- Research article
- Open Access
Presence of intestinal Mycobacterium avium subspecies paratuberculosis(MAP) DNA is not associated with altered MMP expression in ulcerative colitis
BMC Gastroenterology volume 11, Article number: 34 (2011)
Mycobacterium avium subspecies paratuberculosis (MAP) is suspected to be a causative agent in human Crohn's disease (CD). Recent evidence suggests that pathogenic mycobacteria and MAP can induce the expression of Matrix Metalloproteinases (MMP), which are the main proteases in the pathogenesis of mucosal ulcerations in inflammatory bowel disease (IBD). Within this study we assessed the prevalence of intestinal MAP specific DNA in patients with Crohn's disease, ulcerative colitis (UC), and healthy controls. We further analysed regulation patterns of MMPs in mucosal tissues of UC patients with and without intestinal MAP DNA detection.
Colonic biopsy samples were obtained from 63 Norwegian and German IBD patients and 21 healthy controls. RNA was quantified by quantitative real-time polymerase chain reaction (PCR) to study MMP gene expression in both pathological and healthy mucosal specimens. The presence of MAP DNA in colonic mucosa was examined using MAP specific PCR.
MAP DNA was detected in 20% of UC patients and 33% of healthy controls but only in 7% of patients with CD. UC patients treated with corticosteroids exhibited a significantly increased frequency of intestinal MAP DNA compared to those not receiving corticosteroids. Expression of MMP-1, -2, -7, -9, -13, -19, -28 and TNF-α did not differ between UC patients with presence of intestinal MAP DNA compared to those without. MMP-2, MMP-9 and MMP-13 were significantly decreased in UC patients receiving corticosteroids.
The presence of intestinal MAP specific DNA is not associated with altered MMP expression in UC in vivo. Corticosteroids are associated with increased detection of intestinal MAP DNA and decreased expression of certain MMPs. Frequent detection of MAP DNA in healthy controls might be attributable to the wide environmental distribution of MAP and its presence in the food-chain.
Mycobacterium avium strains are widely distributed in the environment and inhabit animal and human intestines. Mycobacterium avium subsp. paratuberculosis (MAP) is the causative agent of Johne's disease, a chronic granulomatous inflammation of the intestines in ruminants like dairy cows and many other species, including primates .
Crohn's disease (CD) and ulcerative colitis (UC) represent the major forms of human idiopathic inflammatory bowel disease (IBD). Accumulating evidence suggests that CD results from an excessive mucosal immune response towards intestinal microbes in a genetically susceptible host . Since the initial description of clinical similarities between Crohn's disease and Johne's disease in cattle in 1913 , it has been hypothesized that MAP might represent a causative agent in CD. Since then, a number of studies and meta-analyses have reported about a more frequent detection of MAP in patients with CD than in controls [4–7]. Nevertheless, it is still a matter of controversy whether MAP represents an etiologic factor for CD or rather a secondary invader of inflamed intestinal mucosa [6, 8, 9]. So far, in vitro studies have identified increased TNF-α levels in mucosal organ culture supernatants from MAP positive CD patients as well as an increased T-cell proliferation upon incubation of peripheral blood mononuclear cells from CD patients with MAP as pathogenic mechanisms and cellular responses [10, 11].
Matrix Metalloproteinases (MMPs) are a family of Zn2+-dependent endopeptidases that are considered to be the most potent proteases in the turnover of the extracellular matrix (ECM) . In addition to their capability of degrading virtually all protein components of the ECM, MMPs regulate a variety of non-matrix substrates such as chemokines, cytokines and growth factors and influence the function and migration of inflammatory cells . They are considered to be the predominant proteases in the pathogenesis of mucosal ulcerations associated with IBD [13–15]. Furthermore, evidence suggests that MMPs are upregulated upon infection with pathogenic mycobacteria and MAP thereby leading to the inflammatory tissue changes associated with mycobacterial infections [16–18].
Within the present study we determined the prevalence of MAP DNA in biopsy samples of patients with UC and CD as well as in patients without IBD using highly sensitive and MAP specific PCRs. To analyse a potential regulation of MMP expression by MAP in vivo, we further assessed the colonic expression of a broad MMP spectrum in UC patients with and without intestinal MAP DNA detection.
Patients and biopsy samples
From June 2007 to July 2008, biopsy samples were obtained from 63 German (n = 21) and Norwegian (n = 42) patients with IBD and from 21 German non-IBD patients during diagnostic colonoscopies. Diagnosis of IBD was confirmed clinically and histologically. Biopsies were taken from areas that macroscopically showed the highest degree of inflammation and were in closest proximity to those biopsies taken for histopathological examinations. Additionally samples were taken in areas with milder signs of inflammation or normally (i.e. unaffected) appearing mucosa. The Mayo endoscopic subscore was utilized for the macroscopic classification of the degree of inflammation .
Biopsy samples from the German IBD patients (n = 21) and the German non-IBD controls (n = 21) for MAP culture were placed in a 1.5-ml sterile screw-cap reaction tube containing 0.5 ml of sterile 0.85% saline and immediately transferred to the laboratory for further investigations. Samples for cultural investigation were not frozen at any time. All biopsies scheduled for MMP analysis were immediately cryopreserved in liquid nitrogen and stored at -80°C until examination. Biopsies underwent a thorough histopathological examination and were classified as "no", "low-grade", or "high-grade" intestinal neoplasia. These examinations were carried out by an experienced pathologist who was neither involved in the study protocol nor aware of the particular MMP measurements. All patients were informed about the study and gave their written consent. In Norway the study was approved by the ethics committee, the data protection commissioner, and the representative for patients' interests and safety (Pasientvernombudet) of the University Bergen. The Norwegian health authority (Helsedirektorat) authorised both, the study and the shipping of the tissue samples from Stavanger, Norway, to Giessen, Germany. In Giessen the study was approved by the local ethic committee (No 75/2009).
Culture of biopsy specimens for MAP detection
The biopsy specimens from 21 German patients with IBD and 21 non-IBD patients was decontaminated when fresh and subsequently cultured in separate MGIT culture tubes at 37°C for up to 18 months. Briefly, 0.5 ml of NaOH-N-acetyl-L-cysteine (Merck, Darmstadt, Germany) was added to each sample in 0.5 ml of saline, and the mixture was incubated at room temperature for 20 min with occasional mixing by inversion. The samples were then centrifuged (10,000 × g for 10 min), and the supernatant was removed. The pellet was resuspended in 0.5 ml of PBS (14.6 mM KH2PO4, 2 mM Na2HPO4 [pH 6.8]) and transferred to the tube containing 4.5 ml of MGIT medium (Becton Dickinson, Heidelberg, Germany) supplemented with 10% oleic acid-albumin-dextrose-catalase (OADC), PANTA (40 U of polymyxin B per ml, 4 μg of amphotericin B per ml, 16 μg of nalidixic acid per ml, 4 μg of trimethoprim per ml, 4 μg of azlocillin per ml [final concentrations]), and 2 μg of mycobactin J (Allied Monitor, Fayette, MO, USA) per ml. After incubation at 37°C for 12 and 52 weeks, the cultures were mixed and 0.5 ml was taken aseptically for testing by the MAP specific PCR as described below. MGIT cultures with visible growth or with a positive PCR result were subcultured onto Herrold's Egg Yolk Medium with ANV (Ampothericin B, Nalidixic acid, Vancomycin) and Mycobactin J and incubated at 37°C for up to 12 months. Biopsy samples from Norwegian patients (n = 42) were processed for direct specific PCR testing.
DNA extraction and PCR analysis for MAP detection
The DNA of the biopsy samples and MGIT cultures after 12 and 52 weeks was extracted using a modified protocol of the DNeasy Blood and Tissue Kit (Qiagen, Hilden, Germany) for the extraction of DNA from Gram-positive bacteria. As a modification to the protocol of the DNeasy Blood and Tissue kit, samples were processed in a spin/rotation instrument for cell lysis (FastPrep-120), with a speed and time setting of 6 and 45 seconds, respectively.
For the molecular detection of MAP, two PCR systems were set up in parallel, a triplex real time-PCR targeting MAP specific genes F57 and ISMav2 and an internal amplification control (IAC) , and a nested PCR  with IS900 oligonucleotide primers. The PCR reaction mixture for the nested PCR (50 μl) contained 1 μl primer 1 (10 pmol/μl), 1 μl primer 2 (10 pmol/μl), 1 μl dNTP (10 mmol, Roche), 5 μl 10 × thermophilic-buffer (Applied Biosystems, Darmstadt, Germany), 0.5 μl MgCl2 (25 mM, Applied Biosystems), 0.5 μl Ampli Taq Gold DNA polymerase (5 U/μl, Applied Biosystems) and 36 μl double-distilled water. Finally, 5 μl of the DNA preparation was added to each reaction tube. The triplex real time-PCR assay was performed as previously described . The fluorescent data were generated by TaqMan® mgb probes applied on the ABI Prism® 7000 Sequence Detection System according to the instructions of the supplier. Briefly, the 50 μl PCR mixture for the triplex real time-PCR assay consisted of 25 μl of the 2xqPCR MasterMix Plus w/o uracil N-glycosylase (UNG, Eurogentec, Seraing, Belgium), 1 μl of each primer (F57, ISMav2), 2 μl of each of the fluorogenic probes (F57, ISMav2, IAC), 1.5 μl of the IAC, 8.5 μl of double-distilled water and a 5-μl aliquot of the DNA sample. The PCRs were performed in a 96well plate format on the ABI Prism® 7000 Sequence Detection System (Applied Biosystems). Thermal cycling conditions comprised a Hot Start DNA Polymerase activation at 95°C for 10 minutes, 50 cycles of denaturation at 95°C for 15 seconds, and an annealing and extension at 60°C for 1 minute. Each measurement was performed in duplicate, and the threshold cycle (Ct) was determined. Primer sequences and fluorogenic probes for MAP detection are presented in Table 1.
RNA Purification, cDNA Synthesis and RT-PCR for MMP analyses
Biopsy samples were homogenized with a polytron homogenizer (Kinematica, Luzern, Switzerland) and total cellular RNA was extracted from shock-frozen single biopsies with RNeasy Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions. First-strand cDNA was synthesized from 1 μg DNA-free total RNA using the oligo-dT-primers and the first-strand cDNA synthesis kit for RT-PCR (Roche Diagnostics, Mannheim, Germany). Real time-PCR was performed using Platinum SYBR Green qPCR Kit (Invitrogen, Karlsruhe, Germany) according to the manufacturer's protocol. Real time-PCR of each gene-specific primer pair was optimized prior to the experiment to confirm the absence of any non-specific amplification product. Primers were purchased from Eurofins (Ebersberg, Germany) and primer sequences are presented in Table 2.
qRT-PCR was performed on the Mx3000P (Stratagene, La Jolla, USA) by using 3-stage program parameters as follows: 1) 10 minutes at 96°C, 2) 40 cycles of 10 seconds at 95°C, 30 seconds at 57°C, and 30 seconds at 73°C, 3) 10 minutes at 73°C. The specificity of the PCR was confirmed by examination of the dissociation reaction plot subsequent to qRT-PCR. PCR products were separated on a 1.5% TAE agarose gel and visualized by staining with ethidium bromide to confirm the appearance of a single band of the correct molecular size. Furthermore, specificity of the PCR reactions and the utilized primers for MMP analyses was verified in sequencing analyses. qRT-PCR data were analysed using the ΔΔCt model .
Prior to more sophisticated statistical calculations, normal distribution of the data was tested using the Kolmogorov-Smirnov test and visualization of histograms. Failing to meet criteria for normal distribution all data were analysed using non-parametric tests. To compare MAP DNA positive detection rates in the three groups CD, UC, and control patients, Fisher's exact test was applied. Individual MMP expression in UC affected colonic mucosa was referred to the respective expression in corresponding healthy mucosa of the same individual in order to account for interindividual differences in colonic MMP expression. Results of MMP expression in relation to the MAP infection status are presented in box-and-whisker-plots. The upper hinge of the box represents the 75th percentile; the lower hinge represents the 25th percentile. The line in the box indicates the median value of the data. The ends of the vertical lines represent the minimum and maximum. Outliers (□) have a distance from 1.5 to 3 box lengths from the upper or lower hinge. Extreme values (Δ) have a distance of >3 box lengths from the upper or lower hinge. Interindividual comparisons of MMP expression were made using Mann-Whitney-U test. A two-sided P < 0.05 was considered significant. Statistical analysis was performed with SPSS 17.0 (SPSS Inc, Chicago, Ill).
Demographic and clinical data of the patient cohort
Intestinal biopsies were obtained during routine colonoscopies from adult patients with CD (n = 14), UC (n = 49) and controls without IBD or other inflammatory disorders within the intestines (n = 21). Diagnosis of CD and UC was confirmed in accordance with the current guidelines based on histopathological examination and clinical findings. Table 3 summarizes the clinical data of these patients.
Detection of MAP in IBD patients and controls
None of the MGIT samples were positive for MAP in the cultural investigation after 12 and 52 weeks of culture.
A total of 63 IBD patients and 21 controls were analysed for the presence of MAP specific DNA in colonic mucosa. To exclude locoregional differences in MAP infection, IBD patients from Germany (n = 21) and Norway (n = 42) were recruited. Despite a more frequent detection of MAP DNA in UC patients (20%) and controls (33%) compared to patients with CD (7%) in the total patient cohort, differences in MAP frequency between these three groups were not statistically significant (CD vs. controls: p = 0.1078, UC vs. controls: p = 0.3615, CD vs. UC: p = 0.4298).
Subgroup analyses considering the German and Norwegian patient cohort separately revealed likewise no significant differences in MAP frequency between patients with CD and UC and controls (Norway: CD vs. controls: p = 0.2945; UC vs. controls: p = 0.1885; CD vs. UC: p = 1.00 and Germany: CD vs. controls: 0.2216; UC vs. controls: p = 1.00; CD vs. UC: 0.3108). Although the MAP detection rate was generally higher in Germany (29%) than in Norway (14%), these differences did not reach the level of statistical significance (p = 0.1828). MAP prevalence in the different cohorts is summarized in Table 4.
We next compared whether the frequency of MAP detection in the IBD and UC patient cohort differed depending on the applied anti-inflammatory therapy (AIT). Comparing IBD and UC patients receiving any kind of AIT to those patients without AIT, no statistical significances in MAP frequency were detected (Figure 1, 2). Similarly, no significant differences in MAP DNA prevalence were observed when patients treated with 5-amino salicylic acid (5-ASA) and its derivatives or immunomodulators (azathioprine and infliximab) were compared to those patients without the respective agents. When comparing patients stratified to the treatment with corticosteroids, MAP DNA was significantly more frequently obtained in UC patients treated with corticosteroids compared to those without corticosteroids in their therapeutic regime (p = 0.043, Figure 2c). However, although not statistically significant, a higher frequency of MAP detection in the corticosteroid group was observed in the total IBD population as well (Figure 1c).
MMP expression in UC patients with and without presence of MAP DNA
For MMP analyses, all determined mRNA values were related to the respective content of 18S rRNA which served as a housekeeping gene. In order to account for interindividual differences in the MMP expression in the colon, MMP expression in diseased colonic mucosa was referred to the respective expression in corresponding healthy mucosa of the same individual.
Gene expression of MMP-1, MMP-2, MMP-7, MMP-9, MMP-13 and MMP-19 was unchanged between UC patients with presence of MAP DNA and those without (Figures 3, 4, 5, 6, 7, 8). Mucosal mRNA expression of MMP-28 and TNF-α did not show any dependency on the presence of MAP DNA either (Figures 9 and 10).
As MAP DNA was detected in only one CD patient, we were unable to analyse MMP expression with regard to MAP status in the CD patient cohort. Since endoscopic evaluation of screening colonoscopy did not reveal any signs of intestinal inflammation, MMP regulation in inflamed mucosa expressed as a multiple of basal expression in healthy mucosa could not be performed in the control cohort either.
Effects of anti-inflammatory agents on MMP and TNF-α expression
To analyse a potential effect of the applied anti-inflammatory therapy on intestinal MMP expression, we further calculated MMP and TNF-α expression in UC patients stratified by the different therapeutic modalities. Gene expression of MMP-1, -2, -7, -9, -13, -19, -28 and TNF-α was unchanged between patients with and without AIT, between patients stratified to 5-ASA and its derivatives and between patients with and without immunomodulators. However, median levels of MMP-2, MMP-9, and MMP-13 were significantly decreased in UC patients treated with corticosteroids compared to those with no corticosteroids in their therapeutic regime (MMP-2: 6.1-fold, p = 0.024; MMP-9: 4.2-fold, p = 0.009; MMP-13: 9.5-fold, p = 0.042, Figures 3, 4, 5, 6, 7, 8, 9, 10).
Based on this finding, we excluded steroid-treated patients in a further analysis and re-calculated the MMP and TNF-α expression in MAP positive and MAP negative IBD patients. However, despite the non-consideration of steroid treated patients, expression of MMP-1, -2, -7, -9, -13, -19, -28 and TNF-α remained unchanged between MAP positive and negative IBD patients (Additional Files 1, 2, 3, 4).
The histopathological and clinical similarities between human chronic granulomatous enteritis, intestinal tuberculosis, and animal paratuberculosis [3, 23] has led to the suspicion that Mycobacterium avium subspecies paratuberculosis is an etiologic factor for the development of Crohn's disease. MAP is fastidious and slow-growing and can therefore only rarely be detected by conventional microbiological techniques . Due to the difficulties in growing MAP in vitro, molecular and serological methods have been developed. Nevertheless, the molecular detection of MAP DNA has also frequently been hampered by insufficient specificity of the selected primers and probes, inadequate DNA extraction methods resulting in insufficient sensitivity, and possible contamination as a consequence of the PCR techniques used . In the current study, we therefore selected a nested PCR system and a real time-PCR method instead of conventional PCR sets, which ensured a sensitive and specific approach. The nested PCR used was developed by Bull et al.  and is based on the widely used MAP reference marker IS900. The oligonucleotide primer sequences were specifically adapted to show no cross reactions with the previously described IS900-like elements [25, 26]. The positive IS900 PCR products detected were sequenced and corresponded to MAP IS900 but not IS900-like sequences. In addition, a triplex real-time PCR assay combining the MAP-specific gene sequences F57, ISMav2, and an internal amplification control for diagnostic quality assurance was applied. The real time-PCR method was carefully validated by using more than 200 references and field strains with different kinds of sample preparation techniques on artificially contaminated and naturally infected samples.
Based on 2 different PCR methods utilized in this study, false-positive results due to an unspecific binding of oligonucleotide primer pairs are therefore highly improbable. The risk of cross-contamination between the samples was also reduced by using sample preparation negative controls. The use of an IAC has been shown to be mandatory for diagnostic PCR applications to exclude false negative results . The included IAC of the real-time PCR assay revealed that none of the real-time PCR reactions was inhibited.
Using this specific and sensitive approach, we explored the detection rate of MAP DNA in colonic biopsies of German and Norwegian patients with IBD and control patients without intestinal inflammation. Within this study, we found no significant differences in MAP DNA detection frequency between patients with UC and CD and controls.
Regarding the literature, reports about the association of MAP and CD are controversial. So far, a number of studies have reported more frequent detection of MAP DNA in CD patients compared with controls using PCR assays [21, 28, 29]. Other authors, in contrast, found no association between CD and the detection of MAP DNA [30–35]. Nevertheless, comparisons between the studies are difficult to make due to heterogeneity in the analysed specimens that vary from fresh [35, 36] to embedded tissue [30, 31] and blood [28, 29, 32–34]. Furthermore, different MAP detection methods are used across the studies including MAP DNA [21, 28, 30, 31, 33–35], MAP culture [29, 32, 34], both DNA and culture , specific antibodies against MAP epitopes  and immunocytochemistry . Although recent meta-analyses were able to confirm the association of MAP infection and CD [4, 6], the pathogenic significance of this association remains unclear. Within our study, we detected MAP DNA in only a low percentage of CD patients. As a limiting factor, our cohort of patients with CD was relatively small. Post hoc power analysis of the CD population against an alpha level of 0.05 estimated a two-tailed statistical power of 0.135. Consequently, appropriate conclusions about an etiologic involvement of MAP in the pathogenesis of CD cannot be drawn from the results of our study.
During the initial phase of our study, we detected MAP DNA in an unexpected high percentage of German UC patients. To exclude a locoregional influence or epiphenomenon, we aimed to confirm this result in a distinct UC population and therefore expanded our analyses to a cohort of Norwegian UC patients. In this cohort, we likewise observed a high frequency of MAP DNA. Data on the frequency of MAP detection in UC in the literature are contradictory as well. In general, MAP is more frequently detected in CD than in UC according to recent meta-analyses [4, 6]. Nevertheless, several studies detected MAP infection in a high percentage of UC patients as well [7, 28, 37–40].
As a further remarkable result, we detected MAP DNA in intact colonic mucosa in a high percentage of German control patients (33%). As both, the Norwegian and German patient population represent an urban population with a comparable demographic and epidemiologic structure and a similar BCG vaccination policy in Germany and Norway, we did not assess the colonic MAP prevalence in healthy Norwegians. In conjunction with our results, previous studies have made similar observations by serologically detecting MAP DNA or specific MAP antibodies in a high percentage of healthy control patients [37, 39–41]. In this context, the following aspects are important to note: MAP has been cultured from chlorinated potable municipal water . Mycobacteria are at least two orders of magnitude more resistant to chlorine purification than Escherichia coli and MAP survives higher concentrations of chlorine than the 1.1 parts per million routinely achieved with first-use municipal water in the USA . Furthermore, MAP has been cultured from pasteurized milk in the USA and Europe [44–46]. Considering these facts, it has been speculated that the frequent detection of MAP in healthy controls is a result of the wide distribution of MAP and its presence in the food-chain. Nevertheless, the biological significance of this finding remains unclear as the detection of MAP DNA might well come from live bacteria but also might merely represent scattered debris from killed bacteria.
Anti-inflammatory agents such as 5-ASA and its derivatives, corticosteroids and immunomodulators are established therapeutic agents for the treatment of IBD. Most interestingly, it has been shown that 5-ASA, thalidomide, methotrexate, 6-mercaptopurine and azathioprine inhibit MAP in vitro in a dose dependent manner [47–50]. Further, recent evidence suggests that 5-ASA decreases the prevalence of MAP DNA from the blood of IBD patients whereas other agents such as 6-mercaptopurin, methotrexate and tacrolimus are associated with clearance of MAP DNA from the blood . To analyse a potential effect of the applied anti-inflammatory therapy on the MAP DNA prevalence in intestinal tissue, we performed subgroup analyses according to the different therapeutic agents in our IBD cohort. However, we were not able to detect significant differences in the MAP DNA prevalence between IBD and UC patients with and without anti-inflammatory therapy and between those patients receiving 5-ASA or immunomodulators compared to patients without the respective agents. Based on the unrefuted data of the anti-MAP activities of IBD medication mentioned above, we assume that the most likely explanation for the lack of association between 5-ASA and immunomodulators and MAP detection rates within our study, apart from the different specimens analysed (tissue vs. blood), is the relative small sample size in our study. Nevertheless, our results provide evidence that UC patients treated with corticosteroids have a higher frequency of intestinal MAP DNA than those not treated with corticosteroids. This result is in accordance with observations from Naser et al. who cultured MAP from blood in 60% (3 of 5) of IBD patients treated with steroids . Although a larger study by Juste and co-workers did not detect a significant increase in MAP prevalence in patients receiving steroids, the authors suggested that the lack of increased MAP DNA frequency in steroid treated IBD patients in their study might be attributable to frequent co-administration of anti-MAP agents in this group . Furthermore, the authors concluded that caution suggests that concomitant anti-MAP agents should always be used when steroids are administered , a position that is strengthened by the results of our study.
To further evaluate a potential contribution of MAP infection to disease manifestation in UC patients, we analysed the expression of Matrix Metalloproteinases with regard to the presence or absence of intestinal MAP DNA. Members of the MMP family have been shown to be upregulated in peripheral blood mononuclear cells from cattle infected with Johne's disease after stimulation with MAP [16, 17]. Furthermore, murine in vitro and in vivo studies provide evidence that upregulation of certain MMPs such as MMP-2 and MMP-9 plays a pathogenic role in infections caused by pathogenic mycobacteria . Most interestingly, enhanced MMP activity after mycobacterial infection was substantially reduced upon treatment with anti-TNFα antibodies , a treatment strategy which has been proven to be highly beneficial in human IBD [51, 52]. On the other hand, in vitro data from Janagama and co-workers demonstrate that MAP strains from diverse hosts differ in their ability to survive intracellularly and that strains with higher intracellular persistence had decreased expression of different cytokines and MMP-3 . Thus, an anti-inflammatory and anti-invasive milieu might facilitate their persistence and survival within macrophages .
On the basis of this evidence, we aimed to analyse the mucosal MMP expression in IBD patients with and without intestinal MAP DNA. Unfortunately, we had to restrict the analysis to the UC patient cohort, as MAP DNA was detected in only one CD patient. Using this approach we focused on MMP gene expression as several studies have shown that expression of MMPs is mainly transcriptional regulated with close correlation between MMP protein concentrations and mRNA expression [54–57]. We analysed a broad spectrum of MMPs including MMP-1, MMP-7 and MMP-13, which have been proven to be major proteases in the pathogenesis of IBD associated mucosal ulcerations [13–15, 58, 59], and MMP-2 and MMP-9, which have been shown to be upregulated upon mycobacterial infection . Furthermore, we determined the expression of MMP-28, the most recent member of the MMP family which is expressed in intact colonic epithelium rather than in UC affected mucosa and therefore is associated with epithelial integrity [14, 60]. Our results provide evidence that neither expression of MMP-1, -2, -7, -9, -13, -19 nor of MMP-28 is altered in UC patients with presence of intestinal MAP DNA compared to those without MAP detection. TNF-α, which regulates MMP-2 and MMP-9 and is part of the cytokine response towards MAP in CD patients [10, 11, 61, 62], was unchanged between UC patients with intestinal MAP DNA detection and those without. Subgroup analyses based on different anti-inflammatory agents applied in our IBD cohort revealed significantly decreased MMP-2, MMP-9, and MMP-13 gene transcripts in UC patients treated with corticosteroids compared to those with no corticosteroids in their therapeutic regime (MMP-2: 6.1-fold, p = 0.024; MMP-9: 4.2-fold, p = 0.009; MMP-13: 9.5-fold, p = 0.042). However, when we excluded steroid-treated patients in a further analysis and re-calculated the MMP and TNF-α expression in MAP positive and MAP negative IBD patients, no significant differences were observed between MAP positive and MAP negative patients (Additional Files 1, 2, 3, 4).
To further elucidate the pathogenic potential of MAP for the development of IBD and its significance in healthy individuals, it seems inevitable to transfer the results of the observed association of MAP and IBD to more functional studies in the future. To understand different susceptibilities towards MAP infections, it will be of great value to determine the presence or absence of certain genetic IBD risk loci in CD and UC patients. Among others, NOD2 and Nramp1 might be of particular interest in the context of MAP infection: approximately 30% of European ancestry have one of three NOD2 polymorphisms and homozygosity for one polymorphism confers an increased risk for CD by factor 11 to 27 . Interestingly, embryonic kidney cells transfected with NOD2 are able to recognize MAP and respond in a dose dependent manner . Defects and mutations in Nrmap (natural-resistance-associated macrophage protein 1) are associated with increased susceptibility to mycobacterial infections in humans and animals and in both, UC and CD patients have a frequency of Nramp1 promoter polymorphisms than healthy controls . Another potential approach might be the use murine models with knock-down of certain IBD susceptibility loci and subsequent controlled infection with MAP strains and other mycobacteria.
Our study provides evidence that MAP can frequently be detected in intestinal mucosa of patients suffering from ulcerative colitis as well as from control patients without intestinal inflammation. This result might well be attributable to the wide environmental distribution of MAP and its presence in the food-chain. Furthermore, we are able to show that corticosteroids are associated with increased detection of intestinal MAP DNA and decreased expression of certain MMPs. The results of this study provide further evidence that the presence of intestinal MAP specific DNA is not associated with altered MMP expression in ulcerative colitis in vivo. Hence, the biological significance of MAP and its contribution to the pathogenesis of IBD remains elusive.
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The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-230X/11/34/prepub
This work was supported by grants from ZooMAP (Bundesministerium für Bildung und Forschung, BMBF) and from the Deutsche Forschungsgemeinschaft (RO 957/7-1 and RO 957/8-1). Dr. Timo Rath has received grants for young researchers ("Anschubfinanzierung") from the Justus-Liebig-University Giessen.
TR has no competing interests to disclose. MR has no competing interests to disclose. SB has no competing interests to disclose. AR has no competing interests to disclose. TB has no competing interests to disclose. ÖA has no competing interests to disclose. AA has no competing interests to disclose. JMH has no competing interests to disclose. RG has no competing interests to disclose. MB has no competing interests to disclose. ER has no competing interests to disclose.
TR participated in the collection the biopsy samples, determined the MMP expression, analysed the data and drafted the manuscript (together with ER). MR, SB and AR participated in study design, collection of the biopsy samples and MMP analyses. ÖA, AA and MB performed the MAP detection and critically revised the manuscript. JMH participated in the collection of the biopsy samples and MMP analyses. TB and RG provided important intellectual content and participated in study design. ER designed the study, analysed the data and drafted the manuscript (together with TR). All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Expression of MMP-1 and MMP-2 in UC patients without corticosteroids with respect to the presence of MAP DNA (n = 41). mRNA results were determined by RT-PCR. MMP-1 and MMP-2 gene expression was not significantly different in steroidfree UC patients with intestinal MAP detection compared to those without. (PDF 59 KB)
Additional file 2: Expression of MMP-7 and MMP-9 in UC patients without corticosteroids with respect to the presence of MAP DNA (n = 41). mRNA results were determined by RT-PCR. MMP-7 and MMP-9 gene expression was not significantly different in steroidfree UC patients with intestinal MAP detection compared to those without. (PDF 61 KB)
Additional file 3: Expression of MMP-13 and MMP-19 in UC patients without corticosteroids with respect to the presence of MAP DNA (n = 41). mRNA results were determined by RT-PCR. MMP-13 and MMP-19 gene expression was not significantly different in steroidfree UC patients with intestinal MAP detection compared to those without. (PDF 58 KB)
Additional file 4: Expression of MMP-28 and TNF-α in UC patients without corticosteroids with respect to the presence of MAP DNA (n = 41). mRNA results were determined by RT-PCR. MMP-28 and TNF-α gene expression was not significantly different in steroidfree UC patients with intestinal MAP detection compared to those without. (PDF 56 KB)
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Rath, T., Roderfeld, M., Blöcher, S. et al. Presence of intestinal Mycobacterium avium subspecies paratuberculosis(MAP) DNA is not associated with altered MMP expression in ulcerative colitis. BMC Gastroenterol 11, 34 (2011). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-230X-11-34
- Inflammatory Bowel Disease
- Inflammatory Bowel Disease Patient
- Ulcerative Colitis Patient
- Mycobacterium Avium Subspecies Paratuberculosis
- Internal Amplification Control