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本文引用的文献

1
The gut microbiome modulates colon tumorigenesis.肠道微生物组调节结肠肿瘤发生。
mBio. 2013 Nov 5;4(6):e00692-13. doi: 10.1128/mBio.00692-13.
2
Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences.基于 16S rRNA 标记基因序列对微生物群落进行功能预测分析。
Nat Biotechnol. 2013 Sep;31(9):814-21. doi: 10.1038/nbt.2676. Epub 2013 Aug 25.
3
Diet, microbiota, and microbial metabolites in colon cancer risk in rural Africans and African Americans.饮食、微生物群和微生物代谢产物与非洲农村居民和非裔美国人结肠癌风险的关系。
Am J Clin Nutr. 2013 Jul;98(1):111-20. doi: 10.3945/ajcn.112.056689. Epub 2013 May 29.
4
Changes of the intestinal microbiota, short chain fatty acids, and fecal pH in patients with colorectal cancer.结直肠癌患者的肠道微生物群、短链脂肪酸和粪便 pH 的变化。
Dig Dis Sci. 2013 Jun;58(6):1717-26. doi: 10.1007/s10620-012-2526-4. Epub 2013 Jan 11.
5
The metabolic activity of gut microbiota in obese children is increased compared with normal-weight children and exhibits more exhaustive substrate utilization.肥胖儿童的肠道微生物群的代谢活性高于正常体重儿童,并且表现出更彻底的底物利用。
Nutr Diabetes. 2011 Jul 18;1(7):e12. doi: 10.1038/nutd.2011.8.
6
The microbiota and its metabolites in colonic mucosal health and cancer risk.肠道黏膜健康和癌症风险中的微生物组及其代谢物。
Nutr Clin Pract. 2012 Oct;27(5):624-35. doi: 10.1177/0884533612452012. Epub 2012 Aug 6.
7
Genomic analysis identifies association of Fusobacterium with colorectal carcinoma.基因组分析鉴定出梭杆菌属与结直肠癌的关联。
Genome Res. 2012 Feb;22(2):292-8. doi: 10.1101/gr.126573.111. Epub 2011 Oct 18.
8
Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma.具核梭杆菌感染在人类结直肠癌中普遍存在。
Genome Res. 2012 Feb;22(2):299-306. doi: 10.1101/gr.126516.111. Epub 2011 Oct 18.
9
Outcomes among black patients with stage II and III colon cancer receiving chemotherapy: an analysis of ACCENT adjuvant trials.接受化疗的 II 期和 III 期结肠癌黑人患者的结局:ACCENT 辅助试验分析。
J Natl Cancer Inst. 2011 Oct 19;103(20):1498-506. doi: 10.1093/jnci/djr310. Epub 2011 Oct 12.
10
Gut microbiota, immunity, and disease: a complex relationship.肠道微生物群、免疫与疾病:复杂的关系。
Front Microbiol. 2011 Sep 5;2:180. doi: 10.3389/fmicb.2011.00180. eCollection 2011.

不同种族/族裔群体中的粪便微生物、短链脂肪酸与结直肠癌

Fecal microbes, short chain fatty acids, and colorectal cancer across racial/ethnic groups.

作者信息

Hester Christina M, Jala Venkatakrishna R, Langille Morgan Gi, Umar Shahid, Greiner K Allen, Haribabu Bodduluri

机构信息

Christina M Hester, K Allen Greiner, Department of Family Medicine Research Division, University of Kansas Medical Center, Kansas City, KS 66160, United States.

出版信息

World J Gastroenterol. 2015 Mar 7;21(9):2759-69. doi: 10.3748/wjg.v21.i9.2759.

DOI:10.3748/wjg.v21.i9.2759
PMID:25759547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4351229/
Abstract

AIM

To investigate differences in microbes and short chain fatty acid (SCFA) levels in stool samples from Hispanic and non-Hispanic African American, American Indian, and White participants.

METHODS

Stool samples from twenty participants were subjected to analysis for relative levels of viable bacteria and for SCFA levels. Additionally, the samples were subjected to 16S rRNA gene pyrosequencing for identification of bacteria present in the stool. We used a metagenome functional prediction technique to analyze genome copy numbers and estimate the abundance of butyrate kinase in all samples.

RESULTS

We found that African Americans had significantly lower levels of acetate, butyrate, and total SCFAs than all other racial/ethnic groups. We also found that participant microbial profiles differed by racial/ethnic group. African Americans had significantly more Firmicutes than Whites, with enriched Ruminococcaceae. The Firmicutes/Bacteroidetes ratio was also significantly higher for African Americans than for Whites (P = 0.049). We found Clostridium levels to be significantly and inversely related to total SCFA levels (P = 0.019) and we found Bacteroides to be positively associated (P = 0.027) and Clostridium to be negatively associated (P = 0.012) with levels of butyrate. We also identified a correlation between copy number for a butyrate kinase predicted from 16S rRNA gene abundance and levels of butyrate in stool.

CONCLUSION

The identified differences in gut flora and SCFA levels may relate to colorectal cancer mortality differentials and may be useful as targets for future clinical and behavioral interventions.

摘要

目的

研究西班牙裔、非西班牙裔非裔美国人、美国印第安人和白人参与者粪便样本中微生物和短链脂肪酸(SCFA)水平的差异。

方法

对20名参与者的粪便样本进行活菌相对水平和SCFA水平分析。此外,对样本进行16S rRNA基因焦磷酸测序以鉴定粪便中存在的细菌。我们使用宏基因组功能预测技术分析基因组拷贝数并估计所有样本中丁酸激酶的丰度。

结果

我们发现非裔美国人的乙酸盐、丁酸盐和总SCFA水平显著低于所有其他种族/族裔群体。我们还发现参与者的微生物谱因种族/族裔群体而异。非裔美国人的厚壁菌门比白人显著更多,瘤胃球菌科富集。非裔美国人的厚壁菌门/拟杆菌门比率也显著高于白人(P = 0.049)。我们发现梭菌水平与总SCFA水平显著负相关(P = 0.019),并且发现拟杆菌与丁酸盐水平呈正相关(P = 0.027),梭菌与丁酸盐水平呈负相关(P = 0.012)。我们还确定了根据16S rRNA基因丰度预测的丁酸激酶拷贝数与粪便中丁酸盐水平之间的相关性。

结论

肠道菌群和SCFA水平的已确定差异可能与结直肠癌死亡率差异有关,并且可能作为未来临床和行为干预的靶点有用。