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Journal of Clinical Microbiology, Sep 1995, 2271-2279, Vol 33, No. 9
LR Washburn, LL Voelker, LJ Ehle, S Hirsch, C Dutenhofer, K Olson and B Beck
Twenty Mycoplasma arthritidis strains or isolates were compared by a
combination of enzyme-linked immunosorbent assay by an antiserum adsorption
technique, Western immunoblotting, and restriction analysis of chromosomal
DNA. Antigenic markers that defined strains related to strains 158p10p9,
PG6, and H606 were identified. In addition, restriction analysis allowed
all 20 strains to be divided into six groups. Results of restriction
analysis corresponded generally with antigenic similarities, although the
former did not allow grouping with as fine a precision as the latter.
However, intrastrain antigenic variability, which is common among many
Mycoplasma species, including M. arthritidis, introduced a complicating
factor into our attempts at antigenic analysis. While serologic and
antigenic analyses remain useful, we recommend that they be used with
caution and in combination with other techniques for identifying and
characterizing new isolates and newly acquired strains. Combinations of
these techniques have proven to be useful in our laboratory for quality
control and for uncovering interesting relationships among strains
subjected to animal passage and their less virulent antecedents and among
strains originally classified as the same but obtained from different
sources and maintained, sometimes for decades, in different laboratories.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Comparison of Mycoplasma arthritidis strains by enzyme-linked immunosorbent assay, immunoblotting, and DNA restriction analysis
Department of Microbiology, School of Medicine, University of South Dakota, Vermillion 57069-2390, USA.
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