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本文引用的文献

1
Crucial role for membrane fluidity in proliferation of primitive cells.膜流动性在原始细胞增殖中的关键作用。
Cell Rep. 2012 May 31;1(5):417-23. doi: 10.1016/j.celrep.2012.03.008. Epub 2012 Apr 26.
2
Daptomycin-mediated reorganization of membrane architecture causes mislocalization of essential cell division proteins.达托霉素介导的膜结构重排导致必需的细胞分裂蛋白定位错误。
J Bacteriol. 2012 Sep;194(17):4494-504. doi: 10.1128/JB.00011-12. Epub 2012 Jun 1.
3
Interaction of type A lantibiotics with undecaprenol-bound cell envelope precursors.A型类细菌素与十一异戊烯基磷酸聚糖结合的细胞包膜前体的相互作用。
Microb Drug Resist. 2012 Jun;18(3):261-70. doi: 10.1089/mdr.2011.0242. Epub 2012 Mar 20.
4
The rod to L-form transition of Bacillus subtilis is limited by a requirement for the protoplast to escape from the cell wall sacculus.枯草芽孢杆菌从杆状到 L 型的转变受到质壁分离这一要求的限制。
Mol Microbiol. 2012 Jan;83(1):52-66. doi: 10.1111/j.1365-2958.2011.07920.x. Epub 2011 Nov 29.
5
The Bacillus subtilis GntR family repressor YtrA responds to cell wall antibiotics.枯草芽孢杆菌 GntR 家族阻遏蛋白 YtrA 响应细胞壁抗生素。
J Bacteriol. 2011 Oct;193(20):5793-801. doi: 10.1128/JB.05862-11. Epub 2011 Aug 19.
6
Reduction in membrane phosphatidylglycerol content leads to daptomycin resistance in Bacillus subtilis.细胞膜磷脂酰甘油含量的降低导致枯草芽孢杆菌对达托霉素产生耐药性。
Antimicrob Agents Chemother. 2011 Sep;55(9):4326-37. doi: 10.1128/AAC.01819-10. Epub 2011 Jun 27.
7
Antimicrobial peptide sensing and detoxification modules: unravelling the regulatory circuitry of Staphylococcus aureus.抗菌肽感应和解毒模块:揭示金黄色葡萄球菌的调控回路。
Mol Microbiol. 2011 Aug;81(3):581-7. doi: 10.1111/j.1365-2958.2011.07747.x. Epub 2011 Jul 12.
8
Bacitracin and nisin resistance in Staphylococcus aureus: a novel pathway involving the BraS/BraR two-component system (SA2417/SA2418) and both the BraD/BraE and VraD/VraE ABC transporters.金黄色葡萄球菌中杆菌肽和乳链菌肽抗性:涉及 BraS/BraR 双组分系统(SA2417/SA2418)和 BraD/BraE 及 VraD/VraE ABC 转运体的新途径。
Mol Microbiol. 2011 Aug;81(3):602-22. doi: 10.1111/j.1365-2958.2011.07735.x. Epub 2011 Jul 4.
9
A recombinant antimicrobial peptide inhibits the growth of oxacillin-induced L-forms of Staphylococcus aureus.一种重组抗菌肽可抑制苯唑西林诱导的金黄色葡萄球菌L型的生长。
Int J Antimicrob Agents. 2011 Aug;38(2):177-8. doi: 10.1016/j.ijantimicag.2011.02.015. Epub 2011 Jun 14.
10
Coevolution of ABC transporters and two-component regulatory systems as resistance modules against antimicrobial peptides in Firmicutes Bacteria.ABC 转运蛋白与双组分调控系统在厚壁菌中对抗抗菌肽的共同进化:耐药模块。
J Bacteriol. 2011 Aug;193(15):3851-62. doi: 10.1128/JB.05175-11. Epub 2011 Jun 10.

枯草芽孢杆菌细胞壁缺陷型 L 形式中的细胞包膜应激反应。

Cell envelope stress response in cell wall-deficient L-forms of Bacillus subtilis.

机构信息

Department Biology I, Ludwig-Maximilians-University Munich, Germany.

出版信息

Antimicrob Agents Chemother. 2012 Nov;56(11):5907-15. doi: 10.1128/AAC.00770-12. Epub 2012 Sep 10.

DOI:10.1128/AAC.00770-12
PMID:22964256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3486569/
Abstract

L-forms are cell wall-deficient bacteria that can grow and proliferate in osmotically stabilizing media. Recently, a strain of the Gram-positive model bacterium Bacillus subtilis was constructed that allowed controlled switching between rod-shaped wild-type cells and corresponding L-forms. Both states can be stably maintained under suitable culture conditions. Because of the absence of a cell wall, L-forms are known to be insensitive to β-lactam antibiotics, but reports on the susceptibility of L-forms to other antibiotics that interfere with membrane-anchored steps of cell wall biosynthesis are sparse, conflicting, and strongly influenced by strain background and method of L-form generation. Here we investigated the response of B. subtilis to the presence of cell envelope antibiotics, with regard to both antibiotic resistance and the induction of the known LiaRS- and BceRS-dependent cell envelope stress biosensors. Our results show that B. subtilis L-forms are resistant to antibiotics that interfere with the bactoprenol cycle, such as bacitracin, vancomycin, and mersacidin, but are hypersensitive to nisin and daptomycin, which both affect membrane integrity. Moreover, we established a lacZ-based reporter gene assay for L-forms and provide evidence that LiaRS senses its inducers indirectly (damage sensing), while the Bce module detects its inducers directly (drug sensing).

摘要

L 型是细胞壁缺陷细菌,可在渗透稳定的培养基中生长和增殖。最近,构建了一种革兰氏阳性模式细菌枯草芽孢杆菌的菌株,该菌株允许在杆状野生型细胞和相应的 L 型之间进行受控切换。在合适的培养条件下,两种状态都可以稳定维持。由于缺乏细胞壁,L 型已知对β-内酰胺类抗生素不敏感,但有关其他抗生素对 L 型的敏感性的报道却很少,并且相互矛盾,并且受到菌株背景和 L 型生成方法的强烈影响。在这里,我们研究了枯草芽孢杆菌对细胞壁抗生素存在的反应,包括抗生素抗性和已知 LiaRS 和 BceRS 依赖性细胞壁应激生物传感器的诱导。我们的结果表明,枯草芽孢杆菌 L 型对干扰巴卡丁醇循环的抗生素(如杆菌肽、万古霉素和麦尔西菌素)具有抗性,但对影响膜完整性的尼生素和达托霉素高度敏感。此外,我们建立了一种基于 lacZ 的报告基因测定法来检测 L 型,并提供证据表明 LiaRS 间接感应其诱导物(损伤感应),而 Bce 模块则直接检测其诱导物(药物感应)。