Determining UV Inactivation of Toxoplasma gondii Oocysts by Using Cell Culture and a Mouse Bioassay

被引:37
作者
Ware, Michael W.
Augustine, Swinburne A. J.
Erisman, David O.
See, Mary Jean [3 ]
Wymer, Larry
Hayes, Samuel L. [2 ]
Dubey, J. P. [4 ]
Villegas, Eric N. [1 ,3 ]
机构
[1] US EPA, Biohazard Assessment Res Branch, Microbiol & Chem Exposure Assessment Res Div, Natl Exposure Res Lab, Cincinnati, OH 45268 USA
[2] US EPA, Natl Risk Management Res Lab, Cincinnati, OH 45268 USA
[3] Univ Cincinnati, McMicken Coll Arts & Sci, Dept Biol Sci, Cincinnati, OH 45220 USA
[4] ARS, Anim Parasit Dis Lab, USDA, Beltsville, MD 20705 USA
基金
美国国家环境保护局;
关键词
CRYPTOSPORIDIUM-PARVUM OOCYSTS; SEVERE ACQUIRED TOXOPLASMOSIS; LOW-PRESSURE ULTRAVIOLET; ENHYDRA-LUTRIS-NEREIS; REAL-TIME PCR; WATERBORNE TOXOPLASMOSIS; DRINKING-WATER; SEA OTTERS; UNITED-STATES; FRENCH-GUIANA;
D O I
10.1128/AEM.00153-10
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The effect of UV exposure on Toxoplasma gondii oocysts has not been completely defined for use in water disinfection. This study evaluated UV-irradiated oocysts by three assays: a SCID mouse bioassay, an in vitro T. gondii oocyst plaque (TOP) assay, and a quantitative reverse transcriptase real-time PCR (RT-qPCR) assay. The results from the animal bioassay show that 1- and 3-log(10) inactivation is achieved with 4 mJ/cm(2) UV and 10 mJ/cm(2) low-pressure UV, respectively. TOP assay results, but not RT-qPCR results, correlate well with bioassay results. In conclusion, a 3-log(10) inactivation of T. gondii oocysts is achieved by 10-mJ/cm(2) low-pressure UV, and the in vitro TOP assay is a promising alternative to the mouse bioassay.
引用
收藏
页码:5140 / 5147
页数:8
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