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Expression of NLRP3 and AIM2 inflammasome in Peripheral blood in Chinese patients with acute and chronic brucellosis
Brucellosis is a zoonotic disease caused by Brucella abortus . An efficient immune response is crucial for curing brucellosis. The inflammasome plays a significant role in the immune response. It is unclear which inflammasome is active in acute and chronic brucellosis and how its levels relate to in...
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Published in: | Scientific reports 2022-09, Vol.12 (1), p.15123-15123, Article 15123 |
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description | Brucellosis is a zoonotic disease caused by
Brucella abortus
. An efficient immune response is crucial for curing brucellosis. The inflammasome plays a significant role in the immune response. It is unclear which inflammasome is active in acute and chronic brucellosis and how its levels relate to inflammatory cytokines. A total of 40 patients with acute or chronic brucellosis and 20 healthy volunteers had peripheral blood samples collected. The expression levels of AIM2, NLRP3, ASC, and Caspase-1 were determined by a real-time polymerase chain reaction from RNA and serum samples, and IL-1β, IL-18, and IFN-γ were measured by enzyme-linked immunosorbent assay. In the acute brucellosis group, AIM2 expression was significantly higher, while ACS expression was significantly lower than that of healthy volunteers. In patients with chronic brucellosis, AIM2 expression was significantly lower, while Caspase-1 expression was significantly higher than that of healthy volunteers. Serum IL-18 and IFN-γ levels were significantly higher in patients with acute brucellosis than in healthy controls. The IFN-γ level was also significantly higher in patients with chronic brucellosis than in healthy controls. The inflammasome responds differently in different stages of brucellosis. The inflammasome may be the site of action of immune escape in brucellosis. |
doi_str_mv | 10.1038/s41598-022-19398-9 |
format | article |
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Brucella abortus
. An efficient immune response is crucial for curing brucellosis. The inflammasome plays a significant role in the immune response. It is unclear which inflammasome is active in acute and chronic brucellosis and how its levels relate to inflammatory cytokines. A total of 40 patients with acute or chronic brucellosis and 20 healthy volunteers had peripheral blood samples collected. The expression levels of AIM2, NLRP3, ASC, and Caspase-1 were determined by a real-time polymerase chain reaction from RNA and serum samples, and IL-1β, IL-18, and IFN-γ were measured by enzyme-linked immunosorbent assay. In the acute brucellosis group, AIM2 expression was significantly higher, while ACS expression was significantly lower than that of healthy volunteers. In patients with chronic brucellosis, AIM2 expression was significantly lower, while Caspase-1 expression was significantly higher than that of healthy volunteers. Serum IL-18 and IFN-γ levels were significantly higher in patients with acute brucellosis than in healthy controls. The IFN-γ level was also significantly higher in patients with chronic brucellosis than in healthy controls. The inflammasome responds differently in different stages of brucellosis. The inflammasome may be the site of action of immune escape in brucellosis.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-022-19398-9</identifier><identifier>PMID: 36068262</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/699 ; 692/699/255 ; 692/699/255/1318 ; Brucellosis ; Caspase-1 ; DNA-directed RNA polymerase ; Enzyme-linked immunosorbent assay ; Humanities and Social Sciences ; IL-1β ; Immune response ; Inflammasomes ; Inflammation ; Interleukin 18 ; multidisciplinary ; Peripheral blood ; Science ; Science (multidisciplinary) ; Zoonoses ; γ-Interferon</subject><ispartof>Scientific reports, 2022-09, Vol.12 (1), p.15123-15123, Article 15123</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. 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><cites>FETCH-LOGICAL-c468t-a432efafbd7bd068870c4876a81961e7908093c58bacc287e234c34288759e7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2710055682/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2710055682?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids></links><search><creatorcontrib>Su, Xiao</creatorcontrib><creatorcontrib>Zhao, Shigang</creatorcontrib><creatorcontrib>Song, Yijun</creatorcontrib><title>Expression of NLRP3 and AIM2 inflammasome in Peripheral blood in Chinese patients with acute and chronic brucellosis</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><description>Brucellosis is a zoonotic disease caused by
Brucella abortus
. An efficient immune response is crucial for curing brucellosis. The inflammasome plays a significant role in the immune response. It is unclear which inflammasome is active in acute and chronic brucellosis and how its levels relate to inflammatory cytokines. A total of 40 patients with acute or chronic brucellosis and 20 healthy volunteers had peripheral blood samples collected. The expression levels of AIM2, NLRP3, ASC, and Caspase-1 were determined by a real-time polymerase chain reaction from RNA and serum samples, and IL-1β, IL-18, and IFN-γ were measured by enzyme-linked immunosorbent assay. In the acute brucellosis group, AIM2 expression was significantly higher, while ACS expression was significantly lower than that of healthy volunteers. In patients with chronic brucellosis, AIM2 expression was significantly lower, while Caspase-1 expression was significantly higher than that of healthy volunteers. Serum IL-18 and IFN-γ levels were significantly higher in patients with acute brucellosis than in healthy controls. The IFN-γ level was also significantly higher in patients with chronic brucellosis than in healthy controls. The inflammasome responds differently in different stages of brucellosis. The inflammasome may be the site of action of immune escape in brucellosis.</description><subject>692/699</subject><subject>692/699/255</subject><subject>692/699/255/1318</subject><subject>Brucellosis</subject><subject>Caspase-1</subject><subject>DNA-directed RNA polymerase</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Humanities and Social Sciences</subject><subject>IL-1β</subject><subject>Immune response</subject><subject>Inflammasomes</subject><subject>Inflammation</subject><subject>Interleukin 18</subject><subject>multidisciplinary</subject><subject>Peripheral blood</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Zoonoses</subject><subject>γ-Interferon</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEolXpH-BkiQuXFH8lsS9I1arASgtUCM6WY082XiV2sJNC_z3eTQWUA77YHr_zaDzzFsVLgq8IZuJN4qSSosSUlkSyfJJPinOKeVVSRunTv85nxWVKB5xXRSUn8nlxxmpcC1rT82K--TlFSMkFj0KHPu2-3DKkvUXX248UOd8Nehx1CiPkC7qF6KYeoh5QO4Rgj7FN7zwkQJOeHfg5oR9u7pE2ywwnkOlj8M6gNi4GhiEkl14Uzzo9JLh82C-Kb-9uvm4-lLvP77eb611peC3mUnNGodNda5vW5oJFgw0XTa0FkTWBRmKBJTOVaLUxVDRAGTeM0yysJDSWXRTblWuDPqgpulHHexW0U6dAiHul4-zMAIowDlyLmlpNOGed1sJYSzphLXAQR9bblTUt7QjW5K_mNjyCPn7xrlf7cKckzzVTkQGvHwAxfF8gzWp06dgR7SEsSdGGEIabPLEsffWP9BCW6HOrjqo8xypPL6voqjIxpBSh-10MweroEbV6RGWPqJNHlMxJbE1KWez3EP-g_5P1C_opvdw</recordid><startdate>20220906</startdate><enddate>20220906</enddate><creator>Su, Xiao</creator><creator>Zhao, Shigang</creator><creator>Song, Yijun</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220906</creationdate><title>Expression of NLRP3 and AIM2 inflammasome in Peripheral blood in Chinese patients with acute and chronic brucellosis</title><author>Su, Xiao ; Zhao, Shigang ; Song, Yijun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-a432efafbd7bd068870c4876a81961e7908093c58bacc287e234c34288759e7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>692/699</topic><topic>692/699/255</topic><topic>692/699/255/1318</topic><topic>Brucellosis</topic><topic>Caspase-1</topic><topic>DNA-directed RNA polymerase</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Humanities and Social Sciences</topic><topic>IL-1β</topic><topic>Immune response</topic><topic>Inflammasomes</topic><topic>Inflammation</topic><topic>Interleukin 18</topic><topic>multidisciplinary</topic><topic>Peripheral blood</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Zoonoses</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Su, Xiao</creatorcontrib><creatorcontrib>Zhao, Shigang</creatorcontrib><creatorcontrib>Song, Yijun</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest 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)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</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><collection>Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Xiao</au><au>Zhao, Shigang</au><au>Song, Yijun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of NLRP3 and AIM2 inflammasome in Peripheral blood in Chinese patients with acute and chronic brucellosis</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><date>2022-09-06</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><spage>15123</spage><epage>15123</epage><pages>15123-15123</pages><artnum>15123</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Brucellosis is a zoonotic disease caused by
Brucella abortus
. An efficient immune response is crucial for curing brucellosis. The inflammasome plays a significant role in the immune response. It is unclear which inflammasome is active in acute and chronic brucellosis and how its levels relate to inflammatory cytokines. A total of 40 patients with acute or chronic brucellosis and 20 healthy volunteers had peripheral blood samples collected. The expression levels of AIM2, NLRP3, ASC, and Caspase-1 were determined by a real-time polymerase chain reaction from RNA and serum samples, and IL-1β, IL-18, and IFN-γ were measured by enzyme-linked immunosorbent assay. In the acute brucellosis group, AIM2 expression was significantly higher, while ACS expression was significantly lower than that of healthy volunteers. In patients with chronic brucellosis, AIM2 expression was significantly lower, while Caspase-1 expression was significantly higher than that of healthy volunteers. Serum IL-18 and IFN-γ levels were significantly higher in patients with acute brucellosis than in healthy controls. The IFN-γ level was also significantly higher in patients with chronic brucellosis than in healthy controls. The inflammasome responds differently in different stages of brucellosis. The inflammasome may be the site of action of immune escape in brucellosis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>36068262</pmid><doi>10.1038/s41598-022-19398-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/699 692/699/255 692/699/255/1318 Brucellosis Caspase-1 DNA-directed RNA polymerase Enzyme-linked immunosorbent assay Humanities and Social Sciences IL-1β Immune response Inflammasomes Inflammation Interleukin 18 multidisciplinary Peripheral blood Science Science (multidisciplinary) Zoonoses γ-Interferon |
title | Expression of NLRP3 and AIM2 inflammasome in Peripheral blood in Chinese patients with acute and chronic brucellosis |
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