Loading…
Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic
Horses that undergo surgery for treatment of primary large colon disease have been reported to be at increased risk of developing recurrent colic episodes postoperatively. The reasons for this are currently unknown. The aim of the current study was to characterise the faecal microbiota of horses wit...
Saved in:
Published in: | BMC veterinary research 2019-12, Vol.15 (1), p.468-468, Article 468 |
---|---|
Main Authors: | , , , , , |
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-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3 |
---|---|
cites | cdi_FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3 |
container_end_page | 468 |
container_issue | 1 |
container_start_page | 468 |
container_title | BMC veterinary research |
container_volume | 15 |
creator | Salem, Shebl E Maddox, Thomas W Antczak, Philipp Ketley, Julian M Williams, Nicola J Archer, Debra C |
description | Horses that undergo surgery for treatment of primary large colon disease have been reported to be at increased risk of developing recurrent colic episodes postoperatively. The reasons for this are currently unknown. The aim of the current study was to characterise the faecal microbiota of horses with colic signs associated with primary large colon lesions treated surgically and to compare the composition of their faecal microbiota to that of a control group of horses undergoing emergency orthopaedic treatment. Faecal samples were collected from horses in both groups on admission to hospital, during hospitalisation and following discharge from hospital for a total duration of 12 weeks. Additionally, colonic content samples were collected from surgical colic patients if pelvic flexure enterotomy was performed during laparotomy. A total of 12 samples were collected per horse. DNA was extracted from samples using a commercial kit. Amplicon mixtures were created by PCR amplification of the V1 - V2 regions of the bacterial 16S rRNA genes and submitted for sequencing using the Ion Torrent PGM next-generation sequencing system. Multivariate data analysis was used to characterise the faecal microbiota and to investigate differences between groups.
Reduced species richness was evident in the colonic samples of the colic group compared to concurrent sampling of the faeces. Alpha and beta diversity differed significantly between the faecal and colonic microbiota with 304 significantly differentially abundant OTUs identified. Only 46 OTUs varied significantly between the colic and control group. There were no significant differences in alpha and beta diversity of faecal microbiota between colic and control horses at admission. However, this lack of significant differences between groups should be interpreted with caution due to a small sample size.
The results of the current study suggest that faecal samples collected at hospital admission in colic cases may not accurately represent changes in upper gut microbiota in horses with colic due to large colon disease. |
doi_str_mv | 10.1186/s12917-019-2205-1 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_708fc278ddd44acb804efb03e1bdf632</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A610324362</galeid><doaj_id>oai_doaj_org_article_708fc278ddd44acb804efb03e1bdf632</doaj_id><sourcerecordid>A610324362</sourcerecordid><originalsourceid>FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3</originalsourceid><addsrcrecordid>eNqFkktv1DAUhSMEoqXwA9ggS2zYpPgVx94gjSoKlSqxgbV1_cp4lImLnVDx73E6pXQQEsoi8fU5X3yvT9O8JvicECneF0IV6VtMVEsp7lrypDklPRetIFw-ffR90rwoZYcx56oXz5sTVt2cCXXauI1dZo_sFqbBFxQnNG_rMo1pihbto83JxDQDguwRlJJshNk7dBvnLRohD756Zl_mOMGIQsr7glJAZclDtLVSSdG-bJ4FGIt_df8-a75dfvx68bm9_vLp6mJz3dpOsblV1HmmMDFBOCOZgtApA6onIDtngFmFMVWWYSa7nirjueTSuJ5aQwBbYGfN1YHrEuz0TY57yD91gqjvCikPGvIc7eh1j2WwtJfOOc7BGom5DwYzT4wLgtHK-nBg3Sxm753105xhPIIe70xxq4f0QwtFOylFBby7B-T0fakT0vtYrB9HmHxaiqacEdWJ2t7_pYxhLDDr1mO9_Uu6S0uus19VnDDWEcn_qAaovcYppHpEu0L1RhDM6r_Fyjr_h6o-zteLT5MPsdaPDORgqKkoJfvwMA6C9ZpIfUikronUayL12tubx3N8cPyOIPsFCDPbNQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2341335184</pqid></control><display><type>article</type><title>Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Salem, Shebl E ; Maddox, Thomas W ; Antczak, Philipp ; Ketley, Julian M ; Williams, Nicola J ; Archer, Debra C</creator><creatorcontrib>Salem, Shebl E ; Maddox, Thomas W ; Antczak, Philipp ; Ketley, Julian M ; Williams, Nicola J ; Archer, Debra C</creatorcontrib><description>Horses that undergo surgery for treatment of primary large colon disease have been reported to be at increased risk of developing recurrent colic episodes postoperatively. The reasons for this are currently unknown. The aim of the current study was to characterise the faecal microbiota of horses with colic signs associated with primary large colon lesions treated surgically and to compare the composition of their faecal microbiota to that of a control group of horses undergoing emergency orthopaedic treatment. Faecal samples were collected from horses in both groups on admission to hospital, during hospitalisation and following discharge from hospital for a total duration of 12 weeks. Additionally, colonic content samples were collected from surgical colic patients if pelvic flexure enterotomy was performed during laparotomy. A total of 12 samples were collected per horse. DNA was extracted from samples using a commercial kit. Amplicon mixtures were created by PCR amplification of the V1 - V2 regions of the bacterial 16S rRNA genes and submitted for sequencing using the Ion Torrent PGM next-generation sequencing system. Multivariate data analysis was used to characterise the faecal microbiota and to investigate differences between groups.
Reduced species richness was evident in the colonic samples of the colic group compared to concurrent sampling of the faeces. Alpha and beta diversity differed significantly between the faecal and colonic microbiota with 304 significantly differentially abundant OTUs identified. Only 46 OTUs varied significantly between the colic and control group. There were no significant differences in alpha and beta diversity of faecal microbiota between colic and control horses at admission. However, this lack of significant differences between groups should be interpreted with caution due to a small sample size.
The results of the current study suggest that faecal samples collected at hospital admission in colic cases may not accurately represent changes in upper gut microbiota in horses with colic due to large colon disease.</description><identifier>ISSN: 1746-6148</identifier><identifier>EISSN: 1746-6148</identifier><identifier>DOI: 10.1186/s12917-019-2205-1</identifier><identifier>PMID: 31864369</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Bacterial genetics ; Biodiversity ; Care and treatment ; Colic ; Colic - microbiology ; Colic - surgery ; Colic - veterinary ; Colon ; Colonic Diseases - microbiology ; Colonic Diseases - surgery ; Colonic Diseases - veterinary ; Colorectal cancer ; Deoxyribonucleic acid ; digestive system diseases ; DNA ; feces ; Feces - microbiology ; Gastrointestinal diseases ; Gastrointestinal Microbiome ; Genes ; high-throughput nucleotide sequencing ; Horse ; Horse Diseases - microbiology ; Horse Diseases - surgery ; Horses ; Hospital admission and discharge ; hospitals ; Infections ; Information management ; Intestinal microflora ; intestinal microorganisms ; Intestinal obstruction ; Intestine ; Laparotomy ; Large colon displacement ; Large colon volvulus ; Medical treatment ; Microbiota ; Microbiota (Symbiotic organisms) ; multivariate analysis ; Next-generation sequencing ; orthopedics ; patients ; polymerase chain reaction ; Postoperative colic ; ribosomal RNA ; RNA ; RNA, Ribosomal, 16S - analysis ; rRNA 16S ; sample size ; Species richness ; Surgery</subject><ispartof>BMC veterinary research, 2019-12, Vol.15 (1), p.468-468, Article 468</ispartof><rights>COPYRIGHT 2019 BioMed Central Ltd.</rights><rights>2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s). 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3</citedby><cites>FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3</cites><orcidid>0000-0001-5315-8934</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925886/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2341335184?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25733,27903,27904,36991,36992,44569,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31864369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salem, Shebl E</creatorcontrib><creatorcontrib>Maddox, Thomas W</creatorcontrib><creatorcontrib>Antczak, Philipp</creatorcontrib><creatorcontrib>Ketley, Julian M</creatorcontrib><creatorcontrib>Williams, Nicola J</creatorcontrib><creatorcontrib>Archer, Debra C</creatorcontrib><title>Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic</title><title>BMC veterinary research</title><addtitle>BMC Vet Res</addtitle><description>Horses that undergo surgery for treatment of primary large colon disease have been reported to be at increased risk of developing recurrent colic episodes postoperatively. The reasons for this are currently unknown. The aim of the current study was to characterise the faecal microbiota of horses with colic signs associated with primary large colon lesions treated surgically and to compare the composition of their faecal microbiota to that of a control group of horses undergoing emergency orthopaedic treatment. Faecal samples were collected from horses in both groups on admission to hospital, during hospitalisation and following discharge from hospital for a total duration of 12 weeks. Additionally, colonic content samples were collected from surgical colic patients if pelvic flexure enterotomy was performed during laparotomy. A total of 12 samples were collected per horse. DNA was extracted from samples using a commercial kit. Amplicon mixtures were created by PCR amplification of the V1 - V2 regions of the bacterial 16S rRNA genes and submitted for sequencing using the Ion Torrent PGM next-generation sequencing system. Multivariate data analysis was used to characterise the faecal microbiota and to investigate differences between groups.
Reduced species richness was evident in the colonic samples of the colic group compared to concurrent sampling of the faeces. Alpha and beta diversity differed significantly between the faecal and colonic microbiota with 304 significantly differentially abundant OTUs identified. Only 46 OTUs varied significantly between the colic and control group. There were no significant differences in alpha and beta diversity of faecal microbiota between colic and control horses at admission. However, this lack of significant differences between groups should be interpreted with caution due to a small sample size.
The results of the current study suggest that faecal samples collected at hospital admission in colic cases may not accurately represent changes in upper gut microbiota in horses with colic due to large colon disease.</description><subject>Analysis</subject><subject>Animals</subject><subject>Bacterial genetics</subject><subject>Biodiversity</subject><subject>Care and treatment</subject><subject>Colic</subject><subject>Colic - microbiology</subject><subject>Colic - surgery</subject><subject>Colic - veterinary</subject><subject>Colon</subject><subject>Colonic Diseases - microbiology</subject><subject>Colonic Diseases - surgery</subject><subject>Colonic Diseases - veterinary</subject><subject>Colorectal cancer</subject><subject>Deoxyribonucleic acid</subject><subject>digestive system diseases</subject><subject>DNA</subject><subject>feces</subject><subject>Feces - microbiology</subject><subject>Gastrointestinal diseases</subject><subject>Gastrointestinal Microbiome</subject><subject>Genes</subject><subject>high-throughput nucleotide sequencing</subject><subject>Horse</subject><subject>Horse Diseases - microbiology</subject><subject>Horse Diseases - surgery</subject><subject>Horses</subject><subject>Hospital admission and discharge</subject><subject>hospitals</subject><subject>Infections</subject><subject>Information management</subject><subject>Intestinal microflora</subject><subject>intestinal microorganisms</subject><subject>Intestinal obstruction</subject><subject>Intestine</subject><subject>Laparotomy</subject><subject>Large colon displacement</subject><subject>Large colon volvulus</subject><subject>Medical treatment</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>multivariate analysis</subject><subject>Next-generation sequencing</subject><subject>orthopedics</subject><subject>patients</subject><subject>polymerase chain reaction</subject><subject>Postoperative colic</subject><subject>ribosomal RNA</subject><subject>RNA</subject><subject>RNA, Ribosomal, 16S - analysis</subject><subject>rRNA 16S</subject><subject>sample size</subject><subject>Species richness</subject><subject>Surgery</subject><issn>1746-6148</issn><issn>1746-6148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkktv1DAUhSMEoqXwA9ggS2zYpPgVx94gjSoKlSqxgbV1_cp4lImLnVDx73E6pXQQEsoi8fU5X3yvT9O8JvicECneF0IV6VtMVEsp7lrypDklPRetIFw-ffR90rwoZYcx56oXz5sTVt2cCXXauI1dZo_sFqbBFxQnNG_rMo1pihbto83JxDQDguwRlJJshNk7dBvnLRohD756Zl_mOMGIQsr7glJAZclDtLVSSdG-bJ4FGIt_df8-a75dfvx68bm9_vLp6mJz3dpOsblV1HmmMDFBOCOZgtApA6onIDtngFmFMVWWYSa7nirjueTSuJ5aQwBbYGfN1YHrEuz0TY57yD91gqjvCikPGvIc7eh1j2WwtJfOOc7BGom5DwYzT4wLgtHK-nBg3Sxm753105xhPIIe70xxq4f0QwtFOylFBby7B-T0fakT0vtYrB9HmHxaiqacEdWJ2t7_pYxhLDDr1mO9_Uu6S0uus19VnDDWEcn_qAaovcYppHpEu0L1RhDM6r_Fyjr_h6o-zteLT5MPsdaPDORgqKkoJfvwMA6C9ZpIfUikronUayL12tubx3N8cPyOIPsFCDPbNQ</recordid><startdate>20191221</startdate><enddate>20191221</enddate><creator>Salem, Shebl E</creator><creator>Maddox, Thomas W</creator><creator>Antczak, Philipp</creator><creator>Ketley, Julian M</creator><creator>Williams, Nicola J</creator><creator>Archer, Debra C</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>3V.</scope><scope>7QG</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5315-8934</orcidid></search><sort><creationdate>20191221</creationdate><title>Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic</title><author>Salem, Shebl E ; Maddox, Thomas W ; Antczak, Philipp ; Ketley, Julian M ; Williams, Nicola J ; Archer, Debra C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Bacterial genetics</topic><topic>Biodiversity</topic><topic>Care and treatment</topic><topic>Colic</topic><topic>Colic - microbiology</topic><topic>Colic - surgery</topic><topic>Colic - veterinary</topic><topic>Colon</topic><topic>Colonic Diseases - microbiology</topic><topic>Colonic Diseases - surgery</topic><topic>Colonic Diseases - veterinary</topic><topic>Colorectal cancer</topic><topic>Deoxyribonucleic acid</topic><topic>digestive system diseases</topic><topic>DNA</topic><topic>feces</topic><topic>Feces - microbiology</topic><topic>Gastrointestinal diseases</topic><topic>Gastrointestinal Microbiome</topic><topic>Genes</topic><topic>high-throughput nucleotide sequencing</topic><topic>Horse</topic><topic>Horse Diseases - microbiology</topic><topic>Horse Diseases - surgery</topic><topic>Horses</topic><topic>Hospital admission and discharge</topic><topic>hospitals</topic><topic>Infections</topic><topic>Information management</topic><topic>Intestinal microflora</topic><topic>intestinal microorganisms</topic><topic>Intestinal obstruction</topic><topic>Intestine</topic><topic>Laparotomy</topic><topic>Large colon displacement</topic><topic>Large colon volvulus</topic><topic>Medical treatment</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>multivariate analysis</topic><topic>Next-generation sequencing</topic><topic>orthopedics</topic><topic>patients</topic><topic>polymerase chain reaction</topic><topic>Postoperative colic</topic><topic>ribosomal RNA</topic><topic>RNA</topic><topic>RNA, Ribosomal, 16S - analysis</topic><topic>rRNA 16S</topic><topic>sample size</topic><topic>Species richness</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salem, Shebl E</creatorcontrib><creatorcontrib>Maddox, Thomas W</creatorcontrib><creatorcontrib>Antczak, Philipp</creatorcontrib><creatorcontrib>Ketley, Julian M</creatorcontrib><creatorcontrib>Williams, Nicola J</creatorcontrib><creatorcontrib>Archer, Debra C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salem, Shebl E</au><au>Maddox, Thomas W</au><au>Antczak, Philipp</au><au>Ketley, Julian M</au><au>Williams, Nicola J</au><au>Archer, Debra C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic</atitle><jtitle>BMC veterinary research</jtitle><addtitle>BMC Vet Res</addtitle><date>2019-12-21</date><risdate>2019</risdate><volume>15</volume><issue>1</issue><spage>468</spage><epage>468</epage><pages>468-468</pages><artnum>468</artnum><issn>1746-6148</issn><eissn>1746-6148</eissn><abstract>Horses that undergo surgery for treatment of primary large colon disease have been reported to be at increased risk of developing recurrent colic episodes postoperatively. The reasons for this are currently unknown. The aim of the current study was to characterise the faecal microbiota of horses with colic signs associated with primary large colon lesions treated surgically and to compare the composition of their faecal microbiota to that of a control group of horses undergoing emergency orthopaedic treatment. Faecal samples were collected from horses in both groups on admission to hospital, during hospitalisation and following discharge from hospital for a total duration of 12 weeks. Additionally, colonic content samples were collected from surgical colic patients if pelvic flexure enterotomy was performed during laparotomy. A total of 12 samples were collected per horse. DNA was extracted from samples using a commercial kit. Amplicon mixtures were created by PCR amplification of the V1 - V2 regions of the bacterial 16S rRNA genes and submitted for sequencing using the Ion Torrent PGM next-generation sequencing system. Multivariate data analysis was used to characterise the faecal microbiota and to investigate differences between groups.
Reduced species richness was evident in the colonic samples of the colic group compared to concurrent sampling of the faeces. Alpha and beta diversity differed significantly between the faecal and colonic microbiota with 304 significantly differentially abundant OTUs identified. Only 46 OTUs varied significantly between the colic and control group. There were no significant differences in alpha and beta diversity of faecal microbiota between colic and control horses at admission. However, this lack of significant differences between groups should be interpreted with caution due to a small sample size.
The results of the current study suggest that faecal samples collected at hospital admission in colic cases may not accurately represent changes in upper gut microbiota in horses with colic due to large colon disease.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>31864369</pmid><doi>10.1186/s12917-019-2205-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5315-8934</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1746-6148 |
ispartof | BMC veterinary research, 2019-12, Vol.15 (1), p.468-468, Article 468 |
issn | 1746-6148 1746-6148 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_708fc278ddd44acb804efb03e1bdf632 |
source | Publicly Available Content Database; PubMed Central |
subjects | Analysis Animals Bacterial genetics Biodiversity Care and treatment Colic Colic - microbiology Colic - surgery Colic - veterinary Colon Colonic Diseases - microbiology Colonic Diseases - surgery Colonic Diseases - veterinary Colorectal cancer Deoxyribonucleic acid digestive system diseases DNA feces Feces - microbiology Gastrointestinal diseases Gastrointestinal Microbiome Genes high-throughput nucleotide sequencing Horse Horse Diseases - microbiology Horse Diseases - surgery Horses Hospital admission and discharge hospitals Infections Information management Intestinal microflora intestinal microorganisms Intestinal obstruction Intestine Laparotomy Large colon displacement Large colon volvulus Medical treatment Microbiota Microbiota (Symbiotic organisms) multivariate analysis Next-generation sequencing orthopedics patients polymerase chain reaction Postoperative colic ribosomal RNA RNA RNA, Ribosomal, 16S - analysis rRNA 16S sample size Species richness Surgery |
title | Acute changes in the colonic microbiota are associated with large intestinal forms of surgical colic |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T18%3A45%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acute%20changes%20in%20the%20colonic%20microbiota%20are%20associated%20with%20large%20intestinal%20forms%20of%20surgical%20colic&rft.jtitle=BMC%20veterinary%20research&rft.au=Salem,%20Shebl%20E&rft.date=2019-12-21&rft.volume=15&rft.issue=1&rft.spage=468&rft.epage=468&rft.pages=468-468&rft.artnum=468&rft.issn=1746-6148&rft.eissn=1746-6148&rft_id=info:doi/10.1186/s12917-019-2205-1&rft_dat=%3Cgale_doaj_%3EA610324362%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c593t-92de3901bf6db839af59ba971a85dba3c90029c30385729be4848bd72cb1a0ca3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2341335184&rft_id=info:pmid/31864369&rft_galeid=A610324362&rfr_iscdi=true |