Identification of age-associated microbial changes via long-read 16S sequencing.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Kai Yee Toh, Tzi Shin Toh, Khi Pin Chua, Priscilla Rajakumar, Jonathan Wei Jie Lee, Chun Wie Chong
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引用次数: 0

Abstract

Background: Age-related gut microbial changes have been widely investigated over the past decade. Most of the previous age-related microbiome studies were conducted on the Western population, and the short-read sequencing (e.g., 16S V4 or V3-V4 region) was the most common microbiota profiling method. We evaluated the gut compositional differences using the long-read sequencing approach (i.e., PacBio sequencing targeting the full-length V1-V9 regions) to enable a deeper taxonomic resolution and better characterize the gut microbiome of Singaporeans from different age groups.

Results: A total of 83 research participants were included in this study. Although no significant differences were detected in alpha and beta diversity, our study demonstrated several bacterial taxa with abundances that were significantly different across age groups. With young individuals as the reference group, Eggerthella lenta and Bacteroides uniformis were found to be significantly altered in the middle-aged group, while Catenibacterium mitsuokai and Bacteroides plebeius were significantly altered in the elderly group. These age-related differences in the gut microbiome were associated with aberrations in several predicted functional pathways, including dysregulations of pathways related to lipopolysaccharide and tricarboxylic acid cycle in older adults.

Conclusions: The utilization of long-read sequencing facilitated the identification of species- and strain-level differences across age groups, which was challenging with the partial 16S rRNA sequencing approach. Nevertheless, replication studies are warranted to confirm our findings, and if confirmed, further in vitro and in vivo studies are crucial to better understand the impact of the altered levels of age-related bacterial taxa. Additionally, the modest performance of strain-level taxonomic classification using 16S-ITS-23S gene sequences, likely due to the limited depth of currently available alignment databases, highlights the need for optimization and refinement in curating these databases for the long-read sequencing approach.

通过长读 16S 测序鉴定与年龄相关的微生物变化。
背景:在过去十年中,与年龄相关的肠道微生物变化已被广泛研究。之前大多数与年龄相关的微生物组研究都是针对西方人群进行的,而短线程测序(如 16S V4 或 V3-V4 区域)是最常用的微生物组分析方法。我们使用长线程测序方法(即以全长 V1-V9 区域为目标的 PacBio 测序)评估了肠道成分的差异,以获得更深的分类分辨率,更好地描述不同年龄段新加坡人肠道微生物组的特征:结果:共有 83 名研究人员参与了这项研究。虽然在阿尔法和贝塔多样性方面没有发现明显差异,但我们的研究表明,几个细菌类群的丰度在不同年龄组之间存在明显差异。以年轻人为参照组,我们发现中年组的 Eggerthella lenta 和 Bacteroides uniformis 有明显变化,而老年组的 Catenibacterium mitsuokai 和 Bacteroides plebeius 则有明显变化。肠道微生物组中这些与年龄相关的差异与几种预测功能通路的畸变有关,包括老年人中脂多糖和三羧酸循环相关通路的失调:结论:长读数测序技术的使用有助于确定不同年龄组的物种和菌株水平差异,而部分 16S rRNA 测序方法则很难做到这一点。尽管如此,我们仍有必要进行重复研究来证实我们的发现,如果得到证实,进一步的体外和体内研究对更好地了解与年龄相关的细菌类群水平变化的影响至关重要。此外,使用 16S-ITS-23S 基因序列进行菌株级分类的效果一般,这可能是由于目前可用的比对数据库深度有限,这突出表明需要优化和完善这些数据库,以用于长读数测序方法。
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来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
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