Department of Pathology, Center for Molecular and Translational Human Infectious Diseases Research, Methodist Hospital Research Institute, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 2010 Mar 9;107(10):4693-8. doi: 10.1073/pnas.0906384107. Epub 2010 Feb 23.
Relatively little is understood about the dynamics of global host-pathogen transcriptome changes that occur during bacterial infection of mucosal surfaces. To test the hypothesis that group A Streptococcus (GAS) infection of the oropharynx provokes a distinct host transcriptome response, we performed genome-wide transcriptome analysis using a nonhuman primate model of experimental pharyngitis. We also identified host and pathogen biological processes and individual host and pathogen gene pairs with correlated patterns of expression, suggesting interaction. For this study, 509 host genes and seven biological pathways were differentially expressed throughout the entire 32-day infection cycle. GAS infection produced an initial widespread significant decrease in expression of many host genes, including those involved in cytokine production, vesicle formation, metabolism, and signal transduction. This repression lasted until day 4, at which time a large increase in expression of host genes was observed, including those involved in protein translation, antigen presentation, and GTP-mediated signaling. The interactome analysis identified 73 host and pathogen gene pairs with correlated expression levels. We discovered significant correlations between transcripts of GAS genes involved in hyaluronic capsule production and host endocytic vesicle formation, GAS GTPases and host fibrinolytic genes, and GAS response to interaction with neutrophils. We also identified a strong signal, suggesting interaction between host gammadelta T cells and genes in the GAS mevalonic acid synthesis pathway responsible for production of isopentenyl-pyrophosphate, a short-chain phospholipid that stimulates these T cells. Taken together, our results are unique in providing a comprehensive understanding of the host-pathogen interactome during mucosal infection by a bacterial pathogen.
目前对于细菌感染黏膜表面时宿主-病原体转录组变化的动态机制还知之甚少。为了验证 A 组链球菌(GAS)感染口咽部会引发宿主转录组明显变化的假设,我们使用实验性咽炎的非人类灵长类动物模型进行了全基因组转录组分析。我们还确定了宿主和病原体的生物过程以及具有相关表达模式的宿主和病原体基因对,表明存在相互作用。在这项研究中,509 个宿主基因和 7 个生物学途径在整个 32 天的感染周期中都表现出差异表达。GAS 感染导致许多宿主基因的表达最初广泛显著下降,包括参与细胞因子产生、囊泡形成、代谢和信号转导的基因。这种抑制持续到第 4 天,此时观察到宿主基因表达的大量增加,包括参与蛋白质翻译、抗原呈递和 GTP 介导的信号转导的基因。互作分析确定了 73 个具有相关表达水平的宿主和病原体基因对。我们发现 GAS 基因中参与透明质酸囊形成和宿主内吞囊泡形成、GAS GTPase 和宿主纤维蛋白溶解基因以及 GAS 对与中性粒细胞相互作用的反应的基因的转录物之间存在显著相关性。我们还发现了一个强烈的信号,表明宿主 gammadelta T 细胞与 GAS 甲羟戊酸合成途径中的基因之间存在相互作用,该途径负责产生异戊烯焦磷酸,这是一种短链磷脂,可刺激这些 T 细胞。总之,我们的研究结果在提供对细菌病原体黏膜感染期间宿主-病原体互作组的全面理解方面是独特的。