Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified on the basis of human clinical data. The mechanisms underlying its beneficial effects are still unknown. Gnotobiotic mice harboring F. prausnitzii (A2-165) and Escherichia coli (K-12 JM105) were subjected to 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced acute colitis. The inflammatory colitis scores and a gas chromatography-time of flight (GC/TOF) mass spectrometry-based metabolomic profile were monitored in blood, ileum, cecum, colon, and feces in gnotobiotic mice. The potential anti-inflammatory metabolites were tested in vitro. We obtained stable E. coli and F. prausnitzii-diassociated mice in which E. coli primed the gastrointestinal tract (GIT), allowing a durable and stable establishment of F. prausnitzii. The disease activity index, histological scores, myeloperoxidase (MPO) activity, and serum cytokine levels were significantly lower in the presence of F. prausnitzii after TNBS challenge. The protective effect of F. prausnitzii against colitis was correlated to its implantation level and was linked to overrepresented metabolites along the GIT and in serum. Among 983 metabolites in GIT samples and serum, 279 were assigned to known chemical reactions. Some of them, belonging to the ammonia (α-ketoglutarate), osmoprotective (raffinose), and phenolic (including anti-inflammatory shikimic and salicylic acids) pathways, were associated with a protective effect of F. prausnitzii, and the functional link was established in vitro for salicylic acid. We show for the first time that F. prausnitzii is a highly active commensal bacterium involved in reduction of colitis through in vivo modulation of metabolites along the GIT and in the peripheral blood.
IMPORTANCE Inflammatory bowel diseases (IBD) are characterized by low proportions of F. prausnitzii in the gut microbiome. This commensal bacterium exhibits anti-inflammatory effects through still unknown mechanisms. Stable monoassociated rodents are actually not a reproducible model to decipher F. prausnitzii protective effects. We propose a new gnotobiotic rodent model providing mechanistic clues. In this model, F. prausnitzii exhibits protective effects against an acute colitis and a protective metabolic profile is linked to its presence along the digestive tract. We identified a molecule, salicylic acid, directly involved in the protective effect of F. prausnitzii. Targeting its metabolic pathways could be an attractive therapeutic strategy in IBD.
INTRODUCTION
The human colonic microbiota is a highly complex microbial ecosystem, and several hundred different species of bacteria are known to colonize the gut (1). The homeostasis established between the host and the resident bacteria plays important functional roles, such as protection against pathogenic organisms, maturation and modulation of the immune system, intestinal maturation, production of short-chain fatty acids (SCFA), mucosal physiology, and production of vitamins, such as vitamin K and biotin (2). Alterations in this homeostasis, named dysbiosis, have a profound impact on human health, as demonstrated in several gastrointestinal diseases, including inflammatory bowel diseases (IBD), irritable bowel syndrome (IBS), and colorectal cancer (CRC) (3–7). For instance, in genetically predisposed subjects, bacterial dysbiosis, including a decrease of Firmicutes, could result in disordered innate immune reactions and lead to IBD (8). Interestingly, in IBD patients that exhibited endoscopic recurrence, the proportion of the most prevalent species from the Clostridium leptum group, Faecalibacterium prausnitzii, was lower than in patients without endoscopic recurrence (7). Since then, it has been observed that F. prausnitzii decreases with the onset of inflammatory status; the relative abundance of F. prausnitzii might be a sensor of intestinal health in adults suffering from Crohn's disease (CD), one of the two major IBD (3). This observation strengthens the paradigm of a mucosal protective role of F. prausnitzii through its anti-inflammatory potential.
The mechanisms leading to the beneficial protection of F. prausnitzii are still poorly understood. F. prausnitzii is predominant in the intestine of many other mammals; such ubiquity suggests that F. prausnitzii plays an important physiological role (3, 9). In humans, F. prausnitzii accounts for more than 3.5% of the total bacterial population (10) and belongs to the functional metagenomic core (11). Because it is one of the most abundant butyrate-producing bacterial species, its beneficial effect had been first attributed to butyrate, well known for its pleiotropic and beneficial effects in the gastrointestinal tract (GIT) (12, 13). However, we showed that F. prausnitzii-mediated butyrate production is not the only host health benefit metabolite linked to this species (7). In fact, in acute or chronic colitis models, the immunomodulation potential of F. prausnitzii involves uncharacterized secreted metabolites that directly impact the host immune response (7, 14). Moreover, we have recently proposed that F. prausnitzii participates in host epithelial homeostasis (15). The establishment of F. prausnitzii along the GIT may result from a combination of environmental factors, such as other commensal bacterial species, redox mediators, oxygen concentration, and mucus layer but also bile salt concentrations, as well as pH (16, 17). In early infancy, the abundance of F. prausnitzii is very low and increases after the establishment of primocolonizing bacteria (18). The complexity of conditions required for F. prausnitzii colonization might explain why the mechanisms accounting for its protection potential in vivo are still poorly understood. Thus, we set up a new model of diassociated mice housing F. prausnitzii and Escherichia coli (as a primocolonizing bacterial companion) to characterize F. prausnitzii's protective role and metabolic profile during a chemically induced acute colitis.
RESULTS
Establishment of a stable E. coli/F. prausnitzii-diassociated mouse model.
We first tried to obtain F. prausnitzii-monocolonized mice by intragastric inoculation of 2 × 108 ± 1 × 108 CFU into germfree (GF) mice. After 24 h, no F. prausnitzii was detected in the feces, indicating that this species was not able to stably colonize the GIT of GF mice after a single oral inoculation. We then tried to establish F. prausnitzii in GF mice by both intragastric and intrarectal inoculations, and as shown in Fig. 1A, we succeeded since the amount of F. prausnitzii A2-165 ranged from 1.5 to 5 × 108 CFU/g of mouse feces. However, this colonization was obtained with a poor yield, with only 5 mice successfully colonized from 18 inoculated. Interestingly, F. prausnitzii exhibited an unusual morphology in the cecum of these 5 F. prausnitzii monoassociated animals, with cell sizes ranging from 6 to 25 µm (Fig. 1B), which is very rarely seen in in vitro cultures.
FIG 1
We thus decided to use E. coli as a bacterial companion in order to get stable F. prausnitzii-colonized mice (hereafter named the E. coli/F. prausnitzii-diassociated mouse model). E. coli strain JM105 rapidly and stably colonized mice gut during at least 4 weeks after oral inoculation (see Fig. S1 in the supplemental material). By “priming” the GIT of mice with E. coli for at least 6 days, a durable and stable implantation of F. prausnitzii was systematically obtained in all mice (n = 29) (Fig. 1C). The population of F. prausnitzii was 10-fold lower (3.4 × 108 to 2 × 109 CFU/g of feces) than that of E. coli (2 × 109 to 1.2 × 1010 CFU/g of feces). Because of their different morphologies, the two bacterial species E. coli and F. prausnitzii could easily be distinguished in the cecal content (Fig. 1D). In addition F. prausnitzii, as a strict anaerobe species, was only mainly present from the cecum to the rectum, whereas E. coli was gradually abundant from the stomach to the colon (Fig. 1E).
Impact of F. prausnitzii on the metabolite profile during inflammation in the gnotobiotic mouse model.
We compared 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in either E. coli-monoassociated or E. coli/F. prausnitzii-diassociated mice in order to establish a metabolite profile under conditions allowing F. prausnitzii to display its anti-inflammatory properties (Fig. 2A). To decipher the impact of F. prausnitzii, after TNBS induction of colitis, metabolite profiling was performed with ileum, cecum, and colon contents, feces, and serum samples using gas chromatography-time of flight (GC/TOF) mass spectrometry (see Text S1 in the supplemental material) (Fig. 2B). Using a system that combines mass spectrometric and biological metadata, 983 metabolic features were validated. The relational database system BinBase was used for automated metabolites annotation (19, 20), with a criterion of presence in 50% or more of the biological replicates (see Text S1 and Table S1 in the supplemental material). Using a stringent 3-fold-intensity criterion, the number of metabolites distinguishing E. coli-monoassociated and E. coli/F. prausnitzii-diassociated animals greatly varied, depending on the GIT segment (Fig. 2B; see Table S1). In the upper part of the GIT, 86 and 142 metabolites were overrepresented in the ileum and cecum, respectively, in the E. coli-monoassociated mice. Conversely, 187 and 482 metabolites were more abundant in the colon and feces from E. coli/F. prausnitzii-diassociated mice, suggesting a metabolic imprinting correlated to the presence of F. prausnitzii (Fig. 1E). A total of 279 metabolic signals were structurally identified and assigned to a compound involved in known chemical reactions (as shown by KEGG number in Table S1). Interestingly, the metabolites identified in the colon mapped onto distinct functional categories (amino acids, energy metabolism, SCFA, lipids, phenolic acid, and sugars), indicating a broad metabolic signature of F. prausnitzii (Table 1). Compared to previous metabolomic data (21), our E. coli/F. prausnitzii-diassociated model displayed many classes of molecules present in conventional animals but absent in axenic animals as energy metabolites, lipids and fatty acids, amino acids, and sugars. Moreover, three metabolites are common: palmitic acid, 3,4-dihydroxyhydrocinnamic acid, and glucuronic acid.
FIG 2
TABLE 1
TABLE 1 Known metabolites statistically overrepresented in the colon of E. coli/F. prausnitzii-diassociated mice compared to E. coli-monoassociated mice after TNBS-induced colitis
Class
Metabolite
KEGG/PubChem ID no.
Dixenic/monoxenic intensity ratio
SEM
P value
Amino acids
Spermidine minor
C00315
7.675
0.69
0.009
N-Acetylaspartic acid
SID 136743417
5.472
0.29
0.000
Quinic acid
C00296
3.682
0.30
0.019
O-Acetylserine
C00979
2.821
0.12
0.0005
Isothreonic acid
SID 103172351
2.220
0.17
0.047
Threonic acid
C01620
2.120
0.11
0.012
Homocystine
C01817
0.490
0.06
0.031
2-Ketoisocaproic acid
C00233
0.402
0.05
0.003
Energy metabolites
Phosphoric acid
C00009
5.334
0.39
0.003
Glucose-6-phosphate
C00092
2.354
0.11
0.005
Fructose-6-phosphate
C00085
2.0364
0.10
0.015
Glycerol
C00116
2.0206
0.07
0.003
β-Sitosterol
C01753
0.0449
0.13
0.020
Lipids and fatty acids
4-Hydroxybutyric acid
C00989
3.277
0.16
0.000
Palmitic acid
C00249
2.765
0.17
0.014
Caprylic acid
SID 11528290
2.637
0.12
0.001
Ethanolamine
C00189
4.854
0.22
0.000
Phytol
C01389
2.4277
0.15
0.015
Squalene
C00751
2.004
0.13
0.046
Phenolic acids
Idonic acid
SID 135170473
3.779
0.40
0.049
trans-Sinapinic acid
C00482
2.618
0.14
0.003
Syringic acid
C10833
2.180
0.11
0.008
Malonic acid
C04025
2.131
0.14
0.037
3-Phenyllactic acid
C05607
2.080
0.10
0.011
3,4-Dihydroxyhydrocinnamic acid
SID 111677818
0.269
0.06
0.001
Pyrimidine
Pseudouridine
C02067
2.556
0.17
0.019
Orotic acid
C00295
0.279
0.09
0.011
Sugars
Fructose
C00095
5.023
0.29
0.001
Mannose
C00159
2.896
0.23
0.025
Glyceric acid
C00258
2.644
0.10
0.000
N-Acetyl-d-hexosamine
C03136
2.591
0.19
0.036
1,5-Anhydroglucitol
C07326
2.484
0.18
0.027
β-Gentiobiose
C08240
2.423
0.11
0.003
Arabinose
C00259
2.356
0.11
0.005
Tagatose
SID 163300922
2.240
0.16
0.037
Ribonic acid
C01685
2.187
0.11
0.013
2-Deoxyerythritol
SID 108236
2.002
0.11
0.023
Glucuronic acid
C00191
0.321
0.02
0.000
Glycero-guloheptose
SID 117585658
0.085
0.07
0.001
Raffinose
C00492
0.024
0.15
0.027
Inulotriose
SID 4849
0.004
0.03
0.000
Other
Indole-3-lactate
C02043
5.427
0.39
0.003
Shikimic acid
C00493
2.220
0.13
0.017
Putrescine
C00134
0.487
0.05
0.015
Protective effect of F. prausnitzii on TNBS-induced colitis is linked to specific metabolic signatures in the colon.
In the E. coli/F. prausnitzii-diassociated mice, all biological markers indicated a decrease of the inflammation level in the presence of F. prausnitzii. After colitis induction, weight loss tended to decrease in the presence of F. prausnitzii (−3.2% ± 1.9% compared to −5.2% ± 1.5%). The disease activity index (DAI), Wallace macroscopic scores, and Ameho microscopic scores (architectural derangements, goblet cell depletion, edema/ulceration, and degree of inflammatory cell infiltrates) were significantly (P < 0.001) decreased in the colons of E. coli/F. prausnitzii-diassociated mice (Fig. 3A, B, and C). A severe disruption of the epithelial architecture was observed in E. coli-infected, TNBS-treated mice in contrast to E. coli/F. prausnitzii-diassociated, TNBS-treated mice (Fig. 3D). E. coli-infected TNBS-treated mouse colon epithelium was characterized by the absence of crypts and massive immune cell infiltrations. Such tissue erosions were less marked in the presence of F. prausnitzii. All of these observations indicated a protective effect of F. prausnitzii in our TNBS-induced-colitis model. Moreover, the F. prausnitzii population level was inversely correlated to the disease activity markers (weight loss, DAI, and Wallace and Ameho scores), suggesting that its anti-inflammatory effects could be dose dependent (see Fig. S2 in the supplemental material).
FIG 3
Regarding metabolic profiles, we obtained strong evidence of the magnitude of the effect of an E. coli/F. prausnitzii microbial context in the TNBS-treated animals. The rarefaction curve showed that 80% of the known metabolites were more represented in the colon content of dixenic mice (see Fig. S3 in the supplemental material). We searched for metabolites segregating the monoxenic and dixenic animals after induction of colitis (t test on the mean). For instance, in the colon, butyrate (4-hydroxybutyric acid) (P = 0.0006), shikimic acid (P = 0.017) related to the salicylic acid pathway (P = 0.2055), and indole-3-lactate (P = 0.0035) were overrepresented in the E. coli/F. prausnitzii-diassociated mice (Table 1 and Fig. 3E). The metabolomic profiles sharply differed according the gut segment (Fig. 2B). For instance, raffinose was more discriminatory in the ileum (P = 0.0091) (data not shown) than in the colon (P = 0.1703) and was negatively related to F. prausnitzii abundance (Fig. 1E).
F. prausnitzii is a metabolically active species in vivo.
The beneficial mitigation effects, observed locally in the colon in the presence of F. prausnitzii, were confirmed in the serum, where systemic inflammation markers were reduced. First, the degree of infiltration by polymorphonuclear neutrophils (estimated by tissue myeloperoxidase [MPO] activity) was significantly decreased during TNBS-induced colitis in the presence of F. prausnitzii (P < 0.001) (Fig. 4A). In the presence of F. prausnitzii after TNBS induction of colitis, the serum cytokine response was globally similar to the one measured without TNBS (see Table S2 in the supplemental material). Interestingly, in the serum, the levels of proinflammatory cytokines, such as interleukin-1α (IL-1α), IL-2, and IL-5, were statistically decreased to a level corresponding to a noninflammatory status (Fig. 4B).
FIG 4
The high number of metabolites detected in the serum samples was noteworthy (Fig. 2B; see Table S1 in the supplemental material). Nineteen metabolites were overrepresented in the serum of E. coli/F. prausnitzii-diassociated mice. Seven were only found in the serum, and 11 were also found in the colon, where F. prausnitzii was most prevalent. Four metabolites were present in ileum, cecum, colon, and feces, but they are so far unknown (BinBase no. ID436364, -269147, -200610, and -310063) (Fig. 4C). The serum metabolome shared 5 entities with both colon and feces (uric acid, elaidic acid, lyxose, and unknown compounds BinBase ID231544 and ID459916). As observed in the colon content, the presence of F. prausnitzii is correlated to high levels of salicylic acid (P = 0.367) and shikimic acid (P = 0.4328) (Fig. 4D). Strikingly, α-ketoglutaric (AKG) acid was 10-fold more abundant in the serum of E. coli/F. prausnitzii-diassociated mice (P = 0.028), together with the linked citric acid and uric acid pathway (P = 0.085 and P = 0.0733, respectively). AKG acid is important in ammonia recycling and is reported to be depleted during gastrointestinal dysbiosis (22). Its involvement in cell proliferation and differentiation through the activity of the AKG-acid-dependent enzymes has recently been reviewed (23). The concomitant analysis of salicylic, shikimic, and AKG acids as standard in the GC mix validated their identification.
The four metabolites specifically associated with the presence of F. prausnitzii possess anti-inflammatory capacities in vitro.
We tested the immunomodulatory properties of four candidate molecules in a human colon adenocarcinoma cell line model (HT-29) by using F. prausnitzii supernatant, butyrate, and the 5-aminosalicylic acid (5-ASA) as controls. As shown in Fig. 5, salicylic acid (10 µM) blocked IL-8 production, as did butyrate (10 mM), F. prausnitzii supernatant, and 5-ASA (20 mM). Shikimic acid, raffinose, and AKG acid (100 µM) did not block IL-8 production, and a mixture of the different molecules did not show any additional effect (data not shown).
FIG 5
DISCUSSION
In this study, we show for the first time that F. prausnitzii is a highly active commensal bacterium involved in the reduction of colitis through in vivo modulation of metabolites along the GIT and in the peripheral blood. This novel approach clearly confirms the anti-inflammatory potential of F. prausnitzii and provides new clues about its ecological lifestyle and mechanisms in intestinal physiopathology.
We showed that efficient F. prausnitzii implantation requires the GIT preparation by E. coli, a primocolonizer of the sterile human newborn gut. Such an implantation kinetic is concordant with previous reports (15, 24) and with the late presence of F. prausnitzii in the human gut 7 months after birth (18). Thus, the time needed for F. prausnitzii colonization could correspond to the decrease of the redox potential (Eh), leading to more reduced conditions in the lower GIT (15, 25). However, other ecological factors should not be excluded, such as physiological modification of nutrient sources by the other species leading to the onset of an efficient trophic chain. Interestingly, sugars and energy metabolisms were deeply modified in the presence of F. prausnitzii (Table 1), suggesting a modification of their availability. While E. coli abundance gradually increased from stomach to colon, F. prausnitzii localization seemed to depend upon anaerobic conditions only found in the lower gut. These observations confirm that gradients in the physiochemical conditions along the GIT influence the biogeography of the colonic mucosal microbiome (26). Thus, our gnotobiotic rodents can be considered a relevant model to provide ecological information about GIT colonization kinetics by extremely oxygen-sensitive species. Moreover, we showed that the colonization pattern of F. prausnitzii in the GIT reflects its metabolic imprinting. F. prausnitzii, abundant in the lower GIT (cecum and colon) (Fig. 1E), had a gradually metabolic impact along the GIT (Fig. 2B). Even if F. prausnitzii was absent in the ileum, metabolic changes were observed in the ileum and at a distance in the serum (Fig. 4C and D). By using ileal content, we counted the F. prausnitzii population, and we cannot exclude that bacteria were present under the detection threshold or in a viable-but-not-culturable state. We detected 86 metabolites specific for E. coli in the ileum and 37 that are linked to the presence of E. coli and F. prausnitzii (Fig. 2B). Twenty-eight are unknown, and 9 could be identified (see Table S1 in the supplemental material). Among them are sugars, an antioxidant (trans-sinapinic acid), and neurotransmitter precursors (5-amino valeric acid lactone, a homologue of γ-aminobutyric acid [GABA] [27], and N-acetyl aspartic acid [28]). In the literature, an impact of F. prausnitzii on ileal physiology and particularly permeability has been already reported (29). These results, and similar findings reported by Velagalpuladi et al. (21), suggest that a direct or indirect effect of F. prausnitzii can be observed at a systemic level and not only where its population level is high.
During dysbiosis, the site-specific colonization and the dominance of F. prausnitzii in the colon are affected, which might contribute to the etiology of diseases of the large intestine (24). We have previously shown that F. prausnitzii presents anti-inflammatory properties in acute and chronic TNBS-induced-colitis models in conventional mice (7, 30), and this result was also observed in simplified gnotobiotic model. Moreover, our model allowed us to compare the population levels of E. coli and F. prausnitzii in feces to assess the impact of TNBS induction of colitis on bacterial populations (see Fig. S2 in the supplemental material). A TNBS challenge decreased the F. prausnitzii population, and the remaining level of F. prausnitzii clustered the mice into two groups (threshold of 108F. prausnitzii cells/g of feces). Inflammation markers were decreased when the F. prausnitzii population was high. Because the level of colitis mitigation was directly correlated to its GIT abundance, our results confirmed that F. prausnitzii might be both a biomarker and a major factor of human health in adults (3). A review suggested that an increase in oxygen tension in the gut, related to the oxidative burst due to inflammatory reaction itself, could be the cause of the dysbiosis in IBD patients (25). Our results allowed us to hypothesize that the decreased F. prausnitzii level observed in IBD patients is a consequence of inflammation but also participates in the inflammation process, leading to the disease's vicious circle (31).
In our simplified microbiota, we identified metabolites that can be produced either by the host or by the bacteria. Moreover, most of those metabolites are not assigned to any functions. This reflects the paucity of knowledge about reciprocal functional adaptation between host and microbes and the high percentage of microbial genes lacking annotation in metagenomic studies (1, 32). Li et al. had identified F. prausnitzii as an active bacterial species in humans, modifying butyrate-derived metabolites in urine (11). Using our metabolomic approach, we confirmed that the amount of 4-hydroxybutyric acid was increased in feces, colon, and cecum, where F. prausnitzii was established (see Table S1 in the supplemental material). Butyrate plays a major role in gut homeostasis, particularly through its anti-inflammatory activities in the colon mucosa (33, 34). This impact was confirmed in vitro using concentrations similar to those found in F. prausnitzii culture supernatants (10 mM) (Fig. 5). However, its role remains controversial since its effects seem to be dose and time dependent but also depend on the cellular model used (14, 35). In our study, butyrate specifically produced by F. prausnitzii (see Fig. S4A in the supplemental material) was not directly linked to health parameters (see Fig. S4B).
Based on our metabolomic approach, we identified metabolites specifically associated with the presence of F. prausnitzii. These findings support the concept that beneficial effects from commensals are linked to their large metabolic impact on host physiology. In fact, salicylic acid, at a concentration close to the one detected in the colon, decreased IL-8 production in vitro (Fig. 5). Interestingly, 40% of Fusobacterium prausnitzii (former nomenclature for F. prausnitzii) strains were able to ferment salicin, an alcoholic β-glucoside that can be converted into salicylic acid (36). In the pharmaceutical industry, salicylic acid is the precursor of 5-ASA, a drug used in the treatment of IBD (37). We showed that salicylic acid was as effective as 20 mM 5-ASA in vitro (38). Furthermore, we identified shikimic acid, a precursor for the biosynthesis aromatic compounds, including salicylic acid through the achorismate synthase pathway (39). Shikimic acid, upstream in the pathway of 5-ASA production, did not have the same anti-inflammatory effect in vitro. However, in vivo, it is demonstrated that 3,4-oxo-eisopropylideneshikimic acid (ISA), a derivative of shikimic acid, protects against TNBS-induced colonic damage in rats (40). We also identified raffinose, an oligosaccharide only fermented by the gut microbiota since monogastric animals do not express pancreatic α-galactosidase (41). Its uptake pathways are affected in celiac disease, whereas only transcellular uptake is affected in CD patients. Mucosal permeability has been found to be an important factor for raffinose permeation (42). Velagapudi et al. detected this metabolite in much higher abundance in GF than in conventional animals (21). F. prausnitzii impacts the host inflammation pattern but could also play a key role in maintaining gut permeability (29, 43), intestinal epithelial homeostasis (15), and energy balance, particularly through sugar pathway (44) (Table 1).
In contrast to the metabolites overrepresented in the presence of F. prausnitzii, underrepresented ones could be involved in anti-inflammatory process (Table 1). For instance, a significant decrease in homocystine was observed in the presence of F. prausnitzii. This amino acid results from the oxidation of homocysteine, which has been reported to be proinflammatory (45). Also, a decrease in putrescine together with an increase in spermidine in the dixenic mice could inhibit the secretion of inflammatory cytokines (46). Our approach provided a lot of hypotheses about the role of F. prausnitzii in intestinal physiopathology for future investigations.
The serum is a biofluid providing an excellent opportunity to assess the extent of interplay between bacterial metabolic and systemic human pathways (47). F. prausnitzii modulated the metabolome of the host blood by decreasing IL-1α, IL-2, and IL-5 concentrations. For instance, α-ketoglutaric (AKG) acid was statistically detected in the serum of mice colonized with F. prausnitzii and E. coli (Fig. 4). This organic acid, important for the proper metabolism of all essential amino acids and the transfer of cellular energy in the citric acid cycle, is a glutamic acid precursor involved in protein synthesis and the regulation of blood glucose levels (48). AKG did not show any significant effect on IL-8 production by HT-29 in our in vitro model (Fig. 5). This may mean that our conditions are not appropriate or that, as reported by Cairns and Mak (23), AKG acid may need a specific transporter/biochemical transformation before being active. Individuals with high protein intake, bacterial infections, or gastrointestinal dysbiosis may benefit from supplemental AKG acid to help metabolic health. Personalized health care investigations could be routinely set up to target inflammation biomarkers or check F. prausnitzii mitigation through salicylic, shikimic, and AKG acid levels in feces or serum.
To conclude, F. prausnitzii is a highly metabolic bacterium that impacts the host via different pathways to preserve its homeostasis. We have identified metabolites, particularly salicylic acid, involved in its anti-inflammatory capacities but also highlighted the complex and dynamic cross talk with the host under inflammation conditions.
MATERIALS AND METHODS
Bacterial culture.
F. prausnitzii A2-165 (DSM 17677), isolated from human fecal stool (49), was grown at 37°C in YBHI medium (brain-heart infusion medium supplemented with 0.5% yeast extract [Difco]) supplemented with cellobiose (1 mg/ml [Sigma]), maltose (1 mg/ml [Sigma]), and cysteine (0.5 mg/ml [Sigma]) in an anaerobic chamber filled with 85% N2, 10% CO2, and 5% H2. Escherichia coli JM105 was grown on LB medium (Difco) at 37°C.
Animals and experimental design.
Germfree 7- to 8-week-old BALB/c mice (male) were obtained from the germfree rodent breeding facilities of Anaxem-Micalis (INRA, Jouy-en-Josas, France). Animals were kept in flexible-film isolators (Getinge-La Calhène, Vendôme, France) in standard cages (5 mice/cage) with sterile wood shavings as animal bedding. Mice were given free access to autoclaved tap water and to a standard diet, R03-40 (Scientific Animal food and Engineering, Augy, France), sterilized by gamma irradiation at 45 kGy (IBA Mediris, Fleurus, Belgium). Isolators were maintained under controlled conditions of light (0730 to 1930 h), temperature (20 to 22°C), and humidity (45 to 55%). All procedures were carried out according to European Community Rules of Animal Care and with authorization 12-092 from the French Veterinary Services.
Inoculation of germfree mice with F. prausnitzii.
To obtain F. prausnitzii-monoassociated mice, germfree animals receive both intragastric and intrarectal inoculations of a 100× concentrated culture of F. prausnitzii A2-165 (109 CFU/inoculation). For intragastric gavages, mice were first treated with 0.1 ml of sodium bicarbonate (0.2 M) and then received 0.5 ml of the bacterial suspension 10 min later. For intrarectal inoculation, mice were first anesthetized by an intraperitoneal injection of a volume (1% of the body weight) of 10% ketamine hydrochloride (Imalgen 500 [Merial]) and 6% xylazine (Rompun [Bayer]) in 0.9% NaCl and then treated with 0.2 ml of the bacterial suspension.
To obtain dixenic E. coli/F. prausnitzii-diassociated mice, germfree mice were orally inoculated with a fresh culture of E. coli JM105 (108 to 109 CFU /ml). Twenty-four hours later, when E. coli was established in the GIT, 109 CFU of F. prausnitzii at 0.2 ml was administered to a donor mouse by intragastric gavage as described above. As soon as F. prausnitzii was established in the donor mouse, its feces were homogenized in water inside the isolator and immediately administered by intragastric gavage to other mice pretreated with sodium bicarbonate.
Viable bacteria in the inoculum were enumerated before and after gavage by plating of appropriate dilutions on supplemented YBHI agar in the anaerobic chamber. To enumerate the A2-165 strain in feces, fresh samples were introduced into the anaerobic chamber, serially 10-fold diluted, and plated on supplemented YBHI agar. In order to selectively enumerate A2-165 in the feces of dixenic mice by eliminating E. coli cells, fecal samples were treated with sodium azide (3%) for 5 min at 37°C and then plated on sodium azide (0.02%) YBHI agar.
TNBS-induced colitis.
Mice were weighed before TNBS administration and anesthetized by an intraperitoneal injection as described above. TNBS (Sigma-Aldrich) was dissolved in 0.9% NaCl–ethanol (50:50 vol/vol). Fifty microliters of TNBS (50 mg/kg body weight) was administered intrarectally (using a 3.5 French catheter [Solomon Scientific]) to mice maintained for 30 s in a vertical position. Control mice received 50 µl of 0.9% NaCl–ethanol solution intrarectally. Inflammation was monitored 48 h after TNBS administration.
Scanning electron microscopy.
Scanning electron microscopy analyses were performed at the MIMA2 platform (INRA, Massy, France) from 0.2 g of cecal samples as previously described (50).
Tissue preparation for histological analysis.
Flushed colons were opened longitudinally, cut into 2-cm sections, and rolled according to the Swiss roll procedure (51). The samples were fixed in 4% paraformaldehyde (4 h, room temperature), dehydrated, and embedded in paraffin according to standard histological protocols. Four-micrometer sections of distal colon were mounted on SuperFrost Plus slides. To assess TNBS-induced colitis, the sections were stained with hematoxylin-eosin and examined blindly according to the Ameho criteria (52).
Inflammation score assessment of TNBS-induced colitis.
The colon was removed without mesenteric fat and mesentery, carefully opened, and cleaned with phosphate-buffered saline (PBS). Colonic damage and inflammation were assessed blindly according to the Wallace score (53).
MPO activity.
MPO activity was measured using the method of Bradley et al. (54), modified as follows. Tissue samples were homogenized (50 mg/ml) in ice-cold 50-mM potassium phosphate buffer (pH 6) containing 5% hexadecyl trimethyl ammonium bromide (Sigma-Aldrich) and hydrogen peroxide. MPO is expressed in units per milligram of wet tissue.
Cytokine analysis.
Colonic samples were homogenized in 400 µl of Tris-HCl buffer containing protease inhibitors (Sigma-Aldrich) in a tissue lyser. Samples were centrifuged for 20 min, and the supernatant was frozen at −80°C until further analysis. Before sacrifice, blood samples were obtained from the retro-orbital venous plexus and centrifuged, and sera were stored at −80°C. Cytokine levels were determined by flow cytometry using Cytometric bead array analysis (mouse inflammation kit) (BD, NJ).
Metabolite extraction and analysis.
Fifty microliters of serum and feces, intestinal content, cecal content, and colonic content were lyophilized and subjected to 10 s of bead beating. Metabolite extraction was performed as previously described (20) with 700 µl of a precooled methanol-isopropanol-water (3:3:2) mixture in an ultrasonic water bath (5 min). After centrifugation, 650 µl of the supernatant was collected (5 min, 15,000 rpm) and dried before derivatization. Metabolite analysis was performed according to Fiehn et al. (55).
In vitro experiments with the HT-29 cell line.
The protocols used in this study were adapted from Kechaou et al. (56). The human colon carcinoma cell line HT-29 was cultured and stimulated with recombinant human tumor necrosis factor alpha (TNF-α) (5 ng/ml; PeproTech, NJ) as described previously. Cell incubations were done in the presence or not of different metabolites tested at the indicated concentration: butyric acid sodium salt, reference 303410, Sigma-Aldrich; shikimic acid, reference S5375, Sigma-Aldrich; salicylic acid, reference 84210, Sigma-Aldrich; d-(+)-raffinose pentahydrate, reference R0514, Sigma-Aldrich; α-ketoglutaric acid disodium salt dihydrate, reference 75892, Sigma-Aldrich; 5-aminosalicylic acid, reference 18858, Sigma-Aldrich. All samples were analyzed in triplicate. After coincubation, cell supernatants were collected and mixed with an antiprotease cocktail according to the manufacturer's instructions (Complete EDTA-free protease inhibitor; Roche Applied Bioscience), and frozen at −80°C until further analysis of interleukin-8 (IL-8) concentrations by an enzyme-linked immunosorbent assay (ELISA) (BioLegend, San Diego, CA, and Mabtech, Sweden, respectively).
Statistical analysis.
Data are reported as means ± standard errors of the means (SEM) and for figures using box-and-whisker plots with the interquartile range, where the top portion of the box represents the 75th percentile and the lower portion represents the 25th percentile. The horizontal bar within the box represents the median, with the mean shown as “+.” The upper horizontal bar outside the box represents the 95th percentile, and the lower horizontal bar outside the box represents the 15th percentile. Statistical analysis was performed using one-way analysis of variance followed by Student-Newman-Keuls multiple comparison post hoc analysis, and with a P value of <0.05 considered significant. For metabolomic analysis, the resulting data sets were imported into the MatLab software for univariate and multivariate statistical analyses. Univariate statistics evaluated the number and percentage of features that are either unique or vary significantly between E. coli-monoassociated and E. coli/F. prausnitzii-diassociated animals. Venn diagrams were constructed as described in reference 57.
ACKNOWLEDGMENTS
This study was a part of the FPARIS collaborative project selected and supported by the Vitagora Competitive Cluster and funded by the French FUI (Fond Unique Interministériel; FUI no. F1010012D), the FEDER (Fonds Européen de Développement Régional; Bourgogne no. 34606), the Burgundy Region, the Conseil Général 21, and the Grand Dijon. This work was also supported by Merck Médication Familiale (Dijon, France) and Biovitis (Saint Étienne de Chomeil, France). R.M. and S.M. received a salary from the same grants.
We thank Sébastien Blugeon for technical assistance and Florian Chain and Olivier Berteau for fruitful discussions and critical reading of the manuscript.
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Commensal and Probiotics-Host Interactions Laboratory, UMR 1319 Micalis, INRA, Jouy-en-Josas, France
AgroParisTech, UMR 1319 Micalis, Jouy-en-Josas, France
AVENIR Team Gut Microbiota and Immunity, ERL, INSERM U 1057/UMR 7203, Faculté de Médecine, Saint-Antoine, Université Pierre et Marie Curie (UPMC), Paris, France
Service de Gastroentérologie, Hôpital Saint-Antoine, Assistance Publique—Hôpitaux de Paris (APHP), Paris, France
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