Kortekangas Emma, Fan Yue-Mei, Chaima David, Lehto Kirsi-Maarit, Malamba-Banda Chikondi, Matchado Andrew, Chingwanda Chilungamo, Liu Zhifei, Ashorn Ulla, Cheung Yin Bun, Dewey Kathryn G, Maleta Kenneth, Ashorn Per
Center for Child, Adolescent and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere 33014, Finland.
School of Public Health and Family Medicine, College of Medicine, University of Malawi, Blantyre, Malawi.
J Trop Pediatr. 2022 Feb 3;68(2). doi: 10.1093/tropej/fmac012.
Environmental enteric dysfunction (EED) is common in low- and middle-income countries and associated with childhood undernutrition. The composition of gut microbiota has been implicated in the pathogenesis of EED. Our aim was to assess the associations between gut microbiota and EED biomarkers in rural Malawian children. We hypothesized that there would be an inverse association between microbiota maturity and diversity and fecal concentrations of EED biomarkers.
We used data from fecal samples collected at 6, 18 and 30 months from 611 children who were followed up during a nutrition intervention trial. The primary time point for analysis was 18 months. Microbiota data were obtained through 16S rRNA sequencing and variables included microbiota maturity and diversity, phylogenetic dissimilarity and relative abundances of individual taxa. EED biomarkers included calprotectin (marker of inflammation), alpha-1 antitrypsin (intestinal permeability) and REG1B (intestinal damage).
There was an inverse association between microbiota maturity and diversity and fecal concentrations of all 3 EED biomarkers at 18 months (p≤0.001). The results were similar at 30 months, while at 6 months inverse associations were found only with calprotectin and alpha-1 antitrypsin concentrations. At 18 months, EED biomarkers were not associated with phylogenetic dissimilarity, but at 6 and 30 months several associations were observed. Individual taxa predicting EED biomarker concentrations at 18 months included several Bifidobacterium and Enterobacteriaceae taxa as well as potentially displaced oral taxa.
Our findings support the hypothesis of an inverse association between microbiota maturity and diversity and EED in rural Malawian children.
环境性肠道功能障碍(EED)在低收入和中等收入国家很常见,并且与儿童营养不良有关。肠道微生物群的组成与EED的发病机制有关。我们的目的是评估马拉维农村儿童肠道微生物群与EED生物标志物之间的关联。我们假设微生物群成熟度和多样性与EED生物标志物的粪便浓度之间存在负相关。
我们使用了在一项营养干预试验中对611名儿童进行随访期间,于6、18和30个月收集的粪便样本数据。分析的主要时间点是18个月。通过16S rRNA测序获得微生物群数据,变量包括微生物群成熟度和多样性、系统发育差异以及各个分类群的相对丰度。EED生物标志物包括钙卫蛋白(炎症标志物)、α-1抗胰蛋白酶(肠道通透性)和REG1B(肠道损伤)。
在18个月时,微生物群成熟度和多样性与所有3种EED生物标志物的粪便浓度之间存在负相关(p≤0.001)。30个月时结果相似,而在6个月时,仅发现与钙卫蛋白和α-1抗胰蛋白酶浓度存在负相关。在18个月时,EED生物标志物与系统发育差异无关,但在6个月和30个月时观察到了几种关联。预测18个月时EED生物标志物浓度的单个分类群包括几种双歧杆菌和肠杆菌科分类群以及可能移位的口腔分类群。
我们的研究结果支持了马拉维农村儿童微生物群成熟度和多样性与EED之间存在负相关的假设。