Nakatsu Geicho, Ko Duhyun, Michaud Monia, Franzosa Eric A, Morgan Xochitl C, Huttenhower Curtis, Garrett Wendy S
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Harvard T.H. Chan Microbiome in Public Health Center, Boston, Massachusetts, USA.
mBio. 2025 Feb 5;16(2):e0373224. doi: 10.1128/mbio.03732-24. Epub 2025 Jan 14.
is a bacterium associated with colorectal cancer (CRC) tumorigenesis, progression, and metastasis. Fap2 is a fusobacteria-specific outer membrane galactose-binding lectin that mediates adherence to and invasion of CRC tumors. Advances in omics analyses provide an opportunity to profile and identify microbial genomic features that correlate with the cancer-associated bacterial virulence factor Fap2. Here, we analyze genomes of colon tumor isolates and find that a family of post-translational modification enzymes containing Fic domains is associated with Fap2 positivity in these strains. We demonstrate that Fic family genes expand with the presence of Fap2 in the fusobacterial pangenome. Through comparative genomic analysis, we find that Fap2 Fusobacteriota are highly enriched with Fic gene families compared to other cancer-associated and human gut microbiome bacterial taxa. Using a global data set of CRC shotgun metagenomes, we show that fusobacterial Fic and Fap2 genes frequently co-occur in the fecal microbiomes of individuals with late-stage CRC. We further characterize specific Fic gene families harbored by Fap2 genomes and detect recombination events and elements of horizontal gene transfer via synteny analysis of Fic gene loci. Exposure of a strain to a colon adenocarcinoma cell line increases gene expression of fusobacterial Fic and virulence-associated adhesins. Finally, we demonstrate that Fic proteins are synthesized by as Fic peptides are detectable in monoculture supernatants. Taken together, our study uncovers Fic genes as potential virulence factors in Fap2 fusobacterial genomes.IMPORTANCEAccumulating data support that bacterial members of the intra-tumoral microbiota critically influence colorectal cancer progression. Yet, relatively little is known about non-adhesin fusobacterial virulence factors that may influence carcinogenesis. Our genomic analysis and expression assays in fusobacteria identify Fic domain-containing genes, well-studied virulence factors in pathogenic bacteria, as potential fusobacterial virulence features. The Fic family proteins that we find are encoded by fusobacteria and expressed by merit future investigation to assess their roles in colorectal cancer development and progression.
是一种与结直肠癌(CRC)的肿瘤发生、进展和转移相关的细菌。Fap2是一种梭杆菌特异性外膜半乳糖结合凝集素,介导对CRC肿瘤的粘附和侵袭。组学分析的进展为剖析和鉴定与癌症相关细菌毒力因子Fap2相关的微生物基因组特征提供了机会。在这里,我们分析了结肠肿瘤分离株的基因组,发现一组含有Fic结构域的翻译后修饰酶与这些菌株中的Fap2阳性相关。我们证明Fic家族基因随着Fap2在梭杆菌泛基因组中的存在而扩展。通过比较基因组分析,我们发现与其他癌症相关和人类肠道微生物组细菌分类群相比,Fap2梭杆菌门高度富集Fic基因家族。使用CRC鸟枪法宏基因组的全球数据集,我们表明梭杆菌Fic和Fap2基因经常共同出现在晚期CRC患者的粪便微生物群中。我们进一步表征了Fap2基因组中包含的特定Fic基因家族,并通过Fic基因座的共线性分析检测重组事件和水平基因转移元件。将一株菌株暴露于结肠腺癌细胞系会增加梭杆菌Fic和毒力相关粘附素的基因表达。最后,我们证明Fic蛋白是由 合成的,因为在单培养上清液中可检测到Fic肽。综上所述,我们的研究发现Fic基因是Fap2梭杆菌基因组中的潜在毒力因子。重要性越来越多的数据支持肿瘤内微生物群的细菌成员对结直肠癌进展有至关重要的影响。然而,对于可能影响致癌作用的非粘附性梭杆菌毒力因子知之甚少。我们在梭杆菌中的基因组分析和表达测定确定了含Fic结构域的基因,这是在病原菌中经过充分研究的毒力因子,作为潜在的梭杆菌毒力特征。我们发现的由梭杆菌编码并由 表达的Fic家族蛋白值得未来进行研究,以评估它们在结直肠癌发生和进展中的作用。