感染、喂养不耐受或坏死性小肠结肠炎早产儿胎便菌群的丰度和组成。

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
YanQiu Jiang, Qiang Yao, YanFeng Zhao, YunWei Kong, Tao Yu, YanFang Wang, Fei Yang, WeiNong Mo
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引用次数: 0

摘要

背景:新生儿肠道微生物菌群的作用具有科学和实际意义。本研究的目的是评估感染、喂养不耐受或坏死性小肠结肠炎(NEC)早产儿胎粪菌群的丰度和组成。方法:84例剖宫产早产儿前瞻性纳入研究。在28例患病婴儿中,23例发生感染,其中败血症8例,肺炎10例,小肠结肠炎1例,NEC 4例。无上述特征的早产儿56例(66.67%)作为对照组。收集一般临床信息(性别、胎龄、出生体重、是否存在胎膜早破、Apgar 1分钟评分、住院时间)。收集首过胎便标本进行16S rRNA微生物学分析。结果:与对照组相比,病儿胎龄低(p < 0.001),体重低(p = 0.014)。患儿住院时间明显长于对照组(p < 0.001)。在α-多样性指标上,两组间物种丰度和多样性均无显著差异;在β-多样性测量上,对两组微生物组成的差异进行PCoA分析,结果表明疾病组与对照组之间存在差异。在门水平上,两组的优势门均为p_Proteobacteria,疾病组的p_Firmicutes丰度更高。在属水平上,两组优势属均为g_Novosphingobium。BugBase的微生物表型预测显示,疾病组微生物表型“革兰氏阳性”和“厌氧”大量增加;两组之间的微生物功能预测在显著功能方面没有差异。结论:感染、喂养不耐受和NEC对宿主的影响是复杂的。剖宫产早产婴儿的优势门为p_变形菌门,疾病组中p_厚壁菌门的丰度更高,这一差异是由g_Peptoniphilus造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abundance and Composition of the Meconium Microbiota in Preterm Infants with Infections, Feeding Intolerance, or Necrotizing Enterocolitis.

Background: The role of the microbial flora of the gut of a newborn is of scientific and practical interest. The aim of this study was to assess the abundance and composition of the meconium microbiota in preterm infants with infections, feeding intolerance, or necrotizing enterocolitis (NEC).

Methods: Eighty-four preterm infants born by cesarean section were prospectively enrolled in this study. Out of the 28 diseased infants, 23 developed infections, including 8 cases of sepsis, 10 cases of pneumonia, 1 case of enterocolitis, and 4 cases of NEC. Fifty-six (66.67%) preterm infants without these characteristics served as control group. General clinical information (gender, gestational age, birth weight, presence of preterm rupture of mem-branes, Apgar 1-minute score, and duration of hospitalization) was collected. First-pass meconium samples were collected for 16S rRNA microbiological analysis.

Results: Compared with the control group, the diseased infants had a lower gestational age (p < 0.001) and lower body weight (p = 0.014). In addition, the hospitalization time of the diseased infants was longer than that of the control group (p < 0.001). On the α-diversity measure, there was no difference in species abundance and diversity between the two groups; on the β-diversity measure, the differences in the microbial composition of the two groups were subjected to PCoA analyses, which showed that there was a difference between the disease group and the control group. At the phylum level, the dominant phylum in both groups was p_Proteobacteria, with higher abundance of p_Firmicutes in the disease group. At the genus level, the dominant genus in both groups was g_Novosphingobium. Microbiome phenotype prediction by BugBase revealed that microbial phenotypes 'Gram-positive' and 'Anaerobic' were abundantly increased in the disease group; microbial function prediction did not differ between the two groups in terms of significant function.

Conclusions: The impact of infections, feeding intolerance, and NEC on a host is complex. Preterm infants delivered by cesarean section have p_Proteobacteria as the dominant phylum, with a higher abundance of p_Firmicutes in the disease group, a difference contributed by g_Peptoniphilus.

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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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