Post-infectious irritable bowel syndrome (PI-IBS) is a common gastrointestinal disorder characterized by persistent abdominal pain despite recovery from acute gastroenteritis. The underlying mechanisms are unclear, although long-term changes in neuronal function, and low grade inflammation of the bowel have been hypothesized. We investigated the presence and mechanism of neuronal sensitization in a unique cohort of individuals who developed PI-IBS following exposure to contaminated drinking water 7 years ago. We provide direct evidence of ongoing sensitization of neuronal signaling in the bowel of patients with PI-IBS. These changes occur in the absence of any detectable tissue inflammation, and instead appear to be driven by pro-nociceptive changes in the gut micro-environment. This is evidenced by the activation of murine colonic afferents, and sensitization responses to capsaicin in dorsal root ganglia (DRGs) following application of supernatants generated from tissue biopsy of patients with PI-IBS. We demonstrate that neuronal signaling within the bowel of PI-IBS patients is sensitized 2 years after the initial infection has resolved. This sensitization appears to be mediated by a persistent pro-nociceptive change in the gut micro-environment, that has the capacity to stimulate visceral afferents and facilitate neuronal TRPV1 signaling.
Infectious gastroenteritis (IGE) is a significant risk factor in the development of irritable bowel syndrome (IBS), a chronic functional gastrointestinal disorder, characterized by abdominal pain and altered bowel habit in the absence of ongoing organic pathology. Up to 36% of patients with gastroenteritis may go on to develop post-infectious IBS (PI-IBS). The majority of PI-IBS patients suffer from increased visceral pain perception or visceral hypersensitivity (VHS) suggesting that long term changes in pain processing occur in PI-IBS1. The underlying mechanisms are still not clear, however it has been proposed that an incomplete resolution of the immune response leads to a persistent microscopic inflammation of the bowel, facilitating activation and sensitization of pain sensing nerves2,3.
Gwee et al. indeed demonstrated increased IL-1β mRNA expression in rectal biopsies following an episode of acute IGE4, while enhanced cytokine release (TNF-α, IL-1β and IL-6) by circulating PI-IBS lymphocytes is reported5. In addition, enterochromaffin cell numbers, intraepithelial lymphocytes and intestinal permeability are increased up to one year after Campylobacter enteritis6. Moreover, mast cell numbers are increased in the terminal ileum of PI-IBS patients following Shigella gastroenteritis7. Mediators released from these cells such as histamine, IL-1β, IL-6 and TNF-α stimulate or sensitize visceral nociceptors consistent with the hypothesis that nociceptor activation by low grade inflammation underpins abdominal pain in PI-IBS8,9,10. Consequently, there is great interest in identifying which specific ion channels are responsible for transducing the depolarization of nociceptors in response to inflammatory mediators.
Despite this compelling evidence, direct functional data from human studies of sensitized neuroimmune signaling in PI-IBS is lacking. The recent failure of 2 large-scale clinical trials with the anti-inflammatory drug mesalazine to show symptom improvement in diarrhea predominant IBS (IBS-D) highlights the urgent need to substantiate this hypothesis. We have recently developed the technical capacity to image calcium transients in human enteric neurons11,12 obtained from gut biopsies, and test the effect of supernatants generated from these biopsies on sensory nerve activity12. We are therefore in the position to examine both, changes in the function of a patient’s own neurons, and changes in the microenvironment of the patient’s bowel, thereby putting our group in the unique position to confirm the sensitization of neuronal signaling in PI-IBS patients. To do this, we have obtained samples from PI-IBS patients, who were exposed to contaminated tap water, 2 years previously13, allowing us to study a unique cohort of PI-IBS patients for whom the duration of disease, and precipitating infectious event, are identical, greatly reducing intra-subject variability.
The aim of this study was to examine neuronal sensitivity in patients with PI-IBS, and to investigate the role of low-grade inflammation in these changes. To our surprise, we found no evidence for low grade inflammation in the bowel of these patients. However, we did find clear evidence for both neuronal sensitization in PI-IBS patients, and a shift in the bowel microenvironment to a pro-nociceptive state. Taken together, our data show for the first-time direct evidence of aberrant neuronal signaling in PI-IBS. Notably, this sensitization of gut function, is not mediated by persistent low grade inflammation, but instead is appears to be mediated by other pro-nociceptive changes in the mucosal micro-environment which modulate TRPV1 signaling.
Sensitization of TRPV1 on submucosal neurons in PI-IBS
To investigate the underlying mechanism of PI-IBS, 8 patients were recruited 2 years following an outbreak in 2 Belgian villages13 (Fig. 1). In addition, 9 healthy volunteers (HVs) were recruited by public advertisement. Of note, 3 individuals who suffered from an infection but did not develop PI-IBS were also recruited (PI-HVs). Demographic data are summarized in Table 1.
Inflammation enhances pain perception via the activation and/or sensitization of TRP channels, including TRPV114,15, and we hypothesized that the persistence of a low-grade inflammation of the bowel in PI-IBS could lead to long term TRPV1 sensitization. Therefore, we performed live Ca2+ imaging of submucosal neurons in rectal biopsies from PI-IBS patients, HVs and PI-HVs12. Application of 0.1 and 1 nM capsaicin induced significantly greater Ca2+ fluxes in submucosal neurons from PI-IBS compared with HVs (0.1 nM: p = 0.012, 1 nM: p = 0.026) or PI-HVs (1 nM: p = 0.024) (Fig. 2A,B). In addition, exposure to 0.1 and 1 nM capsaicin activated significantly more submucosal neurons in PI-IBS compared with HVs (0.1 nM: p < 0.001, 1 nM: p = 0.017) and PI-HVs (1 nM: p < 0.001) (Fig. 2A,B). Responses to capsaicin were blocked by pre-treatment with the selective TRPV1 antagonist SB-366791 (1 µM) confirming specificity for TRPV1 (Supplementary Figure 1).
To assess if the increased Ca2+ response to capsaicin was mediated by increased expression of TRPV1 in PI-IBS, TRPV1 transcript levels in HVs and PI-IBS biopsies were compared. No significant difference was seen between TRPV1 mRNA expression in PI-IBS versus HVs biopsies (Fig. 2C), suggesting that the increased Ca2+ response to capsaicin was due to sensitization of TRPV1 channel function, rather than an increase in channel number.
Biopsy supernatants from PI-IBS patients stimulate murine colonic afferents and DRGs
Having shown that neuronal activity is sensitized in PI-IBS, we next sought to confirm the pro-nociceptive potential of the bowel in PI-IBS patients. Therefore, we examined the effect of tissue biopsy supernatants from PI-IBS patients and HVs on the activity of mouse colonic afferents thought to play a role in visceral nociception, and TRPV1 signaling in DRGs. Application of supernatants from PI-IBS biopsies to the mucosal surface below the receptive field of colonic afferents produced a robust increase in nerve discharge compared with supernatant from HV biopsies (Fig. 3A,B,E) (mean peak increase in firing PI-IBS (n = 8) 2.2 ± 0.4 Hz compared with HV (n = 8) 0.9 ± 0.1 Hz, p = 0.02). Furthermore, responses to von Frey hair (vfH) probing of the receptive field were significantly sensitized following removal of the PI-IBS supernatant, (8.3 ± 0.6 Hz pre-incubation vs. 12.3 ± 1.5 Hz post-incubation; p = 0.016, n = 8) (Fig. 3D,F), and unchanged following removal of supernatant from HV biopsies (9.6 ± 1.1 Hz pre-incubation vs. 8.0 ± 1.1 Hz post-incubation, n = 8, Fig. 3C,F). These findings demonstrating a clear pro-nociceptive change in the bowel from PI-IBS patients.
Consistent with this change, DRG neurons incubated with PI-IBS supernatants demonstrated significantly greater Ca2+ responses to capsaicin compared to neurons incubated with HV supernatants (Fig. 4A), and significantly more DRG neurons responded to capsaicin following incubation with PI-IBS supernatants compared with HV supernatants (Fig. 4B). Taken together, this data demonstrates the presence of bioactive mediators in the bowel of patients with PI-IBS, which have the potential to directly activate colonic afferents and sensitize TRPV1 channels, potentially contributing to VHS in PI-IBS.
Lack of evidence for persistent low grade inflammation or increased cytokine release in PI-IBS
To understand the identity of these mediators we looked at the expression of pro-inflamamatory cytokines in biopsy samples as persistent low grade inflammation of the bowel has been proposed to underlie the production of pain in PI-IBS. Consistent with this hypothesis several cytokines e.g. IL-1β, IL-2 and IL-10 have been shown to stimulate colonic afferents9,10, and TNF-α sensitizes afferent endings and DRG neurons via TRPV1 or TRPA1 channels10,16. However, measurement of cytokine levels in biopsy supernatants failed to show any difference in IL-4, IL-13, IFN-γ, IL-1β, CXCL8, IL-10, IL-17a, TNF-α, MCP-1 and IL-6 levels between HVs and PI-IBS (Fig. 5), and no significant difference was seen in biopsy transcript levels for a panel of pro- and anti-inflammatory cytokines (IFN-γ, TNF-α, IL-6, IL-1β, MCP-1, IL-4, IL-10, IL-17f, IL-5, IL-13 and IL-2) for PI-IBS and HVs (Fig. 6A). Furthermore, no significant differences were seen in plasma cell, B cell, CD3+ T cell or eosinophil numbers in biopsies from PI-IBS and HVs (Table 2, Fig. 6B).
Biopsy supernatants from PI-IBS sensitizes TRPV1 on murine DRG neurons via histamine 1 receptor
As no evidence of low grade inflammation or altered cytokine levels were detected, the potential involvement of mast cell mediators was studied. Recently we reported histamine-mediated sensitization of TRPV1 by IBS supernatants, an effect mediated by activation of histamine 1 receptor (Hrh1). To determine if a similar mechanism is present in PI-IBS, we examined the effect of incubating DRG neurons with PI-IBS supernatants, in the presence of the selective Hrh1 antagonist pyrilamine (1 µM), or in DRGs from Hrh1 knock-out mice. Pyrilamine normalized the sensitized Ca2+ response to capsaicin in DRGs incubated with PI-IBS biopsy supernatants (Fig. 4C), and PI-IBS supernatants were not able to potentiate the capsaicin response in DRGs collected from Hrh1 knock-out mice (Fig. 4C). These data suggest that PI-IBS supernatants contain bioactive compounds, most likely histamine or histamine metabolites that sensitize TRPV1 via Hrh1 activation.
To confirm that histamine sensitizes TRPV1, DRGs were incubated overnight with HVs supernatant supplemented with 10 µM histamine which resulted in an increased Ca2+ response, an effect that was prevented by pyrilamine and absent in Hrh1 knock-out mice (Fig. 4D). Moreover, as previously reported, incubation of HV submucosal neurons with histamine (10 µM) significantly increased the Ca2+ response to capsaicin, confirming that histamine also sensitizes TRPV1 in humans12. Our data indicate that the supernatant of PI-IBS sensitizes TRPV1 via a Hrh1 mediated mechanism.
Finally, we compared histamine levels and mast cell numbers in biopsy supernatants and tissue from HVs and PI-IBS patients. Surprisingly, no difference was seen in histamine concentrations (Fig. 4E), and mast cell counts were reduced in PI-IBS (Table 2; Fig. 6B, Supplementary Figure 1), suggesting that consistent with the absence of low grade inflammation, no overt increase in mast cell function occurs in PI-IBS.
PI-IBS patients suffer from persistent abdominal pain, lasting for many years following clearance of the initial infection. In this study, we provide direct evidence of sensitization of enteric neurons in patients 2 years after a bout of gastroenteritis. Moreover, supernatants generated from PI-IBS patient biopsies stimulate visceral colonic afferents with presumptive nociceptor function and sensitize responses to probing, indicating that an ongoing pro-nociceptive change in the gut micro-environment underlies this abdominal pain. Further investigation, demonstrates that these changes can sensitize TRPV1 channels through a Hrh1 mediated pathway. Our data for the first time provide a mechanism explanation for the abnormal pain perception in patients with PI-IBS, and suggest that histamine receptor blockade may represent a novel analgesic treatment for these patients.
PI-IBS is believed to result from a persistent low-grade inflammation of the bowel triggering symptoms of pain and altered bowel habits, by aberrant activation of intrinsic and extrinsic nerves. Enhanced cytokine signaling4 and increased immune cell numbers7 have been documented in PI-IBS6,17,18,19, however direct evidence of their role in altered neuronal signaling in patients with PI-IBS is lacking. Here, we studied PI-IBS patients from a unique cohort of residents of 2 Belgian villages, who in December 2010, were exposed to tap water contaminated with norovirus, Giardia lamblia and Campylobacter jejuni 13. Rectal biopsies of individuals who developed PI-IBS, all of whom continued to have complaints at the time of biopsy, 2 years after the outbreak, were studied in detail to assess the role of inflammation and neuronal sensitization in PI-IBS. Submucosal neurons from these patients displayed a significant increase in their response to the TRPV1 agonist capsaicin suggesting that long term changes in neuronal signaling occurs in PI-IBS. Submucosal neurons are involved in the regulation of secretion and blood flow in the intestine20, and the increased excitability of these neurons in PI-IBS is in keeping with pro-secretory changes to bowel function, consistent with the patient’s symptoms of diarrhea, and this now needs further study.
To understand the nature of the increased response to capsaicin in these neurons we examined TRPV1 transcript levels in HV and PI-IBS biopsies, observing no change. This observation suggesting that enhanced TRPV1 signaling in PI-IBS was most likely due to a sensitization of TRPV1 channel function, as opposed to an increase in channel numbers, presumably in response to an ongoing change in mediator levels within the bowel. To further explore if a pro-nocieptive change in the gut microenvironment occurs in PI-IBS we examined the effect of PI-IBS biopsy supernatants on murine afferent nerve preparations observing increased ongoing activity and sensitized responses to mechanical probing. Moreover, overnight incubation of mouse DRGs with PI-IBS supernatant resulted in an increased Ca2+ response to capsaicin, confirming that the PI-IBS micro-environment, even 2 years after the infection, contains mediators that activate nociceptive afferents and sensitize TRPV1. TRPV1 is involved in perception of visceral pain triggered by mechanical stimuli, as shown by impaired pain responses to colorectal distention in TRPV1 knock-out compared to WT mice21. Based on these findings, we propose that enhanced TRPV1 function in PI-IBS represents an important mechanism contributing to abdominal pain to bowel distention and altered bowel habits.
Sensitization of TRP channels on sensory neurons is suggested to occur via coupling with G-protein coupled receptors (GPCR) such as histamine receptors, protease receptors or cytokine receptors22 with subsequent activation of multiple intracellular signaling pathways including PLCβ-PI-3 and MAP kinases23. Hughes et al. elegantly showed sensitization of murine mechanosensitive colonic afferents by cytokines, particularly TNF-α10, however, to what extent this mechanism contributes to aberrant neuronal signaling in IBS or PI-IBS remains to be studied. In the present study, we found no evidence of increased inflammatory gene expression or infiltrating inflammatory cells in biopsies from PI-IBS patients, and no increase in biopsy supernatant cytokine levels. It should however be noted that due to the unique nature of the IBS patients studied (contaminated water supply) our sample size is inherently low, and so we should not rule out the possibility that a larger study is required to definitely confirm this observation. Nevertheless, our findings are in line with a previous study by Mearin et al., which also reported no difference in the number of T lymphocytes or pro-inflammatory cytokines between PI-IBS patients and infected HVs 3 years after a Salmonella infection, even though only PI-IBS patients were hypersensitive to rectal distention24. Similarly, no differences in serum cytokines and mucosal cytokine expression were detected between PI-IBS and HVs in a large Swedish cohort25. It is not clear why the presence of low-grade inflammation is an inconsistent finding in PI-IBS, and it is beyond the scope of this study to investigate it further. However, it is notable that the patients we have studied and those of Mearin et al. were examined 2–3 years after the precipitating infectious event. It may therefore be possible that low-grade inflammation is an interim event following gastroenteritis that is superseded by another more persistent change in the gut micro-environment.
Having very recently shown marked clinical efficacy of anti-histamine treatment against symptoms of pain and discomfort, and evidence for histamine mediated sensitization of TRPV1 in IBS-D12, we were keen to understand if a common mechanism of nociceptor activation existed in PI-IBS. Co-incubation of DRGs with the Hrh1 antagonist pyrilamine prevented TRPV1 sensitization by PI-IBS biopsy supernatants highlighting a key role for H1 receptors in TRPV1 sensitization. Moreover, histamine added to HV supernatant mimicked the effect of PI-IBS supernatant and sensitized TRPV1 responses in DRGs. In contrast, supernatant from HV biopsies had no effect on TRPV1 responses in DRGs. This histamine-mediated sensitization of TRPV1 was also blocked by pyrilamine and lacking in DRG neurons from Hrh1 knock-out mice confirming the involvement of Hrh1 activation. Despite displaying a clear histamine receptor mediated effect we could not detect a significant increase in histamine content between biopsy supernatants of PI-IBS compared to HVs, in contrast to previous studies8,26,27. This is likely to be a technical issue as histamine is rapidly degraded into its metabolites. Interestingly, histamine metabolites maintain the capacity to interact with H1 receptors via their aromatic ring28, and to sensitize TRPV1 via activation of the Hrh112, explaining the ability of our PI-IBS supernatants to display stimulatory effects at Hrh1 receptors. In keeping with the overall lack of evidence for low-grade inflammation, we found decreased rather than increased mast cell numbers in biopsies of PI-IBS patients. These findings would suggest that the activity of mast cells rather than an increased number is essential in the pathophysiology of IBS and PI-IBS, as hypothesized previously29. Although it may be that mast cells are not the main source of histamine in biopsy samples, with the microbiome30, representing a significant alternative source of histamine. However, more in depth studies are required to elucidate the exact source of histamine and its metabolites.
In summary, by combining electrophysiological assessment of visceral afferents with presumptive nociceptor function, and state-of-the-art live Ca2+ imaging of neurons in rectal biopsies, from a well-defined group of PI-IBS patients, we have provided direct evidence for long term changes in neuronal sensitivity in patients with PI-IBS, which we believe are driven by pro-nociceptive changes to the gut micro-environment. These changes influence excitability in enteric neurons and extrinsic nociceptors, which in turn are able to drive patient symptoms of diarrhea and abdominal pain. These changes are seen in the distal gut an area remote from the initial precipitating infection (typically upper gut), and most likely represent a global pro-nociceptive change in the bowel, consistent with previous demonstrations of rectal hypersensitivity in PI-IBS patients24. It should be noted that this study was performed in a small cohort of PI-IBS patients, and further work in in a larger cohort of PI-IBS patients is now needed to consolidate these findings.
Significantly, although initiated by inflammation, the pro-nociceptive changes seen in PI-IBS patients are not mediated by altered immune cell numbers or inflammation. Instead, responses are mediated by Hrh1 receptor sensitization of TRPV1 signaling, suggesting that similar to “standard” IBS12, Hrh1 antagonism may represent an interesting new target for treatment of PI-IBS. Taken together, this is the first study using a unique cohort of PI-IBS patients showing histamine-mediated TRPV1 sensitization via Hrh1 as potential mechanism for persistent VHS observed in PI-IBS patients, in absence of low-grade inflammation. Together with the results of our previous clinical trial with the histamine 1 receptor antagonist ebastine12, our data provides the first evidence that peripheral histamine 1 receptor antagonism can serve as a new treatment for PI-IBS.
In 2010, 2 small villages in Antwerp, Hemiksem and Schelle, were exposed to contaminated tap water by which inhabitants were infected with Giardia lamblia, Campylobacter jejuni and Norovirus 13,31. Patients previously identified with PI-IBS13 (n = 34) were re-contacted 2 years after the outbreak. Patients who were still symptomatic and fulfilled the Rome III IBS criteria were invited to participate to this study. Of these 34 patients, 19 were asymptomatic, one did not fulfill ROMEIII criteria, 4 patients moved, one patient was pregnant and one refused to participate. Hence, eight patients (median age: 53 years, IQR: 35–54, 7 F) were included. Also 3 individuals who suffered from an infection but did not develop PI-IBS were recruited (PI-HVs) (median age: 61 years, IQR: 28–64, 0 F). Healthy volunteers (HVs, n = 9, median age: 45 years, IQR: 25–50, 4 F) were recruited by public advertisement. HVs were free of abdominal symptoms and had no history of gastrointestinal disease, no previous gastrointestinal surgery and were not on gastrointestinal medication (Table 1).
All participants were invited to undergo a proctoscopy to collect 7 rectal biopsies (1 for immunohistochemistry, 1 for RNA analysis, 3 for Ca2+ imaging and 2 biopsies were incubated for 24 hours in RPMI (Lonza, Verviers, Belgium) to collect supernatants12). Supernatants were stored at −80 °C until use.
Ca2+ imaging of human submucosal neurons
Biopsies were immediately processed to obtain the submucosal plexus, which was loaded with 1 µM Fluo-4 AM (Molecular Probes, Invitrogen, Merelbeke, Belgium) for Ca2+ imaging as previously described11. Fluorescence intensity recordings (Fi) were normalized to the starting value (Fo) and can therefore be expressed as a % of Fo. The difference (Δ) in amplitude between baseline and peak was calculated (Δ = Fmax/Fo − Fbaseline/Fo) and is therefore expressed as a %. Images were acquired at 2 Hz and collected by TILLVision software (TILL Photonics, Oberhausen, Germany). Data were analyzed by custom-written macros in IGOR-PRO (Wavemetrics, Lake Oswego, Oregon, USA)12. The response of submucosal neurons to capsaicin perfusion (1 ml/min for 5 seconds, 0.1-1-10 nM) (Sigma-Aldrich®, Diegem, Belgium) was compared between HVs, PI-HVs and PI-IBS patients. One µM TRPV1 antagonist SB-366791 (Tocris Bioscience, Bristol, United Kingdom) was used to block the capsaicin response.
Ca2+ imaging of murine dorsal root ganglia neurons
Lumbosacral (L5-S2) DRG neurons from 3 to 4 adult (8–12 weeks) wild type or Hrh1 knock-out mice were bilaterally excised under a dissection microscope, digested and cultured in complete medium (260 µl) on poly-D-lysine/laminin-coated glass coverslips as previously described32. Supernatants (140 µl) derived from either HVs or PI-IBS patients, combined or not with 10 µM histamine (Sigma-Aldrich®, Diegem, Belgium) and/or 1 µM Hrh1 antagonist pyrilamine (Sigma-Aldrich®, Diegem, Belgium), was added overnight. Cultured DRG neurons were subsequently loaded with 2 µM Fura-2AM (Invitrogen, Ghent, Belgium) for 20 minutes at 37 °C.
Intracellular Ca2+ concentration ([Ca2+]i) was measured and quantified as previously described12,32. Neurons were identified by a Krebs–based solution in which the KCl concentration was increased to 45 mM by iso-osmotic substitution of NaCl. The baseline was monitored for 120 s and the chamber was thereafter perfused with 10 nM capsaicin (Sigma-Aldrich®, Diegem, Belgium). TRPV1 positive DRG neurons were identified by a high dose of capsaicin (1 µM).
Afferent nerve recording
These experiments were performed at Queen Mary University of London. Experiments were performed using colons from 12 weeks old male C57BL/6 mice (Charles River UK, Ltd.). Single unit afferent nerve activity was recorded from teased lumbar splanchnic nerve fibers innervating the distal colon, as previously described33. Receptive fields were identified and characterized based on the criteria previously developed by Brierley et al.34,35. Only colonic afferents with presumptive nociceptor function were used. Mechanosensitivity was determined by repeated probing of the receptive field with a 0.6 g von Frey hair (vFh). Thereafter, rectal biopsy supernatants (100 µl) were applied for 12 minutes and mechanosensitivity was re-assessed (0.6 g vFh) post-supernatant. For data analysis, individual single unit discharge was discriminated using template matching wavemark software. For mechanosensitivity to vFh probing, the peak action potential discharge (Hz) over a 2 s period within the 3 s period of probing was determined for each probe and a mean response calculated from each set of 3. For chemosensitivity to biopsy supernatants, nerve discharge of individual fibers was expressed as a rate histogram (20 s) bin width. The peak change in activity during supernatant application was normalized to baseline (mean firing rate over 200 s prior to incubation).
RNA extraction and RT-qPCR
RNA was extracted from 5–10 mg colonic biopsies using RNeasy minikit (Qiagen, Hilden, Germany). cDNA was prepared from 2 µg total RNA using qScript cDNA supermix (Quanta Biosciences, Gaithersburg, Maryland, USA) according to the manufacturer’s instructions. RT-qPCR was performed to quantify inflammatory (IL-1β, IFN-ɣ, TNF-α, IL-2, IL-4, IL-5, IL-6, IL-10, IL-13, IL-17f, MCP-1) and neuronal TRPV1 marker mRNA expression using Probe Master Mix (Sigma-Aldrich®, Diegem, Belgium) or FastStart Essential DNA Green Master (Roche GmBH, Mannheim, Germany) (primer and probe sequences are listed in Supplementary Table 1). Gene expression was normalized to an endogenous reference gene, β-actin and relative gene expression was calculated as 2−∆∆Ct 36.
Immunostaining of rectal biopsies
Immune infiltration was assessed in rectal biopsies using standard immunohistochemistry. Biopsies were fixed in 4% paraformaldehyde (Sigma-Aldrich®, Diegem, Belgium) and put through a sucrose gradient before embedding in OCT-compound (Sakura Finetek, Antwerp, Belgium). Eight µm cryosections were incubated with 1% bovine serum albumin (BSA) (SERVA Electrophoresis GmbH, Heidelberg, Germany) in phosphate-buffered saline containing 0.3% Triton-X (Thermo Fisher Scientific Inc., Leusden, The Netherlands) for 60 min at room temperature (RT) to prevent non-specific antibody binding, followed by overnight incubation with the primary antibody at 4 °C. The following pimary antibodies were used for B cells (1:250 anti-CD20cy L26 (Dako Belgium nv/sa, Heverlee, Belgium)), CD3+-T cells (1:100 anti-CD3 [CA-3] ab82251 (Abcam, Cambridge, United Kingdom)), eosinophils (1:500 anti-major basic protein BMK13 (Merck Millipore, Solna, Sweden)), plasma cells (1:30 anti-Syndecan-1 [B-A38] (Abcam, Cambridge, United Kingdom)), immunoglobulin E+ (IgE+) (1:250 mouse anti-human MHE-18 (BioLegend, Fell, Germany)) and mast cells (1:500 anti-CD117 K963 (Sanbio B.V., Uden, The Netherlands). Plasma cells were detected after heat-mediated antigen-retrieval (2 × 5 minutes at 500 watt) in citrate buffer (pH = 6). For eosinophil staining, sections were pre-treated with 0.1% hydrogen peroxide (VWR, Leuven, Belgium) (10 minutes, RT). After wash, sections were incubated with secondary antibodies (1 hour in the dark, RT) and mounted in SlowFade® Gold (Life Technologies Europe B.V., Gent, Belgium).
Cytokine analysis in supernatants
Biopsy supernatant was collected and stored at −80 °C until analysis as described above. Cytokine levels of IL-4, IL-13, IFN-g, IL-1b, CXCL8, IL-10, IL-17a, TNFα, MCP-1 and IL-6 were quantified by cytometric bead array (BD Bioscience, Erembodegem, Belgium). Samples were acquired on FACSCanto flow cytometer (BD Bioscience) and analysed by FCAP v3.0 analysis software (Soft Flow Inc., Pecs, Hungary).
Enzyme linked immunosorbent assay (ELISA)
Histamine and tryptase levels in rectal biopsy supernatants were assessed by a commercially available histamine (IBL International GmbH, Hamburg, Germany) and tryptase (MyBioSource, San Diego, USA) kit, respectively, according to the manufacturer’s instructions.
All statistical analyses were performed using Graphpad Prism (La Jolla, USA). Continuous data were summarized by their mean and standard deviation. When deviations from normality were observed, medians and interquartile values were presented. Comparisons between groups were made using a t-test or Wilcoxon rank-sum test, as appropriate. Statistical significance is assumed when p ≤ 0.05 after Bonferroni correction for multiple testing.
Statistical analyses of the peak F340/380 ration for the Ca2+ imaging experiments were performed after correction for the individual baseline Ca2+. All values are expressed as means ± SEM from n mice or n cells treated with each of the individual supernatants. Statistical comparisons between 2 groups were performed by a Wilcoxon signed rank test or Mann–Whitney U test as appropriate or ANOVA when comparing more than 2 groups. Categorical data were analyzed by the Fischer’s exact test.
All animal experiments were carried out in accordance to the European Community Council guidelines and were approved by the local ethics committee of the KU Leuven (ECD P157/2014) or the UK Animals Scientific Procedures Act (1986). The human study was approved by the Medical Ethical Committee of the University Hospital of Leuven (study protocol S51573) and all experiments were performed in accordance with relevant guidelines and regulations. All participants gave written informed consent.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Kuiken, S. D., Lindeboom, R., Tytgat, G. N. & Boeckxstaens, G. E. Relationship between symptoms and hypersensitivity to rectal distension in patients with irritable bowel syndrome. Aliment. Pharmacol. Ther 22, 157–164 (2005).
Brierley, S. M. & Linden, D. R. Neuroplasticity and dysfunction after gastrointestinal inflammation. Nat. Rev. Gastroenterol. Hepatol 11, 611–627 (2014).
Spiller, R. & Campbell, E. Post-infectious irritable bowel syndrome. Curr. Opin. Gastroenterol 22, 13–17 (2006).
Gwee, K. A. et al. Increased rectal mucosal expression of interleukin 1beta in recently acquired post-infectious irritable bowel syndrome. Gut 52, 523–526 (2003).
Liebregts, T. et al. Immune activation in patients with irritable bowel syndrome. Gastroenterology 132, 913–920 (2007).
Spiller, R. C. et al. Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute Campylobacter enteritis and in post-dysenteric irritable bowel syndrome. Gut 47, 804–811 (2000).
Wang, L. H., Fang, X. C. & Pan, G. Z. Bacillary dysentery as a causative factor of irritable bowel syndrome and its pathogenesis. Gut 53, 1096–1101 (2004).
Barbara, G. et al. Mast cell-dependent excitation of visceral-nociceptive sensory neurons in irritable bowel syndrome. Gastroenterology 132, 26–37 (2007).
Campaniello, M. A. et al. Activation of colo-rectal high-threshold afferent nerves by Interleukin-2 is tetrodotoxin-sensitive and upregulated in a mouse model of chronic visceral hypersensitivity. Neurogastroenterol. Motil 28, 54–63 (2016).
Hughes, P. A. et al. Sensory neuro-immune interactions differ between Irritable Bowel Syndrome subtypes. Gut (2012).
Cirillo, C., Tack, J. & Vanden Berghe, P. Nerve activity recordings in routine human intestinal biopsies. Gut 62, 227–235 (2013).
Wouters, M. M. et al. Histamine Receptor H1-Mediated Sensitization of TRPV1 Mediates Visceral Hypersensitivity and Symptoms in Patients With Irritable Bowel Syndrome. Gastroenterology 150, 875–887 (2016).
Wouters, M. M. et al. Psychological comorbidity increases the risk for postinfectious IBS partly by enhanced susceptibility to develop infectious gastroenteritis. Gut (2015).
Chen, Y., Yang, C. & Wang, Z. J. Proteinase-activated receptor 2 sensitizes transient receptor potential vanilloid 1, transient receptor potential vanilloid 4, and transient receptor potential ankyrin 1 in paclitaxel-induced neuropathic pain. Neuroscience 193, 440–451 (2011).
Lapointe, T. K. et al. TRPV1 sensitization mediates postinflammatory visceral pain following acute colitis. Am. J Physiol Gastrointest. Liver Physiol 309, G87–G99 (2015).
Jin, X. & Gereau, R. W. Acute p38-mediated modulation of tetrodotoxin-resistant sodium channels in mouse sensory neurons by tumor necrosis factor-alpha. J. Neurosci 26, 246–255 (2006).
Gwee, K. A. et al. The role of psychological and biological factors in postinfective gut dysfunction. Gut 44, 400–406 (1999).
Lee, K. J. et al. The alteration of enterochromaffin cell, mast cell, and lamina propria T lymphocyte numbers in irritable bowel syndrome and its relationship with psychological factors. J. Gastroenterol. Hepatol 23, 1689–1694 (2008).
Chadwick, V. S. et al. Activation of the mucosal immune system in irritable bowel syndrome. Gastroenterology 122, 1778–1783 (2002).
Lomax, A. E., Bertrand, P. P. & Furness, J. B. Electrophysiological characteristics distinguish three classes of neuron in submucosal ganglia of the guinea-pig distal colon. Neuroscience 103, 245–255 (2001).
Jones, R. C. III, Xu, L. & Gebhart, G. F. The mechanosensitivity of mouse colon afferent fibers and their sensitization by inflammatory mediators require transient receptor potential vanilloid 1 and acid-sensing ion channel 3. J Neurosci 25, 10981–10989 (2005).
Blackshaw, L. A. Transient receptor potential cation channels in visceral sensory pathways. Br J Pharmacol 171, 2528–2536 (2014).
Woolf, C. J. & Ma, Q. Nociceptors–noxious stimulus detectors. Neuron 55, 353–364 (2007).
Mearin, F. et al. Pathogenic mechanisms of postinfectious functional gastrointestinal disorders: results 3 years after gastroenteritis. Scand. J Gastroenterol 44, 1173–1185 (2009).
Bennet, S. M. et al. Global Cytokine Profiles and Association With Clinical Characteristics in Patients With Irritable Bowel Syndrome. Am. J Gastroenterol (2016).
Barbara, G. et al. Activated mast cells in proximity to colonic nerves correlate with abdominal pain in irritable bowel syndrome. Gastroenterology 126, 693–702 (2004).
Buhner, S. et al. Neuronal activation by mucosal biopsy supernatants from irritable bowel syndrome patients is linked to visceral sensitivity. Exp. Physiol 99, 1299–1311 (2014).
Ohya, T. & Niitsu, M. Relative reactivities of histamine and indoleamines with acetaldehyde. Biol. Pharm. Bull 26, 1215–1218 (2003).
Wouters, M. M., Vicario, M. & Santos, J. The role of mast cells in functional GI disorders. Gut 65, 155–168 (2016).
Carabotti, M., Scirocco, A., Maselli, M. A. & Severi, C. The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems. Ann Gastroenterol 28, 203–209 (2015).
Braeye, T., DE, S. K., Wollants, E., Van, R. M. & Verhaegen, J. A. large community outbreak of gastroenteritis associated with consumption of drinking water contaminated by river water, Belgium, 2010. Epidemiol. Infect 143, 711–719 (2015).
Vriens, J. et al. Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4. Proc. Natl. Acad. Sci. USA 101, 396–401 (2004).
Hockley, J. R. et al. Multiple roles for NaV1.9 in the activation of visceral afferents by noxious inflammatory, mechanical, and human disease-derived stimuli. Pain 155, 1962–1975 (2014).
Brierley, S. M., Jones, R. C. III, Gebhart, G. F. & Blackshaw, L. A. Splanchnic and pelvic mechanosensory afferents signal different qualities of colonic stimuli in mice. Gastroenterology 127, 166–178 (2004).
Brierley, S. M. et al. Selective role for TRPV4 ion channels in visceral sensory pathways. Gastroenterology 134, 2059–2069 (2008).
Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods 25, 402–408 (2001).
GEB was funded by a governmental grant (Odysseus programme, G·0905·07) of the Research Foundation - Flanders (FWO) and by a KU Leuven university grant (Global Opportunities for Associations GOA 14.011). MMW is supported by a FWO postdoctoral fellowship (1248513 N). DB is supported by a FWO PhD fellowship (1127415 N). This work was funded by FWO research grant G·0699·10 N to GEB and MMW.
The authors declare that they have no competing interests.
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Histamine-mediated potentiation of transient receptor potential (TRP) ankyrin 1 and TRP vanilloid 4 signaling in submucosal neurons in patients with irritable bowel syndrome
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