Techniques for inactivating Toxoplasma gondii oocysts: a systematic review

Técnicas para inativar oocistos de Toxoplasma gondii: uma revisão sistemática

Abstract

The oocyst, a resistant form of Toxoplasma gondii, plays an important role in the transmission of this protozoan. The objective of this review was to report the methods capable of inactivating oocysts through a systematic review of the literature carried out in the Scientific Electronic Library Online, Web of Science, Science Direct, PubMed and Scopus databases. The keywords searched were (((effects OR infectivity OR resistance) AND Toxoplasma) AND oocyst). We selected 16 articles that described 309 different treatments. Among all the protocols evaluated, 35.60% (110/309) were effective in inactivating oocysts. Physical methods were more effective than other methods (p <0.05). Sporulated oocysts and the T. gondii VEG strain were more resistant (p <0.05) to treatments. Although it is effective against viruses and bacteria, the use of disinfectants in water has little or no effect on T. gondii oocysts. The use of radiation and pressure were effective in inactivating oocysts, as these treatments do not include changes in temperature, they can be used in foods for raw consumption, such as vegetables, as it will not cause substantially changes in their physical and chemical characteristics. Therefore, these methods can be viable alternatives for the control of T. gondii.

Keywords:
Chemical; physical; irradiation; decontamination

Resumo

O oocisto, forma resistente do Toxoplasma gondii, desempenha um papel importante na transmissão desse protozoário. O objetivo desta revisão foi relatar os métodos capazes de inativar oocistos por meio de uma revisão sistemática da literatura realizada nas bases de dados Scientific Electronic Library Online, Web of Science, Science Direct, PubMed e Scopus. As palavras-chave pesquisadas foram (((efeitos OR infectividade OR resistência) AND Toxoplasma) AND oocyst). Foram selecionados 16 artigos que descreveram 309 tratamentos diferentes. Dentre todos os protocolos avaliados, 35,60% (110/309) foram eficazes na inativação de oocistos. Os métodos físicos foram mais eficazes do que outros métodos (p <0,05). Oocistos esporulados e a cepa VEG de T. gondii foram mais resistentes (p <0,05) aos tratamentos. Embora seja eficaz contra vírus e bactérias, o uso de desinfetantes na água tem pouco ou nenhum efeito sobre os oocistos de T. gondii. O uso de radiação e pressão foram eficazes na inativação de oocistos. Como esses tratamentos não incluem mudança de temperatura, podem ser utilizados em alimentos de consumo cru, tais como vegetais, pois não acarretarão substancialmente alterações nas suas características físico-químicas. Portanto, esses métodos podem ser alternativas viáveis ​​para o controle de T. gondii.

Palavras-chave:
Química; física; irradiação; descontaminação

Introduction

Toxoplasma gondii infection occur via transplacental transmission or consumption of contaminated food and water. Ingestion of raw or undercooked meat containing tissue cysts (bradyzoites), dairy products containing tachyzoites, and fruits and vegetables that were in contact with soil contaminated with oocysts (sporozoites) can all transmit this protozoan (Tenter et al., 2000; Dabritz & Conrad, 2010; Pinto-Ferreira et al., 2019).

The parasite has a complex life cycle with an asexual phase that occurs in warm-blooded animals, including felines. However, the sexual phase occurs only in felines, which are the definitive hosts, and results in the excretion of oocysts within 3-7 and over 14 days after ingestion of bradyzoites and tachyzoites, respectively (Frenkel et al., 1970; Dubey & Beattie, 1988; Lafferty, 2006; Dubey, 1997). When infected with the tissue cysts, domestic cats can eliminate up to a billion oocysts within a period of one or two weeks (Dubey & Frenkel, 1972). These oocysts get excreted in the non-sporulated form and need to sporulate to become infectious (Dubey et al., 1970b).

In a study on toxoplasmosis outbreaks, Pinto-Ferreira et al. (2019) suggested that the popularization of freezers and improvements in animal handling and hygiene have substantially reduced the formation and viability of meat cysts. Despite these improvements, serum prevalence of antibodies against T. gondii in humans remains relatively high in most countries, suggesting that water, vegetables, and soil could be important routes of transmission (Cole et al., 2011; Ferreira et al., 2018).

The oocyst is an environmentally resistant stage of the protozoan that plays an important role in the epidemiology of this zoonotic parasite (Tenter et al., 2000; Dumètre et al., 2013). The ability of T. gondii oocysts to survive extremely diverse conditions is conferred by its cell wall, which is composed of two complex and resistant layers that protect the protozoan until it is ingested by the host (Dumètre et al., 2013). Although methods for inactivating T. gondii are quite effective in other biological stages of the parasite, no specific recommendations have been made for oocysts. However, decontaminating of drinking water and fresh food that may be carrying oocysts requires greater attention (AWWA, 1999) because the wall of the infectious agent acts as a primary barrier to physical and chemical attacks (Dumètre et al., 2013). The objective of this systematic review was to determine the major techniques used to inactivate T. gondii oocysts.

Materials and Methods

The Scientific Electronic Library Online (SciELO), Web of Science, Science Direct, PubMed, and Scopus databases were used to carry out this systematic review. The keywords used were (((effects OR infectivity OR resistance) AND Toxoplasma) AND oocyst). Two researchers independently collected data in 2019. The main question that we addressed in this review was: what is the most efficient method to inactivate T. gondii oocysts in water and vegetables?

English and Portuguese research articles that mentioned techniques to inactivate T. gondii oocysts in the abstract were included. Articles with inactivation of other biological forms, such as cysts and tachyzoites, were excluded, as well as, only studies that evaluated effectiveness through bioassay in mice were selected. Were considered effective only the protocols that inactivated the oocysts, sporulated or not, to the point of not leading any inoculated mice to death. From each study, the following data were extracted: type of treatment (chemical or physical), number of oocysts inoculated, temperature, concentration of chemical of physical agent, strain of the protozoan, time of exposure, and effectiveness of the protocol. The software program Mendeley (Elsevier, Amsterdam, Netherlands) was used to organize, delete, and research articles.

Microsoft Excel (Microsoft, Redmond, WA, USA) was used to tabulate the different variables and the efficacy of the treatments found in the selected papers. Epi Info 7.2.3.1 (CDC (Centers for Disease Control and Prevention), Atlanta, Georgia, USA) was used to generate data for the frequency tables and bivariate analysis. Only variables with p-values less than 0.20, as determined via Chi-square test or Fisher’s exact test, were included in the logistic regression models. Simple and multiple logistic regression modeling was performed using R Studio 1.2.5033 in the R 3.6.2 environment (R Foundation for Statistical Computing, 2013). Only variables with p-values less than 0.05 were considered statistically significant. The degree of correlation was assessed via the odds ratio (OR) calculation with a 95% confidence interval (CI).

We performed multiple correspondence analysis with the FactoMineR package (http://factominer.free.fr). This technique does not rely on statistical tests and provides visualization of the most relevant relationships in a large set of variables (Lebart et al., 1984).

Results

After searching the search bases with the keywords (((effects OR infectivity OR resistance) AND Toxoplasma) AND oocyst), 625 articles in total were found in the following (the number of articles from each database is given in parentheses): SciELO (1), Web of Science (110), PubMed (117), Science Direct (198), and Scopus (199). Incomplete or duplicate articles, those with missing titles, authors, or abstracts, and those with themes not related to the objective of the study were excluded. For the analysis of the treatment methods, we selected 16 articles, which described 309 different treatments for inactivating T. gondii oocysts.

Of the treatment methods analyzed, 23.62% (73/309) were chemical treatments whereas the remaining 76.38% (236/309) were physical treatments. Physical methods were further divided into temperature-based (63.55%; 150/236), radiation-based (33.05%; 78/236), and pressure-based treatments (3,38%; 8/236) (Table 1). In 83.50% (258/309) of the protocols, sporulated oocysts were treated whereas in the remaining 16.50% (51/309) protocols, non-sporulated oocysts were treated.

Table 1
Frequencies of different physicists and chemicals methods used for the inactivation of Toxoplasma gondii oocysts reported in the literature, 1973-2019.

	Techniques analyzed % (n/N)	Most used techniques	%
		Heating	20.06%
		Ultraviolet	19.74%
		Cooling	14.89%
		Freezing	5.83%
		Irradiation gamma	5.50%
Physical	76.38% (236/309)	Thermal shock	5.18%
		Room temperature	2.59%
		Pressure	2.59%
		Alcohol	6.80%
		Acid	3.24%
		NaCl	3.24%
		Antibiotic	2.91%
Chemicals	23.62% (73/309)	Phenol	2.27%
		Formaldehyde	2.27%
		Base	1.60%
		Antiseptic	0.97%
		Aldehyde	0.32%

• (n/N): n: sample number and N: population number.

We observed that 35.60% (110/309) of the evaluated protocols were effective, among which 85.45% (94/110) employed physical methods and 14.55% (16/110) utilized chemical methods. Of the 110 protocols, we selected those that exhibited rapid effects at low doses in sporulated and non-sporulated oocysts, described in Tables 2 and 3.

Table 2
Treatments against sporulated oocysts of Toxoplasma gondii that were effective with short durations of exposure at low doses, 1973-2019.

Author	Year	Chemical Treatment	Concentration	Time
Ito et al. (1975a)	1975	Ammonium Sulfide PA	HDP	1 h
		Methanol PA	HDP	12 h
		Ethanol 99%	99%	24 h
		Sulfa and Pyrimetramine	1%	3 h
		Ammonium hydroxide	10%	30 min
		Peracetic acid	5%	48 h
		N-Propyl alcohol	HDP	48 h
		Neo Kurehasol (m-Cresol)	1%	48 h
		Formalin	10%	96 h
Lindsay & Dubey (2009)	2009	Salinity	15ppt NaCl	2 years
Physical Thermal
Author	Year	Treatment	Temperature (°C)	Time
Kuticic & Wikerhauser (1996)	1996	Freezing	-20	21 days
Frenkel & Dubey (1973)	1973	Freezing	-21	28 days
Dubey (1998)	1998	Heating	30	107 days
			35	16 days
			40	28 days
			45	3 days
Ito et al. (1975b)	1975	Heating	50	30 min
Dubey (1998)	1998	Heating	55	1 min
Kuticic & Wikerhauser (1996)	1996	Heating	58	15
Dubey (1998)	1998	Heating	60	1 min
Dubey (1998)			65	1 min
			70	1 min
Ito et al. (1975b)		Heating	80	1 min
			90	30 seg
Physical Treatment
Author	Year	Irradiation	Concentration	Time
Dubey et al. (1996a); Lacombe et al. (2017)	1996	Irradiation α	0.20kGy	UR
Ware et al. (2010)	2010	UV continued	10 mj/cm2	UR
Dumètre et al. (2008)	2008	UV continued	20 mJ/cm-2	15 min
Physical Treatment
Author	Year	Pressure	Concentration	Time
Lindsay et al. (2005)	2005	Pressure	400 Mpa	1 min

• HDP= High degree of purity; UR= unreported.

Table 3
Treatments against non-sporulated oocysts of Toxoplasma gondii that were effective with short durations of exposure at low doses, 1973-2019.

CHEMICAL TREATMENTS
Author	Year	Treatments	Concentration	Time
Ito et al. (1975a)	1975	Sulfa and Pyrimetramine	1%	10 min
		Sulfa and Pyrimetramine	5%	5 min
		m-Cresol	1%	120 min
THERMAL TREATMENTS
Author	Year	Treatments	Temperature (°C)	Time
Frenkel & Dubey (1973)	1973	Freezing	-6	14 days
		Freezing	-21	1 day
		Thermal shock	-21 e T° environment	1 day
Ito et al. (1975a)	1975	Heating	37	48 h
			45	60 min
			50	2,5 min
			55	30 sec
			60	10 sec
			70	10 sec

We observed statistically significant correlations between several characteristics of the protocols and their effectiveness from simple logistic regression analysis (Table 4). However, none of the multiple regression models were significant.

Table 4
Results of the simple logistic regression analysis showing the effects of different variables on the effectiveness of inactivation techniques for oocysts of Toxoplasma gondii, 1973-2019.

Variable	n/N	%	p-Wald	OR	(CI 95%)
Method Type
Chemicals	16/73	21.92		1.00
Physicists	94/236	39.83	0.006	2.35	(1.29-4.44)
Physicists Treatment
Room temperature*	0/8	0.00
Cooling	1/45	2.17		1.00
Heating	37/62	59.68	<0.0001	66.60	(8.61-515.02)
Thermal shock	4/16	25.00	0.200	15.00	(1.53-143.93)
Freezing	7/18	38.89	0.003	28.64	(3.18-257.54)
Pressure	4/8	50.00	0.002	45.00	(4.01-505.11)
Gamma irradiation	5/17	29.41	0.010	18.75	(2.00-176.02)
Ultraviolet	36/61	59.02	<0.0001	64.80	(8.37-501.45)
Irradiation Treatment
Dose of oocysts
1 to 100	15/18	83.33		1.00
101 to 1000	7/12	58.33	0.14	0.28	(0.05-1.57)
1001 to 5000	1/9	11.11	0.003	0.03	(0.00-0.28)
5001 to 10000	9/14	64.29	0.226	0.23	(0.07-1.88)
More of 10000	9/25	36.00	0.004	0.11	(0.03-0.50)
Treatment
Gamma irradiation	5/17	29.41		1.00
Ultraviolet	36/61	59.02	0.036	3.46	(1.08-11.04)
Heat treatment
Temperature
-21° to 0°C	11/35	31.43		1.00
1 to 20°C*	0/41	0.00
21°C to 40°C	5/26	19.23	0.288	0.52	(0.16-1.74)
41°C to 90°C	33/48	68.75	0.001	4.80	(1.88-12.28)
Chemical Treatment
Oocyst
Sporulated	12/67	17.91		1.00
No Sporulated	4/6	66.67	0.016	9.20	(1.5-55.9)

• (n/N): n: sample number and N: population number.
• ^*
  Logistic regression was performed without this category.
• CI: Confidence interval.
• OR: Odds ratio.

Comparisons of the two main groups of protocols (chemical and physical) for inactivating T. gondii oocysts revealed that physical methods were 2.35 times more likely than chemical methods to inactivate oocysts (Table 4).

Protocols that involved heat were most effective (p < 0.0001), having a 66.6-fold greater likelihood of inactivating T. gondii oocysts than those that used refrigeration (95% CI = 8.61-515.02). The protocols that used ultraviolet (UV) light (p < 0.0001; OR = 64.8), pressure (p = 0.002; OR = 45.00), freezing (p = 0.003; OR = 28.64), and irradiation (p = 0.010; OR = 18.75) were also effective as treatments (Table 4).

Among the physical methods of irradiation, the protocols that used UV radiation were 3.46 times more likely to inactivate T. gondii oocysts (p = 0.036; 95% CI = 1.08-11.04) when compared to the techniques that used gamma irradiation. When the numbers of oocysts that were used in these studies was considered as a variable, we found that the protocols that treated numbers of oocysts ranging from 1 to 100 were more effective than those performed on numbers ranging from 1,001 to 5,000 (p = 0.003) and those on numbers of more than 10,000 oocysts (p = 0.004) (Table 4). When different genotypes of T. gondii were compared, the genotype III (46.00%; 23/50) was more difficult to inactivate than genotype I (64.29%; 18/28), however there was no statistical significance.

Among the temperature-based treatments that were analyzed, those with temperatures between 41 °C and 90 °C were 4.8 times more likely to inactivate T. gondii oocysts than those that used temperatures between −21 °C and 0 °C (Table 4). When the maturity of oocysts was examined as a factor in the success of the treatment, we found that only 17.91% of the treatments on sporulated oocysts were effective. In contrast, treatment of non-sporulated oocysts was 9.20 times more likely to result in inactivation (p = 0.016; 95% CI = 1.50-55.90) ​​(Table 4).

Discussion

Boiling of milk and cooking and salting of meat are effective techniques for inactivating tachyzoites and bradyzoites, respectively, what makes these foods potentially safer. The consumption of raw vegetables and drinking water containing T. gondii oocysts, in turn, tends to be the main cause of human toxoplasmosis outbreaks worldwide (Pinto-Ferreira et al., 2019) due to the high resistance of the biological form oocyst; no specific recommendations or methods currently exist to limit these routes of transmission. It is noteworthy that both sporulated and non-sporulated oocysts are significant for this study, since by preventing them from sporulating, they do not become infectious (Navarro et al., 1992; Dubey, 2004). After an ordered search, 16 articles that described 309 treatments against oocysts were selected, of which only 35.60% (110/309) were effective. These results were consistent with expectations, as studies indicate that oocysts are difficult to destroy using conventional methods (Dubey et al., 1970a; Dubey, 2004). The parasite naturally encounters harmful environmental conditions, such as variations in humidity, salinity, temperature, solar radiation, and exposure to disinfectants (VanWormer et al., 2013); however, they remain infectious for months or years. This resistance is attributed to the ability of the cell walls of oocysts and sporocysts to largely retain their integrity, despite exposure to chemical and physical stressors (Freppel et al., 2018).

Heat treatment

The protocols that used heat were more effective. Oocysts exposed to 45 °C for 60 minutes, 50 °C for 2.5 minutes, 55 °C for 30 seconds, or 60-70 °C for 10 seconds did not become unviable. However, higher temperatures for longer durations were necessary to inactivate sporulated oocysts. For example, only 50 °C for 30 minutes, 55-60 °C for 15 minutes, 70 °C for 2 minutes, 80 °C for 1 minute, and 90 °C for 30 seconds were effective for this purpose. Hence, upon evaluating all previous studies utilizing heat treatments (Ito et al., 1975b; Kuticic & Wikerhauser, 1996; Dubey, 1998), we may conclude that protocols that used temperatures between 41 °C and 90 °C were 4.8 times more likely to inactivate T. gondii oocysts when compared to techniques that used temperatures between −21 °C and 0 °C. However, the use of high temperatures is not recommended for treating vegetables meant for raw consumption because they are perishable and extremely sensitive to heat.

Frenkel & Dubey (1973) showed that the use of low temperature is an important technique for inactivating oocysts, although adequate time is essential for efficiency. Their study showed that non-sporulated oocysts are much more sensitive to inactivation techniques. When maintained at −21 °C, non-sporulated oocysts were inactivated on day 1, while sporulated oocysts were inactivated only on day 28, and continued to elicit the production of antibodies. Further studies should be carried out to clarify the use of this technique and its real efficiency on oocysts before it is indicated as a food decontamination strategy.

Chemical treatment

Ito et al. (1975a) described various treatments with disinfectants, alcohols, and chemicals. In this study, sporulated oocysts were subjected to treatment with 99% ethanol for 48 hours, 99% methanol for 12 hours, 1% cresol for 48 hours, 10% and 28% liquid ammonia for 30 minutes, and 10% formalin solution for 96 hours. The protocols that used longer exposure times to the chemicals proved to be more effective. However, none of these treatments can be used for the decontamination of water and food, due to the large volume of chemicals required, the long durations of treatment, and the presence of residues.

Physical methods

As T. gondii oocysts are resistant to most chemical disinfectants, irradiation could be an effective method of destroying them in contaminated vegetables and fruits (Dubey et al., 1996a, 1998; Ware et al., 2010; Lacombe et al., 2017). Some previous studies with tachyzoites have shown that, in addition to killing the parasite, radiation can induce the production of antibodies in mice (Seah & Hucal, 1975). The use of UV radiation was also effective in rendering oocysts unviable; moreover, this technique produces less byproducts when compared to chlorination and ozonation (von Gunten, 2003; Wainwright et al., 2007; Dumètre et al., 2008). When evaluating studies that used this technique (Dumètre et al., 2008; Ware et al., 2010), a non-linear sensitivity of oocysts to UV radiation was observed. This may be associated with the ability of the cell walls of oocysts and autofluorescent sporocysts to protect themselves from UV radiation (Lindquist et al., 2003) by using the energy absorbed from UV radiation for their autofluorescence. Although Dumètre et al. (2008) did find 4 log reduction of oocyst infectivity 40 mJ UV treatment, one mouse still got infected when inoculated with 50.000 oocysts, demonstrating a limitation of treatment.

Lacombe et al. (2017) demonstrated that gamma irradiation considerably reduces the viability of T. gondii in blueberries when a minimum dose of 0.2 kGy was used. Other studies have also suggested that gamma radiation can be a successful intervention against the parasite (Dubey et al., 1998) because the high energy of the radiation breaks the chemical bonds in the molecules necessary for their growth and integrity, thus preventing their replication (Dubey et al., 1990). Moreover, low doses of gamma irradiation do not degrade the fruit or negatively affect its texture and color.

High pressure is commercially used to eliminate pathogens in a variety of food products (Flick, 2003). Lindsay et al. (2005) tested whether this method could be used to inactivate T. gondii in raspberries and found that 340 MPa pressure for 60 seconds was sufficient to render the oocysts, present in raspberries, non-infectious for rats. This method should be further explored for treating raw vegetables due to its numerous advantages in terms of increasing their shelf life and maintaining their freshness, flavor, texture, and color (Tewari & Juneja, 2007).

Oocysts and strains of T. gondii

Among the studies that we analyzed, protocols that treated contaminations of 1 to 100 oocysts were more efficient in inactivating oocysts than those that treated higher numbers of oocysts. Such a situation may be associated with the parasite's capacity for infectivity, because when using larger amounts of oocysts, the greater the probability that at least one or more oocysts will be able to infect. However, techniques for decontamination must be efficient regardless of the number of oocysts, as studies have shown that one T. gondii oocyst is sufficient to infect animals (Dubey, 1996; Dubey et al., 1996b).

The existence of three main strains of T. gondii, Type I, II, and III, which differ in their virulence and epidemiology (Sibley & Boothroyd, 1992; AWWA, 1999; Lindsay et al., 2005), has been described in the literature. The VEG strain (Type III) was isolated from the blood of an individual with acquired immunodeficiency syndrome in 1989 and continues to be widely used in scientific studies, because it is a strain that produces large amounts of oocysts in experimental conditions (Dubey, 1998). When we compare the results of the selected articles relating inactivation and genotypes, the VEG strain was found to be more resistant to treatments than genotype I. Proteomics studies have demonstrated similarities in the molecules of the cell walls of genotypes II and III and suggested that the effect of genotype on its environmental resistance is negligible (Fritz et al., 2012; Possenti et al., 2013; Shapiro et al., 2019). However, Zhou et al. (2017) identified differences in protein expression between oocysts derived from an atypical strain and those derived from the Type II strain. Therefore, further studies are needed with different genotypes of oocysts, keeping all other variables constant to determine the association of the genotype with environmental resistance.

Excreted oocysts become infectious after sporulation, a process that results in the formation of two sporocysts, each with four sporozoites (Dubey et al., 1970b; Frenkel et al., 1970). In the present study, we observed that the environmental resistance of T. gondii oocysts is dependent on its maturity, such that the inactivation methodologies are more effective when used on the non-sporulated oocysts. Previous studies corroborate these findings and report that this greater resistance may be due to the additional presence of the sporocyst wall, which serves as a second level of protection (Dumètre et al., 2008; Fritz et al., 2012; Dumètre et al., 2013). Although oocysts have their own defense mechanisms against external stresses, it is known that the oocyst and sporocyst walls are the structures that provide chemical and mechanical protection to them (Dubey, 2004; Dumètre et al., 2013; Freppel et al., 2018). Finding a strategy to destroy this wall is the key to controlling T. gondii infections in humans and animals.

Comparison between treatments

Between the two main groups of treatments, physical treatments were more likely to inactivate oocysts, whereas oocysts were resistant to most chemical inactivation agents. These results may reflect the poor public health in places where supply systems use only chemical disinfectants such as chlorine. For example, many restaurants only use chlorinated aqueous solutions for decontamination of vegetables, without the concomitant use of filtered water (Jones & Dubey, 2010). T. gondii has been isolated from samples of chlorinated drinking water, suggesting that this reagent has no action on the parasite, as it is not capable of permeating or disturbing the oocyst wall (Moura et al., 2006; Dumètre et al., 2013). Diluted solutions of household bleach can destroy the outer wall of the oocyst, but do not markedly alter the structure, mechanics, or permeability of the sporocyst wall or the inner wall of the oocyst. Therefore, exposure to bleach does not affect the infectivity of the sporozoite, but it can make oocysts more adherent than untreated cells (Dumètre et al., 2013). This adherent nature favors the aggregation of oocysts, concentrating them, and increasing the vulnerability of the host (Freppel et al., 2018). Ozone is another chemical that may be more efficient as a disinfectant than chlorine, as it oxidizes organic and inorganic compounds. However, in addition to the formation of undesirable byproducts such as bromate (von Gunten, 2003), ozone use may not be very effective because T. gondii oocysts have a high degree of resistance to it (Dumètre et al., 2008).

The tolerance of oocysts to environmental stressors, including salinity, may be attributed to the robustness, molecular contents, and lack of permeability of the oocyst walls (Shapiro et al., 2019). Lindsay & Dubey (2009) demonstrated that oocysts can survive in seawater (15 ppt of NaCl) at 4 °C for up to two year, and still undergo sporulation in that environment and remain infectious (Lindsay et al., 2003). Thus, techniques with the use of salt, prove to be inefficient for the inactivation of oocysts.

Conclusion

The use of sanitizers in water, although effective against viruses and bacteria, has little or no action on T. gondii oocysts. Heat treatments have been shown to be fast-acting and effective. Their use in treating low volumes of water can be effective for inactivating the parasite. However, despite their effectiveness, heat treatments cause undesirable organoleptic changes in vegetables and therefore, they must be limited to vegetables that need to be cooked prior to consumption.

Among the other methodologies used, treatments with radiation and pressure were effective. Moreover, they do not substantially alter the physicochemical characteristics of food or adversely affect food quality. Thus, such treatments may be viable alternatives for controlling T. gondii and other parasites in vegetables. However, further studies are required before such treatments are used on these foods.

• How to cite: Pinto-Ferreira F, Paschoal ATP, Pasquali AKS, Bernardes JC, Caldart ET, Freire RL, et al. Techniques for inactivating Toxoplasma gondii oocysts: a systematic review. Braz J Vet Parasitol 2021; 30(2): e026420. https://doi.org/10.1590/S1984-29612021040

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Publication Dates

• Publication in this collection
  28 May 2021
• Date of issue
  2021

History

• Received
  09 Dec 2020
• Accepted
  31 Mar 2021