Microorganisms (Jun 2023)

Viable <i>Mycobacterium avium</i> subsp. <i>paratuberculosis</i> Colonizes Peripheral Blood of Inflammatory Bowel Disease Patients

  • Maria Manuela Estevinho,
  • José Cabeda,
  • Mafalda Santiago,
  • Elisabete Machado,
  • Ricardo Silva,
  • Mary Duro,
  • Inês Pita,
  • Rui Morais,
  • Guilherme Macedo,
  • Tim J. Bull,
  • Fernando Magro,
  • Amélia Sarmento

DOI
https://doi.org/10.3390/microorganisms11061520
Journal volume & issue
Vol. 11, no. 6
p. 1520

Abstract

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Pathobionts, particularly Mycobacterium avium subsp. paratuberculosis (MAP) and Escherichia coli isolates with adherence/invasive ability (AIEC) have been associated with inflammatory bowel disease (IBD), particularly Crohn’s disease (CD). This study aimed to evaluate the frequency of viable MAP and AIEC in a cohort of IBD patients. As such, MAP and E. coli cultures were established from faecal and blood samples (with a total n = 62 for each) of patients with CD (n = 18), ulcerative colitis (UC, n = 15), or liver cirrhosis (n = 7), as well as from healthy controls (HC, n = 22). Presumptive positive cultures were tested by polymerase chain reaction (PCR), for a positive confirmation of MAP or E. coli identity. E. coli-confirmed isolates were then tested for AIEC identity using adherence and invasion assays in the epithelial cell line of Caco-2 and survival and replication assays in the macrophage cell line of J774. MAP sub-culture and genome sequencing were also performed. MAP was more frequently cultured from the blood and faecal samples of patients with CD and cirrhosis. E. coli presumptive colonies were isolated from the faecal samples of most individuals, in contrast to what was registered for the blood samples. Additionally, from the confirmed E. coli isolates, only three had an AIEC-like phenotype (i.e., one CD patient and two UC patients). This study confirmed the association between MAP and CD; however, it did not find a strong association between the presence of AIEC and CD. It may be hypothesized that the presence of viable MAP in the bloodstream of CD patients contributes to disease reactivation.

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