Mice Chronically Fed High-Fat Diet Have Increased Mortality and Disturbed Immune Response in Sepsis
Background: Sepsis is a potentially deadly disease that often is caused by gram-positive bacteria, in particular Staphylococcus aureus (S. aureus). As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. Methodology/Principal Findings: The pur...
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description | Background: Sepsis is a potentially deadly disease that often is caused by gram-positive bacteria, in particular Staphylococcus aureus (S. aureus). As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. Methodology/Principal Findings: The purpose of this study was to study the effect of Western diet on mortality induced by intravenous S. aureus inoculation and the immune functions before and after bacterial inoculation. Here we show that C57Bl/6 mice on high-fat diet (HFD) for 8 weeks, like genetically obese Ob/Ob mice on low-fat diet (LFD), have increased mortality during S. aureus-induced sepsis compared with LFD-fed C57Bl/6 controls. Bacterial load in the kidneys 5–7 days after inoculation was increased 10-fold in HFD-fed compared with LFD-fed mice. At that time, HFD-fed mice had increased serum levels and fat mRNA expression of the immune suppressing cytokines interleukin-1 receptor antagonist (IL-1Ra) and IL-10 compared with LFD-fed mice. In addition, HFD-fed mice had increased serum levels of the pro-inflammatory IL-1β. Also, HFD-fed mice with and without infection had increased levels of macrophages in fat. The proportion and function of phagocytosing granulocytes, and the production of reactive oxygen species (ROS) by peritoneal lavage cells were decreased in HFD-fed compared with LFD-fed mice. Conclusions: Our findings imply that chronic HFD disturb several innate immune functions in mice, and impairs the ability to clear S. aureus and survive sepsis. |
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As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. Methodology/Principal Findings: The purpose of this study was to study the effect of Western diet on mortality induced by intravenous S. aureus inoculation and the immune functions before and after bacterial inoculation. Here we show that C57Bl/6 mice on high-fat diet (HFD) for 8 weeks, like genetically obese Ob/Ob mice on low-fat diet (LFD), have increased mortality during S. aureus-induced sepsis compared with LFD-fed C57Bl/6 controls. Bacterial load in the kidneys 5–7 days after inoculation was increased 10-fold in HFD-fed compared with LFD-fed mice. At that time, HFD-fed mice had increased serum levels and fat mRNA expression of the immune suppressing cytokines interleukin-1 receptor antagonist (IL-1Ra) and IL-10 compared with LFD-fed mice. In addition, HFD-fed mice had increased serum levels of the pro-inflammatory IL-1β. Also, HFD-fed mice with and without infection had increased levels of macrophages in fat. The proportion and function of phagocytosing granulocytes, and the production of reactive oxygen species (ROS) by peritoneal lavage cells were decreased in HFD-fed compared with LFD-fed mice. Conclusions: Our findings imply that chronic HFD disturb several innate immune functions in mice, and impairs the ability to clear S. aureus and survive sepsis.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0007605</identifier><identifier>PMID: 19865485</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal Feed ; Animal models ; Animals ; Arthritis ; Bacteria ; Blood ; Carbohydrates ; Congenital diseases ; Critical Care and Emergency Medicine/Sepsis and Multiple Organ Failure ; Cytokines ; Dendritic cells ; Diabetes and Endocrinology/Obesity ; Diet ; Diet, Fat-Restricted ; Dietary Fats - pharmacology ; Disease susceptibility ; Endocrinology ; Experiments ; Fysiologi och anatomi ; Gene expression ; Gram-positive bacteria ; Health aspects ; High fat diet ; Hospitals ; House mouse ; Immune response ; Immune system ; Immunology/Immune Response ; Immunology/Immunity to Infections ; Immunology/Innate Immunity ; Infection ; Infectious Diseases/Bacterial Infections ; Inflammation ; Inflammatory diseases ; Inoculation ; Interleukin ; Interleukin 1 ; Interleukin 1 receptor antagonist ; Interleukin 1 Receptor Antagonist Protein - metabolism ; Interleukin 1 receptors ; Interleukin 10 ; Interleukin-10 - metabolism ; Interleukins ; Intravenous administration ; Kidney - metabolism ; Kidneys ; Leukocytes (granulocytic) ; long term effects ; Macrophages ; Male ; messenger RNA ; Metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Obese ; Models, Genetic ; Mortality ; Neurosciences ; Nosocomial infections ; Nutrition/Obesity ; Obesity ; Obesity - complications ; Obesity - genetics ; Obesity - immunology ; Oxygen ; Peritoneum ; Physiology ; Physiology and Anatomy ; Proteins ; Reactive oxygen species ; Rheumatology ; RNA ; Rodents ; Sepsis ; sepsis (infection) ; Sepsis - complications ; Sepsis - immunology ; Sepsis - mortality ; Serum levels ; signs and symptoms (animals and humans) ; Staphylococcal Infections - complications ; Staphylococcal Infections - mortality ; Staphylococcus aureus ; Staphylococcus aureus - metabolism ; Staphylococcus aureus infections ; Staphylococcus infections ; Sterols ; Studies ; Time Factors ; Weight control</subject><ispartof>PloS one, 2009-10, Vol.4 (10), p.e7605-e7605</ispartof><rights>COPYRIGHT 2009 Public Library of Science</rights><rights>2009 Strandberg et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Strandberg et al. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c867t-6ec62b8c3774087d019caab51be5f99da7886459b6a1589b6ddea501545deab3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765728/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765728/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19865485$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/111473$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://research.chalmers.se/publication/111473$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Strandberg, Louise</creatorcontrib><creatorcontrib>Verdrengh, Margareta</creatorcontrib><creatorcontrib>Enge, Maria</creatorcontrib><creatorcontrib>Andersson, Niklas</creatorcontrib><creatorcontrib>Amu, Sylvie</creatorcontrib><creatorcontrib>Önnheim, Karin</creatorcontrib><creatorcontrib>Benrick, Anna</creatorcontrib><creatorcontrib>Brisslert, Mikael</creatorcontrib><creatorcontrib>Bylund, Johan</creatorcontrib><creatorcontrib>Bokarewa, Maria</creatorcontrib><creatorcontrib>Nilsson, Staffan</creatorcontrib><creatorcontrib>Jansson, John-Olov</creatorcontrib><title>Mice Chronically Fed High-Fat Diet Have Increased Mortality and Disturbed Immune Response in Sepsis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Background: Sepsis is a potentially deadly disease that often is caused by gram-positive bacteria, in particular Staphylococcus aureus (S. aureus). As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. Methodology/Principal Findings: The purpose of this study was to study the effect of Western diet on mortality induced by intravenous S. aureus inoculation and the immune functions before and after bacterial inoculation. Here we show that C57Bl/6 mice on high-fat diet (HFD) for 8 weeks, like genetically obese Ob/Ob mice on low-fat diet (LFD), have increased mortality during S. aureus-induced sepsis compared with LFD-fed C57Bl/6 controls. Bacterial load in the kidneys 5–7 days after inoculation was increased 10-fold in HFD-fed compared with LFD-fed mice. At that time, HFD-fed mice had increased serum levels and fat mRNA expression of the immune suppressing cytokines interleukin-1 receptor antagonist (IL-1Ra) and IL-10 compared with LFD-fed mice. In addition, HFD-fed mice had increased serum levels of the pro-inflammatory IL-1β. Also, HFD-fed mice with and without infection had increased levels of macrophages in fat. The proportion and function of phagocytosing granulocytes, and the production of reactive oxygen species (ROS) by peritoneal lavage cells were decreased in HFD-fed compared with LFD-fed mice. Conclusions: Our findings imply that chronic HFD disturb several innate immune functions in mice, and impairs the ability to clear S. aureus and survive sepsis.</description><subject>Animal Feed</subject><subject>Animal models</subject><subject>Animals</subject><subject>Arthritis</subject><subject>Bacteria</subject><subject>Blood</subject><subject>Carbohydrates</subject><subject>Congenital diseases</subject><subject>Critical Care and Emergency Medicine/Sepsis and Multiple Organ Failure</subject><subject>Cytokines</subject><subject>Dendritic cells</subject><subject>Diabetes and Endocrinology/Obesity</subject><subject>Diet</subject><subject>Diet, Fat-Restricted</subject><subject>Dietary Fats - pharmacology</subject><subject>Disease susceptibility</subject><subject>Endocrinology</subject><subject>Experiments</subject><subject>Fysiologi och anatomi</subject><subject>Gene expression</subject><subject>Gram-positive bacteria</subject><subject>Health aspects</subject><subject>High fat diet</subject><subject>Hospitals</subject><subject>House mouse</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunology/Immune Response</subject><subject>Immunology/Immunity to Infections</subject><subject>Immunology/Innate Immunity</subject><subject>Infection</subject><subject>Infectious Diseases/Bacterial Infections</subject><subject>Inflammation</subject><subject>Inflammatory diseases</subject><subject>Inoculation</subject><subject>Interleukin</subject><subject>Interleukin 1</subject><subject>Interleukin 1 receptor antagonist</subject><subject>Interleukin 1 Receptor Antagonist Protein - metabolism</subject><subject>Interleukin 1 receptors</subject><subject>Interleukin 10</subject><subject>Interleukin-10 - metabolism</subject><subject>Interleukins</subject><subject>Intravenous administration</subject><subject>Kidney - metabolism</subject><subject>Kidneys</subject><subject>Leukocytes (granulocytic)</subject><subject>long term effects</subject><subject>Macrophages</subject><subject>Male</subject><subject>messenger RNA</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Obese</subject><subject>Models, Genetic</subject><subject>Mortality</subject><subject>Neurosciences</subject><subject>Nosocomial infections</subject><subject>Nutrition/Obesity</subject><subject>Obesity</subject><subject>Obesity - complications</subject><subject>Obesity - genetics</subject><subject>Obesity - immunology</subject><subject>Oxygen</subject><subject>Peritoneum</subject><subject>Physiology</subject><subject>Physiology and Anatomy</subject><subject>Proteins</subject><subject>Reactive oxygen species</subject><subject>Rheumatology</subject><subject>RNA</subject><subject>Rodents</subject><subject>Sepsis</subject><subject>sepsis (infection)</subject><subject>Sepsis - complications</subject><subject>Sepsis - immunology</subject><subject>Sepsis - mortality</subject><subject>Serum levels</subject><subject>signs and symptoms (animals and humans)</subject><subject>Staphylococcal Infections - complications</subject><subject>Staphylococcal Infections - mortality</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - metabolism</subject><subject>Staphylococcus aureus infections</subject><subject>Staphylococcus infections</subject><subject>Sterols</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Weight control</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk1Fv1DAMxysEYmPwDRBUQgLxcEfSNEn7gjQNxk7aNGk3eI2c1G0ztc0taQf79uR2B9shkFAeEtk__x1bdpK8pGROmaQfrtzkB-jmKzfgnBAiBeGPkn1asmwmMsIeP3jvJc9CuCKEs0KIp8keLQvB84LvJ-bMGkyPWu8Ga6DrbtNjrNIT27SzYxjTTxbH9ARuMF0MxiOE6DxzfoTOjrcpDFUkwjh5He2Lvp8GTC8wxC8FTO2QLnEVbHiePKmhC_hiex8kl8efL49OZqfnXxZHh6czUwg5zgQakenCMClzUsiK0NIAaE418rosK5BFIXJeagGUF_GqKgROKM95fGh2kLzeyK46F9S2PUHRrMwoy1ieRWKxISoHV2rlbQ_-Vjmw6s7gfKPAj9Z0qCjkGmqeyTqTeS0zTaHihSy1oZQbTqPWcqMVvuNq0jtqHgOCN60yLXQ9-qACqhjPpa6k0jqnKmeUK00pKOAy6saCclFE1dk_VZtppaKpmdZqlNJcssh_3NY86R4rg8PoodsJ2_UMtlWNu1GZFFxm64TvtgLeXU8YRtXbYLDrYEA3BRVziLJkBY_kmz_Iv7d4vqEaiF20Q-1iWhNPhb01cVRrG-2Hecwdz13F73cCIjPij7GBKQS1WF78P3v-bZd9-4BtEbqxDa6bRhuHcxfMN6DxLgSP9e_uUaLWm_arTrXeNLXdtBj26mHn74O2q3U_jjU4BY23QX1dZoQyQgsmOOfsJymBLS0</recordid><startdate>20091028</startdate><enddate>20091028</enddate><creator>Strandberg, Louise</creator><creator>Verdrengh, Margareta</creator><creator>Enge, Maria</creator><creator>Andersson, Niklas</creator><creator>Amu, Sylvie</creator><creator>Önnheim, Karin</creator><creator>Benrick, Anna</creator><creator>Brisslert, Mikael</creator><creator>Bylund, Johan</creator><creator>Bokarewa, Maria</creator><creator>Nilsson, Staffan</creator><creator>Jansson, John-Olov</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>FBQ</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>F1U</scope><scope>F1S</scope><scope>DOA</scope></search><sort><creationdate>20091028</creationdate><title>Mice Chronically Fed High-Fat Diet Have Increased Mortality and Disturbed Immune Response in Sepsis</title><author>Strandberg, Louise ; Verdrengh, Margareta ; Enge, Maria ; Andersson, Niklas ; Amu, Sylvie ; Önnheim, Karin ; Benrick, Anna ; Brisslert, Mikael ; Bylund, Johan ; Bokarewa, Maria ; Nilsson, Staffan ; Jansson, John-Olov</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c867t-6ec62b8c3774087d019caab51be5f99da7886459b6a1589b6ddea501545deab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animal Feed</topic><topic>Animal models</topic><topic>Animals</topic><topic>Arthritis</topic><topic>Bacteria</topic><topic>Blood</topic><topic>Carbohydrates</topic><topic>Congenital diseases</topic><topic>Critical Care and Emergency Medicine/Sepsis and Multiple Organ Failure</topic><topic>Cytokines</topic><topic>Dendritic cells</topic><topic>Diabetes and Endocrinology/Obesity</topic><topic>Diet</topic><topic>Diet, Fat-Restricted</topic><topic>Dietary Fats - pharmacology</topic><topic>Disease susceptibility</topic><topic>Endocrinology</topic><topic>Experiments</topic><topic>Fysiologi och anatomi</topic><topic>Gene expression</topic><topic>Gram-positive bacteria</topic><topic>Health aspects</topic><topic>High fat diet</topic><topic>Hospitals</topic><topic>House mouse</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunology/Immune Response</topic><topic>Immunology/Immunity to Infections</topic><topic>Immunology/Innate Immunity</topic><topic>Infection</topic><topic>Infectious Diseases/Bacterial Infections</topic><topic>Inflammation</topic><topic>Inflammatory diseases</topic><topic>Inoculation</topic><topic>Interleukin</topic><topic>Interleukin 1</topic><topic>Interleukin 1 receptor antagonist</topic><topic>Interleukin 1 Receptor Antagonist Protein - metabolism</topic><topic>Interleukin 1 receptors</topic><topic>Interleukin 10</topic><topic>Interleukin-10 - metabolism</topic><topic>Interleukins</topic><topic>Intravenous administration</topic><topic>Kidney - metabolism</topic><topic>Kidneys</topic><topic>Leukocytes (granulocytic)</topic><topic>long term effects</topic><topic>Macrophages</topic><topic>Male</topic><topic>messenger RNA</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Obese</topic><topic>Models, Genetic</topic><topic>Mortality</topic><topic>Neurosciences</topic><topic>Nosocomial infections</topic><topic>Nutrition/Obesity</topic><topic>Obesity</topic><topic>Obesity - complications</topic><topic>Obesity - genetics</topic><topic>Obesity - immunology</topic><topic>Oxygen</topic><topic>Peritoneum</topic><topic>Physiology</topic><topic>Physiology and Anatomy</topic><topic>Proteins</topic><topic>Reactive oxygen species</topic><topic>Rheumatology</topic><topic>RNA</topic><topic>Rodents</topic><topic>Sepsis</topic><topic>sepsis (infection)</topic><topic>Sepsis - complications</topic><topic>Sepsis - immunology</topic><topic>Sepsis - mortality</topic><topic>Serum levels</topic><topic>signs and symptoms (animals and humans)</topic><topic>Staphylococcal Infections - complications</topic><topic>Staphylococcal Infections - mortality</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - metabolism</topic><topic>Staphylococcus aureus infections</topic><topic>Staphylococcus infections</topic><topic>Sterols</topic><topic>Studies</topic><topic>Time Factors</topic><topic>Weight control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strandberg, Louise</creatorcontrib><creatorcontrib>Verdrengh, Margareta</creatorcontrib><creatorcontrib>Enge, Maria</creatorcontrib><creatorcontrib>Andersson, Niklas</creatorcontrib><creatorcontrib>Amu, Sylvie</creatorcontrib><creatorcontrib>Önnheim, Karin</creatorcontrib><creatorcontrib>Benrick, Anna</creatorcontrib><creatorcontrib>Brisslert, Mikael</creatorcontrib><creatorcontrib>Bylund, Johan</creatorcontrib><creatorcontrib>Bokarewa, Maria</creatorcontrib><creatorcontrib>Nilsson, Staffan</creatorcontrib><creatorcontrib>Jansson, John-Olov</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Göteborgs universitet</collection><collection>SWEPUB Chalmers tekniska högskola</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strandberg, Louise</au><au>Verdrengh, Margareta</au><au>Enge, Maria</au><au>Andersson, Niklas</au><au>Amu, Sylvie</au><au>Önnheim, Karin</au><au>Benrick, Anna</au><au>Brisslert, Mikael</au><au>Bylund, Johan</au><au>Bokarewa, Maria</au><au>Nilsson, Staffan</au><au>Jansson, John-Olov</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mice Chronically Fed High-Fat Diet Have Increased Mortality and Disturbed Immune Response in Sepsis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2009-10-28</date><risdate>2009</risdate><volume>4</volume><issue>10</issue><spage>e7605</spage><epage>e7605</epage><pages>e7605-e7605</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Background: Sepsis is a potentially deadly disease that often is caused by gram-positive bacteria, in particular Staphylococcus aureus (S. aureus). As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. Methodology/Principal Findings: The purpose of this study was to study the effect of Western diet on mortality induced by intravenous S. aureus inoculation and the immune functions before and after bacterial inoculation. Here we show that C57Bl/6 mice on high-fat diet (HFD) for 8 weeks, like genetically obese Ob/Ob mice on low-fat diet (LFD), have increased mortality during S. aureus-induced sepsis compared with LFD-fed C57Bl/6 controls. Bacterial load in the kidneys 5–7 days after inoculation was increased 10-fold in HFD-fed compared with LFD-fed mice. At that time, HFD-fed mice had increased serum levels and fat mRNA expression of the immune suppressing cytokines interleukin-1 receptor antagonist (IL-1Ra) and IL-10 compared with LFD-fed mice. In addition, HFD-fed mice had increased serum levels of the pro-inflammatory IL-1β. Also, HFD-fed mice with and without infection had increased levels of macrophages in fat. The proportion and function of phagocytosing granulocytes, and the production of reactive oxygen species (ROS) by peritoneal lavage cells were decreased in HFD-fed compared with LFD-fed mice. Conclusions: Our findings imply that chronic HFD disturb several innate immune functions in mice, and impairs the ability to clear S. aureus and survive sepsis.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>19865485</pmid><doi>10.1371/journal.pone.0007605</doi><tpages>e7605</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2009-10, Vol.4 (10), p.e7605-e7605 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1292132342 |
source | MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
subjects | Animal Feed Animal models Animals Arthritis Bacteria Blood Carbohydrates Congenital diseases Critical Care and Emergency Medicine/Sepsis and Multiple Organ Failure Cytokines Dendritic cells Diabetes and Endocrinology/Obesity Diet Diet, Fat-Restricted Dietary Fats - pharmacology Disease susceptibility Endocrinology Experiments Fysiologi och anatomi Gene expression Gram-positive bacteria Health aspects High fat diet Hospitals House mouse Immune response Immune system Immunology/Immune Response Immunology/Immunity to Infections Immunology/Innate Immunity Infection Infectious Diseases/Bacterial Infections Inflammation Inflammatory diseases Inoculation Interleukin Interleukin 1 Interleukin 1 receptor antagonist Interleukin 1 Receptor Antagonist Protein - metabolism Interleukin 1 receptors Interleukin 10 Interleukin-10 - metabolism Interleukins Intravenous administration Kidney - metabolism Kidneys Leukocytes (granulocytic) long term effects Macrophages Male messenger RNA Metabolism Mice Mice, Inbred C57BL Mice, Obese Models, Genetic Mortality Neurosciences Nosocomial infections Nutrition/Obesity Obesity Obesity - complications Obesity - genetics Obesity - immunology Oxygen Peritoneum Physiology Physiology and Anatomy Proteins Reactive oxygen species Rheumatology RNA Rodents Sepsis sepsis (infection) Sepsis - complications Sepsis - immunology Sepsis - mortality Serum levels signs and symptoms (animals and humans) Staphylococcal Infections - complications Staphylococcal Infections - mortality Staphylococcus aureus Staphylococcus aureus - metabolism Staphylococcus aureus infections Staphylococcus infections Sterols Studies Time Factors Weight control |
title | Mice Chronically Fed High-Fat Diet Have Increased Mortality and Disturbed Immune Response in Sepsis |
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