Gómez-Couso H, Fontán-Saínz M, Sichel C, Fernández-Ibáñez P, Ares-Mazás E
Laboratorio de Parasitología, Departamento de Microbiología y Parasitología, Universidad de Santiago de Compostela, Spain.
Trop Med Int Health. 2009 Jun;14(6):620-7. doi: 10.1111/j.1365-3156.2009.02281.x.
To investigate the efficacy of the solar water disinfection (SODIS) method for inactivating Cryptosporidium parvum oocysts in turbid waters using 1.5 l polyethylene terephthalate (PET) bottles under natural sunlight.
All experiments were performed at the Plataforma Solar de Almería, located in the Tabernas Desert (Southern Spain) in July and October 2007. Turbid water samples [5, 100 and 300 nephelometric turbidity units (NTU)] were prepared by addition of red soil to distilled water, and then spiked with purified C. parvum oocysts. PET bottles containing the contaminated turbid waters were exposed to full sunlight for 4, 8 and 12 h. The samples were then concentrated by filtration and the oocyst viability was determined by inclusion/exclusion of the fluorogenic vital dye propidium iodide. Results After an exposure time of 12 h (cumulative global dose of 28.28 MJ/m(2); cumulative UV dose of 1037.06 kJ/m(2)) the oocyst viabilities were 11.54%, 25.96%, 41.50% and 52.80% for turbidity levels of 0, 5, 100 and 300 NTU, respectively, being significantly lower than the viability of the initial isolate (P < 0.01).
SODIS method significantly reduced the potential viability of C. parvum oocysts on increasing the percentage of oocysts that took up the dye PI (indicator of cell wall integrity), although longer exposure periods appear to be required than those established for the bacterial pathogens usually tested in SODIS assays. SODIS.
研究在自然阳光下,使用1.5升聚对苯二甲酸乙二酯(PET)瓶,通过太阳能水消毒(SODIS)方法灭活浑浊水中微小隐孢子虫卵囊的效果。
所有实验于2007年7月和10月在位于西班牙南部塔韦纳斯沙漠的阿尔梅里亚太阳能平台进行。通过向蒸馏水中添加红土制备浑浊水样[5、100和300散射浊度单位(NTU)],然后接种纯化的微小隐孢子虫卵囊。将装有受污染浑浊水的PET瓶暴露在充足阳光下4、8和12小时。然后通过过滤浓缩样品,并通过荧光活性染料碘化丙啶的摄入/排除来测定卵囊活力。结果:暴露12小时(累积总剂量为28.28兆焦耳/平方米;累积紫外线剂量为1037.06千焦耳/平方米)后,浊度水平为0、5、100和300 NTU时,卵囊活力分别为11.54%、25.96%、41.50%和52.80%,均显著低于初始分离株的活力(P<0.01)。
SODIS方法显著降低了微小隐孢子虫卵囊的潜在活力,同时增加了摄取染料PI(细胞壁完整性指标)的卵囊百分比,尽管与通常在SODIS试验中测试的细菌病原体相比,似乎需要更长的暴露时间。SODIS。