Tran H L, Fiedler F, Hodgson D A, Kathariou S
Department of Microbiology, University of Hawaii, Honolulu, Hawaii 96822, USA.
Appl Environ Microbiol. 1999 Nov;65(11):4793-8. doi: 10.1128/AEM.65.11.4793-4798.1999.
Teichoic acid-associated N-acetylglucosamine and rhamnose have been shown to serve as phage receptors in Listeria monocytogenes serotype 1/2a. We generated and characterized two single-copy Tn916DeltaE mutants which were resistant to phage A118 and several other serotype 1/2a-specific phages. In one mutant the insertion was immediately upstream of the recently identified ptsHI locus, which encodes two proteins of the phosphoenolpyruvate-dependent carbohydrate uptake system, whereas in the other the insertion was immediately upstream of an operon whose most distal gene was clpC, involved in stress responses and virulence. Transduction experiments confirmed the association of the phage-resistant phenotype of these mutants with the transposon insertion. Phage A118 resistance of the mutants could be attributed to inability of the phage to adsorb onto the mutant cells, and biochemical analysis of cell wall composition showed that the teichoic acids of both mutants were deficient in N-acetylglucosamine. Rhamnose and other teichoic acid and cell wall components were not affected.
已证明,磷壁酸相关的N-乙酰葡糖胺和鼠李糖可作为单核细胞增生李斯特菌1/2a血清型中的噬菌体受体。我们构建并鉴定了两个单拷贝Tn916DeltaE突变体,它们对噬菌体A118和其他几种1/2a血清型特异性噬菌体具有抗性。在一个突变体中,插入位点紧邻最近鉴定出的ptsHI基因座上游,该基因座编码磷酸烯醇丙酮酸依赖性碳水化合物摄取系统的两种蛋白质;而在另一个突变体中,插入位点紧邻一个操纵子上游,该操纵子最远端的基因是clpC,参与应激反应和毒力。转导实验证实了这些突变体的噬菌体抗性表型与转座子插入之间的关联。突变体对噬菌体A118的抗性可归因于噬菌体无法吸附到突变体细胞上,细胞壁成分的生化分析表明,两个突变体的磷壁酸均缺乏N-乙酰葡糖胺。鼠李糖以及其他磷壁酸和细胞壁成分未受影响。