肠道菌群及其与坏死性小肠结肠炎发生关系的研究进展

Q1 Medicine
Michel Hosny, Nadim Cassir, Bernard La Scola
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引用次数: 18

摘要

坏死性小肠结肠炎(NEC)仍然是发病率和死亡率的主要原因,主要影响早产儿。这种肠道疾病的发病机制似乎与细菌定植的破坏或延迟有关,称为肠道生态失调。肠道不成熟、抗生素使用和医院微生物环境是这一病理过程的主要触发因素。相反,肠道共生是通过有益和共生细菌的存在来实现的,这些细菌可以保护未成熟的肠道免受机会性病原体的过度生长和炎症。在此,我们回顾了肠道微生物群与早产儿NEC之间的关系。我们还讨论了属于共生微生物群的特定微生物的作用,强调了NEC发病机制中涉及的产毒机制的可能性。我们总结了旨在提供或恢复有益菌群的干预措施的重要性,以期有效地预防或治疗NEC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Updating on gut microbiota and its relationship with the occurrence of necrotizing enterocolitis

Necrotizing enterocolitis (NEC) remains a leading cause of morbidity and mortality, affecting primarily preterm neonates. The pathogenesis of this intestinal disease appears to be linked to the disruption or delay of bacterial colonization, termed gut dysbiosis. Intestinal immaturity, antibiotic use and hospital microbial environment are the main triggers of this pathological process. Conversely, gut symbiosis is made possible by the presence of beneficial and commensal bacterial species that protect the immature gut from opportunistic pathogens overgrowth and inflammation. Herein, we review the relationships between gut microbiota and NEC in preterm neonates. We also discuss the role of specific microorganisms belonging to the commensal microbiota, highlighting the possibility for a toxigenic mechanism involved in NEC pathogenesis. We conclude on the importance of interventions aimed at providing or restoring beneficial bacteria populations, in view to efficiently preventing or treating NEC.

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来源期刊
Human Microbiome Journal
Human Microbiome Journal Medicine-Infectious Diseases
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期刊介绍: The innumerable microbes living in and on our bodies are known to affect human wellbeing, but our knowledge of their role is still at the very early stages of understanding. Human Microbiome is a new open access journal dedicated to research on the impact of the microbiome on human health and disease. The journal will publish original research, reviews, comments, human microbe descriptions and genome, and letters. Topics covered will include: the repertoire of human-associated microbes, therapeutic intervention, pathophysiology, experimental models, physiological, geographical, and pathological changes, and technical reports; genomic, metabolomic, transcriptomic, and culturomic approaches are welcome.
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