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首页> 外文期刊>Virulence. >Marginal role of von Willebrand factor-binding protein and coagulase in the initiation of endocarditis in rats with catheter-induced aortic vegetations
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Marginal role of von Willebrand factor-binding protein and coagulase in the initiation of endocarditis in rats with catheter-induced aortic vegetations

机译:血管性血友病因子结合蛋白和凝血酶在导管诱发的主动脉植被大鼠心内膜炎发作中的边际作用

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Staphylococcus aureus is the leading cause of infective endocarditis (IE). While the role of S. aureus cell-wall associated protein clumping factor A (ClfA) in promoting IE has been already demonstrated, that of the secreted plasma-clotting factors staphylocoagulase (Coa) and von Willebrand factor-binding protein (vWbp) has not yet been elucidated. We investigated the role of Coa and vWbp in IE initiation in rats with catheter-induced aortic vegetations, using Lactococcus lactis expressing coa, vWbp, clfA or vWbp/clfA, and S. aureus Newman Δcoa, ΔvWbp, ΔclfA or Δcoa/ΔvWbp/ΔclfA mutants. vWbp-expression increased L. lactis valve infection compared to parent and coa-expressing strains (incidence: 62%, versus 0% and 13%, respectively; P??0.05 versus ΔclfA mutant). Coa does not support the initial colonization of IE (in L. lactis) without other key virulence factors and vWbp contributes to initiation of IE (in L. lactis) but is marginal in the present of ClfA.
机译:金黄色葡萄球菌是感染性心内膜炎(IE)的主要原因。尽管已经证明了金黄色葡萄球菌细胞壁相关蛋白聚集因子A(ClfA)在促进IE中的作用,但尚未发现分泌的血浆凝结因子葡萄球菌凝固酶(Coa)和冯·威兰布兰德因子结合蛋白(vWbp)尚未阐明。我们使用表达乳木球菌Coa,vWbp,clfA或vWbp / clfA和金黄色葡萄球菌NewmanΔcoa,ΔvWbp,ΔclfA或Δcoa/ΔvWbp/ΔclfA的乳酸乳球菌研究了Coa和vWbp在导管诱发的主动脉植被大鼠的IE启动中的作用。突变体。与亲本和coa表达菌株相比,vWbp表达增加了乳酸乳球菌感染(发生率:分别为62%,0%和13%;PΔ0.05与ΔclfA突变体相比)。没有其他关键毒力因子时,Coa不支持IE(在乳酸乳球菌)中的最初定植,而vWbp有助于IE(在乳酸乳球菌中)的启动,但在ClfA的存在中是微不足道的。

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