{"title":"Exploring <i>Bifidobacterium</i> species community and functional variations with human gut microbiome structure and health beyond infancy.","authors":"Ruben Ladeira, Julien Tap, Muriel Derrien","doi":"10.20517/mrr.2023.01","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> The human gut <i>Bifidobacterium</i> community has been studied in detail in infants and following dietary interventions in adults. However, the variability of the distribution of <i>Bifidobacterium</i> species and intra-species functions have been little studied, particularly beyond infancy. Here, we explore the ecology of <i>Bifidobacterium</i> communities in a large public dataset of human gut metagenomes, mostly corresponding to adults. <b>Methods:</b> We selected 9.515 unique gut metagenomes from curatedMetagenomicData. Samples were partitioned by applying Dirichlet's multinomial mixture to <i>Bifidobacterium</i> species. A functional analysis was performed on > 2.000 human-associated <i>Bifidobacterium</i> metagenome-assembled genomes (MAGs) paired with participant gut microbiome and health features. <b>Results:</b> We identified several <i>Bifidobacterium</i>-based partitions in the human gut microbiome differing in terms of the presence and abundance of <i>Bifidobacterium</i> species. The partitions enriched in both <i>B. longum</i> and <i>B. adolescentis</i> were associated with gut microbiome diversity and a higher abundance of butyrate producers and were more prevalent in healthy individuals. <i>B. bifidum</i> MAGs harboring a set of genes potentially related to phages were more prevalent in partitions associated with a lower gut microbiome diversity and were genetically more closely related. <b>Conclusion:</b> This study expands our knowledge of the ecology and variability of the <i>Bifidobacterium</i> community, particularly in adults, and its specific association with the gut microbiota and health. Its findings may guide the rational selection of <i>Bifidobacterium</i> strains for gut microbiome complementation according to the individual's endogenous <i>Bifidobacterium</i> community. Our results also suggest that gut microbiome stratification for particular genera may be relevant for studies of variations of species and associations with the gut microbiome and health.</p>","PeriodicalId":75465,"journal":{"name":"Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. Albrecht von Graefe's archive for clinical and experimental ophthalmology","volume":"258 1","pages":"9"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688807/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. Albrecht von Graefe's archive for clinical and experimental ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20517/mrr.2023.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: The human gut Bifidobacterium community has been studied in detail in infants and following dietary interventions in adults. However, the variability of the distribution of Bifidobacterium species and intra-species functions have been little studied, particularly beyond infancy. Here, we explore the ecology of Bifidobacterium communities in a large public dataset of human gut metagenomes, mostly corresponding to adults. Methods: We selected 9.515 unique gut metagenomes from curatedMetagenomicData. Samples were partitioned by applying Dirichlet's multinomial mixture to Bifidobacterium species. A functional analysis was performed on > 2.000 human-associated Bifidobacterium metagenome-assembled genomes (MAGs) paired with participant gut microbiome and health features. Results: We identified several Bifidobacterium-based partitions in the human gut microbiome differing in terms of the presence and abundance of Bifidobacterium species. The partitions enriched in both B. longum and B. adolescentis were associated with gut microbiome diversity and a higher abundance of butyrate producers and were more prevalent in healthy individuals. B. bifidum MAGs harboring a set of genes potentially related to phages were more prevalent in partitions associated with a lower gut microbiome diversity and were genetically more closely related. Conclusion: This study expands our knowledge of the ecology and variability of the Bifidobacterium community, particularly in adults, and its specific association with the gut microbiota and health. Its findings may guide the rational selection of Bifidobacterium strains for gut microbiome complementation according to the individual's endogenous Bifidobacterium community. Our results also suggest that gut microbiome stratification for particular genera may be relevant for studies of variations of species and associations with the gut microbiome and health.