Nailis Heleen, Coenye Tom, Van Nieuwerburgh Filip, Deforce Dieter, Nelis Hans J
Laboratory for Pharmaceutical Microbiology, Ghent University, Harelbekestraat 72, B-9000, Ghent, Belgium.
BMC Mol Biol. 2006 Aug 4;7:25. doi: 10.1186/1471-2199-7-25.
Candida albicans biofilms are commonly found on indwelling medical devices. However, the molecular basis of biofilm formation and development is not completely understood. Expression analysis of genes potentially involved in these processes, such as the ALS (Agglutinine Like Sequence) gene family can be performed using quantitative PCR (qPCR). In the present study, we investigated the expression stability of eight housekeeping genes potentially useful as reference genes to study gene expression in Candida albicans (C. albicans) biofilms, using the geNorm Visual Basic Application (VBA) for Microsoft Excel. To validate our normalization strategies we determined differences in ALS1 and ALS3 expression levels between C. albicans biofilm cells and their planktonic counterparts.
The eight genes tested in this study are ranked according to their expression stability (from most stable to least stable) as follows: ACT1 (beta-actin)/PMA1 (adenosine triphosphatase), RIP (ubiquinol cytochrome-c reductase complex component), RPP2B (cytosolic ribosomal acidic protein P2B), LSC2 (succinyl-CoA synthetase beta-subunit fragment), IMH3 (inosine-5'-monophosphate dehydrogenase fragment), CPA1 (carbamoyl-phosphate synthethase small subunit) and GAPDH (glyceraldehyde-3-phosphate dehydrogenase). Our data indicate that five genes are necessary for accurate and reliable normalization of gene expression data in C. albicans biofilms. Using different normalization strategies, we found a significant upregulation of the ALS1 gene and downregulation of the ALS3 gene in C. albicans biofilms grown on silicone disks in a continous flow system, the CDC reactor (Centre for Disease Control), for 24 hours.
In conclusion, we recommend the use of the geometric mean of the relative expression values from the five housekeeping genes (ACT1, PMA1, RIP, RPP2B and LSC2) for normalization, when analysing differences in gene expression levels between C. albicans biofilm cells and planktonic cells. Validation of the normalization strategies described above showed that the ALS1 gene is overexpressed and the ALS3 gene is underexpressed in C. albicans biofilms grown on silicone in the CDC reactor for 24 hours.
白色念珠菌生物膜常见于植入式医疗设备上。然而,生物膜形成和发展的分子基础尚未完全明确。可使用定量聚合酶链反应(qPCR)对可能参与这些过程的基因进行表达分析,比如ALS(类凝集素序列)基因家族。在本研究中,我们使用适用于Microsoft Excel的geNorm Visual Basic应用程序(VBA),研究了八个管家基因的表达稳定性,这些基因可能作为参考基因用于研究白色念珠菌(C. albicans)生物膜中的基因表达。为验证我们的标准化策略,我们测定了白色念珠菌生物膜细胞与其浮游对应细胞之间ALS1和ALS3表达水平的差异。
本研究中测试的八个基因按其表达稳定性排序(从最稳定到最不稳定)如下:ACT1(β-肌动蛋白)/PMA1(三磷酸腺苷酶)、RIP(泛醇细胞色素c还原酶复合体组分)、RPP2B(胞质核糖体酸性蛋白P2B)、LSC2(琥珀酰辅酶A合成酶β亚基片段)、IMH3(肌苷-5'-单磷酸脱氢酶片段)、CPA1(氨甲酰磷酸合成酶小亚基)和GAPDH(甘油醛-3-磷酸脱氢酶)。我们的数据表明,五个基因对于准确可靠地标准化白色念珠菌生物膜中的基因表达数据是必要的。使用不同的标准化策略,我们发现,在连续流动系统(疾病控制中心(CDC)反应器)中的硅胶盘上生长24小时的白色念珠菌生物膜中,ALS1基因显著上调,ALS3基因下调。
总之,在分析白色念珠菌生物膜细胞与浮游细胞之间的基因表达水平差异时,我们建议使用五个管家基因(ACT1、PMA1、RIP、RPP2B和LSC2)相对表达值的几何平均值进行标准化。上述标准化策略的验证表明,在CDC反应器中的硅胶上生长24小时的白色念珠菌生物膜中,ALS1基因过表达,ALS3基因低表达。