Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2018.00048
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dc.titleSpatial heterogeneity and co-occurrence of mucosal and luminal microbiome across swine intestinal tract
dc.contributor.authorZhang L.
dc.contributor.authorWu W.
dc.contributor.authorLee Y.-K.
dc.contributor.authorXie J.
dc.contributor.authorZhang H.
dc.date.accessioned2020-09-01T00:46:02Z
dc.date.available2020-09-01T00:46:02Z
dc.date.issued2018
dc.identifier.citationZhang L., Wu W., Lee Y.-K., Xie J., Zhang H. (2018). Spatial heterogeneity and co-occurrence of mucosal and luminal microbiome across swine intestinal tract. Frontiers in Microbiology 9 (JAN) : 48. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2018.00048
dc.identifier.issn1664302X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/173743
dc.description.abstractPigs are one of the most important economic livestock. Gut microbiota is not only critical to the health but also the production efficiency of pigs. Manipulating gut microbiota relies on the full view of gut microbiome and the understanding of drive forces shaping microbial communities. 16s rDNA sequencing was used to profile microbiota along the longitudinal and radical axes to obtain the topographical map of microbiome in different intestinal compartments in young pigs. Alpha and beta-diversities revealed distinct differences in microbial compositions between the distal ileum and cecum and colon, as well as between the lumen and mucosa. Firmicutes and Proteobacteria dominated in the ileum, constituting 95 and 80% of the luminal and mucosa-attached microbiome. Transitioning from the small intestine to the large intestine, luminal Bacteroidetes increased from 1.69 to 45.98% in the cecum and 40.09% in the colon, while mucosal Bacteroidetes raised from 9 to 35.36% and 27.96%. Concurrently, luminal Firmicutes and Proteobacteria and mucosal-attached Proteobacteria remarkably decreased. By co-occurrence network analyses, Prevotellaceae, Ruminococcaceae, Lachnospiraceae and Veillonellaceae were recognized as the central nodes of luminal microbial network, and Prevotellaceae and Enterobacteriaceae, Caulobacteraceae, Enterococcaceae, Xanthomonadaceae, Pseudomonadaceae were identified as mucosal central nodes. Co-abundance was uncovered among Prevotellaceae, Lachnospiraceae, and Veillonellaceae in the luminal and mucosal microbiome, while opportunistic pathogens from ?-Proteobacteria in the mucosa. Strong co-exclusion was shown between Enterobacteriaceae with Prevotellaceae-centered microbial groups in the lumen. Redundancy analysis found bile acids and short chain fatty acids explained 37.1 and 41% of variations in the luminal microbial composition, respectively. Primary bile acid, taurine- and glycine- conjugated bile acids were positively correlated with Lactobacillaceae, Enterobacteriaceae, Clostridiaceae_1, Peptostreptococcaceae, whereas secondary bile acids, acetate, propionate, butyrate, and valerate were positively correlated with Prevotellaceae, Acidaminococcaceae, Ruminococcaceae, Lachnospiraceae, Desulfovibronaceae, Veillonellaceae. Functional analyses demonstrated that Prevotella, Veillonellaceae, Lachnospiraceae, and Ruminococcaceae were positively correlated with gene functions related to amino acids, energy, cofactors and vitamins metabolism, which are indispensable for the hosts. These results suggested site specific colonization and co-occurrence of swine gut microbiome closely relate to the microenvironment in each niche. Interactions of core gut microbiome greatly contributed to metabolism and/or immunity in the swine intestine. © 2018 Zhang, Wu, Lee, Xie and Zhang.
dc.sourceUnpaywall 20200831
dc.subjectacetic acid
dc.subjectbile acid
dc.subjectbutyric acid
dc.subjectglycine
dc.subjectisobutyric acid
dc.subjectisovaleric acid
dc.subjectpropionic acid
dc.subjecttaurine
dc.subjectvaleric acid
dc.subjectAcidaminococcaceae
dc.subjectActinobacteria
dc.subjectamino acid metabolism
dc.subjectArticle
dc.subjectBacillaceae
dc.subjectbacterial microbiome
dc.subjectbacterium
dc.subjectBacteroidetes
dc.subjectCampylobacteraceae
dc.subjectcarbohydrate metabolism
dc.subjectCaulobacteraceae
dc.subjectcecum
dc.subjectClostridiaceae
dc.subjectcolon flora
dc.subjectcommunity structure
dc.subjectcyanobacterium
dc.subjectDesulfovibronaceae
dc.subjectenergy metabolism
dc.subjectEnterobacteriaceae
dc.subjectEnterococcaceae
dc.subjectErysipelotrichaceae
dc.subjectFaecalibacterium
dc.subjectFirmicutes
dc.subjectGemmatimonadetes
dc.subjectgene function
dc.subjectHelicobacteraceae
dc.subjectileum
dc.subjectintestine flora
dc.subjectLachnospiraceae
dc.subjectLactobacillaceae
dc.subjectlarge intestine
dc.subjectLawsonia (bacterium)
dc.subjectlipid metabolism
dc.subjectmembrane transport
dc.subjectmicrobial diversity
dc.subjectMycoplasmataceae
dc.subjectnonhuman
dc.subjectPeptostreptococcaceae
dc.subjectpig
dc.subjectPlanctomycetes
dc.subjectPrevotella
dc.subjectPrevotellaceae
dc.subjectProteobacteria
dc.subjectPseudomonadaceae
dc.subjectRuminococcaceae
dc.subjectStreptococcaceae
dc.subjectVeillonellaceae
dc.subjectXanthomonadaceae
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.3389/fmicb.2018.00048
dc.description.sourcetitleFrontiers in Microbiology
dc.description.volume9
dc.description.issueJAN
dc.description.page48
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