Comparative Genomic and Phylogenetic Analyses of Gammaproteobacterial glg Genes Traced the Origin of the Escherichia coli Glycogen glgBXCAP Operon to the Last Common Ancestor of the Sister Orders Enterobacteriales and Pasteurellales

Goizeder Almagro; Alejandro M. Viale; Manuel Montero; Mehdi Rahimpour; Francisco José Muñoz; Edurne Baroja-Fernández; Abdellatif Bahaji; Manuel Zúñiga; Fernando González-Candelas; Javier Pozueta-Romero

doi:10.1371/journal.pone.0115516

Abstract

Production of branched α-glucan, glycogen-like polymers is widely spread in the Bacteria domain. The glycogen pathway of synthesis and degradation has been fairly well characterized in the model enterobacterial species Escherichia coli (order Enterobacteriales, class Gammaproteobacteria), in which the cognate genes (branching enzyme glgB, debranching enzyme glgX, ADP-glucose pyrophosphorylase glgC, glycogen synthase glgA, and glycogen phosphorylase glgP) are clustered in a glgBXCAP operon arrangement. However, the evolutionary origin of this particular arrangement and of its constituent genes is unknown. Here, by using 265 complete gammaproteobacterial genomes we have carried out a comparative analysis of the presence, copy number and arrangement of glg genes in all lineages of the Gammaproteobacteria. These analyses revealed large variations in glg gene presence, copy number and arrangements among different gammaproteobacterial lineages. However, the glgBXCAP arrangement was remarkably conserved in all glg-possessing species of the orders Enterobacteriales and Pasteurellales (the E/P group). Subsequent phylogenetic analyses of glg genes present in the Gammaproteobacteria and in other main bacterial groups indicated that glg genes have undergone a complex evolutionary history in which horizontal gene transfer may have played an important role. These analyses also revealed that the E/P glgBXCAP genes (a) share a common evolutionary origin, (b) were vertically transmitted within the E/P group, and (c) are closely related to glg genes of some phylogenetically distant betaproteobacterial species. The overall data allowed tracing the origin of the E. coli glgBXCAP operon to the last common ancestor of the E/P group, and also to uncover a likely glgBXCAP transfer event from the E/P group to particular lineages of the Betaproteobacteria.

Citation: Almagro G, Viale AM, Montero M, Rahimpour M, Muñoz FJ, Baroja-Fernández E, et al. (2015) Comparative Genomic and Phylogenetic Analyses of Gammaproteobacterial glg Genes Traced the Origin of the Escherichia coli Glycogen glgBXCAP Operon to the Last Common Ancestor of the Sister Orders Enterobacteriales and Pasteurellales. PLoS ONE 10(1): e0115516. https://doi.org/10.1371/journal.pone.0115516

Academic Editor: Gabriel Moreno-Hagelsieb, Wilfrid Laurier University, CANADA

Received: June 17, 2014; Accepted: November 25, 2014; Published: January 21, 2015

Copyright: © 2015 Almagro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Data Availability: All relevant data are within the paper and its Supporting Information files.

Funding: This research was partially supported by the grant [BIO2010-18239] from the Comisión Interministerial de Ciencia y Tecnología and Fondo Europeo de Desarrollo Regional (Spain). MR acknowledges a pre-doctoral JAE fellowship from the Consejo Superior de Investigaciones Científicas. AMV is grateful to the funding of the Programa Campus Iberus de Excelencia Internacional, Ministerio de Educación, Spain. His 2-month visit (January-March 2014) to the Institute of Agrobiotechnology, Public Universtity of Navarra, Pamplona, Spain, was included into the Proyecto financiado por el Ministerio de Educación en el marco del Programa Campus de Excelencia Internacional. FGC was supported by project [BFU2011-24112] from the Ministerio de Ciencia e Innovación (Spain).

Competing interests: The authors have declared that no competing interests exist.

Introduction

Production of large intracellular α-glucans composed of α-1,4-linked glucose units displaying low extents of α-1,6-linked branches (“bacterial glycogen”) represents a common feature observed in many groups of bacteria [1–9]. Glycogen constitutes a major carbon and energy reserve polymer that accumulates to cope with the starvation conditions often occurring in natural environments. The exact role of this polysaccharide in bacteria is not as clear-cut as in eukaryotes [7], but several studies have indicated that glycogen metabolism may confer some adaptive advantages including increased environmental survival and colonization and, in the case of pathogens, increased virulence and immune system evasion [1, 2, 8, 10–15].

Studies conducted for more than 40 years in model bacterial species such as Escherichia coli and Salmonella enterica (family Enterobacteriaceae, order Enterobacteriales, class Gammaproteobacteria) were pivotal to elucidate the glycogen metabolic pathway schematically illustrated in Fig. 1 [6,7]. According to this model, carbon sources are taken up by the bacterial cell and eventually transformed into glucose-6-phosphate (Glc-6-P), which is then converted into glucose-1-phosphate (Glc-1-P) by phosphoglucomutase (PGM). In the presence of Mg²⁺ and ATP, this hexose-P is converted into ADP-glucose (ADPG) and inorganic pyrophosphate by means of ADPG pyrophosphorylase (GlgC), the main regulatory step of glycogen synthesis [16]. ADPG is used by glycogen synthase (GlgA) to incorporate a new α-1,4-linked unit into the growing linear α-glucan. After chain elongation by GlgA, the glycogen branching enzyme (GlgB) catalyzes the formation of branched α-1,6-glycosidic linkages by transferring non-reducing-end oliglucans to the C-6-position of residues within a chain. On the catabolic side, the glycogen phosphorylase (GlgP) and glycogen debranching enzyme (GlgX) are the major determinants of glycogen degradation catalyzing the phosphorolytic cleavage of α-1,4 bonds to generate Glc-1-P at the non-reducing ends and the hydrolysis of α-1,6-glycosidic linkages on limit dextrins (the polysaccharide fragments remaining at the end of exhaustive hydrolysis of glycogen by GlgP), respectively [17,18]. This model is considered to represent the prevalent pathway of glycogen synthesis and degradation in bacteria [6,7]. Still, alternative glycogen synthesis pathways have been identified in some bacterial groups such as the high-G+C Gram-positive actinomycetes [12]. Also, yet unidentified sources of ADPG linked to glycogen biosynthesis have been described in both enterobacterial and cyanobacterial species [14,19,20].

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Figure 1. Schematic model of glycogen metabolism.

Sugar (glucose) is incorporated into the cell and successively transformed to glucose-6-P (Glc-6-P), glucose-1-P (Glc-1-P), ADP-glucose (ADPG) and glycogen. This model involves the coupled reactions of phosphoglucomutase (PGM), ADPG pyrophosphorylase (GlgC) and other (?) ADPG-generating enzyme(s) [19,20], glycogen synthase (GlgA) and glycogen branching enzyme (GlgB). Glycogen catabolism is controlled by both glycogen phosphorylase (GlgP) and glycogen debranching enzyme (GlgX).

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Bacterial genes encoding functionally related proteins are generally clustered in operons [21–23]. This is the case of the five E. coli glg genes coding for the enzymes of the glycogen pathway, which are present in a single copy each and clustered in a single glgBXCAP operon arrangement [24]. However, the evolutionary history of this arrangement and its constituent genes remains unknown. To gain insight into the origin and evolutionary history of E. coli and S. enterica glg genes, we have carried out a detailed comparative analysis of the presence, copy number and arrangement of glg genes present in the different gammaproteobacterial lineages. Our analyses reveal the occurrence of large variations in glg homologs copy number and arrangements within the Gammaproteobacteria, glgBXCAP arrangement being highly conserved in all glg possessing species of the sister orders Enterobacteriales and Pasteurellales (the E/P group). Moreover, the phylogenetic analyses conducted in this work indicated that all glg genes in the E/P group share a common evolutionary origin. Finally, an extended analysis including glg genes of the main bacterial groups outside the Gammaproteobacteria indicates that E/P Glg proteins are more closely related to its counterparts of the phylogenetically distant betaproteobacterial species Variovorax paradoxus S110, Thauera sp. mz1t, Leptothrix cholodnii SP-6 and Thiomonas intermedia K12 than to Glg proteins of other Gammaproteobacteria. Furthermore, the genomic organization of glg genes in these betaproteobacterial species is very similar to that present in the E/P group.

Results

Identification and distribution of glg genes in the Gammaproteobacteria

We first searched for homologs of the five glg genes composing the E. coli glgBXCAP operon in entire genomes of the Gammaproteobacteria available in GenBank. The searches were conducted with the TBLASTN and PSI-BLAST programs on 265 complete gammaproteobacterial genomes representing 63 different genera and 13 orders using the GlgB, GlgX, GlgC, GlgA and GlgP protein sequences of the E. coli K-12 strain MG1655 (S1 Table) as query sequences. Acidithiobacillales were not included in this analysis since this proteobacterial order was recently classified as not belonging to the Gammaproteobacteria [25]. The number of sequenced genomes from the Enterobacteriales is over-represented in the databases as shown by the 115 out of the 265 genomes analyzed which belonged to species of this order (S1 Table).

Our analysis revealed a varied and complex distribution of glg genes in the Gammaproteobacteria (S1 Table). In general, the gammaproteobacterial species analyzed can be grouped into the following four categories: (i) organisms completely lacking glg homologs, (ii) organisms harbouring partial sets of glg homologs, (iii) organisms harbouring more than one copy of a particular glg homolog, and (iv) organisms harbouring all five glg homologs. This classification is not intended to be mutually exclusive since some species can be simultaneously included into categories (ii) and (iii), or (ii) and (iv) (S1 Table). Taking into account that most analyzed species are included in category (iv), in the following lines we will focus on categories (i), (ii) and (iii), and the results will be referenced to a phylogenetic tree based on 16S rRNA sequences (Fig. 2; S1 Fig.).

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Figure 2. Summarized maximum-likelihood phylogenetic tree for 16S rRNA of the analyzed gammaproteobacterial species.

Gammaproteobacterial orders are denoted by brackets. The tree was rooted with the alphaproteobacterial species Azospirillum sp. B510. Species with partial sets or total lack of glg genes are highlighted with blue and red colors, respectively. Support values for the bootstrap analysis by maximum likelihood are given. Red and blue asterisks highlight independent evolutionary events that result in total or partial glg losses, respectively. The complete tree is shown in S1 Fig.

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Gammaproteobacterial species lacking all five glg genes.

Individual species or even complete groups in which no glg homologues could be identified (highlighted in red color in Fig. 2) are interspersed among the different gammaproteobacterial lineages. Among the most recently emerged lineages such as the Enterobacteriales [25,26], organisms lacking all glg genes include endosymbionts of insects or nematodes [27] of the genera Buchnera, Blochmannia, Sodalis, Wigglesworthia and Photorhabdus, as well as Proteus mirabilis HI4320, an inhabitant of the intestinal tract of humans and common cause of urinary infections [26] (Fig. 2).

In the order Pasteurelalles, sister clade of the Enterobacteriales [25,26], two phylogenetically distant species of Haemophilus (i. e., H. influenzae F3031 and H. ducreyi) completely lack glg genes, which contrasts with phylogenetically close relatives such as H. influenzae PittGG (Fig. 2).

Within the order Alteromonodales some species totally lack glg genes, such as the marine psychrophiles Pseudoalteromonas haloplanktis TAC125, Idiomarina loihiensis L2TR, and some species of the genus Shewanella including S. woody ATCC51908, S. sedimis HAW-E4, S. pealeana ANG-SQ1, S. halifaxensis HAW-E4, and S. denitrificans OS217 (S1 Table; Fig. 2). On the contrary, glg genes are present in other species of this order such as the marine Alteromonas isolates and the psychrophiles Pseudoalteromonas atlantica T6c and Pseudoalteromonas sp. SM9913 (S1 Table; Fig. 2).

Among the Pseudomonadales, organisms lacking glg genes include all the analyzed species of the genus Acinetobacter (encompassing both opportunistic human pathogens and harmless soil bacteria), the human pathogen Moraxella catarrhalis RH4, and Psychrobacter sp. PRwf-1 which inhabits extremely cold habitats (S1 Table; Fig. 2).

Finally, concerning the deepest diverging gammaproteobacterial branches, glg genes are totally absent in all analyzed species of the genera Coxiella (obligate intracellular pathogens) and Legionella (facultative intracellular pathogens), both assigned to the order Legionellales, and in Dichelobacter nodosus VCS1703A (aerotolerant anaerobic bacteria causing ovine foot rot) of the order Cardiobacteriales (S1 Table; Fig. 2). The same occurs in the genus Xylella (plant pathogens) and in Stenotrophomonas maltophilia R551-3 (human pathogen) both assigned to the order Xanthomonadales. Also Alcanivorax borkumensis SK2, Hahella chejuensis KCTC2396 and Chromohalobacter salexigens DSM3043 (order Oceanospirillales) inhabiting marine environments completely lack glg genes (S1 Table; Fig. 2).

Gammaproteobacterial species containing partial sets of glg genes.

With the exception of glgA and glgB, differential absences of homologs of all other glg genes were observed in many independent lineages of the Gammaproteobacteria (in blue color in Fig. 2). For instance, among the order Pseudomonadales, all species of the genus Pseudomonas (which include human and plant pathogens) as well as Azotobacter vinelandii DJ (a nitrogen-fixer soil bacterium) contain homologs of all analyzed glg genes with the exception of glgC (S1 Table; Fig. 2). This is not the only example of species or groups totally lacking glgC homologs because, among the order Xanthomonadales, all the species of the genus Xanthomonas also lack glgC and, in addition, glgP (S1 Table; Fig. 2). Among the order Vibrionales, Photobacterium profundum SS9 and all the species of the genus Vibrio (including both marine species and human pathogens) lack glgP, but contain all other glg genes (S1 Table; Fig. 2). All analyzed species of the genus Francisella (order Thiotricales) lack glgX (S1 Table; Fig. 2). Finally, partial sets of glg genes are present in species assigned to the earliest emerging gammaproteobacterial lineages of the order Chromatiales including the phototrophic purple sulfur Halorhodospira halophila SL1, the ammonia-oxidizing chemolithoautotrophs of the genus Nitrosococcus, and the obligate haloalkaliphilic sulfur-oxidizing chemolithoautotroph Thioalkalivibrio sulfidophilus HL-EbGR7 (S1 Table; Fig. 2).

Gammaproteobacterial species possessing more than one copy of a particular glg homolog.

Many gammaproteobacterial species display more than one homolog of a particular glg gene, a situation noted for all five glg genes (S1 Table). More than one homologous copy for a particular glg gene is observed at almost all branching levels, from the most recently emerged to the deepest ones (Fig. 2). Most notable examples in this context are provided by Psychromonas ingrahamii 37 (order Alteromonadales) which contains three glgX homologs, four glgC homologs, and two glgA homologs, besides one copy each of glgB and glgP, and Allochromatium vinosum DSM180 (order Chromatiales) with three copies of glgA, two each of glgC, glgX and glgP, besides one glgB copy (S1 Table). In turn, all the analyzed species of the genus Xanthomonas (order Xanthomonadales) possess two homologous copies of both glgB and glgX (S1 Table). Among the latest emerging gammaproteobacterial groups, all Vibrio species (order Vibrionales) possess two glgC homologs but only one copy of each of the other glg genes, and a similar situation was found in Edwardsiella tarda EIB202 of the order Enterobacteriales (S1 Table). Finally, in the deepest gammaproteobacterial branches (for example the order Chromatiales), Nitrosococcus oceanii ATCC19707 contains two glgA homologs whereas H. halophila SL1 contains two glgC homologs (S1 Table).

Phylogenetic analysis of gammaproteobacterial Glg proteins

To determine the origin and evolutionary history of enterobacterial glg genes we conducted a phylogenetic analysis of Glg proteins in all analyzed gammaproteobacterial species. The data sets including Glg amino acid sequences were aligned using ClustalW and the alignments were subsequently refined with Gblocks. The resulting data sets consisted of 206 sequences with 537 conserved positions for the GlgB alignment, 202 sequences and 384 conserved positions for the GlgX alignment, 181 sequences and 331 conserved positions for the GlgC alignment, 201 sequences and 236 conserved positions for the GlgA alignment and 168 sequences and 631 conserved positions for the GlgP alignment.

ProtTest was used to determine the best-fit model of amino acid substitution. The LG+G+I+F model (see Materials and Methods) was identified as the best model for the five data sets. The phylogenetic information content of the data sets was then evaluated by using likelihood mapping. Briefly, this analysis allows to estimate the suitability for phylogenetic reconstruction of a data set from the proportion of unresolved quartets in a maximum likelihood analysis (for a complete description see Materials and Methods). The analysis was carried out using TreePuzzle with the WAG+G+F [28] model of substitution (the second best model selected by ProtTest since the LG model is not implemented in this program). The likelihood mapping showed that the five data sets possessed a high content of phylogenetic information, with 95%, 93%, 96%, 94% and 97% of fully resolved quartets in GlgB, GlgX, GlgC, GlgA and GlgP, respectively (S2 Fig.).

The phylogenetic reconstructions were performed with PhyML using the LG+G+I+F model (Figs. 3–7). From the inspection of the individual Glg phylogenetic trees some conclusions arose relative to the grouping pattern of the order Enterobacteriales. In agreement with the reference 16S rRNA phylogenetic tree of Fig. 2, all Enterobacteriales Glg sequences clustered with Pasteurellales sequences forming monophyletic Enterobacteriales/Pasteurellales (E/P) groups in the five Glg phylogenetic trees (Figs. 3–7; S3–S7 Figs.). To test whether the topologies of the trees of Glg sequences of the E/P group were compatible with the order of organismal descent inferred from the 16S rRNA phylogenetic analysis, the Shimodaira-Hasegawa test was used. This analysis showed that the topologies of the trees of the five Glg proteins were compatible with the topology of the 16S rRNA phylogenetic tree (p = 0.525, p = 0.462, p = 0.574, p = 0.492 and p = 0.696, for GlgB, GlgX, GlgC, GlgA and GlgP, respectively).

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Figure 3. Summarized maximum-likelihood phylogenetic tree of the GlgB amino acid sequences containing all analyzed gammaproteobacterial species.

The tree was arbitrarily rooted with the alphaproteobacterial species Azospirillum sp. B510. The complete tree is shown in S3 Fig. Bootstrap support values (>70%) are indicated.

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Figure 4. Summarized maximum-likelihood phylogenetic tree of the GlgX amino acid sequences containing all analyzed gammaproteobacterial species.

The tree was arbitrarily rooted with the alphaproteobacterial species Azospirillum sp. B510. The complete tree is shown in S4 Fig. Bootstrap support values (>70%) are indicated.

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Figure 5. Summarized maximum-likelihood phylogenetic tree of the GlgC amino acid sequences containing all analyzed gammaproteobacterial species.

The tree was arbitrarily rooted with the alphaproteobacterial species Azospirillum sp. B510. The complete tree is shown in S5 Fig. Bootstrap support values (>70%) are indicated.

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Figure 6. Summarized maximum-likelihood phylogenetic tree of the GlgA amino acid sequences containing all analyzed gammaproteobacterial species.

The tree was arbitrarily rooted with the alphaproteobacterial species Azospirillum sp. B510. The complete tree is shown in S6 Fig. Bootstrap support values (>70%) are indicated.

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Figure 7. Summarized maximum-likelihood phylogenetic tree of the GlgP amino acid sequences containing all analyzed gammaproteobacterial species.

The tree was arbitrarily rooted with the alphaproteobacterial species Azospirillum sp. B510. The complete tree is shown in S7 Fig. Bootstrap support values (>70%) are indicated.

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As shown in the 16S rRNA reference tree presented in Fig. 2, the E/P group is clustered in a highly supported group (bootstrap support (BS) = 99%) with the orders Vibrionales, Aeromononadales and Alteromonadales forming the Vibrionales/Pasteurellales/Enterobacteriales/Aeromonodales/Alteromonadales (VPEAA) clade. It is worth noting that the monophyly of this VPEAA clade within the Gammaproteobacteria has been described in two independent works analyzing the phylogeny of this class [25,29]. However, similar VPEAA clades are not observed in Glg phylogenetic trees since in all cases the E/P group fails to cluster with Vibrionales, Aeromonadales and Alteromonadales (Figs. 3–7; S3–S7 Figs.). Thus, with the exception of the E/P group, lack of congruence is observed between the evolution of glg genes and the evolution of the rest of gammaproteobacterial lineages.

Phylogenetic relationship of E/P Glg proteins with their counterparts outside the Gammaproteobacteria

We performed a phylogenetic reconstruction including both gammaproteobacterial Glg protein sequences and those of 75 species representing the main bacterial groups outside the Gammaproteobacteria (S2 Table). The Glg sequences thus obtained were aligned with ClustalW and subsequently refined with Gblocks. The resulting data sets consisted of 279 sequences with 406 conserved positions for the GlgB alignment, 257 sequences and 291 conserved positions for the GlgX alignment, 245 sequences and 226 conserved positions for the GlgC alignment, 259 sequences and 157 conserved positions for the GlgA alignment and 217 sequences and 520 conserved positions for the GlgP alignment. The best-fit model for these data sets was LG+G+I+F. The likelihood mapping (using again WAG+G+F) showed a marked decrease in phylogenetic signal compared to the gammaproteobacterial data sets (S8 Fig.). The phylogenetic reconstructions were performed as described for the gammaproteobacterial data sets (Figs. 8–12; S9–S13 Figs.). Moreover, a new 16S rRNA reference tree including both gammaproteobacterial and representative species of the main bacterial groups outside the Gammaproteobacteria was constructed (Fig. 13; S14 Fig.).

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Figure 8. Summarized maximum-likelihood phylogenetic tree of the GlgB amino acid sequences of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

The tree was midpoint rooted. The complete tree is shown in S9 Fig. Bootstrap support values (>70%) are indicated.

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Figure 9. Summarized maximum-likelihood phylogenetic tree of the GlgX amino acid sequences of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

The tree was midpoint rooted. The complete tree is shown in S10 Fig. Bootstrap support values (>70%) are indicated.

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Figure 10. Summarized maximum-likelihood phylogenetic tree of the GlgC amino acid sequences of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

The tree was midpoint rooted. The complete tree is shown in S11 Fig. Bootstrap support values (>70%) are indicated.

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Figure 11. Summarized maximum-likelihood phylogenetic tree of the GlgA amino acid sequences of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

The tree was midpoint rooted. The complete tree is shown in S12 Fig. Bootstrap support values (>70%) are indicated. The branch of GlgA1 and GlgA2 A. pasteurianus IFO3283-01 has been shortened to facilitate its visualization.

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Figure 12. Summarized maximum-likelihood phylogenetic tree of the GlgP amino acid sequences of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

The tree was midpoint rooted. The complete tree is shown in S13 Fig. Bootstrap support values (>70%) are indicated. The branch of GlgP1 G. violaceus PCC7421 has been shortened to facilitate its visualization.

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Figure 13. Summarized maximum-likelihood phylogenetic tree for 16S rRNA of the analyzed gammaproteobacterial species and of the selected species belonging to main bacterial groups.

Support values for the bootstrap analysis by maximum likelihood are given. The Gammaproteobacteria and main bacterial groups are denoted by brackets. The tree was midpoint rooted. The complete tree is shown in S14 Fig.

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The above phylogenetic analyses further confirmed the E/P monophyly for the five glg genes and the lack of congruence between the Glg phylogenetic trees and the 16S rRNA reference tree (Figs. 8–13; S9–S14 Figs.). Remarkably, these analyses also revealed that the Glg proteins of the betaproteobacterial species Variovorax paradoxus S110, Thauera sp. mz1t, Leptothrix cholodnii SP-6 and Thiomonas intermedia K12 all clustered with their corresponding homologs of the E/P group, forming a sister clade of E/P in GlgB, GlgA and GlgP phylogenetic trees (Figs. 8, 11, 12; S9, S12, S13 Figs.). This close relationship among proteins of such distant lineages could be explained by horizontal gene transfer (HGT). HGT events can be detected by nucleotide compositional analyses. Therefore, compositional similarity analyses of V. paradoxus S110, Thauera sp. mz1t, L. cholodnii SP-6 and T. intermedia K12 genomes were carried out using GOHTAM web tool [30]. These analyses showed that glg genes of these betaproteobacterial species did not exhibit atypical compositional features in the context of their respective genomes (S3 Table). Finally, it is worth mentioning that among these betaproteobacterial species only V. paradoxus S110 possesses additional copies of glg genes (glgB2 and glgX2) (see below), which are related with glgB and glgX of other betaproteobacterial lineages (Figs. 8, 9; S9, S10 Figs.).

Genomic arrangement of glg genes

The analysis of the glg genes genomic context showed that the glgBXCAP arrangement exists not only in E. coli but also in all E/P species bearing glg genes (Fig. 14). This is not surprising since previous studies have shown that the gene order in operon structures in the Enterobacteriales and the Pasteurellales is well conserved [31,32]. Thus, 56% of operons of E. coli (order Enterobacteriales) were found to be identical to those of H. influenzae (order Pasteurellales) [31]. Remarkably, the phylogenetically distant betaproteobacterial species V. paradoxus S110, Thauera sp. mz1t, L. cholodnii SP-6 and T. intermedia K12 present a genomic arrangement of glg genes very similar to that of E/P (Fig. 14). In fact, the glg genes in V. paradoxus S110 are arranged following the glgBXCAP order (Fig. 14). No other analyzed species of any bacterial group exhibits the glgBXCAP arrangement.

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Figure 14. Arrangements of glg genes in the specified species.

Colors indicate homologous genes. Arrows indicate the direction of transcription. Black lines indicate a physical separation between the genes and dashed lines indicate pseudogenes.

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As noted above, V. paradoxus S110 possesses additional glgB and glgX copies to those of the glgBXCAP cluster (see above). These copies are arranged in a cluster similar to that occurring in the phylogenetically related betaproteobacterial species Burkholderia sp. 383, Ralstonia eutropha H16 and Bordetella parapertussis 12822 (Figs. 13, 14). Remarkably, T. intermedia K12 and L. cholodnii SP-6 present a phosphohexomutase encoding phx gene between glgX and glgC (Fig. 14).

Our studies of glg arrangements also revealed that glg genes are clustered in glgBXPCA disposition in the genus Shewanella and in the species P. atlantica T6c of the order Alteromonadales (Fig. 14). In addition, species of the orders Aeromonadales and Alteromonadales share the glgBX disposition of glg genes (Fig. 14), whereas the tandem glgCA is conserved in the species belonging to the orders Vibrionales and Aeromonadales (Fig. 14) and glgCAP is present in species of Thiotricales.

Discussion

The aim of this work was to elucidate the origin and evolutionary history of E. coli glg genes. Our analyses indicate that glg genes are present in most gammaproteobacterial lineages, from the earliest to the most recently emerged branches (Fig. 2). This widespread distribution in species displaying a wide range of lifestyles suggests that function(s) linked to glg genes would provide some advantages for survival under varied and varying environmental conditions. Yet, our analyses have also shown large variability in content, copy number and arrangement of glg genes among the different gammaproteobacterial lineages (S1 Table; Fig. 14). The phylogenetic analyses carried out in both the Gammaproteobacteria and other main bacterial groups revealed an important discordance between the evolution of glg genes (Figs. 3–12; S3–S13 Figs.) and the evolution of the analyzed bacterial species (Figs. 2, 13), thus strongly suggesting that HGT has played an important role in the evolutionary history of glg genes. However, a remarkable exception to this rule is constituted by species of the E/P group in which each individual glg gene forms a monophyletic group in the corresponding phylogenetic trees that agrees with the expected order of organismal descent as inferred from 16S rRNA phylogenetic analysis (Figs. 2, 13; S1, S14 Figs.). Our data strongly suggest that (a) E/P glg genes share a common origin in the last common ancestor (LCA) of the E/P group, (b) vertical inheritance has been the primary mode of transmission of these genes throughout evolution in this group and (c) the origin of the glgBXCAP cluster could be traced to the LCA of the E/P group as inferred from the same arrangement found in all analyzed E/P species. The complex evolutionary history of glg genes in the other bacterial lineages prevented us from further tracing the evolutionary history of gammaproteobacterial glg genes.

The most likely evolutionary explanation for the occurrence of species or groups totally or partially lacking glg genes is that both complete and partial losses of glg genes have occurred independently during the evolution of different gammaproteobacterial lineages. In the analyzed data set, partial glg losses are less frequent than the loss of all glg genes. In fact, the observed distribution of partial glg losses in the different gammaproteobacterial lineages can be explained by seven independent evolutionary events, whereas eighteen independent losses are necessary to explain the distribution of the species lacking all five glg genes (indicated by asterisks in Fig. 2). Examples of recent losses of all glg genes are provided by H. influenzae (order Pasteurellales) in which one isolate (F3031) lacks all glg genes whereas complete sets are present in phylogenetically close isolates such 86-028NP and PittGG (S1 Table; Fig. 2). Recent independent losses of all glg genes have also occurred in S. denitrificans OS217, S. halifaxensis HAW-EB4, S. paeleana ANG-SO1, S. sedimis HAW-EB3, S. woodyi ATCC51908, P. haloplanktis TAC125 (order Alteromonadales), S. maltophilia R551-3 (order Xanthomonadales) and Psychrobacter sp. PRwf-1 (order Pseudomonadales) (S1 Table; Fig. 2). The loss of all glg genes is also observed in the marine species belonging to the order Oceanospirillales, in the plant pathogenic species of Xylella, in the Acinetobacter species (which live in the soil and causes infections in humans), in the pathogenic species belonging to the order Legionellales, in P. mirabilis HI4320 or in the insect endosymbionts of the genera Buchnera, Blochmannia, Baumannia, Sodalis, Wigglesworthia and Photorhabdus (all belonging to the order Enterobacteriales) (S1 Table; Fig. 2).

Using 55 complete bacterial genomes (including 11 gammaproteobacterial genomes) Henrissat et al. (2002) [33] reported that bacteria lacking glycogen metabolism are parasitic, symbiotic or fastidious (i. e., difficult to cultivate under laboratory conditions). These authors thus hypothesized that (a) these bacteria rely on their host´s glycogen (or starch) metabolism and (b) the lack of glycogen metabolism is a trait associated with bacterial parasitic or symbiotic behaviors [33]. However, the analysis of a more comprehensive genome set conducted here fails to provide support to this hypothesis at least in the Gammaproteobacteria, since the lack of all glg genes is observed in species with drastically different lifestyles which are not necessarily parasitic, symbiotic or fastidious such as P. mirabilis HI4320, P. haloplanktis TAC125, S. denitrificans OS217, Psychrobacter sp. PRwf-1 or A. borkumensis SK2.

The absence of GlgC and GlgP from some gammaproteobacterial species (S1 Table) would imply the loss of ADPG synthesis and glycogen degradation, respectively. Alternatively, it is possible that the absence of these proteins could be compensated by others that are capable of carrying out the same function(s). In this respect we must emphasize that several reports have shown that multiple bacteria possess still unidentified sources of ADPG, other than GlgC, linked to glycogen biosynthesis [5,14,19,20,34]. In the absence of GlgP, it is likely that maltodextrin phosphorylase (MalP), an α-glucan phosphorylase with high similarity to GlgP, could control glycogen degradation [35–37]. On the other hand, the absence of GlgP in some gammaproteobacterial species could indicate that glg genes are not related to glycogen metabolism in these species but to other functions in which glycogen degrading enzymes are not necessary, such as the synthesis of exopolysaccharides. In this respect, it must be noted that Aeromonas hydrophila (a species lacking GlgP), possesses a GlgA enzyme recognizing both ADPG and UDP-glucose (UDPG) as substrates, and one GlgC homolog displaying UDPG pyrophosphorylase activity rather than ADPG pyrophosphorylase activity involved in the synthesis of a α-branched glucan surface polysaccharide linked to biofilm production [38].

Clustering of genes involved in the same metabolic pathway into a transcriptional unit or operon is frequently observed in bacteria [21–23]. Two models are generally considered to explain operon formation: (i) the selfish operon model postulates that HGT plays a key role in operon evolution [39]; (ii) the co-regulation model proposes that formation of operons facilitates co-regulation [40]. Grouping related genes under a common control mechanism would favour a more efficient regulation of gene expression levels and would allow bacteria to rapidly adapt their metabolism to environmental changes and biochemical needs [41–45]. In the case of glg genes, besides the glgBXCAP operon present in the gammaproteobacterial E/P group, different glg arrangements have been described in other phylogenetically distant bacteria such as in the alphaproteobacterial species Agrobacterium tumefaciens, Rizhobium tropici and Mesorhizobium loti, and also in the Gram-positive species Bacillus subtilis and Bacillus stearothermophilus [7]. In this work we have described the presence of the glgBXPCA arrangement in species of the gammaproteobacterial genus Shewanella and in the species P. atlantica T6c (Fig. 14). It is worth noting that our phylogenetic analyses showed that P. atlantica T6c and Shewanella glg genes are not closely related (Figs. 3–12; S3–S7, S9–S13 Figs.), which suggests an independent assembly of the glgBXPCA cluster in them. Moreover, the glgBX arrangement is shared by species of the orders Aeromonadales and Alteromonadales (Fig. 14), the tandem glgCA is present in Vibrionales and Aeromonadales (Fig. 14), and the glgCAP arrangement is present in Thiotricales. Therefore, it seems that along evolution glg genes have been clustered together in several independent occasions and in different order, probably responding to different metabolic needs imposed by the environment and lifestyles. Needless to say, further research on the glycogen metabolism and evolution of glycogen operons in a wide range of bacterial species is necessary to confirm (or refute) this hypothesis.

Our study has allowed tracing the evolutionary origin of the glgBXCAP operon to the LCA of the E/P group. We can just speculate about the advantages that would account for the widespread preservation of the glgBXCAP arrangement throughout the evolution of the E/P group. The transcription of the glgBXCAP operon implies the combined expression of glycogen synthetic and degradative enzymes, allowing the simultaneous synthesis and degradation of glycogen. It was previously proposed that the balance of parallel synthesis and degradation pathways serves to maintain glycogen structure and to function as a carbon capacitor thus allowing a sensitive regulation of downstream carbon and energy fluxes [17,46,47]. The resulting turnover of glycogen would entail advantages such as dissipation of excess energy, sensitive regulation and rapid channeling of metabolic intermediates toward various metabolic pathways in response to biochemical needs [48,49]. The latter is particularly relevant, especially when considering that previous reports have shown that glycogen metabolism is highly interconnected with a wide variety of cellular processes [19,50,51].

The observed clustering of the E/P group with phylogenetically distant betaproteobacterial species V. paradoxus S110, L. cholodnii SP-6, T. intermedia K12 and Thauera sp. mz1t in the Glg phylogenetic trees (Figs. 8–12; S9–S13 Figs.), along with the presence of glgBXCAP and/or gene clusters similar to glgBXCAP exclusively in these betaproteobacterial species (Fig. 14) can be explained by (i) an ancestral duplication of the glgBXCAP cluster in their LCA and subsequent loss in all intervening lineages, (ii) two independent HGT events of the glgBXCAP cluster from E/P, the first one to the common ancestor of V. paradoxus S110, L. cholodnii SP-6 and T. intermedia K12, and the second one to Thauera sp. mz1t, (iii) an HGT event of the glgBXCAP cluster from E/P to the common ancestor of V. paradoxus S110, L. cholodnii SP-6 and T. intermedia K12 or to Thauera sp. mz1t, and a second HGT event between them, or (iv) an HGT event of the glgBXCAP cluster from E/P to the LCA of the four betaproteobacterial species and followed by subsequent multiple, independent losses in the species Burkholderia sp. 383, R. eutropha H16, B. parapertussis 12822 and Thiobacillus denitrificans ATCC25259 (see Fig. 13). Previous studies based on parametric methods and aimed at predicting horizontally transferred genes did not identify the glg genes as horizontally transferred in the above betaproteobacterial species [52,53], thus favoring the hypothesis of the occurrence of an ancestral duplication of glg genes. Consistently, compositional analysis of V. paradoxus S110, L. cholodnii SP-6, T. intermedia K12 and Thauera sp. mz1t carried out in this work (S3 Table) did not identify glg genes as exhibiting atypical compositional features. However, we must emphasize that HGT events produce a localized nucleotide bias that tends to disappear in a relatively short period of evolutionary time, a process commonly known as amelioration [54]. Thus, failure of parametric methods in identifying glg genes as horizontally transferred in the above four betaproteobacterial species can be explained by this phenomenon in a situation where the putative HGT event(s) would have occurred before the differentiation of these betaproteobacterial lineages. Although data available cannot unequivocally confirm or rule out any of the above scenarios, it must be noted that the second and the third scenarios (both encompassing HGT events) are the most parsimonious since they would imply only two independent evolutionary events whereas the first would imply multiple and independent losses in other lineages, and the fourth requires five independent events (one HGT and four independent losses).

We must emphasize that V. paradoxus S110 possesses additional copies of both glgB and glgX (Figs. 8, 9; S9, S10 Figs.), which are very distant to their own homologs related with the E/P group and located in gene clusters similar to those found in their phylogenetically related betaproteobacterial species Burkholderia sp. 383, R. eutropha H16, and B. parapertussis 12822 (Fig. 14). This reinforces the possibility of an horizontal transfer of the complete glgBXCAP operon from E/P to the ancestor of V. paradoxus S110, L. cholodnii SP-6, T. intermedia K12 and/or to Thauera sp. mz1t. Subsequent gene rearrangements led to the clusters observed in these species. These rearrangements include the relocation of glgB in L. cholodnii SP-6 and of glgP in Thauera mz1t, as well as the acquisition of phx genes in T. intermedia K12 and L. cholodnii SP-6.

In agreement with researchers favoring a view in which HGT has played a major continuous role in evolution [55–59] our results indicate its prevalence in the evolution and distribution of glg genes within Bacteria. Two main pieces of evidence support this conclusion. First, the phylogenetic analysis of the five Glg proteins shows that the evolution of glg genes is in clear conflict with the order of organismal descent, inferred from the 16S rRNA analysis. Second, in species possessing more than one copy of a given glg gene, some of the copies are related to homologous copies of phylogenetically distant species as for example glgX2 of the gammaproteobacterial species Pantoea vagans C9-1 (order Enterobacteriales) which is more related to its homolog present in the alphaproteobacterial species Acetobacter pasteurianus IFO 3283-01 (Fig. 11; S8 Fig.), glgX2 of Cellvibrio gilvus ATCC13127 (gammaproteobacterial order Pseudomonadales) which is more related with homologs from Actinobacteria (Fig. 11; S8 Fig.), and glgC2 of Edwardsiella (gammaproteobacterial order Enterobacteriales) which is more related with homologs of the Pasteurellales (Fig. 12; S9 Fig.). Moreover, our results also suggest the occurrence of an horizontal transfer of the complete glgBXCAP operon from E/P group to some Betaproteobacteria, indicating that HGT is not restricted to individual glg genes, adding more complexity to the evolution of these genes.

Materials and Methods

Sequences

We have analyzed the complete genomes of 265 different gammaproteobacterial species and strains (see S1 Table) and of 75 species of the main bacterial groups outside the Gammaproteobacteria (see S2 Table) retrieved from the NCBI repository. GlgB, GlgX, GlgC, GlgA, and GlgP encoding genes were retrieved from whole genomes by using PSI-BLAST [60]. The PSI-BLAST searches were performed against the GenBank database using the E. coli GlgB, GlgX, GlgC, GlgA and GlgP (accession numbers NP_417890.1, NP_417889.1, NP_417888.1, NP_417887.1 and NP_417886.1 respectively) as query sequences with default settings. From all the sequences retrieved, only those from whole genomes were selected, and these were subsequently filtered attending to a coverage of at least 75% and an identity of at least 35% of the query sequence. The corresponding 16S rRNA sequences from each genome were downloaded using the tools implemented in the Ribosomal Database Project II (RDB-II) [61].

Alignments and phylogenetic information analyses

Multiple alignments were obtained with ClustalW [62] and were manually corrected. Positions of uncertain homology and extensive gaps were removed using GBLOCKS with default settings [63]. The final multiple alignments used for the analyses are available from the authors upon request. The best-fit models of amino acid substitution were determined using the program ProtTest [64]. The Akaike Information Criterion (AIC), which allows for a comparison of likelihoods from non-tested models, was adopted to select the best model [65]. For the five proteins the model LG [66] with a discrete gamma distribution to account for heterogeneity in evolutionary rates among sites, an estimation of the proportion of invariant sites and the empirical frequencies of amino acids (LG+G+I+F) was identified as the best-fit model. The phylogenetic signal contained in the different data sets was assessed by likelihood-mapping [67] using TreePuzzle 5.2 [68]. This method evaluates the resolution in quartets generated from combinations of the different sequences under study. Values below 90% resolved quartets were considered to indicate a low phylogenetic signal. In this evaluation we used the WAG model [28] of amino acid evolution and a discrete gamma distribution to account for heterogeneity in evolutionary rates among positions in the multiple alignments (S2, S8 Figs.).

Phylogenetic reconstructions

The model selected by ProtTest was implemented in PhyML 3.0 [69] to obtain maximum likelihood (ML) trees for the different multiple alignments. Bootstrap support values were obtained from 1000 pseudorandom replicates.

To obtain the phylogenetic reference trees encompassing all the analyzed species, sequences of genes encoding 16S rRNA were obtained using the tools implemented in the RDB-II. The sequences were aligned using the aligner implemented in RDB-II. The best fit-model of nucleotide substitution was selected using jModelTest [70] with the AIC criterion. The phylogenetic relationships were inferred using PhyML with the GTR model of nucleotide substitution and the proportion of invariant and rate heterogeneity categories estimated from the data set. Bootstrap support values were obtained from 1000 pseudorandom replicates.

For the E/P group we carried out a comparison between each glg gene tree and the 16S rRNA (reference tree) topology. The Shimodaira-Hasegawa´s test (SH test) [71] as implemented in the program TreePuzzle 5.2 was used to determine whether the likelihood of the data associated to each tree was significantly different at an alpha level of 0.05 (a value above the threshold indicating a non-significant difference). Phylogenetic trees of 16S rRNA sequences were obtained with the Tree Builder tool of the RDB-II and compared to ML phylogenetic trees of the corresponding Glg sequences from E/P species.

Compositional analyses

Nucleotide compositional analyses were carried out using the GOHTAM web tool [30]. This web tool allows to identify genomic regions and/or genes that exhibit atypical features compared to the rest of the sequence. The detection is based on a combination of the genomic signature [72,73] and a codon usage method [74].

Supporting Information

S1 Table. Summary of gammaproteobacterial species studied in the present work, their assigned order, and number of copies of each glg gene in their genomes.

In the case of endosymbionts of insects, the corresponding host species is also indicated between brackets.

https://doi.org/10.1371/journal.pone.0115516.s001

(DOCX)

S2 Table. Summary of the non-Gammaproteobacteria species studied in the present work and the number of copies of the different glg genes in their genomes.

https://doi.org/10.1371/journal.pone.0115516.s002

(DOCX)

S3 Table. Regions and/or genes of the betaproteobacterial species V. paradoxus S110, T. intermedia K12, L. cholodnii SP-6 and Thauera mz1t that exhibit atypical compositional features compared to the their respective genome.

https://doi.org/10.1371/journal.pone.0115516.s003

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S1 Fig. Maximum likelihood phylogenetic tree for 16S rRNA of the analyzed gammaproteobacterial species.

Support values >70% for the bootstrap analysis by maximum likelihood are given. The tree was rooted with the alphaproteobacterial species Azospirillum sp. B510.

https://doi.org/10.1371/journal.pone.0115516.s004

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S2 Fig. Likelihood mapping analysis of gammaproteobacterial data set.

The regions at the corners of the triangles correspond to the three possible tree topologies for a quartet; the lateral regions to partly resolved trees and the central region to unresolved trees. The numbers indicate the percentage of quartets falling in each region.

https://doi.org/10.1371/journal.pone.0115516.s005

(EPS)