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鉴定四氢嗜热球菌噬菌体敏感性相关荚膜多糖合成基因座。

Identification of Capsular Polysaccharide Synthesis Loci Determining Bacteriophage Susceptibility in Tetragenococcus halophilus.

机构信息

Manufacturing Division, Yamasa Corporation, Choshi, Japan.

NODAI Genome Research Center, Tokyo University of Agriculture, Tokyo, Japan.

出版信息

Microbiol Spectr. 2023 Jun 15;11(3):e0038523. doi: 10.1128/spectrum.00385-23. Epub 2023 May 8.

Abstract

Bacteriophages infecting Tetragenococcus halophilus, a halophilic lactic acid bacterium, have been a major industrial concern due to their detrimental effects on the quality of food products. Previously characterized tetragenococcal phages displayed narrow host ranges, but there is little information on these mechanisms. Here, we revealed the host's determinant factors for phage susceptibility using two virulent phages, phiYA5_2 and phiYG2_4, that infect T. halophilus YA5 and YG2, respectively. Phage-resistant derivatives were obtained from these host strains, and mutations were found at the capsular polysaccharide (CPS) synthesis () loci. Quantification analysis verified that capsular polysaccharide production by the derivatives from YG2 was impaired. Transmission electron microscopy observation confirmed the presence of filamentous structures outside the cell walls of YG2 and their absence in the derivatives of YG2. Phage adsorption assays revealed that phiYG2_4 adsorbed to YG2 but not its derivatives, which suggests that the capsular polysaccharide of YG2 is the specific receptor for phiYG2_4. Interestingly, phiYA5_2 adsorbed and infected derivatives of YG2, although neither adsorption to nor infection of the parental strain YG2 by phiYA5_2 was observed. The plaque-surrounding halos formed by phiYA5_2 implied the presence of the virion-associated depolymerase that degrades the capsular polysaccharide of YA5. These results indicated that the capsular polysaccharide is a physical barrier rather than a binding receptor for phiYA5_2 and that phiYA5_2 specifically overcomes the capsular polysaccharide of YA5. Thus, it is suggested that tetragenococcal phages utilize CPSs as binding receptors and/or degrade CPSs to approach host cells. is a halophilic lactic acid bacterium that contributes to the fermentation processes for various salted foods. Bacteriophage infections of . have been a major industrial problem causing fermentation failures. Here, we identified the loci in . as genetic determinants of phage susceptibility. The structural diversity of the capsular polysaccharide is responsible for the narrow host ranges of tetragenococcal phages. The information provided here could facilitate future studies on tetragenococcal phages and the development of efficient methods to prevent bacteriophage infections.

摘要

噬菌体能感染海栖热袍菌,这种嗜盐乳酸菌是一种主要的工业关注对象,因为它们会对食品的质量产生不利影响。以前所描述的四球菌噬菌体显示出狭窄的宿主范围,但关于这些机制的信息很少。在这里,我们使用两种烈性噬菌体 phiYA5_2 和 phiYG2_4 来揭示噬菌体敏感性的宿主决定因素,这两种噬菌体分别感染 Tetragenococcus halophilus YA5 和 YG2。从这些宿主菌株中获得了抗噬菌体的衍生物,并在荚膜多糖(CPS)合成()基因座中发现了突变。定量分析证实,来自 YG2 的 衍生物的荚膜多糖产生受损。透射电子显微镜观察证实了细胞壁外存在丝状结构,而在 YG2 的 衍生物中不存在。噬菌体吸附实验表明,phiYG2_4 吸附到 YG2 但不吸附其 衍生物,这表明 YG2 的荚膜多糖是 phiYG2_4 的特异性受体。有趣的是,phiYA5_2 吸附并感染了 YG2 的 衍生物,尽管未观察到 phiYA5_2 对亲本菌株 YG2 的吸附和感染。phiYA5_2 形成的噬菌斑周围晕圈表明存在与病毒相关的解聚酶,该酶降解 YA5 的荚膜多糖。这些结果表明,荚膜多糖是 phiYA5_2 的物理屏障而不是结合受体,并且 phiYA5_2 特异性克服了 YA5 的荚膜多糖。因此,建议四球菌噬菌体利用 CPS 作为结合受体和/或降解 CPS 以接近宿主细胞。 是一种嗜盐乳酸菌,它参与各种腌制食品的发酵过程。噬菌体能感染. 一直是导致发酵失败的主要工业问题。在这里,我们确定了. 中的 位点是噬菌体敏感性的遗传决定因素。荚膜多糖的结构多样性是四球菌噬菌体宿主范围狭窄的原因。这里提供的信息可以促进未来对四球菌噬菌体的研究和开发有效预防噬菌体感染的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8012/10269466/d2b821c771d6/spectrum.00385-23-f001.jpg

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