Target Imbalance: Disparity of Borrelia burgdorferi Genetic Material in Synovial Fluid from Lyme Arthritis Patients

Lyme arthritis is a late manifestation of Lyme disease that results in episodic synovial inflammation and swelling. Although this process is thought to be driven directly by the spirochetal etiologic agent, Borrelia burgdorferi, the organism itself has been recovered by culture only twice. In contra...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of infectious diseases Vol. 169; no. 3; pp. 668 - 672
Main Authors: Persing, David H., Rutledge, Barbara J., Rys, Paul N., Podzorski, Diane S., Mitchell, Paul D., ,, Kurt D. Ree, Liu, Bing, Fikrig, Erol, Malawista, Stephen E.
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 01-03-1994
University of Chicago Press
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Lyme arthritis is a late manifestation of Lyme disease that results in episodic synovial inflammation and swelling. Although this process is thought to be driven directly by the spirochetal etiologic agent, Borrelia burgdorferi, the organism itself has been recovered by culture only twice. In contrast, polymerase chain reaction (peR) studies are usually positive. This apparent discrepancy in 19 culture-negative synovial fluid specimens from 18 patients with Lyme arthritis was investigated. In all 19,DNA sequences characteristic of plasmid-encoded genes OspA and OspB were easily detected. However, despite equivalent or even superior analytic sensitivity for detection of cultured organisms, the reactivity of two genomic DNA targets was often weak or absent altogether in the clinical specimens. This apparent overrepresentation of B. burgdorferi plasmid sequences wasfound exclusively in clinical specimensand not in cultured organisms. The physiologic imbalance of genomic and plasmid DNA reactivityin B. burgdorferi infection may signal an underlying pathogenetic mechanism.
Bibliography:ark:/67375/HXZ-1RR6P6R4-B
Reprints or correspondence: Dr. David H. Persing, Mayo Clinic, Divisions of Experimental Pathology and Clinical Microbiology, 200 First St., S.W., 470 Hilton Bldg., Rochester. MN 55905.
istex:AC1D0FB876C6C7FDD17460375F61CEDA5BF0581A
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/169.3.668