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新生儿败血症中的肠道微生物组失调。

Gut microbiome dysbiosis in neonatal sepsis.

机构信息

Molecular Genetics Laboratory, Infection and Immunology Division, Translational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, India.

Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Prog Mol Biol Transl Sci. 2022;192(1):125-147. doi: 10.1016/bs.pmbts.2022.07.010. Epub 2022 Aug 30.

DOI:10.1016/bs.pmbts.2022.07.010
PMID:36280317
Abstract

Sepsis is a highly heterogeneous, life-threatening organ dysfunction primarily caused by a dysregulated immune response to counter bacterial, viral, or fungal infections, resulting in haemodynamic changes and significant morbidity and mortality across all ages. In recent times, it has become one of the foremost causes of morbidity and mortality among newborns globally. The neonates, particularly the preterm neonates, due to their immature immune systems and non-canonical microbial community acquisition in the gastrointestinal tract and other body habitats, are adversely affected compared to the elderly with immunocompromised conditions. The neonates could acquire microbiota in utero or during delivery from the mother's genital tract or postnatally from contact with hospital personnel and the immediate hospital environment after the birth. Other factors that may enhance the risk include early colonization of microbiota by pathogens that trigger dysbiosis of the gut microbiome accompanied by a dysregulated immune response, organ dysfunction, and potential death. The sepsis-linked mortality could be prevented by timely diagnosis, selective antibiotic therapy, and supportive postnatal care. Infections due to antibiotic-resistant bacteria severely restrict possible therapeutic options, thus extending hospital stays. A comprehensive analysis of the infecting pathogens, cognate host responses, and the microbiota present would certainly help formulate appropriate interventions.

摘要

败血症是一种高度异质的、危及生命的器官功能障碍,主要由对细菌、病毒或真菌感染的免疫反应失调引起,导致血流动力学变化,并在所有年龄段都导致发病率和死亡率显著增加。近年来,它已成为全球新生儿发病率和死亡率的首要原因之一。与免疫功能低下的老年人相比,由于免疫系统不成熟和胃肠道及其他身体栖息地中非常规微生物群落的获得,新生儿,特别是早产儿,受到不利影响。新生儿可以在宫内或分娩时从母亲的生殖道中或在出生后通过与医院人员和出生后的立即医院环境接触获得微生物群。其他可能增加风险的因素包括病原体的早期定植,这些病原体引发肠道微生物组的生态失调,随之而来的是免疫反应失调、器官功能障碍和潜在的死亡。通过及时诊断、选择性抗生素治疗和支持性产后护理,可以预防与败血症相关的死亡。抗生素耐药细菌引起的感染严重限制了可能的治疗选择,从而延长了住院时间。对感染病原体、相关宿主反应和存在的微生物组进行全面分析,肯定有助于制定适当的干预措施。

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Gut microbiome dysbiosis in neonatal sepsis.新生儿败血症中的肠道微生物组失调。
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引用本文的文献

1
Antibiotic strategies for neonatal sepsis: navigating efficacy and emerging resistance patterns.新生儿败血症的抗生素治疗策略:应对疗效与新出现的耐药模式
Eur J Pediatr. 2025 Jun 24;184(7):439. doi: 10.1007/s00431-025-06271-w.
2
Gut Pathogen Colonization: A Risk Factor to Bloodstream Infections in Preterm Neonates Admitted in the Neonatal Intensive Care Unit - A Prospective Cohort Study.肠道病原体定植:新生儿重症监护病房收治的早产儿发生血流感染的一个危险因素——一项前瞻性队列研究。
Neonatology. 2025;122(2):151-160. doi: 10.1159/000542335. Epub 2024 Dec 13.
3
Gut microbiota in preterm infants with late-onset sepsis and pneumonia: a pilot case-control study.
早产儿晚发型败血症和肺炎的肠道菌群:一项初步病例对照研究。
BMC Microbiol. 2024 Jul 22;24(1):272. doi: 10.1186/s12866-024-03419-w.