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Infect Immun, March 1998, p. 1149-1158, Vol. 66, No. 3
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Analysis of the Organization of Multicopy Linear-
and Circular-Plasmid-Carried Open Reading Frames in
Borrelia burgdorferi Sensu Lato Isolates
Jason A.
Carlyon,
Crystal
Lavoie,
Shian-Ying
Sung, and
Richard T.
Marconi*
Department of Microbiology and Immunology,
Medical College of Virginia, Virginia Commonwealth University,
Richmond, Virginia 23298-0678
Received 17 April 1997/Returned for modification 2 June
1997/Accepted 31 December 1997
Plasmid cp8.3 of Borrelia afzelii IP21 carries several
open reading frames (ORFs) and a 184-bp inverted repeat (IR) element. It has been speculated that this plasmid may encode factors involved in
virulence or infectivity. In this report, we have characterized the
distribution, molecular variability, and organization of ORFs 1, 2, and
4 and the IR elements among isolates of the Borrelia burgdorferi sensu lato complex. ORFs 1 and 2 are contained within a segment of cp8.3 that is bordered by the IR elements, while ORF 4 resides just outside of the IR-bordered region. By PCR, ORF 4 was
amplified from most isolates while ORFs 1 and 2 were amplified from
only some B. afzelii isolates. However, Southern hybridization analyses with ORF 1, 2, and 4 probes detected related sequences even in some isolates that were PCR negative. The ORF restriction fragment length polymorphism patterns varied widely even
among isolates of the same species. Two-dimensional contour-clamped homogeneous electric field-pulsed-field gel electrophoresis and Southern hybridization detected ORF 1-, 2-, and 4-related sequences on
linear and circular plasmids. In addition, an ORF 4-related sequence
was detected on a previously uncharacterized, circular plasmid that is
greater than 70 kb in size. The IR elements originally identified on
plasmid cp8.3 of B. afzelii IP21 were also analyzed by
Southern hybridization. Related sequences were detected in some but not
all B. burgdorferi sensu lato isolates. These sequences are
carried on plasmids in addition to cp8.3 in some isolates. Single-primer PCR analyses demonstrated that in some isolates these
sequences exist with IR orientation. The data presented here
demonstrate that the IR elements and the ORF 1-, 2-, and 4-related
sequences are multicopy and are variable in organization and in genomic
location among isolates of the B. burgdorferi sensu lato
complex. These analyses provide additional evidence for the highly
variable organization of the plasmid component of the B. burgdorferi sensu lato genome.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Medical College of Virginia, Virginia
Commonwealth University, Box 980678, 1101 East Marshall St., Richmond,
VA 23298-0678. Phone: (804) 828-3779. Fax: (804) 828-9946. E-mail:
RMARCONI{at}HSC.VCU.EDU.
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