Suppr超能文献

肠道特定菌种失衡与中国儿童营养不良的发生相关

Intestinal sp. Imbalance Associated With the Occurrence of Childhood Undernutrition in China.

作者信息

Li Dongfang, Li Yinhu, Dai Wenkui, Wang Huihui, Qiu Chuangzhao, Feng Su, Zhou Qian, Wang Wenjian, Feng Xin, Yao Kaihu, Liu Yanhong, Yang Yonghong, Yang Zhenyu, Xu Ximing, Li Shuaicheng, Wei Jurong, Zhou Ke

机构信息

Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, China.

Department of Microbial Research, WeHealthGene Institute, Shenzhen, China.

出版信息

Front Microbiol. 2019 Nov 29;10:2635. doi: 10.3389/fmicb.2019.02635. eCollection 2019.

Abstract

Undernutrition (UN) is a worldwide concern affecting morbidity and mortality among children, but the safety and long-term efficacy of its current treatments remain controversial. Recent evidence showing the roles of the gut microbiome (GM) in nutrient absorption indicates its usefulness in alternative interventions to treat UN safely with sustainable amelioration. To enhance our understanding of the GM and childhood undernutrition, we deep sequenced the gut metagenomes of 65 children with moderate or severe undernutrition (UN group) and 61 healthy children (HC group) to identify associated taxa and genes using a two-stage validation scheme. At stage I, 54 UN patients and 51 healthy children were enrolled for the discovery of GM markers in UN children. The accuracy of the markers was then tested in an additional 11 UN patients and 10 healthy children at stage II. Compared to the HC group, the UN group had lower richness in microbial genes ( = 0.005, FDR = 0.005) and species ( = 0.002, FDR = 0.002). The distributions of bacterial genes enable the identification of 16 gene markers with which to discriminate UN patients with high accuracy [averaged areas under the receiver operating curve (AUC) = 0.87], including three genes that are responsible for the synthesis of iron transporters. We also identified four species markers that enable the UN patients to be confidently discriminated from the HC children (averaged AUC = 0.91), namely , , , and . In addition, metabolic comparison showed significantly decreased isobutyric acid ( = 0.005, FDR = 0.017) and increased isovaleric acid ( = 0.006, FDR = 0.017) in UN patients. We also identified notable correlations between microbial species and short-chain fatty acids (SCFAs) and several nutritional indicators, including acetic acid and iron ( = 0.436, = 0.029), butyric acid and iron ( = 0.422, = 0.036), butyric acid and lymphocyte ( = -0.309, = 0.011), and acetic acid and total protein ( = -0.303, = 0.043). Taken together, the distinct features of gut microbiota in UN patients highlight the taxonomic and functional shift during the development of UN and provide a solid theoretical basis for intervention in childhood undernutrition through gut microbes.

摘要

营养不良是一个全球性问题,影响着儿童的发病率和死亡率,但其现有治疗方法的安全性和长期疗效仍存在争议。最近有证据表明肠道微生物群(GM)在营养吸收中发挥作用,这表明其在替代干预措施中具有实用性,可安全地治疗营养不良并实现可持续改善。为了加深我们对GM与儿童营养不良的理解,我们对65名中度或重度营养不良儿童(营养不良组)和61名健康儿童(健康对照组)的肠道宏基因组进行了深度测序,采用两阶段验证方案来识别相关的分类群和基因。在第一阶段,纳入了54名营养不良患者和51名健康儿童,以发现营养不良儿童的GM标志物。然后在第二阶段,对另外11名营养不良患者和10名健康儿童进行标志物准确性测试。与健康对照组相比,营养不良组的微生物基因丰富度较低(P = 0.005,FDR = 0.005),物种丰富度也较低(P = 0.002,FDR = 0.002)。细菌基因的分布能够识别出16个基因标志物,可高精度地区分营养不良患者[平均受试者工作特征曲线下面积(AUC)= 0.87],其中包括三个负责铁转运蛋白合成的基因。我们还鉴定出四个物种标志物,能够可靠地区分营养不良患者与健康对照组儿童(平均AUC = 0.91),即、、和。此外,代谢比较显示,营养不良患者的异丁酸显著降低(P = 0.005,FDR = 0.017),异戊酸增加(P = 0.006,FDR = 0.017)。我们还发现微生物物种与短链脂肪酸(SCFAs)以及几种营养指标之间存在显著相关性,包括乙酸与铁(r = 0.436,P = 0.029)、丁酸与铁(r = 0.422,P = 0.036)、丁酸与淋巴细胞(r = -0.309,P = 0.011)以及乙酸与总蛋白(r = -0.303,P = 0.043)。综上所述,营养不良患者肠道微生物群的独特特征突出了营养不良发展过程中的分类学和功能转变,并为通过肠道微生物干预儿童营养不良提供了坚实的理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d56/6895006/94db43a6158a/fmicb-10-02635-g001.jpg

相似文献

1
Intestinal sp. Imbalance Associated With the Occurrence of Childhood Undernutrition in China.
Front Microbiol. 2019 Nov 29;10:2635. doi: 10.3389/fmicb.2019.02635. eCollection 2019.
3
Gut microbiota dysbiosis in Chinese children with type 1 diabetes mellitus: An observational study.
World J Gastroenterol. 2021 May 21;27(19):2394-2414. doi: 10.3748/wjg.v27.i19.2394.
4
Evaluation and comparison of short chain fatty acids composition in gut diseases.
World J Gastroenterol. 2019 Sep 28;25(36):5543-5558. doi: 10.3748/wjg.v25.i36.5543.
5
Bacteroides vulgatus Ameliorates Lipid Metabolic Disorders and Modulates Gut Microbial Composition in Hyperlipidemic Rats.
Microbiol Spectr. 2023 Feb 14;11(1):e0251722. doi: 10.1128/spectrum.02517-22. Epub 2023 Jan 10.
6
Imbalance of Microbacterial Diversity Is Associated with Functional Prognosis of Stroke.
Neural Plast. 2023 May 8;2023:6297653. doi: 10.1155/2023/6297653. eCollection 2023.
7
colonization influences the abundance of intestinal short chain fatty acids and neurotransmitters.
iScience. 2022 Mar 25;25(5):104158. doi: 10.1016/j.isci.2022.104158. eCollection 2022 May 20.
8
Alterations of Gut Microbiota in Cholestatic Infants and Their Correlation With Hepatic Function.
Front Microbiol. 2018 Nov 13;9:2682. doi: 10.3389/fmicb.2018.02682. eCollection 2018.

引用本文的文献

2
The giant panda gut harbors a high diversity of lactic acid bacteria revealed by a novel culturomics pipeline.
mSystems. 2024 Jul 23;9(7):e0052024. doi: 10.1128/msystems.00520-24. Epub 2024 Jun 26.
3
Nutritional assessment in patients with liver cirrhosis.
World J Hepatol. 2022 Sep 27;14(9):1694-1703. doi: 10.4254/wjh.v14.i9.1694.
4
Gut microbes shape microglia and cognitive function during malnutrition.
Glia. 2022 May;70(5):820-841. doi: 10.1002/glia.24139. Epub 2022 Jan 12.
5
Cross-feeding between intestinal pathobionts promotes their overgrowth during undernutrition.
Nat Commun. 2021 Nov 25;12(1):6860. doi: 10.1038/s41467-021-27191-x.
6
Malnutrition in Patients with Liver Cirrhosis.
Nutrients. 2021 Feb 7;13(2):540. doi: 10.3390/nu13020540.

本文引用的文献

1
Microbial regulation of organismal energy homeostasis.
Nat Metab. 2019 Jan;1(1):34-46. doi: 10.1038/s42255-018-0017-4. Epub 2019 Jan 7.
2
SCFAs - the thin microbial metabolic line between good and bad.
Nat Rev Endocrinol. 2019 Jun;15(6):318-319. doi: 10.1038/s41574-019-0205-7.
3
Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases.
Nat Genet. 2019 Apr;51(4):600-605. doi: 10.1038/s41588-019-0350-x. Epub 2019 Feb 18.
4
Alterations of Gut Microbiota in Cholestatic Infants and Their Correlation With Hepatic Function.
Front Microbiol. 2018 Nov 13;9:2682. doi: 10.3389/fmicb.2018.02682. eCollection 2018.
5
You are what you eat: diet, health and the gut microbiota.
Nat Rev Gastroenterol Hepatol. 2019 Jan;16(1):35-56. doi: 10.1038/s41575-018-0061-2.
6
Depicting the composition of gut microbiota in a population with varied ethnic origins but shared geography.
Nat Med. 2018 Oct;24(10):1526-1531. doi: 10.1038/s41591-018-0160-1. Epub 2018 Aug 27.
7
9
Distinct gut microbiota profiles in patients with primary sclerosing cholangitis and ulcerative colitis.
World J Gastroenterol. 2017 Jul 7;23(25):4548-4558. doi: 10.3748/wjg.v23.i25.4548.
10
Gut Microbiota in Obesity and Undernutrition.
Adv Nutr. 2016 Nov 15;7(6):1080-1089. doi: 10.3945/an.116.012914. Print 2016 Nov.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验