School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332.
Emory-Children's Cystic Fibrosis Center, Atlanta, GA 30322.
Proc Natl Acad Sci U S A. 2022 Jan 11;119(2). doi: 10.1073/pnas.2116637119.
Bacterial behavior and virulence during human infection is difficult to study and largely unknown, as our vast knowledge of infection microbiology is primarily derived from studies using in vitro and animal models. Here, we characterize the physiology of , a periodontal pathogen, in its native environment using 93 published metatranscriptomic datasets from periodontally healthy and diseased individuals. transcripts were more abundant in samples from periodontally diseased patients but only above 0.1% relative abundance in one-third of diseased samples. During human infection, highly expressed genes encoding virulence factors such as fimbriae and gingipains (proteases) and genes involved in growth and metabolism, indicating that is actively growing during disease. A quantitative framework for assessing the accuracy of model systems showed that 96% of genes were expressed similarly in periodontitis and in vitro midlogarithmic growth, while significantly fewer genes were expressed similarly in periodontitis and in vitro stationary phase cultures (72%) or in a murine abscess infection model (85%). This high conservation in gene expression between periodontitis and logarithmic laboratory growth is driven by overall low variance in gene expression, relative to other pathogens including and Together, this study presents strong evidence for the use of simple test tube growth as the gold standard model for studying biology, providing biological relevance for the thousands of laboratory experiments performed with logarithmic phase Furthermore, this work highlights the need to quantitatively assess the accuracy of model systems.
在人体感染期间,细菌的行为和毒力很难研究,而且很大程度上是未知的,因为我们对感染微生物学的广泛了解主要来自于使用体外和动物模型进行的研究。在这里,我们使用来自牙周健康和患病个体的 93 个已发表的宏转录组数据集,在其天然环境中描述牙周病原体 的生理学。在牙周病患者的样本中, 转录本更为丰富,但在三分之一的患病样本中仅超过 0.1%的相对丰度。在人类感染期间, 高度表达编码毒力因子(如菌毛和牙龈蛋白酶(蛋白酶))和参与生长和代谢的基因的基因,表明 在疾病期间正在积极生长。用于评估模型系统准确性的定量框架表明,96%的 基因在牙周炎和体外对数生长期表达相似,而在牙周炎和体外静止期培养物(72%)或在鼠脓肿感染模型中(85%)表达相似的基因要少得多。牙周炎和对数期实验室生长之间的这种高基因表达保守性是由 基因表达的总体低方差驱动的,与包括 和 在内的其他病原体相比, 基因表达的方差相对较低。总之,这项研究为使用简单的试管生长作为研究 生物学的黄金标准模型提供了强有力的证据,对数期 进行的数千项实验室实验具有生物学相关性。此外,这项工作强调了需要定量评估模型系统的准确性。