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High Prevalence of Mycoplasma pneumoniae in Intestinal Mucosal Biopsies from Patients with Inflammatory Bowel Disease and Controls

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Abstract

Intestinal microflora are believed to play an important role in the pathogenesis of inflammatory bowel disease (IBD). Mycoplasma have been suggested previously as organisms of ubiquitous distribution with the potential to cause inflammatory diseases, including IBD in susceptible individuals. The aim of this study was to determine the frequency of the presence of M. pneumoniae DNA in intestinal biopsies from patients with IBD and non-IBD controls using a microplate polymerase chain reaction–hybridization assay (PCR-ELISA). A total of 260 endoscopic biopsies (49 from 19 patients with Crohn's disease, 76 from 27 patients with ulcerative colitis, and 135 from 43 non-IBD controls) were used in this study. Overall, M. pneumoniae-specific DNA was detected in 100 endoscopic biopsy samples (38.5%). Among them, the detection rate of M. pneumoniae DNA was significantly higher in biopsies from patients with CD (59.2%) than in those from patients with UC (26.3%) or non-IBD controls (37.7%) (χ2 = 13.65, P ≤ 0.001). The high prevalence of M. pneumoniae in both IBD patients and controls suggest this organism is ubiquitous and may persist in the intestinal mucosa. Epidemiological studies in IBD suggest acquisition of some agents early in life probably during epidemics in temperate latitudes. M. pneumoniae could be one of the ubiquitous agents implicated in the pathogenesis of IBD.

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REFERENCES

  1. Walmsley RS, Anthony A, Sim R, Pounder RE, Wakefield AJ: Absence of Escherichia coli, Listeria monocytogenes, and Klebsiella pneumoniae antigens within inflammatory bowel disease tissues. J Clin Pathol 51:657–661, 1998

    Google Scholar 

  2. Taylor-Robinson D: Infections due to species of Mycoplasma and Ureaplasma: An update. Clin Infect Dis 23:671–682, 1996

    Google Scholar 

  3. Baseman J, Tully J: Mycoplasmas: Sophisticated, reemerging, and burdened by their notoriety. Emerg Infect Dis 3:21–32, 1997

    Google Scholar 

  4. Hoffman R, O'ullivan F, Schafermeyer K, Moore T, Roussell D, Watson-McKown R, et al: Mycoplasma infection and rheumatoid arthritis: Analysis of their relationship using immunoblotting and an ultrasensitive polymerase chain reaction detection method. Arthritis Rheum 40:1219–1228, 1997

    Google Scholar 

  5. Schaeverbeke T, Gilroy C, Bebear C, Dehais J, Taylor-Robinson D: Mycoplasma fermentans, but not M. penetrans, detected by PCR assays in synovium from patients with rheumatoid arthritis and other rheumatic disorders. J Clin Pathol 49:824–828, 1996

    Google Scholar 

  6. Narita M, Matsuzono Y, Togashi T, Kajii N: DNA diagnosis of central nervous system infection by Mycoplasma pneumoniae. Pediatrics 90:550–553, 1992

    Google Scholar 

  7. Miettinen A: Mycoplasma hominis in patients with pelvic inflammatory disease. Isr J Med Sci 23:713–716, 1987

    Google Scholar 

  8. Perez C, Mendoza H, Hernandez R, Valcayo A, Guarch R: Leukocytoclastic vasculitis and polyarthritis associated with Mycoplasma pneumoniae infection. Clin Infect Dis 25:154–155, 1997

    Google Scholar 

  9. Kumada S, Kusaka H, Okaniwa M, Kobayashi O, Kusunoki S: Encephalomyelitis subsequent to mycoplasma infection with elevated serum anti-Gal C antibody. Pediatr Neurol 16:241–244, 1997

    Google Scholar 

  10. Taylor-Robinson D, Schaeverbeke T: Mycoplasmas in rheumatoid arthritis and other human arthritides. J Clin Pathol 49:781–782, 1996

    Google Scholar 

  11. Fleischhauer P, Huben U, Mertens H, Sethi KK, Thurmann D: Demonstration of Mycoplasma pneumoniae in cerebrospinal fluid in acute polyneuritis. Dtsch Med Wochenschr 97:678–682, 1972

    Google Scholar 

  12. Meseguer MA, de Rafael L, Vidal ML: Stevens-Johnson syndrome with isolation of Mycoplasma pneumoniae from skin lesions. Eur J Clin Microbiol 5:167–168, 1986

    Google Scholar 

  13. Prattichizzo FA, Simonetti I, Galetta F: Carditis associated with Mycoplasma pneumoniae infection. Clinical aspects and therapeutic problems. Minerva Cardioangiol 45:447–450, 1997

    Google Scholar 

  14. Kenney RT, Li JS, Clyde WA Jr, Wall TC, O'Connor CM, Campbell PT, et al: Mycoplasmal pericarditis: Evidence of invasive disease. Clin Infect Dis 17:S58–S62, 1993

    Google Scholar 

  15. Jori GP, De Vargas F, Altucci P: Mycoplasmas in chronic ulcerative colitis: A negative study. Pathol Microbiol 31:209–214, 1968

    Google Scholar 

  16. van Kruiningen H, Colombel J, Cartun R, Whitlock R, Koopmans M, Kangr H, et al: An in-depth study of Crohn' disease in two French families. Gastroenterology 104:351–360, 1993

    Google Scholar 

  17. Katseni V, Gilroy C, Ryait B, Ariyoshi K, Bieniasz P, Weber JN et al: Mycoplasma fermentans in individuals seropositive and seronegative for HIV-1. Lancet 341:271–273, 1993

    Google Scholar 

  18. Sharma S, Brousseau R, Kasatiya S: Detection and confirmation of Mycoplasma pneumoniae in urogenital specimens by PCR. J Clin Microbiol 36:277–280, 1998

    Google Scholar 

  19. Goulet M, Dular R, Tully JG, Billowes G, Kasatiya S: Isolation of Mycoplasma pneumoniae from the human urogenital tract. J Clin Microbiol 33:2823–2825, 1995

    Google Scholar 

  20. Haier J, Nasralla M, Franco AR, Nicolson GL: Detection of mycoplasmal infections in blood of patients with rheumatoid arthritis. Br J Rheumatol 38:504–509, 1999

    Google Scholar 

  21. Tully JG, Rose DL, Baseman JB, Dallo SF, Lazzell AL, Davis CP: Mycoplasma pneumoniae and Mycoplasma genitalium mixture in synovial fluid isolate. J Clin Microbiol 33:1851–1855, 1995

    Google Scholar 

  22. Saglie R, Cheng L, Sadighi R: Detection of Mycoplasma pneumoniae DNA within diseased gingiva by in situ hybridization using a biotin-labeled probe. J Periodontol 59:121–123, 1988

    Google Scholar 

  23. Hua J, Birac C, Megraud F: PCR-based RAPD (random amplified polymorphic DNA) ‘fingerprinting’ of clinical isolates of Helicobacter pylori. In Helicobacter pylori: Techniques for Clinical Diagnosis and Basic Research. A Lee, F Megraud (eds). London, WB Saunders, 1996, p; 121–127

    Google Scholar 

  24. Cadieux N, Lebel P, Brousseau R: Use of a triplex polymerase chain reaction for the detection and differentiation of Mycoplasma pneumoniae and Mycoplasma genitalium in the presence of human DNA. J Gen Microbiol 139:2431–2437, 1993

    Google Scholar 

  25. Fink C, Sillis M, Read S, Butler L, Pike M: Neurological disease associated with Mycoplasma penumoniae infection. PCR evidence against a direct invasive mechanism. J Clin Pathol: Mol Pathol 48:M51–M54, 1995

    Google Scholar 

  26. Abele-Horn M, Busch U, Nitschko H, Jacobs E, Bax R, Pfaff F, et al: Molecular approaches to diagnosis of pulmonary diseases due to Mycoplasma pneumoniae. J Clin Microbiol 36:548–551, 1998

    Google Scholar 

  27. Herrmann R, Reiner B: Mycoplasma pneumoniae and Mycoplasma genitalium: A comparison of two closely related bacterial species. Curr Opin Microbiol 1:572–579, 1998

    Google Scholar 

  28. Bowe PS, Van Kruiningen HJ, Rosendal S: Attempts to produce granulomatous colitis in boxer dogs with a mycoplasma. Can J Comp Med 46:430–433, 1982

    Google Scholar 

  29. Rosendal S: Canine mycoplasmas: Their ecologic niche and role in disease. J Am Vet Med Assoc 180:1212–1214, 1982

    Google Scholar 

  30. Jocobs E: Mycoplasma pneumoniae virulence factors and the immune response. Rev Med Microbiol 2:83–90, 1991

    Google Scholar 

  31. Shibata K, Hasebe A, Sasaki T, Watanabe T: Mycoplasma salivarium induces interleukin-6 and interleukin-8 in human gingival fibroblasts. FEMS Immunol Med Microbiol 19: 275–283, 1997

    Google Scholar 

  32. Schaffner E, Opitz O, Pietsch K, Bauer G, Ehlers S, Jacobs E: Human pathogenic Mycoplasma species induced cytokine gene expression in Epstein-Barr virus (EBV)-positive lymphoblastoid cell lines. Microb Pathog 24:257–262, 1998

    Google Scholar 

  33. Brand JM, Neustock P, Kruse A, Alvarez-Ossorio L, Schnabel A, Kirchner H: Stimulation of whole blood cultures in patients with ankylosing spondylitis by a mitogen derived from Mycoplasma arthritidis (MAS) and other mitogens. Rheumatol Int 16:207–211, 1997

    Google Scholar 

  34. Roediger W: A new hypothesis for the aetiology of Crohn' disease-evidence from lipid metabolism and intestinal tuberculosis. Postgrad Med J 67:666–671, 1991

    Google Scholar 

  35. Kangro H, Chong S, Hardiman A, Heath R, Walker-Smith J: A prospective study of viral and mycoplasma infections in chronic inflammatory bowel disease. Gastroenterology 98:549–553, 1990

    Google Scholar 

  36. Bhat P, Boulter EA, Rajan D, Shanthakumari S, Kapadia CR, Baker SJ: Mycoplasma in the upper gastrointestinal tracts of southern Indian control subjects and patients with tropical sprue. Am J Clin Pathol 59:825–828, 1973

    Google Scholar 

  37. Altucci P, Jori GP, Manguso L, Varone GL: Failure to isolate mycoplasmas from upper small intestine of man. Pathol Microbiol 37:181–184, 1971

    Google Scholar 

  38. Leng Z, Kenny GE, Roberts MC: Evaluation of the detection limits of PCR for identification of Mycoplasma pneumoniae in clinical samples. Mol Cell Probes 8:125–130, 1994

    Google Scholar 

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Chen, W., Li, D., Paulus, B. et al. High Prevalence of Mycoplasma pneumoniae in Intestinal Mucosal Biopsies from Patients with Inflammatory Bowel Disease and Controls. Dig Dis Sci 46, 2529–2535 (2001). https://doi.org/10.1023/A:1012352626117

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