TY - JOUR
T1 - Inactivation mechanisms of
T2 - Cryptosporidium parvum oocysts by solar ultraviolet irradiation
AU - Liu, Yuanyuan
AU - Dong, Shengkun
AU - Kuhlenschmidt, Mark S.
AU - Kuhlenschmidt, Theresa B.
AU - Drnevich, Jenny
AU - Nguyen, Thanh H.
N1 - Publisher Copyright:
© 2015 The Royal Society of Chemistry.
PY - 2015
Y1 - 2015
N2 - Cryptosporidium parvum oocysts have been known to cause adverse health effects worldwide, and processes that contribute to their inactivation have gained wide attention in recent years. Solar inactivation is an important process that can improve surface water quality. Solar disinfection (SODIS) can be used to disinfect water as a point-of-use alternative, and disinfect wastewater in waste stabilization ponds. However, a clear understanding of the oocyst solar inactivation mechanisms is lacking. This study systematically investigated the oocyst solar inactivation mechanisms in the presence of a wide range of environmental factors and also provided an insight on the metabolic response of oocysts using the microarray analysis. The result revealed that oocyst inactivation by solar UVA/visible light was dominated by UVA-induced internal radical damages and was sensitive to both the temperature and the oocyst source. External radical producing sensitizers did not enhance the UVA/visible light inactivation of oocysts due to the protection by the oocyst wall. In contrast, UVB was found to directly damage the oocyst genome, ensuring an effective inactivation that correlated only with UV fluence after being corrected for light screening regardless of the oocyst source, temperature, and the presence of external sensitizers. Further microarray analysis suggested that the effective UVB inactivation could be explained by the down-regulation of most of the genes responsible for cellular metabolic activities and the lack of expression of stress protection mechanisms in oocysts after 30 minutes of UVB exposure. These results facilitate the understanding and design of water and wastewater treatment processes that involve natural sunlight exposure.
AB - Cryptosporidium parvum oocysts have been known to cause adverse health effects worldwide, and processes that contribute to their inactivation have gained wide attention in recent years. Solar inactivation is an important process that can improve surface water quality. Solar disinfection (SODIS) can be used to disinfect water as a point-of-use alternative, and disinfect wastewater in waste stabilization ponds. However, a clear understanding of the oocyst solar inactivation mechanisms is lacking. This study systematically investigated the oocyst solar inactivation mechanisms in the presence of a wide range of environmental factors and also provided an insight on the metabolic response of oocysts using the microarray analysis. The result revealed that oocyst inactivation by solar UVA/visible light was dominated by UVA-induced internal radical damages and was sensitive to both the temperature and the oocyst source. External radical producing sensitizers did not enhance the UVA/visible light inactivation of oocysts due to the protection by the oocyst wall. In contrast, UVB was found to directly damage the oocyst genome, ensuring an effective inactivation that correlated only with UV fluence after being corrected for light screening regardless of the oocyst source, temperature, and the presence of external sensitizers. Further microarray analysis suggested that the effective UVB inactivation could be explained by the down-regulation of most of the genes responsible for cellular metabolic activities and the lack of expression of stress protection mechanisms in oocysts after 30 minutes of UVB exposure. These results facilitate the understanding and design of water and wastewater treatment processes that involve natural sunlight exposure.
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U2 - 10.1039/c4ew00079j
DO - 10.1039/c4ew00079j
M3 - Article
AN - SCOPUS:84985026368
SN - 2053-1400
VL - 1
SP - 188
EP - 198
JO - Environmental Science: Water Research and Technology
JF - Environmental Science: Water Research and Technology
IS - 2
ER -