| Literature DB >> 28177794 |
Ling Guo1, Lei Xu1, Tao Wu1, Shulin Fu1, Yinsheng Qiu1, Chien-An Andy Hu1,2, Xinglong Ren3, Rongrong Liu4, Mengdie Ye4.
Abstract
Haemophilus parasuis can cause a severe membrane inflammation disorder. It has been documented that superoxide dismutase (SOD) is a potential target to treat systemic inflammatory diseases. Therefore, we constructed an experimental H. parasuis subunit vaccine SOD and determined the protective efficacy of SOD using a lethal dose challenge against H. parasuis serovar 4 strain MD0322 and serovar 5 strain SH0165 in a mouse model. The results demonstrated that SOD could induce a strong humoral immune response in mice and provide significant immunoprotection efficacy against a lethal dose of H. parasuis serovar 4 strain MD0322 or serovar 5 strain SH0165 challenge. IgG subtype analysis indicated SOD protein could trigger a bias toward a Th1-type immune response and induce the proliferation of splenocytes and secretion of IL-2 and IFN-γ of splenocytes. In addition, serum in mice from the SOD-immunized group could inhibit the growth of strain MD0322 and strain SH0165 in the whole-blood killing bacteria assay. This is the first report that immunization of mice with SOD protein could provide protective effect against a lethal dose of H. parasuis serovar 4 and serovar 5 challenge in mice, which may provide a novel approach against heterogeneous serovar infection of H. parasuis in future.Entities:
Keywords: Glässer’s disease; Haemophilus parasuis; maladie de Glässer; superoxide dismutase; superoxyde dismutase; vaccin; vaccine
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Year: 2016 PMID: 28177794 DOI: 10.1139/cjm-2016-0671
Source DB: PubMed Journal: Can J Microbiol ISSN: 0008-4166 Impact factor: 2.419