Sumby Paul, Porcella Steve F, Madrigal Andres G, Barbian Kent D, Virtaneva Kimmo, Ricklefs Stacy M, Sturdevant Daniel E, Graham Morag R, Vuopio-Varkila Jaana, Hoe Nancy P, Musser James M
Laboratory of Human Bacterial Pathogenesis, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA.
J Infect Dis. 2005 Sep 1;192(5):771-82. doi: 10.1086/432514. Epub 2005 Jul 29.
To better understand the molecular events involved in the origin of new pathogenic bacteria, we studied the evolution of a highly virulent clone of serotype M1 group A Streptococcus (GAS). Genomic, DNA-DNA microarray, and single-nucleotide polymorphism analyses indicated that this clone evolved through a series of horizontal gene transfer events that involved (1) the acquisition of prophages encoding streptococcal pyrogenic exotoxin A and extracellular DNases and (2) the reciprocal recombination of a 36-kb chromosomal region encoding the extracellular toxins NAD+-glycohydrolase (NADase) and streptolysin O (SLO). These gene transfer events were associated with significantly increased production of SLO and NADase. Virtual identity in the 36-kb region present in contemporary serotype M1 and M12 isolates suggests that a serotype M12 strain served as the donor of this region. Multiple horizontal gene transfer events were a crucial factor in the evolutionary origin and emergence of a very abundant contemporary clone of serotype M1 GAS.
为了更好地理解新致病细菌起源过程中涉及的分子事件,我们研究了A群M1型链球菌(GAS)高毒力克隆株的进化。基因组、DNA-DNA微阵列和单核苷酸多态性分析表明,该克隆株通过一系列水平基因转移事件进化而来,这些事件包括:(1)获得编码链球菌致热外毒素A和细胞外DNA酶的原噬菌体;(2)编码细胞外毒素NAD+ - 糖水解酶(NADase)和链球菌溶血素O(SLO)的36kb染色体区域的相互重组。这些基因转移事件与SLO和NADase产量的显著增加相关。当代M1型和M12型分离株中存在的36kb区域的虚拟同一性表明,一株M12型菌株是该区域的供体。多个水平基因转移事件是当代非常常见的M1型GAS克隆株进化起源和出现的关键因素。