马红球菌毒力相关蛋白促毒功能的共性

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Timothy R. Ganderton, Daniel Ghete, Karen Hogg, Graeme J. Park, Christoph G. Baumann, Anthony J. Wilkinson, Paul R. Pryor
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引用次数: 0

摘要

马红球菌是一种革兰氏阳性兼性细胞内病原体,与马驹危及生命的支气管肺炎有关。马鼠在宿主巨噬细胞内存活的关键是毒力相关蛋白(Vaps)的产生。在不同物种分离的毒力质粒上发现了许多vap基因,并且这些vap具有高度的序列同一性。VapA已被广泛研究,尽管来自其他马鼠毒质粒的vapK和vapN基因已被证明对马鼠细胞内存活至关重要,但它们的作用方式却不太明确。因此,我们研究了VapK和VapN是否以与VapA相同的机制起作用。事实上,与VapA一样,VapK和VapN也能中和溶酶体pH值并降低溶酶体水解酶活性。VapK或VapN的存在均可恢复失去的VapA和相等致病性。用VapB也观察到较低程度的酸中和活性。这些促毒Vaps具有不同的活性,其中最具“酸中和”活性的是VapN,然后是VapA和K,最后是VapB。这些数据表明,经常在马感染中发现的VapA的产生可以被VapK和B(由经常在猪物种中发现的质粒产生)或VapN(由经常在牛和人样本中分离的质粒产生)所取代。这些数据表明,VapA用于中和溶酶体酸度的分子机制也应该在VapN和K中看到,这将有助于指导研究人员确定其精确的作用模式,并有助于未来靶向治疗的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Commonality of Virulence-Promoting Function in Rhodococcus equi Virulence Associated Proteins (Vaps)
Rhodococcus equi is a Gram-positive facultative intracellular pathogen associated with life-threatening bronchopneumonial disease in foals. Key to R. equi’s intracellular survival in host macrophages is the production of virulence associated proteins (Vaps). Numerous vap genes are found on virulence plasmids isolated from different species, and the Vaps share a high degree of sequence identity. VapA has been extensively studied, and although vapK and vapN genes from other R. equi virulence plasmids have been shown to be essential for R. equi intracellular survival, their mode of action is less characterised. We, therefore, examined whether VapK and VapN worked mechanistically in the same way as VapA. Indeed, like VapA, VapK and VapN neutralised lysosomal pH and reduced lysosomal hydrolase activity. A loss of VapA and R. equi virulence could be regained by the presence of either VapK or VapN. The acid-neutralisation activity was also observed to a lesser extent with VapB. There was a differential activity across these virulence-promoting Vaps with the most “acid-neutralising” activity found with VapN, then VapA and K, and finally VapB. These data suggest that VapA production, which is often found in equine infections, can be substituted by VapK and B (produced by plasmids often found in porcine species) or VapN (produced by plasmids often isolated in bovine and human samples). These data imply that the molecular mechanism(s) that VapA uses to neutralise lysosomal acidity should also be seen in VapN and K which will help guide researchers in identifying their precise mode of action and aid the future development of targeted therapeutics.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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