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与极早早产儿脑损伤相关的肠道微生物群基因组特征

Gut microbiota genome features associated with brain injury in extremely premature infants.

作者信息

Seki David, Kirkegaard Rasmus, Osvatic Jay, Hausmann Bela, Séneca Joana, Pjevac Petra, Berger Angelika, J Hall Lindsay, Wisgrill Lukas, Berry David

机构信息

Centre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, Division of Microbial Ecology, University of Vienna, Vienna, Austria.

Joint Microbiome Facility of the Medical University of Vienna and the University of Vienna, Vienna, Austria.

出版信息

Gut Microbes. 2024 Jan-Dec;16(1):2410479. doi: 10.1080/19490976.2024.2410479. Epub 2024 Oct 7.

DOI:10.1080/19490976.2024.2410479
PMID:39679616
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11459832/
Abstract

Severe brain damage is common among premature infants, and the gut microbiota has been implicated in its pathology. Although the order of colonizing bacteria is well described, the mechanisms underlying aberrant assembly of the gut microbiota remain elusive. Here, we employed long-read nanopore sequencing to assess abundances of microbial species and their functional genomic potential in stool samples from a cohort of 30 extremely premature infants. We identify several key microbial traits significantly associated with severe brain damage, such as the genomic potential for nitrate respiration and iron scavenging. Members of the were prevalent across the cohort and displayed a versatile metabolic potential, including pathogenic and nonpathogenic traits. Predominance of and were associated with an overall loss of genomic functional redundancy as well as poor neurophysiological outcome. These findings reveal microbial traits that may be involved in exacerbating brain injury in extremely premature infants and provide suitable targets for therapeutic interventions.

摘要

严重脑损伤在早产儿中很常见,肠道微生物群被认为与该病的病理过程有关。尽管定殖细菌的顺序已得到充分描述,但肠道微生物群异常组装的潜在机制仍不清楚。在这里,我们采用长读长纳米孔测序技术,评估了30名极早产儿队列粪便样本中微生物种类的丰度及其功能基因组潜力。我们确定了几个与严重脑损伤显著相关的关键微生物特征,如硝酸盐呼吸和铁清除的基因组潜力。该队列中 的成员普遍存在,并表现出多种代谢潜力,包括致病和非致病特征。 和 的优势与基因组功能冗余的整体丧失以及不良的神经生理结果有关。这些发现揭示了可能参与加重极早产儿脑损伤的微生物特征,并为治疗干预提供了合适的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/eab83df35a20/KGMI_A_2410479_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/b875a8783f73/KGMI_A_2410479_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/00e24970e5cc/KGMI_A_2410479_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/bc3ad8587fc3/KGMI_A_2410479_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/eab83df35a20/KGMI_A_2410479_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/b875a8783f73/KGMI_A_2410479_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/00e24970e5cc/KGMI_A_2410479_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/bc3ad8587fc3/KGMI_A_2410479_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd0/11459832/eab83df35a20/KGMI_A_2410479_F0004_OC.jpg

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Neuroactive metabolites and bile acids are altered in extremely premature infants with brain injury.神经活性代谢物和胆汁酸在脑损伤的极早产儿中发生改变。
Cell Rep Med. 2024 Apr 16;5(4):101480. doi: 10.1016/j.xcrm.2024.101480. Epub 2024 Mar 22.
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Developmental Pharmacokinetics of Antibiotics Used in Neonatal ICU: Focus on Preterm Infants.新生儿重症监护病房使用的抗生素的发育药代动力学:关注早产儿。
Biomedicines. 2023 Mar 17;11(3):940. doi: 10.3390/biomedicines11030940.
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Extending and improving metagenomic taxonomic profiling with uncharacterized species using MetaPhlAn 4.
利用 MetaPhlAn 4 对未鉴定物种进行宏基因组分类分析的扩展和改进。
Nat Biotechnol. 2023 Nov;41(11):1633-1644. doi: 10.1038/s41587-023-01688-w. Epub 2023 Feb 23.
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Why is manganese so valuable to bacterial pathogens?为什么锰对细菌病原体如此有价值?
Front Cell Infect Microbiol. 2023 Feb 3;13:943390. doi: 10.3389/fcimb.2023.943390. eCollection 2023.
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Predicting the pathogenicity of bacterial genomes using widely spread protein families.利用广泛分布的蛋白质家族预测细菌基因组的致病性。
BMC Bioinformatics. 2022 Jun 24;23(1):253. doi: 10.1186/s12859-022-04777-w.
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Ecological Processes Shaping Microbiomes of Extremely Low Birthweight Infants.塑造极低出生体重儿微生物群的生态过程。
Front Microbiol. 2022 Feb 28;13:812136. doi: 10.3389/fmicb.2022.812136. eCollection 2022.
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METABOLIC: high-throughput profiling of microbial genomes for functional traits, metabolism, biogeochemistry, and community-scale functional networks.代谢组学:高通量分析微生物基因组的功能特征、代谢、生物地球化学和群落尺度的功能网络。
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Aberrant gut-microbiota-immune-brain axis development in premature neonates with brain damage.脑损伤早产儿肠道微生物群-免疫-脑轴发育异常。
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Bifidobacteria-mediated immune system imprinting early in life.双歧杆菌在生命早期介导免疫系统印记。
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