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蛔虫的肠道细菌组和代谢组在患者体内。

Gut bacteriome and metabolome of Ascaris lumbricoides in patients.

机构信息

Program in Bioinformatics and Computational Biology, Graduate School, Chulalongkorn University, Bangkok, 10330, Thailand.

Center of Excellence in Systems Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.

出版信息

Sci Rep. 2022 Nov 14;12(1):19524. doi: 10.1038/s41598-022-23608-9.

Abstract

The most frequent intestinal helminth infections in humans are attributed to Ascaris lumbricoides, and there are concerns over the anthelminthic resistance of this species. The gut microbiota has essential roles in host physiology. Therefore, discovering host-parasite-microbiota interactions could help develop alternative helminthiasis treatments. Additionally, these interactions are modulated by functional metabolites that can reveal the mechanisms of infection and disease progression. Thus, we aimed to investigate bacteriomes in the gut of helminths and fecal samples of patients via next-generation sequencing. Our results showed that infection intensity was associated with the bacterial composition of helminth guts but not with the intestinal bacteriome of human hosts. Moreover, the metabolomes of A. lumbricoides in the heavy and light ascariasis cases were characterized using ultra-high performance liquid chromatography/time-of-flight mass spectrometry. Increased levels of essential biomolecules, such as amino acids, lipids, and nucleotide precursors, were found in the guts of helminths isolated from heavily infected patients, implying that these metabolites are related to egg production and ascariasis pathogenicity. These findings are the first step towards a more complete understanding of the mechanisms by which the bacteriome of helminth guts affect their colonization and may reveal novel and more effective approaches to parasitic disease therapy.

摘要

人体最常见的肠道蠕虫感染是由蛔虫引起的,人们担心这种物种会对驱虫剂产生抗药性。肠道微生物群在宿主生理学中起着至关重要的作用。因此,发现宿主-寄生虫-微生物群的相互作用有助于开发替代寄生虫病的治疗方法。此外,这些相互作用受到功能代谢物的调节,这些代谢物可以揭示感染和疾病进展的机制。因此,我们旨在通过下一代测序技术研究蠕虫肠道中的细菌组和患者粪便样本。我们的研究结果表明,感染强度与蠕虫肠道的细菌组成有关,而与人类宿主的肠道细菌组无关。此外,我们使用超高效液相色谱/飞行时间质谱对重度和轻度蛔虫病病例中的蛔虫代谢组进行了表征。在从重度感染患者中分离出的蠕虫肠道中发现了更多必需生物分子(如氨基酸、脂质和核苷酸前体)的水平升高,这表明这些代谢物与产卵和蛔虫病的致病性有关。这些发现是更全面地了解蠕虫肠道细菌组如何影响其定植的机制的第一步,可能揭示治疗寄生虫病的新的、更有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/9663418/7f55588c60e5/41598_2022_23608_Fig1_HTML.jpg

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