Hostname: page-component-7c8c6479df-ws8qp Total loading time: 0 Render date: 2024-03-29T05:01:26.465Z Has data issue: false hasContentIssue false

Risk factors for ocular toxoplasmosis in Brazil

Published online by Cambridge University Press:  18 March 2013

A. I. C. FERREIRA
Affiliation:
Immunogenetics Laboratory, Molecular Biology Department, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil
C. C. BRANDÃO De MATTOS
Affiliation:
Immunogenetics Laboratory, Molecular Biology Department, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil
F. B. FREDERICO
Affiliation:
Outpatient Eye Clinic, Fundação Faculdade Regional de Medicina-Hospital de Base (HB-FUNFARME), São José do Rio Preto, SP, Brazil
C. S. MEIRA
Affiliation:
Parasitology Laboratory, Instituto Adolfo Lutz, São Paulo, SP, Brazil
G. C. ALMEIDA Jr.
Affiliation:
Outpatient Eye Clinic, Fundação Faculdade Regional de Medicina-Hospital de Base (HB-FUNFARME), São José do Rio Preto, SP, Brazil
F. NAKASHIMA
Affiliation:
Immunogenetics Laboratory, Molecular Biology Department, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil
C. R. BERNARDO
Affiliation:
Immunogenetics Laboratory, Molecular Biology Department, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil
V. L. PEREIRA-CHIOCCOLA
Affiliation:
Parasitology Laboratory, Instituto Adolfo Lutz, São Paulo, SP, Brazil
L. C. De MATTOS*
Affiliation:
Immunogenetics Laboratory, Molecular Biology Department, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto, SP, Brazil
*
*Author for correspondence: Professor Dr L. C. de Mattos, Laboratório de Imunogenética, Departamento de Biologia Molecular, Faculdade de Medicina de São José do Rio Preto (FAMERP), Avenida Brigadeiro Faria Lima, 5416, 15090-000– São José do Rio Preto, SP, Brasil. (Email: luiz.carlos@famerp.br)
Rights & Permissions [Opens in a new window]

Summary

The aim of this study was to investigate risk factors for ocular toxoplasmosis (OT) in patients who received medical attention at a public health service. Three hundred and forty-nine consecutive patients, treated in the Outpatient Eye Clinic of Hospital de Base, São José do Rio Preto, São Paulo state, Brazil, were enrolled in this study. After an eye examination, enzyme-linked immunosorbent assay (ELISA) was used to determine anti-Toxoplasma gondii antibodies. The results showed that 25·5% of the patients were seronegative and 74·5% were seropositive for IgG anti-T. gondii antibodies; of these 27·3% had OT and 72·7% had other ocular diseases (OOD). The presence of cats or dogs [odds ratio (OR) 2·22, 95% confidence interval (CI) 1·24–3·98, P = 0·009] and consumption of raw or undercooked meat (OR 1·77, 95% CI 1·05–2·98, P = 0·03) were associated with infection but not with the development of OT. Age (OT 48·2 ± 21·2 years vs. OOD: 69·5 ± 14·7 years, P < 0·0001) and the low level of schooling/literacy (OT vs. OOD: OR 0·414, 95% CI 0·2231–0·7692, P = 0·007) were associated with OT. The presence of dogs and cats as well as eating raw/undercooked meat increases the risk of infection, but is not associated with the development of OT.

Type
Original Papers
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence . The written permission of Cambridge University Press must be obtained for commercial re-use.
Copyright
Copyright © Cambridge University Press 2013

INTRODUCTION

Toxoplasmosis, a disease resulting from infection by the protozoan, Toxoplasma gondii, can be congenital or acquired [Reference Hill and Dubey1]. T. gondii is a versatile parasite for which the prevalence of infection varies between countries, geographical areas and ethnic groups living within a specific region [Reference Tenter, Heckeroth and Weiss2]. In Brazil, infection rates range from 50% to 83% of the population depending on the location of the study [Reference Dubey3]; the high prevalence worldwide is correlated to environmental risk factors and socioeconomic factors [Reference Dubey3, Reference Baldursson and Karanis4].

There are several transmission routes with a large proportion of acquired infections related to the ingestion of cysts in raw or undercooked meat and contact with sporulated oocysts in the environment [Reference Dubey3, Reference Klaren and Kijlstra5].

Manifestations of infection by T. gondii are often subclinical, i.e. asymptomatic, or with non-specific symptoms [Reference Antoniazzi6]. Ocular toxoplasmosis (OT), associated with both congenital and acquired infections, is one of the most common manifestations of the disease [Reference Dubey3, Reference Weiss and Dubey7]. OT is the main cause of posterior uveitis, a disease that can cause serious sequelae including complete loss of vision [Reference Hay and Dutton8].

The prevalence of OT varies in different regions around the world; in Brazil about 30% of patients with eye diseases have OT [Reference Dubey3, Reference Matos9, Reference Arevalo10]. Several studies have investigated risk factors for congenital toxoplasmosis [Reference Spalding11, Reference Barbosa, Holanda and Andrade-Neto12]; however, few studies have evaluated factors related to the occurrence, severity and recurrence of OT.

The aim of this study was to investigate risk factors contributing to infection by T. gondii and to the development of OT in patients who received medical attention in an outpatient eye clinic of a tertiary teaching hospital of a public health service.

MATERIALS AND METHODS

Patient selection

Over a 2-year period (2009–2010), 349 consecutive male and female patients treated in the Outpatient Eye Clinic of Hospital de Base, Fundação Faculdade Regional de Medicina (HB-FUNFARME), a public health service in São José do Rio Preto, São Paulo state, Brazil were enrolled in this study. Each participant signed an informed consent form after receiving details about the objectives of the study and the procedures involved. This study was approved by the Research Ethics Committee of the Medical School in São José do Rio Preto, Brazil (FAMERP; no. 050/2009 dated 9 March 2009).

Epidemiological data

Participants completed a questionnaire on epidemiological data related to T. gondii infection, including social, environmental and economic factors and housing.

Diagnosis of OT

The clinical evaluation of patients was conducted by two experienced physicians (F.B.F. and G.C.A.Jr.), using an indirect binocular ophthalmoscope (Binocular Ophthalmoscope ID10, Topcon Corporation, USA). Subsequently, patients were allocated to either the OT group or the other ocular diseases (OOD) group.

Blood sampling

Serum, obtained for each patient from a peripheral blood sample collected without anticoagulant by venepuncture, was stored at −20°C until use.

Identification of IgG class anti-T. gondii antibodies

After an eye examination, IgG class anti-T. gondii antibodies were investigated by enzyme-linked immunosorbent assay (ELISA) as described previously [Reference Mattos13].

Statistical analysis

The results were analysed using GraphPad version 3.1 software (GraphPad Software Inc., USA). Fisher's exact test, odds ratio (OR) and χ 2 test were used to compare independence between proportions, and ages were compared using Student's t test. Differences were considered statistically significant at P⩽0·05.

RESULTS

The mean age of the 349 patients in this study was 56·9 ± 17·0 years (median 61, minimum 18, maximum 88 years); 187 (53·6%) were male and 16 (46·4%) were female. Ninety-eight percent (n = 342) resided in São Paulo state; 15·5% (n = 53) in São José do Rio Preto and 84·5% (n = 289) in neighbouring towns. Four patients (1·1%) resided in the state of Minas Gerais and three (0·9%) in the state of Mato Grosso do Sul. Based on the data, 73·4% (n = 256) owned a house and only 0·3% (n = 1) lived in wooden shacks.

Table 1 lists the socioeconomic parameters and environmental risk factors of patients who were seronegative and seropositive for IgG anti-T. gondii antibodies.

Table 1. Socioeconomic parameters and environmental risk factors of patients who are seropositive or seronegative for IgG anti-Toxoplasma gondii antibodies in an outpatient eye clinic, São José do Rio Preto, São Paulo state, Brazil*

OR, Odds ratio; CI, confidence interval.

* Univariate analysis; 95% confidence interval, P⩽0·05.

Table 2 shows the socioeconomic parameters and environmental risk factors of seropositive patients with OT and with OOD.

Table 2. Socioeconomic parameters and environmental risk factors of patients seropositive for anti-Toxoplasma gondii IgG antibodies with ocular toxoplasmosis (OT) or other ocular diseases (OOD), in an outpatient eye clinic, São José do Rio Preto, São Paulo state, Brazil*

OR, Odds ratio; CI, confidence interval.

* Univariate analysis; 95% confidence interval, P⩽0·05.

DISCUSSION

This study investigated the risk factors for T. gondii infection and for the development of OT. Several studies have been conducted to ascertain the risk factors contributing to T. gondii infection in pregnant women [Reference Kapperud14Reference Boyer16]; however, there are few studies in outpatient eye clinics that address risk factors, in particular in patients who developed OT.

ELISA was used to detect IgG anti-T. gondii antibodies as recommended, as it is frequently used to determine whether an individual has anti-T. gondii antibodies [Reference Dubey3, Reference Robert-Gangneux and Dardé17].

Patients were examined for the presence of ocular lesions by ophthalmoscopy. The high rate of patients infected by T. gondii in this study is in agreement with the literature reporting that this percentage can be as high as 80% in Brazil [Reference Dubey3], including the region of this study [Reference Gonçalves18Reference Rodrigues20].

The frequency of OT in seropositive patients demonstrates that eye diseases caused by T. gondii are common in individuals with ocular diseases in the study region. Dubey et al. report a lower rate of ocular lesions suggestive of toxoplasmosis than that found in the present study [Reference Dubey3]. Thus the results reported here are not consistent with the findings of Dubey et al., probably due to differences in the sample population and the study region.

Indeed, the prevalence of ocular disease caused by T. gondii in Brazil varies greatly from 1·1% to 27·3% depending on the region but mainly the study population (Table 3). Most research was conducted as population-based studies, whereas in the current study the patients were selected in a referral eye clinic. Similar rates were reported by Gouveia et al. [Reference Gouveia28] in a study at a centre specializing in uveitis care in São Paulo city.

Table 3. Prevalence of ocular disease caused by Toxoplasma gondii in Brazil*

* Adapted from Table Supplement S3 of Dubey et al. [Reference Dubey3], with permission.

The parameters of age, gender, schooling and family income were evaluated in relation to the risk of infection and the development of OT. Comparing the two groups, no statistically significant differences were found between women and men. Aleixo et al. [Reference Aleixo27] found an association between ocular lesions suggestive of toxoplasmosis and women, while Jones et al. [Reference Jones29] reported a higher prevalence of OT in men, possibly due to greater contact with soil on farms and rural settings. These data suggest that the prevalence of OT by gender may be dependent on environmental and biological risk factors that were not present in our population.

No association was found between T. gondii infection and the mean age or the socioeconomic conditions, but the difference in mean age was statistically significant between seropositive patients with OT and those with OOD. Patients with OT had a lower mean age than those with OOD; OT can affect individuals at any stage of life, with 70–90% of cases being due to congenital infections and 2–30% due to infections acquired after birth [Reference Furtado30].

Additional analysis in OT patients showed lower values for the 25th percentile regarding age compared to those with OOD. This observation is consistent with previous reports and suggests that the high incidence of eye disease in congenital toxoplasmosis in Brazil causes patients to seek ophthalmology consultations early [Reference Dubey3, Reference Robert-Gangneux and Dardé17, Reference Abreu23, Reference Joynson and Wreighitt31, Reference Latkany, Weiss and Kim32].

These findings could provide some background for public policies towards maternal fetal and neonatal screening in São Paulo state and postnatal monitoring for the early identification and characterization of toxoplasmosis in children, thereby avoiding later complications and delays in the characterization of OT in children, adolescents and young adults.

In a study conducted in the High-Risk Pregnancy Clinic of Hospital de Base in São José do Rio Preto, the rate of congenital transmission in the region proved to be 2·3% [Reference Mattos33] and the acute infection rate in 556 pregnant women was 3·4% [Reference Gonçalves18].

However, there is no government programme of maternal fetal and neonatal screening in the São Paulo state nor is there postnatal monitoring for the early identification and characterization of toxoplasmosis in children, which complicates and delays the characterization of OT in children, adolescents and young adults.

There was no association between seropositive and seronegative patients and the level of schooling. A lower percentage of OT was observed in those stating that they were illiterate or had few years of schooling. This finding seems paradoxical since less schooling implies greater exposure to risk due to not adopting appropriate measures, such as good hygiene practice, to prevent infection [Reference Varella34]. It would be expected that individuals with a higher level of schooling would have a lower risk of developing OT. It is possible that individuals with better schooling go to eye clinics more frequently and therefore the diagnosis in this group is higher.

The association observed in this study between infection with T. gondii and direct contact with cats and dogs has been reported previously [Reference Barbosa, Holanda and Andrade-Neto12, Reference Lopes35]. This observation is plausible because the cat is the definitive host of the parasite and thus eliminates oocysts in stools, which after maturation, contaminate the environment [Reference Dubey, Lindsay and Speer36]. It is believed that consumption of canine meat may contribute to the spread of the parasite in humans, as has been demonstrated in other diseases [Reference Wertheim37]; however, Brazilians do not have the habit of eating canine meat. However, there is the possibility of contamination due to oocysts in dog fur, as well explained by Frenkel & Parker [Reference Frenkel and Parker38].

It was noted in the current study that infection is strongly associated with the consumption of raw or undercooked meat, a habit believed to be the main infection route of T. gondii. An association was also found in this study, albeit insignificant, between T. gondii infection and regular contact with soil. Direct contact with earth/soil suggests that infection may also occur in this way [Reference Spalding11, Reference Cook39]; and industrialized processed meat and poor hygiene habits also contribute to infection with T. gondii [Reference Bojar and Szymanska40Reference Alvarado-Esquivel42].

No association was found with other factors evaluated and T. gondii infection. No statistically significant differences were observed when environmental risk factors associated with T. gondii infection were analysed in relation to the development of OT. As the risk factors for infection are not associated with OT, it is possible that the risk of developing OT is dependent on the pathogenicity of the infecting strain and/or the immune competence of the host coupled with immunogenetic factors that determine susceptibility. However, these factors are inherent in patients and the parasite requires further study.

In conclusion, the results of this study confirm that the presence of dogs and cats, as well as the consumption of raw or undercooked meat increases the risk of infection, but does not influence the development of OT.

ACKNOWLEDGEMENTS

This study was funded by the Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP (L.C.M., no. 2009/17540-2) (C.S.M., no. 2009/09168-6) (V.L.P.C., no. 2011/13939-8) (F.N. no. 2012/07750-2) (C.R.B., no. 2012/05580-2); Brazilian Ministry of Science, Technology and Inovation–CNPq (L.C.M., no. 473579/2009-0); Brazilian Ministry of Education–CAPES Scholarship (A.I.C.F, C.C.B.M, C.R.B); and BAP-FAMERP (L.C.M).

The authors thank J. P. Dubey and colleagues, for sharing the data in Table 3, previously published in reference [Reference Dubey3]. Thanks are also due to: Dr Lilian Castiglioni (Department of Public Health; FAMERP) for statistical analysis support, and David Hewitt and Jim Henson (AcademicEnglishSolutions.com) for English revision. The authors also thank the Biotechnology Research Institute of Auckland University of Technology, New Zealand, particularly Professor Stephen Henry.

DECLARATION OF INTEREST

None.

References

REFERENCES

1. Hill, D, Dubey, JP. Toxoplasma gondii: transmission, diagnosis and prevention. Clinical Microbiology and Infection 2002; 8: 634640.Google Scholar
2. Tenter, AM, Heckeroth, AR, Weiss, LM. Toxoplasma gondii: from animals to humans. International Journal for Parasitology 2000; 30: 12171258.Google Scholar
3. Dubey, JP, et al. Toxoplasmosis in humans and animals in Brazil: high prevalence, high burden of disease, and epidemiology. Parasitology 2012; 139: 13751424.CrossRefGoogle ScholarPubMed
4. Baldursson, S, Karanis, P. Waterborne transmission of protozoan parasites: review of worldwide outbreaks – an update 2004–2010. Water Research 2011; 45: 66036614.Google Scholar
5. Klaren, VNA, Kijlstra, A. Toxoplasmosis, an overview with emphasis on ocular involvement. Ocular Immunology and Inflammation 2002; 10: 126.Google Scholar
6. Antoniazzi, E, et al. Ocular impaiment of toxoplasmosis. Parassitologia 2008; 50: 3536.Google Scholar
7. Weiss, LM, Dubey, JP. Toxoplasmosis: a history of clinical observations. International Journal for Parasitology 2009; 39: 895901.Google Scholar
8. Hay, J, Dutton, GN. Toxoplasma and the eye. British Medical Journal 1995; 310: 10211022.Google Scholar
9. Matos, K, et al. Correlation between clinical diagnosis and PCR analysis of serum, aqueous, and vitreous samples in patients with inflammatory eye disease. Arquivos Brasileiros de Oftalmologia 2007; 70: 109114.CrossRefGoogle ScholarPubMed
10. Arevalo, JF, et al. Ocular toxoplasmosis in the developing world. International Ophthalmology Clinics 2010; 50: 5769.Google Scholar
11. Spalding, SM, et al. Serological screening and toxoplasmosis exposure factors among pregnant women in South of Brazil. Revista da Sociedade Brasileira de Medicina Tropical 2005; 38: 173177.Google Scholar
12. Barbosa, IR, Holanda, CMCX, Andrade-Neto, VF. Toxoplasmosis screening and risk factors amongst pregnant females in Natal, northeastern Brazil. Transactions of the Royal Society of Tropical Medicine and Hygiene 2009; 103: 377382.Google Scholar
13. Mattos, CCB, et al. Contribution of laboratory methods in diagnosing clinically suspected ocular toxoplasmosis in Brazilian patients. Diagnostic Microbiology and Infectious Disease 2011; 70: 362366.Google Scholar
14. Kapperud, G, et al. Risk factors for Toxoplasma gondii infection in pregnancy. American Journal of Epidemiology 1996; 144: 405412.CrossRefGoogle ScholarPubMed
15. Avelino, MM, et al. Risk factors for Toxoplasma gondii infection in women of childbearing age. Brazilian Journal of Infectious Disease 2004; 8: 164174.CrossRefGoogle ScholarPubMed
16. Boyer, KM, et al. Risk factors for Toxoplasma gondii infection in mothers of infants with congenital toxoplasmosis: implications for prenatal management and screening. American Journal of Obstetrics and Gynecology 2005; 192: 564571.CrossRefGoogle ScholarPubMed
17. Robert-Gangneux, F, Dardé, ML. Epidemiology of and diagnostic strategies for toxoplasmosis. Clinical Microbiology Review 2012; 25: 264.Google Scholar
18. Gonçalves, MAS, et al. Seropositivity rates for toxoplasmosis, rubella, syphilis, cytomegalovirus, hepatitis and HIV among pregnant women receiving care at a Public Health Service, São Paulo State, Brazil. Brazilian Journal of Infectious Disease 2010; 14: 427432.Google Scholar
19. Mattos, CCB, et al. Lack of association between ABO histo-blood groups, secretor and non-secretor phenotypes, and anti-Toxoplasma gondii antibodies among pregnant women from the northwestern region of São Paulo State, Brazil. Archives of Medical Science 2008; 4: 254258.Google Scholar
20. Rodrigues, ACF, et al. Non-association between anti-Toxoplasma gondii antibodies and ABO blood group system. Journal of Venomous Animals and Toxins including Tropical Diseases 2011; 17: 184189.Google Scholar
21. Glasner, PD, et al. An unusually high prevalence of ocular toxoplasmosis in southern Brazil. American Journal of Ophthalmology 1992; 114: 136144.Google Scholar
22. Garcia, JL, et al. Seroprevalence, epidemiology, and ocular evaluation of human toxoplasmosis in a rural area in Jaguapitã, Paraná, Brazil. Revista Panamericana de Salud Pública 1999; 6: 157163.CrossRefGoogle Scholar
23. Abreu, MT, et al. Ocular toxoplasmosis at Venda Nova do Imigrante, ES, Brasil. Arquivos Brasileiros de Oftalmologia 1998; 61: 540545.CrossRefGoogle Scholar
24. Portela, RWD et al. A multihousehold study reveals a positive correlation between age, severity of ocular toxoplasmosis, and levels of glycoinositolphospholipid-specific immunoglobulin A. Journal of Infectious Diseases 2004; 190: 175183.Google Scholar
25. Bahia-Oliveira, LMG, et al. Toxoplasmosis in southeastern Brazil: an alarming situation of highly endemic acquired and congenital infection. In: Petersen, E, Pollak, A, Owona, IR, eds. Recent Trends in Research on Congenital Toxoplasmosis. International Journal for Parasitology 2001; 31: 133136.Google Scholar
26. Amorim, GCA, et al. Socioeconomic conditions as determining factors in the prevalence of systemic and ocular toxoplasmosis in northeastern Brazil. Ophthalmic Epidemiology 2004; 11: 301317.Google Scholar
27. Aleixo, ALQC, et al. Frequency of lesions suggestive of ocular toxoplasmosis among a rural population in the State of Rio de Janeiro. Revista da Sociedade Brasileira de Medicina Tropical 2009; 42: 165169.Google Scholar
28. Gouveia, EB, et al. Causes of uveitis in a tertiary centre in São Paulo city, Brazil. Arquivos Brasileiros Oftalmologia 2004; 67: 139145.Google Scholar
29. Jones, JL, et al. Recently acquired Toxoplasma gondii Infection, Brazil. Emerging Infectious Diseases 2006; 12: 582587.Google Scholar
30. Furtado, JM, et al. Ocular toxoplasmosis I: parasitology, epidemiology and public health. Clinical and Experimental Ophthalmology. Published online 11 July 2012 . doi: 10.1111/j.1442–9071.2012.02821.x Google Scholar
31. Joynson, DHM, Wreighitt, TG. Toxoplasmosis – A Comprehensive Clinical Guide. Cambridge University Press, 2005, pp. 1395.Google Scholar
32. Latkany, P. Ocular disease due to Toxoplasma gondii . In: Weiss, LM, Kim, K, eds. Toxoplasma gondii: The Model Apicomplexan: Perspectives and Methods. Elsevier/Academic Press: Amsterdam, 2007, pp. 117.Google Scholar
33. Mattos, CCB et al. Anti-Toxoplasma gondii antibodies in pregnant women and their newborn infants in the region of São José do Rio Preto, São Paulo, Brazil. Sao Paulo Medical Journal 2011; 129: 261266.CrossRefGoogle Scholar
34. Varella, IS, et al. Seroprevalence of toxoplasmosis in pregnant women. Jornal Pediatria 2003; 79: 6974.Google ScholarPubMed
35. Lopes, FMR, et al. Factors associated with seropositivity for anti-Toxoplasma gondii antibodies in pregnant women of Londrina, Paraná, Brazil. Memórias do Instituto Oswaldo Cruz 2009; 104: 378382.Google Scholar
36. Dubey, JP, Lindsay, DS, Speer, CA. Structures of Toxoplasma gondii tachyzoites, bradyzoites, and sporozoites and biology and development of tissue cysts. Clinical Microbiology Review 1998; 11: 267299.Google Scholar
37. Wertheim, HFL, et al. Furious rabies after an atypical exposure. PLoS Medicine 2009; 6: e1000044.Google Scholar
38. Frenkel, JK, Parker, BB. An apparent role of dogs in the transmission of Toxoplasma gondii: the probable importance of xenosmophilia. Annals of the New York Academy of Science 1996; 791: 402407.CrossRefGoogle ScholarPubMed
39. Cook, AJC, et al. Sources of toxoplasma infection in pregnant women: European multicentre case-control study. British Medical Journal 2000, 321: 142147.Google Scholar
40. Bojar, I, Szymanska, J. Enviromental exposure of pregnant women to infection with Toxoplasma gondii – state of the art. Annals of Agricultural and Environmental Medicine 2010; 17: 209214.Google Scholar
41. Mecca, JN, Meireles, LR, Andrade, HF. Jr. Quality control of Toxoplasma gondii in meat packages: standardization of an ELISA test and its use for detection in rabbit meat cuts. Meat Science 2011; 88: 584589.Google Scholar
42. Alvarado-Esquivel, C, et al. Toxoplasma gondii infection in workers occupationally exposed to raw meat. Occupational Medicine 2011; 61: 265269.Google Scholar
Figure 0

Table 1. Socioeconomic parameters and environmental risk factors of patients who are seropositive or seronegative for IgG anti-Toxoplasma gondii antibodies in an outpatient eye clinic, São José do Rio Preto, São Paulo state, Brazil*

Figure 1

Table 2. Socioeconomic parameters and environmental risk factors of patients seropositive for anti-Toxoplasma gondii IgG antibodies with ocular toxoplasmosis (OT) or other ocular diseases (OOD), in an outpatient eye clinic, São José do Rio Preto, São Paulo state, Brazil*

Figure 2

Table 3. Prevalence of ocular disease caused by Toxoplasma gondii in Brazil*