Gut microbiota drives colon cancer risk associated with diet: a comparative analysis of meat-based and pesco-vegetarian diets.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Carlotta De Filippo, Sofia Chioccioli, Niccolò Meriggi, Antonio Dario Troise, Francesco Vitali, Mariela Mejia Monroy, Serdar Özsezen, Katia Tortora, Aurélie Balvay, Claire Maudet, Nathalie Naud, Edwin Fouché, Charline Buisson, Jacques Dupuy, Valérie Bézirard, Sylvie Chevolleau, Valérie Tondereau, Vassilia Theodorou, Claire Maslo, Perrine Aubry, Camille Etienne, Lisa Giovannelli, Vincenzo Longo, Andrea Scaloni, Duccio Cavalieri, Jildau Bouwman, Fabrice Pierre, Philippe Gérard, Françoise Guéraud, Giovanna Caderni
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引用次数: 0

Abstract

Background: Colorectal cancer (CRC) risk is strongly affected by dietary habits with red and processed meat increasing risk, and foods rich in dietary fibres considered protective. Dietary habits also shape gut microbiota, but the role of the combination between diet, the gut microbiota, and the metabolite profile on CRC risk is still missing an unequivocal characterisation.

Methods: To investigate how gut microbiota affects diet-associated CRC risk, we fed Apc-mutated PIRC rats and azoxymethane (AOM)-induced rats the following diets: a high-risk red/processed meat-based diet (MBD), a normalised risk diet (MBD with α-tocopherol, MBDT), a low-risk pesco-vegetarian diet (PVD), and control diet. We then conducted faecal microbiota transplantation (FMT) from PIRC rats to germ-free rats treated with AOM and fed a standard diet for 3 months. We analysed multiple tumour markers and assessed the variations in the faecal microbiota using 16S rRNA gene sequencing together with targeted- and untargeted-metabolomics analyses.

Results: In both animal models, the PVD group exhibited significantly lower colon tumorigenesis than the MBD ones, consistent with various CRC biomarkers. Faecal microbiota and its metabolites also revealed significant diet-dependent profiles. Intriguingly, when faeces from PIRC rats fed these diets were transplanted into germ-free rats, those transplanted with MBD faeces developed a higher number of preneoplastic lesions together with distinctive diet-related bacterial and metabolic profiles. PVD determines a selection of nine taxonomic markers mainly belonging to Lachnospiraceae and Prevotellaceae families exclusively associated with at least two different animal models, and within these, four taxonomic markers were shared across all the three animal models. An inverse correlation between nonconjugated bile acids and bacterial genera mainly belonging to the Lachnospiraceae and Prevotellaceae families (representative of the PVD group) was present, suggesting a potential mechanism of action for the protective effect of these genera against CRC.

Conclusions: These results highlight the protective effects of PVD while reaffirming the carcinogenic properties of MBD diets. In germ-free rats, FMT induced changes reminiscent of dietary effects, including heightened preneoplastic lesions in MBD rats and the transmission of specific diet-related bacterial and metabolic profiles. Importantly, to the best of our knowledge, this is the first study showing that diet-associated cancer risk can be transferred with faeces, establishing gut microbiota as a determinant of diet-associated CRC risk. Therefore, this study marks the pioneering demonstration of faecal transfer as a means of conveying diet-related cancer risk, firmly establishing the gut microbiota as a pivotal factor in diet-associated CRC susceptibility. Video Abstract.

肠道微生物群驱动与饮食相关的结肠癌风险:肉食和生态素食的比较分析。
背景:大肠癌(CRC)风险受饮食习惯的影响很大,红肉和加工肉类会增加风险,而富含膳食纤维的食物则被认为具有保护作用。膳食习惯也会影响肠道微生物群,但膳食、肠道微生物群和代谢物组合对 CRC 风险的作用仍缺乏明确的定性:为了研究肠道微生物群如何影响与饮食相关的 CRC 风险,我们给 Apc 基因突变的 PIRC 大鼠和偶氮甲烷(AOM)诱导的大鼠喂食了以下饮食:高风险的红肉/加工肉类饮食(MBD)、正常化风险饮食(含 α-生育酚的 MBD,MBDT)、低风险的生态素食饮食(PVD)和对照饮食。然后,我们将PIRC大鼠的粪便微生物群移植(FMT)到用AOM治疗的无菌大鼠身上,并喂食标准饮食3个月。我们分析了多种肿瘤标记物,并使用 16S rRNA 基因测序以及靶向和非靶向代谢组学分析评估了粪便微生物群的变化:结果:在两种动物模型中,PVD组的结肠肿瘤发生率明显低于MBD组,这与各种CRC生物标志物一致。粪便微生物群及其代谢物也显示出明显的饮食依赖性特征。耐人寻味的是,当将喂食这些饮食的 PIRC 大鼠的粪便移植到无菌大鼠体内时,那些移植了 MBD 粪便的大鼠出现了更多的肿瘤前病变,同时还出现了与饮食相关的独特细菌和代谢特征。PVD 确定了至少与两种不同动物模型相关的九种分类标记,这些标记主要属于 Lachnospiraceae 和 Prevotellaceae 家族,其中有四种分类标记是所有三种动物模型共有的。非结合胆汁酸与主要属于Lachnospiraceae和Prevotellaceae科(PVD组的代表)的细菌属之间存在反相关性,这表明这些细菌属对CRC具有保护作用的潜在作用机制:这些结果凸显了 PVD 的保护作用,同时再次证实了 MBD 膳食的致癌特性。在无菌大鼠中,FMT 诱导的变化让人联想到膳食效应,包括 MBD 大鼠肿瘤前病变的加剧以及与膳食相关的特定细菌和代谢特征的传播。重要的是,据我们所知,这是第一项显示与饮食相关的癌症风险可随粪便转移的研究,从而确立了肠道微生物群是与饮食相关的 CRC 风险的决定因素。因此,这项研究开创性地证明了粪便转移是传递膳食相关癌症风险的一种手段,从而牢固确立了肠道微生物群是膳食相关 CRC 易感性的关键因素。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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