- Open Access
A reverse metabolic approach to weaning: in silico identification of immune-beneficial infant gut bacteria, mining their metabolism for prebiotic feeds and sourcing these feeds in the natural product space
Microbiome volume 6, Article number: 171 (2018)
Weaning is a period of marked physiological change. The introduction of solid foods and the changes in milk consumption are accompanied by significant gastrointestinal, immune, developmental, and microbial adaptations. Defining a reduced number of infections as the desired health benefit for infants around weaning, we identified in silico (i.e., by advanced public domain mining) infant gut microbes as potential deliverers of this benefit. We then investigated the requirements of these bacteria for exogenous metabolites as potential prebiotic feeds that were subsequently searched for in the natural product space.
Using public domain literature mining and an in silico reverse metabolic approach, we constructed probiotic-prebiotic-food associations, which can guide targeted feeding of immune health-beneficial microbes by weaning food; analyzed competition and synergy for (prebiotic) nutrients between selected microbes; and translated this information into designing an experimental complementary feed for infants enrolled in a pilot clinical trial (http://www.nourishtoflourish.auckland.ac.nz/).
In this study, we applied a benefit-oriented microbiome research strategy for enhanced early-life immune health. We extended from “classical” to molecular nutrition aiming to identify nutrients, bacteria, and mechanisms that point towards targeted feeding to improve immune health in infants around weaning. Here, we present the systems biology-based approach we used to inform us on the most promising prebiotic combinations known to support growth of beneficial gut bacteria (“probiotics”) in the infant gut, thereby favorably promoting development of the immune system.
The human body is host to 1014 resident microorganisms (bacteria, viruses, fungi, and protozoa)  that live in synergy with human cells influencing health outcomes across lifespan . Depending on micro-environmental conditions, each body site is colonized by specific microbial communities shaped by co-evolution with the host. The majority of those microbes live in our gastrointestinal (GI) tract . At birth, the pristine infant gut is rapidly colonized by millions of bacteria, some beneficial, some not. The first microbial inoculum is acquired at birth with differences in both diversity and abundance driven by host genetics, prenatal and maternal factors, such as the delivery mode, i.e., cesarean or vaginal . The newborn’s microbiome is not yet stable and varies inter-individually . The changes occur as a consequence of exposure to different environmental and health/disease conditions, dietary patterns, and also exposure to antibiotics. A diverse and balanced gut microbiome provides benefits to the host through affecting several physiological processes  ranging from maturation of the immune system, regulation of host metabolism, response to nutrition, metabolism of bioactive molecules and drugs , biosynthesis of vitamins and amino acids, and absorption of iron .
In the first 1000 days of life, the development of the infant’s microbiome is intimately tied to maturation of the immune system . It has long been hypothesized that microbial exposure in early life has a protective effect on the newborn’s health and can influence the health outcomes later in life . The gut microbiota is required for maturation and maintenance of the immune system and has a role in modulation of the immune system. For example, the immune system-microbiota interaction enables induction of protective responses to pathogens and the maintenance of regulatory pathways involved in the tolerance to innocuous antigens .
While several studies support the role of diet in shaping the gut microbial community in adults, only a few focused on understanding the contribution of complementary foods during the weaning period to the modulation of the infant gut microbiome . Weaning is a phase of marked physiological change. The introduction of solid foods and the changes in milk consumption trigger significant GI tract, immune and developmental adaptations. Weaning also exposes infants to non-digestible carbohydrates and provides new substrates for the microbial gut community with resulting growth and dominance of some taxa, such as Bacteroides , and a reduction of others, such as bifidobacteria, enterobacteria, and some Clostridium spp. . Hence, infant nutrition, especially in the complementary feeding period, exerts profound health impacts and careful dietary interventions during weaning can support the development of both a healthy microbiome and immune system, thereby improving child growth and development .
We report on an innovative and integrated pipeline developed to support complementary feeding design with the identification of essential metabolites required by beneficial and protective bacteria (“prebiotic feeds for probiotic bacteria”). After a comprehensive capture of the literature on the infant gut microbiome, the pipeline drives the selection of candidate immune-protective infant GI bacteria. By applying an in silico reverse metabolic approach, which uses the microbial metabolic network to infer its nutritional requirements without prior information, we mined the microbial metabolism to identify exogenous compounds required by candidate bacteria, which were sourced from the chemical composition of foods in order to enable identification of prebiotic ingredients naturally present in food and which can be given safely to infants during weaning. Our systems biology approach has informed the design and development of a complementary prebiotic feeding to nourish the microbiota that supports the immune system of infants and that promotes protection against common infections (http://www.nourishtoflourish.auckland.ac.nz/). Essentially, our methodology addresses and answers the following questions: (i) which immune protection-beneficial infant GI bacteria are present around and after weaning?; (ii) can we interrogate bacterial metabolism by identifying key enzymes involved in exogenous metabolite conversion and what do these preferred bacteria predominantly feed (“prebiotics”)?; (iii) is there an interaction for these metabolites between the selected bacteria and are essential nutrients cross-fed between bacteria?; and (iv) where and how can “prebiotic” whole foods or food components be sourced from the food chain?
Identification of immune-protective bacteria (question i)
The core query (Fig. 1) yielded a total of 3673 unique PubMed IDs by searching titles and abstracts and specifically 1657 PubMed IDs for infant gut microbiome, 608 PubMed IDs for infant nutrition and microbiome metabolism, 583 PubMed IDs for beneficial bacteria supporting immune system development in infant, and 825 PubMed IDs for beneficial bacteria preventing infections in infants.
The PubMed IDs shared by single or multiple research topics are shown in the Venn diagram of Fig. 2.
Fifty PubMed IDs were common to all search criteria. Available full texts (or abstracts when full texts were not available) were automatically annotated for cited biological entities to build dictionaries of relevant terms for the sentence extraction. As detailed in the Methods section, for each of the queries (a), (b), (c) and (d), the pipeline extracted relationships between each pair of the four dictionaries and co-mentions of more than two different dictionaries (Table 1), that were filtered to obtain the final list of sentences (Additional files 1 and 2).
The list of all microbes cited in the extracted sentences for both relationships and co-mentions was then manually curated (Additional files 1 and 2, “*-species” sheets). Examples of relevant sentences and associated PubMed IDs from which the relevant bacterial species are extracted are given in Additional file 3: Table S1.
We firstly concentrated our efforts on outcomes from queries (c) beneficial bacteria supporting immune system development in infants and (d) beneficial bacteria preventing infections in infants. Our pipeline recognized 27 unique species names from the relations of both queries (Additional file 1, “*-species” sheets). Among those lists, the most frequent species were Lactobacillus rhamnosus (appearing in 67 and 72 of the 223 and 235 sentences extracted for queries (c) and (d) respectively) and Lactobacillus casei in query (c) (37/223) and Lactobacillus acidophilus (33/235) in query (d). Queries (a) infant gut microbiome and (b) infant nutrition and microbiome metabolism, which were expected to collect ecological information on the infant microbiome and metabolism, found again L. rhamnosus as the most cited species, 77/260 and 15/60 sentences from query (a) and (b) respectively, and L. acidophilus (35/260) and Bifidobacterium breve (12/60) from query (b) as they are known to be infant gut commensals. As expected, co-mention analysis produced weaker microbial results after manual curation (Additional file 2, “*-species” sheets); we obtained a total of 22 species names from query (c) and 24 from query (d) that confirm the main outcomes from relationships. Based on those lists, the putative probiotic strains implicated in immune defense against infections in infants were evaluated and selected: 14 of the most promising bacteria belonged to bifidobacteria and lactobacilli. Based on our text mining results and from reports of their increasing abundance in healthy babies from 4 to 12 months of age , Akkermansia muciniphila and Faecalibacterium prausnitzii were also selected as potential “probiotics” in our study. General literature mining revealed the presence of Bifidobacterium angulatum in Japanese children at 3 years of age , and Haarman and Knol  found this species harbored by German infants between 28 and 90 days of age, and possible relations with feeding mode: B. angulatum seems to be associated with breast-feeding rather than formula feeding. Bifidobacterium catenulatum was also reported in mother-infant pairs [15, 16]. Both these strains were able to modulate cytokine secretion when tested in vitro in peripheral blood mononuclear cells . We therefore included B. angulatum and B. catenulatum into our selected microbial list to further analyze their interactions with other bacteria.
Identification of exogenous prebiotics for the selected microorganisms (question ii)
For each strain of the 18 selected strains (Table 2), which for simplicity will be referred to as a “community” the metabolic model was retrieved from the Virtual Metabolic Human (VMH) database.
The topology of reconstructed metabolic networks was analyzed with NetSeed to identify exogenously acquired metabolites, and the nutrient profile of each strain was inferred (Additional file 4). We noted oxygen (O2) was included in the requirements of anaerobic bacteria and, while there are studies reporting exogenous oxygen uptake by Bifidobacterium spp. [18, 19], this might be linked to the VMH model reconstruction (see the “Methods” section). Table 2 shows the number of metabolites identified as exogenous on a network topology basis and thus putatively corresponding to essential nutrients required by each strain.
Our in silico study of this microbial community of probiotics identified a total of 632 unique exogenous metabolites which are potentially required for growth under normal circumstances . Among them, 62 are essential for all strains, 200 are required by single microbes in the community, and 398 are shared between different strains. L. casei subsp. casei BL23 requires the most of exogenous metabolites (313), while A. muciniphila ATCC BAA 835 requires only 208 such essential metabolites. Interestingly, F. prausnitzii M21 2 shows highly distinct nutritional requirements compared to the other microorganisms: it needs 99 compounds for its metabolism that are not shared with other members in the community. On the other hand, lactobacilli share the majority of their necessary metabolites and only 5 are specific for the lactobacilli species considered in this study.
Grouping probiotics by genera, Bifidobacterium spp. require 398 nutrients for their growth; among these, 177 are necessary for all nine strains selected in this study, while 52 are strain-specific. Four hundred eighty-six exogenous compounds were detected for Lactobacillus species; 107 are present in the set seed of all seven strains, while 92 appear to be strain-specific. Five hundred seventy-six unique metabolites are required by the bifidobacteria-lactobacilli community; 75 are essential for all strains, and 73 are strain-specific.
Cooperative metabolic bacteria-bacteria and bacteria-host interactions (question iii)
Based on graph theory-based methods , both host-microbe and microbe-microbe cooperation was analyzed for each pair of selected probiotics. The cooperative and competitive interactions within the selected microbial community were investigated adopting a reverse ecology approach. We computed the biosynthetic support scores for each microbe-human host pair and the metabolic complementarity indices as well as the metabolic competition indices for each microbe-microbe pair in our community. Figure 3 graphically depicts the characteristics of these three scores that are abbreviated as support, complementarity, and competition, respectively, in the remaining of the text, for reasons of simplicity.
All probiotic species identified in this study exhibit low support scores versus the human host, ranging from 0.330 to 0.522, confirming that they are indeed gut commensals rather than parasites. Highest support scores were obtained for A. muciniphila and L. acidophilus (0.502 and 0.522), as they are evolved to live in the gut and hence have higher dependence on the host for provision of exogenous metabolites.
Our microbial community (lactobacilli, bifidobacteria, A. muciniphila, F. prausnitzii, B. angulatum, and B. catenulatum) is characterized by low complementarity indices. Lactobacillus paracasei subsp. paracasei is the most “supported” bacterium, while the “altruistic” F. prausnitzii complements most of the community members and is the least “supported.” Bifidobacterium is the taxon showing the lowest complementarity (0.064 for one pair, mean value 0.190 for bifidobacteria group), while lactobacilli show the highest values (0.243 for one specific pair, mean value 0.127 for lactobacilli group). We infer that B. breve and Bifidobacterium bifidum is the least complementing pair within bifidobacteria (complementarity 0.006/0.069), whereas L. rhamnosus and L. casei subsp. casei and L. paracasei subsp. paracasei show a low potential for syntrophy within lactobacilli (complementarity values 0.010/0.150, 0.010/162, respectively). The lactobacilli species most likely to complement each other are L. acidophilus and Lactobacillus reuteri as they show the highest complementarity scores (0.243 and 0.164, respectively).
Overall, we can assume complementarity between lactobacilli and bifidobacteria. Several of our in silico predictions on microbe metabolic cooperativity are supported by experimental studies: (i) for example, our finding of B. breve of enhancing L. paracasei subsp. paracasei (complementarity score 0.239) confirms results from in vitro GI models . (ii) F. prausnitzii shows the highest potential for supporting requirements of a large number of community members (values range 0.036–0.313), from both bifidobacteria and lactobacilli. Several authors reported crossfeeding between (i) acetate-depending butyrate-producing colon bacteria like F. prausnitzii; (ii) lactate- and acetate-producing bacteria, like bifidobacteria [23,24,25]; and (iii) lactobacilli . For example, Rios-Covian et al.  showed experimental evidence of crossfeeding between F. prausnitzii, which requires acetate for the oligofructose breakdown, and Bifidobacterium adolescentis, which produces acetate. B. adolescentis enhances its growth through consumption of carbohydrates, which are in turn released during oligofructose degradation by F. prausnitzii. These interactions are strain-specific and can be either a commensal beneficial relationship or dominated by competition .
A. muciniphila is the least competitive species within our microbial community with metabolic competition values ranging from 0.348 of L. reuteri to 0.644 of L. rhamnosus. Also F. prausnitzii shows values that characterize them as a non-competitive species. By contrast, the closely related species L. casei subsp. casei and L. paracasei subsp. paracasei, which belong to the same phylogenetic group , are the most competitive pair (0.947/0.968).
Within bifidobacteria genera, B. adolescentis and Bifidobacterium longum subsp. longum are the least competitive pair (0.703 and 0.811) while Bifidobacterium pseudocatenulatum and B. catenulatum are the most competitive pair (0.939 and 0.909) followed by Bifidobacterium longum subsp. infantis and B. longum subsp. longum (0.873 and 0.891). However, species pairs within the bifidobacteria genus are generally very competitive (mean competition index of 0.821).
Competition scores for lactobacilli range from 0.419 (L. reuteri/L. acidophilus pair) to 0.968 (L. paracasei subsp. paracasei/L. casei subsp. casei pair). The scarce competitiveness of the unique homo-fermentative L. acidophilus with other lactobacilli, among other factors, might be linked to its exclusive fermentation of hexoses to lactic acid via the Embden-Meyerhof pathway . Indeed, by contrast, several facultative hetero-fermentative species (Lactobacillus plantarum, L. rhamnosus, L. casei subsp. casei, L. paracasei subsp. paracasei), which can ferment both hexoses and pentoses to lactic acid by the phosphogluconate pathway, in our study stand as high competitors (high competition scores), mainly when paired with L. acidophilus.
Considering our whole community, A. muciniphila and F. prausnitzii are the least competitive when paired with species of other genera, possibly due to their very distinct set of exogenous metabolites.
A graphical summary of the metabolic complementarity and competition indices is given in Fig. 4a and b, respectively while numeric data for support, complementarity, and competition is reported in Additional file 5.
Sourcing exogenous feed metabolites (candidate prebiotics) from whole foods (question iv)
Among the 632 identified exogenous metabolites, each needed by at least one of the bacteria in our probiotic community, there are 218 name-matched compounds in the food compound list of the Foods database (FooDB)—candidate prebiotics—in 894 whole foods (Fig. 5).
The VMH database includes internal metabolites (1101 out of a total of 1689 metabolites for the 773 gut microbes reported by Magnúsdóttir et al. ), which are not present in other databases: therefore, these metabolites do not have a match in FooDB. Moreover, not all metabolites might be present as compound in foods and for this reason only 218 over 632 metabolites from VMH were found in FooDB. Interestingly, around 60% of the candidate prebiotics are present in several common fruits and vegetables: specifically, 62.7% are present in potatoes, 61.0% in cucumbers, and 59.3% in spinaches, broccoli, and common pea. Minerals, such as potassium, sodium, magnesium, and zinc, are the most commonly found (between 95.4 and 92.3%), and also vitamins, such as pyridoxine and β-carotenes, are widely present in most of the foods (98.5 and 80.7%, respectively).
For further analysis, metabolites were then categorized into oligosaccharides, monosaccharides, amino acids, vitamins, nitrogenous compounds, bioactive substances, and non-standard nutritive compounds (see Additional file 3: Supplemental Information 1). For each compound category, the mean metabolite concentration was calculated. The relationship between metabolite categories and foods, after removing non-standard nutritive compounds (NSN) and removing foods with metabolites below the limit of quantification (LOQ), is shown in the circular visualization of Fig. 6a. Figure 6b shows the Circos between those exogenous metabolites that are shared among microbes in our community and could be found in FooDB and the associated foods (13 metabolites after removing NSN).
A metabolite pathway enrichment analysis was performed for our probiotic community using bStyle . Pathways were considered significant if a hypergeometric p value lower than 0.05 was obtained. The histogram in Fig. 7a and the heatmap in Fig. 7b show pathways whose average overrepresentation significance is less than 0.05 (full results for each microorganism are available in Additional file 6).
The highest enriched pathways are glyoxylate, dicarboxylate, and carbon metabolism (hypergeometric p value of 0.0000119 and 0.0000185, respectively) appearing in all members of the microbial community selected in our study. Seven additional pathways are also significantly enriched: alanine, aspartate, and glutamate metabolism (p = 0.00054); arginine biosynthesis (p = 0.00084); glycine, serine and threonine metabolism (p = 0.0021); pyruvate metabolism (p = 0.0037); microbial metabolism in diverse environments (p = 0.0058); biosynthesis of antibiotics (p = 0.0061); and biosynthesis of secondary metabolites (p = 0.0075). The metabolic pathways of carbohydrates, co-factors, vitamins, and amino acids are also overrepresented, even with lower, but still significant, p values. Our analysis also revealed four pathways that are overrepresented in only one species each, and these are fatty acid metabolism in L. plantarum (p = 0.0015), C5-branched dibasic acid metabolism in Lactobacillus fermentum (p = 0.0022), starch and sucrose metabolism in A. muciniphila (p = 0.0023), and lysine degradation in B. longum subsp. longum (p = 0.0027). The metabolic enrichment analysis confirmed the role of essential compounds (see Additional file 4) in vitamin B and amino acid metabolism as growth factors for the selected microbial community of 18 probiotics [31, 32].
The foods were then sorted according to their nutritive content (Additional file 7 and top 20 foods and their content in Table 3). At the top of the food list, there is “honey” that is much enriched in monosaccharides and bioactive substances, while “Red bell pepper” is characterized by high amounts of vitamins and amino acids.
From the whole body of sentences extracted by the natural language processing (NLP) pipeline, after a manual curation, we defined a final gut microbial sub-community composed of 18 bacteria (Table 2 and Additional file 3: Table S1) that should as a community have a beneficial effect on the infant health.
This prompted us to investigate cooperative and competitive interactions within the community and its assembly rules applying a reverse ecology approach. Pair-wise microbial interaction mainly depends on the environment, into which two considered species are placed, and the availability of nutrients for their growth . In a given ecological model with limited nutrient supply, high complementarity and low competition between two microbial species can suggest potential syntrophy or niche complementarity , but not necessarily a coexistence. Niche complementarity may occur in different forms according to different relations of predation susceptibility and resource dependence—including different forms of the same chemical resource—in a community of coexisting bacterial species where no one predominates . Moreover, in closely related species, which are expected to share specific metabolic traits that help adapt to a specific habitat, a “habitat filtering” effect may be observed and nutrients available from the environment rather than crossfeeding between bacteria shape their community . Nevertheless, lactis acid bacteria can produce antimicrobial peptides, i.e., bacteriocines, which play a role in the competitive exclusion of pathogens , as well as interference competition among closely related species , helping producers to colonize and establish a niche in the environment . In summary, complementarity and competition metrics could reveal the pressure of the habitat on the gut community assembly.
Competition and complementarity scores were calculated for each microbe-microbe pair in the community, and support scores were calculated for each microbe-human host pair. The low support scores (~ 0.54) observed between each microbial strain and the human host supports the premise that these bacteria are non-pathogenic for humans, because pathogens (specifically intracellular organisms) typically show high support values (> 0.7) . Competition and complementarity were used to capture species interactions within the community; indeed, complementarity is a measure of potential syntrophy between two species, while competition index provides a proxy for niches overlap.
Reverse ecology analysis revealed generally low complementarity (< 0.32) and high competition scores (~ 0.97) for probiotic species pairs in our microbial community. We interpreted the results assuming the co-occurrence of these species in our ecology model. Low complementarity combined with high competition values observed for bacteria pairs belonging to the same genus suggest that these pairs are close relatives with similar nutrient needs, although the contribution of bacteriocines to modulate the microbial community could also be a major determinant. These nutrients are mainly acquired from the environment rather than via crossfeeding, and, hence, the bacteria may compete with each other, but do not necessarily exclude one another. Species pairs within the genus bifidobacteria are the most competitive and show the lowest potential for syntrophy; in particular, B. longum subsp. infantis is the most competitive. The highest competition scores were obtained for evolutionary closely related pairs. Among bifidobacteria, B. pseudocatenulatum exerts the highest competitive interaction when paired with B. catenulatum. Among lactobacilli, L. paracasei subsp. paracasei and L. casei subsp. casei are the most competitive pair. Interestingly, the least competitive pair among bifidobacteria, B. longum subsp. longum and B. adolescentis, consists of species belonging to two phylogenetically distinct bifidobacteria groups as evident by their distant positions on the recently reconstructed phylogenetic tree for the Bifidobacterium taxon .
A. muciniphila and F. prausnitzii, which have nutritional needs very different from the others and L. acidophilus, show low competition values. Hence, we can assume they do not compete with other species in our selected microbial community. Those species might be able to grow mutualistically with the other microbes because their nutritional needs could be met by crossfeeding . While A. muciniphila is not affected by competitiveness from other microbes, L. acidophilus can encounter competition from facultative hetero-fermentative lactobacilli. The low competition and the relatively high complementarity value of A. muciniphila suggests its important metabolic role within our selected microbial community; a capable mucin degrader and butyrate producer, it is involved in crossfeeding supporting the growth of several other species. Mutualistic interactions might also occur between some lactobacilli and bifidobacteria species pairs, e.g., B. catenulatum, B. longum subsp. longum, B. longum subsp. infantis, and B. pseudocatenulatum. On the other hand, B. breve and B. adolescentis, which show comparatively high competition values and are not much involved in potential syntrophic relations (low complementarity), might exert competitive behavior in the community. From the results, we might suppose the possible competition between F. prausnitzii, with Bifidobacterium animalis subsp. lactis and with B. bifidum. In a nutshell, our reverse ecology analysis provided information on potential  competitions and/or complementations between selected species in our community. These potential outcomes are strain-dependent as revealed by Moens and co-authors . Performing co-culture fermentations, they found a strain-dependent interaction between bifidobacteria strains and F. prausnitzii, which can be either commensal or competitive depending on the inulin-type fructanse degradation capacity of the former.
The most over-represented metabolic pathways covered by these compounds are classified into the Kyoto Encyclopedia of Genes and Genomes (KEGG)  classes of carbohydrate and amino acid metabolism. Among carbohydrates, the galactose metabolism and the pentose phosphate pathway are enriched by seeds from 10 out of 18 species of the community. The metabolic pathway enrichment analysis showed d-glucose, sucrose, lactose, d-sorbitol, galactitol, d-mannose, N-Acetyl-d-galactosamine, alpha-d-galactose, and myo-inositol as associated to the galactose metabolism. Moreover, the fundamental role played by microbial growth factors found in the vitamin B and amino acid metabolism has been underlined.
The aim of introducing prebiotics into the diet is to stimulate growth of specific indigenous, health-beneficial gut bacteria, i.e., probiotics. Oligosaccharides are established prebiotic substrates because they are carbohydrates non-digestible for the human host and can therefore reach the colon, where they can be selectively fermented by indigenous beneficial bacteria . Other substrates used as prebiotics include fibers, cellulose, hemicellulose, pectins, gums, β-glucans, inulin, fructose-oligosaccharides, and galacto-oligosaccharides . In addition to these prebiotics, specific growth factors are also required by gut microbes, such as B vitamins and amino acids, essential for both bifidobacteria  and lactobacilli . The metabolic pathway enrichment analysis shows that most of the exogenous metabolites identified for lactobacilli and bifidobacteria belong to vitamin B and amino acid pathways.
In order to inform the design of a prebiotic complementary infant feeding, the metabolites that are essential for at least one member of the selected microbial community (i.e., a total of 632 metabolites) were sourced into the FooDB. All 218 matching compounds were associated with a final number of 575 foods. The foods were sorted (Additional file 7) for facilitating the selection of the most promising food groups suitable to nourish and support the growth (prebiotic food) of these selected bacterial species (probiotics). We propose the top 20 foods (Table 3) that include vegetables and fruits, which are natural resources of prebiotic compounds, and moreover, most of them are normally recommended as complementary foods which can provide infants a large proportion of micronutrients such as iron, zinc, phosphorus, magnesium, calcium, and vitamin B6 . Among the foods showing the highest amounts of vitamins and amino acids, sweet potato (Kumara) appears as a practical choice for the formulation of infant complementary foods. Kumara powder is therefore proposed for the pilot clinical trials on infants aged 6–12 months, where each subject will receive a fixed quantity that could be mixed with the infant’s complementary foods.
This proof-of-concept of a health benefit-driven, public domain mining reverse metabolic approach to identifying candidate pro- and prebiotics and matching food sources comes with some limitations: For example, we initially encountered a number of false positives from the “text mining” due to the complexity of the search criteria; we have largely overcome this limitation by optimizing our dictionaries and adopting additional filters to exclude non-relevant articles. For our proof-of-concept, we deliberately selected a probiotic microbial community for gut ecology analysis. However, the infant gut harbors many more microbes apart from those selected by us and, hence, the interactions predicted by NetCooperate will be much more complex and may even differ for our selected community when embedded into a larger microbial context. Our exogenous metabolite (prebiotic) identification was targeted towards the strains that are available in VMH (which again depends mainly on literature for metabolite reconstruction). From the literature, it is evident that the prebiotic requirement is strain-specific. Hence, the full potential of growth-promoting function of this complementary feeding may not be realized fully in clinical studies conducted with a heterogeneous population. Moreover, we encountered some nomenclature limitations while mapping metabolites between VMH and FooDB databases, that calls for an increased effort in unifying the identifiers and give researchers full instruments for the inter-resources data integration. However, to the best of our knowledge, this is the first in silico study to identify prebiotics for the growth of potential probiotics that beneficially impact on the immune system development in infants during weaning.
In conclusion, deploying complex public domain mining and developing an in silico reverse metabolic approach, we have (i) constructed probiotic-prebiotic-food correlation matrices that can guide targeted feeding of immune health-beneficial microbes by weaning food in infants; (ii) analyzed competition and synergy for (prebiotic) nutrients between microbes; and (iii) translated this information into designing an experimental complementary feed for infants enrolled in a pilot clinical trial (http://www.nourishtoflourish.auckland.ac.nz/). The presented, benefit-oriented microbiome research strategy is in our opinion nutritionally more actionable than large-scale descriptive studies in humans and has potential to be more translational than microbiomics in rodent models, be they mouse strains, genetically engineered models, or gnotobiotic mice seeded with a limited set of microbes. Our reverse metabolic pipeline aimed at leveraging in silico-generated data into clinical relevance. We have tried to extend from “classical” to molecular nutrition, with the aim of identifying nutrients, bacteria, and mechanisms that point towards crossfeeding to improve immune health in infants around weaning. Our “seeding through feeding” approach differs fundamentally from classical prebiotic candidate testing (feeding baby to assert microbial changes and clinical outcomes). We deliver here the proof-of-concept showing that the in silico mining indeed yields new pro- and prebiotics related to healthy infant immunity but also “positive controls,” i.e., bacteria we expect to find, such as bifidobacteria and lactobacilli. Overall, we present an innovative, translational systems biology-based methodology to inform feeding the infant gut with the optimum prebiotics to facilitate the growth of beneficial gut bacteria that help the maturation and development of immune system in human infants.
To identify exogenous metabolites required by gut microorganisms potentially capable of enhancing the immune system against infant infections and to detect those metabolites in foods/food components, we developed an integrated pipeline based on literature searching, text mining, reverse metabolic analysis, and food database exploration.
Identification of immune-protective bacteria (question i)
The workflow for the identification of immune-protective bacteria is shown in Fig. 1. As a preliminary step, all context-relevant concepts and keywords were identified. To prioritize and focus on the research aims, the initial concepts were organized into four research topics: (a) infant gut microbiome, (b) infant nutrition and microbiome metabolism, (c) beneficial bacteria supporting immune system development in infants, and (d) beneficial bacteria preventing infections in infants. For each topic, a specific literature query was formulated (see Additional file 3: Supplemental Information 3 for explanations). To enhance the specificity of the queries, keywords specifically excluding non-human/non-infant data were taken into consideration. However, some of those keywords, especially “rat/mice model” and “in vitro” study, occur frequently in literature to provide context for the article. Hence, those excluding terms were retained in the queries and used downstream for further manual filtering of the results, therefore yielding both fewer false-positive and false-negative articles.
The literature was queried (31 October 2017) for each of the four research topics to retrieve eligible MEDLINE abstracts and/or full texts from the PMC Open Access Subset and PMC Author Manuscript Collection repositories in PubMed Central. The obtained collection of documents, representing the relevant literature corpus (3673 PubMed IDs), was annotated for key biological entities, (genes, chemicals, species, DNA mutations, SNPs, protein mutations, and diseases) using state-of-the-art biomedical annotation tools: DNorm , tmVar , tmChem , and GNormPlus . The tools are the same as utilized in the Pubtator database, which was deployed for abstract annotations , as it allows the downloading of the data (revision date: 26 June 2017).
All biomedical annotations were retrieved from the relevant literature corpus of abstracts and full texts and were manually inspected to improve both understanding and extent of the potential biological concepts involved in the weaning period. Pertinent annotations and entity lists of terms were therefore collected in three dictionaries: (i) immunity-infant related, (ii) infant infection-disease related, and (iii) chemical related (Additional file 3: Supplemental Information 4). Moreover, a fourth microorganism dictionary was included with names of human gut microorganisms. To build this dictionary, a complete list of microbes at genus level colonizing the human GI tract was used from the Human Microbiome Project catalogue . Two further lactic acid bacteria genera, Oenococcus and Lactococcus, were included. The former, Oenococcus, which is commonly used in wine fermentation, was not reported as a gut commensal in the HMP catalogue, but appears in the Metagenomics of the Human Intestinal Tract (MetaHit) catalogue, and it is present in 13.5% of subjects of the Danish and Spanish cohort (249 individuals) . The latter, Lactococcus, is a genus dominating in the baby gut microbiota . Furthermore, the complete list of microbes at species level was downloaded from the NCBI taxonomy  and manually curated for non-pathogenic species relevant to human gut alone. Opportunistic pathogens and other non-relevant bacterial species (those not described at genus level in the Human Microbiome Project) were excluded from the final list.
The four dictionaries were combined with the literature corpus and submitted to natural language processing (NLP) methods to extract relevant information for the four research topics of the project. The CoreNLP API  was used to parse the scientific text in the corpus, and an analytical pipeline was developed to identify the linguistic relations between the concepts found in our dictionaries. This is the most important step: all abstracts and full texts of the literature corpus were automatically annotated and analyzed to identify relevant linguistic relationships between at least one pair of terms from each pair of dictionaries. Co-mention between at least one term related to more than two dictionaries, for all combinations, was also obtained. Table 1 contains the combinations of the four dictionaries used for NLP relationship and co-mention identification. Out of 3673 papers in our literature corpus of abstracts and full texts, the NLP pipeline extracted 348 unique relevant sentences for relations among two dictionaries and 129 for co-mentions among three or four dictionaries (an excerpt is shown in Additional file 3: Table S1). These were manually curated to ensure coherence, exclude false positives, and identify relevant bacteria at species/strain level, wherever possible. The latter step was carried out by exploiting the manually revised list of human gut microorganisms containing only non-pathogenic and, putative, probiotic bacteria. Results from text mining were filtered to exclude articles published before 2000, sentences from title journal section and from full texts containing unrelated terms (e.g., animals except mice…), “pathogen” or “not-relevant” species at genera level (e.g., species level). The role of the identified microorganisms in supporting the development of the immune system during early life was manually evaluated to define a set of putative probiotic bacteria for further analysis. The evidence on beneficial effects of those microbes was mainly obtained from clinical studies, with some relevant articles on in vitro effects being included in the manual curation process. The full list of sentences identified with text mining is available in Additional files 1 and 2.
Identification of exogenous metabolites for selected microorganisms (question ii)
Exogenous metabolites required by beneficial microbes (putative probiotics) were identified by reverse metabolic analysis of their metabolic models. The metabolic models were those published in the Virtual Metabolic Human  database, which contains the in silico metabolic reconstructions of microbes commonly found in the gut . Those are automatically reconstructed using ModelSeed  starting from the two aerobic bacteria Bacillus subtilis and Escherichia coli to evaluate stoichiometric coefficients for all gram-positive and gram-negative bacteria respectively and may thus represents a bias for anaerobic metabolism. A Perl script was implemented to transform these metabolic models, which are distributed in the Systems Biology Markup Language (SBML) format, into text-based metabolic networks best suited for the downstream analyses. The resulting text-based models are directed graphs, represented with the nodes corresponding to compounds and the edges corresponding to reactions linking reagents to products. Furthermore, the tool harmonizes in a detailed tabular representation all metabolic reactions of each organism, including enzymes and name identifiers from the universal metabolite names and CHEBI identifiers converted using the BiGG Models database . To infer the nutritional profile of each beneficial microbe, the metabolic topologies so far obtained were analyzed with NetSeed , a tool to identify the minimal subset of nodes (in this case, compounds) that cannot be synthesized from other compounds in the network and therefore need to be acquired exogenously (see Fig. 3).
Cooperative metabolic interactions between bacteria and between host and bacteria (question iii)
To deepen the insights into potential ecological microbial interactions between species in our selected community composed of selected candidate probiotics from the text mining analysis, a reverse ecology analysis was applied to predict the ecological structure of this community. For determining host-microbe and microbe-microbe cooperative and competitive potential in a pair-wise manner, NetCooperate  and the R package RevEcoR version 0.99.3 , in R version 3.4.1, were used. Three reverse ecology measures for species interactions were calculated.
The biosynthetic support score provides a measure for the capacity of a potential host to meet the metabolic requirements of a microbe and can be also regarded as a cooperation index . The support represents the fraction of exogenous metabolites of the bacterium, i.e., the nutrients or precursors that cannot be produced by the bacterium itself, that are found in the metabolic interaction network of the host. Its value ranges from 0, no cooperation, to 1, full cooperation. While parasites “egoistically” exploit the host’s metabolism, commensal bacteria have a mutualistic relationship with the host, i.e., they both benefit and contribute. High support scores (> 0.75) are reported for parasites whereas low scores (< 0.75) are reported for commensals .
The metabolic complementarity index between two species measures the ratio (range 0–1) of exogenously acquired compounds in one species that are found in the metabolic network, although not as its feed, of the other species . As such compounds are used by both species, niche complementarity and syntrophy are likely to happen and, typically, high complementary species are able to coexist in contrast to low complementary ones that do rather not co-occur .
The metabolic competition index of two species is the fraction of compounds exogenously required by both species and is therefore a measure of potential nutritional competition  with values ranging from 0 (no competition) to 1 (high competition).
Sourcing exogenous metabolites from whole foods (question iv)
Exogenous compounds, which may inform dietary-based interventions, were used to interrogate the Canadian Foods database (FooDB), a resource of whole foods and food components, as well as their chemistry and biology. The exact chemical name of the metabolites from VMH was sourced into the compound database (1689 metabolites for the 773 gut microbes by Magnúsdóttir et al. ), and the identified compounds were linked to foods. We encountered a limitation in matching the nomenclatures used in VMH as it provides an extensive number of metabolites whose names, to the best of the authors’ knowledge, cannot be retrieved elsewhere (see the “Results” section for details). The list was manually filtered to exclude processed foods, alcohol, and those foods that do not contain clearly defined products (belonging to “Other …” categories, see Additional file 3: Supplemental Information 5). “Baby foods” category (see Additional file 3: Supplemental Information 2, for description) was selected as positive control for this study.
A metabolic enrichment set analysis was performed using the identified exogenous metabolites for which VMH reported a KEGG identifier. The hypergeometric distribution is used to evaluate how likely specific KEGG-available exogenously identified chemical compounds are associated to microbial-specific pathways and help identify those biological processes and pathways that best explain the meaning of the exogenous compounds. All analyses were performed using the graphical environment bStyle , which automated and simplified the entire integration and analytical process (Additional file 3: Figure S1). bStyle also proved to be much faster than analogous R implementations. All selected strains were available in the KEGG database , except F. prausnitzii M21 2 that was replaced by F. prausnitzii SL3/3 as it belongs to the same phylogroup  and B. longum subsp. infantis CCUG 52486 that was replaced by the closely related B. longum subsp. longum strain BBMN68 . Only pathways in the “metabolism” KEGG class, which includes biochemical transformations—essential for growth, reproduction, maintenance of physiological structures, and response to environmental changes—were considered in bStyle. A hypergeometric p value lower than 0.05 was defined as the threshold for considering significant the enriched pathways.
To better classify the foods for further selection and trial in infant weaning studies, metabolites were grouped in seven categories: oligosaccharides, monosaccharides, vitamins, amino acids, other bioactive substances, organic nitrogen compounds, and non-standard nutritive compounds (NSN; see Additional file 3: Supplemental Information 1). The NSN category includes trace elements such as nickel, cadmium, and other heavy metals, plus compounds like acetaldehyde, ethanol. While some of these trace elements are co-factors, they exhibit very narrow concentration ranges for bioactivity, above which they can be or are toxic. Acetaldehyde and ethanol are common small organic compounds in human metabolism but not regarded as nutrients. Furthermore, those substances have been associated to health complications [62, 63]. This is why we termed this category as NSN.
The value of metabolite categories was computed, for each food, as the mean concentration (in mg/100 g) of their compounds normalized to the range [0–1]. The sum of the metabolic categories provides a nutritional-oriented ranking for the foods, and to prioritize foods rich in essential growth factors (vitamins and amino acids) that are usually found in very low concentrations, the weights 10, 8, 6, 4, 2, 1, and − 100 were used respectively for vitamins, amino acids, oligosaccharides, bioactive substances, N-compounds, monosaccharides, and NSNs.
Based on this sorting, the most promising whole-food source containing several of the identified candidate prebiotics can be chosen to be incorporated in an experimental complementary feeding for infants to support and enhance the growth of immune-protective beneficial microbes. This experimental weaning food will be administered in a pilot clinical trial to demonstrate the role of prebiotic complementary feeding in modulating the infant gut microbial composition and abundance (http://www.nourishtoflourish.auckland.ac.nz/).
Chemical Entities of Biological Interest
Human Microbiome Project
Kyoto Encyclopedia of Genes and Genomes
Limit of detection
Limit of quantification
Metagenomics of the Human Intestinal Tract
Natural language processing
Systems Biology Markup Language
Virtual Metabolic Human
Singh RK, Chang H-W, Yan D, Lee KM, Ucmak D, Wong K, et al. Influence of diet on the gut microbiome and implications for human health. J Transl Med. 2017;15:73. https://doi.org/10.1186/s12967-017-1175-y.
Yang I, Corwin EJ, Brennan PA, Jordan S, Murphy JR, Dunlop A. The infant microbiome: implications for infant health and neurocognitive development. Nurs Res. 2016;65:76–88. https://doi.org/10.1097/NNR.0000000000000133.
Gerritsen J, Smidt H, Rijkers GT, de Vos WM. Intestinal microbiota in human health and disease: the impact of probiotics. Genes Nutr. 2011;6:209.
Tamburini S, Shen N, Wu HC, Clemente JC. The microbiome in early life: implications for health outcomes. Nat Med. 2016;22:713–22. https://doi.org/10.1038/nm.4142.
Hill CJ, Lynch DB, Murphy K, Ulaszewska M, Jeffery IB, O’Shea CA, et al. Evolution of gut microbiota composition from birth to 24 weeks in the INFANTMET cohort. Microbiome. 2017;5:4. https://doi.org/10.1186/s40168-016-0213-y.
Wu H, Tremaroli V, Bäckhed F. Linking microbiota to human diseases: a systems biology perspective. Trends Endocrinol Metab. 2015;26:758–70.
Groer MW, Luciano AA, Dishaw LJ, Ashmeade TL, Miller E, Gilbert JA. Development of the preterm infant gut microbiome: a research priority. Microbiome. 2014;2:38. https://doi.org/10.1186/2049-2618-2-38.
Belkaid Y, Hand TW. Role of the microbiota in immunity and inflammation. Cell. 2014;157:121–41. https://doi.org/10.1016/j.cell.2014.03.011.
Fallani M, Amarri S, Uusijarvi A, Adam R, Khanna S, Aguilera M, et al. Determinants of the human infant intestinal microbiota after the introduction of first complementary foods in infant samples from five European centres. Microbiology. 2011;157:1385–92. https://doi.org/10.1099/mic.0.042143-0.
Koenig JE, Spor A, Scalfone N, Fricker AD, Stombaugh J, Knight R, et al. Succession of microbial consortia in the developing infant gut microbiome. Proc Natl Acad Sci U S A. 2011;108(Suppl 1):4578–85. https://doi.org/10.1073/pnas.1000081107.
Rodríguez JM, Murphy K, Stanton C, Ross RP, Kober OI, Juge N, et al. The composition of the gut microbiota throughout life, with an emphasis on early life. Microb Ecol Heal Dis. 2015;26. https://doi.org/10.3402/mehd.v26.26050.
Bäckhed F, Roswall J, Peng Y, Feng Q, Jia H, Kovatcheva-Datchary P, et al. Dynamics and stabilization of the human gut microbiome during the first year of life. Cell Host Microbe. 2015;17:690–703. https://doi.org/10.1016/j.chom.2015.04.004.
Nagpal R, Kurakawa T, Tsuji H, Takahashi T, Kawashima K, Nagata S, et al. Evolution of gut Bifidobacterium population in healthy Japanese infants over the first three years of life: a quantitative assessment. Sci Rep. 2017;7:10097. https://doi.org/10.1038/s41598-017-10711-5.
Haarman M, Knol J. Quantitative real-time PCR assays to identify and quantify fecal Bifidobacterium species in infants receiving a prebiotic infant formula. Appl Environ Microbiol. 2005;71:2318–24. https://doi.org/10.1128/AEM.71.5.2318-2324.2005.
Duranti S, Lugli GA, Mancabelli L, Armanini F, Turroni F, James K, et al. Maternal inheritance of bifidobacterial communities and bifidophages in infants through vertical transmission. Microbiome. 2017;5:66. https://doi.org/10.1186/s40168-017-0282-6.
Makino H, Kushiro A, Ishikawa E, Kubota H, Gawad A, Sakai T, et al. Mother-to-infant transmission of intestinal Bifidobacterial strains has an impact on the early development of vaginally delivered Infant’s microbiota. PLoS One. 2013;8:e78331. https://doi.org/10.1371/journal.pone.0078331.
Pozo-Rubio T, Mujico JR, Marcos A, Puertollano E, Nadal I, Sanz Y, et al. Immunostimulatory effect of faecal Bifidobacterium species of breast-fed and formula-fed infants in a peripheral blood mononuclear cell/Caco-2 co-culture system; 2018. https://doi.org/10.1017/S0007114511001656.
Gonzalez R, Blancas A, Santillana R, Azaola A, Wacher C. Growth and final product formation by Bifidobacterium infantis in aerated fermentations. Appl Microbiol Biotechnol. 2004;65:606–10. https://doi.org/10.1007/s00253-004-1603-9.
Shimamura S, Abe F, Ishibashi N, Miyakawa H, Yaeshima T, Araya T, et al. Relationship between oxygen sensitivity and oxygen metabolism of Bifidobacterium species. J Dairy Sci. 1992;75:3296–306. https://doi.org/10.3168/jds.S0022-0302(92)78105-3.
Mendes-Soares H, Chia N. Community metabolic modeling approaches to understanding the gut microbiome: bridging biochemistry and ecology. Free Radic Biol Med. 2017;105:102–9. https://doi.org/10.1016/J.FREERADBIOMED.2016.12.017.
Levy R, Carr R, Kreimer A, Freilich S, Borenstein E. NetCooperate: a network-based tool for inferring host-microbe and microbe-microbe cooperation. BMC Bioinformatics. 2015;16:164. https://doi.org/10.1186/s12859-015-0588-y.
Adamberg S, Sumeri I, Uusna R, Ambalam P, Kondepudi KK, Adamberg K, et al. Survival and synergistic growth of mixed cultures of bifidobacteria and lactobacilli combined with prebiotic oligosaccharides in a gastrointestinal tract simulator. Microb Ecol Health Dis. 2014;25. https://doi.org/10.3402/MEHD.V25.23062.
Rios-Covian D, Gueimonde M, Duncan SH, Flint HJ, de los Reyes-Gavilan CG. Enhanced butyrate formation by cross-feeding between Faecalibacterium prausnitzii and Bifidobacterium adolescentis. FEMS Microbiol Lett. 2015;362:fnv176. https://doi.org/10.1093/femsle/fnv176.
Moens F, Verce M, De Vuyst L. Lactate- and acetate-based cross-feeding interactions between selected strains of lactobacilli, bifidobacteria and colon bacteria in the presence of inulin-type fructans. Int J Food Microbiol. 2017;241:225–36. https://doi.org/10.1016/J.IJFOODMICRO.2016.10.019.
De Vuyst L, Leroy F. Cross-feeding between bifidobacteria and butyrate-producing colon bacteria explains bifdobacterial competitiveness, butyrate production, and gas production. Int J Food Microbiol. 2011;149:73–80. https://doi.org/10.1016/j.ijfoodmicro.2011.03.003.
Moens F, Weckx S, De Vuyst L. Bifidobacterial inulin-type fructan degradation capacity determines cross-feeding interactions between bifidobacteria and Faecalibacterium prausnitzii. Int J Food Microbiol. 2016;231:76–85. https://doi.org/10.1016/J.IJFOODMICRO.2016.05.015.
Zhang C, Yin A, Li H, Wang R, Wu G, Shen J, et al. Dietary modulation of gut microbiota contributes to alleviation of both genetic and simple obesity in children. EBioMedicine. 2015;2:968–84.
Holzapfel WH, Wood BJB. Lactic acid bacteria in contemporary perspective. In: The genera of lactic acid Bacteria. Boston, MA: Springer US; 1995. p. 1–6. https://doi.org/10.1007/978-1-4615-5817-0_1.
Magnúsdóttir S, Heinken A, Kutt L, Ravcheev DA, Bauer E, Noronha A, et al. Generation of genome-scale metabolic reconstructions for 773 members of the human gut microbiota. Nat Biotechnol. 2016;35:81–9. https://doi.org/10.1038/nbt.3703.
Lombardo R, Priami C. Graphical modeling meets systems pharmacology. Gene Regul Syst Bio. 2017;11:1177625017691937. https://doi.org/10.1177/1177625017691937.
Mattarelli P, Biavati B, Holzapfel WH, Wood BJ. The Bifidobacteria and related organisms: biology, taxonomy, applications. 2017.
Holdeman LV, Kelley RW, Moore WEC, Krieg NR, Holt JH. Bergey’s manual of systematic bacteriology: Springer; 1984. https://doi.org/10.1007/978-0-387-68489-5.
Levy R, Borenstein E. Metabolic modeling of species interaction in the human microbiome elucidates community-level assembly rules. Proc Natl Acad Sci. 2013;110:12804–9. https://doi.org/10.1073/pnas.1300926110.
Chesson P, Kuang JJ. The interaction between predation and competition. Nature. 2008;456:235–8. https://doi.org/10.1038/nature07248.
Umu ÖCO, Rudi K, Diep DB. Modulation of the gut microbiota by prebiotic fibres and bacteriocins. Microb Ecol Health Dis. 2017;28:1348886. https://doi.org/10.1080/16512235.2017.1348886.
Dobson A, Cotter PD, Ross RP, Hill C. Bacteriocin production: a probiotic trait? Appl Environ Microbiol. 2012;78:1–6. https://doi.org/10.1128/AEM.05576-11.
Zheng J, Gänzle MG, Lin XB, Ruan L, Sun M. Diversity and dynamics of bacteriocins from human microbiome. Environ Microbiol. 2015;17:2133–43. https://doi.org/10.1111/1462-2920.12662.
Milani C, Turroni F, Duranti S, Lugli GA, Mancabelli L, Ferrario C, et al. Genomics of the genus Bifidobacterium reveals species-specific adaptation to the glycan-rich gut environment. Appl Environ Microbiol. 2015;82:980–91. https://doi.org/10.1128/AEM.03500-15.
Takemoto K, Aie K. Limitations of a metabolic network-based reverse ecology method for inferring host-pathogen interactions. BMC Bioinformatics. 2017;18:278. https://doi.org/10.1186/s12859-017-1696-7.
Ogata H, Goto S, Sato K, Fujibuchi W, Bono H, Kanehisa M. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 1999;27:29–34. https://doi.org/10.1093/nar/27.1.29.
Parracho H, McCartney AL, Gibson GR. Probiotics and prebiotics in infant nutrition. Proc Nutr Soc. 2007;66:405–11. https://doi.org/10.1017/S0029665107005678.
Rolim PM, Rolim PM. Development of prebiotic food products and health benefits. Food Sci Technol. 2015;35:3–10. https://doi.org/10.1590/1678-457X.6546.
Abeshu MA, Lelisa A, Geleta B. Complementary feeding: review of recommendations, feeding practices, and adequacy of homemade complementary food preparations in developing countries – lessons from Ethiopia. Front Nutr. 2016;3:41. https://doi.org/10.3389/fnut.2016.00041.
Leaman R, Islamaj Dogan R, Lu Z. DNorm: disease name normalization with pairwise learning to rank. Bioinformatics. 2013;29:2909–17. https://doi.org/10.1093/bioinformatics/btt474.
Wei C-H, Harris BR, Kao H-Y, Lu Z. tmVar: a text mining approach for extracting sequence variants in biomedical literature. Bioinformatics. 2013;29:1433–9. https://doi.org/10.1093/bioinformatics/btt156.
Leaman R, Wei C-H, Lu Z. tmChem: a high performance approach for chemical named entity recognition and normalization. J Cheminform 2015;7 Suppl 1 Text mining for chemistry and the CHEMDNER track:S3. doi:https://doi.org/10.1186/1758-2946-7-S1-S3.
Wei C-H, Kao H-Y, Lu Z. GNormPlus: an integrative approach for tagging genes, gene families, and protein domains. Biomed Res Int. 2015;2015:1–7. https://doi.org/10.1155/2015/918710.
Wei C-H, Kao H-Y, Lu Z. PubTator: a web-based text mining tool for assisting biocuration. Nucleic Acids Res. 2013;41(Web Server issue):W518–22. https://doi.org/10.1093/nar/gkt441.
NIH HMP Working Group TNHW, Peterson J, Garges S, Giovanni M, McInnes P, Wang L, et al. The NIH human microbiome project. Genome Res. 2009;19:2317–23. https://doi.org/10.1101/gr.096651.109.
Li J, Jia H, Cai X, Zhong H, Feng Q, Sunagawa S, et al. An integrated catalog of reference genes in the human gut microbiome. Nat Biotechnol. 2014;32:834–41. https://doi.org/10.1038/nbt.2942.
Yatsunenko T, Rey FE, Manary MJ, Trehan I, Dominguez-Bello MG, Contreras M, et al. Human gut microbiome viewed across age and geography. Nature. 2012;486:222–7. https://doi.org/10.1038/nature11053.
Resource Coordinators NCBI. Database resources of the National Center for biotechnology information. Nucleic Acids Res. 2017;45:D12–7. https://doi.org/10.1093/nar/gkw1071.
Manning C, Surdeanu M, Bauer J, Finkel J, Bethard S, McClosky D. The Stanford CoreNLP natural language processing toolkit. Proc 52nd Annu Meet Assoc Comput Linguist Syst Demonstr. 2014:55–60. https://doi.org/10.3115/v1/P14-5010.
VMH. http://vmh.uni.lu/. Accessed 22 Dec 2017.
Henry CS, DeJongh M, Best AA, Frybarger PM, Linsay B, Stevens RL. High-throughput generation, optimization and analysis of genome-scale metabolic models. Nat Biotechnol. 2010;28:977–82. https://doi.org/10.1038/nbt.1672.
King ZA, Lu J, Dräger A, Miller P, Federowicz S, Lerman JA, et al. BiGG models: a platform for integrating, standardizing and sharing genome-scale models. Nucleic Acids Res. 2016;44:D515–22. https://doi.org/10.1093/nar/gkv1049.
Carr R, Borenstein E. NetSeed: a network-based reverse-ecology tool for calculating the metabolic interface of an organism with its environment. Bioinformatics. 2012;28:734–5. https://doi.org/10.1093/bioinformatics/btr721.
Cao Y, Wang Y, Zheng X, Li F, Bo X. RevEcoR: an R package for the reverse ecology analysis of microbiomes. BMC Bioinformatics. 2016;17:294. https://doi.org/10.1186/s12859-016-1088-4.
Borenstein E, Feldman MW. Topological signatures of species interactions in metabolic networks. J Comput Biol. 2009;16:191–200. https://doi.org/10.1089/cmb.2008.06TT.
Lopez-Siles M, Khan TM, Duncan SH, Harmsen HJM, Garcia-Gil LJ, Flint HJ. Cultured representatives of two major Phylogroups of human colonic Faecalibacterium prausnitzii can utilize pectin, Uronic acids, and host-derived substrates for growth. Appl Environ Microbiol. 2012;78:420–8. https://doi.org/10.1128/AEM.06858-11.
Altmann F, Kosma P, O’Callaghan A, Leahy S, Bottacini F, Molloy E, et al. Genome analysis and characterisation of the exopolysaccharide produced by Bifidobacterium longum subsp. longum 35624™. PLoS One. 2016;11:e0162983. https://doi.org/10.1371/journal.pone.0162983.
von Ehrenstein OS, Heck JE, Park AS, Cockburn M, Escobedo L, Ritz B. In utero and early-life exposure to ambient air toxics and childhood brain tumors: a population-based case-control study in California, USA Environ Health Perspect 2016;124:1093–1099. doi:https://doi.org/10.1289/ehp.1408582.
Edmunds SM, Ajizian SJ, Liguori A. Acute obtundation in a 9-month-old patient: ethanol ingestion. Pediatr Emerg Care. 2014;30:739–41. https://doi.org/10.1097/PEC.0000000000000240.
We show gratitude to Professor Elhanan Borenstein for his thoughtful comments about NetCooperate and microbial interactions. We thank Alan Ramponi and Alessio Paris for the technical assistance.
The work was funded by the New Zealand National Science Challenge “High-Value Nutrition”: “Complementary Infant Feeding”, Research Funding Module (RFM) Project no.: 3713256.
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Relevant relationship for PubMed IDs. (XLSX 225 kb)
Relevant co-mention for PubMed IDs. (XLSX 109 kb)
Table S1. Example of relevant sentences from the pipeline for selected microbes. Supplemental Information 1 List of metabolites in each metabolite category. Supplemental Information 2 Description and motivation for “Baby Food” category. Supplemental Information 3 Literature queries for each topic. Supplemental Information 4 List of terms in each dictionaries. Supplemental Information 5 List of manually filtered foods, which excludes processed foods, alcohol and those foods that do not contain clearly defined products. Figure S1 Metabolic enrichment set analysis description. (PDF 1050 kb)
Nutrient profile of each microbes in the community in exam as resulted from NetSeed. (XLSX 59 kb)
Data for support, complementarity and competition. (XLSX 72 kb)
Metabolite pathway enrichment analysis results for each selected microbes. (XLSX 108 kb)
Foods sorted according to their nutritive content. (XLSX 27 kb)
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Michelini, S., Balakrishnan, B., Parolo, S. et al. A reverse metabolic approach to weaning: in silico identification of immune-beneficial infant gut bacteria, mining their metabolism for prebiotic feeds and sourcing these feeds in the natural product space. Microbiome 6, 171 (2018). https://doi.org/10.1186/s40168-018-0545-x
- Infant gut microbiome
- Reverse ecology
- Knowledge extraction
- Complementary feeding
- Systems biology