Abstract

Borrelia burgdorferi, the spirochetal agent of Lyme disease, is maintained in nature in a cycle involving a tick vector and a mammalian host. Adaptation to the diverse conditions of temperature, pH, oxygen tension and nutrient availability in these two environments requires the precise orchestration of gene expression. Over 25 microarray analyses relating to B. burgdorferi genomics and transcriptomics have been published. The majority of these studies has explored the global transcriptome under a variety of conditions and has contributed substantially to the current understanding of B. burgdorferi transcriptional regulation. In this review, we present a summary of these studies with particular focus on those that helped define the roles of transcriptional regulators in modulating gene expression in the tick and mammalian milieus. By performing comparative analysis of results derived from the published microarray expression profiling studies, we identified composite gene lists comprising differentially expressed genes in these two environments. Further, we explored the overlap between the regulatory circuits that function during the tick and mammalian phases of the enzootic cycle. Taken together, the data indicate that there is interplay among the distinct signaling pathways that function in feeding ticks and during adaptation to growth in the mammal.

Highlights

  • The spirochete Borrelia burgdorferi is the causative agent of Lyme disease, the most commonly reported arthropod-borne disease in the United States [1,2,3]

  • The principal application of microarray technology to B. burgdorferi has been for global transcriptome analysis

  • These studies have informed our understanding of regulation of B. burgdorferi gene expression under different environmental conditions and, most importantly, elucidation of the roles for several transcriptional regulators in this process

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Summary

Introduction

The spirochete Borrelia burgdorferi is the causative agent of Lyme disease, the most commonly reported arthropod-borne disease in the United States [1,2,3]. B. burgdorferi is maintained in a natural enzootic cycle involving small mammals and a tick vector of the Ixodes species [3,4] These two diverse host environments vary with respect to temperature, pH, oxygen tension and nutrients [5]. Several groups have employed other custom glass slide or chip designs representing the complete genome or smaller sub-arrays of selected ORFs [13,14,15]. The steps for studying global gene expression changes in the B. burgdorferi transcriptome are as follows: RNA isolation, generation of labeled cDNA, array hybridization and scanning, data acquisition and analysis. The results of virtually all published microarray studies reported to date have been validated by quantitative reverse transcription polymerase chain reaction (qRT-PCR)

Comparative Genomic Studies
Global Transcriptome Studies
Response to Temperature
Transcriptional Regulation
Rrp2-RpoN-RpoS Regulatory Cascade
Borrelia Oxidative
Hk1-Rrp1 Regulatory Circuit
Interaction between the Rrp2-RpoN-RpoS-BosR and Hk1-Rrp1 Regulatory Circuits
Conclusions and Prospects for the Future
Findings
Methods
Full Text
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