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肠炎沙门氏菌鼠伤寒血清型中可溶性溶菌转糖基酶失活导致对美西林产生高水平耐药性。

High-level resistance to mecillinam produced by inactivation of soluble lytic transglycosylase in Salmonella enterica serovar Typhimurium.

作者信息

Costa Cristina S, Antón Dora N

机构信息

Departamento de Radiobiología, Comisión Nacional de Energía Atómica, San Martín, Argentina.

出版信息

FEMS Microbiol Lett. 2006 Mar;256(2):311-7. doi: 10.1111/j.1574-6968.2006.00133.x.

Abstract

By screening for high-level mecillinam resistant derivatives of a low-level resistant strain (cysB403 galE1922 relA21::Tn10) of Salmonella enterica serovar Typhimurium, a MudJ insertion in the gene for soluble lytic transglycosylase (slt) was isolated. This insertion (slt-1::MudJ) increased the resistance to mecillinam of cysB and cysE strains (MIC: about 20-40 microg mL(-1)) to a strikingly high level (MIC: 160 microg mL(-1)). As in Escherichia coli K-12, the slt mutation slightly increased the sensitivity of the wild type and of several strains that carried mutations that did not increase mecillinam resistance. All the strains acquired a spherical cell shape when treated with mecillinam. The effect of slt-1::MudJ was limited to mecillinam, the response to several other antibiotics remaining unaltered by the insertion. The results presented in this paper demonstrate that soluble lytic transglycosylase performs an important role in the response to mecillinam, which only becomes evident when failure of CysB/CysE function causes medium-level resistance. The results also suggest that soluble lytic transglycosylase interacts with, and is partially inhibited by normal lipopolysaccharide.

摘要

通过筛选鼠伤寒沙门氏菌低水平耐药菌株(cysB403 galE1922 relA21::Tn10)的高水平美西林耐药衍生物,分离出了可溶性溶菌转糖基酶(slt)基因中的一个MudJ插入突变。该插入突变(slt-1::MudJ)使cysB和cysE菌株对美西林的耐药性(MIC:约20 - 40μg mL(-1))显著提高到高水平(MIC:160μg mL(-1))。与大肠杆菌K-12一样,slt突变使野生型以及一些携带未增加美西林耐药性突变的菌株的敏感性略有增加。用美西林处理时,所有菌株均呈现球形细胞形态。slt-1::MudJ的作用仅限于美西林,插入突变对其他几种抗生素的反应没有改变。本文给出的结果表明,可溶性溶菌转糖基酶在对美西林的反应中起重要作用,只有当CysB/CysE功能失效导致中等水平耐药时这一作用才变得明显。结果还表明,可溶性溶菌转糖基酶与正常脂多糖相互作用并部分受其抑制。

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