Klein Pavel, Cirioni Oscar, Giacometti Andrea, Scalise Giorgio
Institute of Animal Science, Praha 10, Uhrineves, Czech Republic.
J Antimicrob Chemother. 2008 Nov;62(5):1101-4. doi: 10.1093/jac/dkn303. Epub 2008 Jul 23.
The aim of this study was to assess the effect of commercial aurintricarboxylic acid (ATA) against Cryptosporidium parvum.
The anticryptosporidial effect of ATA was evaluated in vitro using cell culture and double fluorogenic staining, and in vivo in experimentally infected neonatal C57BL/6 mice. Mice were orally treated for 9 consecutive days starting on the day of infection with daily ATA doses of 50 and 100 micromol/kg. Paromomycin (100 mg/kg) was used as a positive control.
In both in vitro models, ATA at concentrations of 100 and 10 micromol/L completely inhibited sporozoites within 10 and 60 min, respectively. Viability of oocysts exposed to 100 micromol/L and assessed by flow cytometry and in cell culture was reduced by 65% and 61%, respectively. The treatment of neonatal mice with a daily ATA dose of 100 micromol/kg led to 97-99% inhibition of infection without any observable negative effects on the animals. In comparison, the mean reduction of infection for paromomycin was 79-84%.
ATA exerted high anticryptosporidial activity and should be considered for further study.
本研究旨在评估商用金精三羧酸(ATA)对微小隐孢子虫的作用。
使用细胞培养和双荧光染色在体外评估ATA的抗隐孢子虫作用,并在实验性感染的新生C57BL/6小鼠体内进行评估。从感染当天开始,小鼠连续9天每天口服ATA,剂量分别为50和100微摩尔/千克。巴龙霉素(100毫克/千克)用作阳性对照。
在两种体外模型中,浓度为100和10微摩尔/升的ATA分别在10分钟和60分钟内完全抑制子孢子。通过流式细胞术和细胞培养评估,暴露于100微摩尔/升的卵囊活力分别降低了65%和61%。每天给新生小鼠口服100微摩尔/千克的ATA可导致感染抑制率达97%-99%,且对动物无任何明显负面影响。相比之下,巴龙霉素的平均感染降低率为79%-84%。
ATA具有较高的抗隐孢子虫活性,应考虑进一步研究。