Salmonella-triggered reactive arthritis - Use of polymerase chain reaction, immunocytochemical staining, and gas chromatography mass spectrometry in the detection of bacterial components from synovial fluid

Citation
S. Nikkari et al., Salmonella-triggered reactive arthritis - Use of polymerase chain reaction, immunocytochemical staining, and gas chromatography mass spectrometry in the detection of bacterial components from synovial fluid, ARTH RHEUM, 42(1), 1999, pp. 84-89
Citations number
13
Categorie Soggetti
Rheumatology,"da verificare
Journal title
ARTHRITIS AND RHEUMATISM
ISSN journal
00043591 → ACNP
Volume
42
Issue
1
Year of publication
1999
Pages
84 - 89
Database
ISI
SICI code
0004-3591(199901)42:1<84:SRA-UO>2.0.ZU;2-H
Abstract
Objective. To investigate whether microbial components are present in the c ells of synovial fluid or peripheral blood from patients with Salmonella-tr iggered reactive arthritis (ReA). Methods. Synovial fluid cells and/or peripheral blood cells from 23 patient s with Salmonella-triggered ReA and from 19 control patients with newly dia gnosed rheumatoid arthritis were studied using 3 different polymerase chain reaction (PCR) techniques and immunocytochemical staining. Muramic acid fr om the synovial fluid was studied btv gas chromatography-mass spectrometry, Results. Salmonella chromosomal DNA was not detectable in the synovial flui d cells and peripheral blood leukocytes of patients with Salmonella ReA. In itially, positive reactions were observed in the synovial. fluid cells and peripheral blood leukocytes of 3 of 17 and 3 of 18 patients with ReA respec tively, but in the subsequent PCR studies, these findings were not reproduc ible. Salmonella-specific antigen was detectable by immunofluorescence in t he synovial fluid cells and peripheral blood leukocytes of 4 of 11 and 2 of 7 patients dth ReA, respectively. Muramic acid was present in 2 of 15 syno vial fluid samples from patients with ReA, but the bacterial cultures from synovial fluid were negative. Conclusion. These findings indicate the presence of bacterial degradation p roducts, but not bacterial DNA, in the inflamed joints of patients with Sal monella triggered ReA.