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. Author manuscript; available in PMC: 2014 Feb 8.
Published in final edited form as: N Engl J Med. 2013 Aug 8;369(6):517–528. doi: 10.1056/NEJMoa1211115

Figure 3. Abundance of Bradyrhizobium enterica in Samples Obtained from Patients with Cord Colitis, as Compared with Control Samples.

Figure 3

B. enterica was more abundant in samples obtained from patients with the cord colitis syndrome (CCS) than in samples obtained from healthy controls, patients with colon cancer, or patients with graft-versus-host disease (GVHD). In addition, B. enterica was present in colon-biopsy samples from three additional patients with cord colitis. In Panels A through F, the top lanes show amplification of a B. enterica target after 35 cycles of a polymerase-chain-reaction (PCR) assay, and the bottom lanes show amplification of a human actin target after 35 PCR cycles. A lane containing reagents but no DNA (no-template control) is indicated by 0. Shown are results for five healthy control specimens (p1 through p5) (Panel A), five colon-cancer specimens (c1 through c5) (Panel B), three colon-biopsy specimens from patients with pathologically confirmed GVHD (g1 through g3) (Panel C), and DNA from temporally distinct colon-biopsy samples from Patient 4 (4a, 4b, 4c, and 4e) (Panel D), from Patient 9 (9b through 9f) (Panel E), and from Patient 6 (6a and 6b) (Panel F). Samples are displayed chronologically. Milestones in therapy for the three patients with cord colitis are indicated by colored arrowheads. Microscopical images of colon tissue obtained from a patient with cord colitis are shown, including a section stained with hematoxylin and eosin (Panel G) and a corresponding section (Panels H through K), along with colon tissue from healthy controls (Panels L and M) stained with either a universal eubacterial probe (EUB, yellow) or a bradyrhizobium-specific probe (Brady) and counterstained with 4',6-diamidino-2-phenylindole (DAPI, orange).