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首页> 外文期刊>Microbiology >Hyaluronidase expression and biofilm involvement in Staphylococcus aureus UAMS-1 and its sarA, agr and sarA agr regulatory mutants
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Hyaluronidase expression and biofilm involvement in Staphylococcus aureus UAMS-1 and its sarA, agr and sarA agr regulatory mutants

机译:透明质酸酶表达和生物膜参与金黄色葡萄球菌UAMS-1及其sarA,agr和sarA agr调控突变体

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摘要

In a previous study, two proteins identified as hyaluronidases were detected in spent media by MS and found to be in greater quantity in the sarA and sarA agr mutant strains when compared with the parent and agr mutant strains of Staphylococcus aureus UAMS-1. In the present study, spent media and total RNA were isolated from UAMS-1 and its regulatory mutants and analysed for hyaluronidase activity and steady-state hyaluronidase (hysA) RNA message levels. Hyaluronidase activity was observed throughout all time points examined regardless of the regulatory effects of sarA and agr but activity was always substantially higher in the sarA and sarA agr mutant strains than in the UAMS-1 parent and agr mutant strains. Northern analysis did not detect hysA message for either the UAMS-1 parent or the agr mutant strains at any time point examined, while steady-state hysA message levels were detected throughout growth for the sarA mutant strain, but only at exponential and early post-exponential growth for the sarA agr mutant strain. An in vitro biofilm plate assay, pre-coated with human plasma as a source of hyaluronic acid, demonstrated no significant increase in biofilm for a sarA mutant strain of S. aureus UAMS-1 defective in hyaluronidase activity when compared with the sarA mutant strain. These data indicate that, while hysA message levels and hyaluronidase activity are elevated in the sarA mutant strains of S. aureus UAMS-1, the increase in activity did not contribute to the biofilm-negative phenotype observed in the sarA mutant strain of S. aureus UAMS-1.
机译:在先前的研究中,通过质谱在废培养基中检测到两种被鉴定为透明质酸酶的蛋白质,与金黄色葡萄球菌UAMS-1的亲本和agr突变株相比,在sarA和sarA agr突变株中含量更高。在本研究中,从UAMS-1及其调节突变体中分离了用过的培养基和总RNA,并分析了透明质酸酶活性和稳态透明质酸酶(hysA)RNA信息水平。不论sarA和agr的调节作用如何,在所有检查的时间点均观察到透明质酸酶活性,但sarA和sarA agr突变株的活性始终比UAMS-1亲本和agr突变株的活性高得多。 Northern分析在任何检查的时间点均未检测到UAMS-1亲本或agr突变株的hysA信息,而在整个sarA突变株的整个生长过程中均检测到稳态的hysA信息水平,但仅在指数和早期sarA agr突变株的指数生长。预先涂有人血浆作为透明质酸来源的体外生物膜平板测定表明,与sarA突变株相比,透明质酸酶活性缺陷的金黄色葡萄球菌UAMS-1的sarA突变株的生物膜没有明显增加。这些数据表明,虽然在金黄色葡萄球菌UAMS-1的sarA突变株中hysA信息水平和透明质酸酶活性升高,但活性的增加并没有促进在金黄色葡萄球菌sarA突变株中观察到的生物膜阴性表型。 UAMS-1。

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