McLauchlin J, Pedraza-Díaz S, Amar-Hoetzeneder C, Nichols G L
Food Hygiene Laboratory, Division of Gastrointestinal Infections, PHLS Central Public Health Laboratory, London NW9 5HT, United Kingdom.
J Clin Microbiol. 1999 Oct;37(10):3153-8. doi: 10.1128/JCM.37.10.3153-3158.1999.
Samples of whole feces in which Cryptosporidium oocysts were recognized by hospital laboratories were collected from 218 patients with diarrhea. All samples were reexamined by light microscopy, and oocysts were detected in 211 samples. A simple and rapid procedure for the extraction of DNA from whole feces was developed, and this was used to amplify fragments of the Cryptosporidium outer wall protein (COWP), the thrombospondin-related adhesive protein C1 (TRAP-C1), and the 18S rRNA genes by PCR. For seven samples oocysts were not detected by microscopy and DNA failed to be amplified by the three PCR procedures. Among the 211 samples "positive" by microscopy, the sensitivities of PCRs for the 18S rRNA, COWP, and TRAP-C1 gene fragments were 97, 91, and 66%, respectively. The sensitivities of all three PCR procedures increased with increasing numbers of oocysts as observed by microscopy. Two genotypes of the COWP and TRAP-C1 genes can be detected by PCR-restriction fragment length polymorphism analysis. With this series of samples, the same genotypes of the COWP and TRAP-C1 genes always segregated together. A combined genotyping data set was produced for isolates from 194 samples: 74 (38%) were genotype 1 and 120 (62%) were genotype 2. Genotype 2 was detected in a significantly greater proportion of the samples with small numbers of oocysts, and genotype 1 was detected in a significantly greater proportion of the samples with larger numbers of oocysts. There were no significant differences in the distribution of the genotypes by patient sex and age. The distribution of the genotypes was significantly different both in patients with a history of foreign travel and in those from different regions in England.
从218例腹泻患者中收集了经医院实验室鉴定出隐孢子虫卵囊的全粪便样本。所有样本均通过光学显微镜重新检查,在211个样本中检测到了卵囊。开发了一种从全粪便中提取DNA的简单快速方法,并用于通过聚合酶链反应(PCR)扩增隐孢子虫外壁蛋白(COWP)、血小板反应蛋白相关粘附蛋白C1(TRAP-C1)和18S rRNA基因的片段。有7个样本在显微镜下未检测到卵囊,并且三种PCR方法均未能扩增出DNA。在显微镜检查为“阳性”的211个样本中,针对18S rRNA、COWP和TRAP-C1基因片段的PCR敏感性分别为97%、91%和66%。如显微镜观察所示,所有三种PCR方法的敏感性均随着卵囊数量的增加而提高。通过PCR-限制性片段长度多态性分析可检测到COWP和TRAP-C1基因的两种基因型。对于这一系列样本,COWP和TRAP-C1基因的相同基因型总是一起分离。为194个样本的分离株生成了一个联合基因分型数据集:74个(38%)为基因型1,120个(62%)为基因型2。在卵囊数量较少的样本中,基因型2的检测比例显著更高,而在卵囊数量较多的样本中,基因型1的检测比例显著更高。患者的性别和年龄在基因型分布上无显著差异。在有国外旅行史的患者和来自英格兰不同地区的患者中,基因型分布均存在显著差异。