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10.1186/s40635-014-0021-2 http://scihub22266oqcxt.onion/10.1186/s40635-014-0021-2 C4678137!4678137 !26215706     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26215706 &cmd=llinks): Failed to open stream: HTTP request failed! 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Neutrophil extracellular traps in the host defense against sepsis induced by Burkholderia pseudomallei (melioidosis) |pdf=|usr=}}{{26215706 }} gab.com Text Neutrophil extracellular traps in the host defense against sepsis induced by Burkholderia pseudomallei (melioidosis) JO: Intensive Care Med Exp http://www.kidney.de/pget.php?&tw=1&pmid=26215706 #FOAvip BACKGROUND: Neutrophil extracellular traps (NETs) are a central player in the host response to bacteria: neutrophils release extracellular DNA (nucleosomes) and neutrophil elastase to entrap and kill bacteria. We studied the role of NETs in Burkholderia pseudomallei infection (melioidosis), an important cause of Gram-negative sepsis in Southeast Asia. METHODS: In a prospective observational study, circulating nucleosomes and neutrophil elastase were assayed in 44 patients with Gram-negative sepsis caused by B. pseudomallei (melioidosis) and 82 controls. Functional assays included human neutrophil stimulation and killing assays and a murine model of B. pseudomallei infection in which NET function was compromised using DNase. Specified pathogen-free 8- to 12-week-old C57BL/6 mice were sacrificed post-infection to assess bacterial loads, inflammation, and pathology. RESULTS: Nucleosome and neutrophil elastase levels were markedly elevated in patients compared to controls. NETs killed B. pseudomallei effectively, and neutrophils stimulated with B. pseudomallei showed increased elastase and DNA release in a time- and dose-dependent matter. In mice, NET disruption with intravenous DNase administration resulted in decreased nucleosome levels. Although DNase treatment of mice resulted in diminished liver inflammation, no differences were observed in bacterial dissemination or systemic inflammation. CONCLUSION: B. pseudomallei is a potent inducer of NETosis which was reflected by greatly increased levels of NET-related components in melioidosis patients. Although NETs exhibited antibacterial activity against B. pseudomallei, NET formation did not protect against bacterial dissemination and inflammation during B. pseudomallei-induced sepsis. Twit Text FOAVip Neutrophil extracellular traps in the host defense against sepsis induced by Burkholderia pseudomallei (melioidosis) ????Intensive Care Med Exp http://www.kidney.de/pget.php?&tw=1&pmid=26215706 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26215706 #FOAvip English Wikipedia <ref>{{Cite pmid|26215706 }}</ref> Neutrophil extracellular traps in the host defense against sepsis induced by Burkholderia pseudomallei (melioidosis) #MMPMID26215706 de Jong HK ; Koh GC ; Achouiti A ; van der Meer AJ ; Bulder I ; Stephan F ; Roelofs JJ ; Day NP ; Peacock SJ ; Zeerleder S ; Wiersinga WJ Intensive Care Med Exp 2014[Dec]; 2 (1 ): 21 PMID26215706 show ga BACKGROUND: Neutrophil extracellular traps (NETs) are a central player in the host response to bacteria: neutrophils release extracellular DNA (nucleosomes) and neutrophil elastase to entrap and kill bacteria. We studied the role of NETs in Burkholderia pseudomallei infection (melioidosis), an important cause of Gram-negative sepsis in Southeast Asia. METHODS: In a prospective observational study, circulating nucleosomes and neutrophil elastase were assayed in 44 patients with Gram-negative sepsis caused by B. pseudomallei (melioidosis) and 82 controls. Functional assays included human neutrophil stimulation and killing assays and a murine model of B. pseudomallei infection in which NET function was compromised using DNase. Specified pathogen-free 8- to 12-week-old C57BL/6 mice were sacrificed post-infection to assess bacterial loads, inflammation, and pathology. RESULTS: Nucleosome and neutrophil elastase levels were markedly elevated in patients compared to controls. NETs killed B. pseudomallei effectively, and neutrophils stimulated with B. pseudomallei showed increased elastase and DNA release in a time- and dose-dependent matter. In mice, NET disruption with intravenous DNase administration resulted in decreased nucleosome levels. Although DNase treatment of mice resulted in diminished liver inflammation, no differences were observed in bacterial dissemination or systemic inflammation. CONCLUSION: B. pseudomallei is a potent inducer of NETosis which was reflected by greatly increased levels of NET-related components in melioidosis patients. Although NETs exhibited antibacterial activity against B. pseudomallei, NET formation did not protect against bacterial dissemination and inflammation during B. pseudomallei-induced sepsis. äNeutrophil extracellular traps in the host defense against sepsis indu(epmc).pdf DeepDyve Pubget Overpricing