BioMed Research International

BioMed Research International / 2014 / Article
Special Issue

Advances in Computational Genomics

View this Special Issue

Research Article | Open Access

Volume 2014 |Article ID 694967 | 11 pages |

Metabolic Modeling of Common Escherichia coli Strains in Human Gut Microbiome

Academic Editor: Zhixi Su
Received21 Apr 2014
Revised11 Jun 2014
Accepted13 Jun 2014
Published13 Jul 2014


The recent high-throughput sequencing has enabled the composition of Escherichia coli strains in the human microbial community to be profiled en masse. However, there are two challenges to address: (1) exploring the genetic differences between E. coli strains in human gut and (2) dynamic responses of E. coli to diverse stress conditions. As a result, we investigated the E. coli strains in human gut microbiome using deep sequencing data and reconstructed genome-wide metabolic networks for the three most common E. coli strains, including E. coli HS, UTI89, and CFT073. The metabolic models show obvious strain-specific characteristics, both in network contents and in behaviors. We predicted optimal biomass production for three models on four different carbon sources (acetate, ethanol, glucose, and succinate) and found that these stress-associated genes were involved in host-microbial interactions and increased in human obesity. Besides, it shows that the growth rates are similar among the models, but the flux distributions are different, even in E. coli core reactions. The correlations between human diabetes-associated metabolic reactions in the E. coli models were also predicted. The study provides a systems perspective on E. coli strains in human gut microbiome and will be helpful in integrating diverse data sources in the following study.

1. Introduction

Escherichia coli (E. coli) is the most widely studied prokaryotic model organism and an important species in the fields of biotechnology and microbiology. E. coli constitutes about 0.1% of human gut flora [1], which benefits human beings by providing supplemental nutrition, by enhancing nutrient acquisition, and by preventing the establishment of pathogenic bacteria within the intestine [2]. The study of this bacterium is both of importance for applications, such as environmental testing and metabolic engineering [3], and of interest as a fundamental physical problem. For example, a recent study demonstrated an obvious increase in the number of E. coli in the stool, while diarrhea was apparent [4].

In the recent five years, the flood of deep sequencing data has set the latest wave of microbiome research apart from earlier studies, with the ability to enumerate all of the cells in a complex microbial community at once [5]. For instance, using deep sequencing, the Human Microbiome Project (HMP) was launched to characterize the microbial communities found at several different sites on the human body and to analyze the role of these microbes in human health and disease [6, 7]. This switch from the low-throughput technique, culture-based enumeration, to the high-throughput technology of deep sequencing offers several advantages, including high accuracy, culture-free sampling, and comprehensive information. However, there are still two challenges to address. First, due to the huge data size and high complexity of the different algorithms, it is difficult to determine the exact roles of the various species in human microbiome, let alone strains of the same species. The composition of E. coli strains is of value to human health; for example, changes in the E. coli composition were observed associated with intestinal inflammatory disorders in human and mice [8, 9]. Second, most of the microbiota community structures obtained from sequencing were “static,” while the human microbiomes are diverse and dynamic. The diet changes, individual differences, sampling sites, and physical conditions are responsible for the dynamic responses of human microbiome [1012]. However, the comprehensive responses of microbiome to the dynamic microenvironments can hardly be obtained from one or several samples.

To solve these problems, considerable efforts have been made to develop metabolic networks of E. coli [3, 13, 14]. These in silico models have been successfully applied in many fields. For example, they were frequently used in prediction of steady-state or dynamic responses of cells to changes in ecosystems [3]. In addition, the metabolic models can be easily integrated with other data sources, such as DNA sequencing [15], expression profiles [16], proteomics [17], or metabolomics [18]. Goals of such data integration efforts are (1) to gain a better understanding of the observable phenotypes of the cell, (2) to predict potential functions of molecular signatures, and (3) to apply these in silico models for biological discovery and engineering applications. As a result, integration of relevant omics data with metabolic models as a representative species in the human gut microbiota elucidates the changes in the gut microbiota.

In this study, we performed in silico modeling of metabolic networks of E. coli strains in human gut microbiome. First, we determined E. coli strains in human gut microbiome using 148 fecal metagenomes. Next, we reconstructed genome-wide metabolic network of common E. coli strains in human gut. Then, the cellular phenotypes were predicted and validated using the genome variation of E. coli and diet changes. The findings of the study will help in developing new technologies and tools for computational analysis and exploring the relationship between disease and changes in the human microbiome.

2. Materials and Methods

2.1. Human Gut Metagenomes and Reference Genomes

High-quality short reads of 148 human gut samples were retrieved from Human Microbiome Project (HMP, The sequenced and well-annotated E. coli genomes (totally 61 genomes) deposited in GenBank were downloaded from NCBI database (, to build a reference genome database. The reads were aligned against the E. coli reference genome using BLASTN (version 2.2.27+) with , minimal 99% identity cutoff and considering the reads that were aligned onto only a single position in the reference genome.

2.2. De Novo Assembly and Identification of Genes

The reads of human gut samples were assembled by Newbler (454/Roche GS Mapper/Assembler), following the protocol in HMP [19]. The assembled scaffolds were aligned against E. coli genomes using BLASTN with minimal 99% identity cutoff and best hit output.

2.3. Reconstruction of Strain-Specific Metabolic Network

The E. coli pan-genome (the union of the gene sets of all the strains of a species) metabolic network has been generated in a recent study [20]. The strain-specific metabolic model could be reconstructed based on the pan-genome metabolic network. We generated metabolic networks for the common E. coli strains in human gut microbiome based on the pan-genome metabolic network.

In the process, we derived the strain-specific metabolic models using two commonly used algorithms of top-down metabolic reconstructions, including GIMME [21] and iMAT [22]. These two algorithms are different: the GIMME is a linear programming procedure, while the iMAT is a mixed integer linear programming procedure.

2.4. Predictions of Cellular Phenotypes Using Metabolic Network

Fluxes through reactions in the metabolic models can be predicted using flux balance analysis (FBA) [23]. In the process, fluxes are constrained by steady-state mass balances, enzyme capacities, and reaction directionality, which yield a solution space of possible flux values. Besides, FBA uses an objective function to identify flux distributions that maximize (or minimize) the physiologically relevant predicted solution. Cellular growth rate (biomass production in another word) was used as an objective function for FBA analyses performed in this study. The same biomass equation, growth (GAM) and nongrowth (NGAM) associated ATP requirement values, and PO (number of ATP molecules produced per pair of electrons donated to the electron transport system) ratio were used for all the E. coli models and were the same as that in iAF1260 model [24]. When the metabolic models were used to simulate the change of carbon source (e.g., from glucose to succinate), we obtained the corresponding optimal growth rates and flux distributions for all the reactions. If the uptake/secretion flux for a reaction in the optimal flux solution was reduced or increased by over 10% ( or ) between two conditions, we defined the reactions to be associated with the diet stress.

Uniform random sampling of the solution space for E. coli metabolic models in any environmental condition is a rapid and scalable way to characterize the structure of the allowed space of metabolic fluxes [25]. The set of flux distributions obtained from sampling can be interrogated further to answer a number of questions related to the metabolic network function. In the study, we studied how dependent two reactions within the E. coli network were on each other.

2.5. Flux Variability Analysis (FVA)

Biological systems often contain redundancies that contribute to their robustness. FVA can be used to examine these redundancies by calculating the full range of numerical values for each reaction flux in a network [26]. In FVA, the process is carried out by optimizing for a particular objective, while still satisfying the given constraints set on biological systems. In the study, FVA was applied to determine the ranges of fluxes that correspond to an optimal solution of the E. coli models determined through FBA. The maximum value of the objective function is first computed and this value is used with multiple optimizations to calculate the maximum and minimum flux values through each reaction.

3. Results

3.1. E. coli in Human Gut Microbiome

Deep metagenomic sequencing provides us the opportunity to explore the existence of a common set of E. coli species in human gut microbiome.

To obtain this goal, we built a nonredundant database of 61 sequenced and well-annotated E. coli genomes. After aligning the reads of each human gut microbial sample onto the reference database, we determined the proportion of the genomes covered by the reads (Methods). At a 99% identity threshold and 10-fold coverage (the genomes of E. coli strains are 5 M on average), we detected one in all gut samples, three in 80%, and seven in 60% of the 148 human gut samples (Table 1). We focused on the three common E. coli strains, including E. coli HS, UTI89, and CFT073. Other recent studies support our findings, including studies from human [27] and animal models [28].

Escherichia coli strainsSamples countaGenome sizeGene countsProtein countGenes by de novo assembly

E. coli HS1484.6 M462943773606
E. coli UTI891345.0 M512750173435
E. coli CFT0731255.2 M557953693406
E. coli KO11FL1154.9 M475645333512
E. coli NA114945.0 M497548733381
E. coli 536904.9 M477946193488
E. coli O127:H6 str. E2348/69905.0 M489045523179

aThere are 148 individual samples in the analysis.

Besides the genome-guided methods, the reads were used to perform de novo assembly, which can recover transcript fragments from regions missing in the genome assembly [29]. We first assembled metagenomes in 148 human gut microbiome samples using over 10 billion reads. Then, we mapped the 15 million gut scaffolds to the 293663 genes (target genes) of the 61 E. coli genomes in the human gut. At a 99% identity threshold, over 60% of the target genes of the seven E. coli in Table 1 had at least 80% of their length covered by a single scaffold, indicating that the genes of these E. coli strains were significantly enriched in the gut scaffolds (Fisher’s exact test, ).

3.2. In Silico Metabolic Models of E. coli Strains

We generated genome-wide metabolic network of three common E. coli (E. coli HS, UTI89, and CFT073) from metabolic model of E. coli pan-genome using GIMME and iMAT algorithms.

The results indicate that the metabolic networks obtained with the two algorithms are identical (TEXT S1–S3 available online at We then explored the differences in network properties among the three models. It shows that these models are different in network structure (Figure 1(a), Table S1). For example, compared with E. coli CFT073 and E. coli UTI89, E. coli HS model has 41 specific metabolic reactions catalyzed by 36 genes (Figure 1(b)). These reactions are associated with alternate carbon metabolism, murein recycling, nitrogen metabolism, and inner membrane transport. Most of the reactions tend to form a subnetwork rather than are scattered in an apparently random manner in the metabolic network. We also observed 32 different metabolites not included in all the three models (Table 2). Only three of the metabolites (including allantoate, tRNA-Ala, and tRNA-Phe) can be detected in the human metabolic model Recon2 [30], suggesting that most of these different metabolites are not involved in direct interactions of gut microbiome host. However, some of these metabolites are of importance to strain-specific characteristics and closely related to human-microbe interactions. For example, GDP-L-fucose plays important roles in microbial infection and numerous ontogenic events [31].


all6pD-Allose 6-phosphateC6H11O9P−2
allul6pAllulose 6-phosphateC6H11O9P−2
dhcinnm2,3-Dihydroxicinnamic acidC9H7O4−1
frulyspFructoselysine phosphateC12H24N2O10P−1
gg4abutGamma-glutamyl-gamma aminobutyric acidC9H15O5N2−1
malt6pMaltose 6′-phosphateC12H21O14P−2
pacPhenylacetic acidC8H7O2−1
urdglyc (-)-UreidoglycolateC3H5N2O4−1

The genome-wide metabolic networks for E. coli CFT073 and UTI89 have recently been reconstructed based on the comparative genomics analysis [20]. We compared our models (TEXT S1–S3) with the previous ones and found that our models included more metabolic genes because the deep sequencing has been proven to lead to the identification of large populations of novel as well as missing transcripts that might reflect Hydra-specific evolutionary events [32].

3.3. Optimal Flux Distributions for E. coli Strains

In the previous studies, one of the most fundamental genome-scale phenotypic calculations is the simulation of cellular growth using flux balance analysis (FBA) [25]. As a result, we defined biomass composition of the cell as the biomass objective function and performed FBA on the model in order to maximize the objective function. It shows that the optimal biomass flux for the three models are pretty close (optimal flux = 0.7287 for CFTO73, while optimal flux = 0.7367 for HS and UTI89). However, the optimal flux distributions are of different in the networks. Figure 2 shows the optimal flux distribution map of core metabolic network in three E. coli strains. It shows that the fluxes of ACS (acetyl-CoA synthetase), PTAr (phosphotransacetylase), and ACKr (acetate kinase) in CFTO73 model are obviously different from that in the other two models.

We then estimated the effect of reducing flux through metabolic reactions on biomass production of three models. Two reactions ACOAD6F (acyl-CoA dehydrogenase, tetradecanoyl-CoA) and PGK (phosphoglycerate kinase) were taken as examples here (Figure S1). It shows that the growth rate is sustained near the optimal value over a range of values for PGK in all three models, indicating the same network robustness with respect to flux changes in the reaction (Figure S1A). However, the effects of reducing flux through ACOAD6F on growth are different between E. coli CFTO73 and the other two models (Figure S1B). Besides, the growth rate is sharply reduced after reaching the optimal value in HS and UTI89 models.

3.4. Dynamic Responses of Metabolic Networks to Changes in Carbon Sources

Although a few human gut microbiome projects have been launched, the interrelationships between our diets and the structure and operations of our gut microbial communities are poorly understood. Here, we predicted the human gut E. coli’s response to diet using metabolic modeling.

We simulated the optimal growth rates for three models on carbon source as acetate, ethanol, glucose, and succinate, respectively (uptake rate sets all changed to 9 mmol gDW−1 h−1). The average growth rates of three metabolic models corresponding to four diet conditions are shown in Figure 3(a). We can see that the growth rates for three models are similar in different conditions. Besides, it demonstrates substantially decreased anaerobic growth as compared with aerobic (18 mmol gDW−1 h−1) growth with the same glucose uptake rate, which was supported by recent studies that E. coli requires aerobic respiration to compete successfully in the mouse intestine [8, 9]. For E. coli strains in human gut, carbon sources are diverse, but glucose is most suitable for their growth.

These responses of E. coli to the diet changes involve many metabolic genes and pathways. We explored the perturbations in the metabolic networks and found 10 genes (including ADH5, ALDH5A1, DLD, FECH, GCLC, GPT, GSR, KARS, MPST, and TST) closely associated with the diet stress (Figure 3(b)). The glycolysis, gluconeogenesis, and glycerophospholipid metabolism were enriched in the metabolic reactions catalyzed by these genes ( using Fisher’s exact test). Besides, we found that these enzymes were evolutionarily conserved from E. coli to human and were involved in the interactions between human and E. coli [14, 33]. Especially, nine out of these 10 genes (except GPT, glutamic-pyruvate transaminase) were found to be increased in human obesity [34].

3.5. Analyzing Flux Correlations in Diabetes-Associated Pathways in E. coli Using Sampling

Assessment and characterization of gut microbiota (E. coli acts as an integral component) has become a major research area in human type 2 diabetes, the most prevalent endocrine disease worldwide. A recent metagenomic research identified and validated over 400 type-2-diabetes-associated markers in E. coli, including over 100 metabolic genes [35]. In the study, we performed uniform random sampling for three models under glucose-limiting aerobic growth conditions to explore the relationships between the diabetes-associated pathways.

We detected 158 metabolic reactions in E. coli models that were associated with human type 2 diabetes (Table S2). It shows that these reactions participate in many subsystems, of which over 30% are associated with lipid metabolism and cofactor/prosthetic group biosynthesis. Correlation ships between some metabolic reactions can be observed in Figure 4. For example, PGL (6-phosphogluconolactonase) and GND (phosphogluconate dehydrogenase) fluxes are positively correlated in the E. coli HS model, whereas PGL shows negative correlation with RPI (ribose-5-phosphate isomerase) fluxes. The correlation ships between these diabetes-associated reaction fluxes are the same in other two models.

3.6. Flux Variability Analysis (FVA) of E. coli Models

FBA returns a single flux distribution that corresponds to maximal biomass production under given growth conditions. However, alternate optimal solutions may exist, which correspond to maximal growth. As a result, we performed FVA for the three E. coli models under glucose-limited aerobic growth conditions (glucose and oxygen were changed to 10 and 18 mmol gDW−1 h−1, resp.).

It shows that the minimum and maximum fluxes for the reactions in E. coli models are different. Figure 5 illustrates FVA result for the seven reactions in pyrimidine biosynthesis. All the reactions have different flux range in three networks, especially carbamate kinase and dihydroorotic acid dehydrogenase.

4. Discussion and Conclusion

In our study, we determined the common E. coli strains in human gut microbial communities based on HMP datasets. We applied two widely used algorithms (GIMME and iMAT) to reconstruct genome-wide metabolic models for three common E. coli strains (E. coli HS, UTI89, and CFT073) and compared the network characteristics of these models. These models were then used to predict the cellular phenotypes and dynamic responses to the diverse gut microenvironment. The models were also applied in exploring the relationships between E. coli and human diabetes. The results will be helpful in exploring the dynamic responses of gut microbiome to the environmental perturbations.

The E. coli strains have been proven to be significantly different among individuals, although the species is abundant in human gut [36]. Although it is well accepted that the composition of E. coli strains in human gut flora is associated with health status, the exact molecular mechanism is still unclear. We detected the common E. coli strains in human gut and systematically compared their functions through in silico modeling, which have two advantages over the traditional methods. First, the sequencing data allows for a much more accurate determination of microbiome composition. The advent of next-generation sequencing (NGS) enabled several high-profile collaborative projects including the HMP Consortium ( and MetaHIT Consortium (, which have released a wide range of data on the human microbiome. Using these datasets, we applied different methods (genome-guided mapping and de novo assembly) to determine the common E. coli strains, making the following study of interconnectivity between gut microbiota, diet, and cell molecular responses available. Second, the metabolic modeling can allow us to see how a biological system might respond [37]. This will guide the wet lab experiments and avoid most of the mistakes in the process. In fact, developing computational methods capable of predicting metabolic flux by integrating these data sources with a metabolic network is a major challenge of systems biology [18]. For example, the predicted behaviors of diabetes-associated reactions in E. coli (Table S2) can be integrated with experimental validations to detect the causal genes in human diabetes.

The E. coli is regarded as the prototypical pluripotent pathogens capable of causing a wide variety of illnesses in a broad array of species, including pyelonephritis, diarrhea, dysentery, and the hemolytic-uremic syndrome [38]. In particlar, human gut E. coli and its relationship to complex diseases, such as cancer [39] and diabetes [40], has attracted increasing interest in the last few years. A question then arises: “How is it possible for this Jekyll and Hyde species to both coexist peacefully with its host and cause devastating illness?” [38]. The answer mainly lies in the existence of different strains of E. coli with variable pathogenic potential [41]. However, we can hardly draw a complete picture of how the E. coli strains respond physiologically to the complex gut microenvironment. Our study can provide valuable information based on the systematic comparisons of different E. coli strains. It shows that although the optimal growth rates are similar for three E. coli strains, the optimal flux distributions are different for three models, even in E. coli core reactions. The detected different reactions, such as ACS (acetyl-CoA synthetase) and PTAr (phosphotransacetylase) were approved to be involved in the virulence of E. coli and be associated with human complex diseases [35, 42]. The results can be integrated with other data sets, such as human clinical trials and virulence profiles, which will help establish the extent of commonality between food-source and human gut E. coli [43] and estimate the contribution of strain-specific reactions or genes to infections in humans.

We found that the E. coli responded distinctly to different gut diets and the stress-associated genes were closely associated with obesity. With the high prevalence of diet-induced health concerns, such as diabetes and obesity, there remains a need for approaches that treat the causal factors. Among these factors, gut microbiome is drawing more attention [35, 44] for it is suitable as disease markers and drug targets. For example, Qin et al. carried out a metagenome-wide association study which indicated that patients with type 2 diabetes have only moderate intestinal dysbiosis but that butyrate-producing bacteria are less abundant and opportunistic pathogens are more abundant in these individuals than in healthy controls [35]. The underlying mechanisms of interactions between gut microbiome and human health are complicated; however the stress-associated pathways (such as the detected the gluconeogenesis, and glycerophospholipid metabolism) may play important roles in the disease development. The diet changes first induced changes of involved metabolic genes (such as ADH5, alcohol dehydrogenase 5), which trigger the downstream signaling pathways. These signaling pathways mainly associated with immune responses and development [44, 45]. It is commonly accepted that the gut microbiota interacts with the immune system, providing signals to promote the maturation of immune cells and the normal development of immune functions [46]. The dynamic interactions between all components of the microbiota and host tissue over time will be crucial for building predictive models for diagnosis and treatment of diseases linked to imbalances in our microbiota.

In summary, the findings here represent a significantly expanded and comprehensive reconstruction of the E. coli metabolic network in human gut. This work will enable a wider spectrum of studies focused on microbe-host interactions and serve as a means of integrating other omics sets in systems biology.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


This work was supported by the National Natural Science Foundation of China (Grant no. 31123005) and the Instruments Function Deployment Foundation of CAS (Grants nos. yg2010044 and yg2011057).

Supplementary Materials

Figure S1: Robustness analysis of metabolic reactions in E. coli models.

Table S1: The reactions and metabolites in three E. coli metabolic networks.

Table S2: Metabolic reactions associated with human type 2 diabetes.

TEXT S1: Metabolic model for E. coli CFTO73 in SBML format.

TEXT S2: Metabolic model for E. coli HS in SBML format.

TEXT S3: Metabolic model for E. coli UTI89 in SBML format.

  1. Supplementary Material


  1. P. B. Eckburg, E. M. Bik, C. N. Bernstein et al., “Microbiology: diversity of the human intestinal microbial flora,” Science, vol. 308, no. 5728, pp. 1635–1638, 2005. View at: Publisher Site | Google Scholar
  2. G. Reid, J. Howard, and B. S. Gan, “Can bacterial interference prevent infection?” Trends in Microbiology, vol. 9, no. 9, pp. 424–428, 2001. View at: Publisher Site | Google Scholar
  3. D. McCloskey, B. Ø. Palsson, and A. M. Feist, “Basic and applied uses of genome-scale metabolic network reconstructions of Escherichia coli,” Molecular Systems Biology, vol. 9, no. 1, article 661, 2013. View at: Publisher Site | Google Scholar
  4. S. Nakamura, T. Nakaya, and T. Iida, “Metagenomic analysis of bacterial infections by means of high-throughput DNA sequencing,” Experimental Biology and Medicine, vol. 236, no. 8, pp. 968–971, 2011. View at: Publisher Site | Google Scholar
  5. M. S. Donia and M. A. Fischbach, “Dyeing to learn more about the gut microbiota,” Cell Host and Microbe, vol. 13, no. 2, pp. 119–120, 2013. View at: Publisher Site | Google Scholar
  6. L. Rup, “The human microbiome project,” Indian Journal of Microbiology, vol. 52, no. 3, p. 315, 2012. View at: Publisher Site | Google Scholar
  7. P. J. Turnbaugh, R. E. Ley, M. Hamady, C. M. Fraser-Liggett, R. Knight, and J. I. Gordon, “The human microbiome project,” Nature, vol. 449, no. 7164, pp. 804–810, 2007. View at: Publisher Site | Google Scholar
  8. S. A. Jones, F. Z. Chowdhury, A. J. Fabich et al., “Respiration of Escherichia coli in the mouse intestine,” Infection and Immunity, vol. 75, no. 10, pp. 4891–4899, 2007. View at: Publisher Site | Google Scholar
  9. S. E. Winter, M. G. Winter, M. N. Xavier et al., “Host-derived nitrate boosts growth of E. coli in the inflamed gut,” Science, vol. 339, no. 6120, pp. 708–711, 2013. View at: Publisher Site | Google Scholar
  10. I. Cho and M. J. Blaser, “The human microbiome: at the interface of health and disease,” Nature Reviews Genetics, vol. 13, no. 4, pp. 260–270, 2012. View at: Publisher Site | Google Scholar
  11. C. Huttenhower, D. Gevers, R. Knight et al., “Structure, function and diversity of the healthy human microbiome,” Nature, vol. 486, no. 7402, pp. 207–214, 2012. View at: Google Scholar
  12. C. F. Maurice, H. J. Haiser, and P. J. Turnbaugh, “Xenobiotics shape the physiology and gene expression of the active human gut microbiome,” Cell, vol. 152, no. 1-2, pp. 39–50, 2013. View at: Publisher Site | Google Scholar
  13. A. Heinken, S. Sahoo, R. M. Fleming, and I. Thiele, “Systems-level characterization of a host-microbe metabolic symbiosis in the mammalian gut,” Gut Microbes, vol. 4, no. 1, pp. 28–40, 2013. View at: Publisher Site | Google Scholar
  14. S. Shoaie, F. Karlsson, A. Mardinoglu, I. Nookaew, S. Bordel, and J. Nielsen, “Understanding the interactions between bacteria in the human gut through metabolic modeling,” Scientific Reports, vol. 3, article 2532, 2013. View at: Publisher Site | Google Scholar
  15. C. Lozupone, K. Faust, J. Raes et al., “Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts,” Genome Research, vol. 22, no. 10, pp. 1974–1984, 2012. View at: Publisher Site | Google Scholar
  16. Y. Q. Zhao and J. F. Huang, “Reconstruction and analysis of human heart-specific metabolic network based on transcriptome and proteome data,” Biochemical and Biophysical Research Communications, vol. 415, no. 3, pp. 450–454, 2011. View at: Publisher Site | Google Scholar
  17. J. Zhao, C. Geng, L. Tao et al., “Reconstruction and analysis of human liver-specific metabolic network based on CNHLPP data,” Journal of Proteome Research, vol. 9, no. 4, pp. 1648–1658, 2010. View at: Publisher Site | Google Scholar
  18. K. Yizhak, T. Benyamini, W. Liebermeister, E. Ruppin, and T. Shlomi, “Integrating quantitative proteomics and metabolomics with a genome-scale metabolic network model,” Bioinformatics, vol. 26, no. 12, pp. i255–i260, 2010. View at: Publisher Site | Google Scholar
  19. B. A. Methe, K. E. Nelson, M. Pop et al., “A framework for human microbiome research,” Nature, vol. 486, no. 7402, pp. 215–221, 2012. View at: Publisher Site | Google Scholar
  20. D. J. Baumler, R. G. Peplinski, J. L. Reed, J. D. Glasner, and N. T. Perna, “The evolution of metabolic networks of E. coli,” BMC Systems Biology, vol. 5, article 182, 2011. View at: Publisher Site | Google Scholar
  21. S. A. Becker and B. O. Palsson, “Context-specific metabolic networks are consistent with experiments,” PLoS Computational Biology, vol. 4, no. 5, Article ID e1000082, 2008. View at: Publisher Site | Google Scholar | MathSciNet
  22. H. Zur, E. Ruppin, and T. Shlomi, “iMAT: an integrative metabolic analysis tool,” Bioinformatics, vol. 26, no. 24, pp. 3140–3142, 2010. View at: Publisher Site | Google Scholar
  23. J. D. Orth, I. Thiele, and B. O. Palsson, “What is flux balance analysis?” Nature Biotechnology, vol. 28, no. 3, pp. 245–248, 2010. View at: Publisher Site | Google Scholar
  24. A. M. Feist, C. S. Henry, J. L. Reed et al., “A genome-scale metabolic reconstruction for Escherichia coli K-12 MG1655 that accounts for 1260 ORFs and thermodynamic information,” Molecular Systems Biology, vol. 3, article 121, 2007. View at: Publisher Site | Google Scholar
  25. S. A. Becker, A. M. Feist, M. L. Mo, G. Hannum, B. Ø. Palsson, and M. J. Herrgard, “Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox,” Nature Protocols, vol. 2, no. 3, pp. 727–738, 2007. View at: Publisher Site | Google Scholar
  26. R. Mahadevan and C. H. Schilling, “The effects of alternate optimal solutions in constraint-based genome-scale metabolic models,” Metabolic Engineering, vol. 5, no. 4, pp. 264–276, 2003. View at: Publisher Site | Google Scholar
  27. S. L. Chen, M. Wu, J. P. Henderson et al., “Genomic diversity and fitness of E. coli strains recovered from the intestinal and urinary tracts of women with recurrent urinary tract infection,” Science Translational Medicine, vol. 5, no. 184, 2013. View at: Publisher Site | Google Scholar
  28. J. S. Ayres, N. J. Trinidad, and R. E. Vance, “Lethal inflammasome activation by a multidrug-resistant pathobiont upon antibiotic disruption of the microbiota,” Nature Medicine, vol. 18, no. 5, pp. 799–806, 2012. View at: Publisher Site | Google Scholar
  29. P. Jain, N. M. Krishnan, and B. Panda, “Augmenting transcriptome assembly by combining de novo and genome-guided tools,” PeerJ, vol. 1, article e133, 2013. View at: Publisher Site | Google Scholar
  30. I. Thiele, N. Swainston, R. M. T. Fleming et al., “A community-driven global reconstruction of human metabolism,” Nature Biotechnology, vol. 31, no. 5, pp. 419–425, 2013. View at: Publisher Site | Google Scholar
  31. D. J. Becker and J. B. Lowe, “Fucose: biosynthesis and biological function in mammals,” Glycobiology, vol. 13, no. 7, pp. 41R–53R, 2003. View at: Publisher Site | Google Scholar
  32. Y. Wenger and B. Galliot, “RNAseq versus genome-predicted transcriptomes: a large population of novel transcripts identified in an Illumina-454 Hydra transcriptome,” BMC Genomics, vol. 14, no. 1, article 204, 2013. View at: Publisher Site | Google Scholar
  33. Z. Qi and M. R. O'Brian, “Interaction between the bacterial iron response regulator and ferrochelatase mediates genetic control of heme biosynthesis,” Molecular Cell, vol. 9, no. 1, pp. 155–162, 2002. View at: Publisher Site | Google Scholar
  34. S. Greenblum, P. J. Turnbaugh, and E. Borenstein, “Metagenomic systems biology of the human gut microbiome reveals topological shifts associated with obesity and inflammatory bowel disease,” Proceedings of the National Academy of Sciences of the United States of America, vol. 109, no. 2, pp. 594–599, 2012. View at: Publisher Site | Google Scholar
  35. J. J. Qin, Y. R. Li, Z. M. Cai et al., “A metagenome-wide association study of gut microbiota in type 2 diabetes,” Nature, vol. 490, no. 7418, pp. 55–60, 2012. View at: Publisher Site | Google Scholar
  36. M. Martinez-Medina, X. Aldeguer, M. Lopez-Siles et al., “Molecular diversity of Escherichia coli in the human gut: new ecological evidence supporting the role of adherent-invasive E. coli (AIEC) in Crohn's disease,” Inflammatory Bowel Diseases, vol. 15, no. 6, pp. 872–882, 2009. View at: Publisher Site | Google Scholar
  37. J. R. Karr, J. C. Sanghvi, D. N. MacKlin et al., “A whole-cell computational model predicts phenotype from genotype,” Cell, vol. 150, no. 2, pp. 389–401, 2012. View at: Publisher Site | Google Scholar
  38. M. Donnenberg, Escherichia coli: Pathotypes and Principles of Pathogenesis, Academic Press, New York, NY, USA, 2013.
  39. H. Tlaskalová-Hogenová, R. Tpánková, H. Kozáková et al., “The role of gut microbiota (commensal bacteria) and the mucosal barrier in the pathogenesis of inflammatory and autoimmune diseases and cancer: Contribution of germ-free and gnotobiotic animal models of human diseases,” Cellular and Molecular Immunology, vol. 8, no. 2, pp. 110–120, 2011. View at: Publisher Site | Google Scholar
  40. N. Larsen, F. K. Vogensen, F. W. J. van den Berg et al., “Gut microbiota in human adults with type 2 diabetes differs from non-diabetic adults,” PLoS ONE, vol. 5, no. 2, Article ID e9085, 2010. View at: Publisher Site | Google Scholar
  41. R. M. Robins-Browne, “Traditional enteropathogenic Escherichia coli of infantile diarrhea,” Reviews of Infectious Diseases, vol. 9, no. 1, pp. 28–53, 1987. View at: Publisher Site | Google Scholar
  42. K. Guan and Y. Xiong, “Regulation of intermediary metabolism by protein acetylation,” Trends in Biochemical Sciences, vol. 36, no. 2, pp. 108–116, 2011. View at: Publisher Site | Google Scholar
  43. J. R. Johnson, M. A. Kuskowski, K. Smith, T. T. O'Bryan, and S. Tatini, “Antimicrobial-resistant and extraintestinal pathogenic Escherichia coli in retail foods,” Journal of Infectious Diseases, vol. 191, no. 7, pp. 1040–1049, 2005. View at: Publisher Site | Google Scholar
  44. J. C. Clemente, L. K. Ursell, L. W. Parfrey, and R. Knight, “The impact of the gut microbiota on human health: an integrative view,” Cell, vol. 148, no. 6, pp. 1258–1270, 2012. View at: Publisher Site | Google Scholar
  45. P. D. Gluckman, K. A. Lillycrop, M. H. Vickers et al., “Metabolic plasticity during mammalian development is directionally dependent on early nutritional status,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 31, pp. 12796–12800, 2007. View at: Publisher Site | Google Scholar
  46. J. Chow, S. M. Lee, Y. Shen, A. Khosravi, and S. K. Mazmanian, “Host-bacterial symbiosis in health and disease,” Advances in Immunology, vol. 107, pp. 243–274, 2010. View at: Publisher Site | Google Scholar

Copyright © 2014 Yue-Dong Gao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

2996 Views | 3878 Downloads | 7 Citations
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19.