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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682

Rev. Soc. Bras. Med. Trop. vol.44 no.3 Uberaba May/June 2011 Epub July 01, 2011

http://dx.doi.org/10.1590/S0037-86822011005000040 

Seroepidemiological study of human cysticercosis with blood samples collected on filter paper, in Lages, State of Santa Catarina, Brazil, 2004-2005

 

Estudo soroepidemiológico da cisticercose humana com amostras de sangue total coletado em papel filtro, em Lages, Estado de Santa Catarina, 2004-2005

 

 

Maria Márcia Imenes IshidaI; Marília Sirianni dos Santos AlmeidaII; Noeli Maria EspíndolaIII; Alberto IhaIII; Diana Ana PereiraI; Jean Gabriel de SouzaI; Theopi Rados VarvakisI; Adelaide José VazIII

IDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de Santa Catarina, Florianópolis, SC
IILaboratório Experimental de Esquistossomose, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, RJ
IIIDepartamento de Análises Clínicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo, SP

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ABSTRACT

INTRODUCTION: Human serofrequency of antibodies against Taenia solium antigens was determined and risk factors for cysticercosis transmission were identified.
METHODS: Individuals (n=878) from periurban and rural locations of Lages, SC, were interviewed to gather demographic, sanitary and health information. Interviews and blood sample collections by finger prick on Whatman filter paper were performed from August 2004 to May 2005. Observation determined that 850 samples were suitable for analysis and were tested by ELISA using vesicular fluid of Taenia crassiceps heterologous antigen. To ensure the reliability of the results, 77 samples of the dried blood were matched with sera. The reactive samples were submitted to a serum confirmatory immunoblot (IB) test using purified Taenia crassiceps glycoproteins.
RESULTS: The ELISA results for the dried blood and serum samples were statistically consistent. ELISA was positive in 186 (21.9%) out of 850 individuals. A group of 213 individuals were asked to collect vein blood for IB (186 with positive result in ELISA and 27 with inappropriate whole blood samples) and 130 attended the request. The IB was positive in 29 (3.4%) out of 850 individuals. A significant correlation (p = 0.0364) was determined among individuals who tested positive in the IB assay who practiced both pig rearing and kitchen gardening.
CONCLUSIONS: ELISA with dried blood eluted from filter paper was suitable for cysticercosis population surveys. In Lages, human infection was associated with pig rearing and kitchen gardening. The prevalence index was compatible with other Latin American endemic areas.

Keywords: Cysticercosis. Taenia crassiceps. Immunodiagnosis. Epidemiology.


RESUMO

INTRODUÇÃO: O primeiro levantamento sobre cisticercose humana e identificação dos fatores de risco associados à transmissão, foram realizados em Lages, SC.
MÉTODOS: Oitocentos e setenta e sete voluntários de regiões periurbana e rural foram entrevistados e forneceram informações demográficas e condições sanitárias e de saúde. Amostras de sangue foram coletadas por meio de punção digital em papel filtro entre agosto 2004 e maio 2005. Verificou-se que 850 amostras estavam adequadas para análise. No ELISA, utilizou-se o antígeno heterólogo liquido vesicular de Taenia crassiceps. Para assegurar a confiabilidade dos resultados de ELISA, foram pareadas 77 amostras de soro e sangue eluido do papel filtro. A confirmação do diagnóstico sorológico foi feita por immunoblot (IB) com glicoproteínas purificadas de Taenia crassiceps.
RESULTADOS: A reatividade de IgG eluída de sangue em papel filtro mostrou-se compatível com a dos soros correspondentes. A triagem por ELISA de 850 indivíduos revelou 186 (21,9%) positivos. De 213 pessoas convidadas a colher soro para IB (186 ELISA positivo e 27 com amostras de sangue total inadequadas), compareceram 130. O IB foi positivo em 29 (3,4%) de 850 amostras. Houve correlação significativa entre IB positivo e a prática de criação de suínos e de horta caseira (p = 0,0364).
CONCLUSÕES: ELISA com sangue total em papel filtro mostrou-se adequado para inquéritos populacionais para cisticercose. A transmissão da cisticercose humana na área estudada mostrou correlação com criação suína domestica e horta caseira. A prevalência obtida foi semelhante à relatada em áreas endêmicas da América Latina.

Palavras-chaves: Cisticercose. Taenia crassiceps. Imunodiagnóstico. Epidemiologia.


 

 

INTRODUCTION

Serology is an appropriate screening technique for identifying possible carriers of specific parasitic infections. Although the first report of an immunodiagnosis method for cysticercosis was presented by the Brazilian researcher Arthur Moses in 19111, Brazil still lacks well defined human prevalence figures for cysticercosis, although the Ministry of Health made it compulsory to report cases after 19962.

Human cysticercosis is prevalent in many developing countries and is reemerging in societies where human migration is intense3. Despite the worldwide distribution of this parasite, the prevalence of neurocysticercosis (NC) is rarely higher than 10% and the number of symptomatic NC cases is even lower4,5.

Difficulties related to acquiring expensive equipment for diagnosis, such as computed tomography (CT) scanners, inhibit current knowledge of the real prevalence of the disease in some Brazilian states6. Immunological assays for the detection of specific Taenia solium cysticercus antibodies are a valuable tool when used together with brain imaging exams7-9. However, false-negative results can be obtained in the enzyme-linked immunosorbent assay (ELISA) with serum or cerebrospinal fluid (CSF) from proven NC patients, as well as false-positive results due to cross-reactivity with other parasites8,10. The currently accepted gold standard antibody-based diagnostic assay was developed by the Centers for Disease Control and Prevention (CDC), Atlanta, USA11,12. The enzyme-linked immunoelectrotransfer blot (EITB) test, which uses seven purified glycoproteins as antigens13, is highly sensitive and specific for the detection of active multiple lesions but, conversely, the sensitivity for detecting single and calcified lesions is low11,12,14. All of the components of these diagnosis antigens have been previously characterized, expressed and cloned, eliminating the need for parasite material as a source of antigens15,16. Attempts to adapt these antigens to the ELISA rather than the EITB format, to make it less work intensive and suitable for use in large scale screening assays, have resulted in a considerable reduction in specificity17.

Some authors have demonstrated that larvae from Taenia solium and Taenia crassiceps (laboratory strain) share antigenic components18,19, such as the 18 and 14kDa fractions from which have been considered specific for the immunodiagnosis of NC20.

This paper reports the use of purified 18/14kDa proteins obtained by immunoaffinity chromatography, which provided good performance and high specificity for serum samples21.

Studies concerning neurocysticercosis have been conducted on epileptic patients10,22,23. Ishida et al10 reported the first correlation between tomography exam results and a serological survey on epileptic neurocysticercosis patients conducted in the State of Santa Catarina, indicating the good features of ELISA and the immunoblot assay in discriminating active lesions from inactive (calcified) lesions.

In ELISA, blood serum is generally used to detect antibodies. Using microquantities of whole blood as specimens is more practical for large scale studies in seroepidemiological surveys with regard to preservation, storage and costs24- 26.

The aims of this study were to assess the frequency of cysticercosis in a population from the State of Santa Catarina by ELISA, using Taenia crassiceps vesicular fluid as antigen and dried blood on filter paper as source of anti-cysticercus antibodies, in association with confirmatory immunoblot serum test, using 18-14kDa fractions from Taenia crassiceps cysticercus and establish an association between infection and sociodemographic and environmental factors.

 

METHODS

Study site

This study was conducted in the rural and periurban areas of Lages, a town in the State of Santa Catarina (SC), Brazil (27º48'S; 50º20'W) located around 200km southeast of the State capital Florianópolis, in southern Brazil. The main economic activity of the region is livestock production on small farms and other types of farming. The annual temperature varies from 7.4 to 35ºC with an annual mean of 15ºC. The subtropical climate has one rainy season from May to December and the average annual rainfall is 120mm. The total population of the municipality is 162,000.

This region has been identified as important in terms of cysticercosis23 and, as with many other towns and cities in Brazil, it has inadequate sanitary and socioeconomic conditions that can facilitate the transmission of Taenia solium through open air defecation, fecal contamination of the environmental, rustic pig rearing methods, poor person hygiene and dietary habits and pork consumption without proper inspection by the authorities.

Study subjects

The population studied was a total of 877 individuals belonging to 580 families from eight locations in the rural area and 29 districts in the periurban area, located around the center of the town. In the periurban areas, the survey was conducted door to door by our staff, always accompanied by a community health worker from the Family Health Program of the Health Ministry. The rural inhabitants were interviewed at community health centers during their visits. All individuals in the study were interviewed using a questionnaire. Demographic information concerning age, sex, education and occupation were collected, together with any history of teniasis/cysticercosis and personal hygiene habits. A family questionnaire was applied to each household with questions relating to pig-rearing, the origin of vegetables consumed, sanitation facilities in the home, among other information. The data were collected from August 2004 to May 2005.

Terms of free, informed consent were signed by all participant subjects or from parents or legal guardians of minors or individuals with mental illness. The exam results were sent to the Family Health Program Office. Individuals identified as immunoreactive for cysticercosis were advised to inform their local health service in a subsequent visit.

Samples

All 877 (594 females and 283 males) interviewees provided a blood sample collected on Whatman filter paper-3 (0.5cm x 1cm) by finger prick until each strip was completely soaked with blood on both sides. The Whatman filter paper samples were air dried at room temperature, labeled, sealed in airtight packets and stored at -20ºC until use. For elution, the specimens were cut out and antibodies were eluted by soaking the samples in 240µl of PBS for 24h at 4ºC. Since 27 samples were determined as inappropriate, these volunteers, along with those who were ELISA positive, were invited to attend to a health center to collect vein blood for a confirmatory immunoblot.

Of these, 130 individuals responded to the invitation and blood samples were obtained by vein puncture collected in sterile screw-capped bottles. The samples were allowed to clot at room temperature and the serum was then separated, labeled and stored in a deep freezer (-20ºC) until testing (herein referred to as the classical method). A group of 77 individuals were tested for both sources of antibody by ELISA, serum and whole blood, in order to verify the agreement between the results.

Control samples: six serum samples from patients with NC confirmed by imaging exams (CT and/or MRI) and serological assays (ELISA and IB), obtained from the Immunology Laboratory of the Department of Clinical Analyses of São Paulo University (Laboratório de Imunologia, Departamento de Analises Clinicas, Universidade de São Paulo) serum collection, were used as a positive control group. Twenty six serum samples from blood donors collected from Hemotherapy Service of the University Hospital of the Federal University of Santa Catarina (Universidade Federal de Santa Catarina, UFSC), Brazil, were used as a negative control group.

All samples were examined at the Microbiology and Parasitology Department of the UFSC, Brazil.

Antigens

Cysts of the Ontario Research Foundation (ORF), Canada, strain of Taenia crassiceps were obtained from the peritoneal cavity of experimental infected Balb/C mice, as described by Vaz et al27. Vesicular fluid of the Taenia crassiceps antigen (Tcra-vf) was produced according to the method described by Espíndola et al19. The 18-and 14-kDa proteins from Taenia crassiceps cysticerci (18/14-Tcra) were purified by immunoaffinity chromatography using a sepharose column coupled with monoclonal antibody anti-Taenia crassiceps, as described by Espíndola et al21.

Enzyme-linked immunosorbent assay

ELISA was performed with 850 total blood samples and 77 matched sera, according to previously standardized protocols with Tcra-vf18. Each well of the plates was coated with 10µg/ml of Tcra-vf antigen. The sera samples and whole blood were diluted 1:100 and 1:2.5, respectively, in a 1% skim milk saline solution containing 0.05% Tween 20®. Conjugate peroxidase-labeled sheep anti-human immunoglobulin G was used at titers 1:5,000 for both sera and total blood sample and chromogen substrate ortho-phenylenediamine and H2O2 in citrate buffer (pH 5.0). The reaction was read with a plate spectrophotometer at 492nm. The cutoff value for the ELISA-Tcra-vf was determined with sera from 6 proven NC patients (positive controls) and from 68 healthy individuals (negative controls) following the same ELISA serum protocol18. Each plaque assay was performed with the inclusion of one positive and one negative serum sample as controls, from the same group of samples used in the standardization. The results were expressed as the ratio between the optical density (OD) of the sample and the cutoff value. Ratio values > 1 were considered as positive.

In order to compare the results obtained for the filter paper-eluted blood with those obtained for the serum samples, a dilution factor for the filter paper samples was defined based on the volume of blood soaked in the delimited paper area26,28.

Immunoblot assay

The 18/14-Tcra antigen obtained by elution from the immunoaffinity chromatography with specific monoclonal antibodies was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)29. Then (3µg/mm) was solubilized with sample buffer (0.01M Tris-HCl, pH 6.8, containing 2% SDS, 5% 2-mercaptoethanol, and 10% glycerol) at 100ºC for 5min and separated electrophoretically on 15% polyacrylamide gel. The separated antigen was transferred to a 0.22-µm-pore size membrane of polyvinylidene difluoride (Millipore Corp., Bedford, Mass). The membrane was blocked by treatment with 5% skim milk in PBS for 2h, washed in PBS containing 0.05% Tween 20, and then incubated for 18h at 4ºC with serum in 1:50, in 1% skim milk in PBS. Following further washes, the strips were incubated for 1h with goat anti-human immunoglobulin G (IgG)-biotin/avidin peroxidase (Sigma) conjugate (1:3,000). Following additional washes, the antigen-antibody complexes were obtained by incubation with an appropriate substrate: 4-chloro-1-naphthol (Sigma) predissolved in methanol (20% of the volume) and then diluted to 0.05% with Tris-buffered saline (0.01 M Tris, 0.15 M NaCl, pH 7.4) containing 0.06% H2O2 (for the peroxidase conjugate).

Statistical analysis

The Kappa coefficient (k) was calculated to evaluate the agreement between the ELISA results for the serum and whole blood30.

The Chi square test with significance set at p < 0.05 and metaanalysis were used in order to verify the correlation between the immunological test results and risk factors31.

The results of the seroepidemiological studies focusing on cysticercosis were sent to the health authorities of the municipality, in order to contribute to the collection of information on endemicity and on risk factors for transmission.

Ethical considerations

Ethical approval for the study was granted by the Research Ethics Committee of UFSC, Brazil, under protocol no. 211/03.

 

RESULTS

Data obtained from 877 questionnaires answered orally provided a demographic profile of this population regarding age, sex, residential location, education and information related to the epidemiology of teniasis/cysticercosis in the area, as shown on Table 1.

 

 

The results for ELISA using whole blood were in agreement with those using serum samples (k= 0.73) up to one year after collection. A total of 850 samples of whole blood collected in filter paper were able to be analyzed by ELISA using Tcra-vf as antigens and positive reactions were obtained in 186 (21.9%) individuals. A total of 213 volunteers were asked to collect blood samples for use in the immunoblot assay (IB) confirmatory assay (186 positive for ELISA and 27 whose initial sample was considered inappropriate). The IB test was performed on 130 samples collected from people who showed up to provide a blood sample and 29 presented a positive reaction. Considering that these individuals are putative holders of cysticerci, analysis of their socioeconomic profiles was conducted in an attempt to relate infection with known factors that predispose human populations to cysticercosis.

The prevalence encountered in the population of Lages (SC) was 3.4%, since the immunoblot confirmatory test was positive in 29 samples out of 850 tested individuals. A significant correlation was determined among individuals tested positive by IB who practice both pig rearing and kitchen gardening (p = 0.0364).

 

DISCUSSION

The use of filter paper proved to be an appropriate option for field work where no facilities to collect vein blood or to obtain serum from whole blood are available. The data obtained were in agreement with results reported by Peralta et al26 and Fleury et al25, and thus epidemiological studies on cysticercosis can be successfully conducted using this method.

The results obtained using immunoglobulin G (IgG) eluted from dried blood were consistent with most of the IgG concentrations in the corresponding serum samples. The overall prevalence of 3.4% encountered in this population is compatible with reports from other seroepidemiological surveys conducted in Brazil32.

Bragazza et al20 reported a serum prevalence of 2.1% for cysticercosis in individuals from a rural population in the State of São Paulo, associated with the consumption of untreated water. Prestes-Carneiro et al33 verified a frequency of 0.6% of anti-Taenia solium cysticerci, confirmed by the immunoblot method, in a rural settlement in the State of São Paulo. According to the authors, the index was considered low and was a consequence of continued investment in public health care and private institutions to improve the infrastructure services and education.

In this study, pig rearing and kitchen gardening were determined as risk factors associated with Taenia solium infection in the population studied (p = 0.0364). The highest prevalence (65% of the confirmatory IB) was verified in the areas known as Rancho de Tábuas and Tributo, a rural and periurban area, respectively. Rancho de Tábuas is an area where pigs are reared for domestic consumption and the transmission of Tania solium to pigs requires access to human feces and human consumption of improperly cooked pork. These conditions are still very common in the developing world.

More than 80% of the population of Lages lives in urban areas, which account for only 10% of the area of the municipality34. This intense urbanization results in crowded areas around the town center with poor sanitation and precarious housing and is commonly associated with low education and economic levels of the inhabitants. Tributo is a locality with the conditions necessary for the maintenance of teniasis/cysticercosis transmission. Its population lives on the border between the urban and rural areas, maintaining some rural habits, such as domestic rearing of a small number of pigs in the backyard fed with leftover food and often in free contact with domestic sewage.

This study was conducted by visiting houses or at community health centers during the day, when most men are at work and women, mostly housewives, are at home taking care of children. This explains the higher frequency of women in the population sample.

The findings provided data which will be useful to the authorities when planning interventions in routine healthcare practices and, more importantly, in preventive healthcare practices. Moreover, it was suggested that the positive results obtained in this study were registered in the medical records of each participant to improve medical care in cases of the appearance of related symptoms.

In conclusion, the local seroprevalence of cysticercosis verified among volunteers from rural and periurban areas of Lages, SC, was similar to that reported in others studies in Latin America. Among all the risk factors analyzed, pig rearing and kitchen garden were positively associated with cysticercosis markers.

 

ACKNOWLEDGMENTS

The authors would like to thank all the health professionals who contributed directly or indirectly to collecting data, in particular to the Health Authorities and Community Health Agents of the town of Lages.

 

CONFLICT OF INTEREST

The authors declare that there is no conflict of interest.

 

FINANCIAL SUPPORT

This work was supported by the Fundação de Amparo à Pesquisa no Estado de Santa Catarina, project # 4663/2004

 

REFERENCES

1. Moses A. Dos métodos biolójicos de diagnóstico nas cisticercozes. Mem Inst Oswaldo Cruz 1911; 3:322-326.         [ Links ]

2. Fundação Nacional de Saúde. Projeto para controle do complexo teníase/cisticercose no Brasil. Brasília: Ministério da Saúde; 1996.         [ Links ]

3. Fleury A, Morales J, Bobes RJ, Dumas M, Yánez O, Piña J, et al. An epidemiological study of familial neurocysticercosis in an endemic Mexican community. Trans Royal Soc Trop Med Hyg 2006; 100:551-558.         [ Links ]

4. Cruz ME, Schantz PM, Cruz I, Espinosa P, Preux PM, Cruz A, et al. Epilepsy and neurocysticercosis in an Andean community. Int J Epidemiol 1999; 28:799-803.         [ Links ]

5. Fleury A, Gómez T, Alvarez I, Meza D, Huerta M, Chavaria A, et al. High prevalence of calcified silent neurocysticercosis in a rural village of México. Neuroepidemiology 2003; 22:139-145.         [ Links ]

6. Agapejev S. Clinical and epidemiological aspects of neurocysticercosis in Brazil: a critical approach. Arq Neuro-Psiquiatr 2003; 61:822-828.         [ Links ]

7. Garcia HH, Herrera G, Gilman RH, Tsang VCW, Pilcher JB, Diaz JF, et al. Discrepancies between cerebral computed tomography and western blot in the diagnosis of neurocysticercosis. The Cysticercosis Working Group in Peru (Clinical Studies Coordination Board). Am J Trop Med Hyg 1994; 50:152-157.         [ Links ]

8. Sciutto E, Fragoso G, Fleury A, Laclette JP, Sotelo J, Aluja A, et al. Taenia solium disease in humans and pigs: an ancient parasitosis disease rooted in developing countries and emerging as a major health problem of global dimensions. Microbes Infect 2000; 2:1875-1890.         [ Links ]

9. Bueno EC, Scheel CM, Vaz AJ, Machado LR, Livramento JA, Takayanagui OM, et al. Application of synthetic 8-kD and recombinant GP50 antigens in the diagnosis of neurocysticercosis by enzyme-linked immunosorbent assay. Am J Trop Med Hyg 2005; 72:278-283.         [ Links ]

10. Ishida MM, Peralta RH, Livramento JA, Hoshino-Shimizu S, Peralta JM, Vaz AJ. Serodiagnosis of neurocysticercosis in patients with epileptic seizure using ELISA and immunoblot assay. Rev Inst Med Trop S Paulo 2006; 48:343-346.         [ Links ]

11. Bern C, Garcia HH, Evans C, Gonzalez AE, Verastegui M, Tsang VCW, et al. Magnitude of the disease burden from neurocysticercosis in a developing country. Clin Infect Dis 1999; 29:1203-1209.         [ Links ]

12. Wilson M, Bryan RT, Fried JA, Ware DA, Schantz PA, Pilcher JB, et al. Clinical evaluation of the cysticercosis enzyme-linked immunoelectrotransfer blot in patients with neurocysticercosis. J Infect Dis 1991; 164:1007-1009.         [ Links ]

13. Tsang VCW, Brand JA, Boyer AE. An enzyme-linked immunoelectrotransfer blot assay and glycoprotein antigens for diagnosing human cysticercosis (Taenia solium). J Infect Dis 1989; 159:50-59.         [ Links ]

14. Flisser A, Gyorkos TW. Contribution of immunodiagnostic tests to epidemiological/intervention studies of cysticercosis/taeniosis in México. Parasite Immunol 2007; 29:637-649.         [ Links ]

15. Greene RM, Hancock K, Wilkins PP, Tsang VCW. Taenia solium: molecular cloning and serologic evaluation of 14- and 18-kDa related, diagnostic antigens. J Parasitol 2000; 86:1001-1007.         [ Links ]

16. Hancock K, Khan A, Williams FB, Yushak ML, Pattabhi S, Noh J, et al. Characterization of the 8-kilodalton Antigens of Taenia solium Metacestodes and Evaluation of Their Use in an Enzyme-Linked Immunosorbent Assay for Serodiagnosis. J Clin Microbiol 2003; 41:2577-2586.         [ Links ]

17. Hancock K, Pattabhi S, Whitfield FW, Yushak ML, Lane WS, Garcia HH, et al. Characterization and cloning of T24, a Taenia solium antigen diagnostic for cysticercosis. Mol Bioch Parasitol 2006; 147:109-117.         [ Links ]

18. Bueno EC, Vaz AJ, Machado LR, Livramento JA, Mielle SR. Specific Taenia crassiceps and Taenia solium antigenic peptides for neurocysticercosis immunodiagnosis using serum samples. J Clin Microbiol 2000; 38:146-151.         [ Links ]

19. Espíndola NM, Vaz AJ, Pardini AX, Fernandes I. Excretory/secretory antigens (ES) from in-vitro cultures of Taenia crassiceps cysticerci, and use of an anti-ES monoclonal antibody for antigen detection in samples of cerebrospinal fluid from patients with neurocysticercosis. Ann Trop Med Parasitol 2002; 96:361-368.         [ Links ]

20. Bragazza LM, Vaz AJ, Passos ADC, Takayanagui OM, Nakamura PM, Espíndola NM, et al. Frequency of serum anti-cysticercus antibodies in the population of a rural brazilian community (Cássia dos Coqueiros, SP) determined by ELISA and immunoblotting using Taenia crassiceps antigens. Rev Inst Med Trop S Paulo 2002; 44:7-12.         [ Links ]

21. Espíndola NM, Iha AH, Fernandes I, Takayanagui OM, Machado LR, Livramento JA. Cysticercosis immunodiagnosis using 18- and 14- kilodalton proteins from Taenia crassiceps cysticercus antigens obtained by immunoaffinity chromatography. J Clin Microbiol 2005; 4:3178-3184.         [ Links ]

22. Trevisol-Bittencourt PC, Silva NC, Figueiredo R. Neurocisticercose em pacientes internados por epilepsia no Hospital Regional de Chapecó, região oeste do Estado de Santa Catarina. Arq Neuropsiquiatr 1998; 56:53-58.         [ Links ]

23. Pfuetzenreiter MR, Avila-Pires FD. Clinical manifestations in patients with computerized tomography diagnosis of neurocysticercosis. Arq Neuropsiquiatr 1999; 57:653-658.         [ Links ]

24. Jafri HS, Torrico F, Noh JC, Bryan RT, Balderrama F, Pilcher JB, et al. Application of the enzyme-linked immunoelectrotransfer blot to filter paper blood spots to estimate seroprevalence of cysticercosis in Bolivia. Am J Trop Med Hyg 1998; 58:313-315.         [ Links ]

25. Fleury A, Bouteille B, Garcia E, Marquez C, Preux PM, Escobedo F, et al. Neurocysticercosis: validity of ELISA after storage of whole blood and cerebrospinal fluid on paper. Trop Med Intern Health 2001; 6:688-693.         [ Links ]

26. Peralta RHS, Macedo HW, Vaz AJ, Machado LR, Peralta JM. Detection of anti-cysticercus antibodies by ELISA using whole blood collected on filter paper. Trans R Soc Trop Med Hyg 2001; 95:35-36.         [ Links ]

27. Vaz AJ, Nunes CM, Piazza RM, Livramento JA, Da Silva MV, Nakamura PM, et al. Immunoblot with cerebrospinal fluid from patients with neurocysticercosis using antigen from cysticerci of Taenia solium and Taenia crassiceps. Am J Trop Med Hyg 1997; 57:354-357.         [ Links ]

28. Evengard B, Linder E, Lundberg P. Standardization of a filter-paper technique for blood sampling. Ann Trop Med Parasitol 1988; 82:295-303.         [ Links ]

29. Lambin P, Rochu D, Fine JM. A new method for determination of molecular weights of protein by electrophoresis across a sodium dodecyl sulfate (SDS)-polyacrylamide gradient gel. Anal Biochem 1976; 74:567-575.         [ Links ]

30. Ayres M, Ayres Jr M, Ayres DL Santos AS. Bio Estat 5.0 Aplicações Estatísticas nas Áreas das Ciências Biológicas e Médicas, Belém: Sociedade Civil Mamirauá. Conselho Nacional de Desenvolvimento Científico e Tecnológico; 2007.         [ Links ]

31. Nist Sematech. e-Handbook of Statistical Methods [Internet]. 2010 - [cited 2010 April 25th]. Available from: http://www.itl.nist.gov/div898/handbook/.         [ Links ]

32. Prestes-Carneiro LE, Freitas SBZ, Zago SCS, Miguel NA, Primo OB, Iha AH, et al. Taeniosis-cysticercosis complex in individuals of a peasants' settlement (Teodoro Sampaio, Pontal of Paranapanema, SP, Brazil). Mem Inst Oswaldo Cruz 2005; 101:1-6.         [ Links ]

33. Prestes-Carneiro LE, Souza DHP, Moreno GC, Troiani C, Santarém V, Zago SCS, et al. Toxocariasis/cysticercosis seroprevalence in a long-term rural settlement, São Paulo, Brazil. Parasitology 2009; 136:681-689.         [ Links ]

34. City of Lages, State of Santa Catarina. Official website [Internet]. Lages (SC): Lages Cityhall; 2009. [cited 2009 Sep 16th]. Available from: http://www.lages.sc.gov.br/perfil.php/.         [ Links ]

 

 

Address to:
Dr Maria Márcia Imenes Ishida.
Deptº MIP/UFSC. Campus Universitário, Trindade
88040-900 Florianópolis, SC, Brasil
Phone: 55 48 3721-5209
e-mail: imenes@ccb.ufsc.br

Received in 18/10/2010
Accepted in 07/02/2011