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Herd-level based seroprevalence and associated factors for Toxoplasma gondii in cows in the state of Paraíba, Northeastern Brazil

Soroprevalência em nível de rebanho e fatores associados para Toxoplasma gondii em vacas no estado da Paraíba, Nordeste do Brasil

Abstract

We aimed to determine the herd and animal levels seroprevalence and associated factors for Toxoplasma gondii infections in cattle from the state of Paraíba, Northeastern Brazil. Herds (n = 434) and cows aged ≥ 24 months (n = 1,895) were randomly selected, and serum samples were tested with the immunofluorescence antibody test (IFAT) using as cutoff of 64. Of the 434 farms investigated, 197 had at least one seropositive cow (prevalence of 49.0%; 95% CI = 44.3%-53.8%), and the prevalence at animal level was 18.0% (95% CI = 5.3%-21.1%). The antibody titers ranged from 64 to 1024, with the most frequent titers being 64 (10.8%) and 128 (3.7%). The risk factors identified were property located in Sertão region (odds ratio [OR] = 3.07), property located in Agreste/Zona da Mata regions (OR = 2.00), animal purchasing (OR = 2.68), herd size of 34-111 animals (OR = 2.91) and herd size > 111 animals (OR = 6.97). The results suggest the wide distribution of T. gondii infections in cattle throughout the state of Paraíba, and the risk factors identified are not possible to correct.

Keywords:
Zoonosis; toxoplasmose; two-stage sample survey; cattle herd; T. gondii infection

Resumo

Objetivou-se determinar a soroprevalência do rebanhos e de animais e os fatores associados à infecção por Toxoplasma gondii em bovinos do estado da Paraíba, Nordeste do Brasil. Rebanhos (n = 434) e vacas com idade ≥ 24 meses (n = 1.895) foram selecionados aleatoriamente, e as amostras de soro foram testadas com o teste de imunofluorescência (RIFI), usando-se como ponto de corte 64. Das 434 fazendas investigadas, 197 tiveram pelo menos uma vaca soropositiva (prevalência de 49%; IC 95% = 44,3%-53,8%), e a prevalência em nível de animais foi de 18% (IC 95% = 5,3%-21,1%). Os títulos de anticorpos variaram de 64 a 1024, sendo os títulos mais frequentes 64 (10,8%) e 128 (3,7%). Os fatores de risco identificados foram na propriedade localizada na região do Sertão ("odds ratio" [OR] = 3,07), na propriedade localizada na região do Agreste/Zona da Mata (OR = 2,00), na compra de animais (OR = 2,68), no tamanho do rebanho de 34-111 animais (OR = 2,91) e no tamanho do rebanho > 111 animais (OR = 6,97). Os resultados sugerem a ampla distribuição de infecções por T. gondii em bovinos em todo o estado da Paraíba, e os fatores de risco identificados não são passíveis de correção.

Palavras-chave:
Zoonose; toxoplasmosis; amostragem em dois estágios; rebanho bovino; infecção por T. gondii

Introduction

Toxoplasmosis is a parasitic zoonosis, caused by the obligate intracellular protozoan Toxoplasma gondii, which is capable of infecting most homeothermic species, including humans, by forming tissue cysts. The infection is generally asymptomatic and does not cause clinical disease in several animal species, but in some, it causes acute life-threatening illness (Smith et al., 2021Smith NC, Goulart C, Hayward JA, Kupz A, Miller CM, van Dooren GG. Control of human toxoplasmosis. Int J Parasitol 2021; 51(2-3): 95-121. http://dx.doi.org/10.1016/j.ijpara.2020.11.001. PMid:33347832.
http://dx.doi.org/10.1016/j.ijpara.2020....
). Humans can become infected mainly by eating undercooked, contaminated meat (especially pork, lamb, and venison) or shellfish (like oysters, clams, and mussels); accidentally ingesting undercooked, contaminated meat or shellfish after handling it and not washing hands thoroughly; eating food that was contaminated by knives, utensils, cutting boards or other foods that had contact with raw, contaminated meat or shellfish; and drinking unpasteurized goat’s milk (Dubey, 2010Dubey JP. Toxoplasmosis of animals and humans. Florida: CRC Press; 2010.; CDC, 2023Centers for Disease Control and Prevention - CDC. Toxoplasmosis: epidemiology & risk factors [online]. 2023 [cited 2023 Feb 22]. Available from: https://www.cdc.gov/parasites/toxoplasmosis/epi.html
https://www.cdc.gov/parasites/toxoplasmo...
).

Felids are important in the life cycle of T. gondii because they are definitive hosts and, therefore, the only ones that can contaminate the environment with oocysts, which after sporulating, become infective, spreading through soil, water and vegetation, and because they are resistant they can survive in humid environments for several months (Dubey et al., 2020Dubey JP, Cerqueira-Cézar CK, Murata FHA, Kwok OCH, Yang YR, Su C. All about toxoplasmosis in cats: the last decade. Vet Parasitol 2020; 283: 109145. http://dx.doi.org/10.1016/j.vetpar.2020.109145. PMid:32645556.
http://dx.doi.org/10.1016/j.vetpar.2020....
). The risk factors associated with T. gondii infection in animals is similar to that in humans, and depends on the type of geographical region, the sanitary conditions and management of the farms, and the animal's diet (origin of the water and food offered). The most common source of infection in animals is through the ingestion of sporulated oocysts, either through food or water. Carnivores are infected most commonly by oral route (more than 80% of cases), through consumption of raw or undercooked meat containing tissue cysts, or vegetables and fruits contaminated with oocysts shed by felids (Jones & Dubey, 2012Jones JL, Dubey JP. Foodborne toxoplasmosis. Clin Infect Dis 2012; 55(6): 845-851. http://dx.doi.org/10.1093/cid/cis508. PMid:22618566.
http://dx.doi.org/10.1093/cid/cis508...
; Hill & Dubey, 2013Hill DE, Dubey JP. Toxoplasma gondii prevalence in farm animals in the United States. Int J Parasitol 2013; 43(2): 107-113. http://dx.doi.org/10.1016/j.ijpara.2012.09.012. PMid:23201235.
http://dx.doi.org/10.1016/j.ijpara.2012....
).

In veterinary medicine, toxoplasmosis represents a serious problem and is considered a major cause of reproductive losses in sheep, goats and pigs (Ferra et al., 2020Ferra B, Holec-Gasior L, Graźlewska W. Toxoplasma gondii recombinant antigens in the serodiagnosis of toxoplasmosis in domestic and farm animals. Animals 2020; 10(8): 1245. http://dx.doi.org/10.3390/ani10081245. PMid:32707821.
http://dx.doi.org/10.3390/ani10081245...
). Although it is considered a poor host for T. gondii, natural and experimental infections in cattle have been reported (Dubey, 2010Dubey JP. Toxoplasmosis of animals and humans. Florida: CRC Press; 2010.; Costa et al., 2011Costa GHN, Costa AJ, Lopes WDZ, Bresciani KDS, Santos TR, Esper CR, et al. Toxoplasma gondii: infection natural congenital in cattle and an experimental inoculation of gestating cows with oocysts. Exp Parasitol 2011; 127(1): 277-281. http://dx.doi.org/10.1016/j.exppara.2010.08.005. PMid:20736009.
http://dx.doi.org/10.1016/j.exppara.2010...
). Vertical transmission should also be considered, since in experimental infection, inoculated pregnant females aborted or gave birth to congenitally infected offspring (without apparent clinical signs), favoring the maintenance of the agent in the herd (Wiengcharoen et al., 2011Wiengcharoen J, Thompson RCA, Nakthong C, Rattanakorn P, Sukthana Y. Transplacental transmission in cattle: is Toxoplasma gondii less potent than Neospora caninum? Parasitol Res 2011; 108(5): 1235-1241. http://dx.doi.org/10.1007/s00436-010-2172-8. PMid:21203773.
http://dx.doi.org/10.1007/s00436-010-217...
).

The Brazilian cattle herd has reached 218.2 million heads and the data from the Brazilian Institute of Geography and Statistics report that by the third quarter of 2021, 20,614,976 million cattle were slaughtered, taking into account establishments under federal, state or municipal health inspection, in which 40,420 of these cattle correspond to the state of Paraíba (IBGE, 2021Instituto Brasileiro de Geografia e Estatística - IBGE. Pesquisa trimestral do abate de animais [online]. 2021 [cited 2023 Jan 13]. Available from: https://sidra.ibge.gov.br/tabela/1092#resultado
https://sidra.ibge.gov.br/tabela/1092#re...
), which shows the importance of this food. Due to the isolation of this protozoan in bovine tissues, the importance of this infection in the epidemiological chain of toxoplasmosis cannot be neglected (Gomes et al., 2020Gomes DFC, Krawczak FS, Oliveira CHS, Ferreira A Jr, Fernandes EKK, Lopes WDZ, et al. Toxoplasma gondii in cattle in Brazil: a review. Rev Bras Parasitol Vet 2020; 29(1): e015719. http://dx.doi.org/10.1590/s1984-29612019106. PMid:32049142.
http://dx.doi.org/10.1590/s1984-29612019...
).

Studies on bovine toxoplasmosis are of utmost importance due to the zoonotic potential. Therefore, the objective of this study was to determine the seroprevalence of toxoplasmosis in cows in the state of Paraíba, Northeastern Brazil, using a planned sampling targeting herds and animals, as well as to identify the risk factors associated with herd-level seroprevalence.

Material and Methods

Characterization of the study area

The study was carried out in Paraíba state, Northeast region of Brazil. The state was stratified according to the operational capacity of the Animal Defense Service of the State of Paraíba (SEDAP) based on the areas of operation of its regional offices to ensure that the agency could perform the field work. It was divided into three sampling groups: sampling stratum 1 (mesoregion of Sertão), sampling stratum 2 (mesoregion of Borborema) and sampling stratum 3 (mesoregions of Zona da Mata and Agreste) (Figure 1).

Figure 1
Division of Paraíba state into three sample strata (Sertão, Borborema, and Agreste/Zona da Mata) and distribution of positive and negative cattle herds for T. gondii infections.

Sampling

The serum samples used in this study were obtained from a bovine brucellosis study in the state of Paraíba, conducted by the National Program for the Control and Eradication of Brucellosis and Tuberculosis (Clementino et al., 2016Clementino IJ, Dias RA, Amaku M, Ferreira F, Telles EO, Heinemann MB, et al. Epidemiological situation of bovine brucellosis in the state of Paraiba, Brazil. Semina: Ciênc Agrár 2016; 37(5): 3403-3412. http://dx.doi.org/10.5433/1679-0359.2016v37n5Supl2p3403.
http://dx.doi.org/10.5433/1679-0359.2016...
), and the sampling design was adjusted for bovine toxoplasmosis. For each sampling stratum, the prevalence of herds and the prevalence of seropositive animals were estimated by two-stage sample survey. In the first stage, a predetermined number of herds (primary sampling units) were randomly selected; in the second stage, a predetermined number of cows aged ≥ 24 months were randomly selected (secondary sampling units).

The selection of the primary sampling units was random (random draw) and was based on the SEDAP farm registers. The number of herds selected per sampling stratum was determined using the formula for simple random sampling (Thrusfield & Christley, 2018Thrusfield M, Christley R. Veterinary epidemiology. Oxford: John Wiley & Sons; 2018. http://dx.doi.org/10.1002/9781118280249.
http://dx.doi.org/10.1002/9781118280249...
). The parameters adopted for the calculation were as follows: confidence level of 95%, estimated prevalence of 71% (Santos et al., 2009Santos TR, Costa AJ, Toniollo GH, Luvizotto MCR, Benetti AH, Santos RR, 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(3-4): 324-326. http://dx.doi.org/10.1016/j.vetpar.2009.01.017. PMid:19232473.
http://dx.doi.org/10.1016/j.vetpar.2009....
) and 5% error. In addition, the operational and financial capacity of SEDAP was taken into account in determining the sample size.

For the secondary units, the minimum number of animals to be examined within each herd was estimated in order to allow their classification as positive. For this, the concept of aggregate sensitivity and specificity was used (Dohoo et al., 2003Dohoo IR, Martin W, Stryhn H. Veterinary epidemiologic research. Charlottetown: Atlantic Veterinary College; 2003.). For the calculations, we adopted 100% for the sensitivity and specificity of the serological test (Sunanta et al., 2009Sunanta C, Inpankaew T, Pinyopanuwat N, Chimnoi W, Kengradomkij C, Arunwipas P, et al. Comparison of diagnostic technique for detection of Toxoplasma gondii infection in dairy cows in Thailand. Witthayasan Kasetsat Witthayasat 2009; 43(5): 48-52.), and 71% for the estimated intra-herd prevalence (Santos et al., 2009Santos TR, Costa AJ, Toniollo GH, Luvizotto MCR, Benetti AH, Santos RR, 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(3-4): 324-326. http://dx.doi.org/10.1016/j.vetpar.2009.01.017. PMid:19232473.
http://dx.doi.org/10.1016/j.vetpar.2009....
). Herdacc version 3 software (Jordan, 1995Jordan D. Herdacc: a program for calculating herd level (aggregate) sensitivity and specificity. Guelph: University of Guelph; 1995.) was used during this process and the sample size was selected so that the herd sensitivity and specificity values were ≥ 90%. Therefore, 10 animals were sampled in herds with up to 99 cows older than 24 months; 15 animals were sampled in herds with 100 or more cows older than 24 months; and all animals were sampled in those with up to 10 cows older than 24 months. The selection of cows within herds was systematic.

Field activites

The field activities included blood collection, application of an epidemiological questionnaire, and sending the samples to the laboratory. SEDAP veterinarians and agricultural and livestock technicians were involved in the field work. Blood samples (10 mL volume) were collected from September 2012 to January 2013, from cows aged ≥ 24 months by puncture of the jugular vein with disposable needle and vacuum tube with 15 mL capacity (without anticoagulant).

Immunofluorescence antibody test (IFAT)

Serological analyses were performed in the Laboratory of Immunology and Infectious Diseases (LIID) of the Adílio Santos Azevedo Veterinary Hospital (ASA) of the Federal Institute of Paraíba (IFPB), Sousa-PB. For detection of anti-T. gondii antibodies, serum samples were submitted to IFAT, considering the dilution of 1:64 as cutoff point (Santos et al., 2009Santos TR, Costa AJ, Toniollo GH, Luvizotto MCR, Benetti AH, Santos RR, 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(3-4): 324-326. http://dx.doi.org/10.1016/j.vetpar.2009.01.017. PMid:19232473.
http://dx.doi.org/10.1016/j.vetpar.2009....
). Tachyzoites of T. gondii strain ME-49, maintained in mice, were used as antigens. Positive and negative control bovine sera were kindly provided by Prof. Dr. Rinaldo Aparecido Mota, Universidade Federal Rural de Pernambuco (UFRPE), Brazil. The conjugate used in the reactions was anti-bovine IgG (whole molecule with FITC, produced in rabbits, Sigma/F-7887), at a dilution of 1:400 in PBS 7.2 solution containing 10% Evan’s Blue. Reactions were considered positive when tachyzoites showed full peripheral fluorescence. Reactive serum samples were titrated in serial dilutions until the highest positive dilution was obtained.

Calculation of prevalence

The target condition was a seropositive animal in an infected herd. The herd-level case definition was based on population size (cows aged ≥ 24 months), number of females sampled, an apparent intra-herd prevalence of 71% (Santos et al., 2009Santos TR, Costa AJ, Toniollo GH, Luvizotto MCR, Benetti AH, Santos RR, 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(3-4): 324-326. http://dx.doi.org/10.1016/j.vetpar.2009.01.017. PMid:19232473.
http://dx.doi.org/10.1016/j.vetpar.2009....
), and the sensitivity and specificity of serology, with the goal of obtaining herd sensitivity and specificity ≥90%. After several simulations with the Herdacc software, a herd was deemed positive for toxoplasmosis if it had at least one seropositive animal.

EpiInfo 6.04 software was used to calculate apparent prevalences and their confidence intervals (Dean et al., 1996Dean AG, Dean JA, Coulombier D, Brendel KA, Smith DC, Burton AH, et al. Epi Info, version 6: a word processing, database, and statistics program for public health on IBM Compatible microcomputers. Atlanta: Center for Diseases Control and Prevention; 1996.). Stratified random sampling was used to calculate herd-level prevalence in Paraíba state (Thrusfield & Christley, 2018Thrusfield M, Christley R. Veterinary epidemiology. Oxford: John Wiley & Sons; 2018. http://dx.doi.org/10.1002/9781118280249.
http://dx.doi.org/10.1002/9781118280249...
). Required parameters were (a) herd condition (positive or negative), (b) sampling stratum to which the herd belonged, and (c) statistical weight. The statistical weight was determined by applying the following formula (Dean et al., 1996Dean AG, Dean JA, Coulombier D, Brendel KA, Smith DC, Burton AH, et al. Epi Info, version 6: a word processing, database, and statistics program for public health on IBM Compatible microcomputers. Atlanta: Center for Diseases Control and Prevention; 1996.):

W e i g h t = number of herds in the stratum number of herds sampled in the stratum (1)

The calculation of herd-level prevalence per sampling stratum employed a simple random sample design using the following parameters: (a) number of positive herds and (b) number of herds sampled in the stratum. The sampling design for the calculation of animal-level prevalence in Paraíba state used a two-stage stratified cluster sampling and a two-stage cluster sampling in each stratum (Thrusfield & Christley, 2018Thrusfield M, Christley R. Veterinary epidemiology. Oxford: John Wiley & Sons; 2018. http://dx.doi.org/10.1002/9781118280249.
http://dx.doi.org/10.1002/9781118280249...
), and each herd was considered a cluster. The following parameters were used: (a) animal status (seropositive or seronegative), (b) sample stratum to which the animal belonged, (c) herd code (to identify each cluster), and (d) statistical weight. The statistical weight was calculated with the following formula (Dean et al., 1996Dean AG, Dean JA, Coulombier D, Brendel KA, Smith DC, Burton AH, et al. Epi Info, version 6: a word processing, database, and statistics program for public health on IBM Compatible microcomputers. Atlanta: Center for Diseases Control and Prevention; 1996.):

W e i g h t = cows 24 months in the stratum cows 24 months in the sampled herds × cows 24 months in the herd cows 24 months sampled in the herd (2)

Risk fator analysis

The variables obtained with the epidemiological questionnaires were organized for presentation in increasing or decreasing order as to the scale of risk. The variable herd size was categorized according to quartiles. The lowest risk category was considered the basis of comparison for the other categories. An initial exploratory data analysis (univariable) was performed by the chi-square test or Fisher's exact test, and variables with P ≤ 0.2 were selected for logistic regression analysis (Hosmer & Lemeshow, 2000Hosmer DW, Lemeshow S. Applied logistic regression. New York: John Wiley & Sons; 2000. http://dx.doi.org/10.1002/0471722146.
http://dx.doi.org/10.1002/0471722146...
). The final model fit was verified with the Hosmer and Lemeshow test and collinearity between the independent variables was checked by correlation analysis; for variables with strong collinearity (correlation coeficiente > 0.9), one of the two variables was excluded from the multiple analysis according to biological plausibility (Dohoo et al., 2003Dohoo IR, Martin W, Stryhn H. Veterinary epidemiologic research. Charlottetown: Atlantic Veterinary College; 2003.). The confounding variables was assessed by monitoring changes in model parameters when adding new variables. If substantial changes (i.e. greater than 20%) were observed in the regression coefficients, this was considered an indication of confounding. The significance level in final model was 5%, and the calculations were performed in SPSS software version 20.0.

Results

The census data and the sample studied in each sampling stratum are presented in Table 1. In total, 1,895 animals were sampled in 434 farms. Herd and animal level prevalences are presented in Table 2; in addition, the geographic distribution of positive and negative herds is shown in Figure 1. Of the 434 farms investigated, 197 had at least one seropositive cow (prevalence of 49.0%; 95% CI = 44.3%-53.8%). In Sertão, the prevalence was 60.3% (95% CI = 52.1%-67.9%), 26.5% (95% CI = 19.7%-34.6%) in Borborema and 48.3% (95% CI = 40.2%-56.5%) in Agreste/Zona da Mata. The prevalence at animal level was 18.0% (95% CI = 5.3%-21.1%) in Paraíba state, 18.5% (95% CI = 15.2%-22.5%) in Sertão, 15.7% (95% CI = 7.6%-29.5%) in Borborema and 18.3% (95% CI = 14%-23.4%) in Agreste/Zona da Mata. The titers of anti-T. gondii antibodies ranged from 64 to 1024, with the most frequent titers being 64 (10.8%) and 128 (3.7%).

Table 1
Census data on the cattle population in Paraíba state, Northeastern Brazil, according to sampling stratum.
Table 2
Herd and animal levels prevalence of T. gondii infections in cattle from the state of Paraíba, Northeastern Brazil, according to sampling stratum.

The results of the univariable analysis for the risk factors are presented in Table 3. The variables selected (P ≤ 0.2) for the multiple analysis were region, management system, herd size, presence of wild animals, occurrence of abortions, animal purchasing, sharing of pastures, sharing of water sources, use of maternity pens, veterinary assistance and type of property. In the final logistic regression model (Table 4), the risk factors identified were property located in Sertão (odds ratio [OR] = 3.07), property located in Agreste/Zona da Mata (OR = 2.00), animal purchasing (OR = 2.68), herd size of 34-111 animals (OR = 2.91) and herd size > 111 animals (OR = 6.97). The final model had a good fit (Hosmer and Lemeshow test: chi-square = 1.498; P = 0.983).

Table 3
Univariable analysis for factors associated with the herd-level prevalence of T. gondii infections in cattle, in the state of Paraiba, Northeastern Brazil.
Table 4
Logistic regression final model with factors associated with the herd-level prevalence of T. gondii infections in cattle from the state of Paraíba, Northeastern Brazil.

Discussion

In this study, a comprehensive epidemiological survey for toxoplasmosis was performed with planned sampling to determine the seroprevalence at herd and animal levels in cattle in Paraíba state. Only samples from cows aged ≥ 24 months were used because there was a pre-existing serum bank. In addition, females are animals that remain longer in the herd and can provide a more accurate profile of infection, and are animals that contribute to the maintenance of the agent circulating in herds due to the possibility of vertical transmission.

Despite we used serum samples collected between September 2012 to January 2013, a serum bank is ‘a planned catalogued collection of serum forming a random sample that is as representative as possible of a population and that is stored to preserve its immunological and biochemical characteristics’ (Thrusfield & Christley, 2018Thrusfield M, Christley R. Veterinary epidemiology. Oxford: John Wiley & Sons; 2018. http://dx.doi.org/10.1002/9781118280249.
http://dx.doi.org/10.1002/9781118280249...
).

This survey was carried out in all regions of the state of Paraíba, with herd-level prevalence of 49% (95% CI = 44.3%-53.8%) and positive herds covering all mesoregions. This suggests broad capacity of dissemination and adaptability of T. gondii (Tenter et al., 2000Tenter AM, Heckeroth AR, Weiss LM. Toxoplasma gondii: from animals to humans. Int J Parasitol 2000; 30(12-13): 1217-1258. http://dx.doi.org/10.1016/S0020-7519(00)00124-7. PMid:11113252.
http://dx.doi.org/10.1016/S0020-7519(00)...
) and hypothesizes environmental contamination by the parasite. The occurrence of infection due to T. gondii in the Brazilian cattle herd is variable with frequencies from 1% (Gondim et al., 1999Gondim LFP, Barbosa Jr HV, Ribeiro CHA Fo, Saeki H. Serological survey of antibodies to Toxoplasma gondii in goats, sheep, cattle and water buffaloes in Bahia State, Brazil. Vet Parasitol 1999; 82(4): 273-276. http://dx.doi.org/10.1016/S0304-4017(99)00033-3. PMid:10384902.
http://dx.doi.org/10.1016/S0304-4017(99)...
) to 89.1% (Santin et al., 2017Santin API, Juliano RS, Silva AC, Oliveira VSF, Junqueira-Kipnis AP, Brito WMED, et al. Soroepidemiologia de Neospora caninum e Toxoplasma gondii em bovinos da raça Curraleiro. Cienc Anim Bras 2017; 18: e44649. http://dx.doi.org/10.1590/1089-6891v18e-44649.
http://dx.doi.org/10.1590/1089-6891v18e-...
), however studies should be compared with caution due to the use of different diagnostic techniques with different cutoff points (Gomes et al., 2020Gomes DFC, Krawczak FS, Oliveira CHS, Ferreira A Jr, Fernandes EKK, Lopes WDZ, et al. Toxoplasma gondii in cattle in Brazil: a review. Rev Bras Parasitol Vet 2020; 29(1): e015719. http://dx.doi.org/10.1590/s1984-29612019106. PMid:32049142.
http://dx.doi.org/10.1590/s1984-29612019...
).

In Brazil, studies on the frequency of anti- T. gondii antibodies in cattle have been based mainly on IFAT (Dubey et al., 2012Dubey JP, Lago EG, Gennari SM, Su C, Jones JL. Toxoplasmosis in humans and animals in Brazil: high prevalence, high burden of disease, and epidemiology. Parasitology 2012; 139(11): 1375-1424. http://dx.doi.org/10.1017/S0031182012000765. PMid:22776427.
http://dx.doi.org/10.1017/S0031182012000...
), and in a review (Gomes et al., 2020Gomes DFC, Krawczak FS, Oliveira CHS, Ferreira A Jr, Fernandes EKK, Lopes WDZ, et al. Toxoplasma gondii in cattle in Brazil: a review. Rev Bras Parasitol Vet 2020; 29(1): e015719. http://dx.doi.org/10.1590/s1984-29612019106. PMid:32049142.
http://dx.doi.org/10.1590/s1984-29612019...
) of the 35 studies conducted in Brazil 24 (68.5%) used IFAT as diagnostic method, among which 22 (91.6%) established 64 as the cutoff point, as in this study. The most frequent antibody titer obtained in this study was 64, corresponding to 10.8%, followed by 128 (3.7%), results similar to those obtained by Gomes et al. (2020)Gomes DFC, Krawczak FS, Oliveira CHS, Ferreira A Jr, Fernandes EKK, Lopes WDZ, et al. Toxoplasma gondii in cattle in Brazil: a review. Rev Bras Parasitol Vet 2020; 29(1): e015719. http://dx.doi.org/10.1590/s1984-29612019106. PMid:32049142.
http://dx.doi.org/10.1590/s1984-29612019...
. Dubey & Thulliez (1993)Dubey JP, Thulliez PH. Persistence of tissue cysts in edible tissues of cattle fed Toxoplasma gondii oocysts. Am J Vet Res 1993; 54(2): 270-273. PMid:8430937. support that because of resistance to toxoplasmosis, antibody titers lower than 1,024 are indicative of chronic infection, suggesting the presence of tissue cysts.

Although the role of cattle in the transmission of the parasite to humans is not completely known, beef is often eaten undercooked and may pose a risk to the population (Gomes et al., 2020Gomes DFC, Krawczak FS, Oliveira CHS, Ferreira A Jr, Fernandes EKK, Lopes WDZ, et al. Toxoplasma gondii in cattle in Brazil: a review. Rev Bras Parasitol Vet 2020; 29(1): e015719. http://dx.doi.org/10.1590/s1984-29612019106. PMid:32049142.
http://dx.doi.org/10.1590/s1984-29612019...
). Cattle can be readily infected with T. gondii, but are considered poor hosts because they develop a more effective immune response to T. gondii infection than other animals (Esteban-Redondo & Innes, 1997Esteban-Redondo I, Innes EA. Toxoplasma gondii infection in sheep and cattle. Comp Immunol Microbiol Infect Dis 1997; 20(2): 191-196. http://dx.doi.org/10.1016/S0147-9571(96)00039-2. PMid:9208205.
http://dx.doi.org/10.1016/S0147-9571(96)...
). However, T. gondii has been isolated from bovine tissues and unpasteurized milk (Dubey, 1986Dubey JP. A review of toxoplasmosis in cattle. Vet Parasitol 1986; 22(3-4): 177-202. http://dx.doi.org/10.1016/0304-4017(86)90106-8. PMid:3551316.
http://dx.doi.org/10.1016/0304-4017(86)9...
), indicating that consumption of meat and milk can be source of T. gondii transmission. The ingestion of beef of questionable provenance increases the risk of T. gondii infection to the consumer (Millar et al., 2008Millar PR, Sobreiro LG, Bonna ICF, Amendoeira MRR. A importância dos animais de produção na infecção por Toxoplasma gondii no Brasil. Semina: Ciênc Agrár 2008; 29(3): 693-706. http://dx.doi.org/10.5433/1679-0359.2008v29n3p693.
http://dx.doi.org/10.5433/1679-0359.2008...
), and due to the informality of slaughterhouses and food markets in Brazil, especially in Paraíba where there is no federal inspection for cattle (Maia et al., 2017Maia ARA, Fernandes LG, Pinto PS, Guimarães-Peixoto RP, Silva LF, Santos CSAB, et al. Herd-level seroprevalence and associated risk factors for bovine cysticercosis in the State of Paraiba, Northeastern Brazil. Prev Vet Med 2017; 142: 51-57. http://dx.doi.org/10.1016/j.prevetmed.2017.05.008. PMid:28606366.
http://dx.doi.org/10.1016/j.prevetmed.20...
), the clandestine slaughter is a worrisome factor.

T. gondii infection is often more common in areas with warm, humid climates and lower altitudes (Dubey, 2010Dubey JP. Toxoplasmosis of animals and humans. Florida: CRC Press; 2010.), characteristics of the entire state of Paraíba. The average temperatures of the Northeast region are between 26º and 28 ºC, with low annual variability, and the state of Paraíba, due to its location within the Equatorial belt, is subjected to the incidence of high solar radiation with a large number of hours of insolation. Such condition determines a warm climate and average annual temperature of 26 ºC, also with low intra-annual variation (AESA, 2016Agência Executiva de Gestão das Águas do Estado da Paraíba - AESA. Caracterização do clima, da pluviometria e da fluviometria [online]. 2016 [cited 2023 Mar 1]. Available from: http://www.aesa.pb.gov.br/aesa-website/wp-content/uploads/2016/11/PE_10.pdf
http://www.aesa.pb.gov.br/aesa-website/w...
). In this study, the Sertão and Agreste/Zona da Mata mesoregions presented association with T. gondii prevalence. It is known that T. gondii infection in herbivores is more prevalent in humid areas, which favor sporulation conditions and maintenance of oocyst viability in vegetation (Dubey, 2010Dubey JP. Toxoplasmosis of animals and humans. Florida: CRC Press; 2010.). Brejo Paraibano, a microregion that belongs to Agreste, has characteristics with the presence of Atlantic Forest fragments, high rainfall, and a wide variety of fauna, which may favor the viability of oocysts in this region.

Sertão is an area bordering the states of Rio Grande do Norte, Ceará and Pernambuco, where there is an intense trade of animals without the knowledge of their sanitary condition, which may justify this region as risk factor. It is noteworthy that, despite the climatic conditions of the Sertão being different from the Agreste, which presents favorable abiotic factors for T. gondii, the family farm production in the Sertão, with low technification level of the properties, and without the support of important general sanitary measures for the control of infectious diseases, as quarantine of animals coming from other regions (Clementino et al., 2015Clementino IJ, Pimenta CRM, Fernandes LG, Bezerra CS, Alves CJ, Dias RA, et al. Caracterização da pecuária bovina no Estado da Paraíba, Nordeste do Brasil. Semina: Ciênc Agrár 2015; 36(1): 557-570. http://dx.doi.org/10.5433/1679-0359.2015v36n1p557.
http://dx.doi.org/10.5433/1679-0359.2015...
) are possible factors that may be generating this risk association. In addition, primary clusters of positive herds for important cattle infectious diseases (such as Bovine Viral Diarrhea Virus, Bovine Herpesvirus type 1 and Vesicular Stomatitis) covering the Sertão region were detected in previous surveys (Bezerra et al., 2018Bezerra CS, Cargnelutti JF, Sauthier JT, Weiblen R, Flores EF, Alves CJ, et al. Epidemiological situation of vesicular stomatitis virus infection in cattle in the state of Paraíba, semiarid region of Brazil. Prev Vet Med 2018; 160: 68-75. http://dx.doi.org/10.1016/j.prevetmed.2018.09.027. PMid:30389000.
http://dx.doi.org/10.1016/j.prevetmed.20...
; Fernandes et al., 2018Fernandes LG, Pituco EM, Romaldini AHCN, De Stefano E, Clementino IJ, Maia ARA, et al. Spatial analysis for bovine viral diarrhea virus and bovine herpesvirus type 1 infections in the state of Paraíba, northeastern Brazil. BMC Vet Res 2018; 14(1): 102. http://dx.doi.org/10.1186/s12917-018-1412-5. PMid:29554912.
http://dx.doi.org/10.1186/s12917-018-141...
).

Animal purchasing was also identified as associate with T. gondii prevalence. This variable is a classical risk fator for infectious diseases and is related to acquisition of animals without previous testing for diseases. In fact, the serological testing of cattle for toxoplasmosis prior to introducting into the herd is not a common procedure anywhere, which facilitates the introduction of infected animals. The producer often purchases animals without knowing the origin, and some diseases are not previously diagnosed due to the high cost and difficult accessibility of diagnostic tests. In Brazil, this variable has been identified as risk factor for several bovine diseases, such as toxoplasmosis (Gomes et al., 2021Gomes DFC, Mendes LA, Dias JM, Ribeiro-Andrade M, Oliveira PRF, Mota RA, et al. Seroprevalence, spatial distribution and risk factors associated with Toxoplasma gondii infection among cattle in a quilombola community in the Brazilian cerrado. Rev Bras Parasitol Vet 2021; 30(1): e018720. http://dx.doi.org/10.1590/s1984-296120201080. PMid:33729314.
http://dx.doi.org/10.1590/s1984-29612020...
) in the Brazilian cerrado, leptospirosis (Hashimoto et al., 2012Hashimoto VY, Dias JA, Spohr KAH, Silva MCP, Andrade MGB, Müller EE, et al. Prevalência e fatores de risco associados à Leptospira spp. em rebanhos bovinos da região centro-sul do estado do Paraná. Pesq Vet Bras 2012; 32(2): 99-105. http://dx.doi.org/10.1590/S0100-736X2012000200001.
http://dx.doi.org/10.1590/S0100-736X2012...
) and neosporosis (Gindri et al., 2018Gindri PC, Mion B, Pradieé J, Bialves TS, Souza GN, Dellagostin OA, et al. Seroprevalence estimate and associated risk factors for neosporosis in dairy cattle in the northwest region of Rio Grande do Sul State, Brazil. Cienc Rural 2018; 48(7): e20170921. http://dx.doi.org/10.1590/0103-8478cr20170921.
http://dx.doi.org/10.1590/0103-8478cr201...
) in Rio Grande do Sul, as well as in Northeastern Brazil for brucellosis (Silva et al., 2009Silva VGSO, Dias RA, Ferreira F, Amaku M, Costa ELS, Lôbo JR, et al. Situação epidemiológica da brucelose bovina no Estado de Sergipe. Arq Bras Med Vet Zootec 2009; 61(Suppl. 1): 109-117. http://dx.doi.org/10.1590/S0102-09352009000700014.
http://dx.doi.org/10.1590/S0102-09352009...
), neosporosis (Silva et al., 2008Silva MIS, Ornelas MAA, Mota RA, Pinheiro JW Jr, Rabelo SSA. Fatores de riscos associados à infecção por Neospora caninum em matrizes bovinas leiteiras em Pernambuco. Cienc Anim Bras 2008; 9(2): 455-461.), bovine viral diarrhea (Fernandes et al., 2016Fernandes LG, Nogueira AHC, De Stefano E, Pituco EM, Ribeiro CP, Alves CJ, et al. Herd-level prevalence and risk factors for bovine viral diarrhea virus infection in cattle in the State of Paraíba, Northeastern Brazil. Trop Anim Health Prod 2016; 48(1): 157-165. http://dx.doi.org/10.1007/s11250-015-0937-x. PMid:26498460.
http://dx.doi.org/10.1007/s11250-015-093...
) and cysticercosis (Maia et al., 2017Maia ARA, Fernandes LG, Pinto PS, Guimarães-Peixoto RP, Silva LF, Santos CSAB, et al. Herd-level seroprevalence and associated risk factors for bovine cysticercosis in the State of Paraiba, Northeastern Brazil. Prev Vet Med 2017; 142: 51-57. http://dx.doi.org/10.1016/j.prevetmed.2017.05.008. PMid:28606366.
http://dx.doi.org/10.1016/j.prevetmed.20...
). Herd size ≥ 34 animals was associated with herd-level prevalence, indicating that the larger the herd size the greater the odds of herd positivity. In fact, properties with a great number of animals tended to introduce new animals more often, a practice that, without sanitary precautions, may predispose the introduction of toxoplasmosis into the herd.

In conclusion, the results found here suggest the wide distribution of T. gondii infections in cattle throughout the state of Paraíba, Northeastern Brazil, and the risk factors identified are not possible to correct.

Acknowledgements

This study was funded by the National Council for Scientific and Technological Development (CNPq), under codes 471571/2011-3, 302131/2012-4 and 476596/2013-0.

  • How to cite: Maia ARA, Bezerra RA, Silva SS, Álvares FBV, Santos CSAB, Alves CJ, et al. Herd-level based seroprevalence and associated factors for Toxoplasma gondii in cows in the state of Paraíba, Northeastern Brazil. Braz J Vet Parasitol 2023; 32(2): e017222. https://doi.org/10.1590/S1984-29612023025

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Publication Dates

  • Publication in this collection
    22 May 2023
  • Date of issue
    2023

History

  • Received
    29 Nov 2022
  • Accepted
    03 Apr 2023
Colégio Brasileiro de Parasitologia Veterinária FCAV/UNESP - Departamento de Patologia Veterinária, Via de acesso Prof. Paulo Donato Castellane s/n, Zona Rural, , 14884-900 Jaboticabal - SP, Brasil, Fone: (16) 3209-7100 RAMAL 7934 - Jaboticabal - SP - Brazil
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