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
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
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.