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不同营养状况印度儿童的肠道细菌特征:一项比较性初步研究。

Gut bacterial profile in Indian children of varying nutritional status: a comparative pilot study.

机构信息

Molecular Biology Unit, Dairy Microbiology Division, ICAR-National Dairy Research Institute, Karnal, Haryana, 132001, India.

Advanced Paediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.

出版信息

Eur J Nutr. 2021 Oct;60(7):3971-3985. doi: 10.1007/s00394-021-02571-7. Epub 2021 Apr 30.

Abstract

PURPOSE

Childhood malnutrition is a multifactorial disease, responsible for nearly half of all deaths in children under five. Lately, the probable association of a dysbiotic gut to malnutrition is also being eagerly investigated. The current study is an attempt to investigate this purported association through assessing the abundance of major gut bacterial phyla (Firmicutes, Bacteroidetes, Actinobacteria and Proteobacteria), probionts (Bifidobacteria and Lactobacillus), butyrogens (Faecalibacterium and Roseburia) and pathogens (Escherichia and Klebsiella).

METHODS

The study was conducted in the suburbs of Chandigarh, India in the year 2017. The children enrolled in the study were part of Anganwadis (Rural Child Care Centres) set up under Integrated Child Development Scheme (ICDS) of Government of India where community-based management approach is being widely used for treatment of malnutrition. We used qPCR based absolute quantification as well as the 16S rRNA amplicon sequencing approach for our study. The study population included 30 children in the age group of 2-5 years who were categorized into three groups Healthy, Moderate Acute Malnutrition (MAM) and Severe Acute Malnutrition (SAM), with 10 children in each group. The selection of participants was made based on Z scores. Further, statistical tools like the One-way ANOVA, PCA and PLSDA were employed to analyze and compare the gut bacterial profile.

RESULTS

Our investigation through the qPCR (Absolute quantification) approach revealed a significantly higher abundance of Actinobacteria in healthy, in comparison to children suffering from Severe Acute Malnutrition (SAM). Consequently, the same trend was also reflected with respect to Bifidobacterium, a prominent member of the Actinobacteria phylum. Conversely, a significant higher abundance of Lactobacillus with the diminishing nutritional status was recorded. Escherichia showed a significant higher abundance in healthy subjects compared to the malnourished; however, no such difference in abundance of Klebsiella was observed. The other target phyla [Bacteroidetes, Firmicutes and Proteobacteria] and genera (Faecalibacterium and Roseburia) showed differences in abundance; however, these were non-significant. Similarly, the bacterial taxonomy analysis of 16S rRNA gene amplicon sequencing data revealed the higher abundance of phylum Actinobacteria and its member Bifidobacterium with lower prevalence of Lactobacillus in healthy children.

CONCLUSION

The pattern of gut microbiota profile in malnourished subjects suggests a dysbiotic gut depleted in Bifidobacteria, a core member of the consortia of beneficial anaerobes of the healthy child gut.

摘要

目的

儿童营养不良是一种多因素疾病,导致五岁以下儿童近半数死亡。最近,肠道菌群失调与营养不良之间的可能关联也在被积极研究。本研究试图通过评估主要肠道细菌门(Firmicutes、Bacteroidetes、Actinobacteria 和 Proteobacteria)、益生菌(双歧杆菌和乳酸杆菌)、丁酸产生菌(Faecalibacterium 和 Roseburia)和病原体(Escherichia 和 Klebsiella)的丰度来研究这种假定的关联。

方法

该研究于 2017 年在印度昌迪加尔郊区进行。参与研究的儿童是印度政府综合儿童发展计划(ICDS)下的安格班迪(农村儿童保育中心)的一部分,该计划广泛采用基于社区的管理方法来治疗营养不良。我们使用基于 qPCR 的绝对定量和 16S rRNA 扩增子测序方法进行研究。研究人群包括 30 名 2-5 岁的儿童,分为三组:健康组、中度急性营养不良(MAM)组和严重急性营养不良(SAM)组,每组 10 名儿童。参与者的选择是根据 Z 分数进行的。此外,还使用 One-way ANOVA、PCA 和 PLSDA 等统计工具来分析和比较肠道细菌谱。

结果

通过 qPCR(绝对定量)方法的研究发现,与患有严重急性营养不良(SAM)的儿童相比,健康儿童的放线菌丰度显著更高。同样,放线菌的主要成员双歧杆菌的丰度也呈现出相同的趋势。相反,随着营养状况的恶化,乳酸杆菌的丰度显著增加。与营养不良的儿童相比,健康儿童的大肠杆菌丰度显著更高;然而,没有观察到克雷伯氏菌丰度的差异。其他目标门(Bacteroidetes、Firmicutes 和 Proteobacteria)和属(Faecalibacterium 和 Roseburia)的丰度存在差异,但无统计学意义。同样,16S rRNA 基因扩增子测序数据分析的细菌分类学表明,健康儿童的肠道中放线菌及其成员双歧杆菌的丰度较高,而乳酸杆菌的丰度较低。

结论

营养不良儿童的肠道微生物群谱模式表明,肠道菌群失调,双歧杆菌减少,而双歧杆菌是健康儿童肠道有益厌氧菌联合体的核心成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b73/8085102/670e1f82547a/394_2021_2571_Fig1_HTML.jpg

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