Salmonella is a major foodborne pathogen which successfully infects animal species for human consumption such as swine. The pathogen has a battery of virulence factors which it uses to colonise and persist within the host. The host microbiota may play a role in resistance to, and may also be indirectly responsible from some of the consequences of, Salmonella infection. To investigate this, we used 16S rRNA metagenomic sequencing to determine the changes in the gut microbiota of pigs in response to infection by Salmonella Typhimurium at three locations: ileum mucosa, ileum content and faeces. Early infection (2 days post-infection) impacted on the microbiome diversity at the mucosa, reflected in a decrease in representatives of the generally regarded as desirable genera (i.e., Bifidobacterium and Lactobacillus). Severe damage in the epithelium of the ileum mucosa correlated with an increase in synergistic (with respect to Salmonella infection; Akkermansia) or opportunistically pathogenic bacteria (Citrobacter) and a depletion in anaerobic bacteria (Clostridium spp., Ruminococcus, or Dialliser). Predictive functional analysis, together with metabolomic analysis revealed changes in glucose and lipid metabolism in infected pigs. The observed changes in commensal healthy microbiota, including the growth of synergistic or potentially pathogenic bacteria and depletion of beneficial or competing bacteria, could contribute to the pathogen’s ability to colonize the gut successfully. The findings from this study could be used to form the basis for further research aimed at creating intervention strategies to mitigate the effects of Salmonella infection.
Salmonella is a major foodborne pathogen with a significant number of cases and outbreaks every year1. Poultry meat, eggs and pork are the main sources of human salmonellosis. As a consequence of the successful establishment of control programmes in poultry, the relative proportion of human cases attributed to pork consumption has increased2.
Swine are a natural host for Salmonella spp. Apart from infections caused by S. Cholerasuis, the host adapted serovar to swine, Salmonella infections in pigs usually vary from subclinical to a self-limiting diarrhoea3. Among serovars affecting swine, Salmonella Typhimurium stands out due to its zoonotic importance in human salmonellosis1 and its widespread distribution in pork production4,5. The relevance of S. Typhimurium infections in swine is reflected by the vast literature published with respect to the pathogenesis6, the host immune response7,8, epidemiology of infections3 and control9,10 of this serotype in pigs. Notably, it has been reported that within a few hours of ingestion, the pathogen is detected in high concentrations in faeces11. Early after infection, epithelial damage and inflammation can be observed, principally at the ileum mucosa12, together with a migration of the pathogen to the gut associated lymphoid tissue via monocyte-derived cells13.
High throughput sequencing methods have provided an opportunity to study the porcine microbiota with unprecedented detail through sequencing of the 16S rRNA gene as a phylogenetic marker14,15,16. Indeed, these high throughput sequencing methods offer the chance to understand how infections such as swine salmonellosis impact the gut microbiota. For instance, this approach has been employed to identify differences in the microbiota among high and low Salmonella shedders17. In their study, Bearson and colleagues revealed a higher abundance of representatives of the family Ruminococcaceae in low-shedder pigs and also depletion of Prevotella in high shedder pigs early after infection. Another recent study, where pigs were challenged with S. Typhimurium, showed that strain virulence and the resulting intensity of the inflammatory response following infection by Salmonella caused a reduction in the abundance of short-chain fatty acids-producing bacteria18.
Understanding the changes occurring in the host microbiome due to Salmonella infection is of paramount importance with respect to developing a better understanding of Salmonella pathogenesis and disease. Here we characterise for the first time how the gut microbiome is modified after a Salmonella Typhimurium challenge in recently weaned pigs within three target locations of the gastrointestinal tract, i.e., faeces, ileum content and ileum mucosa. By studying changes in the diversity, taxonomy and abundance, and by combining this information with the predicted functionality of the microbiome and metabolite analysis, we aimed to expand on previous studies17,18,19, and provide a greater insight into the mechanisms underlying successful colonization of the gut by Salmonella17,18,19. Ultimately, it is hoped that identification of the groups of bacteria affected by disruption of gut homeostasis following Salmonella infection, could serve as a preliminary step to design strategies to limit the alteration of the microbiota by Salmonella infection and to increase resistance to gut colonization by this pathogen.
58014 operational taxonomic units (OTUs) were detected among the samples following matching of the 16S rRNA sequencing data to the Greengenes database. After filtering low abundance OTUs using a 0.005% threshold, a final number of 1192 taxa across seven taxonomic ranks were retained for further analysis.
Factors affecting microbiome richness
Sample richness was estimated by Chao1 and Shannon indices while Simpson index was used to estimate sample evenness (Fig. 1; Supplementary file 1). By repeated measure of analysis of variance (ANOVA), it was apparent that there were no significant differences in richness or evenness between infected and control pigs (p = 0.977; p = 0.75) or across sampling time points, (p = 0.96; p = 0.67). However, when ileum mucosa samples were specifically analysed, differences in richness among sampling time points were close to significance (Shannon index; p = 0.061). Across sample type, significant differences were observed in the richness estimators between faeces, ileum content and ileum mucosa (p < 0.001). Faecal samples showed higher richness than ileum content or ileum mucosa regardless of the estimator used (Fig. 1).
Ordination of the pig gut microbiota varies according to the location in the gut from which samples are collected and between Day 0 and Day 2 samples
Two factors, i.e., type of sample (p < 0.001) and individual pig (p < 0.01), influenced the ordination of samples (Fig. 2a). The effect was maintained even after splitting samples by sampling day (Fig. 2b). Considering this output, the next ordination analyses were split by type of sample and the analysis of faeces, ileum mucosa and ileum content samples separately revealed that both infection (p < 0.01) and sampling day (p < 0.05) had a significant influence (Fig. 2). When samples from Day 0 (control group) and 2 days post-infection (d.p.i.) were specifically compared, significant differences in Bray-Curtis non-linear multi-dimensional scaling (NMDS) ordination were detected at within the ileum mucosa microbiota (p < 0.001) and close to significant differences (p = 0.053) were apparent in faecal samples (Fig. 2c and d).
Taxonomic differences in faeces, ileum content and mucosa microbiomes at the time points evaluated
We compared the relative abundances of bacteria present in faeces, ileum content and ileum mucosa at different time points, including late infection sampling (14 d.p.i. and 30 d.p.i.; Fig. 3). OTUs were ranked by relative abundance, selecting up to the 10th most abundant taxa (families and genera) in each sample type (faeces, ileum mucosa and ileum content) at each sampling point (Day 0, Day 2, Day 14 and Day 30). Overall, we observed large differences among samples across a variety of variables. On Day 0, Lactobacillaceae (Lactobacillus) dominated the bacteria present within the ileum contents. At the ileum mucosa Lactobacillus, Helicobacteraceae (Flexispira) and Ruminococcaceae (Ruminococcus) were the most abundant bacteria. In faeces, proportions of Lactobacillaceae were lower and the dominant family was Ruminococcaceae. Clear changes in dominant families and genera were observed in infected pigs at Days 2, 14 and 30 across intestinal locations. These differences were evident within ileum content and ileum mucosa samples, and are described in greater depth below. In contrast, the dominant families Prevotellaceae (Prevotella), Lachnospirceae (Rosseburia and Coprococcus) and Ruminococcaceae (Ruminococcus) remained relatively stable in faeces at different sampling points.
Changes in the abundance of OTUs as a consequence of the S. Typhimurium infection
The analysis of changes in microbiota abundance at 2 d.p.i. revealed 60 differentially abundant OTUs (FDR-value < 0.05) in the ileum mucosa (Supplementary file 2), when compared with the corresponding samples from the control group (0 d.p.i.). Similarly, 25 and 10 OTUs were found to be differentially abundant (FDR-value < 0.05) across the ileum content (Supplementary file 3) and faecal samples (Supplementary file 4), respectively. Particular OTUs differed significantly in abundance across the gut regions analysed, as depicted in Fig. 4a. Table 1 summarises the principal increased and decreased OTUs in the ileum mucosa, ileum content and in faeces after two days of infection. Notably, a decrease in abundance of OTUs belonging to the class Clostridia was apparent across all three locations analysed. Specifically, genera such as Clostridium (FDR = 0.037) and Dialister (FDR = 0.002) in the ileum mucosa, Megasphaera (FDR = 0.017) and Mitsuokella (FDR = 0.035) in the ileum content and two OTUs from families Lachnospiraeae (FDR = 0.033) and Ruminococcaceae (FDR = 0.027) in faeces, were all present in decreased proportions after two days of infection. In addition, OTUs from the genus Lactobacillus were also decreased in the ileum mucosa and content samples (FDR = 0.007, FDR = 0.042; respectively) at this time point.
The proportions of a number of taxa also increased at this time point (i.e., 2 dpi pigs). Genera such as Candidatus arthromitus (FDR < 0.001), Akkermansia (FDR = 0.016) and Odoribacter (FDR = 0.035) were increased within the mucosa of infected pigs, one OTU belonging to the Enterobacteriaceae family (genera unclassified) (FDR = 0.027) was significantly increased in ileum content samples and OTUs that were significantly increased in faeces were assigned to the families Mogibacteriaceae (FDR = 0.025) and Ruminococcaceae (FDR = 0.08).
Hierarchical clustering of pig samples according to the relative count of differentially abundant OTUs in the ileum mucosa, clustered pigs on the basis of infection (Fig. 4b). Samples collected from the four necropsied pigs at 2 d.p.i. (infected pigs) exhibited a similar pattern of OTUs abundance that diverged from the control pigs necropsied on Day 0. This clustering of pigs by the relative abundance of OTUs was not observed either in the ileum content or faeces for Day 0 and Day 2 pigs (Supplementary Figure S1a and b respectively).
Correlation between histopathology scoring and mucosa-associated microbiota
Histological lesions in ileum mucosa samples from pigs necropsied on Day 0 and Day 2 were scored and correlated with OTU proportions at the mucosa (Fig. 5; Supplementary file 5). Severe epithelial damage was positively correlated to taxa from the phyla Proteobacteria, such as Citrobacter (Spearman’s ρ = 0.97 and p < 0.001), Verrucomicrobia such as Akkermansia muciniphila (Spearman’s ρ = 0.93 and p < 0.001), Firmicutes, such as Allobaculum (Spearman’s ρ = 0.92 and p < 0.001) or Roseburia (Spearman’s ρ = 0.88 and p < 0.01), and Bacteroidetes, such as Bacteroides (Spearman’s ρ = 0.87 and p < 0.01).
In contrast, the integrity of the intestinal epithelial cell wall was positively associated with different Firmicutes, such as Lactobacillus (Spearman’s ρ = −0.90 and p < 0.01), Clostridium (Spearman’s ρ = −0.88 and p < 0.01), Bulleidia (Spearman’s ρ = −0.87 and p < 0.01) and Ruminococcus (Spearman’s ρ = −0.87 and p < 0.01), Proteobacteria, such as Campylobacter (Spearman’s ρ = −0.88 and p < 0.01) and Flexispira (Spearman’s ρ = −0.87 and p < 0.01), and the genus Bifidobacterium (phylum Actinobacteria) (Spearman’s ρ = −0.88 and p < 0.01).
Analysis of modulation of predicted microbiome functionality by Salmonella infection
The PICRUSt tool was used to predict Kegg Orthology group (KOs) abundances based on 16S rRNA sequences. The analysis yielded a prediction of 5441 KOs. As for OTU-based analysis, Bray-Curtis compositional dissimilarity highlighted significant differences in predicted functions (p < 0.001) by type of sample (faeces, ileum content or ileum mucosa (Supplementary Figure S2). Further analyses focused on differences between ileum mucosa samples from Day 0 and Day 2 pigs. No significant differences in metagenome functions were observed at KO level 2 functions although a tendency (p < 0.1) was observed in functions such as membrane transport or biosynthesis of secondary metabolites, all with lower abundance in infected pigs (Supplementary Figure S3). Analyses of functions at L3 in these samples identified 1138 differentially abundant KOs among control pigs (Day 0) and infected pigs (2 d.p.i) (Supplementary file 6). The inclusion of differentially expressed KOs in the software Interactive pathway explorer (Ipath2) showed an increased abundance of genes linked with the metabolism of lipids (biosynthesis of fatty acids) and nucleotide metabolism, and a decreased abundance of genes associated with bacterial chemotaxis, glycolysis and gluconeogenesis pathways in the ileum mucosa of Day 2 infected pigs.
Ileum content samples from control pigs (Day 0) and infected pigs (Day 2) were also analysed by liquid and gas chromatography. The analysis targeted fatty acids, fatty acyls and short-chain fatty acids compounds, carboxylic acid compounds and sugar derivatives. Table 2 summarises the 19 compounds that were significantly changed between control and infected pigs. Among fatty acids, there was a remarkable increase in concentration of dihydroxybutanoic (p = 0.026) acid, octanoic acid (p = 0.026) and acetoacetic acid (p = 0.002) in 2 dpi infected pigs. Among carboxylic acids, the levels of pyruvic (p = 0.002) and aconitic (p = 0.015) acids were significantly decreased in the ileum contents of infected pigs. Finally, glycerol, a sugar derivate, was also significantly decreased (p = 0.002) in the ileum content of Day 2 infected pigs.
This study involved an in-depth investigation of the microbial changes that occur in the gut environment at target locations, ileum content and mucosa as well as faeces, after a S. Typhimurium infection in swine. S. Typhimurium, either under controlled or field conditions, is able to succesfully infect pigs in a short time-frame, with relatively high concentrations of the pathogen being present in faeces within a few hours of exposure11,20. A number of studies agree that the local inflamation, resulting from the immune response elicited by Salmonella, triggers changes in the gut environment which favour the survival of Salmonella and prompt changes in the gut microbiota composition18,21,22. This inflamatory response is thought to enable Salmonella to compete with the resident microbiota through the use of tetrathionate produced by the oxidation of thiosulfate by reactive oxygen species (ROS)23 or due to its resistance to defensive molecules such as ROS or lipocalin-2, which is secreted by neutrophils and limits the acquisition of iron24. As a result, changes in the composition of the microbiota and gut functionality were anticipated. Our study included a limited number of pigs per sampling day. Although, ideally, a larger sample size would have been employed, our investigation with the limited number of pigs available, together with the appropiate statistical analysis, allow us to report, for the first time to our knowledge, that Salmonella’s biggest impact on microbiota composition takes places at the ileum mucosa as early as 2 d.p.i.
Methods of evaluating microbial diversity include α-diversity indexes such as richness (the total number of unique species within a community) and the relative abundance of different species that make up the richness in that community, and as well as β-diversity, dissimilarity-based ordinations. These metriceswere clearly influenced by the origin of the sample (ileum content, ileum mucosa or faeces) in accordance with previous results25,26. When samples were split by sample type, the influence of the infection on the ordination of the microbiota at the ileum mucosa was particulalrly apparent. In contrast, it was surprising to note that although challenged pigs exhibited clinical signs, such as mild to watery diarrhoea and low-grade fever, as well as the steady shedding of Salmonella during the first week (data not shown), no clear significant differences in diversity were observed in faeces (only a trend), or ileum content samples. Although the sample size limits the power to detect differences in diversity in faeces, our observation is consistent with the results obtained by Bearson and colleagues17, who observed that neither alpha nor beta diversity were affected when challenged pigs shed Salmonella at low concentrations in faeces. Furthemore, Drumo et al.18 showed that Salmonella strain virulence influences the observed changes of diversity results in faeces. In our results, we establish for the first time that the major diversity differences occur at the ileum mucosa and that this effect is less apparent within the ileum content or the downstream segments of the intestine (i.e., faeces).
In agreement with previous studies in pigs17,18,19, we found that Salmonella infection triggered changes in the relative abundance of certain bacteria at 2 d.p.i. The shift in the microbiota was apparent at the ileum mucosa (see dendogram in Fig. 4b), where samples from 2 d.p.i. infected pigs clustered together in the same clade, influenced by the drop in abundance of genera from the family Veillonellaceae (Mitsuokella, Dialister and Megasphaera). Since the ileum constitutes the principal target for Salmonella invasion in the gut27, it can be inferred from our results that the aforementioned impacts on epithelial cell damage, inflammation, defensive molecules and metabolites principally affect the microbiota associated to the ileum mucosa, while the effect on ileum content or faeces is more limited.
To evaluate the effect of the infection on the relative abundance of the microbiota, relative changes in taxa abundance between Day 0 and Day 2 were evaluated. In agreement with previous studies, we observed dissimilarities in OTU changes at different locations after Salmonella infection19. Although the microbiota is not stable and evolves through the pigs’ life26, the short time-frame between challenge and infection (2 days) ensures that the changes observed cannot be attributed to age-related influences. Notably, our results demonstrated a decrease in abundance of beneficial gut bacteria such as Clostridium spp., Lactobacillus spp., Prevotella, Bifidobacterium or Megaesphera in the ileum (mucosa and content) after infection. The decrease in Lactobacillus was one of the most robust results with respect to the microbiota of the ileum content and ileum mucosa, with a number of different OTUs of these species ranking among the most decreased. S. Typhimurium infection in pigs prompts an early inflamatory response which is associated with a decreased expressionof genes coding for apical sodium-dependent bile acid transporter (ASBT) and the fatty and bile acid transporters FABP2 and FABP6, impairing normal bile absorption in the ileum8. As a result, higher concentrations of bile salts are present in the lumen of the small intestine. As some beneficial species such as Lactobacillus and Bifidobacterium, are susceptible to bile salts28,29, the marked drop of abundance of these bacteria in the ileum could be the consequence of the disruption of the entero-hepatic circulation of the biliary acids. However, it remains to be seen if these changes are transitory, i.e., as a consequence of the challenge with a high dose of Salmonella, or if they persist for longer periods. It is notable that previous work does show that the changes in microbiome community structure persist over the first week post-challenge17,19.
We also observed taxa changes specific to each location, e.g., Dialister only changed at the mucosa, Veillonella at the ileum content and Treponema in faeces. Even if divergences in changes in the microbiota at different locations could be explained by the differences of the background microbiota25, we propose that a diluted effect in faeces compared to the ileum may also be a contributory factor. Through the analysis of the most abundant taxa in samples Day 14 and Day 30, it was apparent that the faecal microbiome was more stable throughout the course of the study than was the case for the ileal microbiomes14. This result highlights that the microbiome is more susceptible to changes in targeted locations (e.g. ileum mucosa) than in faeces (which can be considered a global picture of the gut microbiome), a fact that is particularly notable in light of the fact that faeces is regularly used in microbiome studies due to the fact that sample procurement is non-invasive30. Although our results may be limited by the study sample size, we illustrate that the interpretation of the results should be validated in the context of the anatomical location of the studied effect when faeces are used as proxy samples.
Damage of ileal mucosa was correlated to an increase of bacteria that are synergistic to the infectious process, i.e., bacteria that boost the damage caused by the pathogen, and/or opportunistic pathogens, such as Akkermansia muciniphila and Citrobacter, respectively. Previous studies have reported an increase in levels of other Enterobacteriaceae, such as Citrobacter, arising from Salmonella infection22,31. Our study confirms that the modification of the intestinal environment at the ileum favours the expansion of closely related microorganisms22,32,33. Akkermansia is an opportunistic bacterium which develops synergistic relationships with Salmonella by disturbing mucus secretion and silfation19. Similarly to our study, Borton et al.22 detected an increase in the proportions of the genus Akkermansia genera in Salmonella infection with inflamed murine gut samples. In contast, typically regarded as beneficial, anaerobic, Gram-positive gut bacteria such as Lactobacillus, Ruminococcus, Clostridium or Allobaculum abundance decreased in severe damaged ileum mucosa samples. The release of RNS and ROS during intestinal non-typhoidal Salmonella infection creates a highly oxidative environment which is not permissive for the growth of anaerobic bacteria34, while transitient aerotolerant bacteria such as Bacteroides35 might take an advantage of the disruption in the gut enviromental conditions.
Finally, based on PICRUSt predictions and metabolomic analysis, we inferred changes in functional pathways encoded within the ileum mucosa microbiome associated with infection. Ordination of predicted functions by Bray-Curtis dissimilarity clustered samples by tissue, similarly to 16S rRNA OTU results. At KEGG level 2, there were no clear differences in microbiome functions among control and early infected pigs at the ileum mucosa. The sample size together with the overlapping of functions among different bacteria are two possibly limiting factors in finding potential differences30. Nevertheless, some functions related to basal metabolism (secondary metabolism, metabolism of enzymes, amino acids and biosynthesis of lipids) demonstrated a tendency to be reduced at 2 d.p.i., an observation that suggests a general downshift in microbial intestinal activity. These results are in accordance with a study of induced colitis in pigs36, which described a reduced capacity for energy acquisition and dysregulated microbial signaling and repair pathways after inflammation. Further analysis of functions at KEGG level 3 interestingly revealed that chemotaxis and glucose metabolism (glycolysis and gluconeogenesis) functions were more abundant at the ileum mucosa prior to Salmonella infection (control pigs). The activation of the glucose metabolism could be associated with the degradation of oligo- and polysacharides by lactic acid bacteria. Levels of glycerol, a sugar derivative, and pyruvate, a carboxylic acid, were decreased in infected pigs, acording to the predictions in the metabolism of glucose and its derivatives. In contrast, levels of pantothenic acid were increased in the ileum contents of infected pigs at 2 d.p.i. Analysis of predicted metabolic routes in Interactive Pathways Explorer (Ipath2) showed an activation of valine, leucine and isoleucine metabolism, all of which result in the production of pantothenic acid. At 2 d.p.i., an increase of fatty acid metabolism KOs was observed, with particular activation of fatty acid biosynthesis routes. Levels of methylvaleric, oxovaleric, acetoacetic, butenedioic and octanoic acids were increased in ileum contents from 2 d.p.i. pigs, confirming the activation of biosynthesis of fatty acids by the gut microbiota early after infection. The link between the microbiota and fatty acid metabolism could be attributed to changes in the nutrients available in the gut environment. Salmonella infection disrupts the entero-hepatic circulation of the billiary acids as mentioned above8,30, which in turn alters the lipid metabolism. As a result, we can expect higher concentrations of available fatty acids in the gut lumen, favouring the growth of bacteria that use them in their metabolism. Overall, these results illustrate that S. Typhimurium infection triggers impairment of metabolic funtions, which in turn can affect the physiology of digestive processes in the gut30.
The present study demonstrates that Salmonella infection modifies the microbiota in the gut early after infection, and shows for the first time that the major changes occur in the ileum mucosa and are less evident in the faeces and even the ileum lumen, highlighting the merits of study host mucosal samples, where practical. Ironically, host response to infection (immune response and metabolic changes) could be a major contributor to the depletion of commensal/beneficial inhabitants of the intestinal tract (Lactobacillus, Bifidobacterium, Prevotella or Megasphaera), and the increase of synergists of infection such as Akkermansia or Citrobacter. Indeed, the relative abundance of these synergists in the ileal microbial ecosystem is positively correlated to the degree of epitelium damage in the ileum. Finally, we illustrate that the disruption of microbiota composition triggered by infection also has apparent consequences for the microbiome function, with a general downshift of activities early after infection and additional changes in relevant metabolic routes. Future research should focus on identifying the key host response-related factors that prompt changes in the microbiome structure, which might help to establish novel microbiome restoration strategies to limit the impact of Salmonella infection in pigs and, ultimately, zoonotic infections in humans.
Salmonella challenge outline
Sixteen crossbred commercial weaned female pigs of approximately four weeks of age from a Salmonella-free herd were moved into the isolation facilities at the University of León (Spain). After an adaptation period of seven days, four pigs were euthanized and necropsied (control group). The remaining twelve pigs were orally challenged with 5 ml of a broth containing 108 cfu/ml of S. Typhimurium phage type DT104 and subsequently necropsied in groups of four at 2 days post-infection (d.p.i.), 14 d.p.i., and 30 d.p.i.
Faeces and ileum (approx., 20 cm backwards from ileocaecal junction) were collected from each animal. Ileum luminal content (approx. 5 g) was poured in a plastic tube and the ileum wall was preserved in another tube. All samples were collected aseptically and frozen in liquid nitrogen immediately. Frozen samples were kept at −80 °C until further processing. A subsample of faeces was cultured by the current ISO:6579/2007 to detect the presence/absence of Salmonella in all pigs included in the study. Another sub-sample of ileum wall was fixed in formalin and embedded in paraffin wax for further processing.
All procedures involving animals were performed in accordance with the European regulations regarding the protection of animals used for experimental and other scientific purposes, under the supervision of the Ethical and Animal Welfare Committee of the University of León (Spain).
Histopathology and immunohistochemistry
Two paraffin sections (5 μm) from each formalin fixed samples were routinely processed and stained with hematoxylin and eosin (H&E) to evaluate tissue morphology. For immunohistochemistry assays, a standard avidin-biotin peroxidase method was performed as described elsewhere37 employing 1F12 monoclonal antibody and a biotinylated anti-mouse IgG (Dako, Barcelona, Spain) as a secondary antibody. Sections were evaluated by microscopy and scored (from 0 to 5) by adding up the following parameters: no lesions = 0; villi shorten = 1; complete villi erosion = 1; presence of Salmonella = 1; high concentration of Salmonella = 1; inflammatory cells infiltration = 1.
Frozen ileum wall (5–10 cm of ileum) was opened using a scalpel, mucosa wall was rinsed carefully with sterile Phosphate Saline Buffer to remove any faecal matter and its surface was scraped without excessive pressure using a sterile slide.
Purelink Genomic DNA mini-kit (Invitrogen) was used to extract DNA from 200 mg ileum mucosa (IM) while Purelink Microbiome DNA Extraction kit (Invitrogen) was used for Ileum content (200 mg) and faeces (200 mg) samples. Both kits were used in accordance with manufacturer’s instructions. After extraction, DNA was quantified (Nanodrop®, ThermoFisher) and the presence of microbial DNA was confirmed by 16S rRNA amplification by conventional PCR38.
16S rRNA amplicon sequencing
All samples were prepared for MiSeq compositional sequencing using the specifications outlined by Illumina Inc. (Illumina Inc., Cambridge, UK). The V3–V4 region of the 16S rRNA gene was amplified and Illumina index primers attached in two separate PCR reactions39. All PCR reaction conditions and clean up procedures using AMPure XP (Labplan, Kildare, Ireland) were followed as outlined by Illumina Inc. Quantified samples were then sequenced using an Illumina MiSeq system at the Teagasc Sequencing Centre (Moorepark, Fermoy, Ireland).
Bioinformatic processing and analysis
Raw sequence reads generated by MiSeq sequencing were processed using the version 1.9.1 of the Quantitative Insights Into Microbial Ecology (QIIME) pipeline40 by using the subsampled open-reference OTU calling approach41. Demultiplexing and trimming of Miseq reads was done with the default QIIME parameters42. After trimming, the reads were merged into a single fasta file and clustered into OTU against the GreenGenes database43 (release 2013-08: gg_13_8_otus) by using the parallel uclust_ref method. Reads that failed this step were clustered to de novo OTU with the uclust44 method. The filtering of chimeric OTU was performed by using ChimeraSlayer45 against the GreenGenes reference alignment. After removing singletons and doubletons OTUs, only those OTUs representing more than 0.005% of the total filtered were retained as suggested by Bokulich et al.42. For the genera analyses, OTU were collapsed into genera taxonomic level by using the tax_glom funciont in PhyloSeq46. The full data sets have been submitted to NCBI Sequence Read Archive (SRA) under accession: SRP111505, (BioProject:PRJNA393762).
Functional metagenomic predictions
A functional prediction based on 16S rRNA marker gene sequences was performed using PICRUSt47. After excluding the unknown OTUs from the GreenGenes 13.5 reference database and normalizing by 16S rRNA gene copy number, functional metagenomes for each sample were predicted from the Kyoto Encyclopedia of Genes and Genomes (KEGG) catalogue and categorised to a specified KEGG level. In addition, Kegg orthology groups (KOs) were mapped to KEGG and visualized using the Interactive Pathway Explorer (iPath2.0) web-based tool48.
Detection of metabolites by metabolomics
Detection of metabolites was performed from 160 mg of ileum content samples from Day 0 and Day 2 pigs by liquid chromatography time-of-flight mass spectrometry (LC–QTOF MS/MS) and Gas chromatography time-of-flight mass spectrometry (GC–QTOF MS). Prior to the analysis, an extraction of the metabolites was carried out with methanol and dichloromethane.
LC–QTOF MS/MS was run in Agilent 1200 Series LC system coupled to an Agilent 6540 UHD Accurate-Mass QTOF hybrid mass spectrometer (Santa Clara, CA, USA). Chromatographic separation was performed by using a Poroshell 120 EC-C18 column (50 mm × 2.1 mm i.d., 2.7 μm particle size) from Agilent Technologies. The mobile phases were 95:5 water:ACN (phase A) and 95:5 ACN:water (phase B), both containing 0.1% (v/v) formic acid and 5 mM ammonium acetate as ionization agents. The LC pump was programmed at a flow rate of 0.25 mL min−1 and the elution gradient was as follows: from min 0 to 30, the percentage of phase B was modified from 50% to 100%, and then the final percentage was held for 20 min. Thus, the total analysis time per sample was 61 min (including postprocessing). Accurate mass spectra in MS scan were acquired in the m/z range 40–1200. MassHunter Workstation software (version B7.00 Qualitative Analysis, Agilent Technologies, Santa Clara, CA, USA) was used to process all data obtained by LC–QTOF in auto MSMS mode. Identification of the metabolites was supported on MS and MS/MS information and search in the METLIN MS and MS/MS databases (http://metlin.scripps.edu), the Human Metabolome Database (HMDB, 3.6 version) and the LIPID MAPS website ((http://www.lipidmaps.org), using in all cases the MFs obtained in the previous step. A table with the peak area of all identified compounds in the different samples injected was obtained as a result.
GC–QTOF/MS analysis was performed by Agilent 7890 A Series GC system coupled to an Agilent 7200 UHD Accurate-Mass QTOF hybrid mass spectrometer equipped with an electron impact (EI) source (Santa Clara, CA, USA). The samples were analyzed by EI ionization mode at 70 eV. Chromatographic separation was carried out with a fused silica DB-5MS-UI 30 m × 0.25 mm i.d, × 0.25 μm film thickness capillary column. The GC oven temperature program started at 60 °C (1 min held), followed by a temperature ramp of 10 °C min−1 to final 300 °C (2 min held). Post-run time was programmed for 4 min up to 310 °C to assure complete elution of the injected sample. MassHunter Workstation software (version B7.00 Qualitative Analysis, Agilent Technologies, Santa Clara, CA, USA) was used to process all data obtained by GC–TOF/MS in full scan mode. The list of MFs obtained for each analysis was exported as data files in compound exchange format (.cef files). Tentative identification of compounds was performed by searching each mass spectrum in the NIST 11 and Fiehn databases using the retention index or retention time value, respectively.
Further analyses were performed in R v3.1.1. Microbiota and study variables (type of sample, sampling, infection) were included in the estimation of alpha diversity (Shannon and Chao1 indexes) and beta diversity (Simpson index) analysis by Vegan R package49. Potential differences in richness of factors included in the study were estimated by analysis of variance (ANOVA). Dissimilarities between pairs of samples were estimated with the Bray-Curtis dissimilarity index50 and weighted unifrac index51 and analysed with non-linear multi-dimensional scaling (NMDS) in Vegan. The Vegan envfit function was used to evaluate if the factors of study (i.e. sampling day and infection status) where associated to the NMDS ordinations; the significance of the fitted factors was estimated by using 999 permutations.
Normalisation of OTUs counts is recommended for further statistical processing52. The metagenomeSeq R package53 was used for data normalisation and further statistical analysis of differences in OTUs abundance. By using the fitZig function, a zero-inflated Gaussian mixture model, OTUs counts were normalised by calculating the scaling factors equal to the sum of counts. The parameters for the mixture model were estimated with an expectation-maximization algorithm, coupled with a moderated t statistic. Individual pig was used as a covariate in the analyses. Differences in OTUs threshold was fixed at a false discovery rate (FDR) value of 0.05. Finally, KO abundance obtained from PICRUSt was introduced into R using PhyloSeq and statistical differences were estimated using Deseq 254 using the Wald-test and a FDR threshold of 0.05. The relationship between histopathological lesions and abundance of bacteria in the ileum mucosa was explored by non-parametric Spearman’s rank correlation coefficient test implemented in Qiime.
Metabolites abundance were measured by the normalised area under the curve. For each metabolite, comparisons were made by the non-parametric Wilcoxon-test in R with a significant threshold of 0.05.
All procedures involving animals were approved by the institutional bioethical committee fo the University of Leon (license number ULE_003_2015) and performed according to European regulations regarding animal welfare and protection of animals used for experimental and other scientific purposes.
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We want to acknowledge the staff from the Genomics and Animal breeding group at the University of Córdoba for their technical support to carry out this study. This article is based upon work from COST Action FA1401 (PiGutNet), supported by COST (European Cooperation in Science and Technology. This work was supported by the Spanish Ministry of Economy and Competitiveness (AGL2014-54089-R/AGL2017-87415-R). HA was funded by the PiGutNet COST action (FA1401) for a Short-Term Scientific Mission at INRA’s GABI laboratory (Jouy-en-Josas, France). SZL is a postdoctoral researcher supported by the Postdoctoral Trainee Program of the Spanish Ministry of Economy and Competitiveness (FPDI-2013-15619). HA is a postdoctoral researcher supported by the Juan de la Cierva Postdoctoral Trainee Program of the Spanish Ministry of Economy and Competitiveness (FJCI-2014-22877).
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Pathobiont release from dysbiotic gut microbiota biofilms in intestinal inflammatory diseases: a role for iron?
Journal of Biomedical Science (2019)
Journal of Animal Science and Biotechnology (2019)