Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
mBio. 2018 Nov 20;9(6):e02248-18. doi: 10.1128/mBio.02248-18.
Human viruses (those that infect human cells) have been associated with many cancers, largely due to their mutagenic and functionally manipulative abilities. Despite this, cancer microbiome studies have focused almost exclusively on bacteria instead of viruses. We began evaluating the cancer virome by focusing on colorectal cancer, a primary cause of morbidity and mortality throughout the world and a cancer linked to altered colonic bacterial community compositions but with an unknown association with the gut virome. We used 16S rRNA gene, whole shotgun metagenomic, and purified virus metagenomic sequencing of stool to evaluate the differences in human colorectal cancer virus and bacterial community composition. Through random forest modeling, we identified differences in the healthy and colorectal cancer viromes. The cancer-associated virome consisted primarily of temperate bacteriophages that were also predicted to be bacterium-virus community network hubs. These results provide foundational evidence that bacteriophage communities are associated with colorectal cancer and potentially impact cancer progression by altering the bacterial host communities. Colorectal cancer is a leading cause of cancer-related death in the United States and worldwide. Its risk and severity have been linked to colonic bacterial community composition. Although human-specific viruses have been linked to other cancers and diseases, little is known about colorectal cancer virus communities. We addressed this knowledge gap by identifying differences in colonic virus communities in the stool of colorectal cancer patients and how they compared to bacterial community differences. The results suggested an indirect role for the virome in impacting colorectal cancer by modulating the associated bacterial community. These findings both support the idea of a biological role for viruses in colorectal cancer and provide a new understanding of basic colorectal cancer etiology.
人类病毒(感染人类细胞的病毒)与许多癌症有关,主要是因为它们具有诱变和功能操纵能力。尽管如此,癌症微生物组研究几乎完全集中在细菌上,而不是病毒上。我们开始通过关注结直肠癌来评估癌症病毒组,结直肠癌是全世界发病率和死亡率的主要原因,是一种与结肠细菌群落组成改变相关但与肠道病毒组未知关联的癌症。我们使用 16S rRNA 基因、全 shotgun 宏基因组和粪便纯化病毒宏基因组测序来评估人类结直肠癌病毒和细菌群落组成的差异。通过随机森林模型,我们确定了健康人和结直肠癌病毒组之间的差异。与癌症相关的病毒组主要由温和噬菌体组成,这些噬菌体也被预测为细菌-病毒群落网络的枢纽。这些结果提供了基础证据,表明噬菌体群落与结直肠癌有关,并可能通过改变细菌宿主群落来影响癌症进展。结直肠癌是美国和全球癌症相关死亡的主要原因。其风险和严重程度与结肠细菌群落组成有关。尽管人类特异性病毒与其他癌症和疾病有关,但对结直肠癌病毒群落知之甚少。我们通过识别结直肠癌患者粪便中结肠病毒群落的差异以及它们与细菌群落差异的比较来解决这一知识空白。结果表明,病毒组通过调节相关细菌群落间接影响结直肠癌。这些发现既支持病毒在结直肠癌中的生物学作用的观点,也为结直肠癌的基本病因提供了新的认识。