- Research article
- Open Access
Nature of bacterial colonization influences transcription of mucin genes in mice during the first week of life
© Bergström et al.; licensee BioMed Central Ltd. 2012
Received: 16 November 2011
Accepted: 12 July 2012
Published: 2 August 2012
Postnatal regulation of the small intestinal mucus layer is potentially important in the development of adult gut functionality. We hypothesized that the nature of bacterial colonization affects mucus gene regulation in early life.
We thus analyzed the influence of the presence of a conventional microbiota as well as two selected monocolonizing bacterial strains on the transcription of murine genes involved in mucus layer development during the first week of life.
Mouse pups (N = 8/group) from differently colonized dams: Germ-free (GF), conventional specific pathogen free (SPF), monocolonized with either Lactobacillus acidophilus NCFM (Lb) or Escherichia coli Nissle (Ec) were analyzed by qPCR on isolated ileal tissue sections from postnatal days 1 and 6 (PND1, PND6) after birth with respect to: (i) transcription of specific genes involved in mucus production (Muc1-4, Tff3) and (ii) amounts of 16S rRNA of Lactobacillus and E. coli. Quantification of 16S rRNA genes was performed to obtain a measure for amounts of colonized bacteria.
We found a microbiota-independent transcriptional increase of all five mucus genes from PND1 to PND6. Furthermore, the relative level of transcription of certain mucus genes on PND1 was increased by the presence of bacteria. This was observed for Tff3 in the SPF, Ec, and Lb groups; for Muc2 in SPF; and for Muc3 and Muc4 in Ec and Lb, respectively.
Detection of bacterial 16S rRNA genes levels above the qPCR detection level occurred only on PND6 and only for some of the colonized animals. On PND6, we found significantly lower levels of Muc1, Muc2 and Muc4 gene transcription for Lb animals with detectable Lactobacillus levels as compared to animals with Lactobacillus levels below the detection limit.
In summary, our data show that development of the expression of genes encoding secreted (Muc2/Tff3) and membrane-bound (Muc1/Muc3/Muc4) mucus regulatory proteins, respectively, is distinct and that the onset of this development may be accelerated by specific groups of bacteria present or absent at the mucosal site.
The interplay between the microbiota of the gut and the intestinal mucus layer in early life is important in the development of the epithelial barrier as part of the innate immune defense . The first weeks and months after birth are believed to be crucial for establishment of the gut microbiota and consequently for the health and integrity of the epithelium throughout life [2, 3]. In this period, a development regulated by endogenous factors such as hormones, in parallel with gene regulation caused by the microorganisms present in the gut, takes place [4, 5]. The presence and composition of the microbiota has been shown to be directly involved in the regulation of gene transcription in the intestinal epithelium, including the mucin genes, Muc1-4 and the trefoil factor Tff3[4, 6].
In the human intestines, MUC1-4 are the most prevalent  of the different mucin gene transcripts described to date [1, 7, 8]. In the gastrointestinal tract, specific mucins show coordinated expression and localization with the viscosity regulating trefoil factors (TFF’s), in particular TFF3 . Epithelial linings contain both membrane-bound (MUC1, MUC3, MUC4) and secreted gel-forming mucins (MUC2) expressing highly specific oligosaccharide side chains, which are important in relation to filtering the entry of various moieties e.g. bacteria and food to the underlying tissue. The membrane-bound mucins act as cell-surface receptors and sensors, mediating signals to trigger cell proliferation, apoptosis, differentiation and specific secretions, when relevant . The four human mucin genes (MUC1-4) all share a fairly high degree of sequence, distribution and functional homology to the mouse mucin genes Muc1-4[9–12].
As facultative anaerobes, lactobacilli and E. coli strains have been recognized as successful early life colonizers of the sterile gastro-intestinal tract [13, 14]. Strains of Lactobacillus acidophilus are known to stimulate transcription of mucin genes in vitro[15, 16]. Moreover administrations of probiotic lactobacilli and bifidobacteria have been shown to increase ileal gene and protein levels of Muc3 in adult rats  and cell cultures , respectively. Certain E. coli strains have been associated with increased production of MUC2 MUC3 and MUC4 in human ileal cells .
In order to elucidate the role of microbial colonization in the postnatal regulation of Muc1-4 and Tff3, we investigated the expression of these genes in mouse ileal segments isolated at the first day after birth (PND1) and six days after birth (PND6), respectively, from specific pathogen free, conventionally bred mice (SPF), mice monocolonized with either Lactobacillus acidophilus NCFM (Lb)  or E. coli Nissle (Ec) [20, 21], and from germ free (GF) mice [15, 22]. Specifically, samples were collected and analyzed at PND1 and PND6 to examine the immediate postnatal effects, which are relevant for immune system priming [22, 23]. Quantification of bacterial 16S rRNA gene levels was performed to obtain a measure of bacterial colonization levels in the different animal groups on PND1 and PND6.
Results and discussion
We introduced several new primers in this study, all scoring successfully on our validation criteria. LinRegPCR [24, 25] was utilized for qPCR analysis, as it enables individual PCR efficiencies to be calculated. The standard curve assumption, that in all samples the PCR efficiency/amplicon, based on one “representative” DNA sample is constant, is replaced by an assumption-free method based on linear regression in the exponential phase of the fluorescence of the actual individual samples analyzed . Further, by including in the subsequent calculation of average efficiency/amplicon, only successful samples within 5 % of the mean efficiency/amplicon, contributions from diverging samples to the final results are excluded.
We tested the choice of reference gene, but interestingly found no significant difference in the results between beta-actin [26, 27], neuroplastin (Genevestigator recommendation) nor the geometrical mean of them both.
Effect of time and bacterial colonization on regulation of Muc1-4 and Tff3 transcription
The higher level of Muc2 and Tff3 transcriptions at PND1, both encoding secreted proteins with goblet cell origin , indicates that the presence of bacteria affects gene transcription onset in these exocytotic cells. While both gene products play protective roles during gut inflammatory conditions, at sites of epithelial damage [18, 29–34] and during postnatal development [35, 36], Muc2, unlike Tff3, polymerizes into a protective gel-like structure . Based on the obtained results, it is however not possible to determine whether there is a connection between this difference in functionality and the corresponding gene regulation.
Previously, we demonstrated how microbiota affects ileal gene expression of a number of immune related genes (specific cytokines and chemokines) during the first week after birth . As seen for Muc2 in the present study, and also for a number of Toll-like receptor signaling pathway related genes such as Tlr2/4 Irak1 and the chemokine Cxcl2, encoding MIP-2, the presence of a full microbiota was required to influence gene expression on PND1, which was only to a limited degree affected by monocolonization with either Lactobacilli or E. coli.
Increased transcription of Muc3 and Muc4 on PND1 was observed in Ec and Lb pups, respectively, but not in SPF (Figure 1). Although specific probiotic bacteria, including Lactobacillus acidophilus NCFM , Lactobacillus rhamnosus, Bifidobacterium bifidum, Lactobacillus plantarum[16, 17] as well as two atypical, enteropathogenic E.coli strains , have previously been shown to stimulate mucin gene expression, this study is to our knowledge the first to address such effects at a very early stage of life. Muc1 transcription levels were in this study apparently not affected by the presence of bacteria.
Bacterial 16S rRNA abundance on PND1 and PND6
16S rRNA measured presence vs. absence of all 4 animal groups on each of days PND1 and PND6
It has been established by others that degradation of mucin in adult rats  as well as gene expression of Muc1-4 and Tff3 in six week old mice , is different when comparing GF and conventional animals. Clearly, gene regulation induced by the colonizing microbiota is a complex and continuous process occurring throughout the first weeks of life, and as a more stable and adult-like microbiota is probably not achieved until the end of weaning process at approximately 21 days after birth , the expression of the mucus regulating genes may change not only in newborn animals, but also later in life in response to periodic changes in the microbiota
In this manuscript, we show distinct differences between the expression patterns of secreted (Muc2/Tff3) and membrane-bound (Muc1/Muc3/Muc4) mucus-regulatory genes in the very first days after birth. Presence of a full microbiota (SPF) increased the relative level of transcription of Muc2 and Tff3, which implies the two corresponding secreted gene products, Muc2 and Tff3, to play protective roles in the postnatal intestinal layer development. The immediate activation of Muc2/Tff3 transcription may provide a coating of the new born ileal epithelial layer, allowing only passage of certain substances or organisms.
GF Swiss Webster mice and SPF mice, containing conventional microbiota, were purchased from Taconic (Lille Skensved, Denmark) and kept in GF isolators or under specific pathogen-free conditions, respectively . Fecal samples from GF mice, taken at sampling i.e. once a week, were cultivated on non-selective LB medium and under aerobic and anaerobic conditions to confirm sterility of isolators. For breeding, pairs of female mice were housed with one male until plugs were observed. Mono-colonization of pregnant mice with Ec and Lb was performed 7 days after mating by applying 5x108 CFU ml-1 in 0.5 ml PBS suspension orally using a pipette and 0.5 ml to the abdominal skin. Lb was grown anaerobically in de Man, Rogosa, and Sharpe broth (MRS, Merck, Darmstadt, Germany) and Ec aerobically in Luria-Bertani broth (LB, Merck) overnight at 37°C. The cultures were harvested, washed twice in sterile phosphate-buffered saline (PBS) (Lonza, Basel, Switzerland), re-suspended in 1/50 of the original culture volume and frozen at −80 °C until use. Prior to administering bacteria to the mice, Ec suspensions were diluted tenfold in PBS immediately to obtain 5x108 CFU ml-1. Lb suspensions were not diluted. Four litters spontaneously delivered from 4 different mothers in each group; SPF, GF, Lb and Ec, were used for the experiment. At post-natal days 1 and 6, the pups were put down and the distal ileum (segment from cecum and 3 cm up) was removed from the small intestine of two pups per litter and frozen in RNAlater (Qiagen, Hilden, Germany). No separation of mucosal from luminal content was performed.
The mouse experiment was performed under a license to Department of Microbiology, National Food Institute, from the Danish Council for Animal Experimentation.
Tissues were removed from RNAlater and homogenized by a rotor strator in RLT buffer (Qiagen). RNA from tissue homogenate was extracted using RNeasy Mini Kit from Qiagen following the supplier's protocol.
Primer design and validation
Primers used for qPCR
Modified from 
Modified from 
Modified from 
Lactobacillus 16S rRNA
E. coli 16S rRNA
Quantitative PCR (qPCR)
Isolated ileal RNA was reverse transcribed into cDNA using SuperScript® VILO™ cDNA Synthesis Kit from Invitrogen, Denmark. After verifying the quality of the cDNA by spectroscopy (A260/A280 = 1.8 ± 10 %) measured on a NanoDrop ND-1000 Spectrophotometer (Saveen Werner, Limhamn, Sweden), it was used as template in quantitative real-time PCR using the ABI prism 7900HT from Applied Biosystems. All cDNA concentrations were within the range of 90-100 ng μl-1. The amplification reactions were carried out in a total volume of 20 μl containing 10 μl master mix (2x PerfeCTaTM SYBR® Green SuperMix, ROX from Quanta Biosciences TM), 0.4 μl of each primer (10 μM), 2 μl template cDNA, and 7.2 μl nuclease-free water (Qiagen GmbH, Germany) purified for PCR. The amplification program consisted of one cycle of 50 °C for 2 min; one cycle of 95 °C for 10 min; 40 cycles of 95 °C for 15 s and 60 °C for 1 min; and finally one cycle of dissociation curve analysis for assessing the amplification products (95 °C for 15 s, 60 °C for 20s and increasing ramp rate by 2 % until 95 °C for 15 s). These conditions were selected based on preliminary qPCR experiments on target DNA with similar concentrations (100 ng μl-1). Samples of all amplification products were further subjected to gel electrophoresis in 2 % agarose, followed by ethidium bromide staining in order to verify amplicon sizes.
Three separate qPCR experiments on ileal cDNA were performed; 1) and 2) were separate replications of relative quantifications on mucus gene transcription (Muc1-4 and Tff3) with selected reference genes (see next paragraph) and 3) on presence or absence of specific bacterial 16S rRNA analysis (Lactobacillus, E.coli).
qPCR data analysis
All qPCR analysis was performed with the freely available LinRegPCR tool developed by Ruijter et al. [24, 25]. The raw fluorescence data were exported from the ABI prism 7900HT SDS-software, and the LinRegPCR program was used to estimate baselines and individual PCR efficiencies in order to calculate output as target starting concentration, expressed in arbitrary fluorescence units N0, for each PCR sample by the formula N0 = threshold / (EffmeanCt), where Effmean denotes the optimal PCR mean efficiency/amplicon, threshold the optimal “cutoff” in the exponential region and Ct is the number, where each PCR sample exceeds this threshold. Samples with no amplification, baseline error, too much noise or without plateau were automatically excluded by the LinRegPCR software. Subsequently, for each amplicon the average of all remaining, successful samples within 5 % of the mean value of all successful samples/amplicon were used in the calculation of Effmean for each amplicon. All N0-values were calculated as means of double qPCR determinations.
For relative quantification of mucus gene transcripts, two different eukaryotic reference genes were used namely beta-actin  and neuroplastin, the latter suggested by the Genevestigator software (https://www.genevestigator.com) [41, 42] based on microarray data on similar organism (M. musculus) and tissue (ileum). We used the geometric mean of the two reference genes as previously suggested . Normalization to relevant reference gene expression was then calculated according to the formula: Ra =Ratio = N0Sample/ N0Reference and averaged over the two qPCR experiments.
Unspecific amplification of 16S rRNA bacterial genes from GF mice was used to specify detection limits for specific amplifications (Lactobacillus, E .coli). Cutoffs for presence of either bacterium were defined by at least 5 Ct-values difference from the GF samples. No normalization to reference genes and thus relative quantification was used for the 16S analysis, since the purpose was only to determine presence vs. absence of detectable bacteria.
All statistics was performed with GraphPad Prism 5. One-way ANOVA followed by Dunnett’s post hoc test with GF as control group and Student’s t-test was used to compare mucus gene expression between the four animal groups and development from PND1 to PND6, respectively. P-values lower than p = 0.05 were considered statistically significant. Welch’s correction for unequal variances was applied, when necessary.
The work was supported by Globalization Funds obtained from the Technical University of Denmark, through The National Food Institute, and a post doc grant for Anders Bergström from The Danish Agency for Science, Technology and Innovation.
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