Schwarz E, Plum G, Mauff G, Hasbach H, Eidt S, Schrappe M, Kruis W
Institut für Medizinische Mikrobiologie und Hygiene, Universität zu Köln, Germany.
Zentralbl Bakteriol. 1997 Feb;285(3):368-78. doi: 10.1016/s0934-8840(97)80003-5.
Infection with Helicobacter pylori causes chronic active gastritis and has been associated with gastric and duodenal ulcer disease. In biopsy samples of 110 patients with clinical symptoms of active gastritis, H. pylori was detected by means of the polymerase chain reaction (PCR), using species-specific primers defining a 858 bp DNA fragment of H. pylori urease beta-subunit. Sensitivity and specificity of the PCR was compared with culture, histology and Warthin-Starry stain (WSs), detection of H. pylori urease antibodies in serum and urease testing with the Campylobacter-like organism (CLO) test. PCR yielded specific amplification products in 53 cases, whereas culture of the organisms was positive in a subset of 50 cases. Only direct detection in histological sections of biopsy specimens had a higher sensitivity, with 65 positive samples. In contrast, the CLO test was negative in eleven culture-positive and PCR-positive cases. Significant urease antibody titres were found in 39 patients with histologically confirmed diagnosis. These results placed the sensitivity of PCR between tat of the Warthin-Starry stain (WSs) and that of culture. Therefore, PCR can be proposed as a useful rapid and time-saving technique for the detection of H.pylori in gastritis. For epidemiological purposes, fingerprinting with arbitrarily chosen primers by AP-PCR was evaluated. Strain-specific patterns with up to 13 fragments were achieved with 10-nucleotide or longer primers (21-nt) with a G + C content > or = 55%. Thirty-five of 40 strains investigated by this method were distinguishable with a single primer. These results suggest a high level of DNA sequence diversity within this species with the possibility of confirming the clonality in consecutive isolates from a single individual. Alternatively, an increased in-vivo mutation rate could be responsible for DNA divergence, resulting in specific strains for each individual patient.
幽门螺杆菌感染可导致慢性活动性胃炎,并与胃溃疡和十二指肠溃疡疾病相关。在110例有活动性胃炎临床症状的患者活检样本中,使用定义幽门螺杆菌脲酶β亚基858 bp DNA片段的种特异性引物,通过聚合酶链反应(PCR)检测幽门螺杆菌。将PCR的敏感性和特异性与培养、组织学和沃辛-斯塔里染色(WSs)、血清中幽门螺杆菌脲酶抗体检测以及弯曲杆菌样菌(CLO)试验的脲酶检测进行比较。PCR在53例中产生特异性扩增产物,而该菌的培养在50例的一个亚组中呈阳性。只有活检标本组织学切片中的直接检测具有更高的敏感性,有65个阳性样本。相比之下,CLO试验在11例培养阳性和PCR阳性病例中呈阴性。在39例经组织学确诊的患者中发现了显著的脲酶抗体滴度。这些结果使PCR的敏感性介于沃辛-斯塔里染色(WSs)和培养之间。因此,PCR可被认为是一种用于检测胃炎中幽门螺杆菌的有用的快速且节省时间的技术。为了流行病学目的,评估了通过任意选择引物的AP-PCR进行指纹分析。使用10个核苷酸或更长(21个核苷酸)且G + C含量≥55%的引物可获得多达13个片段的菌株特异性图谱。用这种方法研究的40株菌株中有35株可通过单一引物区分。这些结果表明该物种内存在高水平的DNA序列多样性,有可能确认来自单个个体的连续分离株中的克隆性。或者,体内突变率的增加可能导致DNA差异,从而导致每个患者有特定的菌株。