Objectives-To evaluate the value of broad range bacterial FCR in the diagno
sis of joint infection and to find out if there are bacteria causing arthri
tis which are not cultivable by the present methods.
Methods-Polymerase chain reaction (PCR) with broad range bacterial primers
and DNA sequencing (bacterial PCR) was used to analyse 154 synovial fluid (
SF) samples from patients with different arthritic diseases.
Results-Bacterial DNA was detected in 18 SF samples, including samples from
six patients with culture proven purulent arthritis, and from three patien
ts with possible purulent arthritis. Three samples from patients with cultu
re confirmed purulent arthritis remained negative in bacterial PCR.
Conclusions-The results indicate that in the usual diagnostic laboratory se
tting bacterial PCR does not offer any obvious advantage over bacterial cul
ture in the microbiological diagnosis of joint infection.