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PBP2b 突变可促进缺乏多糖荚膜的噬菌体抗性的生长。

PBP2b Mutations Improve the Growth of Phage-Resistant Lacking Polysaccharide Pellicle.

机构信息

Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.

Université Paris-Saclay, INRAE, MaIAGE, Jouy-en-Josas, France.

出版信息

Appl Environ Microbiol. 2023 Jun 28;89(6):e0210322. doi: 10.1128/aem.02103-22. Epub 2023 May 24.

Abstract

Lactococcus lactis and Lactococcus cremoris are Gram-positive lactic acid bacteria widely used as starter in milk fermentations. Lactococcal cells are covered with a polysaccharide pellicle (PSP) that was previously shown to act as the receptor for numerous bacteriophages of the class. Thus, mutant strains lacking PSP are phage resistant. However, because PSP is a key cell wall component, PSP-negative mutants exhibit dramatic alterations of cell shape and severe growth defects, which limit their technological value. In the present study, we isolated spontaneous mutants with improved growth, from PSP-negative mutants. These mutants grow at rates similar to the wild-type strain, and based on transmission electron microscopy analysis, they exhibit improved cell morphology compared to their parental PSP-negative mutants. In addition, the selected mutants maintain their phage resistance. Whole-genome sequencing of several such mutants showed that they carried a mutation in , a gene encoding a penicillin-binding protein involved in peptidoglycan biosynthesis. Our results indicate that lowering or turning off PBP2b activity suppresses the requirement for PSP and ameliorates substantially bacterial fitness and morphology. Lactococcus lactis and Lactococcus cremoris are widely used in the dairy industry as a starter culture. As such, they are consistently challenged by bacteriophage infections which may result in reduced or failed milk acidification with associated economic losses. Bacteriophage infection starts with the recognition of a receptor at the cell surface, which was shown to be a cell wall polysaccharide (the polysaccharide pellicle [PSP]) for the majority of lactococcal phages. Lactococcal mutants devoid of PSP exhibit phage resistance but also reduced fitness, since their morphology and division are severely impaired. Here, we isolated spontaneous, food-grade non-PSP-producing mutants resistant to bacteriophage infection with a restored fitness. This study provides an approach to isolate non-GMO phage-resistant L. cremoris and L. lactis strains, which can be applied to strains with technological functionalities. Also, our results highlight for the first time the link between peptidoglycan and cell wall polysaccharide biosynthesis.

摘要

乳球菌(Lactococcus lactis)和乳球菌(Lactococcus cremoris)是革兰氏阳性的乳酸菌,广泛用作牛奶发酵的起始剂。乳球菌细胞表面覆盖有一层多糖荚膜(PSP),先前的研究表明,该多糖荚膜是许多噬菌体的受体。因此,缺乏 PSP 的突变株对噬菌体具有抗性。然而,由于 PSP 是细胞壁的关键成分,PSP 阴性突变株的细胞形状发生剧烈变化,生长缺陷严重,限制了其技术价值。在本研究中,我们从 PSP 阴性突变株中分离出具有生长改善特性的自发突变株。这些突变株的生长速度与野生型菌株相似,并且基于透射电子显微镜分析,与亲本 PSP 阴性突变株相比,它们的细胞形态得到了改善。此外,所选的突变株保持其对噬菌体的抗性。对几个这样的突变株进行全基因组测序显示,它们携带一个基因的突变,该基因编码参与肽聚糖生物合成的青霉素结合蛋白 2b(PBP2b)。我们的研究结果表明,降低或关闭 PBP2b 的活性可以抑制对 PSP 的需求,并大大改善细菌的适应性和形态。乳球菌(Lactococcus lactis)和乳球菌(Lactococcus cremoris)在乳制品行业中被广泛用作起始培养物。因此,它们经常受到噬菌体感染的挑战,这可能导致牛奶酸化减少或失败,从而带来经济损失。噬菌体感染始于细胞表面受体的识别,先前的研究表明,该受体是大多数乳球菌噬菌体的细胞壁多糖(多糖荚膜[PSP])。缺乏 PSP 的乳球菌突变株对噬菌体具有抗性,但适应性也降低,因为它们的形态和分裂受到严重损害。在这里,我们分离到了自发产生的、食品级的非 PSP 生产突变株,它们对噬菌体感染具有抗性,并且恢复了适应性。本研究提供了一种分离非转基因噬菌体抗性乳球菌(Lactococcus cremoris)和乳球菌(Lactococcus lactis)菌株的方法,可应用于具有技术功能的菌株。此外,我们的研究结果首次强调了肽聚糖和细胞壁多糖生物合成之间的联系。

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