Previous Article | Next Article ![]()
Journal of Clinical Microbiology, 09 1995, 2304-2315, Vol 33, No. 9
RN Picken, Y Cheng, D Han, JA Nelson, AG Reddy, MK Hayden, MM Picken, F Strle, JK Bouseman and GM Trenholme
We have characterized 33 isolates of Borrelia burgdorferi from northern
Illinois (32 isolates) and Wisconsin (1 isolate) representing the largest
series of midwestern isolates investigated to date. The techniques used for
molecular analysis of strains included (i) genospecies typing with
species-specific PCR primers, (ii) plasmid profiling by pulsed-field gel
electrophoresis of total genomic DNA, (iii) large-restriction-fragment
pattern (LRFP) analysis by pulsed- field gel electrophoresis of
MluI-digested genomic DNA (J. Belfaiza, D. Postic, E. Bellenger, G.
Baranton, and I. Saint Girons, J. Clin. Microbiol. 31:2873-2877, 1993),
(iv) sodium dodecyl sulfate- polyacrylamide gel electrophoresis of total
proteins, (v) microsequencing of high-performance liquid
chromatography-purified peptides derived from proteins showing high levels
of expression, (vi) amino acid composition analysis of proteins, and (vii)
immunological analysis of proteins with a polyclonal antiserum of human
origin. Five reference strains as well as two atypical tick isolates from
California (DN127) and New York (25015) were included for comparison. All
of the Illinois and Wisconsin isolates were typed as B. burgdorferi sensu
stricto with genospecies-specific PCR primers. The isolates were found to
be heterogeneous with regard to their plasmid and protein profiles. One
isolate from Illinois possessed two large-molecular-size plasmids instead
of the usual 49-kb plasmid. Fragment patterns resulting from MluI digestion
of genomic DNA from the 33 isolates and strains DN127 and 25015 were
separable into six distinct LRFPs, five of which have not previously been
described. Strain 25015 and an isolate from Illinois (CT39) shared an
unusual LRFP that is not typical of other B. burgdorferi sensu stricto
strains, suggesting that they may represent a fifth species of B.
burgdorferi sensu lato. Five of the 33 isolates and strains DN127 and 25015
showed high-level expression of proteins with molecular masses of
approximately 22 kDa. Investigation of these proteins by microsequencing of
individual peptides and total amino acid composition analysis indicated
that the 22-kDa proteins expressed by the seven strains were polymorphic
OspC proteins. By using a polyclonal serum of human origin, expression of
OspC could be detected in all 33 Illinois and Wisconsin isolates.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Genotypic and phenotypic characterization of Borrelia burgdorferi isolated from ticks and small animals in Illinois
Department of Immunology/Microbiology, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612, USA.
This article has been cited by other articles:
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. |
|---|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|