Luo Xiao-Feng, Jiao Jian-Hua, Zhang Wen-Yue, Pu Han-Ming, Qu Bao-Jin, Yang Bing-Ya, Hou Min, Ji Min-Jun
Xiao-Feng Luo, Wen-Yue Zhang, Bing-Ya Yang, Min Hou, Min-Jun Ji, Department of Pathogen Biology, Nanjing Medical University, Nanjing 211166, Jiangsu Province, China.
World J Gastroenterol. 2016 Jul 7;22(25):5822-30. doi: 10.3748/wjg.v22.i25.5822.
To investigate clarithromycin resistance positions 2142, 2143 and 2144 of the 23SrRNA gene in Helicobacter pylori (H. pylori) by nested-allele specific primer-polymerase chain reaction (nested-ASP-PCR).
The gastric tissue and saliva samples from 99 patients with positive results of the rapid urease test (RUT) were collected. The nested-ASP-PCR method was carried out with the external primers and inner allele-specific primers corresponding to the reference strain and clinical strains. Thirty gastric tissue and saliva samples were tested to determine the sensitivity of nested-ASP-PCR and ASP-PCR methods. Then, clarithromycin resistance was detected for 99 clinical samples by using different methods, including nested-ASP-PCR, bacterial culture and disk diffusion.
The nested-ASP-PCR method was successfully established to test the resistance mutation points 2142, 2143 and 2144 of the 23SrRNA gene of H. pylori. Among 30 samples of gastric tissue and saliva, the H. pylori detection rate of nested-ASP-PCR was 90% and 83.33%, while the detection rate of ASP-PCR was just 63% and 56.67%. Especially in the saliva samples, nested-ASP-PCR showed much higher sensitivity in H. pylori detection and resistance mutation rates than ASP-PCR. In the 99 RUT-positive gastric tissue and saliva samples, the H. pylori-positive detection rate by nested-ASP-PCR was 87 (87.88%) and 67 (67.68%), in which there were 30 wild-type and 57 mutated strains in gastric tissue and 22 wild-type and 45 mutated strains in saliva. Genotype analysis showed that three-points mixed mutations were quite common, but different resistant strains were present in gastric mucosa and saliva. Compared to the high sensitivity shown by nested-ASP-PCR, the positive detection of bacterial culture with gastric tissue samples was 50 cases, in which only 26 drug-resistant strains were found through analyzing minimum inhibitory zone of clarithromycin.
The nested-ASP-PCR assay showed higher detection sensitivity than ASP-PCR and drug sensitivity testing, which could be performed to evaluate clarithromycin resistance of H. pylori.
通过巢式等位基因特异性引物聚合酶链反应(nested-ASP-PCR)研究幽门螺杆菌(H. pylori)23SrRNA基因2142、2143和2144位点的克拉霉素耐药情况。
收集99例快速尿素酶试验(RUT)结果为阳性患者的胃组织和唾液样本。采用与参考菌株和临床菌株对应的外部引物和内部等位基因特异性引物进行巢式-ASP-PCR方法。检测30例胃组织和唾液样本以确定巢式-ASP-PCR和ASP-PCR方法的敏感性。然后,使用不同方法检测99例临床样本的克拉霉素耐药性,包括巢式-ASP-PCR、细菌培养和纸片扩散法。
成功建立巢式-ASP-PCR方法检测幽门螺杆菌23SrRNA基因2142、2143和2144位点的耐药突变点。在30例胃组织和唾液样本中,巢式-ASP-PCR检测幽门螺杆菌的阳性率分别为90%和83.33%,而ASP-PCR的阳性率仅为63%和56.67%。特别是在唾液样本中,巢式-ASP-PCR在幽门螺杆菌检测和耐药突变率方面显示出比ASP-PCR更高的敏感性。在99例RUT阳性的胃组织和唾液样本中,巢式-ASP-PCR检测幽门螺杆菌的阳性率分别为87例(87.88%)和67例(67.68%),其中胃组织中有30例野生型和57例突变株,唾液中有22例野生型和45例突变株。基因型分析表明三点混合突变很常见,但胃黏膜和唾液中存在不同的耐药菌株。与巢式-ASP-PCR显示的高敏感性相比,胃组织样本细菌培养的阳性检测为50例,通过分析克拉霉素的最小抑菌圈仅发现26例耐药菌株。
巢式-ASP-PCR检测法显示出比ASP-PCR和药敏试验更高的检测敏感性,可用于评估幽门螺杆菌的克拉霉素耐药性。