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首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Homologous role of CovRS two-component regulatory system in NAD(+)-glycohydrolase activity in Streptococcus dysgalactiae subsp. equisimilis as in Streptococcus pyogenes
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Homologous role of CovRS two-component regulatory system in NAD(+)-glycohydrolase activity in Streptococcus dysgalactiae subsp. equisimilis as in Streptococcus pyogenes

机译:CoVR双组分调节系统在链球菌患者中NAD(+) - 甘油糖酶活性中的同源作用。 等于链球菌Pyogenes

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摘要

Streptococcal toxic shock syndrome (STSS) is primarily caused by Streptococcus pyogenes, but it may also be caused by Streptococcus dysgalactiae subsp. equisimilis (SDSE). The analyses of S.pyogenes have revealed the important roles of NAD(+)-glycohydrolase (Nga) and CovR/CovS, a two-component regulatory system. We examined these factors in SDSE by analyzing mainly two isogenic SDSE strains (12-10-1 and 12-10-3) from the blood of a patient with STSS. The Nga activities were measured and the nucleotide sequences of covR and covS genes were determined. We detected one nucleotide difference between the covR gene of 12-10-1 and that of 12-10-3, and the Nga activity of 12-10-1 was approximately 6.8-fold more than that of 12-10-3. The introduction of covR of 12-10-3 into 12-10-1 significantly reduced the Nga activity, but the introduction of 12-10-1 covR into itself had only a little effect. In addition, the knockout of covR or covS of 12-10-3 remarkably increased the Nga activity. We are the first to report that strains with wild-type and mutated covR were isolated simultaneously from an SDSE STSS patient and that the CovR/CovS two-component regulatory system is involved in the Nga activity in SDSE as well as in S.pyogenes.
机译:链球菌毒性休克综合征(STSS)主要是由嗜盐剂引起的,但它也可能是由链球菌患者引起的。 Equisimilis(SDSE)。 S.pyogenes的分析揭示了NAD(+) - 甘油糖酶(NGA)和CoVR / COV,双组分调节系统的重要作用。我们通过用STSS的患者的血液分析,在SDSE中检查了这些因素。测量NGA活性,测定CoVR和COVS基因的核苷酸序列。我们检测到12-10-1的CoVR基因之间的一种核苷酸差异,即12-10-3,NGA活性为12-10-1的活性比12-10-3的12-10-1的活性约为6.8倍。将12-10-3的COVR引入12-10-1显着降低了NGA活性,但引入12-10-1 CoVR进入本身只有一点效果。此外,12-10-3的CoVR或CoV的敲除显着增加了NGA活性。我们是第一个报告野生型和突变的CoVR的菌株从SDSE STSS患者同时分离,并且CoVR / CoVs双组分调节系统参与SDSE中的NGA活性以及S.Pyogenes。

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