Nago Tamami T, Tokashiki Yoshino T, Kisanuki Kyoko, Nakasone Isamu, Yamane Nobuhisa
Clinical Laboratories, University Hospital of the Ryukyus, Nakagami-gun, Okinawa-pref. 903-0215, Japan.
Rinsho Byori. 2010 Aug;58(8):765-71.
To establish an alternative and more sensitive test method to detect oocyst of Cryptosporidium parvum and cyst of Giardia lamblia in clinical stool specimens, loop-mediated isothermal amplification (LAMP) was evaluated. Minimum cell concentrations at which LAMP assay could detect C. parvum oocyst and G. lamblia cyst were determined as 6.25 x 10(-1) and 3.12 x 10(-1) cells/assay when the stool specimens were spiked with the respective parasites. The results indicated 400 times higher sensitivities or more when compared to the microscopic readings. Twenty and nineteen diarrhea stool specimens spiked with C. parvum oocyst or G. lamblia cyst were assayed by LAMP. The results indicated that 14 (70%) and 16 (84%) samples successfully resulted in positive readings. But the remaining 6 and 3 samples were read as negative probably due to residual stool color. However, further dilutions of DNA extraction samples and addition of bovine serum albumin to LAMP reaction mixture showed positive effects on the occurrence of false-negative readings. With these results, we can conclude that the LAMP assay provides us an accurate and highly sensitive test method to detect C. parvum oocyst and cyst of G. lamblia, in place of labor-intensive and experience-dependent microscopic examination, in clinical laboratories.
为建立一种替代的、更灵敏的检测方法,用于检测临床粪便标本中微小隐孢子虫卵囊和蓝氏贾第鞭毛虫包囊,对环介导等温扩增技术(LAMP)进行了评估。当粪便标本中分别加入相应寄生虫时,LAMP检测微小隐孢子虫卵囊和蓝氏贾第鞭毛虫包囊的最低细胞浓度分别确定为6.25×10⁻¹和3.12×10⁻¹个细胞/检测。结果表明,与显微镜读数相比,灵敏度提高了400倍或更高。对20份添加微小隐孢子虫卵囊和19份添加蓝氏贾第鞭毛虫包囊的腹泻粪便标本进行LAMP检测。结果表明,分别有14份(70%)和16份(84%)样本检测结果为阳性。但其余6份和3份样本检测结果为阴性,可能是由于粪便颜色残留所致。然而,对DNA提取样本进行进一步稀释,并在LAMP反应混合物中添加牛血清白蛋白,对假阴性读数的出现有积极影响。基于这些结果,我们可以得出结论,LAMP检测为临床实验室提供了一种准确且高度灵敏的检测方法,可用于检测微小隐孢子虫卵囊和蓝氏贾第鞭毛虫包囊,以取代劳动强度大且依赖经验的显微镜检查。