Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies
Studies indicate that the gut microbiota (GM) can significantly influence both local and systemic host physiologic processes. With rising concern for optimization of experimental reproducibility and translatability, it is essential to consider the GM in study design. However, GM profiles can vary be...
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description | Studies indicate that the gut microbiota (GM) can significantly influence both local and systemic host physiologic processes. With rising concern for optimization of experimental reproducibility and translatability, it is essential to consider the GM in study design. However, GM profiles can vary between rodent producers making consistency between models challenging. To circumvent this, we developed outbred CD1 mouse colonies with stable, complex GM profiles that can be used as donors for a variety of GM transfer techniques including rederivation, co-housing, cross-foster, and fecal microbiota transfer (FMT). CD1 embryos were surgically transferred into CD1 or C57BL/6 surrogate dams that varied by GM composition and complexity to establish four separate mouse colonies harboring GM profiles representative of contemporary mouse producers. Using targeted 16S rRNA amplicon sequencing, subsequent female offspring were found to have similar GM profiles to surrogate dams. Furthermore, breeding colonies of CD1 mice with distinct GM profiles were maintained for nine generations, demonstrating GM stability within these colonies. To confirm GM stability, we shipped cohorts of these four colonies to collaborating institutions and found no significant variation in GM composition. These mice are an invaluable experimental resource that can be used to investigate GM effects on mouse model phenotype. |
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C. Kent ; Grimsrud, Kristin N. ; Rogala, Allison R. ; Godfrey, Virginia L. ; Nielsen, Judith N. ; Franklin, Craig L.</creator><creatorcontrib>Hart, Marcia L. ; Ericsson, Aaron C. ; Lloyd, K. C. Kent ; Grimsrud, Kristin N. ; Rogala, Allison R. ; Godfrey, Virginia L. ; Nielsen, Judith N. ; Franklin, Craig L.</creatorcontrib><description>Studies indicate that the gut microbiota (GM) can significantly influence both local and systemic host physiologic processes. With rising concern for optimization of experimental reproducibility and translatability, it is essential to consider the GM in study design. However, GM profiles can vary between rodent producers making consistency between models challenging. To circumvent this, we developed outbred CD1 mouse colonies with stable, complex GM profiles that can be used as donors for a variety of GM transfer techniques including rederivation, co-housing, cross-foster, and fecal microbiota transfer (FMT). CD1 embryos were surgically transferred into CD1 or C57BL/6 surrogate dams that varied by GM composition and complexity to establish four separate mouse colonies harboring GM profiles representative of contemporary mouse producers. Using targeted 16S rRNA amplicon sequencing, subsequent female offspring were found to have similar GM profiles to surrogate dams. Furthermore, breeding colonies of CD1 mice with distinct GM profiles were maintained for nine generations, demonstrating GM stability within these colonies. To confirm GM stability, we shipped cohorts of these four colonies to collaborating institutions and found no significant variation in GM composition. These mice are an invaluable experimental resource that can be used to investigate GM effects on mouse model phenotype.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-28448-0</identifier><identifier>PMID: 29973630</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/1647/767 ; 631/326/2565/2134 ; Animal models ; Colonies ; Embryos ; Fecal microflora ; Genetic crosses ; Humanities and Social Sciences ; Intestinal microflora ; Microbiota ; multidisciplinary ; Offspring ; Phenotypes ; rRNA 16S ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2018-07, Vol.8 (1), p.10107-11, Article 10107</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-4adc88941d9eea378ce308fc59d01931ef090f9f382d423d0ae7c01d593a40d53</citedby><cites>FETCH-LOGICAL-c511t-4adc88941d9eea378ce308fc59d01931ef090f9f382d423d0ae7c01d593a40d53</cites><orcidid>0000-0002-5318-4144</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/PMC6031694/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031694/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29973630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hart, Marcia L.</creatorcontrib><creatorcontrib>Ericsson, Aaron C.</creatorcontrib><creatorcontrib>Lloyd, K. C. Kent</creatorcontrib><creatorcontrib>Grimsrud, Kristin N.</creatorcontrib><creatorcontrib>Rogala, Allison R.</creatorcontrib><creatorcontrib>Godfrey, Virginia L.</creatorcontrib><creatorcontrib>Nielsen, Judith N.</creatorcontrib><creatorcontrib>Franklin, Craig L.</creatorcontrib><title>Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Studies indicate that the gut microbiota (GM) can significantly influence both local and systemic host physiologic processes. With rising concern for optimization of experimental reproducibility and translatability, it is essential to consider the GM in study design. However, GM profiles can vary between rodent producers making consistency between models challenging. 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Kent</creatorcontrib><creatorcontrib>Grimsrud, Kristin N.</creatorcontrib><creatorcontrib>Rogala, Allison R.</creatorcontrib><creatorcontrib>Godfrey, Virginia L.</creatorcontrib><creatorcontrib>Nielsen, Judith N.</creatorcontrib><creatorcontrib>Franklin, Craig L.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science 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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hart, Marcia L.</au><au>Ericsson, Aaron C.</au><au>Lloyd, K. C. Kent</au><au>Grimsrud, Kristin N.</au><au>Rogala, Allison R.</au><au>Godfrey, Virginia L.</au><au>Nielsen, Judith N.</au><au>Franklin, Craig L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-07-04</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>10107</spage><epage>11</epage><pages>10107-11</pages><artnum>10107</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Studies indicate that the gut microbiota (GM) can significantly influence both local and systemic host physiologic processes. With rising concern for optimization of experimental reproducibility and translatability, it is essential to consider the GM in study design. However, GM profiles can vary between rodent producers making consistency between models challenging. To circumvent this, we developed outbred CD1 mouse colonies with stable, complex GM profiles that can be used as donors for a variety of GM transfer techniques including rederivation, co-housing, cross-foster, and fecal microbiota transfer (FMT). CD1 embryos were surgically transferred into CD1 or C57BL/6 surrogate dams that varied by GM composition and complexity to establish four separate mouse colonies harboring GM profiles representative of contemporary mouse producers. Using targeted 16S rRNA amplicon sequencing, subsequent female offspring were found to have similar GM profiles to surrogate dams. Furthermore, breeding colonies of CD1 mice with distinct GM profiles were maintained for nine generations, demonstrating GM stability within these colonies. To confirm GM stability, we shipped cohorts of these four colonies to collaborating institutions and found no significant variation in GM composition. These mice are an invaluable experimental resource that can be used to investigate GM effects on mouse model phenotype.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29973630</pmid><doi>10.1038/s41598-018-28448-0</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-5318-4144</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/1647/767 631/326/2565/2134 Animal models Colonies Embryos Fecal microflora Genetic crosses Humanities and Social Sciences Intestinal microflora Microbiota multidisciplinary Offspring Phenotypes rRNA 16S Science Science (multidisciplinary) |
title | Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies |
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