Microevolution analysis of Bacillus coahuilensis unveils differences in phosphorus acquisition strategies and their regulation

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Abstract

Bacterial genomes undergo numerous events of gene losses and gains that generate genome variability among strains of the same species (microevolution). Our aim was to compare the genomes and relevant phenotypes of three Bacillus coahuilensis strains from two oligotrophic hydrological systems in the Cuatro Ciénegas Basin (México), to unveil the environmental challenges that this species cope with, and the microevolutionary differences in these genotypes. Since the strains were isolated from a low P environment, we placed emphasis on the search of different phosphorus acquisition strategies. The three B. coahuilensis strains exhibited similar numbers of coding DNA sequences, of which 82% (2,893) constituted the core genome, and 18% corresponded to accessory genes. Most of the genes in this last group were associated with mobile genetic elements (MGEs) or were annotated as hypothetical proteins. Ten percent of the pangenome consisted of strain-specific genes. Alignment of the three B. coahuilensis genomes indicated a high level of synteny and revealed the presence of several genomic islands. Unexpectedly, one of these islands contained genes that encode the 2-keto-3-deoxymannooctulosonic acid (Kdo) biosynthesis enzymes, a feature associated to cell walls of Gram-negative bacteria. Some microevolutionary changes were clearly associated with MGEs. Our analysis revealed inconsistencies between phenotype and genotype, which we suggest result from the impossibility to map regulatory features to genome analysis. Experimental results revealed variability in the types and numbers of auxotrophies between the strains that could not consistently be explained by in silico metabolic models. Several intraspecific differences in preferences for carbohydrate and phosphorus utilization were observed. Regarding phosphorus recycling, scavenging, and storage, variations were found between the three genomes. The three strains exhibited differences regarding alkaline phosphatase that revealed that in addition to gene gain and loss, regulation adjustment of gene expression also has contributed to the intraspecific diversity of B. coahuilensis.

Figures

  • FIGURE 1 | Core and accessory genomes of three Bacillus coahuilensis strains (m4-4, m2-6, and p1.1.43). Ortholog identification was performed using the bidirectional best hit (BBH) approach with mutual coverage or a shared length of 60% and an e-value ≥10−6. The core genome is indicated by the numbers in black font. Accessory gene numbers are in blue font. The number of predicted genes is shown in parenthesis for each genome.
  • TABLE 1 | General characteristics of the Bacillus coahuilensis genomes.
  • FIGURE 2 | Mobile genetic elements (MGEs) identified in the B. coahuilensis genomes (strains m4-4, m2-6, and p1.1.43). Axis Y indicates the number of genes related to MGEs per genome, axis X indicates different MGEs coding in the genomes (IS, transposons, phage-related genes, and CRISPR).
  • FIGURE 3 | Mauve alignment of the B. coahuilensis genomes (strains m4-4, m2-6, and p1.1.43). Colored rounded boxes represent syntenic regions and white/gray areas represent unique regions in the three genomes. Blue rectangular boxes indicate genomic islands that include phage-related genes. Rectangular pink boxes indicate unique areas that include genes related to transposons. Rectangular red boxes indicate unique areas that include insertion sequences. The rectangular yellow box indicates a genomic island with genes associated with the biosynthesis of cell wall lipopolysaccharide, common only in Gram-negative bacteria. The rectangular green box indicates a unique region encoding genes related to phosphonate transport in the B. coahuilensis m2-6 genome.
  • FIGURE 4 | Genomic island (GIm2d) of Bacillus coahuilensis m2-6 and phylogenetic reconstruction of KdsB. (A) Genes arrangement in GIm2d. Red arrows indicate insertion sequences (IS643); orange arrows indicate genes coding for glycosyltransferase; light blue arrows indicate genes encoding hypothetical proteins; green arrows indicate genes associated with Kdo biosynthesis; purple arrows indicate genes coding for membrane proteins; the dark blue arrow indicates a gene coding for N-acetylmuramoyl-L-alanine amidase; the pink arrow indicates a gene coding for gamma-D-glutamyl-L-diamino acid endopeptidase I. Name of the genes associated with Kdo biosynthesis: kdsB, CMP-Kdo synthetase; kpsC, capsular polysaccharide export system protein; kdsD, D-arabinose-5-phosphate isomerase; kdsC, Kdo-8-P phosphatase; kdsA, Kdo-8-P synthase. (B) The phylogenetic reconstruction of the KdsB associated with Kdo biosynthesis was based on a maximum likelihood method. Numbers next to the branches represent bootstrap values expressed as percentages of 100 replications; only the values >70% are indicated. Bar represents 0.1 substitutions per nucleotide position. The Arabidopsis thaliana KdsB was used as outgroup. Colors represent bacterial lineages.
  • TABLE 2 | Utilization of different amino acid sources by each Bacillus coahuilensis strain.
  • FIGURE 5 | Observed variability in the utilization of carbon sources in three B. coahuilensis strains. (A) Biolog results for the use of poly- and oligosaccharides. Compounds were clustered according to how the strains (m4-4, m2-6, and p1.1.43) used poly- and oligosaccharides. (B) Biolog results for the use of monosaccharides. Data were clustered according to bacterial utilization, as in (A). (C) Biolog results for the use of carboxylic acids and aromatic compounds. Data were clustered according to bacterial utilization, as in (A). Carbohydrates names in red font indicate that in silico metabolic models have missing genes in the three genomes. ∗ Indicates that genes are missing only in B. coahuilensis m4-4. In all cases, lighter green areas indicate greater evidence of source utilization, and black green indicates no utilization for poly- and oligosaccharides (A), monosaccharides (B), and carboxylic acids and aromatic compounds (C), respectively.
  • FIGURE 6 | Differences in swim capabilities and lack of swarm ability of three B. coahuilensis strains. The control is marine medium (MM) containing 2% agar. Swarm was evaluated on MM containing 0.6% agar. Swim was evaluated on MM containing 0.3% agar.

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Gómez-Lunar, Z., Hernández-González, I., Rodríguez-Torres, M. D., Souza, V., & Olmedo-álvarez, G. (2016). Microevolution analysis of Bacillus coahuilensis unveils differences in phosphorus acquisition strategies and their regulation. Frontiers in Microbiology, 7(FEB). https://doi.org/10.3389/fmicb.2016.00058

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