对自闭症患者肠道微生物组的全面多样性分析:从α、β到γ多样性。

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Hongju Daisy Chen, Lianwei Li, Fubing Yu, Zhanshan Sam Ma
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引用次数: 0

摘要

据估计,自闭症谱系障碍(ASD)影响着全球多达 1%的儿童,但其病因仍不清楚。有研究认为,肠道微生物组在调节与自闭症谱系障碍相关的异常行为方面发挥着重要作用。微生物组相关疾病的事实标准分析是多样性分析,然而,现有关于 ASD 与微生物组关系的研究尚未达成共识。在此,我们基于已发表的 8 个数据集,包括 898 个 ASD 样本和 467 个健康对照(HC)的 16S-rRNA 测序结果,对 ASD 相关的多样性变化进行了全面分析,涉及α、β和γ-多样性指标。我们的研究结果包括(i) 就阿尔法多样性而言,在大约 1/3 的研究案例中,ASD 患者表现出明显高于 HC 的阿尔法多样性,这似乎与多样性-疾病关系(DDR)的 "1/3 猜想 "一致。 (ii) 就贝塔多样性而言,AKP(安娜-卡列尼娜原则)预测所有健康微生物组都应该是相似的,而每个患病微生物组都应该有其自身的不同之处,这在大约 1/2 到 3/4 的研究案例中似乎是正确的。(iii) 在伽马多样性方面,DAR(多样性-面积关系)模型表明,ASD 患者的多样性-面积比例参数似乎比 HC 患者大,这与 AKP 的结果一致。然而,MAD(最大应计多样性)和RIP(个体与群体多样性之比)参数并未表明ASD患者与HC之间存在显著差异。在整个研究过程中,我们采用希尔数来衡量多样性,并根据稀有度-常见度-优势度频谱对多样性指标进行了分层。看来,ASD 患者和 HC 之间的差异在稀有物种方面比在优势物种方面更有说服力。最后,我们讨论了不同案例研究中多样性与自闭症之间明显不一致的关系,并推测这种关系不是单调的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comprehensive diversity analysis on the gut microbiomes of ASD patients: from alpha, beta to gamma diversities.

Autism spectrum disorder (ASD) is estimated to influence as many as 1% children worldwide, but its etiology is still unclear. It has been suggested that gut microbiomes play an important role in regulating abnormal behaviors associated with ASD. A de facto standard analysis on the microbiome-associated diseases has been diversity analysis, and nevertheless, existing studies on ASD-microbiome relationship have not produced a consensus. Here, we perform a comprehensive analysis of the diversity changes associated with ASD involving alpha-, beta-, and gamma-diversity metrics, based on 8 published data sets consisting of 898 ASD samples and 467 healthy controls (HC) from 16S-rRNA sequencing. Our findings include: (i) In terms of alpha-diversity, in approximately 1/3 of the studies cases, ASD patients exhibited significantly higher alpha-diversity than the HC, which seems to be consistent with the "1/3 conjecture" of diversity-disease relationship (DDR). (ii) In terms of beta-diversity, the AKP (Anna Karenina principle) that predict all healthy microbiomes should be similar, and every diseased microbiome should be dissimilar in its own way seems to be true in approximately 1/2 to 3/4 studies cases. (iii) In terms of gamma-diversity, the DAR (diversity-area relationship) modeling suggests that ASD patients seem to have large diversity-area scaling parameter than the HC, which is consistent with the AKP results. However, the MAD (maximum accrual diversity) and RIP (ratio of individual to population diversity) parameters did not suggest significant differences between ASD patients and HC. Throughout the study, we adopted Hill numbers to measure diversity, which stratified the diversity measures in terms of the rarity-commonness-dominance spectrum. It appears that the differences between ASD patients and HC are more propounding on rare-species side than on dominant-species side. Finally, we discuss the apparent inconsistent diversity-ASD relationships among different case studies and postulate that the relationships are not monotonic.

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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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