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Journal of Clinical Microbiology, June 1998, p. 1646-1652, Vol. 36, No. 6
Departments of
Urology1 and
Pathobiology,2 Schools of Medicine
and Public Health, University of Washington, Seattle, Washington
Received 11 November 1997/Returned for modification 20 January
1998/Accepted 17 March 1998
Treatment of chronic prostatitis/chronic pelvic pain syndrome is
often empirical because clinical culture methods fail to detect
prostate-associated pathogens in >90% of patients. Previously, we
tested a variety of specific-microorganism PCRs and began a DNA
sequence study after we found that 77% of prostatitis patients were
PCR positive for prokaryotic rRNA-encoding DNA sequences (rDNAs)
despite negative cultures using optimal techniques. In the present
study, 36 rDNA clones from 23 rDNA-positive patients were
sequenced. This study represents more than twice the total rDNA
sequence and more than twice the number of patients in the previous
study. The increased number of patients and clones sequenced allowed
enhanced phylogenetic analyses and refinements in our view of
rDNA species inhabiting the prostate. A continuum of related rDNAs that might be arbitrarily described as two major groups of
rDNAs and several minor groups was found. Sequences termed Pros A,
identified in 8 (35%) of 23 rDNA-positive patients, grouped with
Aeromonas spp. in phylogenetic studies. Sequences termed Pros B, identified in 17 (74%) of 23 rDNA-positive patients, were distinct from previously reported sequences, although all were >90%
similar to known gram-negative bacteria. Of the nine patients for whom
multiple rDNAs were sequenced, six had biopsy specimens containing
rDNAs from more than one species. Four (17%) patients had
rDNAs different from those of the Pros A and Pros B groups. Of
these four, one patient had rDNA similar to that of
Flavobacterium spp., another had rDNA similar to that
of Pseudomonas testosteroni, and two patients had rDNAs
<70% similar to known rDNAs. These findings suggest that the
prostate can harbor bacteria undetectable by traditional approaches.
Most of these diverse sequences are not reported in environments
outside the prostate. The sequence similarities suggest adaptation of
limited groups of bacteria to the microenvironment of the prostate.
Further studies may elucidate the relationship of prostate-associated
bacteria to chronic prostatitis/chronic pelvic pain syndrome.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Diverse and Related 16S rRNA-Encoding DNA Sequences
in Prostate Tissues of Men with Chronic Prostatitis
*
Corresponding author. Mailing address: Department of
Urology, School of Medicine, University of Washington, Health Sciences, Pacific Ave., Seattle, WA 98195. Phone: (206) 685-3346. Fax: (206) 543-3272. E-mail: dri{at}u.washington.edu.
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