Brooks Chad S, Hefty P Scott, Jolliff Sarah E, Akins Darrin R
Department of Microbiology and Immunology, The University of Oklahoma Health Sciences Center, Oklahoma City 73104, USA.
Infect Immun. 2003 Jun;71(6):3371-83. doi: 10.1128/IAI.71.6.3371-3383.2003.
Lyme disease is a tick-borne infection that can lead to chronic, debilitating problems if not recognized or treated appropriately. Borrelia burgdorferi, the causative agent of Lyme disease, is maintained in nature by a complex enzootic cycle involving Ixodes ticks and mammalian hosts. Many previous studies support the notion that B. burgdorferi differentially expresses numerous genes and proteins to help it adapt to growth in the mammalian host. In this regard, several studies have utilized a dialysis membrane chamber (DMC) cultivation system to generate "mammalian host-adapted" spirochetes for the identification of genes selectively expressed during mammalian infection. Here, we have exploited the DMC cultivation system in conjunction with microarray technology to examine the global changes in gene expression that occur in the mammalian host. To identify genes regulated by only mammal-specific signals and not by temperature, borrelial microarrays were hybridized with cDNA generated either from organisms temperature shifted in vitro from 23 degrees C to 37 degrees C or from organisms cultivated by using the DMC model system. Statistical analyses of the combined data sets revealed that 125 genes were expressed at significantly different levels in the mammalian host, with almost equivalent numbers of genes being up- or down-regulated by B. burgdorferi within DMCs compared to those undergoing temperature shift. Interestingly, during DMC cultivation, the vast majority of genes identified on the plasmids were down-regulated (79%), while the differentially expressed chromosomal genes were almost entirely up-regulated (93%). Global analysis of the upstream promoter regions of differentially expressed genes revealed that several share a common motif that may be important in transcriptional regulation during mammalian infection. Among genes with known or putative functions, the cell envelope category, which includes outer membrane proteins, was found to contain the most differentially expressed genes. The combined findings have generated a subset of genes that can now be further characterized to help define their role or roles with regard to B. burgdorferi virulence and Lyme disease pathogenesis.
莱姆病是一种由蜱传播的感染病,如果未得到正确识别或治疗,可能会导致慢性、使人衰弱的问题。莱姆病的病原体伯氏疏螺旋体,通过一个涉及硬蜱和哺乳动物宿主的复杂的动物流行病循环在自然界中得以维持。许多先前的研究支持这样一种观点,即伯氏疏螺旋体差异表达众多基因和蛋白质以帮助其适应在哺乳动物宿主中的生长。在这方面,多项研究利用透析膜腔室(DMC)培养系统来产生“适应哺乳动物宿主的”螺旋体,以鉴定在哺乳动物感染期间选择性表达的基因。在此,我们利用DMC培养系统并结合微阵列技术来研究在哺乳动物宿主中发生的基因表达的整体变化。为了鉴定仅受哺乳动物特异性信号而非温度调控的基因,将伯氏疏螺旋体微阵列与从体外温度从23摄氏度转变为37摄氏度的生物体或使用DMC模型系统培养的生物体产生的cDNA进行杂交。对合并数据集的统计分析表明,125个基因在哺乳动物宿主中的表达水平存在显著差异,与经历温度转变的生物体相比,在DMC内伯氏疏螺旋体上调或下调的基因数量几乎相等。有趣的是,在DMC培养期间,在质粒上鉴定出的绝大多数基因被下调(79%),而差异表达的染色体基因几乎全部被上调(93%)。对差异表达基因的上游启动子区域的整体分析表明,有几个基因共享一个共同基序,这在哺乳动物感染期间的转录调控中可能很重要。在具有已知或推定功能的基因中,包括外膜蛋白的细胞包膜类别被发现含有差异表达最多的基因。这些综合发现产生了一组基因,现在可以对其进行进一步表征,以帮助确定它们在伯氏疏螺旋体毒力和莱姆病发病机制方面的作用。