Changes in bacterial enzymes and PCR profiles of fecal bacteria from a patient with ulcerative colitis before and after antimicrobial treatments

Citation
F. Rafii et al., Changes in bacterial enzymes and PCR profiles of fecal bacteria from a patient with ulcerative colitis before and after antimicrobial treatments, DIG DIS SCI, 44(3), 1999, pp. 637-642
Citations number
28
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
DIGESTIVE DISEASES AND SCIENCES
ISSN journal
01632116 → ACNP
Volume
44
Issue
3
Year of publication
1999
Pages
637 - 642
Database
ISI
SICI code
0163-2116(199903)44:3<637:CIBEAP>2.0.ZU;2-9
Abstract
A 26-year-old female patient, suffering from recurrent attacks of ulcerativ e colitis accompanied by extraintestinal symptoms (erythema nodosum and pyo derma gangrenosum), was evaluated for the effect of antibacterial agents on the intestinal bacteria and their enzymatic activities. The enzymes were a ssayed both at the onset of disease symptoms and after treatment with each of five drug regimens (fluconazole and cefadroxil, cefuroxime axetil and ce striaxone sodium, ciprofloxacin and cestriaxone sodium, ciprofloxacin alone , and ciprofloxacin, metronidazole, and cephalexin). The activities of azor eductase, nitroreductase, oxidoreductase, glucuronidase, and sulfatase were generally lower following all of the treatments, especially when ciproflox acin was included. The DNA from each sample was amplified by PCR, using ran dom primers. Profiles of amplified DNA on agarose gels showed different pat terns, indicating differences in the microflora before and after the antimi crobial treatments. The clinical response to antibacterial therapy was cons istent with the decreased bacterial enzymatic activities and changes in the microbial population. Ciprofloxacin, which was associated with the most dr amatic falls in enzymatic activity, also had the best clinical results. We conclude that intestinal bacteria and their enzymes play important roles in ulcerative colitis and that population changes can be monitored using PCR profiles.