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. Author manuscript; available in PMC: 2015 Nov 2.
Published in final edited form as: Mamm Genome. 2015 Feb 27;26(0):222–234. doi: 10.1007/s00335-015-9560-4

Cystic fibrosis mouse model-dependent intestinal structure and gut microbiome

Mark Bazett 1, Lisa Honeyman 2, Anguel N Stefanov 3, Christopher E Pope 4, Lucas R Hoffman 5,6, Christina K Haston 7
PMCID: PMC4629800  NIHMSID: NIHMS732114  PMID: 25721416

Abstract

Mice with a null mutation in the cystic fibrosis transmembrane conductance regulator (Cftr) gene show intestinal structure alterations and bacterial overgrowth. To determine whether these changes are model-dependent and whether the intestinal microbiome is altered in cystic fibrosis (CF) mouse models, we characterized the ileal tissue and intestinal microbiome of mice with the clinically common ΔF508 Cftr mutation (FVB/N Cftrtm1Eur) and with Cftr null mutations (BALB/c Cftrtm1UNC and C57BL/6 Cftrtm1UNC). Intestinal disease in 12-week-old CF mice, relative to wild-type strain controls, was measured histologically. The microbiome was characterized by pyrosequencing of the V4–V6 region of the 16S rRNA gene and intestinal load was measured by RT-PCR of the 16S rRNA gene. The CF-associated increases in ileal crypt to villus axis distention, goblet cell hyperplasia, and muscularis externa thickness were more severe in the BALB/c and C57BL/6 Cftrtm1UNC mice than in the FVB/N Cftrtm1Eur mice. Intestinal bacterial load was significantly increased in all CF models, compared to levels in controls, and positively correlated with circular muscle thickness in CF, but not wild-type, mice. Microbiome profiling identified Bifidobacterium and groups of Lactobacillus to be of altered abundance in the CF mice but overall bacterial frequencies were not common to the three CF strains and were not correlative of major histological changes. In conclusion, intestinal structure alterations, bacterial overgrowth, and dysbiosis were each more severe in BALB/c and C57BL/6 Cftrtm1UNC mice than in the FVB/N Cftrtm1Eur mice. The intestinal microbiome differed among the three CF mouse models.

Introduction

Cystic fibrosis (CF) is an autosomal recessive disease caused by defects in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Although over 1500 different mutations in CFTR have been documented, a deletion of a phenylalanine at position 508 (ΔF508) accounts for 70 % of those found among people with CF (O'Sullivan and Freedman 2009). CF patients have well-described pathologies affecting the lung and pancreas, and can also develop intestinal disease which manifests as meconium ileus and distal intestinal obstruction syndrome in this population (van der Doef et al. 2011). Small intestinal bacterial overgrowth has been reported as a feature of clinical CF intestinal disease (Lisowska et al. 2009).

Intestinal phenotypes resembling meconium ileus (Snouwaert et al. 1992) and distal intestinal obstruction syndrome (Durie et al. 2004) develop in mice with a null mutation in Cftr (Cftrtm1Unc mice) and in the mice these traits are characterized by mucous build up and the presence of lethal intestinal plugs (Durie et al. 2004; Snouwaert et al. 1992). Histologically, Cftrtm1Unc mice, on either the C57BL/6 J (Durie et al. 2004; Kent et al. 1996) or BALB/ cJ (Bazett et al. 2011; Canale-Zambrano et al. 2010) genetic background, have intestinal goblet cell hyperplasia, and crypt dilation and elongation. Our studies of C57BL/J x BALBc/J F2 Cftrtm1Unc mice also demonstrated the intestinal submucosa to be thicker in the Cftr-deficient mice (Canale-Zambrano and Haston 2011). Finally, intestinal bacterial overgrowth is a feature of the Cftrtm1Unc model (Canale-Zambrano et al. 2010; Clarke et al. 2004; Norkina et al. 2004).

In addition to Cftrtm1Unc mice, cystic fibrosis has been modeled with FVB/N Cftrtm1Eur mice (van Doorninck et al. 1995) which carry the clinically common ΔF508 mutation. These mice express the mutant allele at the same level at which wild-type (WT) mice express the wild-type allele in assayed tissues including the intestine (French et al. 1996). This CF mouse model has been used to assay CFTR function in the lung (Gavina et al. 2013; Lubamba et al. 2009), salivary glands (Droebner and Sandner 2013) and intestine (Dekkers et al. 2013; Dhooghe et al. 2013) but the intestinal disease in these mice has not been quantified. An early report indicated Cftrtm1Eur mice to have an intestinal phenotype of goblet cell hyperplasia with limited crypt distention and intestinal obstructions (van Doorninck et al. 1995), at 5–7 weeks of age, but the extent of disease in adults, and whether Cftrtm1Eur mice also develop bacterial overgrowth is unknown.

The bacterial overgrowth phenotype is potentially of interest to the development of CF pathology in the intestine but clinical studies of this interaction are likely to be confounded by the prevalence of antibiotic treatment in the CF patient population. Specifically, non-CF studies have shown that the introduction of specific bacteria to mice can result in increased crypt depth (Preidis et al. 2012), and that gastroenterological patients with small intestinal bacterial overgrowth also have a decreased villus to crypt ratio (Lappinga et al. 2010) which is consistent with the CF intestinal change. High throughput microbiome sequencing has been applied to CF, most commonly of respiratory samples, and has shown there to be an effect of antibiotic treatment on the pulmonary microbiome (Zhao et al. 2012). The clinical CF intestinal microbiome has not been characterized, but limited investigation of fecal samples from CF patients (Duytschaever et al. 2011, 2013; Hoffman et al. 2014; Lynch et al. 2013; Scanlan et al. 2012) has suggested an intestinal dysbiosis exists, and features alterations in the abundance of individual bacterial groups including Bifidobacterium (Duytschaever et al. 2013; Scanlan et al. 2012) and Escherichia coli (Hoffman et al. 2014), which may be associated with disease (Hoffman et al. 2014). An evaluation of the intestinal microbiome of the differing CF mouse models has not been completed.

CF mouse models thus recapitulate important aspects of the gastrointestinal pathology observed in patients and can be studied in the absence of antibiotics. The current study was undertaken to determine whether differences exist in the intestinal disease phenotype among three different CF mouse models- BALB/c Cftrtm1Unc, C57BL/6 Cftrtm1Unc and FVB/N Cftrtm1Eur mice, and, if so, to investigate whether these changes are associated with specific constituents of the intestinal microbiome.

Materials and methods

Mice

Cftr+/tm1Eur heterozygous mice (van Doorninck et al. 1995), which had been backcrossed for 13 generations to the FVB/N strain, were obtained from Dr. B. Scholte of the Erasmus University Medical Centre Rotterdam, the Netherlands. These mice were bred together to produce Cftrtm1Eur mice and wild-type Cftr +/+ controls and were genotyped as previously described (Paradis et al. 2010), Cftr+/tm1UNC heterozygous mice on either C57BL/6 or BALB/c background were used to generate knockout (Cftrtm1UNC) mice as previously described (Bazett et al. 2012; Haston et al. 2006). All mice were bred and maintained at the Meakins-Christie Laboratories of McGill University. To circumvent possible premature death due to intestinal disease, all mice (CF and WT) were fed standard chow and received PEGLYTE® (17.8 mmol/L polyethylene glycol, Pharma Science, DIN:00777838) in their drinking water as described previously (Bazett et al. 2012; Clarke et al. 1996; Haston et al. 2006; Paradis et al. 2010). Mice were weaned at 3 weeks of age and grouped in ventilated cages of 1–3 mice based on their sex. CF and WT mice were co-housed. At 12 weeks of age the mice were weighed and euthanized with a lethal dose of anesthetic. At dissection, the entire small intestine was removed, flushed with phosphate buffered saline containing a mucolytic agent (10 mM dithiothreitol), the contents collected, and the tissue was fixed in formalin before being submitted for standard histological processing. All animal procedures were performed in accordance with McGill University guidelines set by the Canadian Council on Animal Care.

Histology

Paraffin-embedded Sects. (5 lm) were stained with hematoxylin and eosin for evaluation of general histological structure. The crypt to villus axis (CVA) height was measured, from 25 complete and intact CVAs within each ileum, using image analysis of the histological sections (Olympus BX51, Image-Pro Plus 5.1, Media Cybernetics) as in previous studies (Bazett et al. 2011; Canale-Zambrano et al. 2010; Canale-Zambrano et al. 2007). Separate measurements of villus height and crypt depth were also taken. The number of goblet cells was counted for an average of 20–25 CVAs per section from Periodic acid-Schiff/Alcian blue stained sections. For muscle thickness, both the circular and longitudinal muscle layers of the muscularis externa were measured at 50 regular intervals throughout the section, and nuclei per mm2 were enumerated in ten regions located throughout the section. All sections were scored by an observer blinded to mouse strain and Cftr genotype.

Bacterial load measurement

DNA for bacterial load quantification was extracted from 200 mg of the centrifuged small intestinal contents using a Stool DNA Kit (Qiagen, #51504). The bacterial load was quantified by real-time PCR amplification of the 16S (small ribosomal subunit) gene as previously described (Canale-Zambrano et al. 2010; Ott et al. 2004). A standard curve of the number of 16S rRNA gene copies present was created by extracting and quantifying DNA from a known number of E. coli D5Hα, which has seven 16S rRNA copies per bacteria.

Bacterial DNA extraction and PCR amplification of the 16S rRNA gene

DNA was isolated from small intestinal contents by repeated bead beating followed by a column extraction as previously described (Hoffman et al. 2014; Yu and Morrison 2004). FLX Pyrosequencing of the V4–V6 variable region of the bacterial 16S rRNA gene (Primers: 530-F: GTGCCAGC MGCNGCGG and 1100-R: GGGTTNCGNTCGTTG) was completed by MrDNA as previously described (Dowd et al. 2008). 10,000 reads were sequenced per sample and a total of 548,576 reads were collected. Raw sequences were analyzed using Mothur (Schloss et al. 2009) version 1.28, a publicly available online computational microbiomics resource which has previously been used to analyze the microbiome in CF patients (Zhao et al. 2012) and mice (Russell et al. 2012), with a pipeline similar to that described previously (Schloss et al. 2011). Raw sequences were cleaned using the Mothur implementation of PyroNoise (Quince et al. 2009) and analyzed sequences were retained based on read lengths of >200 bp, fewer than two barcode mismatches, fewer than three primer mismatches and no homopolymer stretches >8 nucleotides. Sequences were aligned using the SILVA reference database (Pruesse et al. 2007) and unique sequences were defined as having no more than two bases apart. Chimeras were removed using the Mothur implementation of UChime (Edgar et al. 2011). The resulting 355,187 sequences were assigned to operational taxonomic units (OTUs) based on 97 % sequence similarity with the most abundant read serving as the representative read. Taxonomic assignment of reads was completed with the Ribosomal Database Project classifier (Wang et al. 2007). The sequencing data was rarefied to 5457 sequences per sample.

Statistical analysis

Weight, histological and bacterial load phenotypes are expressed as the mean ± SD and differences in phenotype between mice grouped by Cftr genotype were determined using Student's t test. To assess the significance of differences among models, ANOVA was used with Tukey's post hoc test. Correlations between bacterial load and histological features were defined with Pearson's correlation coefficient.

Phylogenetic trees were constructed using Clearcut (Evans et al. 2006) via Mothur. Alpha diversity, Chao1 richness estimator, Simpson Evenness and Shannon's Diversity were calculated in Mothur (Schloss et al. 2009). Correlations between these population measures and phenotypes of histological features, bacterial load and body weight were defined with Pearson's correlation coefficient. To investigate the compositional similarity between samples, Bray-Curtis dissimilarities were calculated for each model, data were visualized using two dimensional non-metric dimensional scaling (NMDS) ordination, and significant differences between groups were determined by Adonis, using vegan package 2.0–10 in R (http://CRAN.R-project.org/package=vegan). Differences in abundance of OTUs between mice grouped by Cftr genotype were determined by the Mothur implementation of the Metastats program (White et al. 2009). The abundance of OTUs which had reads in more than two CF mice was correlated with histological features and with body weight. Correlations were completed on the CF mice with all three strains considered together and were evaluated using Pearson's correlation coefficient with the Bonferroni-corrected P < 0.0011 taken as the level of significance.

Results

Survival and body weight phenotype

A population of mice was bred from a cross of FVB/N Cftr+/tm1Eur progenitors and of the mice produced 28 % were homozygous for the ΔF508-Cftr allele at weaning, which is consistent with expected Mendelian ratios. Greater than 89 % of Cftrtm1Eur mice survived to the experimental age of 12 weeks and no intestinal blockages were apparent at necropsy. As seen in Fig. 1a, the average weight of the Cftrtm1Eur mice at 12 weeks of age was not significantly different from that of wild-type controls (P = 0.11), in agreement with previous data of this strain (Bazett and Haston 2014; Paradis et al. 2010). This is in contrast to Cftrtm1UNC mice, also bred from heterozygous progenitors, which had less than the expected 25 % homozygous Cftrtm1UNC mouse production rates at weaning (BALB/c = 9.2 %, C57BL/6 = 6.9 %). Cftrtm1UNC mice were significantly smaller than controls for BALB/c (P = 0.0008), and C57BL/6 (P = 0.04) strains, in agreement with previous reports (Bazett et al. 2011; Canale-Zambrano et al. 2010; Haston et al. 2002; Norkina et al. 2004). There was a significant difference in weight among the strains of CF mice with the FVB/N Cftrtm1Eur mice weighing more than the BALB/c Cftrtm1UNC mice. The strain-dependent difference in body weight among CF mice was not evident within the wild-type mice; Fig. 1a.

Fig. 1.

Fig. 1

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Body weight and ileal goblet cell counts of FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and WT control mice at 12 weeks of age. a Weights of mice at sacrifice. b Number of goblet cells per crypt to villus axis (CVA), (villus open square; crypt filled square). Data are presented as the mean ± SD (n = 5–13 mice/group). Horizontal bars indicate groups compared by ANOVA (NS not significant). *Indicates a significant difference, P < 0.05, by Tukey's post hoc test. # Indicates a significant difference, P < 0.05, between CF and WT mice within each strain by Student's t test. Representative ileal sections of c a wild-type control mouse from each strain, and d FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC and C57BL/6 Cftrtm1UNC mice featuring hyperplasia of goblet cells (arrows). Periodic acid-Schiff//Alcian Blue stain, magnification ×400

Ileal histology

To determine whether adult FVB/N mice with the ΔF508 mutation in Cftr presented with intestinal disease, and if so, how this intestinal disease related to that of Cftrtm1UNC mice, measures of crypt-villus axis (CVA) height, muscularis externa thickness, and goblet cell count were made in ileal tissue procured from FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and wild-type control mice. As shown in Fig. 1b–d, the ilea of each of the three CF mouse models contained significantly more goblet cells per CVA than those of wild-type control mice (P = 0.001 for FVB/N; P = 8.4 × 10−6 for BALB/c, P = 6.4 × 10−5 for C57BL/6). Among the CF models, there was a significant difference in goblet cell hyperplasia, with FVB/N Cftrtm1Eur mice having fewer goblet cells per CVA than the BALB/c Cftrtm1UNC mice. This trait did not vary by strain in wild-type mice, as shown in Fig. 1b.

Secondly, the average CVA height in all three CF mouse models exceeded that of wild-type mice (P = 0.004 for FVB/N; P = 3.6 × 10−6 for BALB/c, P = 6.4 × 10−6 for C57BL/6; Fig. 2a, b). The CVA height did not differ by strain among wild-type mice, but in the CF mice the CVA distention of FVB/N Cftrtm1Eur mice was significantly reduced compared to that of the BALB/c Cftrtm1UNC and C57BL/6 Cftrtm1UNC mice; Fig. 2c.

Fig. 2.

Fig. 2

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Crypt to villus axis (CVA) height and muscularis externa thickness and cell density of the ileal tissue of FVB/N Cftrtm1Eur, BALB/cCftrtm1UNC, C57BL/6 Cftrtm1UNC, and WT control mice at 12 weeks of age. Representative ileal sections of a a wild-type control mouse from each strain, and b FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC and C57BL/6 Cftrtm1UNC mice showing distended CVA and increased muscle thickness. Hematoxylin and Eosin stain, magnification ×200. LM longitudinal muscle, CM circular muscle. c CVA height, (villus open square; crypt filled square) was measured by image analysis of histological sections for 25 ileal CVAs per mouse. d Muscle layer thickness was measured by image analysis of ileal histological sections (longitudinal muscle filled square; circular muscle open square) LM longitudinal muscle, CM circular muscle. e Number of nuclei per unit area (mm2) of muscularis externa. Data are presented as the mean ± SD (n = 5–13 mice/group); Horizontal bars indicate groups compared by ANOVA (NS not significant). *Indicates a significant difference, P < 0.05, by Tukey's post hoc test. # Indicates a significant difference, P < 0.05, between CF and WT mice within each strain by Student's t test

Finally, to investigate whether the ΔF508 mutation in Cftr caused an increase in the muscularis externa layer of the ileum, and how this compared to the null mutation models of Cftr, measurements of the muscle layers in the ileal tissue were completed in these mice. As shown in Fig. 2, both the circular and longitudinal muscle layers of the muscularis externa in the ileum were significantly thicker in the FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC and C57BL/6 Cftrtm1UNC mice compared to strain controls (P = 0.005 for FVB/N; P = 2.2 × 10−7 for BALB/c, P = 2.8 × 10−7 for C57BL/6). Among strains, there was no difference in total muscle thickness for the wild-type mice, but there was a significant difference in this trait for CF mouse models (P = 1.5 × 10−7) wherein the total muscle layer thickness, circular muscle thickness, and longitudinal muscle thickness were each significantly reduced in the FVB/N ΔF508 mice compared to the Cftrtm1UNC models; Fig. 2d. Finally, tissue from all three CF mouse models had significantly fewer nuclei per mm2 of muscularis externa compared to controls, indicating that hypertrophy of smooth muscle cells contributed to the increased muscle thickness; Fig. 2e.

Bacterial load quantification

To determine whether the CF mouse models presented with similar increases in bacterial load, the intestinal contents from FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and wild-type control mice were evaluated with quantitative real time RT-PCR. As shown in Fig. 3a, all three CF mouse models had significantly increased bacterial density compared to the levels in wild-type strain controls (P = 0.044 for FVB/N; P = 0.006 for BALB/c, P = 0.018 for C57BL/6). While the bacterial load was similar in all strains of wild-type mice, there was a significant difference by strain in the CF mice, with bacterial loads in C57BL/6 Cftrtm1UNC mice significantly exceeding those of FVB/N Cftrtm1Eur mice. The bacterial load of BALB/c Cftrtm1UNC mice was not significantly different from that of either of FVB/N Cftrtm1Eur mice or C57BL/6 Cftrtm1UNC mice.

Fig. 3.

Fig. 3

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Small intestinal bacterial load of FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and WT control mice at 12 weeks of age and correlation to circular muscle thickness. a Bacterial load was measured using quantitative RT-PCR of the 16S rRNA of DNA isolated from small intestinal contents. Average ± SD is shown (n = 7–14 mice/group). Horizontal bars indicate groups compared by ANOVA (NS not significant). *Indicates a significant difference, P < 0.05, by Tukey's post hoc test. # Indicates a significant difference, P < 0.05, between CF and WT mice within each strain by Student's t test. Correlation between bacterial load and circular muscle thickness in b CF mice (n = 8–13 per strain) and c WT mice (n = 7–13 per strain)

To determine whether bacterial load was related to extent of histological disease, correlation analyses were performed. Bacterial load was significantly correlated with circular muscle thickness (r = 0.36; P = 0.04), in CF, but not WT, mice as illustrated in Fig. 3b, c. There was also a suggestive, but non-significant, correlation between bacterial load and CVA height in CF mice (r = 0.31; P = 0.09, data not shown). Neither goblet cell count per CVA nor body weight of CF mice correlated significantly with bacterial load (P > 0.22, data not shown).

Intestinal microbiome of CF mice

To investigate whether the bacterial microbiome within the small intestine differed among mice grouped by Cftr genotype within each strain, DNA extracted from intestinal content samples was evaluated by 454 pyrosequencing of the V4–V6 region of the bacterial 16S rRNA gene.

The effect of a Cftr mutation on the overall compositional similarity for each strain was investigated using Bray-Curtis dissimilarity and is presented in Fig. 4a–c with two dimensional non-metric multidimensional scaling (NMDS). As seen in this figure, samples from FVB/N Cftrtm1Eur mice clustered with those from FVB/N wild-type mice (Adonis test, P = 0.20) as did samples from BALB/c Cftrtm1UNC with their in strain wild-type mice (Adonis test, P = 0.14). C57BL/6 Cftrtm1UNC derived samples clustered separately from C57BL/6 wild-type-derived samples (Adonis test P = 0.002).

Fig. 4.

Fig. 4

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Small intestinal microbiome community metrics for FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and WT control mice. Two dimensional non-metric multidimensional scaling (NMDS) of the Bray-Curtis dissimilarity between samples for a FVB/N Cftrtm1Eur mice, b BALB/c Cftrtm1UNC mice, c C57BL/6 Cftrtm1UNC mice, and respective wild-type mice. d Richness was measured using the Chao 1 estimator. e Evenness defined by Simpson's Evenness. f Diversity, measured with Shannon's Diversity Index. Data are presented as mean ± SD (n = 4–9 per group). Horizontal bars indicate groups compared by ANOVA (NS not significant). *Indicates a significant difference, P < 0.05, by Tukey's post hoc test. # Indicates a significant difference, P < 0.05, between CF and WT mice within each strain by Student's t test

Next, we determined whether there were community structure differences in the intestinal microbiome either between each line of CF mice and respective controls, or among the CF models. Richness, which represents the number of microbial taxa in a sample, was calculated with the Chao 1 estimator. This parameter was decreased (P = 0.06) in samples from BALB/c Cftrtm1UNC mice, but not in FVB/N Cftrtm1Eur (P = 0.60) or C57BL/6 Cftrtm1UNC (P = 0.41) mice, when compared to in strain controls, as shown in Fig. 4d. Further, there was a significant difference in the Chao 1 estimates among the CF models, which was not evident within the wild-type mice, as the FVB/N Cftrtm1Eur mice were estimated to have greater richness than the BALB/c Cftrtm1UNC mice. Community evenness, or the relative distribution of taxa within the samples, was evaluated with Simpsons Evenness Index. As shown in Fig. 4e, community evenness was significantly increased compared to controls in samples from BALB/c Cftrtm1UNC (P = 0.005) and C57BL/6 Cftrtm1UNC mice (P = 0.0001) but not from FVB/N Cftrtm1Eur mice (P = 0.61). Variability in evenness among CF mouse strains, but not wild-type mice, was also evident, as the FVB/N Cftrtm1Eur mice differed from the BALB/c and C57BL/6 Cftrtm1UNC mice for this parameter. Diversity, a combination of the richness and evenness of a population, which was measured with Shannon's index, was higher (P = 0.06), in samples from C57BL/6 Cftrtm1UNC mice relative to wild-type levels. No differences in diversity were evident for comparisons between any of the remaining wild-type or CF mouse strains, as illustrated in Fig. 4f.

To determine whether any of the microbiome community measures was related to extent of histological disease, body weight, or to bacterial load, correlation analyses were performed. The histological features of CVA height (r = 0.60; P = 0.008), goblet cells/CVA (r = 0.57; P = 0.014), circular muscle thickness (r = 0.65; P = 0.003), longitudinal muscle thickness (r = 0.55; P = 0.018), circular muscle cell density (r = −0.70; P = 0.001), and longitudinal muscle cell density (r = −0.54; P = 0.018) were each correlated with Simpson's evenness index in CF, but not WT, mice as shown in Supplemental Fig. 1. Similarly, the richness measure (Chao1) was suggestively to significantly correlated with intestinal disease in CF mice, as illustrated in Supplemental Fig. 2, while not correlated in WT mice, with the possible exception of Chao 1 estimates correlated to goblet cells/CVA (r = 0.51; P = 0.09) in intestines of WT mice. Shannon's Diversity measures were not significantly correlated with the histological features in CF or WT mice (P > 0.19), data not shown, but were correlated (r = 0.51; P = 0.09) to bacterial load in CF (r = 0.67; P > 0.009), but not WT mice (P = 0.24), data not shown. None of the microbiome community measures was related to body weight in either of CF (P > 0.33), or WT mice (P > 0.17), data not shown.

Regarding the microbiome composition, for both the CF and wild-type mice of each of the three strains, the major phyla present were Firmicutes, Actinobacteria and Proteobacteria (Fig. 5), in agreement with the expected microbiome in mouse intestines (Hildebrand et al. 2013; Ivanov et al. 2009; O'Connor et al. 2014; Rehman et al. 2011; Russell et al. 2012). At the phylum level C57BL/6 Cftrtm1UNC mice had a significantly decreased abundance of Firmicutes (P = 0.02) and an increased abundance of Actinobacteria (P = 0.003), compared to levels in C57BL/6 WT mice. While similar trends in those two phyla were apparent in the other models, BALB/c Cftrtm1UNC and FVB/N Cftrtm1Eur mice did not have significantly altered abundances of specific bacteria at the phylum level when compared to wild-type mice.

Fig. 5.

Fig. 5

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Small intestinal microbiome community composition of FVB/N Cftrtm1Eur, BALB/c Cftrtm1UNC, C57BL/6 Cftrtm1UNC, and wild-type strain control mice at 12 weeks of age. a Phylum level classification. Firmicutes were significantly decreased (P = 0.02) and Actinobacteria (P = 0.003) were significantly increased in C57BL/6 Cftrtm1UNC mice compared to C57BL/6 WT mice. No other significant differences in bacterial abundance at the genus level, between CF mice and WT in strain controls, were detected. The group “other” contains the phylum Tm7, Tenericutes, Fusobacteria and unclassified bacteria. b 16S rRNA gene frequencies of the most abundant operational taxonomic unit (OTU) classified to the closest related taxon. Classifications: o order, f family, g genus

Further, to investigate whether specific taxa within the phyla were affected by the Cftr deficiency, the 16S rRNA gene reads were mapped into operational taxonomic units (OTUs). As shown in Fig. 5b and Table 1, OTUs which were largely specific to each model differed in abundance between samples from CF and wild-type mice of each strain. The relative abundance of an OTU corresponding to Bifidobacterium was the only bacterial group increased in CF mice of all three strains (FVB/N, P = 0.04; BALB/c, P = 0.07; C57BL/6, P = 0.002) compared to wild-type levels. In FVB/N Cftrtm1Eur mice, the other major microbiome difference was increased levels of an OTU corresponding to a group of Lactobacillus, compared to levels in FVB/N wild-type mice. In the BALB/c strain, two distinct OTUs that both corresponded to Lactobacillus were altered in abundance between Cftrtm1UNC and wild-type mice. In C57BL/6 mice, OTUs for Lactobacillus and Erysipelotrichaceae, were of altered abundance in mice grouped by Cftrtm1UNC genotype.

Table 1.

Operational taxonomic units (OTUs) differing in intestinal abundance between CF and WT mice by nearest classification

Group Nearest classification FVB/N WT (%) FVB/N CF (%) P value BALB/c WT (%) BALB/c CF (%) P value C57BL/6 WT (%) C57BL/6 CF (%) P value
OTU1 Lactobacillus 27.3 ± 6.5 47.8 ± 7.0 0.02 89.9 ± 11.5 24.6 ± 8.4 0.01 10.1 ± 1.5 25.8 ± 5.0 0.008
OTU2 Erysipelotrichaceae 13.9 ± 11.3 0.18 ± 0.15 0.20 6.0 ± 5.8 14.1 ± 8.3 0.64 67.3 ± 6.6 32.2 ± 4.4 0.0009
OTU3 Lactobacillus 26.7 ± 9.0 15.4 ± 4.1 0.23 6.8 ± 3.3 29.2 ± 9.9 0.03 0.51 ± 1.5 6.00 ± 1.91 0.009
OTU6 Bifidobacterium 1.0 ± 0.9 5.6 ± 2.3 0.04 0 0.8 ± 0.4 0.07 2.3 ± 0.8 8.0 ± 1.2 0.002
OTU14 Anaerostipes 1.8 ± 1.1 0.7 ± 0.2 0.57 0.03 ± 0.03 2.0 ± 1.1 0.04 0.38 ± 0.05 0.31 ± 0.09 0.64
OTU21 Streptococcus 0.23 ± 0.16 0.21 ± 0.16 0.95 0.53 ± 0.23 0.05 ± 0.02 0.03 0.055 ± 0.037 0.096 ± 0.040 0.58
OTU29 Clostridium_X1 0.007 ± 0.004 0.160 ± 0.062 0.01 0.03 ± 0.03 0.03 ± 0.02 0.90 0.018 ± 0.013 0.047 ± 0.019 0.24
OTU31 Gemella 0 0 N/A 0.43 ± 0.15 0.03 ± 0.01 0.01 0.018 ± 0.013 0.0041 ± 0.0041 0.37
OTU35 Erysipelotrichaceae 0.037 ± 0.037 0 0.35 0.009 ± 0.009 0.03 ± 0.03 0.64 0.142 ± 0.045 0.043 ± 0.008 0.04
OTU38 Coriobacteriaceae 0.033 ± 0.020 0.032 ± 0.036 0.98 0.03 ± 0.03 0.03 ± 0.02 0.93 0.087 ± 0.029 0.008 ± 0.008 0.02
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Abundance in % ±SD

Bold values indicate P < 0.05

We analyzed whether the intestinal abundance of specific bacteria was correlative of the CF traits. In this analysis, the correlation for each OTU detected in more than two CF mice was completed, using data from the CF mice of all three strains considered together. This investigation of OTU abundance with each of the histological features, and with the phenotype of body weight, revealed no significant correlations after correction for multiple testing between OTU frequencies and traits of CVA distension, goblet cell hyperplasia, and muscle thickness in CF mice (P > 0.002, data not shown). A significant correlation between the number of nuclei per mm2 in the circular muscle layer and OTU17, which corresponds to an unclassified Porphyromonadaceae (r = 0.82; P < 0.0001) was detected.

Discussion

Our investigation of intestinal disease in CF mice revealed all three models to develop bacterial overgrowth with histological features of crypt to villus axis distention, goblet cell hyperplasia, and increased muscle thickness. Secondly these traits, although significantly increased compared to measures from wild type, were less severe in adult FVB/N Cftrtm1Eur mice relative to BALB or C57BL/6 J Cftrtm1UNC mice. Finally, microbiome profiling identified CF intestinal dysbiosis to be model specific in mice.

CF related intestinal structure changes were evident in all models, and these phenotypes were reduced in magnitude in the FVB/N ΔF508 mice. Indeed, the extent of CVA distention and goblet cell hyperplasia reported here agree well with prior findings for BALB/c (Bazett et al. 2011; Canale-Zambrano et al. 2010) and C57BL/6 (Durie et al. 2004; Kent et al. 1996) Cftrtm1UNC mice and the trait of increased intestinal muscle thickness, originally reported in BALB x C57BL/6 J F2 Cftrtm1UNC mice (Canale-Zambrano and Haston 2011), was also evident in the BALB/c and C57BL/6 Cftrtm1UNC models. The findings of increased longitudinal and circular muscle thickness in the intestines of C57BL/6 Cftrtm1UNC mice may contradict those of prior reports (De Lisle et al. 2010; Risse et al. 2012) but as in the latter work normalized area of alpha smooth muscle staining was reported, differences in methods of histological assessment may have contributed to the discrepancy. The intestinal disease measured here had not been comprehensively studied in adult FVB/N ΔF508 mice although indications of goblet cell hyperplasia have been reported (van Doorninck et al. 1995; Wilke et al. 2011) without “dramatic” CVA distention (van Doorninck et al. 1995). The cause of CVA distention in CF mice is unknown but it has been proposed to depend on increased proliferation in the intestinal crypts (Canale-Zambrano and Haston 2011; Gallagher and Gottlieb 2001) which, in turn, may be related to their alkaline environment (Liu et al. 2012; Putney and Barber 2003). The milder CF phenotype of FVB/N ΔF508 mice extended to the microbiome, in terms of population characteristics, where standard metrics for these mice did not differ from those of wild-type mice in contrast to samples from the Cftrtm1UNC models. Given how the models were constructed, however, we cannot discern whether the reduced phenotype of FVB/N ΔF508 mice, compared to the BALB and C57BL/6 J Cftrtm1UNC mice, is the influence of the Cftr mutation (ΔF508 compared to Cftr null) or of genetic background (FVB/N, BALB, C57BL/6 J) which itself is known to affect both CF traits (Haston et al. 2002), and microbiome composition (Campbell et al. 2012; Hildebrand et al. 2013; O'Connor et al. 2014).

We identified intestinal bacterial overgrowth to be a feature of the Cftrtm1Eur model, as it is in Cftrtm1UNC mice, and for the circular muscle layer of the intestine to be increased with greater bacterial load in CF mice. The correlation of muscle layer thickness on bacteria may indicate this intestinal phenotype to occur as an adaptive response in CF mice (Barbara et al. 2005). Supporting the potential of an adaptive response wherein muscle layer thickness increases with intestinal bacterial load, parasitic infection of the small intestine of rats has been shown to induce hyperplasia and hypertrophy of intestinal circular muscle (Blennerhassett et al. 1992). Alternatively, as experimentally induced intestinal obstruction is associated with an increased circular muscle layer (Zhao et al. 2010), the correlation of load and muscle thickness in CF mice may indicate these traits to be related to developing intestinal obstruction.

The observations of altered smooth muscle thickness, goblet cells, and small bowel bacterial content in the intestines of these mouse models support observations made in people with CF. For example, people with CF tend to have small bowel bacterial overgrowth (Fridge et al. 2007) as well as an abundance of viscid mucous material in the intestinal lumen (Kreda et al. 2012). De Lisle et al. (2010) hypothesized that enteric microbiota impact smooth muscle activity and intestinal transit time through a prostaglandin-dependent mechanism, a pathway which could have contributed to the correlation we observed between muscle thickness and small intestinal bacterial load. Together, these results support close relationships between intestinal mucus secretion, dysbiosis, and dysmotility, indicating that treatments that address one of these abnormalities (e.g., laxatives, antibiotics, and pro kinetic agents, respectively) could positively impact the others and possibly improve overall intestinal function.

In each of the three CF models studied here, the relative abundance of specific CF microbiome constituents was uniquely changed compared to those of wild-type mice. Such variability has also been recorded in CF children (Madan et al. 2012) and CF ferrets (Sun et al. 2014a, b), where intestinal samples from each of studied subjects had a largely unique microbiome profile. This finding may suggest that a dysfunctional or deficient Cftr creates an intestinal environment which includes lower luminal pH (De Lisle et al. 2001), increased transit time (De Lisle 2007), increased mucus production (Malmberg et al. 2006) and abnormal paneth cell dissolution (Clarke et al. 2004) that is permissive for dysbiosis, but does not create a CF specific dysbiosis. The existence of strain-dependent profiles is also likely the reason we were unable to identify specific microbiome constituents which correlated with histological features of intestinal disease in this panel of mice. The intervention used to reduce the incidence of lethal intestinal plugs in the mice, the laxative PEGLYTE, may also have affected the microbiome data observed in CF and WT mice (van der Wulp et al. 2013). Finally, although work to document the CF intestinal and pulmonary microbiomes is ongoing (O'Sullivan and Freedman 2009; Sun et al. 2014a; Zhao et al. 2012, Madan et al. 2012), to date increased E. coli levels in fecal samples from CF children (Hoffman et al. 2014) and for the lung, CF-associated bacteria including Pseudomonas aeruginosa and Staphylococcus aureus (Goddard et al. 2012), as well as Streptococcus and Prevotella (Filkins et al. 2012) have been reported, these bacteria were not prominent in the samples from CF mice studied here. The lack of commonality is likely due to known microbiome variation by tissue sample site (Costello et al. 2009; Human Microbiome Project C 2012). The increase in Bifidobacterium evident in CF mice may have clinical relevance as it has also been reported as a significant component of the fecal microbiome in CF children (Madan et al. 2012).

In conclusion, mice deficient in Cftr exhibited intestinal structure abnormalities and bacterial overgrowth which were of reduced magnitude in FVB/N Cftrtm1Eur mice. Further, in CF mice bacterial overgrowth correlated with the increased circular muscle thickness in the intestine. Our data also support the hypothesis that intestinal microbial dysbiosis is prevalent in CF, and we specifically showed the intestinal microbiome in CF mice to be model-dependent.

Supplementary Material

Supplement

Acknowledgments

This work was supported by Cystic Fibrosis Canada and the National Institutes of Health (P30 DK089507 and K02 HL105543). Maintenance of the Cftrtm1Eur mouse colony at Erasmus MC was supported by the EUROCAFECF EU concerted action program and the Dutch CF Foundation (NCFS).

Footnotes

Electronic supplementary material The online version of this article (doi:10.1007/s00335-015-9560-4) contains supplementary material, which is available to authorized users.

Disclosures No conflicts to disclose.

Contributor Information

Mark Bazett, Meakins-Christie Laboratories, Departments of Medicine and Human Genetics, McGill University, 3626 St. Urbain, Montreal, QC H2X 2P2, Canada.

Lisa Honeyman, Meakins-Christie Laboratories, Departments of Medicine and Human Genetics, McGill University, 3626 St. Urbain, Montreal, QC H2X 2P2, Canada.

Anguel N. Stefanov, Meakins-Christie Laboratories, Departments of Medicine and Human Genetics, McGill University, 3626 St. Urbain, Montreal, QC H2X 2P2, Canada

Christopher E. Pope, Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA

Lucas R. Hoffman, Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA Department of Microbiology, University of Washington School of Medicine, Seattle, WA, USA.

Christina K. Haston, Meakins-Christie Laboratories, Departments of Medicine and Human Genetics, McGill University, 3626 St. Urbain, Montreal, QC H2X 2P2, Canada

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