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肺炎链球菌 cpoA 突变体中脂质组成的改变。

Altered lipid composition in Streptococcus pneumoniae cpoA mutants.

机构信息

Department of Microbiology, University of Kaiserslautern, Gottlieb-Daimler-Strasse, Gebäude 23, D-67663 Kaiserslautern, Germany.

出版信息

BMC Microbiol. 2014 Jan 20;14:12. doi: 10.1186/1471-2180-14-12.

Abstract

BACKGROUND

Penicillin-resistance in Streptococcus pneumoniae is mainly due to alterations in genes encoding the target enzymes for beta-lactams, the penicillin-binding proteins (PBPs). However, non-PBP genes are altered in beta-lactam-resistant laboratory mutants and confer decreased susceptibility to beta-lactam antibiotics. Two piperacillin resistant laboratory mutants of Streptococcus pneumoniae R6 contain mutations in the putative glycosyltransferase gene cpoA. The CpoA gene is part of an operon including another putative glycosyltransferase gene spr0982, both of which being homologous to glycolipid synthases present in other Gram-positive bacteria.

RESULTS

We now show that the cpoA mutants as well as a cpoA deletion mutant are defective in the synthesis of galactosyl-glucosyl-diacylglycerol (GalGlcDAG) in vivo consistent with the in vitro function of CpoA as α-GalGlcDAG synthase as shown previously. In addition, the proportion of phosphatidylglycerol increased relative to cardiolipin in cpoA mutants. Moreover, cpoA mutants are more susceptible to acidic stress, have an increased requirement for Mg(2+) at low pH, reveal a higher resistance to lysis inducing conditions and are hypersensitive to bacitracin.

CONCLUSIONS

The data show that deficiency of the major glycolipid GalGlcDAG causes a pleitotropic phenotype of cpoA mutant cells consistent with severe membrane alterations. We suggest that the cpoA mutations selected with piperacillin are directed against the lytic response induced by the beta-lactam antibiotic.

摘要

背景

肺炎链球菌对青霉素的耐药性主要是由于编码青霉素结合蛋白(PBPs)等β-内酰胺类靶酶的基因发生改变所致。然而,β-内酰胺类耐药的实验室突变株中非 PBP 基因也发生了改变,导致对β-内酰胺类抗生素的敏感性降低。肺炎链球菌 R6 的两种哌拉西林耐药的实验室突变株含有假定糖基转移酶基因 cpoA 的突变。CpoA 基因是一个操纵子的一部分,该操纵子还包括另一个假定的糖基转移酶基因 spr0982,它们都与其他革兰氏阳性菌中的糖脂合成酶同源。

结果

我们现在表明,cpoA 突变体以及 cpoA 缺失突变体在体内合成半乳糖基-葡萄糖基-二酰基甘油(GalGlcDAG)方面存在缺陷,这与先前显示的 CpoA 作为α-GalGlcDAG 合酶的体外功能一致。此外,cpoA 突变体中磷脂酰甘油与心磷脂的比例相对于野生型增加。此外,cpoA 突变体对酸性应激更敏感,在低 pH 值时对 Mg2+的需求增加,对诱导裂解的条件具有更高的抗性,并且对杆菌肽更敏感。

结论

这些数据表明,主要糖脂 GalGlcDAG 的缺乏导致 cpoA 突变体细胞的多效表型,与严重的膜改变一致。我们认为,哌拉西林选择的 cpoA 突变是针对β-内酰胺类抗生素诱导的裂解反应的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62bf/3901891/ec954bd9d39a/1471-2180-14-12-1.jpg

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