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Prevalence of Mycobacterium avium subspecies paratuberculosis IS 900 DNA in biopsy tissues from patients with Crohn’s disease: histopathological and molecular comparison with Johne’s disease in Fars province of Iran

BMC Infectious Diseases volume 19, Article number: 23 (2019) Cite this article

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Abstract

Background

Crohn’s disease is a chronic enteritis of humans that affects the gastrointestinal tract, especially the terminal ileum, cecum and colon. The etiology of this disease is still unknown but seems to be multifactorial. There are reports about the potential link between Crohn’s disease in humans and the causative agent of Johne’s disease in ruminants. Because of the prevalence of Johne’s disease in the Fars Province of Iran, the aim of this study was to investigate the prevalence of MAP in the biopsy tissues of patients affected by Crohn’s disease in this area.

Methods

The study was performed from April 2015 to June 2017 at Namazi Hospital, Shiraz University of Medical Sciences, and School of Veterinary Medicine, Shiraz University, Shiraz, Iran. Intestinal biopsies of 30 patients (12 male and 18 female; mean age, 34 years; range 4–77 years) with the confirmed diagnosis of Crohn’s disease and 30 patients diagnosed as non-inflammatory bowel disease (19 male and 11 female; mean age, 38 years; range 13–68 years) were studied by molecular, histopathological and histochemical methods. Also, similar numbers of adult goats affected by Johne’s disease were studied, comparatively. DNA extractions of tissue specimens were subjected to PCR to amplify a 413-bp sequence of the IS900 gene.

Results

Using IS900-PCR, the overall prevalence of MAP in patients affected by Crohn’s disease and non-inflammatory bowel disease were 47 and 13%, respectively. In addition, the prevalence of MAP in goats affected by Johne’s disease was 70%. Using acid-fast histochemical staining, only 7% of Crohn’s disease patients were weakly positive as paucibacillary and 43% of Johne’s disease cases were moderate to strongly positive as multibacillary. Histopathologically, granulomatous enteritis (83 and 90%), lymphoplasmacytic enteritis (17 and 14%), edema and lymphangiectasia (67 and 96%), and vasculitis (20 and 73%) were common findings in Crohn’s and Johne’s diseases, respectively.

Conclusion

Our findings demonstrate a remarkable association between MAP and CD in this population, and support an etiologic relationship between MAP infection in humans and the development of CD. MAP infection in human tissue may display species-specific pathologic findings, as occurs with other zoonotic pathogens.

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Background

Crohn’s disease (CD) is an idiopathic chronic regional enteritis of human that most commonly affects terminal ileum and has the potential to affect any part of the gastrointestinal tract. The etiology of this disease is still unknown but seems to be multifactorial. The results of recent investigations have highlighted the potential link between CD in humans and Mycobacterium avium subspecies paratuberculosis or MAP [1, 2]. Millions of people all over the world are affected by CD and the rate of this disease is increasing in Iran [2]. The causative agent of Johne’s disease (JD) or paratuberculosis in ruminants is MAP which is characterized by chronic granulomatous enteritis [3]. Secretion of MAP from infected animals into their milk and excretion of MAP into their feces and therefore into the environment (feed, water, bedding and soil) make possible multiple vehicles for the transmission of MAP from infected animals to humans. MAP is able to form heat-resistant spores and persist in the host and environment [4]. MAP can survive the process of pasteurization due to its thick, waxy cell wall. MAP may lead to the development of CD in people with genetic predisposition [5]. MAP has been isolated from both raw and pasteurized milk [6,7,8,9,10] and from tissue biopsies and blood of Crohn’s patients [11, 12]. Even inhalation of MAP aerosols can result in infection [13]. Intestinal tissue (ileum, cecum and colon) is the most suitable site for detecting MAP bacteria. It is supposed that MAP in humans is in an obligate intracellular spheroplast form residing in the macrophages [9]. Acid-fast staining is a routine method for showing the presence of MAP in feces and tissue samples of JD [14,15,16,17,18,19,20]. An insertion sequence of IS900 is considered specific for MAP [21]. Therefore, IS900 polymerase chain reaction (PCR) is a rapid and routine method for MAP detection from different sources including feces, milk, intestinal tissues and mesenteric lymph nodes [22,23,24,25,26,27]. Because of the prevalence of JD in small ruminants of the Fars province of Iran, the present study was carried out to investigate the prevalence of MAP in the biopsy tissues of patients affected by CD in this area with regard to histopathological and molecular comparison with prevalent JD.

Methods

Study settings

The study was performed from April 2015 to June 2017 at Namazi Hospital, Shiraz University of Medical Sciences, and School of Veterinary Medicine, Shiraz University, Shiraz, Iran. We examined paraffin embedded archival tissues of 30 patients (12 male and 18 female; mean age, 34 years; range 4–77 years) with the confirmed diagnosis of CD and 30 patients diagnosed as non-inflammatory bowel disease (19 male and 11 female; mean age, 38 years; range 13–68 years) –using molecular, histopathological and histochemical methods. Also, 30 goats affected by JD and 30 healthy goat kids as control group were collected from Shiraz and Marvdasht slaughterhouses of Fars province, Iran. Ethical approval was obtained from the Ethical Committees of Shiraz University and Shiraz University of Medical Sciences. There have been no live animals used or tested on in this study. Also, we used only paraffin embedded tissues and the names and characteristics of the patients were confidential.

Collection of samples

Intestinal biopsy samples including ileum, or cecum and colon from 30 patients with confirmed diagnosis of CD (12 male and 18 female; mean age, 34 years; range 4–77 years) and also 30 patients (19 male and 11 female; mean age, 38 years; range 13–68 years) affected by non-inflammatory bowel disease (nIBD) as the control group were selected. Thirty paraffin embedded blocks of Crohn’s patients which were diagnosed before by histopathology were selected from Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran. These samples were used for acid-fast staining and molecular evaluations.

Also, fresh intestinal tissues including ileum, cecum and colon from 30 goats affected by JD and 30 healthy goat kids as control group were collected from Shiraz and Marvdasht slaughterhouses of Fars province, Iran. The double samples were coded and their characteristics were recorded. For molecular method, the tissue samples were stored at − 20 °C until further analysis. For histopathological confirmation and acid-fast staining, tissue samples were fixed in 10% neutral buffered formalin, processed routinely, embedded in paraffin, sectioned at 5 μm and used for hematoxylene eosin (H&E) staining.

Acid-fast staining method

Five μm tissue sections from paraffin blocks of all samples were used for acid-fast or Zeihl-Neelsen stain. Routinely, tissue specimens were deparaffinized and rinsed with consecutive dilutions of alcohol (96 to 70% ethanol). Slides were placed in hot Carbol fuchsin solution for 5 min. They were washed in running tap water and 1% acid alcohol until light pink and the color stopped. The slides were washed for 5 min and then rinsed in distilled water. Counterstaining was done using Methylene blue for 30 s. After rinsing in cold water, samples were allowed to dehydrate, and then cleared and coverslipped. According to a positive control slide of acid-fast stain (tissue samples of confirmed paratuberculosis) as represents mycobacteria, all fields of the stained tissue slides were observed under magnifications of × 400 and × 1000 oil immersion by light microscopy (Olympus, Tokyo, Japan). Visualization of any pink to red material with bacterial like morphology (especially inside cells) under 1000 magnification was interpreted as positive for acid-fast bacteria (AFB).

DNA extraction

DNA was extracted from formalin fixed paraffin embedded blocks of CD samples using GeneRead™DNA Formalin Fixed Paraffin Embedded Kit (QIAGEN®) and stored at −20_°C for PCR assays.

Total genomic DNA was extracted from goat samples for PCR assays. About 2 g of intestinal tissue was chopped with a sterile scalpel and transferred to a 2 ml sterile microtube. Then sterile distilled water was added to the chopped tissue to 2 ml volume and centrifuged at 13000 g for 30 s. The supernatant layer was discarded and this stage was repeated twice. Afterward, 500 μl of lysis buffer and 50 μl of proteinase k (CinnaGene) were added and it was stirred gently. After remaining overnight at 37 °C, 500 μl of phenol-chloroform isopropanol (25:24:1) was added to the sample and it was stirred for 15 min. After centrifuging for 10 min at 10000 g, the supernatant layer was transferred to another sterile micro tube and the equal volume of chloroform-isopropanol (24:1) was added and it was stirred for 2 min then centrifuged at 10000 g for 1 min. The supernatant layer was transferred to another sterile micro tube and ethanol 100% was added 2.5 times its volume. After storing at − 70 °C for 1 h, samples were left at room temperature until thawed, then centrifuged at 10000 g for 1 min. The supernatant fluid was removed and the pellet was washed in 1 ml ethanol 70% followed by centrifuging at 10000 g for 1 min. The supernatant fluid was removed and sample was left at room temperature until total ethanol evaporated and the pellet was dry. Finally, DNA extracted pellet was resuspended in 50 μl sterile distilled water and stored at −20_°C for PCR assays.

PCR of internal fragment of IS900

IS900 PCR was performed as described by Corti and Stephan with minor modifications [22]. DNA extractions were subjected to PCR in order to amplify a 413-bp sequence of the IS900 insertion element containing the probe target sequence. The PCR was carried out by final volume of 25 μl, containing 1× reaction buffer (CinnaGen), 5 mM MgCl2, 40 μM 2 deoxyribonucleoside- 5-triphosphate (dNTP; CinnaGen), 20 pmol of each primers (P90 5- GAA GGG TGT TCG GGG CCG TCG CTT AGG -3, P91 5- GGC GTT GAG GTC GAT CGC CCA CGT GAC -3) [26, 27], 0.5 U Tag DNA polymerase and 2 μl extracted DNA. Samples were amplified as follows: 94 °C for 5 min (1 cycle); 94 °C for 1 min, 59 °C for 1 min, 72 °C for 2 min (30 cycles); 72 °C for 7 min (1 cycle). The PCR products were finally electrophoresed on 1.5% safe stain agarose gel and the specific DNA fragment with the desired size of 413 bp was observed. DNA of the already identified positive case and sterilized distilled water were used as positive and negative controls, respectively.

Results

Histopathological findings

The most common histopathologic lesions of CD in the present study were chronic lymphoplasmacytic enteritis, granulomatous enteritis, mucosal ulceration, pyloric gland metaplasia, lymphoid hyperplasia, Paneth cell hyperplasia, lymphangiectasia, edema and goblet cell hyperplasia. Granulomatous enteritis was observed in 83% of CD patients. Among them, 63% of biopsies were seen with noncryptolytic granulomas without central necrosis and caseation (Fig. 1a) and 20% of CD patients were observed with diffuse granulomatous enteritis (Fig. 1b) as infiltration of many lymphocytes, plasma cells and macrophages in the mucosa and submucosa of affected intestines. Lymphoplasmacytic enteritis (Fig. 1c) was diagnosed in 17% of cases of CD with infiltration of many lymphocytes and plasma cells in the mucosa and submucosa of affected intestines. Epithelial aphthoid ulcerations and mucosal microulcerations were observed in 73% of cases (Fig. 1d). Also, intraepithelial lymphocytes and neutrophils were seen in the epithelium adjacent to ulcer. Infiltration of neutrophils in the affected crypts as cryptitis and crypt abscess were also found in 40 and 33% of cases, respectively. Neuronal hyperplasia was seen in 36% cases of Crohn’s biopsies.

Fig. 1
figure1

Histopathological lesions of Crohn’s disease, a Granulomatous ileitis: granuloma formation in the mucosa (arrow). b Mixed granulomatous enteritis is seen with Infiltration of lymphocytes and plasma cells in the mucosa. c Chronic lymphoplasmacytic enteritis: Infiltration of lymphocytes and plasma cells in the mucosa. d Epithelial patchy necrosis or ulceration of mucosal of ileum (arrow). e Pyloric gland metaplasia: compound acinar glands lined by antral type mucosa of stomach are observed in the lamina propria (arrow). f Paneth cell hyperplasia: These cells with numerous cytoplasmic granules are situated at the base of crypts of Liberkuhen glands (arrow) .H & E, ileum, human

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Increased size and diameter of lymphoid follicles in the Peyer’s patches of ileum were considered as lymphoid hyperplasia. It was seen in 33% of cases. Architectural abnormalities of the mucosa such as irregularity and blunting of the villi, atrophy of crypts and cystic dilation were also commonly found in the affected intestines. Replacement of the normal mucosal crypts of Leiberkuhn glands with antral type of stomach mucosa was diagnosed as pyloric gland metaplasia (Fig. 1e) in 40% of cases. In 17% of cases, Paneth cell hyperplasia in the ileum (Fig. 1f) was observed abnormally in the cecum and colon. These cells were situated at the base of crypts, the Leiberkuhn glands and filled with numerous prominent apical secretory acidophilic cytoplasmic granules. Lymphangiectasia and edema of mucosa and submucosa were seen as a common alteration in 67% of cases. Vasculitis in 20% and fibrinous thrombi in 30% of cases were diagnosed in mucosal and submucosal vessels. Goblet cell hyperplasia was diagnosed in 14% of cases in the ileum. Other less common findings included hypertrophy and hyperplasia of neural ganglia of the submucosa.

Most common microscopic lesions of JD were multifocal to diffuse granulomatous enteritis (multibacillary and paucibacillary forms), lymphangiectasia, edema, and lymphangitis. Granulomatous enteritis (Fig. 2a, b) was diagnosed in 90% cases of JD. Diffuse granulomatous enteritis as diffuse infiltration of epithelioid macrophages in the mucosa and submucosa of affected intestines. Diffuse mixed granulomatous enteritis (Fig. 2c) as mixed infiltration of epithelioid macrophages, lymphocytes and plasma cells in the mucosa and submucosa of affected intestines. Multinucleated giant cells were rarely seen in the affected tissues. In some villi, infiltration and aggregation of many epithelioid macrophages in the apical part make a drumstick like appearance to affected villi. By using acid-fast staining, diffuse granulomatous enteritis were divided to two forms including: multibacillary and paucibacillary lesions in 43 and 33% of cases, respectively. Also, a few of the neutrophils and eosinophils were admixed with other inflammatory cells in the lesions. Lymphoplasmacytic enteritis (Fig. 2d) was reported in 14% of JD cases as infiltration of lymphocytes and plasma cells in the mucosa and submucosa of affected intestines. Other common findings included lymphangiectasia (Fig. 2e) and edema of mucosa and submucosa in 96% and lymphangitis (Fig. 2f) in 73% of cases. Presence of lymphocytes in the submucosal neural ganglions (Fig. 2)f as lymphocytic neuritis (43%) was diagnosed. Increased size and diameter of lymphoid follicles in the Peyer’s patches of ileum were considered as lymphoid hyperplasia in 43% of cases. Atrophy of crypts associated with irregularity and blunting of the villi, were found commonly in the affected ilei. Other less common findings included reactive fibrosis in the mesenteric lymph nodes (10%), cryptitis (14%) and crypt abscess (10%). Comparative histopathological results between CD and JD are summarized in the Table 1.

Fig. 2
figure2

Histopathological lesions of Johne’s disease, a and b Granulomatous ileitis. Infiltration of epithelioid macrophages are seen in the mucosa. c Mixed granulomatous ileitis: Infiltration of epithelioid macrophages, lymphocytes and plasma cells in the mucosa and submucosa of ileum. d Lymphoplasmacytic enteritis. Diffuse infiltration of lymphocytes and plasma cells in the mucosa and submucosa. e Lymphangiectasia. Lymphatic dilation in the mucosa and submucosa. f Lymphangitis (starisk) and lymphocytic neuritis (arrow). H & E, ileum, goat

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Table 1 The comparative histopathological lesions of intestines between Crohn’s and Johne’s diseases
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Findings of acid-fast staining

The comparative results of acid-fast histochemical staining in the CD and JD samples are shown in the Table 2. All fields of each acid fast stained slide were observed for at least 30 min with total magnifications of × 400 and × 1000 (oil immersion) by light microscopy. Weakly positive acid-fast staining as paucibacillary form of granulomatous inflammation was observed in 7% of CD (Fig. 3a, b) and moderately to strongly positive in 47% of JD cases. Multibacillary form of granulomatous inflammation was not observed in CD samples (0%) whereas 43% of JD cases (Fig. 3c, d) were positive as multibacillary lesion.

Table 2 Comparative results of acid fast staining and IS900 PCR
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Fig. 3
figure3

Positive acid-fast staining of affected intestines as paucibacillary in Crohn’s disease (a and b) and multibacillary in Johne’s disease (c and d). Presence of pink to red material with bacterial like morphology are seen, especially inside cells. ZN staining, human, (× 1000)

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IS900 PCR findings

MAP specific IS900 gene with 413 bp was detected in 47% of CD patients (Fig. 4) and also in 70% of JD cases (Fig. 5). In the control groups, all of the samples of healthy control goat kids were PCR negative (0%), but MAP specific IS900 gene was detected in 13% of nIBD patients (Table 2).

Fig. 4
figure4

Gel electrophoresis of IS900 PCR products from Crohn’s patients. Lane M: 1 KB DNA ladder. Lane 1: Positive control MAP, Lane 2: Negative control, Lanes 3, 4, 5, 6, 7, 8 and 9: PCR products of 413 bp from Crohn’s biopsies samples, Lane 10: No product from biopsies samples

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Fig. 5
figure5

Gel electrophoresis of IS900 PCR products from intestinal tissue samples of Johne’s disease in goats. Lane M: 1 KB DNA ladder. Lane 1: Negative control, Lane 2: Positive control MAP, Lanes 4, 11,13,14,15,16,20,21 and 23: PCR product of 413 bp from tissue samples. Lanes 3,5,6,7,8,9,10,1217,18,19,25 and 26: No product from tissue samples

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Discussion

The results of this study showed a relatively high prevalence (47%) of MAP DNA in biopsies of CD patients and low prevalence (13%) in control nIBD patients in Fars province of Iran. Zamani et al. (2017) reported positivity for IS900 PCR in 64% of CD, 33% of ulcerative colitis (UC) and 9.7% of control nIBD samples from patients biopsies in Tehran province of Iran [2]. Speculation has existed for many years. JD is zoonotic and somehow causative of CD in human beings [3, 28]. CD as one of the main types of inflammatory bowel disease (IBD) is described as a relapsing disorder with high morbidity and uncertain pathogenesis that can occur from early childhood to late adulthood. Although the etiology of CD is largely complex and unknown, it is thought to be caused by a combination of genetic and environmental factors that affect the immune responses. Among environmental factors, MAP seems to have the important role in the pathogenesis of CD, despite conflicting reports. Some researchers showed the involvement of MAP in CD [2, 15, 24, 26, 29] whereas a number of reports could not confirm such association [6, 30,31,32]. In genetically susceptible individuals cell-mediated immune responses to intestinal bacteria seems to play an important role in its etiology.

In different provinces of Iran, prevalence of JD and presence of MAP in farms of small or large ruminants have been reported [33,34,35]. Therefore, during subclinical or clinical stages of JD, MAP is shed through feces and milk which can contaminate the environment and dairy products. The nature and pathology of CD in human is somehow similar to JD in ruminants. In the present study, similar histopathological changes including granulomatous enteritis, lymphoplasmacytic enteritis, edema, lymphangiectasia, fibrosis, vasculitis, cryptitis and crypt abscess were observed in both CD and JD. Also, other reported diagnostic features of CD such as patchy necrosis of epithelium, Paneth cell hyperplasia, nerve fiber hyperplasia, and architectural distortion associated with increased intraepithelial lymphocytes were in accordance with our results [36,37,38,39,40]. In spite of remarkable histopathologic similarities between CD and JD in our study, specific pathologic findings of CD patients (that were not found in JD) include ulceration, fibrosis, goblet cell hyperplasia, Paneth cell hyperplasia, thrombosis, nerve fiber hyperplasia, and architectural distortion. Although, there is no discussion in the veterinary literature of MAP infection causing these pathologic findings, there are some reports such as goblet cell hyperplasia of ileum in acute and chronic MAP infection in cattle [41, 42], thrombosis of lymphatic vessels in ileum of deer JD [43], multiple foci of ulceration in sheep JD [44]. MAP infection in human tissue may display species-specific pathologic findings, as occurs with other zoonotic pathogens. Van Kruiningen (1999) in a review report, concluded that presence of a little or superficial pathologic similarity between CD in humans and JD of animals, provides no support for association between MAP and CD [45].

In the present study, fibrosis of intestinal mucosa was found in 53% of CD patients and in 10% of mesenteric lymph nodes of JD cases. In agreement with our study, reactive fibrosis of affected mesenteric lymph nodes was reported in JD deer and sheep [44, 46]. Crypt abscesses as focal aggregation of neutrophils within the intestinal crypts was diagnosed in 33 and 10% of CD and JD cases, respectively. This lesion was reported by other studies in cattle and sheep affected by paratuberculosis [41, 46], and also in non-human primates MAP infection [47].

Infiltration of lymphocytes and macrophages in the mucosa and submucosa, crypts atrophy, lymphoid hyperplasia and the presence of microgranulomas in the mucosa of affected intestines were observed similarly in both CD and JD and are in agreement with other reports [18, 19, 48, 49]. In the present study, using acid-fast histochemical staining, only 7% of CD patients were weakly positive as paucibacillary and 43% of JD cases were moderate to strongly positive as multibacillary. Our findings about paucibacillary and multibacillary forms of granulomatous enteritis in JD are in agreement with previous reports [48, 49]. There are not many MAP organisms in the tissues of CD patients and only small quantities of the microorganism may be present. In these tissues, MAP occur in a round, coccoid form that stains with acid fast stains. Detection of MAP in tissues requires oil immersion microscopy and microscopic detection limit is governed more by bacterial burden than by staining method [17, 50]. In the JD cases with multibacillary lesions, mucosal atrophy and replacement of epithelioid macrophages instead of intestinal glands have been reported in other studies [51,52,53]. It has been suggested that paucibacillary and multibacillary lesions are associated with strong cell mediated and humoral immune responses, respectively [54, 55].

In this study, infiltration of neutrophils was more common in CD lesions than JD. Marks et al. (2006) described when the numbers of functional neutrophils are not enough for the effective clearance of bacteria; bacteria will be phagocytized by macrophages to make the granuloma and chronic inflammation typical of CD [56]. Similar to JD, granulomas without central caseous necrosis which were observed in the lamina propria of affected intestines in CD patients of our studies are in agreement with others [37, 53, 57]. These granulomas are not cryptolytic or dependent on crypt injury [56] but cryptolytic granulomas in ulcerative colitis patients was reported [58].

In our study, crypt irregularity was observed in CD biopsies. Crypt irregularity is characterized by crypt distortion (non-parallel crypts, variable diameter or cystically dilated crypts), crypt branching and crypt shortening [40]. Tanaka et al. (1999) have reported that crypts should be regarded as abnormal if more than two branched crypts exist in a well-orientated biopsy specimen [58]. While focal architectural abnormalities favor CD, pseudovillous appearance of the colorectal surface, crypt irregularity, and reduced crypt numbers and crypt epithelial polymorphs is proposed more consistent with a diagnosis of ulcerative colitis [59, 60].

In the present study, unlike JD, pyloric gland metaplasia was diagnosed in 40% of CD cases. It is referred as pseudopyloric gland metaplasia or glandular mucoid metaplasia that is a feature of chronic mucosal inflammation and related to mucosal ulceration and repair [38, 61]. In our study, Paneth cell metaplasia was diagnosed in 17% of cecal biopsies of CD patients. Tanaka et al. found a correlation between Paneth cell metaplasia and crypt architectural distortion of chronic IBD [62]. It is reported that Paneth cell numbers were significantly increased in IBD at all sites except the rectosigmoid in ulcerative colitis and the caecum and rectum in CD [63].

Nancy and Buckley (2008) stated that reports of significant number of positive MAP CD patients revealed that an association between MAP and CD does exist [29]. Unlike ruminants paratuberculosis, CD is not a lepromatoid disease with an abundance of MAP laden macrophages. Also, in initial stage of MAP infection, no macroscopic and histological lesions including acid-fast organism can be detected [64]. This study showed, unlike in JD cases, most of the CD intestinal lesions (93%) were acid-fast negative. Acid-fast stain is necessary for demonstrating the mycobacterial bacilli. Detection of one or more mycobacteria in an area of granulomatous inflammation is highly specific and indicative of infection. It is believed that more than 10 mycobacteria per milligram of tissue are usually necessary to detect the organism by light microscopy, so a negative stain does not exclude a diagnosis of mycobacterial infection [65]. This level of MAP in the tissue is needed in order for histochemical stains to show the organism, and there are not many MAP organisms in the tissue, because of the strong cell wall mediated immune response. In the present study, the acid-fast bacilli were detected in most of the JD intestinal lesions. This finding is in agreement with other investigations [7, 16,17,18]. Only small quantities of the microorganism are present in the tissues of CD [20]. The absence or sparcing of MAP in the mucosal lesions is related to strong cell-mediated immune response with poor or absent humoral response. The intracellular phenotype of MAP in Crohn’s patients does not illustrate an acid-fast-positive lipid rich mycobacterial cell wall. MAP in its protease resistant acid-fast negative phenotype parasitized immunoregulatory macrophage and other cells. It is associated with a variable immune dysregulation [50]. This matter describes why histological examinations cannot detect acid-fast cells in tissues of CD patients [28]. Paucibacillary form infections revealed that mycobacteria could only be visualized by careful examination under 1000 oil immersion [66].

Unlike CD, MAP in JD samples has intact cell walls and abundant acid-fast bacilli can be observed in multibacillary lesions. Hence, infected ruminants with JD, shed numerous MAP from feces and increase the risk of its transmission to humans. Bharathy et al. have detected MAP DNA in milk samples of goats [10]. This organism is a resistant bacterium to pasteurization temperature for having thick lipid cell wall [66, 67]. Consumption of milk and different dairy products like cheese can increase the risk of transmission to human [10, 21,22,23, 33, 67].

Several studies have revealed MAP DNA in intestinal biopsies, peripheral blood and breast milk samples of CD patients [5, 14, 30, 31, 68]. There are reports about confirmation of contamination of water sources, aerosols, dairy products, river waters, and even domestic tap water and survival from chlorine disinfection of MAP [69, 70]. The isolation and detection of MAP in breast milk of CD patients supports the possibility that it can be a systemic infection in humans [68]. It results in activation of immune system to development of inflammatory bowel disease [71].

In this study, despite the presence granulomatous lesions, MAP could not be detected by PCR in a number of CD patients. The absence of MAP DNA in the majority of our Crohn’s paraffin blocks may be explained by a strong cell-mediated immune response to MAP in humans with CD as discussed above, which results in paucibacillary lesions. Collins et al. (2000) used different methods including IS900 PCR to detect MAP in IBD patients and in controls and found IS900 was positive significantly in CD patients (19.0%) and UC patients (26.2%) than from controls (6.3%). The complex interplay of potential age-dependent effects, host genetic effects, immune responses, immunosuppressive drug therapy effects, BCG vaccination, rate of exposure to MAP or other risk factors on infection susceptibility to MAP must be taken into consideration in future studies [72]. The effect of anti-mycobacterial therapy on CD is unclear [73]. Also, McNees et al. (2015) expressed that MAP is widespread in dairy cattle and because of resistance to pasteurization and chlorination, humans are frequently exposed through contamination of food and water [74].

Also, PCR amplification can create false-negative results [75]. False-negative results (the specific error at issue) can be caused by a low number of MAP targets and/or PCR inhibitors.

Schwartz et al. (2000) described a higher frequency of MAP in CD patients (37%) than healthy controls (5.6%). They found MAP DNA at a higher percentage (86%) in surgically resected tissue samples in comparison to tissue biopsies (20%) and suggested that MAP may be located below the mucosal layer than on the apical surface area [31]. Therefore, larger specimens that contained the deeper portions of the bowel wall are more apt to yield positive results.

Our study supports the possible role of MAP in triggering CD, whereas low IS900 PCR detection rates were observed in the control nIBD group. Similar to results of this study, some researchers have obtained low prevalence of MAP in the intestinal tissues of nIBD patients [20, 76,77,78]. No study has done a long-term follow up on such persons to see if they remain healthy or are in the early stage of a disease induced by MAP. This could be CD or any number of other diseases linked with MAP such as sarcoidosis, Blau syndrome, type 1 diabetes, Hashimoto thyroiditis, and multiple sclerosis [79].

Conclusion

Our findings demonstrate a remarkable association between MAP and CD in this population, and support an etiologic relationship between MAP infection in humans and the development of CD. MAP infection in human tissue may display species-specific pathologic findings, as occurs with other zoonotic pathogens.

Abbreviations

AFS:

Acid-fast staining

CD:

Crohn’s disease

IBD:

Inflammatory bowel disease

JD:

Johne’s disease

MAP:

Mycobacterium avium subspecies paratuberculosis

nIBD:

Non-inflammatory bowel disease

PCR:

Polymerase chain reaction

UC:

Ulcerative colitis

References

  1. 1.

    Liverani E, Scaioli E, Cardamone C, Dal Monte P, Belluzzi A. Mycobacterium avium subspecies paratuberculosis in the etiology of Crohn’s disease, cause or epiphenomenon? World J Gastroenterol. 2014;20(36):1360–70.

  2. 2.

    Zamani S, Zali MR, Asadzadeh Aghdaei H, Sechi LA, Niegowska M, Caggiu E, et al. Mycobacterium avium subsp. paratuberculosis and associated risk factors for inflammatory bowel disease in Iranian patients. Gut Pathog. 2017;9:1–10.

  3. 3.

    Gelberg HB. Alimentary system and the peritoneum, omentum, mesentery, and peritoneal cavity. In: Zachary JF, editor. Pathologic basis of veterinary disease, 6th edition, Vol 1. St. Louis: Elsevier, Inc; 2017. p. 398–9.

  4. 4.

    Lamont EA, Bannantine JP, Armie’n A, Ariyakumar DS, Sreevatsan S. Identification and characterization of a spore-like morphotype in chronically starved Mycobacterium avium Subsp. paratuberculosis cultures. PLoS One. 2012;7(1):e30648.

  5. 5.

    Naser SA, Sagramsingh SR, Naser AS, Thanigachalam S. Mycobacterium avium subspecies paratuberculosis causes Crohn’s disease in some inflammatory bowel disease patients. World J Gastroenterol. 2014;20:7403–15.

  6. 6.

    Ellingson JL, Cheville JC, Brees D, Miller JM, Cheville NF. Absence of Mycobacterium avium subspecies paratuberculosis components from Crohn’s disease intestinal biopsy tissues. Clin Med Res. 2003;1(3):217–26.

  7. 7.

    Hruska K, Bartos M, Kralik P, Pavlik I. Mycobacterium avium subsp. paratuberculosis in powdered infant milk: paratuberculosis in cattle – the public health problem to be solved. Vet Med. 2005;50:327–35.

  8. 8.

    ZoiDimareli-Malli Z. Detection of Mycobacterium avium subsp. paratuberculosis in milk from clinically affected sheep and goats. Int J Appl Res Vet. 2010;8:44–50.

  9. 9.

    Patel A, Shah N. Mycobacterium avium subspecies paratuberculosis- incidence in milk and milk product, their isolation, enumeration, characterization, and role in human health. J Microbiol Immunol Infect. 2011;44:473–9.

  10. 10.

    Bharathy S, Gunaseelan L, Porteen K, Prabu K. Goat milk as a non - invasive sample for confirmation of Mycobacterium avium subspecies paratuberculosis by IS900 PCR. J Adv Vet Anim Res. 2017;1(3):136–9.

  11. 11.

    Sipos F, Galamb O, Wichmann B, Krenács T, Tóth K, Leiszter K, et al. Peripheral blood based discrimination of ulcerative colitis and Crohn's disease from non-IBD colitis by genome-wide gene expression profiling. Dis Markers. 2011;30(1):1–17.

  12. 12.

    Khan IA, Pilli S, Surendranath A, Rampal R, Chauhan SK, Tiwari V, et al. Prevalence and association of Mycobacterium avium subspecies paratuberculosis with disease course in patients with ulcero-constrictive ileocolonic disease. PLoS One. 2016;11(3):e0152063.

  13. 13.

    Eisenberg SWF, Koets ADP, Nielen M, Heederik D, Mortier R, Buck JD, et al. Intestinal infection following aerosol challenge of calves with Mycobacterium avium subspecies paratuberculosis. Vet Res. 2011;42:117.

  14. 14.

    Chiodini RJ, Chamberlin WM, Sarosiek J, McCallum RW. Crohn’s disease and the mycobacterioses: a quarter century later causation or simple association? Crit Rev Microbiol. 2012;38:52–93.

  15. 15.

    Sechi LA, Mura M, Tanda F, Amelia L, Antonello S, Giovanni F, et al. Identification of Mycobacterium avium subsp. paratuberculosis in biopsy specimens from patients with Crohn’s disease identified by in situ hybridization. J Clin Microbiol. 2001;39(12):4514–7.

  16. 16.

    Romero C, Hamdi A, Valentine JF, Naser SA. Evaluation of surgical tissue from patients with Crohn’s disease for the presence of Mycobacterium avium subspecies paratuberculosis DNA by in situ hybridization and nested polymerase chain reaction. Inflamm Bowel Dis. 2005;11(2):116–25.

  17. 17.

    Jeyanathan M, Boutros-Tadros O, Radhi J, Semret M, Bitton A, Behr MA. Visualization of Mycobacterium avium in Crohn’s tissue by oil-immersion microscopy. Microb Infect. 2007;9(14–15):1567–73.

  18. 18.

    Kheirandish R, Khodakaram-Tafti A, Hosseini A. The comparative evaluation of immunohistochemical and acid-fast staining with histopathological changes in naturally occurring paratuberculosis in sheep. Comp Clin Path. 2008;17:111–6.

  19. 19.

    Kheirandish R, Khodakaram-Tafti A, Hosseini A. Classification of lesions and comparison of immunohistochemical and acid-fast staining in diagnosis of naturally occurring paratuberculosis in goats. Small Ruminant Res. 2009;87:81–5.

  20. 20.

    Carvalho IA, Gonçalves Schwarz DG, Grasse Pietralonga PA, Silva Faria AC, Espechit Braga IF, Carvalho GD, et al. Presence of Mycobacterium avium subsp. paratuberculosis (MAP) in Brazilian patients with inflammatory bowel diseases and in controls. Sao Paulo Med J. 2016;134(1):13–29.

  21. 21.

    Selim A, El-Haig M, Galila ES, Gaede W. Direct detection of Mycobacterium avium subsp. paratuberculosis in bovine milk by multiplex real time PCR. Anim Sci Pap Rep. 2013;31(4):291–301.

  22. 22.

    Corti S, Stephan R. Detection of Mycobacterium avium subsp. paratuberculosis specific IS900 insertion sequences in bulk-tank milk samples obtained from different regions throughout Switzerland. BMC Microbiol. 2002;2:15.

  23. 23.

    O'Reilly CE, O'Connor L, Anderson W, Harvey P, Grant IR, Donaghy J, et al. Surveillance of bulk raw and commercially pasteurized cows’ milk from approved Irish liquid-milk pasteurization plants to determine the incidence of Mycobacterium paratuberculosis. Appl Environ Microbiol. 2004;70(9):5138–44.

  24. 24.

    Autschbach F, Eisold S, Hinz U, Zinser S, Linnebacher M, Giese T, et al. High prevalence of Mycobacterium avium subspecies paratuberculosis IS900 DNA in gut tissues from individuals with Crohn’s disease. Gut. 2005;54:944–9.

  25. 25.

    Wells JE, Bosilevac JM, Kalchayanand N, Arthur TM, Shackelford SD, Wheeler TL, et al. 2009. Prevalence of Mycobacterium avium subsp. paratuberculosis in ileocecal lymph nodes and on hides and carcasses from cull cows and fed cattle at commercial beef processing plants in the United States. J Food Prot. 2009;72:1457–62.

  26. 26.

    Mendoza JL, San-Pedro A, Culebras E, Cíes R, Taxonera C, Lana R, et al. High prevalence of viable Mycobacterium avium subspecies paratuberculosis in Crohn’s disease. World J Gastroenterol. 2010;16:4558–63.

  27. 27.

    Grant IR, Foddai ACG, Tarrant JC, Kunkel B, Hartmann FA, McGuirk S, et al. Viable Mycobacterium avium subspecies paratuberculosis isolated from calf milk replacer. J Dairy Sci. 2017;100:9723–35.

  28. 28.

    Grant IR. Zoonotic potential of Mycobacterium avium subsp. paratuberculosis: the current position. Appl Environ Microbiol. 2005;98:1282–93.

  29. 29.

    Nancy C, Buckley M. Mycobacterium avium paratuberculosis: infrequent human pathogen or public health threat? Washington DC: American Academy of Microbiology; 2008. p. 1–37.

  30. 30.

    Naser SA, Ghobrial G, Romero C, Valentine JF. Culture of Mycobacterium avium subspecies paratuberculosis from the blood of patients with Crohn’s disease. Lancet. 2004;364:1039–44.

  31. 31.

    Schwartz D, Shafran I, Romero C, Piromalli C, Biggerstaff J, Naser N, et al. Use of short-term culture for identifcation of Mycobacterium avium subsp. paratuberculosis in tissue from Crohn’s disease patients. Clin Microbiol Infect. 2000;6:303–7.

  32. 32.

    Ricanek P, Lothe SM, Szpinda I, Jorde AT, Brackmann S, Perminow G, et al. Paucity of mycobacteria in mucosal bowel biopsies from adults and children with early inflammatory bowel disease. J Crohns Colitis. 2010;4:561–6.

  33. 33.

    Khodakaram-Tafti A, Rashidi K. The pathology of goat paratuberculosis: gross and histopathological lesions in the intestines and mesenteric lymph nodes. J Vet Med. 2000;47:487–95.

  34. 34.

    Sadati R, Jafarpour M, Mirinargesi M, Nazemi A, Barghi A. Prevalence of Mycobacterium avium subsp. paratuberculosis in dairy cattle breed in northern Iran by nested-PCR. Global Vet. 2012;8(3):259–63.

  35. 35.

    Nemati M. Detection of Mycobacterium avium subsp. paratuberculosisin the mesenteric lymph nodes of goats by PCR and culture. J Livestock Sci Technol. 2015;3(2):56–60.

  36. 36.

    Bentley E, Jenkins D, Campbell F, Warren B. How could pathologists improve the initial diagnosis of colitis? Evidence from an international workshop. J Clin Pathol. 2002;55:955–60.

  37. 37.

    Seldenrijk CA, Morson BC, Meuwissen SGM, Schipper NW, Lindeman J, Meijer CJLM. Histopathological evaluation of colonic mucosal biopsy specimens in chronic inflammatory bowel disease: diagnostic implications. Gut. 1991;32:1514–20.

  38. 38.

    Buisine MP, Desreumaux P, Leteurtre E, Copin MC, Colombel JF, Porchet N, et al. Mucin gene expression in intestinal epithelial cells in Crohn’s disease. Gut. 2001;49:544–51.

  39. 39.

    Geboes K, Collins S. Structural abnormalities of the nervous system in Crohn’s disease and ulcerative colitis. Neurogastroenterol Mot. 1998;10:189–202.

  40. 40.

    Jenkins D, Balsitis M, Gallivan S, Dixon MF, Gilmour HM, Shepherd NA, et al. Guidelines for the initial biopsy diagnosis of suspected chronic idiopathic inflammatory bowel disease. The British Society of Gastroenterology Initiative. J Clin Pathol. 1997;50:93–105.

  41. 41.

    Khare S, Nunes JS, Figueiredo JF, Lawhon SD, Rossetti CA, Gull T, et al. Early phase morphological lesions and transcriptional responses of bovine ileum infected with Mycobacterium avium subsp. paratuberculosis. Vet Pathol. 2009;46:717–28.

  42. 42.

    Charavaryamath C, Gonzalez-Cano P, Fries P, Gomis S, Doig K, Scruten E, et al. Host responses to persistent Mycobacterium avium subspecies paratuberculosis infection in surgically isolated bovine ileal segments. Clin Vaccine Immunol. 2012;20(2):156–65.

  43. 43.

    Balseiro A, Garcia Marin JF, Solano P, Garrido JM, Prieto JM. Histopathological classification of lesions observed in natural cases of paratuberculosis in free-ranging fallow deer (Dama dama). J Comp Pathol. 2008;138:180–8.

  44. 44.

    Clarke CJ, Little D. The pathology of ovine paratuberculosis: gross and histological changes in the intestine and other tissues. Comp Path. 1996;114:419–37.

  45. 45.

    Van Kruiningen HJ. Lack of support for a common etiology in Johne’s disease of animals and Crohn’s disease in humans. Inflam Bowel Dis. 1999;5(3):183–91.

  46. 46.

    Nyange JFC, Gilmour NJL, Buxton D, Reid HW. Paratuberculosis in deer. In: Brown RD, editor. The biology of deer. New York: Springer; 1992.

  47. 47.

    McClure HM, Chiodini RJ, Anderson DC, Swenson RB, Thayer WR, Coutu JA. Mycobacterium paratuberculosis infection in a colony of stumptail macaques (Macaca arctoides). J Infect Dis. 1987;155(5):1011–9.

  48. 48.

    Hailat NQ, Hananeh W, Metekia AS, Stabe JR, Al-Majali A, Lafi S. Pathology of subclinical paratuberculosis (Johne’s disease) in Awassi sheep with reference to its occurrence in Jordan. Vet Med. 2010;55(12):590–602.

  49. 49.

    Kheirandish R, Sami M, Khalili M, Shafaei K, Azizi S. Diagnosis of paratuberculosis in fresh and paraffin embedded samples by histopathology, PCR and immunohistochemistry techniques. Bulg J Vet Med. 2017;20(4):339–7.

  50. 50.

    Hermon-Taylor J, Bull TJ. Crohn’s disease caused by Mycobacterium avium subspecies parauberculosis: a public health tragedy whose resolution is long overdue. J Med Microbiol. 2002;51:3–6.

  51. 51.

    Dennis MM, Reddacliff LA Whittington RJ. Longitudinal study of clinicopathological features of Johne’s disease in sheep naturally exposed to Mycobacterium avium subspecies paratuberculosis. Vet Pathol. 2011;48:565–75.

  52. 52.

    Gulliver EL, Plain KM, Begg DJ, Whittington RJ. Histopathological characterization of cutaneous delayed- type hypersensitivity and correlations with intestinal pathology and systemic immune responses in sheep with paratuberculosis. J Comp Pathol. 2015;153:67–80.

  53. 53.

    Awadin WF, Moustafa SH, Abd El-Mottaleb E, EL-Morshidy Y. Pathological studies on Johne's disease induced enteritis in Egyptian cattle. Int J Agri Sci Vet Med. 2016;4:4.

  54. 54.

    Chiodini RJ. Immunology: resistance to pratuberculosis. In: Sweeny RW, editor. Veterinary clinics of North America: food animal practice. Paratuberculosis (Johne’s disease). Philadelphia: WB Saunders Company; 1996. p. 313–43.

  55. 55.

    Burrells C, Clarke CJ, Colston A, Kay JM, Porter J, Little D, et al. A study of immunological responses of sheep clinically-affected with paratuberculosis (Johne’s disease), the relationship of blood, mesenteric lymph node and intestinal lymphocyte responses to gross and microscopic pathology. Vet Immunol Immunopathol. 1998;66:343–58.

  56. 56.

    Marks DJ, Harbord MW, MacAllister R, Rahman FZ, Young J, Al-Lazikani B, et al. Defective acute inflammation in Crohn’s disease: a clinical investigation. Lancet. 2006;367:668–78.

  57. 57.

    Dundas SA, Dutton J, Skipworth P. Reliability of rectal biopsy in distinguishing between chronic inflammatory bowel disease and acute self-limiting colitis. Histopathol. 1997;31:60–6.

  58. 58.

    Tanaka M, Riddell RH, Saito H, Soma Y, Hidaka H, Kudo H. Morphologic criteria applicable to biopsy specimens for effective distinction of inflammatory bowel disease from other forms of colitis and of Crohn’s disease from ulcerative colitis. Scand J Gastroenterol. 1999;34:55–67.

  59. 59.

    Magro F, Langner C, Driessen A, Ensari A, Geboes K, Mantzaris GJ, et al. European consensus on the histopathology of inflammatory bowel disease on behalf of the European Society of Pathology (ESP) and the European Crohn’s and colitis organisation (ECCO). J Crohn's Colitis. 2013;7:827–51.

  60. 60.

    Mahadeva U, Martin JP, Patel NK, Price AB. Granulomatous ulcerative colitis: a re-appraisal of the mucosal granuloma in the distinction of Crohn’s disease from ulcerative colitis. Histopathol. 2002;41:50–5.

  61. 61.

    Goldstein N, Dulai M. Contemporary morphologic definition of backwash ileitis in ulcerative colitis and features that distinguish it from Crohn’s disease. Am J Surg Pathol. 2006;126:365–76.

  62. 62.

    Tanaka M, Saito H, Kusumi T, Fukuda SH, Shimoyama T, Sasaki Y, et al. Spatial distribution and histogenesis of colorectal Paneth cell metaplasia in idiopathic inflammatory bowel disease. J Gastroenerol Hepatol. 2001;16:12.

  63. 63.

    Simmonds N, Furman M, Karanika E, Phillips A, WH Bates A. Paneth cell metaplasia in newly diagnosed inflammatory bowel disease in children. BMC Gastroenterol. 2014;14:93.

  64. 64.

    Waters WR, Miller JM, Palmer MV, Stabel JR, Jones DE, Koistinen KA, et al. Early induction of humoral and cellular immune responses during experimental Mycobacterium avium subsp. paratuberculosis infection of calves. Infect Immunol. 2013;71:5130–8.

  65. 65.

    Jeyanathan M, Alexander DC, Turenne CY, Girard C, Behr MA. Evaluation of in situ methods used to detect Mycobacterium avium subsp. paratuberculosis in samples from patients with Crohn's disease. J Clin Microbiol. 2006;44(8):2942–50.

  66. 66.

    Grant IR, Ball HJ, Rowe MT. Incidence of Mycobacterium paratuberculosis in bulk raw and commercially pasteurized cows’ milk from approved dairy processing establishments in the United Kingdom. Appl Environ Microbiol. 2002;68:2428–35.

  67. 67.

    Anzabi Y, Hanifian S. Detection of Mycobacterium avium subspecies paratuberculosis in pasteurized milk by IS900 PCR and culture method. Afr J Microbiol Res. 2012;6:1453–6.

  68. 68.

    Naser SA, Schwartz D, Shafran I. Isolation of Mycobacterium avium subsp paratuberculosis from breast milk of Crohn’s disease patients. Am J Gastroenterol. 2000;95:1094–5.

  69. 69.

    Gill CO, Saucier L, Meadus WJ. Mycobacterium avium subsp. paratuberculosis in dairy products, meat, and drinking water. J Food Prot. 2011;74:480–99.

  70. 70.

    Rhodes G, Richardson H, Hermon-Taylor J, Weightman A, Higham A, Pickup R. Mycobacterium avium subspecies paratuberculosis: human exposure through environmental and domestic aerosols. Pathogens. 2014;3:577–95.

  71. 71.

    Baumgart DC, Sandborn WJ. Crohn’s disease. Lancet. 2012;380:1590–605.

  72. 72.

    Collins MT, Lisby G, Moser C, Chicks D, Christensen S, Reichelderfer M, et al. Results of multiple diagnostic tests for Mycobacterium avium subsp. paratuberculosis in patients with inflammatory bowel disease and in controls. J Clin Microbiol. 2000;38(12):4373–81.

  73. 73.

    Peyrin-Biroulet L, Neut C, Colombel LF. Antimycobacterial therapy in Crohn’s disease: game over? Gastroenterol. 2007;132(7):2594–8.

  74. 74.

    McNees AL, Markesich D, Zayyani NR, Graham DY. Mycobacterium paratuberculosis as a cause of Crohn's disease. Expert Rev Gastroenterol Hepatol. 2015;9(12):1523–34.

  75. 75.

    Acharya KR, Dhand NK, Whittington RJ, Plain KM. PCR inhibition of a quantitative pcr for detection of Mycobacterium avium subspecies paratuberculosis DNA in feces: diagnostic implications and potential solutions. Front Microbiol. 2017;8:115.

  76. 76.

    Bull TJ, McMinn EJ, Sidi-Boumedine K, Skull A, Durkin D, Neild P, et al. Detection and verification of Mycobacterium avium subsp. paratuberculosis in fresh ileocolonic mucosal biopsy specimens from individuals with and without Crohn’s disease. J Clin Microbiol. 2003;41:2915–23.

  77. 77.

    Feller M, Huwiler K, Stephan R, Altpeter E, Shang A, Furrer H, et al. Mycobacterium avium subspecies paratuberculosis and Crohn’s disease: a systematic review and meta-analysis. Lancet Infect Dis. 2007;7:607–13.

  78. 78.

    Abubakar I, Myhill D, Aliyu SH, Hunter PR. Detection of Mycobacterium avium subspecies paratuberculosis from patients with Crohn’s disease using nucleic acid-based techniques: a systematic review and meta-analysis. Inflamm Bowel Dis. 2008;14:401–10.

  79. 79.

    Sechi LA, Dow CT. Mycobacterium avium subspecies paratuberculosis zoonosis the hundred year war-beyond Crohn’s disease. Front Immunol. 2015;6:96.

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Acknowledgments

The authors would like to appreciate the financial support of Shiraz University and Shiraz University of Medical Sciences, Iran. We wish to thank Mrs. Jokar, Mr. Zare also Mrs. Mansouri for their technical assistance.

Funding

This work was supported by funds from Shiraz University, Shiraz, Iran (94GRD1M1310). The funder had no role in study design, data collection and analysis, decision to publish or preparation of manuscript.

Availability of data and materials

The datasets used and/or analyzed during this study are available from the corresponding author on reasonable request.

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Affiliations

  1. Department of Pathology, School of Veterinary Medicine, Shiraz University, PO Box 71345-1731, Shiraz, Iran

    • Forough Zarei-Kordshouli
    •  & Azizollah Khodakaram-Tafti

  2. Department of Pathology, Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

    • Bita Geramizadeh

Authors

  1. Search for Forough Zarei-Kordshouli in:

  2. Search for Bita Geramizadeh in:

  3. Search for Azizollah Khodakaram-Tafti in:

Contributions

AKHT and BG conceived and designed the study and critically revised the manuscript. FZK contributed to sample collection and performed laboratory tests. AKHT, BG and FZK analyzed the data and drafted the manuscript. AKHT, BG and FZK participated in the study investigation. All the authors have read and approved the final manuscript.

Corresponding author

Correspondence to Azizollah Khodakaram-Tafti.

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Ethical approval was obtained from the Ethical Committees of Shiraz University and Shiraz University of Medical Sciences. A written informed consent was signed before enrollment, for participants under 18 years old the informed consent was signed by their respective guardians before enrollment. There have been no live animals used or tested on in this study. Also, we used only paraffin embedded tissues and the name and characteristics of the patients have not been revealed. Confidentiality of the information was assured through handling the information by locking the document with a password, storing in a file by assigning a code number to it and omitting the name of participants. Written informed consent has been obtained from the patients.

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Zarei-Kordshouli, F., Geramizadeh, B. & Khodakaram-Tafti, A. Prevalence of Mycobacterium avium subspecies paratuberculosis IS 900 DNA in biopsy tissues from patients with Crohn’s disease: histopathological and molecular comparison with Johne’s disease in Fars province of Iran. BMC Infect Dis 19, 23 (2019) doi:10.1186/s12879-018-3619-2

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Keywords

  • IS900-PCR
  • Crohn’s disease
  • Johne’s disease
  • Mycobacterium avium subsp. paratuberculosis

BMC Infectious Diseases

ISSN: 1471-2334

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