Department of Basic Sciences, New York University College of Dentistry, New York, NY 10010-4086, USA.
FEMS Microbiol Lett. 2010 Nov;312(1):63-70. doi: 10.1111/j.1574-6968.2010.02100.x. Epub 2010 Sep 10.
Protease inhibitor cocktails are routinely added to clinical samples used for proteomic studies to inactivate proteases. As these same samples are often used for microbial studies, we determined whether the addition of protease inhibitors could affect the quantitative or qualitative assessment of microbial profiles. Twenty-two saliva samples were collected and processed immediately with or without the addition of a protease inhibitor cocktail. Conventional cultivation methods were used to evaluate total bacterial growth. Total genomic DNA was isolated and a specific 16S rRNA gene-targeted region was PCR-amplified and separated by denaturing gradient gel electrophoresis. A combination of 1D sodium dodecyl sulfate polyacrylamide gel electrophoresis and LC-MS/MS methods was used to determine the effect of the protease inhibitors on the integrity of salivary proteins and peptides. Interestingly, no significant differences were observed in either the bacterial growth and composition or the integrity of salivary proteins between the two groups. Correlation coefficients between the paired samples for total cultivable microbiota (r(2) =0.847), total mutans streptococci (r(2) =0.898), total oral lactobacilli (r(2) =0.933), and total Streptococcus mutans (r(2) =0.870) also exceeded expected values. The results suggest that the addition of a protease inhibitor cocktail in saliva samples does not impact the growth of oral microbiota or compromise the ability to characterize its composition.
蛋白酶抑制剂混合物通常添加到用于蛋白质组学研究的临床样本中以灭活蛋白酶。由于这些相同的样本通常也用于微生物研究,因此我们确定添加蛋白酶抑制剂是否会影响微生物谱的定量或定性评估。收集了 22 份唾液样本,并立即在添加或不添加蛋白酶抑制剂混合物的情况下进行处理。使用常规培养方法评估总细菌生长。分离总基因组 DNA,并对 16S rRNA 基因靶向区域进行 PCR 扩增和变性梯度凝胶电泳分离。使用 1D 十二烷基硫酸钠聚丙烯酰胺凝胶电泳和 LC-MS/MS 方法的组合来确定蛋白酶抑制剂对唾液蛋白和肽完整性的影响。有趣的是,两组之间的细菌生长和组成或唾液蛋白的完整性均无显着差异。总可培养微生物群(r²=0.847)、总变异链球菌(r²=0.898)、总口腔乳杆菌(r²=0.933)和总变异链球菌(r²=0.870)的配对样本之间的相关系数也超过了预期值。结果表明,在唾液样本中添加蛋白酶抑制剂混合物不会影响口腔微生物群的生长或损害其组成特征的能力。