STERIS SA R&D, Fontenay-aux-Roses, France.
J Eukaryot Microbiol. 2012 May-Jun;59(3):198-205. doi: 10.1111/j.1550-7408.2012.00612.x. Epub 2012 Feb 21.
Despite increasing concerns of direct pathogenicity and/or their role as hosts for other microorganisms there are currently no standard methods for the inactivation of amoebae that belong to the genus Acanthamoeba. Methods used to grow amoebae and produce cysts for these tests may be important as they can dramatically modify cyst susceptibility. We compared resistance of cysts produced from trophozoites grown in peptone-yeast extract-glucose broth or by feeding on HEp-2 cells and then encysted in Neff's medium. We observed that trophozoites grown using HEp-2 cells as a nutrient source produce cysts that are significantly more resistant to SDS and to most biocides tested, including heat. Increased resistance is likely due to a higher proportion of mature cysts presenting thicker cell walls as demonstrated using transmission electron microscopy. This was confirmed by calcofluor white staining demonstrating higher cellulose content in cysts produced from trophozoites grown using HEp-2 cells as a feeding source. These results demonstrate that not only methods used to produce cysts from trophozoites are critical, but that methods used to grow trophozoites before encystment should also be chosen carefully. This should be taken into account for the development of protocols to evaluate biocides and antimicrobials against amoebal cysts.
尽管人们越来越关注直接致病性和/或它们作为其他微生物宿主的作用,但目前尚无针对属于棘阿米巴属的阿米巴原虫的标准灭活方法。用于培养阿米巴虫和产生用于这些测试的胞囊的方法可能很重要,因为它们可以极大地改变胞囊的敏感性。我们比较了在蛋白胨-酵母提取物-葡萄糖肉汤中生长的滋养体或通过在 HEp-2 细胞上进食然后在 Neff 培养基中包囊化产生的滋养体产生的胞囊的抗性。我们观察到,使用 HEp-2 细胞作为营养源生长的滋养体产生的胞囊对 SDS 和大多数测试的生物杀灭剂(包括热)具有显著更高的抗性。更高的抗性可能是由于成熟胞囊的比例更高,细胞壁更厚,如透射电子显微镜所示。这通过钙荧光白染色得到证实,该染色显示出从使用 HEp-2 细胞作为饲养源生长的滋养体产生的胞囊中的纤维素含量更高。这些结果表明,不仅从滋养体产生胞囊的方法至关重要,而且在包囊之前生长滋养体的方法也应谨慎选择。在制定评估针对阿米巴胞囊的消毒剂和抗菌剂的方案时,应考虑到这一点。