High prevalence of viable Mycobacterium avium subspecies paratuberculosis in Crohn's disease
Juan L Mendoza1, Amparo San-Pedro, Esther Culebras
1Department of Gastroenterology, Hospital Clinico San Carlos, Martin Lagos s/n, 28040 Madrid, Spain. jmendozah@meditex.es
Aim:
To examine the detection rate of viable Mycobacterium avium subspecies paratuberculosis (MAP) in patients with inflammatory bowel disease [Crohn's disease (CD) and ulcerative colitis (UC)].
Methods:
Thirty patients with CD (15 with at least one NOD2/CARD15 mutation), 29 with UC, and 10 with no inflammatory bowel disease (IBD). were tested for MAP by polymerase chain reaction (specific IS900 fragment) and blood culture.
Results:
MAP DNA was detected in all original blood samples and 8-wk blood cultures (CD, UC and non-IBD). Positive MAP DNA status was confirmed by dot blot assays. All 69 cultures were negative by acid-fast Ziehl-Neelsen staining. Viable MAP, in spheroplast form, was isolated from the 18-mo blood cultures of all 30 CD patients, one UC patient, and none of the non-IBD controls. No association was found between positive MAP cultures and use of immunosuppressive drugs or CD-associated single nucleotide polymorphisms.
Conclusion:
MAP is widely present in our area and MAP DNA can be recovered from the blood of CD, UC and non-IBD patients. However, MAP spheroplasts were only found in CD patients.
Insights
Viable Mycobacterium avium subspecies paratuberculosis (MAP) was found in blood cultures of all Crohn's disease patients, but not in healthy controls. MAP DNA was detected in all inflammatory bowel disease patients.
Area of Science:
- Microbiology
- Gastroenterology
- Immunology
Background:
- Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), presents diagnostic challenges.
- The potential role of Mycobacterium avium subspecies paratuberculosis (MAP) in IBD pathogenesis remains a subject of investigation.
Purpose of the Study:
- To investigate the prevalence and viability of MAP in patients diagnosed with IBD.
- To compare MAP detection rates between CD, UC, and non-IBD control groups.
Main Methods:
- MAP detection utilized polymerase chain reaction (PCR) for IS900 fragment and blood cultures.
- Samples included 30 CD patients (15 with NOD2/CARD15 mutations), 29 UC patients, and 10 non-IBD controls.
- Viability assessed through prolonged blood cultures and confirmed with dot blot and Ziehl-Neelsen staining.
Main Results:
- MAP DNA was detected in blood samples and initial cultures of all participant groups (CD, UC, non-IBD).
- Acid-fast staining was negative for all samples.
- Viable MAP spheroplasts were exclusively isolated from 18-month blood cultures of all CD patients and one UC patient, but none from controls.
Conclusions:
- MAP DNA is frequently detected in the blood of individuals with and without IBD.
- Viable MAP, in a spheroplast form, was specifically identified in Crohn's disease patients, suggesting a potential association.
- No correlation was observed between MAP detection and immunosuppressive drug use or CD-associated genetic mutations.
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