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Dynamic changes of inflammatory response and oxidative stress induced by methicillin-resistant Staphylococcus aureus in mice
This study is to analyze the dynamic changes of inflammation and oxidative stress in mice infected with MRSA and to provide experimental basis for clinically formulating reasonable treatment plans. We established a model of MRSA infection in mice, detected the fluctuations in the concentration of pr...
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Published in: | European journal of clinical microbiology & infectious diseases 2022, Vol.41 (1), p.79-86 |
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description | This study is to analyze the dynamic changes of inflammation and oxidative stress in mice infected with MRSA and to provide experimental basis for clinically formulating reasonable treatment plans. We established a model of MRSA infection in mice, detected the fluctuations in the concentration of proinflammatory cytokines and oxidative stress factors with time, and combined with the results of microscopic examination of tissue sections to explain the infection in vivo caused by MRSA. The results showed that on the 1st, 3rd, and 7th day of MRSA infection, the number of leukocytes and eosinophils decreased at first and then increased, monocytes increased continuously, and neutrophils and basophils decreased. At the same time, the levels of proinflammatory cytokines IL-1β, IL-6, and TNF-α increased. The concentration of glutathione peroxide decreased, and the oxidative metabolites increased. Tissue sections also showed that inflammation and oxidative stress occurred in mice. It is obvious that MRSA infection can lead to significant inflammation and oxidative stress. Therefore, while treating MRSA infection, attention should be paid to the levels of inflammation and oxidative stress in different periods to achieve better treatment effects. |
doi_str_mv | 10.1007/s10096-021-04349-5 |
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We established a model of MRSA infection in mice, detected the fluctuations in the concentration of proinflammatory cytokines and oxidative stress factors with time, and combined with the results of microscopic examination of tissue sections to explain the infection in vivo caused by MRSA. The results showed that on the 1st, 3rd, and 7th day of MRSA infection, the number of leukocytes and eosinophils decreased at first and then increased, monocytes increased continuously, and neutrophils and basophils decreased. At the same time, the levels of proinflammatory cytokines IL-1β, IL-6, and TNF-α increased. The concentration of glutathione peroxide decreased, and the oxidative metabolites increased. Tissue sections also showed that inflammation and oxidative stress occurred in mice. It is obvious that MRSA infection can lead to significant inflammation and oxidative stress. Therefore, while treating MRSA infection, attention should be paid to the levels of inflammation and oxidative stress in different periods to achieve better treatment effects.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/s10096-021-04349-5</identifier><identifier>PMID: 34562152</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Cytokines ; Drug resistance ; Eosinophils ; Female ; Glutathione ; Glutathione - immunology ; Humans ; IL-1β ; Inflammation ; Inflammatory response ; Interleukin 6 ; Interleukin-1beta - genetics ; Interleukin-1beta - immunology ; Interleukin-6 - genetics ; Interleukin-6 - immunology ; Internal Medicine ; Leukocytes ; Leukocytes (basophilic) ; Leukocytes (eosinophilic) ; Leukocytes (neutrophilic) ; Male ; Medical Microbiology ; Metabolites ; Methicillin ; Methicillin-Resistant Staphylococcus aureus - genetics ; Methicillin-Resistant Staphylococcus aureus - physiology ; Mice ; Mice, Inbred ICR ; Monocytes ; Original Article ; Oxidation resistance ; Oxidative Stress ; Staphylococcal Infections - genetics ; Staphylococcal Infections - immunology ; Staphylococcal Infections - microbiology ; Staphylococcus infections ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - immunology ; Tumor necrosis factor-α</subject><ispartof>European journal of clinical microbiology & infectious diseases, 2022, Vol.41 (1), p.79-86</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-4db234259eaee30573b4c41c72d77fb406918170b9a237fc7b77fc9f36973dcf3</citedby><cites>FETCH-LOGICAL-c375t-4db234259eaee30573b4c41c72d77fb406918170b9a237fc7b77fc9f36973dcf3</cites><orcidid>0000-0002-4988-9002</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34562152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Long, Nana</creatorcontrib><creatorcontrib>Zhang, Yanjiao</creatorcontrib><creatorcontrib>Qiu, Min</creatorcontrib><creatorcontrib>Deng, Jingzhu</creatorcontrib><creatorcontrib>Sun, Fenghui</creatorcontrib><creatorcontrib>Dai, Min</creatorcontrib><title>Dynamic changes of inflammatory response and oxidative stress induced by methicillin-resistant Staphylococcus aureus in mice</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>This study is to analyze the dynamic changes of inflammation and oxidative stress in mice infected with MRSA and to provide experimental basis for clinically formulating reasonable treatment plans. We established a model of MRSA infection in mice, detected the fluctuations in the concentration of proinflammatory cytokines and oxidative stress factors with time, and combined with the results of microscopic examination of tissue sections to explain the infection in vivo caused by MRSA. The results showed that on the 1st, 3rd, and 7th day of MRSA infection, the number of leukocytes and eosinophils decreased at first and then increased, monocytes increased continuously, and neutrophils and basophils decreased. At the same time, the levels of proinflammatory cytokines IL-1β, IL-6, and TNF-α increased. The concentration of glutathione peroxide decreased, and the oxidative metabolites increased. Tissue sections also showed that inflammation and oxidative stress occurred in mice. It is obvious that MRSA infection can lead to significant inflammation and oxidative stress. Therefore, while treating MRSA infection, attention should be paid to the levels of inflammation and oxidative stress in different periods to achieve better treatment effects.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cytokines</subject><subject>Drug resistance</subject><subject>Eosinophils</subject><subject>Female</subject><subject>Glutathione</subject><subject>Glutathione - immunology</subject><subject>Humans</subject><subject>IL-1β</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Interleukin 6</subject><subject>Interleukin-1beta - genetics</subject><subject>Interleukin-1beta - immunology</subject><subject>Interleukin-6 - genetics</subject><subject>Interleukin-6 - immunology</subject><subject>Internal Medicine</subject><subject>Leukocytes</subject><subject>Leukocytes (basophilic)</subject><subject>Leukocytes (eosinophilic)</subject><subject>Leukocytes (neutrophilic)</subject><subject>Male</subject><subject>Medical Microbiology</subject><subject>Metabolites</subject><subject>Methicillin</subject><subject>Methicillin-Resistant Staphylococcus aureus - genetics</subject><subject>Methicillin-Resistant Staphylococcus aureus - physiology</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Monocytes</subject><subject>Original Article</subject><subject>Oxidation resistance</subject><subject>Oxidative Stress</subject><subject>Staphylococcal Infections - genetics</subject><subject>Staphylococcal Infections - immunology</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcus infections</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor necrosis factor-α</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kc2KFDEUhYMoTs_oC7iQgBs30fzfzlLGXxhwoa5DKpWyM1QlbZIaLPDhzdijggs3CeR8597Ah9ATRl8wSuFl7afRhHJGqBTSEHUP7ZgUikgB4j7aUSMkMcDFGTqv9Zr20h7gIToTUmnOFN-hH6-35JbosT-49DVUnCcc0zS7ZXEtlw2XUI851YBdGnH-HkfX4k3AtfWgdnRcfRjxsOEltEP0cZ5jIj2LtbnU8Kfmjodtzj57v1bs1hLW2xruO8Mj9GBycw2P7-4L9OXtm8-X78nVx3cfLl9dES9ANSLHgQvJlQkuBEEViEF6yTzwEWAaJNWG7RnQwTguYPIw9GdvJqENiNFP4gI9P809lvxtDbXZJVYf5tmlkNdquQKtlQTQHX32D3qd15L67yzXTMNeMEU7xU-UL7nWEiZ7LHFxZbOM2ls39uTGdjf2lxureunp3eh1WML4p_JbRgfECag96jLK393_GfsTwBeb0g</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Long, Nana</creator><creator>Zhang, Yanjiao</creator><creator>Qiu, Min</creator><creator>Deng, Jingzhu</creator><creator>Sun, Fenghui</creator><creator>Dai, Min</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4988-9002</orcidid></search><sort><creationdate>2022</creationdate><title>Dynamic changes of inflammatory response and oxidative stress induced by methicillin-resistant Staphylococcus aureus in mice</title><author>Long, Nana ; Zhang, Yanjiao ; Qiu, Min ; Deng, Jingzhu ; Sun, Fenghui ; Dai, Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-4db234259eaee30573b4c41c72d77fb406918170b9a237fc7b77fc9f36973dcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cytokines</topic><topic>Drug resistance</topic><topic>Eosinophils</topic><topic>Female</topic><topic>Glutathione</topic><topic>Glutathione - 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Academic</collection><jtitle>European journal of clinical microbiology & infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Long, Nana</au><au>Zhang, Yanjiao</au><au>Qiu, Min</au><au>Deng, Jingzhu</au><au>Sun, Fenghui</au><au>Dai, Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic changes of inflammatory response and oxidative stress induced by methicillin-resistant Staphylococcus aureus in mice</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2022</date><risdate>2022</risdate><volume>41</volume><issue>1</issue><spage>79</spage><epage>86</epage><pages>79-86</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>This study is to analyze the dynamic changes of inflammation and oxidative stress in mice infected with MRSA and to provide experimental basis for clinically formulating reasonable treatment plans. We established a model of MRSA infection in mice, detected the fluctuations in the concentration of proinflammatory cytokines and oxidative stress factors with time, and combined with the results of microscopic examination of tissue sections to explain the infection in vivo caused by MRSA. The results showed that on the 1st, 3rd, and 7th day of MRSA infection, the number of leukocytes and eosinophils decreased at first and then increased, monocytes increased continuously, and neutrophils and basophils decreased. At the same time, the levels of proinflammatory cytokines IL-1β, IL-6, and TNF-α increased. The concentration of glutathione peroxide decreased, and the oxidative metabolites increased. Tissue sections also showed that inflammation and oxidative stress occurred in mice. It is obvious that MRSA infection can lead to significant inflammation and oxidative stress. Therefore, while treating MRSA infection, attention should be paid to the levels of inflammation and oxidative stress in different periods to achieve better treatment effects.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34562152</pmid><doi>10.1007/s10096-021-04349-5</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4988-9002</orcidid></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Cytokines Drug resistance Eosinophils Female Glutathione Glutathione - immunology Humans IL-1β Inflammation Inflammatory response Interleukin 6 Interleukin-1beta - genetics Interleukin-1beta - immunology Interleukin-6 - genetics Interleukin-6 - immunology Internal Medicine Leukocytes Leukocytes (basophilic) Leukocytes (eosinophilic) Leukocytes (neutrophilic) Male Medical Microbiology Metabolites Methicillin Methicillin-Resistant Staphylococcus aureus - genetics Methicillin-Resistant Staphylococcus aureus - physiology Mice Mice, Inbred ICR Monocytes Original Article Oxidation resistance Oxidative Stress Staphylococcal Infections - genetics Staphylococcal Infections - immunology Staphylococcal Infections - microbiology Staphylococcus infections Tumor Necrosis Factor-alpha - genetics Tumor Necrosis Factor-alpha - immunology Tumor necrosis factor-α |
title | Dynamic changes of inflammatory response and oxidative stress induced by methicillin-resistant Staphylococcus aureus in mice |
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