Abstract:Elongation of many rod-shaped bacteria occurs by peptidoglycan synthesis at discrete foci along the sidewall of the cells. However, within the Rhizobiales, there are many budding bacteria, in which new cell growth is constrained to a specific region. The phylogeny of the Rhizobiales indicates that this mode of zonal growth may be ancestral. We demonstrate that the rod-shaped bacterium
Agrobacterium tumefaciens
grows unidirectionally from the new pole generated after cell division and ha… Show more
“…However, in the latter strain the knockout leads to elongated cells. Polar growth has been described for representatives of Rhizobiales, Caulobacterales and Rhodobacterales and may be ancient in Alphaproteobacteria (Brown et al, 2012); the core genes of cell cycle control are conserved throughout the phylum (Brilli et al, 2010). This is the first time that the mode of cell division has been shown to be controlled by QS in Alphaproteobacteria.…”
Dinoroseobacter shibae, a member of the Roseobacter clade abundant in marine environments, is characterized by a pronounced pleomorphism. Cell shapes range from variable-sized ovoid rods to long filaments with a high copy number of chromosomes. Time-lapse microscopy shows cells dividing either by binary fission or by budding from the cell poles. Here we demonstrate that this morphological heterogeneity is induced by quorum sensing (QS). D. shibae utilizes three acylated homoserine lactone (AHL) synthases (luxI 1-3 ) to produce AHLs with unsaturated C18 side chains. A DluxI 1 -knockout strain completely lacking AHL biosynthesis was uniform in morphology and divided by binary fission only. Transcriptome analysis revealed that expression of genes responsible for control of cell division was reduced in this strain, providing the link between QS and the observed phenotype. In addition, flagellar biosynthesis and type IV secretion system (T4SS) were downregulated. The wild-type phenotype and gene expression could be restored through addition of synthetic C18-AHLs. Their effectiveness was dependent on the number of double bonds in the acyl side chain and the regulated trait. The wild-type expression level of T4SS genes was fully restored even by an AHL with a saturated C18 side chain that has not been detected in D. shibae. QS induces phenotypic individualization of D. shibae cells rather than coordinating the population. This strategy might be beneficial in unpredictably changing environments, for example, during algal blooms when resource competition and grazing exert fluctuating selective pressures. A specific response towards non-native AHLs might provide D. shibae with the capacity for complex interspecies communication.
“…However, in the latter strain the knockout leads to elongated cells. Polar growth has been described for representatives of Rhizobiales, Caulobacterales and Rhodobacterales and may be ancient in Alphaproteobacteria (Brown et al, 2012); the core genes of cell cycle control are conserved throughout the phylum (Brilli et al, 2010). This is the first time that the mode of cell division has been shown to be controlled by QS in Alphaproteobacteria.…”
Dinoroseobacter shibae, a member of the Roseobacter clade abundant in marine environments, is characterized by a pronounced pleomorphism. Cell shapes range from variable-sized ovoid rods to long filaments with a high copy number of chromosomes. Time-lapse microscopy shows cells dividing either by binary fission or by budding from the cell poles. Here we demonstrate that this morphological heterogeneity is induced by quorum sensing (QS). D. shibae utilizes three acylated homoserine lactone (AHL) synthases (luxI 1-3 ) to produce AHLs with unsaturated C18 side chains. A DluxI 1 -knockout strain completely lacking AHL biosynthesis was uniform in morphology and divided by binary fission only. Transcriptome analysis revealed that expression of genes responsible for control of cell division was reduced in this strain, providing the link between QS and the observed phenotype. In addition, flagellar biosynthesis and type IV secretion system (T4SS) were downregulated. The wild-type phenotype and gene expression could be restored through addition of synthetic C18-AHLs. Their effectiveness was dependent on the number of double bonds in the acyl side chain and the regulated trait. The wild-type expression level of T4SS genes was fully restored even by an AHL with a saturated C18 side chain that has not been detected in D. shibae. QS induces phenotypic individualization of D. shibae cells rather than coordinating the population. This strategy might be beneficial in unpredictably changing environments, for example, during algal blooms when resource competition and grazing exert fluctuating selective pressures. A specific response towards non-native AHLs might provide D. shibae with the capacity for complex interspecies communication.
“…Indeed, our bioinformatics searches revealed that Agrobacterium and related Rhizobiales species have more genes encoding LD-transpeptidases in their genome than other rod-shaped bacteria that predominantly encode DD-transpeptidases, and LD-transpeptidases are generally insensitive to β-lactam antibiotics (24). That PG biosynthesis in Agrobacterium is distinct is supported by its unique muropeptide profile (4). Also, in contrast to polar growth, midcell PG synthesis before division is significantly affected by Cb and results in striking tire-like expansions at this site.…”
Section: Discussionmentioning
confidence: 88%
“…Finally, cells expressing FtsA-GFP were pulse-labeled with Texas red-X succinimidyl ester (TRSE), which binds cell-surface proteins (4). Following short or long chases in media without TRSE, TRSE remained at the old pole, and FtsA-GFP was at the opposite end of the cell, namely the growth pole ( Fig.…”
Section: Growth Poles and Old Poles Of Agrobacterium Exhibit Differenmentioning
confidence: 99%
“…First, a specific unipolar polysaccharide (UPP) is secreted from one pole and mediates attachment of cells to the substrate, and this activity is required for the formation of biofilms (3). Second, Agrobacterium (and other members of the Rhizobiales) grows by the addition of PG primarily at one end of the cell, the growth pole (4). After cell division, unipolar growth resumes in both daughter cells from the new cell poles generated at the division site.…”
mentioning
confidence: 99%
“…Recent studies with another rod-shaped α-proteobacterium, Agrobacterium tumefaciens, revealed additional novel modes of bacterial growth and cell division (3,4). First, a specific unipolar polysaccharide (UPP) is secreted from one pole and mediates attachment of cells to the substrate, and this activity is required for the formation of biofilms (3).…”
Growth and cell division in rod-shaped bacteria have been primarily studied in species that grow predominantly by peptidoglycan (PG) synthesis along the length of the cell. Rhizobiales species, however, predominantly grow by PG synthesis at a single pole. Here we characterize the dynamic localization of several Agrobacterium tumefaciens components during the cell cycle. First, the lipophilic dye FM 4-64 predominantly stains the outer membranes of old poles versus growing poles. In cells about to divide, however, both poles are equally labeled with FM 4-64, but the constriction site is not. Second, the cell-division protein FtsA alternates from unipolar foci in the shortest cells to unipolar and midcell localization in cells of intermediate length, to strictly midcell localization in the longest cells undergoing septation. Third, the cell division protein FtsZ localizes in a cell-cycle pattern similar to, but more complex than, FtsA. Finally, because PG synthesis is spatially and temporally regulated during the cell cycle, we treated cells with sublethal concentrations of carbenicillin (Cb) to assess the role of penicillin-binding proteins in growth and cell division. Cb-treated cells formed midcell circumferential bulges, suggesting that interrupted PG synthesis destabilizes the septum. Midcell bulges contained bands or foci of FtsA-GFP and FtsZ-GFP and no FM 4-64 label, as in untreated cells. There were no abnormal morphologies at the growth poles in Cb-treated cells, suggesting unipolar growth uses Cb-insensitive PG synthesis enzymes.agrobacterium cell cycle | bacterial cell growth | bacterial cell division | peptidoglycan synthesis
Among the myriad of cyanobacterial shapes and sizes, Stigonematales show the highest complexity as they present different cell shapes and sizes within a single cyanobacterial strain. By studying the main cytoskeletal components in these cyanobacteria, we aim to understand how cells undergo these changes. We provide the first insights on the role of the cytoskeletal proteins MreB and FtsZ in cyanobacterial morphogenesis.
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