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通过转座子和单基因缺失筛选鉴定影响沙门氏菌噬菌体 P22 感染进展的基因。

Genes affecting progression of bacteriophage P22 infection in Salmonella identified by transposon and single gene deletion screens.

机构信息

Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824, USA.

Department of Microbiology and Molecular Genetics, University of California, School of Medicine, Irvine, California 92697, USA.

出版信息

Mol Microbiol. 2018 May;108(3):288-305. doi: 10.1111/mmi.13936. Epub 2018 Mar 30.

Abstract

Bacteriophages rely on their hosts for replication, and many host genes critically determine either viral progeny production or host success via phage resistance. A random insertion transposon library of 240,000 mutants in Salmonella enterica serovar Typhimurium was used to monitor effects of individual bacterial gene disruptions on bacteriophage P22 lytic infection. These experiments revealed candidate host genes that alter the timing of phage P22 propagation. Using a False Discovery Rate of < 0.1, mutations in 235 host genes either blocked or delayed progression of P22 lytic infection, including many genes for which this role was previously unknown. Mutations in 77 genes reduced the survival time of host DNA after infection, including mutations in genes for enterobacterial common antigen (ECA) synthesis and osmoregulated periplasmic glucan (OPG). We also screened over 2000 Salmonella single gene deletion mutants to identify genes that impacted either plaque formation or culture growth rates. The gene encoding the periplasmic membrane protein YajC was newly found to be essential for P22 infection. Targeted mutagenesis of yajC shows that an essentially full-length protein is required for function, and potassium efflux measurements demonstrated that YajC is critical for phage DNA ejection across the cytoplasmic membrane.

摘要

噬菌体依赖宿主进行复制,许多宿主基因通过噬菌体抗性对病毒产物的产生或宿主的成功起着关键作用。使用沙门氏菌肠炎亚种 240,000 个突变体的随机插入转座子文库来监测单个细菌基因缺失对噬菌体 P22 裂解感染的影响。这些实验揭示了改变噬菌体 P22 繁殖时间的候选宿主基因。使用错误发现率 < 0.1,235 个宿主基因的突变要么阻断要么延迟 P22 裂解感染的进展,其中包括许多以前未知的具有这种作用的基因。77 个基因的突变减少了感染后宿主 DNA 的存活时间,包括参与肠杆菌共同抗原 (ECA) 合成和渗透压调节周质聚糖 (OPG) 的基因的突变。我们还筛选了 2000 多个沙门氏菌单基因缺失突变体,以确定影响菌斑形成或培养物生长速率的基因。发现编码周质膜蛋白 YajC 的基因对 P22 感染是必需的。yajC 的靶向诱变表明,功能需要基本上全长的蛋白质,钾流出测量表明 YajC 对于噬菌体 DNA 穿过细胞质膜的排出至关重要。

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