非洲儿童的真核体受地理位置、肠道生物地理和营养状况的影响。

microLife Pub Date : 2023-01-01 DOI:10.1093/femsml/uqad033
Pascale Vonaesch, Vincent Billy, Allison E Mann, Evan Morien, Azimdine Habib, Jean-Marc Collard, Michel Dédé, Nathalie Kapel, Philippe J Sansonetti, Laura Wegener Parfrey
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摘要

真核生物历来被研究为寄生虫,但最近的证据表明它们可能是健康肠道生态系统的指标。在这里,我们描述了2-5岁儿童胃肠道的真核体,并测试了与贫血、肠道炎症、慢性营养不良和年龄等临床因素的关联。儿童于2016年12月至2018年5月在中非共和国班吉和马达加斯加塔那那利佛入学。我们分析了总共1104份样本,其中212份是胃样本,187份是十二指肠样本,705份是粪便样本,我们采用了一种针对真菌的ITS2全区和针对整个真核体的18S rRNA基因的V4高变区的元条形码方法。大约一半的粪便样本显示微真核生物。我们发现高主体间变异性,只有少数分类群可能是胃肠道的居民,真核生物在个体内经常共存。我们还发现,胃、十二指肠和粪便的真核体不同,并受到原产国的强烈影响。我们的数据显示,与未发育不良的对照组相比,发育不良儿童的镰孢菌(一种产生霉菌毒素的真菌)水平较高,原生囊胚菌水平较低。总体而言,真核体与临床变量相关性较差。我们的研究是迄今为止分析人类肠道真核体的最大队列之一,也是第一个比较胃肠道不同隔室真核体的队列。我们的研究结果强调了研究世界各地的人群以揭示健康真核体的共同特征的重要性。
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The eukaryome of African children is influenced by geographic location, gut biogeography, and nutritional status.

Eukaryotes have historically been studied as parasites, but recent evidence suggests they may be indicators of a healthy gut ecosystem. Here, we describe the eukaryome along the gastrointestinal tract of children aged 2-5 years and test for associations with clinical factors such as anaemia, intestinal inflammation, chronic undernutrition, and age. Children were enrolled from December 2016 to May 2018 in Bangui, Central African Republic and Antananarivo, Madagascar. We analyzed a total of 1104 samples representing 212 gastric, 187 duodenal, and 705 fecal samples using a metabarcoding approach targeting the full ITS2 region for fungi, and the V4 hypervariable region of the 18S rRNA gene for the overall eukaryome. Roughly, half of all fecal samples showed microeukaryotic reads. We find high intersubject variability, only a handful of taxa that are likely residents of the gastrointestinal tract, and frequent co-occurrence of eukaryotes within an individual. We also find that the eukaryome differs between the stomach, duodenum, and feces and is strongly influenced by country of origin. Our data show trends towards higher levels of Fusarium equiseti, a mycotoxin producing fungus, and lower levels of the protist Blastocystis in stunted children compared to nonstunted controls. Overall, the eukaryome is poorly correlated with clinical variables. Our study is of one of the largest cohorts analyzing the human intestinal eukaryome to date and the first to compare the eukaryome across different compartments of the gastrointestinal tract. Our results highlight the importance of studying populations across the world to uncover common features of the eukaryome in health.

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