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Revista de Salud Animal

Print version ISSN 0253-570XOn-line version ISSN 2224-4700

Rev Salud Anim. vol.37 no.1 La Habana Jan.-Apr. 2015

 

ORIGINAL ARTICLE

 

Detection of a high prevalence of antibodies against Toxoplasma gondii in cattle in Northern and Midwestern Brazil

Detección de alta prevalencia de anticuerpos contra Toxoplasma gondii en bovinos del Norte y Medio Oeste de Brasil

 

 

Jenevaldo Barbosa da SilvaI, Gustavo Nunes de Santana CastroII, Priscilla Nunes dos SantosII, Adivaldo Henrique da FonsecaII, Danillo Henrique da Silva LimaIII, Henrique dos Anjos BomjardimIII, Alessandra dos Santos Belo ReisIII, Susiane de Oliveira SoaresIII, José Diomedes BarbosaIII

ILaboratório de Imunoparasitologia, Departamento de Patologia Veterinária, Faculdade de Ciências Agrárias e Veterinárias FCAV-UNESP, Via de Acesso Prof. Paulo Donato Castellane s/n, 14884-900, Jaboticabal, SP, Brazil. E-mail: jenevaldo@hotmail.com.
II
Laboratório de Doenças Parasitárias, Departamento de Epidemiologia e Saúde Pública, Universidade Federal Rural de Rio de Janeiro (UFRRJ), Br 465, Km 7, 23890-000, Seropédica, RJ, Brazil. E-mail: adivaldo@ufrrj.br.
IIIInstituto de Medicina Veterinária, Universidade Federal do Pará, Rodovia BR 316 Km 61, Bairro Saudade, 68740-970, Castanhal, PA, Brazil. E-mail: diomedes@ufpa.br.

 

 


ABSTRACT

The aim of this study was to determine the prevalence of Toxoplasma gondii in cattle from the Northern and Midwestern regions of Brazil. Serum samples were collected from 1789 animals and tested by indirect enzyme-linked immunosorbent assay (ELISA). The overall prevalence of T. gondii was 83.40% (1492/1789). The prevalence rates of T. gondii-seropositive animals observed in the states of Pará, Tocantins and, Mato Grosso were 87.45%, 87.79% and 73.06%, respectively. The detection of high prevalence rates of T. gondii in cattle deserves special attention because they are the main source of high biological value protein for humans. This finding indicates the need for further studies on the risk that these animals may pose to public health.

Key words: cattle, ELISA, IFAT, Toxoplasma gondii.


RESUMEN

El objetivo del presente estudio fue determinar la prevalencia de Toxoplasma gondii en bovinos de las regiones del Norte y Medio Oeste de Brasil. Las muestras de suero se colectaron de 1789 animales y se testaron por ELISA. La prevalencia total de T. gondii fue de 83.40% (1492/1789). La proporción de animales seropositivos a T. gondii, observados en los estados de Pará, Tocantins y Mato Grosso, fue de 87.45%, 87.79% y 73.06%, respectivamente. La detección de alta prevalencia a T. gondii en bovinos merece atención especial, porque ellos son la principal fuente biológica de valor proteico para los humanos. Estos hallazgos indican la necesidad de estudios posteriores sobre el riesgo que estos animales pueden significar para la salud pública.

Palabras clave: bovino, ELISA, IFAT, Toxoplasma gondii.


 

 

INTRODUCTION

Toxoplasma gondii, the etiological agent of toxoplasmosis (1), is a protozoan with a heteroxenous life cycle that includes an asexual stage in omnivorous and herbivorous hosts and a sexual stage in carnivorous hosts (2). The infection is normally asymptomatic (3); however, clinical signs such as fever, adenopathy and apathy are observed in immunosuppressed animals (4), and spontaneous abortion is an important detrimental effect in both humans and ruminants.

Toxoplasma gondii is transmitted by the ingestion of oocytes shed in the feces of definitive hosts, or by the ingestion of meat from intermediate hosts containing bradyzoites (4). Serological studies have shown T. gondii infection in several animal species around the world (5-7). Brazil is the largest meat exporter in the world (8) and serological studies for this important zoonosis must be pursued because of the frequent reports on T. gondii circulation in livestock in many regions of the country (9-11). However, there is still a shortage of epidemiological data regarding T. gondii circulation in Brazilian beef cattle.

Beef cattle production in Brazil is distributed across all the states, and the Midwestern and Northern states alone hold approximately 115 million cattle, representing 55% of the entire Brazilian cattle herd (12). Thus, this study was significant given that its goal was to evaluate the seroprevalence of T. gondii in cattle from the states in Northern and Midwestern Brazil.

 

MATERIALS AND METHODS

Animals and areas studied

The evaluated animals were selected in Midwestern and Northern Brazil. All the animals were Nelore cattle (Bos indicus) and of approximately three years of age. They were raised predominantly in an extensive farming system, grazing pasture and receiving supplementation in the feeding trough. The sample size was determined using the Epi-Info software considering a 5% error margin and an infection frequency of 50% in the cattle population of Brazil.

Sampling

For this study, 1879 animals were selected. The samples were collected between January and March 2013. The farms selected were authorized for cattle export. These cattle routinely undergo a rigorous health protocol involving screening for brucellosis (Brucella abortus), tuberculosis (Mycobacterium bovis), leptospirosis (Leptospira spp.) and bovine viral diarrhea (Pestivirus sp).

Blood samples were collected from cattle from 15 towns in the state of Mato Grosso (Tangará, Denise, Nova Marilândia, São Felix do Araguaia, Santa Cruz do Xingu, Castanheira, Primavera do Leste, Brasnorte, Canarana, Espigão do Norte, Campo Novo, Vila Rica, Juína, Luciara and São José do Xingu), 8 towns in the state of Pará (Marabá, Itupiranga, Xinguara, Rio Maria, Água Azul do Norte, Curionópolis, Santa Maria das Barreiras and Bannach) and 14 towns in the state of Tocantins (Miranorte, Bernardo Sayão, Porto Nacional, Santa Fé do Araguaia, Alvorada, Talismã, Bandeirantes do Tocantins, Colinas, Divinópolis do Tocantins, Araguanã, Pium, Miracema, Couto Magalhães and Gurupi). At least three different farms were selected in each town, and at least 20 samples were taken from each farm.

Enzyme-linked immunosorbent assay (ELISA)

The blood of the animals was collected by jugular venipuncture and later centrifuged to obtain the serum. IgG antibodies against T. gondii were detected by ELISA as described by Voller et al. (13).

The anti-Toxoplasma gondii antibodies were searched by ELISA. The ``RH'' strain was used to obtain the antigens as described by Camargo (14). The ELISA test was established using an optimal concentration of the T. gondii antigen (10 µg/ml) in a 0.05 M carbonate/bicarbonate buffer, pH 9.6. The single dilution of the ELISA test was 1: 200 in PBS-Tween (phosphate buffered saline, pH 7.2, and 0.05% Tween 20) for the positive- and negative-reference sera and test sera, and the conjugate serum was used at a 1:25,000 dilution in PBS-Tween, according to the manufacturer's guidelines (Sigma-Aldrich Chemical Company, St. Louis, Missouri, U.S.A.). The plates were read by using an ELISA reader (Dynex-Technologies®, Virginia, U.S.A.) with a 405-nm filter. Under these conditions, the lowest mean optical density (OD) of the negative sera was 0.90±0.013. The highest mean reactivity observed for the positive-reference sera was 1.13±0.065.

Thirty positive and 30 negative controls were used to determine the cut-off, which was calculated based on the sera of negative animals and analyzed using the statistic software MedCalc (version 11.4, http://www.medcalc.be). Serological detection based on ELISA and IFAT test has been proven to provide reliable results with high sensitivity and specificity in detection of T. gondii, particularly when the parasitemia is very low. The tests showed no cross-reaction with any other microorganism.

Statistical analysis

The data were analyzed using the chi-square and Kruskal-Wallis tests with a 95% confidence interval using the R software, version 2.2.1 (R Development Core Team, 2005).

 

RESULTS AND DISCUSSION

Of the 1789 samples evaluated by the ELISA test for T. gondii, 1492 were seropositive, which corresponded to a prevalence of 83.40%. The prevalence rates for T. gondii observed in Pará, Tocantins and Mato Grosso were 87.45%, 87.79% and 73.06%, respectively (Table 1).

All of the farms evaluated had at least one positive animal, and on some farms, 100% of the animals were positive for T. gondii. Thus, considering the farm as an epidemiological unit, the prevalence of T. gondii was 100%. The prevalence of T. gondii was significantly higher (p<0.05) in the states of Pará and Tocantins compared with Mato Grosso.

Several studies have been performed to investigate the serological prevalence of T. gondii in cattle because they are one of the main sources of animal protein consumed by humans around the world (9). A wide variation in the frequency of this agent has been observed in cattle in Brazil (9, 10, 15, 16) and other parts of the world (6, 17).

Recent studies in Brazil have shown both a low (9) and a high (18) prevalence of T. gondii in cattle. However, few studies have been performed in Midwestern and Northern Brazil, where the largest cattle herd for export in the world is found. Because these regions have a herd of 115 million cattle, studies in this area are more than justifiable. The high prevalence of T. gondii in cattle observed in the studied region constitutes a public health issue because this protozoan is capable of causing infection through the ingestion of meat products containing cysts. Our results showed a prevalence value higher than all those other values reported for Brazil.

Garcia et al. (19), Daguer et al. (20) and Santos et al. (18) reported T. gondii prevalences of 25.8%, 41.4% and 17.4%, respectively, for Brazilian cattle. In Southeastern Brazil, Fajardo et al. (9) observed that only 2.68% of animals were positive, while Gondin et al. (21) reported that 1.03% of animals were positive in the Northeastern region of Brazil. However, few studies have been performed in Midwestern and Northern Brazil. A recent study performed in Northern Brazil showed a prevalence of 41.6% for T. gondii-seropositive buffalo (22). Other studies indicated a T. gondii prevalence of 71.0% in cattle from Midwestern Brazil (23).

The prevalence of T. gondii also varies greatly in other parts of the world. A total of 83.3% of the cattle in Spain were diagnosed as positive (6), and 44.8% were positive in Sudan (24); conversely, only 5.7% of the animals in China were seropositive for T. gondii (25). These results demonstrate that the presence of this agent is highly variable, and comprehensive health safety measures are necessary in areas where the prevalence is higher because we still do not know the connection between T. gondii seroprevalence in cattle and the potential infection of other hosts such as humans. Cattle showed a significant serological prevalence of T. gondii using both of the techniques evaluated. These results suggest that cattle, when exposed to the same risks for T. gondii infection, have a high antibody mediated response.

 

CONCLUSIONS

The detection of high prevalence rates of T. gondii in livestock deserves special attention because cattle are the most important source of animal protein for humans. This finding indicates the need for further studies on the risk that such animals may pose to public health.

Conflict of interest statement

None of the authors of this work has a financial or personal relationship with other people or organizations that could inappropriately influence or bias the contents of this paper.

 

ACKNOWLEDGMENTS

We are grateful to the Office of the Dean for Research and Graduate Education of the Federal University of Pará (Pró-Reitoria de Pesquisa e Pós- Graduação da Universidade Federal do Pará - PROPESP/UFPA) for typing the manuscript. This study was supported by Pará State Research Foundation (Fundação de Amparo e Desenvolvimento da Pesquisa do Estado - FADESP). We also thank the Brazilian Federal Agency for the Support and Evaluation of Graduate Education (CAPES) and the National Council for Scientific and Technological Development (CNPq) for financial support.

 

REFERENCES

1. Uggla A. Toxoplasma gondii in farm animals: some immunodiagnostic methods and their potential use. Uppsala: Merkantil-Tryckeriet. 1986; pp. 1-56.

2. Tenter AM, Heckeroth AR, Weiss LM. Toxoplasma gondii: from animals to humans. Int J Parasitol. 2000;30(1):1217-1258.

3. Dubey JP. Toxoplasma, Neospora, Sarcocystis and other tissue cyst-forming coccidia of human and animals. In: Krier, J.P. Parasitic Protozoa. 2nd ed. San Diego: Academic Press.1993:1-157.

4. Black MW, Boothroyd JC. Lytic Cycle of Toxoplasma gondii. Microbiol Mol Biol R. 2000;64(3):607.

5. Dubey JP, Jones JL. Toxoplasma gondii infection in humans and animals in the United States. Int J Parasitol. 2008;38:1257-1278.

6. García-Bocanegra I, Cabezón O, Hernández E, Martínez-Cruz MS, Martínez-Moreno Á, Martínez-Moreno J. Toxoplasma gondii in Ruminants Species (Cattle, Sheep, and Goats) from Southern Spain. J Parasitol. 2013;99(3):438-440.

7. Yang N, Mu MY, Yuan GM, Zhang GX, Li HK, He JB. Seroprevalence of Toxoplasma gondii in slaughtered horses and donkeys in Liaoning province, northeastern China. Parasite Vector. 2013;6:140-143.

8. Ministério da Agricultura, Pecuária e Abastecimento (in Portuguese), http://www.agricultura.gov.br/animal/especies/bovinos-e -bubalinos/. Brasil, 2013.

9. Fajardo HV, D'ávila S, Bastos RR, Cyrino CD, Detoni ML, et al. Seroprevalence and risk factors of toxoplasmosis in cattle from extensive and semi-intensive rearing systems at Zona da Mata, Minas Gerais state, Southern Brazil. Parasite Vector. 2013; 6:191-198.

10.Santos SL, Costa KS, Gondim LQ, Silva MSA, Uzêda RS, et al. Investigation of Neospora caninum, Hammondia sp, and Toxoplasma gondii in tissues from slaughtered beef cattle in Bahia, Brazil. Parasitol Res. 2010;106:457-461.

11.Andrade MMC, Carneiro M, Medeiros AD, Andrade Neto V, Vitor RWA. Seroprevalence and risk factors associated with ovine toxoplasmosis in Northeast Brazil. Parasite. 2013; 20:20-24.

12. Ministério da Agricultura, Pecuária e Abastecimento. Dados de rebanho bovino e bubalino do Brasil (Data pertaining to cattle and buffalo herds in Brazil) (in Portuguese). Brasil, 2012.

13.Voller AD, Bidwell DE, Bartlett A. Microplate immunoassay for the immunodiagnosis of virus infections. Handbook of Clinical Immunology, American Society for Microbiology, Washington, D.C. 1976:506-512.

14. Camargo ME. Improved technique of indirect immunofluorescence for serological diagnosis of toxoplasmosis. Rev Inst Med Trop Saão Paulo. 1974; 6:117-118.

15.Spagnol FH, Paranhos EB, Oliveira LLS, Medeiros SM, Lopes CWG, Albuquerque GR. Prevalência de anticorpos anti-Toxoplasma gondii em bovinos abatidos em matadouros do estado da Bahia, Brasil (Anti-Toxoplasma gondii antibody prevalence in cattle slaughtered in slaughterhouses in the state of Bahia, Brazil). Rev Bras Parasitol Vet. 2009;18:42-45.

16.Moura AB, Osaki SC, Zulpo DL, Garcia JL, Teixeira EB. Detecção de anticorpos contra Toxoplasma gondii em bovinos de corte abatidos em Guarapuava, PR, Brasil (Anti-Toxoplasma gondii antibody detection in beef cattle slaughtered in Guarapuava, PR, Brazil) (in Portuguese with English abstract). Arch Vet Sci. 2010;15(2):94-99.

17.Inpankaew T, Pinyopanuwut N, Chimnoi W, Kengradomkit C, Sunuta C, Zhang G, et al. Serodiagnosis of Toxoplasma gondii infection in dairy cows in Thailand. Transbound Emerg Dis. 2010;57:42-45.

18.Santos LMJF, Damé MCF, Cademartori BG, Cunha Filho NA, Farias NAR, Ruas J L. Occurrence of antibodies to Toxoplasma gondii in water buffaloes and meat cattle in Rio Grande do Sul State, southern Brazil. Acta Parasitol. 2013;58(3):334-336.

19.Garcia JL, Navarro IT, Ogawa L, Oliveira RC. Soroprevalência do Toxoplasma gondii, em suínos, bovinos, ovinos e equinos, e sua correlação com humanos, felinos e caninos, oriundos de propriedades rurais do norte do Paraná-Brasil (Toxoplasma gondii seroprevalence in pigs, cattle, sheep and horses and its correlation with humans, cats and dogs from rural areas of Northern Paraná, Brazil) (in Portuguese with English abstract). Cienc Rural. 1999;29(1):91-97.

20.Daguer H, Vicente RT, Costa T, Virmond MP, Hamann W, Amendoeira MRR. Soroprevalência de anticorpos anti-Toxoplasma gondii em bovinos e funcionários de matadouro da microrregião de Pato Branco, Paraná, Brasil (Seroprevalence of anti-Toxoplasma gondii antibodies in cattle and slaughterhouse workers in the region of Pato Branco, Paraná, Brazil) (in Portuguese with English abstract). Cienc Rural. 2004;34(4):1133-1137.

21.Gondim LFP, Barbosa JrHV, Ribeiro Filho CHA, Sakei H. Serological survey of antibodies to Toxoplasma gondii in goats, sheep, cattle and water buffaloes in Bahia State, Brazil. Vet Parasitol. 1999; 82:273-276.

22.Silva JB, Fonseca AH, Andrade SJT, Silva AGM, Oliveira CMC, Barbosa JD. Prevalência de anticorpos anti-Toxoplasma gondii em búfalos (Bubalus bubalis) no Estado do Pará (Prevalence of anti-Toxoplasma gondii antibodies in buffalo (Bubalus bubalis) in the state of Pará) (in Portuguese with English abstract). Pesquisa Vet Brasil. 2013;5:581-585.

23.Santos TR, Costa AJ, Toniollo GH, Luvizotto MCR, Benetti AH, et al. Prevalence of anti-Toxoplasma gondii antibodies in dairy cattle, dogs, and humans from the Jauru micro-region, Mato Grosso state, Brazil. Vet Parasitol. 2009;161:324-326.

24.Elfahal AM, Hussien MO, Enan KA, Musa AB, El Hussein AM. Seroprevalence of Toxoplasma gondii in Dairy Cattle with Reproductive Problems in Sudan. Vet Sci. 2013;1:1-4.

25.Zhou DH, Zhao FR, Lu P, Xia HY, Xu MJ, et al. Seroprevalence of Toxoplasma gondii infection in dairy cattle in southern China. Parasite Vector. 2012;5:48-51.

 

 

Recibido: 7-2-2014.
Aceptado: 27-8-2014.

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