Loading…

Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing

Summary It is well recognized that a dynamic biofilm develops upon plant biomass in the herbivore gastrointestinal tract, but this component of the microbiome has not previously been specifically sampled, or directly compared with the biodiversity present in the planktonic fraction of digesta. In th...

Full description

Saved in:
Bibliographic Details
Published in:Environmental microbiology 2005-04, Vol.7 (4), p.530-543
Main Authors: Larue, Ross, Yu, Zhongtang, Parisi, Victoria A., Egan, Adrian R., Morrison, Mark
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3
cites cdi_FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3
container_end_page 543
container_issue 4
container_start_page 530
container_title Environmental microbiology
container_volume 7
creator Larue, Ross
Yu, Zhongtang
Parisi, Victoria A.
Egan, Adrian R.
Morrison, Mark
description Summary It is well recognized that a dynamic biofilm develops upon plant biomass in the herbivore gastrointestinal tract, but this component of the microbiome has not previously been specifically sampled, or directly compared with the biodiversity present in the planktonic fraction of digesta. In this study, the digesta collected from four sheep fed two different diets was separated into three fractions: the planktonic phase, and the microbial populations either weakly or tightly adherent to plant biomass. The community DNA prepared from each fraction was then subjected to both ribosomal intergenic spacer analysis (RISA) and denaturing gradient gel electrophoresis (DGGE). Both types of analysis showed that dietary factors influence community structure, and that the adherent fractions produced more complex profiles. The RIS‐clone libraries prepared from the planktonic and adherent populations were then subjected to restriction fragment length polymorphism (RFLP) and DNA sequence analyses, which resulted in a far greater degree of discrimination among the fractions. Although many of the sequenced clones from the adherent populations were assigned to various clusters within the low G+C Gram‐positive bacteria, the clone libraries from animals consuming an all‐grass diet were largely comprised of novel lineages of Clostridium, while in animals consuming the starch‐containing diet, Selenomonas and Ruminococcus spp. were the dominant low G+C Gram‐positive bacteria. Additionally, the libraries from hay‐fed animals also contained clones most similar to asaccharolytic Clostridia, and other Gram‐positive bacteria that specialize in the transformation of plant phenolic compounds and the formation of cinnamic, phenylacetic and phenylpropionic acids. These results reveal, for the first time, the phylogeny of adherent subpopulations that specialize in the transformation of plant lignins and other secondary compounds, which potentiate polysaccharide hydrolysis by other members of the biofilm.
doi_str_mv 10.1111/j.1462-2920.2005.00721.x
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67717786</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67717786</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3</originalsourceid><addsrcrecordid>eNqNUctuEzEUHSEQLYVfQHfFihlsz8OOxAaqUiq1RYIglpbHcyd1mEfwdULmj_hMPCQKS_DGR7rnoXtPkgBnGY_vzTrjRSVSsRAsE4yVGWNS8Gz_KDk_DR6fMBdnyTOiNWNc5pI9Tc54qXi1yNl58ut-3GEHvbN-rJ3poHE79OTCBKZ5QI9DgDDCpjMR1G7sDRG4AcIDQhzXbjd6hJWh4Ec3BKTghugSvLHhNRgCjzs0HTZQT-BdPVK06GCm-hUOzgJtjEUPJsomchRBA94TxCkC4Y8tDtYNq-fJk9Z0hC-O_0Xy9cPV8vJjevvp-uby3W1qS8Z5qnKpFLaqiqZNbbnBQjApS4Vla-KN0CizELIs7ULmLTOilbbBpsCcK9GWdX6RvDr4bvwYsyno3pHFLh4Axy3pSkoupar-SeRSFUVMjkR1IMYTE3ls9ca73vhJc6bnOvVaz03puTU916n_1Kn3UfrymLGte2z-Co_9RcLbA-Gn63D6b2N9dXcTQZSnB7mjgPuT3Pjvcc9clvrb_bVevhdfPqvlneb5b2o9we8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17844775</pqid></control><display><type>article</type><title>Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Larue, Ross ; Yu, Zhongtang ; Parisi, Victoria A. ; Egan, Adrian R. ; Morrison, Mark</creator><creatorcontrib>Larue, Ross ; Yu, Zhongtang ; Parisi, Victoria A. ; Egan, Adrian R. ; Morrison, Mark</creatorcontrib><description>Summary It is well recognized that a dynamic biofilm develops upon plant biomass in the herbivore gastrointestinal tract, but this component of the microbiome has not previously been specifically sampled, or directly compared with the biodiversity present in the planktonic fraction of digesta. In this study, the digesta collected from four sheep fed two different diets was separated into three fractions: the planktonic phase, and the microbial populations either weakly or tightly adherent to plant biomass. The community DNA prepared from each fraction was then subjected to both ribosomal intergenic spacer analysis (RISA) and denaturing gradient gel electrophoresis (DGGE). Both types of analysis showed that dietary factors influence community structure, and that the adherent fractions produced more complex profiles. The RIS‐clone libraries prepared from the planktonic and adherent populations were then subjected to restriction fragment length polymorphism (RFLP) and DNA sequence analyses, which resulted in a far greater degree of discrimination among the fractions. Although many of the sequenced clones from the adherent populations were assigned to various clusters within the low G+C Gram‐positive bacteria, the clone libraries from animals consuming an all‐grass diet were largely comprised of novel lineages of Clostridium, while in animals consuming the starch‐containing diet, Selenomonas and Ruminococcus spp. were the dominant low G+C Gram‐positive bacteria. Additionally, the libraries from hay‐fed animals also contained clones most similar to asaccharolytic Clostridia, and other Gram‐positive bacteria that specialize in the transformation of plant phenolic compounds and the formation of cinnamic, phenylacetic and phenylpropionic acids. These results reveal, for the first time, the phylogeny of adherent subpopulations that specialize in the transformation of plant lignins and other secondary compounds, which potentiate polysaccharide hydrolysis by other members of the biofilm.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/j.1462-2920.2005.00721.x</identifier><identifier>PMID: 15816930</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject><![CDATA[Animals ; Bacteria - classification ; Bacteria - genetics ; Bacteria - isolation & purification ; Biodiversity ; Biofilms ; Biomass ; Clostridium ; Clostridium - classification ; Clostridium - genetics ; Clostridium - isolation & purification ; DNA Fingerprinting ; DNA, Bacterial - chemistry ; DNA, Bacterial - isolation & purification ; DNA, Ribosomal Spacer - analysis ; DNA, Ribosomal Spacer - isolation & purification ; Electrophoresis, Polyacrylamide Gel ; Gastrointestinal Tract - microbiology ; Molecular Sequence Data ; Phylogeny ; Polymorphism, Restriction Fragment Length ; Ruminococcus ; Ruminococcus - classification ; Ruminococcus - genetics ; Ruminococcus - isolation & purification ; Selenomonas ; Selenomonas - classification ; Selenomonas - genetics ; Selenomonas - isolation & purification ; Sequence Analysis, DNA ; Sheep - microbiology]]></subject><ispartof>Environmental microbiology, 2005-04, Vol.7 (4), p.530-543</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3</citedby><cites>FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15816930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Larue, Ross</creatorcontrib><creatorcontrib>Yu, Zhongtang</creatorcontrib><creatorcontrib>Parisi, Victoria A.</creatorcontrib><creatorcontrib>Egan, Adrian R.</creatorcontrib><creatorcontrib>Morrison, Mark</creatorcontrib><title>Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary It is well recognized that a dynamic biofilm develops upon plant biomass in the herbivore gastrointestinal tract, but this component of the microbiome has not previously been specifically sampled, or directly compared with the biodiversity present in the planktonic fraction of digesta. In this study, the digesta collected from four sheep fed two different diets was separated into three fractions: the planktonic phase, and the microbial populations either weakly or tightly adherent to plant biomass. The community DNA prepared from each fraction was then subjected to both ribosomal intergenic spacer analysis (RISA) and denaturing gradient gel electrophoresis (DGGE). Both types of analysis showed that dietary factors influence community structure, and that the adherent fractions produced more complex profiles. The RIS‐clone libraries prepared from the planktonic and adherent populations were then subjected to restriction fragment length polymorphism (RFLP) and DNA sequence analyses, which resulted in a far greater degree of discrimination among the fractions. Although many of the sequenced clones from the adherent populations were assigned to various clusters within the low G+C Gram‐positive bacteria, the clone libraries from animals consuming an all‐grass diet were largely comprised of novel lineages of Clostridium, while in animals consuming the starch‐containing diet, Selenomonas and Ruminococcus spp. were the dominant low G+C Gram‐positive bacteria. Additionally, the libraries from hay‐fed animals also contained clones most similar to asaccharolytic Clostridia, and other Gram‐positive bacteria that specialize in the transformation of plant phenolic compounds and the formation of cinnamic, phenylacetic and phenylpropionic acids. These results reveal, for the first time, the phylogeny of adherent subpopulations that specialize in the transformation of plant lignins and other secondary compounds, which potentiate polysaccharide hydrolysis by other members of the biofilm.</description><subject>Animals</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation &amp; purification</subject><subject>Biodiversity</subject><subject>Biofilms</subject><subject>Biomass</subject><subject>Clostridium</subject><subject>Clostridium - classification</subject><subject>Clostridium - genetics</subject><subject>Clostridium - isolation &amp; purification</subject><subject>DNA Fingerprinting</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - isolation &amp; purification</subject><subject>DNA, Ribosomal Spacer - analysis</subject><subject>DNA, Ribosomal Spacer - isolation &amp; purification</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Gastrointestinal Tract - microbiology</subject><subject>Molecular Sequence Data</subject><subject>Phylogeny</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Ruminococcus</subject><subject>Ruminococcus - classification</subject><subject>Ruminococcus - genetics</subject><subject>Ruminococcus - isolation &amp; purification</subject><subject>Selenomonas</subject><subject>Selenomonas - classification</subject><subject>Selenomonas - genetics</subject><subject>Selenomonas - isolation &amp; purification</subject><subject>Sequence Analysis, DNA</subject><subject>Sheep - microbiology</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNUctuEzEUHSEQLYVfQHfFihlsz8OOxAaqUiq1RYIglpbHcyd1mEfwdULmj_hMPCQKS_DGR7rnoXtPkgBnGY_vzTrjRSVSsRAsE4yVGWNS8Gz_KDk_DR6fMBdnyTOiNWNc5pI9Tc54qXi1yNl58ut-3GEHvbN-rJ3poHE79OTCBKZ5QI9DgDDCpjMR1G7sDRG4AcIDQhzXbjd6hJWh4Ec3BKTghugSvLHhNRgCjzs0HTZQT-BdPVK06GCm-hUOzgJtjEUPJsomchRBA94TxCkC4Y8tDtYNq-fJk9Z0hC-O_0Xy9cPV8vJjevvp-uby3W1qS8Z5qnKpFLaqiqZNbbnBQjApS4Vla-KN0CizELIs7ULmLTOilbbBpsCcK9GWdX6RvDr4bvwYsyno3pHFLh4Axy3pSkoupar-SeRSFUVMjkR1IMYTE3ls9ca73vhJc6bnOvVaz03puTU916n_1Kn3UfrymLGte2z-Co_9RcLbA-Gn63D6b2N9dXcTQZSnB7mjgPuT3Pjvcc9clvrb_bVevhdfPqvlneb5b2o9we8</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Larue, Ross</creator><creator>Yu, Zhongtang</creator><creator>Parisi, Victoria A.</creator><creator>Egan, Adrian R.</creator><creator>Morrison, Mark</creator><general>Blackwell Science Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>200504</creationdate><title>Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing</title><author>Larue, Ross ; Yu, Zhongtang ; Parisi, Victoria A. ; Egan, Adrian R. ; Morrison, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Bacteria - classification</topic><topic>Bacteria - genetics</topic><topic>Bacteria - isolation &amp; purification</topic><topic>Biodiversity</topic><topic>Biofilms</topic><topic>Biomass</topic><topic>Clostridium</topic><topic>Clostridium - classification</topic><topic>Clostridium - genetics</topic><topic>Clostridium - isolation &amp; purification</topic><topic>DNA Fingerprinting</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - isolation &amp; purification</topic><topic>DNA, Ribosomal Spacer - analysis</topic><topic>DNA, Ribosomal Spacer - isolation &amp; purification</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Gastrointestinal Tract - microbiology</topic><topic>Molecular Sequence Data</topic><topic>Phylogeny</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Ruminococcus</topic><topic>Ruminococcus - classification</topic><topic>Ruminococcus - genetics</topic><topic>Ruminococcus - isolation &amp; purification</topic><topic>Selenomonas</topic><topic>Selenomonas - classification</topic><topic>Selenomonas - genetics</topic><topic>Selenomonas - isolation &amp; purification</topic><topic>Sequence Analysis, DNA</topic><topic>Sheep - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Larue, Ross</creatorcontrib><creatorcontrib>Yu, Zhongtang</creatorcontrib><creatorcontrib>Parisi, Victoria A.</creatorcontrib><creatorcontrib>Egan, Adrian R.</creatorcontrib><creatorcontrib>Morrison, Mark</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Larue, Ross</au><au>Yu, Zhongtang</au><au>Parisi, Victoria A.</au><au>Egan, Adrian R.</au><au>Morrison, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2005-04</date><risdate>2005</risdate><volume>7</volume><issue>4</issue><spage>530</spage><epage>543</epage><pages>530-543</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary It is well recognized that a dynamic biofilm develops upon plant biomass in the herbivore gastrointestinal tract, but this component of the microbiome has not previously been specifically sampled, or directly compared with the biodiversity present in the planktonic fraction of digesta. In this study, the digesta collected from four sheep fed two different diets was separated into three fractions: the planktonic phase, and the microbial populations either weakly or tightly adherent to plant biomass. The community DNA prepared from each fraction was then subjected to both ribosomal intergenic spacer analysis (RISA) and denaturing gradient gel electrophoresis (DGGE). Both types of analysis showed that dietary factors influence community structure, and that the adherent fractions produced more complex profiles. The RIS‐clone libraries prepared from the planktonic and adherent populations were then subjected to restriction fragment length polymorphism (RFLP) and DNA sequence analyses, which resulted in a far greater degree of discrimination among the fractions. Although many of the sequenced clones from the adherent populations were assigned to various clusters within the low G+C Gram‐positive bacteria, the clone libraries from animals consuming an all‐grass diet were largely comprised of novel lineages of Clostridium, while in animals consuming the starch‐containing diet, Selenomonas and Ruminococcus spp. were the dominant low G+C Gram‐positive bacteria. Additionally, the libraries from hay‐fed animals also contained clones most similar to asaccharolytic Clostridia, and other Gram‐positive bacteria that specialize in the transformation of plant phenolic compounds and the formation of cinnamic, phenylacetic and phenylpropionic acids. These results reveal, for the first time, the phylogeny of adherent subpopulations that specialize in the transformation of plant lignins and other secondary compounds, which potentiate polysaccharide hydrolysis by other members of the biofilm.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15816930</pmid><doi>10.1111/j.1462-2920.2005.00721.x</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1462-2912
ispartof Environmental microbiology, 2005-04, Vol.7 (4), p.530-543
issn 1462-2912
1462-2920
language eng
recordid cdi_proquest_miscellaneous_67717786
source Wiley-Blackwell Read & Publish Collection
subjects Animals
Bacteria - classification
Bacteria - genetics
Bacteria - isolation & purification
Biodiversity
Biofilms
Biomass
Clostridium
Clostridium - classification
Clostridium - genetics
Clostridium - isolation & purification
DNA Fingerprinting
DNA, Bacterial - chemistry
DNA, Bacterial - isolation & purification
DNA, Ribosomal Spacer - analysis
DNA, Ribosomal Spacer - isolation & purification
Electrophoresis, Polyacrylamide Gel
Gastrointestinal Tract - microbiology
Molecular Sequence Data
Phylogeny
Polymorphism, Restriction Fragment Length
Ruminococcus
Ruminococcus - classification
Ruminococcus - genetics
Ruminococcus - isolation & purification
Selenomonas
Selenomonas - classification
Selenomonas - genetics
Selenomonas - isolation & purification
Sequence Analysis, DNA
Sheep - microbiology
title Novel microbial diversity adherent to plant biomass in the herbivore gastrointestinal tract, as revealed by ribosomal intergenic spacer analysis and rrs gene sequencing
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T23%3A59%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20microbial%20diversity%20adherent%20to%20plant%20biomass%20in%20the%20herbivore%20gastrointestinal%20tract,%20as%20revealed%20by%20ribosomal%20intergenic%20spacer%20analysis%20and%20rrs%20gene%20sequencing&rft.jtitle=Environmental%20microbiology&rft.au=Larue,%20Ross&rft.date=2005-04&rft.volume=7&rft.issue=4&rft.spage=530&rft.epage=543&rft.pages=530-543&rft.issn=1462-2912&rft.eissn=1462-2920&rft_id=info:doi/10.1111/j.1462-2920.2005.00721.x&rft_dat=%3Cproquest_cross%3E67717786%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5011-83788ef86acedbc1ae4207758e5fa721ea8a92755c973f0a2f7cded4e3182f5b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=17844775&rft_id=info:pmid/15816930&rfr_iscdi=true