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Applied and Environmental Microbiology, March 2007, p. 1501-1513, Vol. 73, No. 5
0099-2240/07/$08.00+0 doi:10.1128/AEM.02454-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
,
Andrew T. Revel,2,
Alexandra H. Smith,1
Gulnaz N. Bachlani,1 and
Michael V. Norgard1*
Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390,1 Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 021152
Received 19 October 2006/ Accepted 28 December 2006
The development of new genetic systems for studying the complex regulatory events that occur within Borrelia burgdorferi is an important goal of contemporary Lyme disease research. Although recent advancements have been made in the genetic manipulation of B. burgdorferi, there still remains a paucity of basic molecular systems for assessing differential gene expression in this pathogen. Herein, we describe the adaptation of two powerful genetic tools for use in B. burgdorferi. The first is a Photinus pyralis firefly luciferase gene reporter that was codon optimized to enhance translation in B. burgdorferi. Using this modified reporter, we demonstrated an increase in luciferase expression when B. burgdorferi transformed with a shuttle vector encoding the outer surface protein C (OspC) promoter fused to the luciferase reporter was cultivated in the presence of fresh rabbit blood. The second is a lac operator/repressor system that was optimized to achieve the tightest degree of regulation. Using the aforementioned luciferase reporter, we assessed the kinetics and maximal level of isopropyl-ß-D-thiogalactopyranoside (IPTG)-dependent gene expression. This lac-inducible expression system also was used to express the gene carried on lp25 required for borrelial persistence in ticks (bptA). These advancements should be generally applicable for assessing further the regulation of other genes potentially involved in virulence expression by B. burgdorferi.
Published ahead of print on 12 January 2007.
Supplemental material for this article may be found at http://aem.asm.org/.
J.S.B. and A.T.R. contributed equally to this work.
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