a significant economic threat to citrus crops globally.
- Understanding bacterial cell division is essential for developing effective disease control strategies.
Purpose of the Study:
- To investigate the role of the MinC protein in Xac cell division, chromosome segregation, and peptidoglycan incorporation.
- To characterize the phenotypic consequences of minC deletion in Xac.
Main Methods:
- Gene deletion of minC using allele exchange in Xac.
- Complementation of the minC deletion mutant by integrating gfp-minC.
- Microscopic analysis of cell morphology, nucleoid organization, and divisome formation.
Main Results:
- Xac lacking minC exhibited minicells, short filamentation, and branching, a phenotype dependent on growth medium.
- Complemented strains restored a wild-type phenotype, and GFP-MinC showed pole-to-pole oscillations.
- Branching cells displayed disrupted nucleoid organization, divisome formation, and peptidoglycan incorporation.
Conclusions:
- MinC plays a critical role in regulating Xac cell division and morphology.
- The observed branching phenotype is linked to disruptions in fundamental cellular processes and may be influenced by nutrient availability.
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