Table of Contents
International Scholarly Research Notices
Volume 2014, Article ID 525719, 7 pages
http://dx.doi.org/10.1155/2014/525719
Research Article

Giardia duodenalis: Number and Fluorescence Reduction Caused by the Advanced Oxidation Process (H2O2/UV)

1Department of Sanitation and the Environment, School of Civil Engineering, Architecture and Urbanism, University of Campinas (UNICAMP), CP 6021, 13083-852 Campinas, SP, Brazil
2Department of Animal Biology, Biology Institute, University of Campinas (UNICAMP), CP 6109, 13083-970 Campinas, SP, Brazil
3Padre Anchieta University Center, UNIANCHIETA, Bom Jesus de Pirapora Street 100/140, 13207-270 Jundiaí, SP, Brazil

Received 1 September 2014; Accepted 4 November 2014; Published 7 December 2014

Academic Editor: Erick R. Bandala

Copyright © 2014 José Roberto Guimarães et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

This study evaluated the effect of peroxidation assisted by ultraviolet radiation (H2O2/UV), which is an advanced oxidation process (AOP), on Giardia duodenalis cysts. The cysts were inoculated in synthetic and surface water using a concentration of 12 g H2O2 L−1 and a UV dose ( nm) of 5,480 mJcm−2. The aqueous solutions were concentrated using membrane filtration, and the organisms were observed using a direct immunofluorescence assay (IFA). The AOP was effective in reducing the number of G. duodenalis cysts in synthetic and surface water and was most effective in reducing the fluorescence of the cyst walls that were present in the surface water. The AOP showed a higher deleterious potential for G. duodenalis cysts than either peroxidation (H2O2) or photolysis (UV) processes alone.

1. Introduction

The constant environmental degradation of watersheds near densely populated areas has greatly altered the quality of public water sources. Although access to safe drinking water is a priority, providing safe drinking water is challenging due to the potential for severe contamination and the lack of access to sanitary infrastructure. One billion people lack access to improved water supplies and 2.6 billion people lack adequate sanitation [1]. Waterborne diseases that are caused by microorganisms such as viruses, bacteria, and protozoa have been documented throughout the world. Parasitic protozoan diseases that are transmitted through water have caused 62.5 million disability adjusted life years (DALYs) worldwide. Giardia duodenalis (also known as Giardia lamblia) is parasite responsible for approximately 35% of gastrointestinal disease outbreaks caused by waterborne protozoa in Australia, Europe, and North America [2]. The economic losses, both direct and indirect, caused by G. duodenalis infection are considerable. Children are most at risk for the clinical consequences of G. duodenalis infection, particularly children in developing countries [3].

This protozoan is responsible for intestinal infection and diarrhea that may lead to nutritional deficiencies and significant morbidity and mortality, especially among children and the elderly. In areas where G. duodenalis is endemic, the emergence of resistant strains has led to a high rate of clinical failure of treatment [4].

Symptoms include diarrhea, malaise, flatulence, foul-smelling greasy stools, abdominal cramps, bloating, nausea, anorexia, and weight loss. Extraintestinal symptoms (urticaria, angioedema, and atopic dermatitis) have been reported, and a deficiency in the appropriate treatment of giardiasis has been identified [5]. Asymptomatic infection also occurs frequently (50–75% of infected persons). The absence of symptoms may result in a low clinical index of suspicion for diagnosis [6, 7].

Giardia spp. cysts (the environmentally resistant stage of the parasite) are transmitted by a fecal-oral route and are particularly suited to waterborne transmission because they are widely present in surface water, sewage, and drinking and recreational water [8]. Following ingestion, excystation takes place shortly after cysts leave the stomach and leads to rapid colonisation of the duodenum and jejunum, where the excysted trophozoites attach to the intestinal mucosa and multiply rapidly. Attachment is mediated by the ventral adhesive disc and is an essential feature of the relationship between Giardia spp. and its host and a prerequisite to sustained infection [9].

Infectious diseases remain a public health problem in Brazil. Although approximately 91.5% of the population has access to treated drinking water, the sewage generated from only 41.2% receives some treatment [10]. Giardia spp. cysts were detected in many Brazilian environmental samples: wastewater, water (superficial and recreational), and bivalve mollusks [6, 1114].

These cysts are highly prevalent in wastewater throughout various parts of the world, which may reflect the infection rate in the population. Although wastewater treatment plants are designed to produce effluents that carry low health-risk levels for the exposed population, treated wastewater can carry pathogens [6, 7].

The presence of Giardia spp. cysts can be reduced with wastewater treatment processes; however, it is difficult to achieve protozoa inactivation with the concentration of chlorine that is typically used for water and wastewater disinfection [7]. The disinfection step of treated sewage is crucial; however, most processes do not efficiently inactivate the resistant stages of the pathogens.

New procedures for pathogen disinfection, such as microwaves, high-intensity pulsed UV light radiation (PUV), and advanced oxidation processes (AOPs), have been evaluated (Guimarães et al., unpublished data) [15, 16].

The concept of the AOP, which originated in 1976 [17], entails processes that have the ability to generate elevated concentrations of hydroxyl radicals (OH). Due to its high oxidative and nonselective character, (OH) is a strong oxidant that is capable of complete oxidation of most organic compounds [18]. AOPs are also capable of promoting degradation of pharmaceutical compounds [19] and can inactivate bacteria such as Escherichia coli and the spore-forming bacteria Clostridium perfringens [20, 21].

The most direct method for generating hydroxyl radicals is the breaking of hydrogen peroxide by photolysis (H2O2/UV), as described in The destruction of microorganisms occurs as a function of oxidation of the cell wall and the subsequent cellular damage caused by the hydroxyl radical. This action leads to cell leakage and diffusion of the radical throughout the cell; the radical thus damages enzymes that affect protein synthesis [21, 22]. Few studies investigating the use of AOPs for the inactivation of protozoa in water have been reported [23, 24]. The use of UV photocatalysis/titanium dioxide (TiO2) for the inactivation of Cryptosporidium spp. oocysts has been evaluated [24].

The objective of the present study was to evaluate the efficiency of peroxidation associated with ultraviolet light (H2O2/UV) in reducing the number and fluorescence of G. duodenalis cysts.

2. Material and Methods

2.1. Experimental Method

The experimental system consisted of a reactor designed by Guimarães and Barretto [20] (Figure 1) with a net volume of 190 mL (82 mL min−1). The photoreactors were operated in a one-way ascending passage mode for the three processes: advanced oxidation processing (AOP), peroxidation (H2O2), and photolysis (UV). The UV and peroxidation processes were used as a control to evaluate the synergistic effect of AOP (H2O2/UV).

525719.fig.001
Figure 1: Experimental system: magnetic stirrer, (2) reservoir (1 L), (3) peristaltic pump, and (4) reactor.

All experiments were repeated six times for each process (), and the experimental system was decontaminated after each experiment with an elution solution of hypochlorite and ultrapure water (Milli-Q).

2.2. Samples Evaluated (Synthetic and Surface Water)

The aqueous solution (known as synthetic water) was formulated according to the proceedings of the American Public Health Association [25] using ultrapure water. Surface water was collected from the Atibaia River, which is the source of 95% of the water supply in Campinas (southeastern Brazil); these water samples were collected from the intake pipe in the Campinas water treatment plant of the municipal Society for Water Supply and Sanitation (SANASA). The plastic bottles that were used to obtain water samples were washed with 0.1% Tween 80 prior to collection to avoid the adherence of Giardia spp. cysts, which were naturally present in the water. In all the experiments 1 liter of raw water without artificial inoculation of Giardia spp. was processed. When the samples were positive, this number of cysts was subtracted for calculation of the reduction of organisms by processes.

The samples were transported to the laboratory under refrigeration at 10°C for same-day processing. Both water samples were seeded (under constant stirring) with 103 G. duodenalis cysts that had been purified from fecal samples (A. L. Smith and H. V. Smith 1989 [26]). A hydrogen peroxide concentration of 12 g L−1 [2729] and a UV radiation ( nm) dosage of 5,480 mJ cm−2 were used in the experiments [30, 31]. Six experiments were performed for each of the three processes evaluated. We assessed two kinds of water, totaling 36 experiments.

2.3. Artificial Contamination of Samples with Giardia spp. Cysts

The cysts were taken from feces samples, according to A. L. Smith and H. V. Smith [26], and were diluted in PBS (1 : 9) in order to enumerate and prepare the inoculum. Enumeration was performed using RID, obtaining the number of cysts at 5 μL (triplicate). The reading of these three aliquots was performed by 3 microscopists, without prior knowledge of the result of each count; the average number of Giardia spp. cysts was calculated for all conditions. Both samples of synthetic and superficial water were artificially contaminated with 103 Giardia spp. cysts and submitted the processes studied (H2O2/UV, H2O2, and UV).

2.4. Sample Concentration

One liter of water samples (synthetic and surface) was filtrated by membrane cellulose ester membranes (Merck Millipore) with a diameter of 47 mm and a 3 μm nominal porosity [32]. The filtrate was transferred to Petri dishes. The membranes were then scraped with a soft plastic loop and manually rinsed for 20 minutes with the eluting solution with Tween 80 (0.1%), which is a nonionic detergent that decreases the surface tension of water, allowing for the accommodation of nonpolar functional groups in the aqueous environment. It has been widely used as a component of eluting solutions to enhance protozoa recovery from filters surface. The resulting liquid was concentrated for 10 minutes (1,050 ×g), and the pellet was rinsed with ultrapure water for 10 minutes (1,050 ×g). Aliquots of 5 μL of the two samples were dyed (fluorescein isothiocyanate, FITC), and the G. duodenalis cysts were enumerated using IFA staining followed by epifluorescence microscopy.

2.5. Molecular Identification

Molecular identification of Giardia in the samples was performed by polymerase chain reaction (PCR) of fragments of the Giardia β-giardin gene [33]. Characterization of the genotype of the G. duodenalis cysts that were present in the samples was performed through amplification and sequencing of a fragment of the glutamate dehydrogenate gene (GDH) [34].

2.6. Enumeration and Visualization of G. duodenalis Cysts Using an IFA

The IFA is based on the reaction of anti-Giardia monoclonal antibodies with epitopes on the cyst walls. These antibodies are conjugated to a fluorochrome FITC used with a filter block (excitation 490 nm; emission 510 nm). The fluorochrome generates a predominant bright apple green color on the walls of the organism (Figure 2).

525719.fig.002
Figure 2: Scheme of the immunofluorescence assay (IFA): after AOP modification in epitope: reduction of anti-Giardia mAb-FITC conjugated binding.

However, if the parasite cyst wall is damaged, antibody binding with the surface epitope will be hampered, and staining of the parasite will be reduced or eliminated. The lack of color suggests damage to the cyst wall surface. The IFA was performed with a Merifluor kit (Meridian Bioscience, Cincinnati, Ohio) according to the manufacturer’s instructions, and the observational criteria described by Method 1623.1 of the United States Environmental Protection Agency [35] were used. The lower the recovery efficiency of G. duodenalis cysts, the higher the efficacy of the disinfection process.

2.7. Statistical Methods

The reduction means of the number of cysts were compared using Student’s -test and -test both with .

3. Results and Discussion

3.1. Molecular Identification

Amplification of fragments of the β-giardin gene and the 220-bp fragment of the GDH gene demonstrated the presence of G. duodenalis in the fecal samples from the University of Campinas (UNICAMP) Clinical Hospital.

Although G. duodenalis infects humans, a wide range of species can be found in many other mammals [27]. Based on genetic analysis, G. duodenalis can be considered a complex species, whose members exhibit little variation in their morphology (designated assemblages A to G). The sequencing reaction that was performed for the amplified fragment from the GDH gene, using DNA from a positive sample in this study, confirmed the presence of G. duodenalis assemblage A.

Assemblages A and B are broadly distributed responsible for human infection and are found in a range of mammals; however, the role of animals in the epidemiology of human infection remains unclear, despite the fact that the zoonotic potential of Giardia spp. was recognized by the World Health Organization (WHO) 30 years ago [3].

3.2. Occurrence of Giardia spp. Cysts in Atibaia River Samples

Giardia spp. cysts were detected, with 97.5% of surface water samples with average 7,9 × 105 cysts L−1. Only one sample resulted negative for cysts detection. Giardia spp. are constantly found in Atibaia River; this is because the load of fecal material discharged in this river through domestic effluents is significant [12].

3.3. Reduction in the Number of G. duodenalis Cysts

A reduction in the number of organisms that were initially inoculated, in relation to the number of organisms recovered after the water treatment process is applied, may be considered a measure of the efficiency of the processes [36, 37]. An average of 2.5 × 103 G. duodenalis cysts were inoculated in all experiments. According to the results obtained in this study, AOP treatment was responsible for a greater reduction in G. duodenalis cysts in comparison to chemical or physical processes evaluated alone (Figure 3).

525719.fig.003
Figure 3: Average number (and standard deviation) of G. duodenalis cysts recovered from synthetic and surface water.

As shown in Table 1, AOP resulted in the highest reduction in G. duodenalis cysts counted in every condition tested.

tab1
Table 1: Efficiency (%) of the three processes in reducing the number of G.  duodenalis cysts, for each water type evaluated.

However, for surface water, AOP and UV showed higher efficiency in reducing the number of organisms only when compared with peroxidation (Table 1). When comparing photolysis to AOP, the results presented no statistically significant difference (AOP = UV > H2O2).

Efficiencies for every process were calculated considering inoculum and reductions in cysts count (Table 1).

AOP is capable of degrading organic compounds by promoting chemical modifications of the substrate, which enables their complete mineralization in some cases [38]. Thus, due to the nonselective character of the hydroxyl radical, the organic matter present in water most likely sequesters part of these radicals that were generated by the AOP, which causes a reduction of its action on the G. duodenalis cyst walls.

Three main effects of particulate matter can impact the ability of UV radiation to inactivate G. duodenalis: (a) the number and size of particles, which could cause the dispersion of radiation and the shading of certain areas; (b) the nature of the particles (whether organic or inorganic); and (c) the degree of association between the parasitic stage and the particles, which exerts a protective effect on the pathogenic organisms [3840].

The surface water samples turbidity was from 22 to 34 NTU, with a mean value of 27 NTU. The interference of the particulate matter with the efficiency of UV radiation is complex; all previously described issues can explain the higher efficiency of the AOP when driven in synthetic water and the decrease in efficiency when applied to surface water.

The efficiency in the reduction of cysts in synthetic and surface water achieved by photolysis presented no statistically significant difference.

A wide range of UV doses is reported in related research: 1 mJ cm−2 to 40,000 mJ cm−2 is considered effective in inactivating protozoa [30, 41]; thereby, the evaluation of different doses of radiation is relevant.

Based on research related to protozoan inactivation and considering the high resistance of protozoa to disinfection, a high concentration of hydrogen peroxide was chosen [28, 29, 42]. However, this concentration may have underestimated the efficiency of the AOP in reducing the number of G. duodenalis cysts present in surface water. When excessive H2O2 is present, it may become a significant competitor for the OH radicals and a generator of hydroperoxide radicals (), which have less reactive potential than the OH radicals. These reactions consume the hydroxyl radical, which decreases the oxidation potential of the medium [43]. An optimum concentration of hydrogen peroxide is recommended to improve process efficiency.

3.4. Fluorescence Reduction in G. duodenalis Cysts

In synthetic water, 35,5%, 23,4%, and 55,4% of the cysts exhibited weak fluorescence when using the AOP, peroxidation, and photolysis processes, respectively, suggesting that the sequence of process efficiency damaging the wall of the protozoa is UV > AOP = H2O2 (no statistically significant difference between AOP and H2O2 process was observed).

When surface water was evaluated, AOP was more effective in decreasing the fluorescence of the wall surfaces of G. duodenalis cysts. By using the AOP, peroxidation, and photolysis processes, 98,7%, 62,6%, and 79,7%, respectively, of the G. duodenalis cysts presented weak fluorescence (AOP > UV = H2O2).

During the disinfection process, the destruction of the microorganisms is directly related to disinfectant concentration and time of exposure of the cells to the disinfectant. This damage is caused by reactions that involve intracellular and extracellular biomolecules. Inactivation will occur when vital constituents suffer a certain level of irreversible damage [44].

The ability of hydroxyl radicals to destroy many types of macromolecules, including carbohydrates, nucleic acids, lipids, and amino acids, is very strong. Previous studies of the filamentous walls of Giardia spp. cysts have confirmed the presence of materials such as carbohydrates and protein in a ratio of 3 : 2 (w/w) [45]. The decrease of fluorescence of cysts is an evidence of serious damage to the cysts wall due to hydroxyl radicals (Figures 4(a) and 4(b)).

fig4
Figure 4: G. duodenalis cysts: (a) typical fluorescence (400x) and (b) weak fluorescence (600x).

França [46] also observed a reduction in the number of organisms and a decrease in the fluorescence of G. duodenalis cysts that were submitted to photoelectrochemical treatment for 90 minutes.

The AOP (H2O2/UV) using lower concentration of hydrogen peroxide (15 and 21 mg L−1) and lower dose of UV radiation (44 mJ cm−2) has shown itself as a technology capable of causing damage in Cryptosporidium spp. oocysts and G. duodenalis cysts [47].

Evaluation of the efficiency of the disinfection processes in the environmental samples is a difficult task due to the presence of interfering material dispersed in the medium. AOP was more efficient than peroxidation and photolysis in reducing the number and/or fluorescence of the G. duodenalis cyst wall, suggesting protozoan inactivation. Studies with low concentrations of hydrogen peroxide and a low dose of UV AOP to increase the efficiency of hydroxyl radicals are needed to elucidate the AOP action in resistant forms of protozoa.

4. Conclusion

AOP (H2O2/UV) was effective in reducing the number of cysts of G. duodenalis when they were inoculated in synthetic water and in damaging the wall of cysts when present in surface water with 86,2% and 98,7%, respectively.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors thank FAPESP (no. 2007/57068-5) and CNPq (no. 471487/2007-4) for their financial support of this work.

References

  1. C. L. Moe and R. D. Rheingans, “Global challenges in water, sanitation and health,” Journal of Water and Health, vol. 4, no. 1, pp. 41–58, 2006. View at Publisher · View at Google Scholar · View at Scopus
  2. S. Baldursson and P. Karanis, “Waterborne transmission of protozoan parasites: Review of worldwide outbreaks—an update 2004–2010,” Water Research, vol. 45, no. 20, pp. 6603–6614, 2011. View at Publisher · View at Google Scholar · View at Scopus
  3. H. Sprong, S. M. Cacciò, J. W. van der Giessen, and ZOOPNET network and partners, “Identification of zoonotic genotypes of Giardia duodenalis,” PLoS Neglected Tropical Diseases, vol. 3, no. 12, p. e558, 2009. View at Publisher · View at Google Scholar
  4. M. Machado, A. M. Dinis, L. Salgueiro, J. B. A. Custódio, C. Cavaleiro, and M. C. Sousa, “Anti-Giardia activity of Syzygium aromaticum essential oil and eugenol: effects on growth, viability, adherence and ultrastructure,” Experimental Parasitology, vol. 127, no. 4, pp. 732–739, 2011. View at Publisher · View at Google Scholar · View at Scopus
  5. P. T. Cantey, S. Roy, B. Lee et al., “Study of nonoutbreak giardiasis: novel findings and implications for research,” The American Journal of Medicine, vol. 124, no. 12, pp. 1175.e1–1175.e8, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. R. C. Neto, J. U. Santos, and R. M. B. Franco, “Evaluation of activated sludge treatment and the efficiency of the disinfection of Giardia species cysts and Cryptosporidium oocysts by UV at a sludge treatment plant in Campinas, South-East Brazil,” Water Science and Technology, vol. 54, no. 3, pp. 89–94, 2006. View at Publisher · View at Google Scholar · View at Scopus
  7. A. M. Nasser, D. Vaizel-Ohayon, A. Aharoni, and M. Revhun, “Prevalence and fate of giardia cysts in wastewater treatment plants,” Journal of Applied Microbiology, vol. 113, no. 3, pp. 477–484, 2012. View at Publisher · View at Google Scholar · View at Scopus
  8. L. J. Robertson, L. Hermansen, B. K. Gjerde, E. Strand, J. O. Alvsvåg, and N. Langeland, “Application of genotyping during an extensive outbreak of waterborne giardiasis in Bergen, Norway, during autumn and winter 2004,” Applied and Environmental Microbiology, vol. 72, no. 3, pp. 2212–2217, 2006. View at Publisher · View at Google Scholar
  9. R. C. A. Thompson and P. Monis, “Giardia—from genome to proteome,” Advances in Parasitology, vol. 78, pp. 57–95, 2012. View at Publisher · View at Google Scholar · View at Scopus
  10. “Ministério das Cidades (MC)-Sistema Nacional de Informação sobre Saneamento (SNIS)-Diagnóstico dos Serviços de Água e Esgoto-2011,” 2013.
  11. R. S. Araújo, M. Dropa, L. N. Fernandes et al., “Genotypic characterization of cryptosporidium hominis from water samples in São Paulo, Brazil,” The American Journal of Tropical Medicine and Hygiene, vol. 85, no. 5, pp. 834–838, 2011. View at Publisher · View at Google Scholar · View at Scopus
  12. R. C. Neto, L. U. dos Santos, M. I. Z. Sato, and R. M. B. Franco, “Cryptosporidium spp. and Giardia spp. in surface water supply of Campinas, Southeast Brazil,” Water Science & Technology, vol. 62, no. 1, pp. 217–222, 2010. View at Publisher · View at Google Scholar
  13. A. G. Leal Diego, A. P. Dores Ramos, D. S. Marques Souza et al., “Sanitary quality of edible bivalve mollusks in Southeastern Brazil using an UV based depuration system,” Ocean and Coastal Management, vol. 72, pp. 93–100, 2013. View at Publisher · View at Google Scholar · View at Scopus
  14. L. U. Santos, T. R. Bonatti, R. Cantusio Neto, and R. M. B. Franco, “Occurrence of Giardia cysts and Cryptosporidium oocysts in activated sludge samples in Campinas, SP, Brazil,” Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 46, no. 6, pp. 309–313, 2004. View at Publisher · View at Google Scholar · View at Scopus
  15. J. C. Hayes, M. Garvey, A. M. Fogarty, E. Clifford, and N. J. Rowan, “Inactivation of recalcitrant protozoan oocysts and bacterial endospores in drinking water using high-intensity pulsed UV light irradiation,” Water Science and Technology: Water Supply, vol. 12, no. 4, pp. 513–522, 2012. View at Publisher · View at Google Scholar · View at Scopus
  16. S. Mun, S. H. Cho, T. S. Kim, B. T. Oh, and J. Yoon, “Inactivation of Ascaris eggs in soil by microwave treatment compared to UV and ozone treatment,” Chemosphere, vol. 77, no. 2, pp. 285–290, 2009. View at Publisher · View at Google Scholar · View at Scopus
  17. J. Hoigne and H. Bader, “The role of hydroxyl radical reactions in ozonation processes in aqueous solutions,” Water Research, vol. 10, no. 5, pp. 377–386, 1976. View at Publisher · View at Google Scholar · View at Scopus
  18. M. Sievers, “Advanced oxidation processes,” Treatise on Water Science, vol. 4, pp. 377–408, 2011. View at Google Scholar
  19. C. R. da Silva, M. G. Maniero, S. Rath, and J. R. Guimarães, “Antibacterial activity inhibition after the degradation of flumequine by UV/H2O2,” Journal of Advanced Oxidation Technologies, vol. 14, no. 1, pp. 106–114, 2011. View at Google Scholar · View at Scopus
  20. J. R. Guimarães and A. S. Barretto, “Photocatalytic inactivation of Clostridium perfringens and coliphages in water,” Brazilian Journal of Chemical Engineering, vol. 20, no. 4, pp. 403–411, 2003. View at Google Scholar · View at Scopus
  21. C. P. Rodrigues, R. L. Ziolli, and J. R. Guimarães, “Inactivation of Escherichia coli in water by TiO2-assisted disinfection using solar light,” Journal of the Brazilian Chemical Society, vol. 18, no. 1, pp. 126–134, 2007. View at Publisher · View at Google Scholar · View at Scopus
  22. J. R. Guimarães, J. Ibáñez, M. I. Litter, and R. Pizarro, Eliminación de contaminantes por fotocatálisis heterogénea, Ciemat, Madrid, Spain, 1st edition, 2004.
  23. T. P. Curtis, G. W. Alker, B. M. Dowling, and P. A. Christensen, “Fate of Cryptosporidium oocysts in an immobilised titanium dioxide reactor with electric field enhancement,” Water Research, vol. 36, no. 9, pp. 2410–2413, 2002. View at Publisher · View at Google Scholar · View at Scopus
  24. H. Ryu, D. Gerrity, J. C. Crittenden, and M. Abbaszadegan, “Photocatalytic inactivation of Cryptosporidium parvum with TiO2 and low-pressure ultraviolet irradiation,” Water Research, vol. 42, no. 6-7, pp. 1523–1530, 2008. View at Publisher · View at Google Scholar · View at Scopus
  25. APHA-AWWA-WEF, Standard Methods for the Examination of Water and Wastewater, American Public Health Association, Washington, DC, USA, 20th edition, 1998.
  26. A. L. Smith and H. V. Smith, “A comparison of fluorescein diacetate and propidium iodide staining and in vitro excystation for determining Giardia intestinalis cyst viability,” Parasitology, vol. 99, no. 3, pp. 329–331, 1989. View at Publisher · View at Google Scholar · View at Scopus
  27. S. L. Barbee, D. J. Weber, M. D. Sobsey, and W. A. Rutala, “Inactivation of Cryptosporidium parvum oocyst infectivity by disinfection and sterilization processes,” Gastrointestinal Endoscopy, vol. 49, no. 5, pp. 605–611, 1999. View at Publisher · View at Google Scholar · View at Scopus
  28. F. Hernández, D. Hernández, Z. Zamora et al., “Giardia duodenalis: effects of an ozonized sunflower oil product (Oleozon) on in vitro trophozoites,” Experimental Parasitology, vol. 121, no. 3, pp. 208–212, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. S. C. Weir, N. J. Pokorny, R. A. Carreno, J. T. Trevors, and H. Lee, “Efficacy of common laboratory disinfectants on the infectivity of Cryptosporidium parvum oocysts in cell culture,” Applied and Environmental Microbiology, vol. 68, no. 5, pp. 2576–2579, 2002. View at Publisher · View at Google Scholar · View at Scopus
  30. J. L. Clancy, Z. Bukhari, T. M. Hargy, J. R. Bolton, B. W. Dussert, and M. M. Marshall, “Using UV to inactivate Cryptosporidium,” American Water Works Association, vol. 92, no. 9, pp. 97–104, 2000. View at Google Scholar · View at Scopus
  31. H. Gómez-Couso, M. Fontán-Sainz, K. G. McGuigan, and E. Ares-Mazás, “Effect of the radiation intensity, water turbidity and exposure time on the survival of Cryptosporidium during simulated solar disinfection of drinking water,” Acta Tropica, vol. 112, no. 1, pp. 43–48, 2009. View at Google Scholar
  32. R. M. B. Franco, R. Rocha-Eberhardt, and R. Cantusio Neto, “Occurrence of Cryptosporidium oocysts and Giardia cysts in raw water from the Atibaia river, Campinas, Brazil,” Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 43, no. 2, pp. 109–111, 2001. View at Google Scholar · View at Scopus
  33. M. H. Mahbubani, A. K. Bej, M. H. Perlin, F. W. Schaefer III, W. Jakubowski, and R. M. Atlas, “Differentiation of Giardia duodenalis from other Giardia spp. by using polymerase chain reaction and gene probes,” Journal of Clinical Microbiology, vol. 30, no. 1, pp. 74–78, 1992. View at Google Scholar · View at Scopus
  34. N. Abe, I. Kimata, and M. Iseki, “Identification of genotypes of Giardia intestinalis isolates from dogs in Japan by direct sequencing of the PCR amplified glutamate dehydrogenase gene,” Journal of Veterinary Medical Science, vol. 65, no. 1, pp. 29–33, 2003. View at Publisher · View at Google Scholar · View at Scopus
  35. U.S. Environmental Protection Agency (EPA), Method 1623.1: Cryptosporidium and Giardia in Water by Filtration/IMS/FA, EPA-816-R-12-001, Office of Water. US Environmental Protection Agency, Washington, DC, USA, 2012.
  36. W. A. M. Hijnen, E. F. Beerendonk, and G. J. Medema, “Inactivation credit of UV radiation for viruses, bacteria and protozoan (oo)cysts in water: a review,” Water Research, vol. 40, no. 1, pp. 3–22, 2006. View at Google Scholar
  37. M. Otaki, T. Hirata, and S. Ohgaki, “Aqueous microorganisms inactivation by photocatalytic reaction,” Water Science and Technology, vol. 42, no. 3-4, pp. 103–108, 2000. View at Google Scholar · View at Scopus
  38. X. Doménech, W. F. Jardim, and M. I. Litter, “Procesos avanzados de oxidación para la eliminación de contaminantes,” in Eliminación de Contaminantes por Fotocatálisis Heterogenea, La Plata, X. Doménech, W. F. Jardim, and M. I. Litter, Eds., pp. 3–25, 2001. View at Google Scholar
  39. E. Caron, G. Chevrefils Jr., B. Barbeau, P. Payment, and M. Prevost, “Impact of microparticles on UV disinfection of indigenous aerobic spores,” Water Research, vol. 41, pp. 4546–4556, 2007. View at Publisher · View at Google Scholar
  40. A. Vogelpohl, “Applications of AOPs in wastewater treatment,” Water Science and Technology, vol. 55, no. 12, pp. 207–211, 2007. View at Publisher · View at Google Scholar · View at Scopus
  41. G.-A. Shin, K. G. Linden, and G. Faubert, “Inactivation of Giardia lamblia cysts by polychromatic UV,” Letters in Applied Microbiology, vol. 48, no. 6, pp. 790–792, 2009. View at Publisher · View at Google Scholar · View at Scopus
  42. J. Quilez, C. Sanchez-Acedo, C. Avendaño, E. del Cacho, and F. Lopez-Bernad, “Efficacy of two peroxygen-based disinfectants for inactivation of Cryptosporidium parvum oocysts,” Applied and Environmental Microbiology, vol. 71, no. 5, pp. 2479–2483, 2005. View at Publisher · View at Google Scholar · View at Scopus
  43. Q. Hu, C. Zhang, Z. Wang et al., “Photodegradation of methyl tert-butyl ether (MTBE) by UV/H2O2 and UV/TiO2,” Journal of Hazardous Materials, vol. 154, no. 1–3, pp. 795–803, 2008. View at Publisher · View at Google Scholar · View at Scopus
  44. W. J. Fernando, “Theoretical considerations and modeling of chemical inactivation of microorganisms: inactivation of Giardia Cysts by free chlorine,” Journal of Theoretical Biology, vol. 259, no. 2, pp. 297–303, 2009. View at Publisher · View at Google Scholar · View at MathSciNet · View at Scopus
  45. M. Sökmen, S. Degerli, and A. Aslan, “Photocatalytic disinfection of Giardia intestinalis and Acanthamoeba castellani cysts in water,” Experimental Parasitology, vol. 119, no. 1, pp. 44–48, 2008. View at Publisher · View at Google Scholar
  46. R. B. França, Cryptosporidium spp., Giardia spp. e ovos de helmintos em esgoto hospitalar: destruição e análise do dano estrutural dos protozoários após o processo fotoeletroquímico, Dissertação (Mestrado em Parasitologia) [M.S. thesis], UNICAMP-Universidade Estadual de Campinas, Campinas, Brazil, 2007.
  47. J. R. Guimarães, L. U. Santos, R. M. B. Franco, and R. A. Guadagnini, “Peroxidation and peroxidation assisted by ultraviolet radiation in the inactivation of Giardia duodenalis (Peroxidação e peroxidação assistida por radiação ultravioleta na inativação de cistos de Giardia duodenalis),” Revista Engenharia Sanitária e Ambiental. In press.