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Biofilm formation by group A Streptococcus: a role for the streptococcal regulator of virulence (Srv) and streptococcal cysteine protease (SpeB)

机译:Biofilm组由链球菌组形成:毒力(SRV)和链球菌半胱氨酸蛋白酶(SPEB)的中风调节剂的作用

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Recently, biofilms have become a topic of interest in the study of the human pathogen group A Streptococcus (GAS). In this study, we sought to learn more about the make-up of these structures and gain insight into biofilm regulation. Enzymic studies indicated that biofilm formation by GAS strain MGAS5005 required an extracellular protein and DNA component(s). Previous results indicated that inactivation of the transcriptional regulator Srv in MGAS5005 resulted in a significant decrease in virulence. Here, inactivation of Srv also resulted in a significant decrease in biofilm formation under both static and flow conditions. Given that production of the extracellular cysteine protease SpeB is increased in the srv mutant, we tested the hypothesis that increased levels of active SpeB may be responsible for the reduction in biofilm formation. Western immunoblot analysis indicated that SpeB was absent from MGAS5005 biofilms. Complementation of MGAS5005Δsrv restored the biofilm phenotype and eliminated the overproduction of active SpeB. Inhibition of SpeB with E64 also restored the MGAS5005Δsrv biofilm to wild-type levels.
机译:最近,生物膜已成为对人病原菌群的研究感兴趣的话题(气体)。在这项研究中,我们试图了解更多有关这些结构的化妆,并进入生物膜监管的洞察力。酶学研究表明,气体菌株Mgas5005的生物膜形成需要细胞外蛋白和DNA组分。以前的结果表明,MGAS5005中转录调节器SRV的失活导致毒力显着降低。这里,在静态和流动条件下,SRV的失活也导致生物膜形成显着降低。鉴于细胞外半胱氨酸蛋白酶SPEB的产生在SRV突变体中增加,我们测试了升高的活性SPEB水平可能对生物膜形成的降低负责的假设。 Western免疫斑分析表明SPEB不存在Mgas5005生物膜。 MGAS5005ΔSRV的互补恢复生物膜表型并消除了活性SPEB的过量生产。用E64的SPEB的抑制还将MGAS5005ΔSRV生物膜恢复到野生型水平。

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