Terry Courtney E, McGinnis Lisa M, Madigan Katharine C, Cao Ping, Cover Timothy L, Liechti George W, Peek Richard M, Forsyth Mark H
Department of Biology, The College of William & Mary, 214 Millington Hall, Landrum Drive, Williamsburg, VA 23187-8795, USA.
Infect Immun. 2005 Jun;73(6):3794-8. doi: 10.1128/IAI.73.6.3794-3798.2005.
In an analysis of Helicobacter pylori genomic DNA by macroarray methodology, genomic DNA from a panel of cag pathogenicity island (PAI)-negative H. pylori clinical isolates failed to hybridize with 27 genes located outside the cag PAI in a cag PAI-positive reference strain. PCR analyses confirmed that HP0217 (encoding a lipopolysaccharide biosynthetic protein) and HP1079 (encoding a protein of unknown function) were present significantly more frequently in cagA-positive strains than in cagA-negative strains. A low G+C content of these two genes suggests they were acquired by horizontal transfer events.
在用宏阵列方法分析幽门螺杆菌基因组DNA时,一组cag致病岛(PAI)阴性的幽门螺杆菌临床分离株的基因组DNA未能与cag PAI阳性参考菌株中位于cag PAI之外的27个基因杂交。PCR分析证实,HP0217(编码一种脂多糖生物合成蛋白)和HP1079(编码一种功能未知的蛋白)在cagA阳性菌株中出现的频率明显高于cagA阴性菌株。这两个基因的低G+C含量表明它们是通过水平转移事件获得的。