强化母乳后极早产儿肠道微生物群的发育。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-03-18 Epub Date: 2025-02-21 DOI:10.1128/msystems.00916-24
Lin Yang, Yan Hui, Per Torp Sangild, Witold Piotr Kot, Lise Aunsholt, Gitte Zachariassen, Ping-Ping Jiang, Dennis Sandris Nielsen
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引用次数: 0

摘要

极早产儿(vpi)出生时肠道发育不成熟,易患肠道微生物群失调相关疾病,例如坏死性小肠结肠炎。虽然这些婴儿需要强化母乳,但最佳强化剂仍不确定。牛初乳(BC)富含蛋白质和生物活性成分,可作为传统强化剂(CF)的替代品。采用16S rRNA基因扩增子测序方法,对225名喂食加了BC或CF的母乳的vpi (FortiColos研究,NCT03537365)在强化前、强化1周和强化2周后收集的粪便样本进行了肠道微生物群(GM)分析。出生方式对出生后不久的微生物群落结构有短暂的影响,剖宫产出生的VPIs以厚壁菌门为主,而顺产出生的VPIs以变形菌门为主。这种出生方式导致的差异随着年龄的增长而减少,并在出生后1个月左右消失。强化物类型对微生物群落结构有一定影响,但在BC和CF两组间没有显著差异。BC升高的粪便pH与葡萄球菌和棒状杆菌呈正相关,与双歧杆菌丰度呈负相关。葡萄球菌相对丰度的变化与体重增加呈负相关。总的来说,用BC或CF强化母乳确实会影响vpi的GM,但在生命早期只有适度的程度。在此期间,出生方式似乎对转基因有显著但暂时的影响。生命早期是肠道微生物群(GM)建立的关键时期,其中肠内喂养起着重要作用。早产婴儿也是如此,由于他们的肠道不成熟,他们患转基因生物失调相关疾病的风险很高。母乳是早产儿的最佳饲料,但它需要强化以达到足够的水平,尤其是蛋白质。只有少数研究调查了强化剂对早产儿转基因发育的影响。在这里,我们证明了两种不同的牛乳强化剂,牛初乳和基于成熟牛乳的传统强化剂,对极早产儿的微生物群落结构的影响有限。这些发现表明,尽管在早产儿GM最佳成熟方面应该采取非常谨慎的措施,但选择强化剂的影响有限。在临床实践中,强化剂的选择因此可以充分集中在优化早产儿营养。临床试验:该研究已在ClinicalTrials.gov注册为NCT03537365。
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Gut microbiota development in very preterm infants following fortification of human milk.

Very preterm infants (VPIs) are born with an immature gut and predisposed to gut microbiota dysbiosis-related diseases, for example, necrotizing enterocolitis. Although fortification of human milk is required for these infants, the optimal fortifier remains uncertain. Bovine colostrum (BC), rich in protein and bioactive components, could serve as an alternative to conventional fortifiers (CF). The gut microbiota (GM) of 225 VPIs fed human milk fortified with either BC or CF (FortiColos study, NCT03537365) was profiled by 16S rRNA gene amplicon sequencing of fecal samples collected before, and after 1 and 2 weeks of fortification. Birth mode exhibited transient effects on the microbial community structure shortly after birth, with cesarean section-born VPIs dominated by Firmicutes, whereas vaginally born VPIs were dominated by Proteobacteria. This birth mode-derived difference diminished with age and disappeared around 1 month after birth. Fortifier type affected the microbial community structure to a modest extent, but no specific taxa significantly differed between the BC and CF groups. Fecal pH, increased by BC, was positively correlated with Staphylococcus and Corynebacterium and negatively with Bifidobacterium abundance. Change in the relative abundance of Staphylococcus was negatively correlated with body weight gain. Collectively, fortification of human milk with BC or CF does influence the GM of VPIs but only to a modest extent during early life. Birth mode appears to have a significant, but temporary influence on the GM during this period.IMPORTANCEEarly life is a key period for gut microbiota (GM) establishment, where enteral feeding plays a significant role. This is also the case for infants born preterm, who, due to their immature gut, are at a high risk of developing GM dysbiosis-related diseases. Human milk is the optimal feed for preterm infants, but it requires fortification to reach adequate levels of especially protein. Only a few studies have investigated the impact of fortifiers on GM development in preterm infants. Here, we demonstrate that two different bovine milk-based fortifiers, bovine colostrum and a conventional fortifier based on mature bovine milk, exhibit limited effects on the microbial community structure of very preterm infants. These findings suggest that although great care in terms of optimally maturing the preterm infant GM should be taken, the choice of fortifier only has limited impact. In clinical practice, the choice of fortifier can thus be fully focussed on optimizing preterm infant nutrition.CLINICAL TRIALSThis study is registered with ClinicalTrials.gov as NCT03537365.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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