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Profiling of Temperature-induced Changes in Borrelia Burgdorferi Gene Expression by Using Whole Genome Arrays

Abstract

Borrelia burgdorferi is the etiologic agent of Lyme disease, the most prevalent arthropod-borne disease in the United States. The genome of the type strain, B31, consists of a 910,725-bp linear chromosome and 21 linear and circular plasmids comprising 610,694 bp. During its life cycle, the spirochete exists in distinctly different environments, cycling between a tick vector and a mammalian host. Temperature is one environmental factor known to affect B. burgdorferi gene expression. To identify temperature-responsive genes, genome arrays containing 1,662 putative B. burgdorferi open reading frames (ORFs) were prepared on nylon membranes and employed to assess gene expression in B. burgdorferi B31 grown at 23 and 35 degrees C. Differences in expression of more than 3.5 orders of magnitude could be readily discerned and quantitated. At least minimal expression from 91% of the arrayed ORFs could be detected. A total of 215 ORFs were differentially expressed at the two temperatures; 133 were expressed at significantly greater levels at 35 degrees C, and 82 were more significantly expressed at 23 degrees C. Of these 215 ORFs, 134 are characterized as genes of unknown function. One hundred thirty-six (63%) of the differentially expressed genes are plasmid encoded. Of particular interest is plasmid lp54 which contains 76 annotated putative genes; 31 of these exhibit temperature-regulated expression. These findings underscore the important role plasmid-encoded genes may play in adjustment of B. burgdorferi to growth under diverse environmental conditions.

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References
1.
Suk K, Das S, Sun W, Jwang B, Barthold S, Flavell R . Borrelia burgdorferi genes selectively expressed in the infected host. Proc Natl Acad Sci U S A. 1995; 92(10):4269-73. PMC: 41925. DOI: 10.1073/pnas.92.10.4269. View

2.
Tao H, Bausch C, Richmond C, Blattner F, Conway T . Functional genomics: expression analysis of Escherichia coli growing on minimal and rich media. J Bacteriol. 1999; 181(20):6425-40. PMC: 103779. DOI: 10.1128/JB.181.20.6425-6440.1999. View

3.
Orloski K, Hayes E, Campbell G, Dennis D . Surveillance for Lyme disease--United States, 1992-1998. MMWR CDC Surveill Summ. 2000; 49(3):1-11. View

4.
Hagman K, Yang X, Wikel S, Schoeler G, Caimano M, Radolf J . Decorin-binding protein A (DbpA) of Borrelia burgdorferi is not protective when immunized mice are challenged via tick infestation and correlates with the lack of DbpA expression by B. burgdorferi in ticks. Infect Immun. 2000; 68(8):4759-64. PMC: 98430. DOI: 10.1128/IAI.68.8.4759-4764.2000. View

5.
Porcella S, Fitzpatrick C, Bono J . Expression and immunological analysis of the plasmid-borne mlp genes of Borrelia burgdorferi strain B31. Infect Immun. 2000; 68(9):4992-5001. PMC: 101720. DOI: 10.1128/IAI.68.9.4992-5001.2000. View