Interfakultäres Institut für Mikrobiologie und Infektionsmedizin, Universität Tübingen, Elfriede-Aulhorn-Str. 6, 72076 Tübingen, Germany.
Virology. 2010 Oct 25;406(2):322-7. doi: 10.1016/j.virol.2010.07.017. Epub 2010 Aug 13.
Temperate bacteriophages play a critical role in the pathogenicity of the human pathogen Staphylococcus aureus by mediating positive lysogenic conversion for different virulence factors such as Panton-Valentine leukocidin (PVL) or by interrupting chromosomal virulence genes. PVL-encoding phages are integrated in the S. aureus genome within a conserved ORF which is surrounded by a cluster of tandemly repeated genes. Here we demonstrate that in S. aureus clonal complex ST80 strains PVL-phage induction led to the acquisition of host DNA into the phage genome probably due to a homologous recombination event between direct repeats of the two paralogous genes adjacent to the phage integration site. Phage excision was accompanied by an additional chromosomal deletion in this region. This so far unrecognized mechanism of DNA uptake into the phage genome may play an important role in the co-evolution of phages and bacteria.
温和噬菌体在人类病原体金黄色葡萄球菌的致病性中发挥着关键作用,它们可以通过介导不同毒力因子(如 Panton-Valentine 白细胞毒素(PVL))的正溶原性转化,或通过中断染色体毒力基因来实现。编码 PVL 的噬菌体整合在金黄色葡萄球菌基因组内的一个保守 ORF 中,该 ORF 被一组串联重复基因包围。在这里,我们证明在 ST80 克隆复合体的金黄色葡萄球菌菌株中,PVL 噬菌体的诱导导致宿主 DNA 进入噬菌体基因组,这可能是由于噬菌体整合位点附近两个旁系同源基因的直接重复之间发生了同源重组事件。噬菌体的切除伴随着该区域内的额外染色体缺失。这种迄今为止尚未被识别的将 DNA 摄取到噬菌体基因组中的机制,可能在噬菌体和细菌的共同进化中发挥重要作用。