Virulence factor discovery identifies associations between the Fic gene family and Fap2+ fusobacteria in colorectal cancer microbiomes.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-02-05 Epub Date: 2025-01-14 DOI:10.1128/mbio.03732-24
Geicho Nakatsu, Duhyun Ko, Monia Michaud, Eric A Franzosa, Xochitl C Morgan, Curtis Huttenhower, Wendy S Garrett
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引用次数: 0

Abstract

Fusobacterium is a bacterium associated with colorectal cancer (CRC) tumorigenesis, progression, and metastasis. Fap2 is a fusobacteria-specific outer membrane galactose-binding lectin that mediates Fusobacterium 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 Fusobacterium 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+ Fusobacterium animalis genomes and detect recombination events and elements of horizontal gene transfer via synteny analysis of Fic gene loci. Exposure of a F. animalis 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 F. animalis as Fic peptides are detectable in F. animalis 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 Fusobacterium animalis merit future investigation to assess their roles in colorectal cancer development and progression.

毒力因子的发现确定了Fic基因家族与结直肠癌微生物群中Fap2+梭菌之间的关联。
梭杆菌是一种与结直肠癌(CRC)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,介导梭杆菌粘附和CRC肿瘤的侵袭。组学分析的进步为描述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,我们分析了大肠梭杆菌肿瘤分离株的基因组,发现含有Fic结构域的翻译后修饰酶家族与这些菌株的Fap2阳性相关。我们证明了Fic家族基因在梭菌泛基因组中随着Fap2的存在而扩增。通过比较基因组分析,我们发现Fap2+梭杆菌与其他癌症相关和人类肠道微生物群细菌类群相比,具有高度富集的Fic基因家族。使用CRC霰弹枪宏基因组的全球数据集,我们发现梭杆菌Fic和Fap2基因经常在晚期CRC患者的粪便微生物组中共同出现。我们进一步表征了Fap2+ Fusobacterium animalis基因组中特定的Fic基因家族,并通过Fic基因位点的synteny分析检测了重组事件和水平基因转移的元素。将动物F.菌株暴露于结肠腺癌细胞系可增加梭杆菌Fic和毒力相关黏附素的基因表达。最后,我们证明了Fic蛋白是由F. animalis合成的,因为在F. animalis单一培养的上清液中可以检测到Fic肽。综上所述,我们的研究揭示了Fap2+梭菌基因组中Fic基因是潜在的毒力因子。越来越多的数据支持肿瘤内微生物群的细菌成员严重影响结直肠癌的进展。然而,对可能影响癌变的非黏附性梭杆菌毒力因子的了解相对较少。我们在梭杆菌中的基因组分析和表达测定鉴定了含有Fic结构域的基因,这些基因是致病菌中得到充分研究的毒力因子,是潜在的梭杆菌毒力特征。我们发现由梭杆菌编码并由动物梭杆菌表达的Fic家族蛋白值得进一步研究,以评估其在结直肠癌发生和进展中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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