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Host Prdx6 contributing to the intracellular survival of Brucella suis S2 strain
Background Brucellosis is a worldwide zoonotic infectious disease that is transmitted in various ways and causes great harm to humans and animals. The brucellosis pathogen is Brucella, which mainly resides in macrophage cells and survives and replicates in host cells. However, the mechanisms underly...
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Published in: | BMC Veterinary Research 2019, Vol.15 (1) |
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creator | Wang, Lu-Lu Chen, Xiao-Feng Hu, Pan Lu, Shi-Ying Fu, Bao-Quan Li, Yan-Song Zhai, Fei-Fei Ju, Dan-Di Zhang, Shi-Jun Shui, Yi-Ming Chang, Jiang Ma, Xiao-Long Su, Bing Zhou, Yu Liu, Zeng-Shan Ren, Hong-Lin |
description | Background Brucellosis is a worldwide zoonotic infectious disease that is transmitted in various ways and causes great harm to humans and animals. The brucellosis pathogen is Brucella, which mainly resides in macrophage cells and survives and replicates in host cells. However, the mechanisms underlying Brucella survival in macrophage cells have not been thoroughly elucidated to date. Peroxiredoxin 6 (Prdx6) is a bifunctional protein that shows not only GSH peroxidase activity but also phospholipase A2 activity and plays important roles in combating oxidative damage and regulating apoptosis. Results Recombinant mouse (Mus musculus) Prdx6 (MmPrdx6) was expressed and purified, and monoclonal antibodies against MmPrdx6 were prepared. Using the Brucella suis S2 strain to infect RAW264.7 murine macrophages, the level of intracellular Prdx6 expression first decreased and later increased following infection. Overexpressing Prdx6 in macrophages resulted in an increase in B. suis S2 strain levels in RAW264.7 cells, while knocking down Prdx6 reduced the S2 levels in cells. Conclusions Host Prdx6 can increase the intracellular survival of B. suis S2 strain and plays a role in Brucella infection. Keywords: Host, Prdx6, Brucella, Macrophage, Intracellular survival |
doi_str_mv | 10.1186/s12917-019-2049-8 |
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The brucellosis pathogen is Brucella, which mainly resides in macrophage cells and survives and replicates in host cells. However, the mechanisms underlying Brucella survival in macrophage cells have not been thoroughly elucidated to date. Peroxiredoxin 6 (Prdx6) is a bifunctional protein that shows not only GSH peroxidase activity but also phospholipase A2 activity and plays important roles in combating oxidative damage and regulating apoptosis. Results Recombinant mouse (Mus musculus) Prdx6 (MmPrdx6) was expressed and purified, and monoclonal antibodies against MmPrdx6 were prepared. Using the Brucella suis S2 strain to infect RAW264.7 murine macrophages, the level of intracellular Prdx6 expression first decreased and later increased following infection. Overexpressing Prdx6 in macrophages resulted in an increase in B. suis S2 strain levels in RAW264.7 cells, while knocking down Prdx6 reduced the S2 levels in cells. Conclusions Host Prdx6 can increase the intracellular survival of B. suis S2 strain and plays a role in Brucella infection. Keywords: Host, Prdx6, Brucella, Macrophage, Intracellular survival</description><identifier>ISSN: 1746-6148</identifier><identifier>EISSN: 1746-6148</identifier><identifier>DOI: 10.1186/s12917-019-2049-8</identifier><language>eng</language><publisher>BioMed Central Ltd</publisher><subject>Antibodies ; Brucella ; Brucellosis ; Communicable diseases ; Disease transmission ; Gene expression ; Genetic aspects ; Health aspects ; House mouse ; Identification and classification ; Macrophages ; Monoclonal antibodies ; Monocytes ; Peroxidase ; Phospholipases ; Plasmids ; Zoonoses</subject><ispartof>BMC Veterinary Research, 2019, Vol.15 (1)</ispartof><rights>COPYRIGHT 2019 BioMed Central Ltd.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Wang, Lu-Lu</creatorcontrib><creatorcontrib>Chen, Xiao-Feng</creatorcontrib><creatorcontrib>Hu, Pan</creatorcontrib><creatorcontrib>Lu, Shi-Ying</creatorcontrib><creatorcontrib>Fu, Bao-Quan</creatorcontrib><creatorcontrib>Li, Yan-Song</creatorcontrib><creatorcontrib>Zhai, Fei-Fei</creatorcontrib><creatorcontrib>Ju, Dan-Di</creatorcontrib><creatorcontrib>Zhang, Shi-Jun</creatorcontrib><creatorcontrib>Shui, Yi-Ming</creatorcontrib><creatorcontrib>Chang, Jiang</creatorcontrib><creatorcontrib>Ma, Xiao-Long</creatorcontrib><creatorcontrib>Su, Bing</creatorcontrib><creatorcontrib>Zhou, Yu</creatorcontrib><creatorcontrib>Liu, Zeng-Shan</creatorcontrib><creatorcontrib>Ren, Hong-Lin</creatorcontrib><title>Host Prdx6 contributing to the intracellular survival of Brucella suis S2 strain</title><title>BMC Veterinary Research</title><description>Background Brucellosis is a worldwide zoonotic infectious disease that is transmitted in various ways and causes great harm to humans and animals. The brucellosis pathogen is Brucella, which mainly resides in macrophage cells and survives and replicates in host cells. However, the mechanisms underlying Brucella survival in macrophage cells have not been thoroughly elucidated to date. Peroxiredoxin 6 (Prdx6) is a bifunctional protein that shows not only GSH peroxidase activity but also phospholipase A2 activity and plays important roles in combating oxidative damage and regulating apoptosis. Results Recombinant mouse (Mus musculus) Prdx6 (MmPrdx6) was expressed and purified, and monoclonal antibodies against MmPrdx6 were prepared. Using the Brucella suis S2 strain to infect RAW264.7 murine macrophages, the level of intracellular Prdx6 expression first decreased and later increased following infection. Overexpressing Prdx6 in macrophages resulted in an increase in B. suis S2 strain levels in RAW264.7 cells, while knocking down Prdx6 reduced the S2 levels in cells. Conclusions Host Prdx6 can increase the intracellular survival of B. suis S2 strain and plays a role in Brucella infection. Keywords: Host, Prdx6, Brucella, Macrophage, Intracellular survival</description><subject>Antibodies</subject><subject>Brucella</subject><subject>Brucellosis</subject><subject>Communicable diseases</subject><subject>Disease transmission</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>House mouse</subject><subject>Identification and classification</subject><subject>Macrophages</subject><subject>Monoclonal antibodies</subject><subject>Monocytes</subject><subject>Peroxidase</subject><subject>Phospholipases</subject><subject>Plasmids</subject><subject>Zoonoses</subject><issn>1746-6148</issn><issn>1746-6148</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2019</creationdate><recordtype>report</recordtype><sourceid/><recordid>eNqVjs0KwjAQhIMo-PsA3vYFokkb0-aoongU9C7RproSG0hS8fGN4MGr7GGXj9mZIWTK2YzzUs4DzxQvKOOKZkwoWnbIgBdCUslF2f25-2QYwp0xIVQhB2S_cyHC3lcvCRfXRI_nNmJzhegg3gxgQvpirG2t9hBa_8SntuBqWPn2w3WCGOCQQUhKbMakV2sbzOS7R2S23RzXO3rV1pywqd3HME1lHpgSTY2JLxepjcxFpvK_H96_bk30</recordid><startdate>20190822</startdate><enddate>20190822</enddate><creator>Wang, Lu-Lu</creator><creator>Chen, Xiao-Feng</creator><creator>Hu, Pan</creator><creator>Lu, Shi-Ying</creator><creator>Fu, Bao-Quan</creator><creator>Li, Yan-Song</creator><creator>Zhai, Fei-Fei</creator><creator>Ju, Dan-Di</creator><creator>Zhang, Shi-Jun</creator><creator>Shui, Yi-Ming</creator><creator>Chang, Jiang</creator><creator>Ma, Xiao-Long</creator><creator>Su, Bing</creator><creator>Zhou, Yu</creator><creator>Liu, Zeng-Shan</creator><creator>Ren, Hong-Lin</creator><general>BioMed Central Ltd</general><scope/></search><sort><creationdate>20190822</creationdate><title>Host Prdx6 contributing to the intracellular survival of Brucella suis S2 strain</title><author>Wang, Lu-Lu ; Chen, Xiao-Feng ; Hu, Pan ; Lu, Shi-Ying ; Fu, Bao-Quan ; Li, Yan-Song ; Zhai, Fei-Fei ; Ju, Dan-Di ; Zhang, Shi-Jun ; Shui, Yi-Ming ; Chang, Jiang ; Ma, Xiao-Long ; Su, Bing ; Zhou, Yu ; Liu, Zeng-Shan ; Ren, Hong-Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_infotracacademiconefile_A5976634293</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antibodies</topic><topic>Brucella</topic><topic>Brucellosis</topic><topic>Communicable diseases</topic><topic>Disease transmission</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>House mouse</topic><topic>Identification and classification</topic><topic>Macrophages</topic><topic>Monoclonal antibodies</topic><topic>Monocytes</topic><topic>Peroxidase</topic><topic>Phospholipases</topic><topic>Plasmids</topic><topic>Zoonoses</topic><toplevel>online_resources</toplevel><creatorcontrib>Wang, Lu-Lu</creatorcontrib><creatorcontrib>Chen, Xiao-Feng</creatorcontrib><creatorcontrib>Hu, Pan</creatorcontrib><creatorcontrib>Lu, Shi-Ying</creatorcontrib><creatorcontrib>Fu, Bao-Quan</creatorcontrib><creatorcontrib>Li, Yan-Song</creatorcontrib><creatorcontrib>Zhai, Fei-Fei</creatorcontrib><creatorcontrib>Ju, Dan-Di</creatorcontrib><creatorcontrib>Zhang, Shi-Jun</creatorcontrib><creatorcontrib>Shui, Yi-Ming</creatorcontrib><creatorcontrib>Chang, Jiang</creatorcontrib><creatorcontrib>Ma, Xiao-Long</creatorcontrib><creatorcontrib>Su, Bing</creatorcontrib><creatorcontrib>Zhou, Yu</creatorcontrib><creatorcontrib>Liu, Zeng-Shan</creatorcontrib><creatorcontrib>Ren, Hong-Lin</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Lu-Lu</au><au>Chen, Xiao-Feng</au><au>Hu, Pan</au><au>Lu, Shi-Ying</au><au>Fu, Bao-Quan</au><au>Li, Yan-Song</au><au>Zhai, Fei-Fei</au><au>Ju, Dan-Di</au><au>Zhang, Shi-Jun</au><au>Shui, Yi-Ming</au><au>Chang, Jiang</au><au>Ma, Xiao-Long</au><au>Su, Bing</au><au>Zhou, Yu</au><au>Liu, Zeng-Shan</au><au>Ren, Hong-Lin</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Host Prdx6 contributing to the intracellular survival of Brucella suis S2 strain</atitle><jtitle>BMC Veterinary Research</jtitle><date>2019-08-22</date><risdate>2019</risdate><volume>15</volume><issue>1</issue><issn>1746-6148</issn><eissn>1746-6148</eissn><abstract>Background Brucellosis is a worldwide zoonotic infectious disease that is transmitted in various ways and causes great harm to humans and animals. The brucellosis pathogen is Brucella, which mainly resides in macrophage cells and survives and replicates in host cells. However, the mechanisms underlying Brucella survival in macrophage cells have not been thoroughly elucidated to date. Peroxiredoxin 6 (Prdx6) is a bifunctional protein that shows not only GSH peroxidase activity but also phospholipase A2 activity and plays important roles in combating oxidative damage and regulating apoptosis. Results Recombinant mouse (Mus musculus) Prdx6 (MmPrdx6) was expressed and purified, and monoclonal antibodies against MmPrdx6 were prepared. Using the Brucella suis S2 strain to infect RAW264.7 murine macrophages, the level of intracellular Prdx6 expression first decreased and later increased following infection. Overexpressing Prdx6 in macrophages resulted in an increase in B. suis S2 strain levels in RAW264.7 cells, while knocking down Prdx6 reduced the S2 levels in cells. Conclusions Host Prdx6 can increase the intracellular survival of B. suis S2 strain and plays a role in Brucella infection. Keywords: Host, Prdx6, Brucella, Macrophage, Intracellular survival</abstract><pub>BioMed Central Ltd</pub><doi>10.1186/s12917-019-2049-8</doi></addata></record> |
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subjects | Antibodies Brucella Brucellosis Communicable diseases Disease transmission Gene expression Genetic aspects Health aspects House mouse Identification and classification Macrophages Monoclonal antibodies Monocytes Peroxidase Phospholipases Plasmids Zoonoses |
title | Host Prdx6 contributing to the intracellular survival of Brucella suis S2 strain |
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