Go M F, Cissell L, Graham D Y
Dept. of Medicine, Veterans Affairs Medical Center and Baylor College of Medicine, Houston, Texas 77030, USA.
Scand J Gastroenterol. 1998 Feb;33(2):132-6. doi: 10.1080/00365529850166842.
Mosaicism of the Helicobacter pylori vac A gene comprises two families of allelic variations of the signal sequence region (s1, s2) and of the mid-region (m1, m2). Initial studies suggested that peptic ulcer disease correlated with the s1 subtype of vac A. We compared the prevalence of various vac A genotypes of H. pylori isolates obtained from duodenal ulcer (DU) patients and subjects with simple gastritis. Those isolates with s1 type were further examined to determine whether the specific vac A s1 (s1a versus s1b) genotype enabled prediction of gastroduodenal disease.
H. pylori isolates were obtained from 38 patients with endoscopically documented DU and 39 individuals with asymptomatic H. pylori gastritis from Houston, Texas. The vac A genotype of each isolate was determined by polymerase chain reaction (PCR) amplification of genomic DNA for specific regions of the vac A gene. Those isolates with s1 vac A subtype were further examined to determine whether they had s1a or s1b mosaicism.
There was no difference in frequency of the s1 genotype of isolates obtained from patients with duodenal ulcer or asymptomatic H. pylori gastritis in this sample (84% versus 79%, respectively; P = 0.77). The s1/m1 vac A genotype was detected in isolates from 16 duodenal ulcer patients versus 15 with H. pylori gastritis (P = 0.82). Detailed analysis of the s1 region failed to show a correlation of either s1a or s1b with duodenal ulcer. Both s1a and s1b genotypes were detected in 24 strains, and both m1 and m2 mid-gene PCR amplicons were seen in 16 strains.
We were unable to use H. pylori vac A genotyping to predict type of gastroduodenal disease in our patient sample. This failure to confirm an association of vac A genotype and duodenal ulcer disease differs from samples from other regions. This most likely represents an example of differences in H. pylori strains infecting host populations in different geographic regions. This study confirms the importance of establishing statistical associations with isolates from widely separate geographic regions before concluding that disease-related associations exist.
幽门螺杆菌空泡毒素A(VacA)基因的镶嵌体由信号序列区(s1、s2)和中间区(m1、m2)的两个等位基因变异家族组成。初步研究表明,消化性溃疡病与VacA的s1亚型相关。我们比较了从十二指肠溃疡(DU)患者和单纯性胃炎患者中分离出的幽门螺杆菌各种VacA基因型的流行情况。对那些s1型分离株进一步检查,以确定特定的VacA s1(s1a与s1b)基因型是否能够预测胃十二指肠疾病。
从得克萨斯州休斯顿的38例经内镜证实为DU的患者和39例无症状幽门螺杆菌胃炎患者中分离出幽门螺杆菌。通过聚合酶链反应(PCR)扩增VacA基因特定区域的基因组DNA来确定每个分离株的VacA基因型。对那些s1 VacA亚型的分离株进一步检查,以确定它们是否具有s1a或s1b镶嵌体。
在本样本中,从十二指肠溃疡患者或无症状幽门螺杆菌胃炎患者中分离出的菌株的s1基因型频率没有差异(分别为84%和79%;P = 0.77)。在16例十二指肠溃疡患者的分离株中检测到s1/m1 VacA基因型,而幽门螺杆菌胃炎患者中有15例(P = 0.82)。对s1区域的详细分析未能显示s1a或s1b与十二指肠溃疡之间的相关性。在24株菌株中检测到s1a和s1b基因型,在16株菌株中同时看到m1和m2中间基因PCR扩增产物。
在我们的患者样本中,我们无法使用幽门螺杆菌VacA基因分型来预测胃十二指肠疾病的类型。未能证实VacA基因型与十二指肠溃疡病之间的关联与其他地区的样本不同。这很可能代表了不同地理区域感染宿主人群的幽门螺杆菌菌株差异的一个例子。这项研究证实了在得出疾病相关关联存在的结论之前,与来自广泛不同地理区域的分离株建立统计关联的重要性。