interrogans serovar Copenhageni in response to serum that were differentially expressed due to the effect of: serum only, serum and temperature

shift, serum and osmolarity shift, and all three conditions; in each general COG grouping. Interestingly, ligB was the only gene of known or predicted function that was up-regulated in response to all three conditions [11, 13, 15, 16]. Therefore, this gene is most likely induced during early bloodstream infection upon exposure to serum and temperature and osmolarity shift. This finding correlates with previous studies showing that anti-LigB Bromosporine order IgM was found in more than 95% www.selleckchem.com/products/cb-839.html of patients with acute leptospiral infection [93]. It is therefore intriguing that ligB is not essential for acute infection of hamsters or for rat kidney colonization [58]. Interestingly, no gene of known or predicted function was down-regulated by all three signals. In addition, expression of genes encoding proteins

known to be temperature regulated, such as LipL36 [8] and Qlp42 [14], was not altered in our study, a finding consistent with previous work on the effect of temperature on these genes [11]. Validation of selleck chemicals microarray data by quantitative RT-PCR To validate the microarray data, 12 genes were selected for quantitative RT-PCR. Genes encoding flagella subunits, flaB and flaA2 did not show any transcriptional changes under different temperature or osmolarity conditions and were used for normalization of RT-PCR data in those studies [11, 13]. Likewise, flaB transcription was not altered by the presence of serum and therefore, flaB was used for normalization of RT-PCR data in this study.

The correlation coefficient (R2) between expression measured by microarray and real-time quantitative PCR was 0.812 [Additional file 3]. Conclusions We studied global changes at the transcriptional level of L. interrogans serovar Copenhageni in response to serum, thus mimicking the early bacteremic phase of infection. Out of a total of 3,711 ORFs, 168 genes (4.5%) were selleck inhibitor found to be differentially expressed. To adapt to stress signals in serum, several genes involved in transcriptional regulation, translational process, signal transduction systems, cell or membrane biogenesis, enzymes in various metabolic pathways, and unknown genes were differentially expressed. Serum appeared to be a unique stimulus for leptospires, resulting in a distinct pattern of gene expression compared with genes found to be regulated by only temperature or osmolarity shifts.