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Seroprevalence and associated factors with Neospora caninum infection in sheep and goats slaughtered in the state of Paraíba, Brazil

Soroprevalência e fatores associados à infecção por Neospora caninum em ovinos e caprinos abatidos no Estado da Paraíba, Brasil

Abstract

The objective was to describe the seroprevalence of anti-Neospora caninum antibodies in goats and sheep slaughtered in the state of Paraíba and to identify possible associated factors with the infections. Two hundred twenty-nine samples from goats and two hundred five from sheep were analyzed by Indirect Immunofluorescence Reaction (IFAT) using a cutoff point of 1:50. The presence of anti-N. caninum antibodies was identified in 28.4% (65/ 229; 95% Confidence Interval: 22.6-34.2) of the goat samples and in 12.7% (26/ 205; 95% CI: 8.2 – 17.2) of the sheep samples. Contact between goats and dogs (Odds ratio 4.81; CI 1.13 – 2.67; p = 0.041) and cattle (OR. 1.87; CI 1.13 – 2.67; p = 0.002) was identified as a risk factor for goats and contact between sheep and dogs (OR 2.32; CI 1.58 – 3.14; p = 0.026) and history of abortion (OR 1.94; CI 1.28 – 2.90; p = 0.001) was considered a risk factor for sheep. The study revealed a high seroprevalence of anti-N. caninum antibodies in slaughtered goats and sheep in Paraíba. Risk factors such as contact with dogs/cattle and abortion history underscore the need for preventive measures to control infection and enhance animal health management.

Keywords:
Neosporosis; small ruminants; semi-arid

Resumo

O objetivo deste estudo foi descrever a soroprevalência de anticorpos anti-Neospora caninum em caprinos e ovinos abatidos em abatedouros públicos do Estado da Paraíba, e identificar os possíveis fatores associados às infecções. Foram analisadas 229 amostras de soro de caprinos e 205 de ovinos pela Reação de Imunofluorescência Indireta (RIFI), utilizando-se ponto de corte de 1:50. A presença de anticorpos anti-Neospora caninum foi identificada em 28,4% (65/229; Intervalo de confiança 95%: 22,6-34,2) das amostras de caprinos e em 12,7% (26/205; IC 95%: 8,2-17,2%) das amostras de ovinos. O contato de caprinos com cães (Odds ratio 4,81; IC 2,07-8,87; p = 0,041) e bovinos (OR. 1,87; IC 1,13 – 2,67; p = 0,002) foram identificados como fatores de risco para caprinos; e o contato de ovinos com cães (OR. 2,32; IC 1,58-3,14; p = 0,026) e o histórico de aborto (OR. 1,94; IC 1,28-2,90; p = 0,001) foram considerados fatores de risco para ovinos. O estudo revelou alta soroprevalência de anticorpos anti-N. caninum em caprinos e ovinos abatidos na Paraíba. Fatores de risco, como contato com cães/bovinos e histórico de aborto, destacam a necessidade de medidas preventivas para conter a infecção e melhorar o manejo da saúde animal.

Palavras-chave:
Neosporose; pequenos ruminantes; semiárido

Introduction

Neosporosis is a disease caused by the protozoan Neospora caninum, which has domestic and wild canids as its definitive host (Lindsay et al., 1999Lindsay DS, Dubey JP, Duncan RB. Confirmation that the dog is a definitive host for Neospora caninum. Vet Parasitol 1999; 82(4): 327-333. http://dx.doi.org/10.1016/S0304-4017(99)00054-0. PMid:10384909.
http://dx.doi.org/10.1016/S0304-4017(99)...
; Dubey et al., 2011Dubey JP, Jenkins MC, Rajendran C, Miska K, Ferreira LR, Martins J, et al. Gray wolf (Canis lupus) is a natural definitive host for Neospora caninum. Vet Parasitol 2011; 181(2-4): 382-387. http://dx.doi.org/10.1016/j.vetpar.2011.05.018. PMid:21640485.
http://dx.doi.org/10.1016/j.vetpar.2011....
). As intermediate hosts are species such as sheep, goats, and cattle. Although cattle are considered more susceptible to neosporosis, abortions, placental necrosis, fetal death, stillbirths, and other reproductive problems have also been reported in sheep and goats, although these animals may have some resistance to the disease (Buxton et al., 2002Buxton D, McAllister MM, Dubey JP. The comparative pathogenesis of neosporosis. Trends Parasitol 2002; 18(12): 546-552. http://dx.doi.org/10.1016/S1471-4922(02)02414-5. PMid:12482540.
http://dx.doi.org/10.1016/S1471-4922(02)...
; Mesquita et al., 2018Mesquita LP, Costa RC, Nogueira CI, Abreu CC, Orlando DR, Ascari I Jr, et al. Placental lesions associated with abortion and stillbirth in goats naturally infected by Neospora caninum. Pesq Vet Bras 2018; 38(3): 444-449. http://dx.doi.org/10.1590/1678-5150-pvb-4598.
http://dx.doi.org/10.1590/1678-5150-pvb-...
). In small ruminants, N. caninum can be transmitted horizontally or vertically, and the association of the two forms of transmission is often identified as a way of perpetuating the disease in herds (Nunes et al., 2017Nunes ACBT, Yamasaki EM, Kim PCP, Melo RPB, Ribeiro-Andrade M, Porto WJN, et al. Transplacental transmission of Neospora caninum in naturally infected small ruminants from northeastern Brazil. Pesq Vet Bras 2017; 37(9): 921-925. http://dx.doi.org/10.1590/s0100-736x2017000900004.
http://dx.doi.org/10.1590/s0100-736x2017...
; Pereira et al., 2021Pereira KAG, Sousa RS, Varaschin MS, Becker APBB, Monteiro ALG, Koch MO, et al. Transplacental transmission of Neospora caninum to lambs in successive pregnancies of naturally infected sheep in Southern Brazil. Vet Parasitol Reg Stud Rep 2021; 23: 100537. http://dx.doi.org/10.1016/j.vprsr.2021.100537. PMid:33678390.
http://dx.doi.org/10.1016/j.vprsr.2021.1...
; Bezerra et al., 2022aBezerra RA, Lima BA, Alvares FBV, Rossi GAM, Braga FR, Melo RPB, et al. Detection of Anti-Neospora caninum IgG in blood serum and colostrum samples in naturally infected sheep and in their newborn offspring. Pathogens 2022a; 11(11): 1263. http://dx.doi.org/10.3390/pathogens11111263. PMid:36365014.
http://dx.doi.org/10.3390/pathogens11111...
, bBezerra RA, Valencio BA, Alvares FBV, Alcântara ET, Sarmento WF, Melo RPB, et al. Dynamics of Neospora caninum transmission in naturally infected sheep under semiarid conditions. Small Rumin Res 2022b; 217: 106843. http://dx.doi.org/10.1016/j.smallrumres.2022.106843.
http://dx.doi.org/10.1016/j.smallrumres....
).

The occurrence of a high rate of endogenous vertical transmission in naturally infected sheep (6/ 19 – 31.6%) was observed in the semi-arid region of the state of Paraíba, Brazil, in which chronically infected females gave birth to clinically healthy animals, but infected and with potential for transmissibility to future offspring or to the definitive host (Feitosa et al., 2021Feitosa TF, Costa FTR, Bezerra RA, Álvares FBV, Ferreira LC, Mota RA, et al. Vertical transmission and kinetic of antibodies anti-Neospora caninum in naturally infected lambs in the semiarid region of Brazil. Rev Bras Parasitol Vet 2021; 30(3): e010621. http://dx.doi.org/10.1590/s1984-29612021073. PMid:34495126.
http://dx.doi.org/10.1590/s1984-29612021...
). Vertical transmission seems to be of greater importance in the perpetuation of the parasite in small ruminants when compared to horizontal transmission, since the same female can transmit the protozoan to several subsequent generations, making the occurrence and maintenance of the disease in the herd possible even in the absence of the definitive host (Pereira et al., 2021Pereira KAG, Sousa RS, Varaschin MS, Becker APBB, Monteiro ALG, Koch MO, et al. Transplacental transmission of Neospora caninum to lambs in successive pregnancies of naturally infected sheep in Southern Brazil. Vet Parasitol Reg Stud Rep 2021; 23: 100537. http://dx.doi.org/10.1016/j.vprsr.2021.100537. PMid:33678390.
http://dx.doi.org/10.1016/j.vprsr.2021.1...
).

However, horizontal transmission may be favored due to the eating habits of dogs, which may involve the ingestion of animal’s tissues such as placental remains (Lindsay et al., 1999Lindsay DS, Dubey JP, Duncan RB. Confirmation that the dog is a definitive host for Neospora caninum. Vet Parasitol 1999; 82(4): 327-333. http://dx.doi.org/10.1016/S0304-4017(99)00054-0. PMid:10384909.
http://dx.doi.org/10.1016/S0304-4017(99)...
; Robbe et al., 2016Robbe D, Passarelli A, Gloria A, Di Cesare A, Capelli G, Lorio R, et al. Neospora caninum seropositivity and reproductive risk factors in dogs. Exp Parasitol 2016; 164: 31-35. http://dx.doi.org/10.1016/j.exppara.2016.02.003. PMid:26873272.
http://dx.doi.org/10.1016/j.exppara.2016...
). Contact with dogs increases the risk of infection in small ruminants, although other factors such as a history of abortion, contact with other species, and water supply are also associated with the infection. It is essential to consider these factors when identifying reproductive problems within the herd (Machado et al., 2011Machado GP, Kikuti M, Langoni H, Paes AC. Seroprevalence and risk factors associated with neosporosis in sheep and dogs from farms. Vet Parasitol 2011; 182(2-4): 356-358. http://dx.doi.org/10.1016/j.vetpar.2011.05.021. PMid:21676548.
http://dx.doi.org/10.1016/j.vetpar.2011....
; Topazio et al., 2014Topazio JP, Weber A, Camillo G, Vogel FF, Machado G, Ribeiro A, et al. Seroprevalence and risk factors for Neospora caninum in goats in Santa Catarina state, Brazil. Rev Bras Parasitol Vet 2014; 23(3): 360-366. http://dx.doi.org/10.1590/S1984-29612014062. PMid:25271457.
http://dx.doi.org/10.1590/S1984-29612014...
; Rodrigues et al., 2020Rodrigues AA, Reis SS, Sousa ML, Moraes ES, Garcia JL, Nascimento TVC, et al. A systematic literature review and meta-analysis of risk factors for Neospora caninum seroprevalence in goats. Prev Vet Med 2020; 185: 105176. http://dx.doi.org/10.1016/j.prevetmed.2020.105176. PMid:33129022.
http://dx.doi.org/10.1016/j.prevetmed.20...
). Thus, control and prevention measures should be focused simultaneously on reducing vertical transmission and reducing horizontal transmission.

These facts make diagnosis and regional epidemiological knowledge important tools to better understand the dynamics of neosporosis transmission in herds. In addition, knowledge of seroprevalence and factors associated with N. caninum infection is necessary for the development of an effective control and prophylaxis methodology. Current knowledge about the seroprevalence of neosporosis in small ruminants in Brazil is still scarce. Faced with this gap, the objective of this study was to describe the seroprevalence of N. caninum in sheep and goats slaughtered in public slaughterhouses in two cities in the semi-arid region of the state of Paraíba and to identify the risk factors related to these infections.

Material and Methods

Sampling

To determine the number of samples to be evaluated, simple random sampling was performed according to Thrusfield (2007)Thrusfield M. Veterinary Epidemiology. Oxford: Blackwell Science; 2007.:

n = Z 2 × P 1 P d 2 (1)

n = number of samples

Z = normal distribution value for the confidence level of 95%

P = expected prevalence of 17.4% in goats and 4.7% in sheep (Moraes et al., 2011Moraes LMB, Raimundo JM, Guimarães A, Santos HA, Macedo GL Jr, Masssard CL, et al. Occurrence of anti-Neospora caninum and anti-Toxoplasma gondii IgG antibodies in goats and sheep in western Maranhão, Brazil. Rev Bras Parasitol Vet 2011; 20(4): 312-317. http://dx.doi.org/10.1590/S1984-29612011000400010. PMid:22166386.
http://dx.doi.org/10.1590/S1984-29612011...
).

d = sampling error of 5%

The minimum number of samples to be evaluated determined by the sample calculation was 220 samples for goats and 69 sheep. However, for safety and due to the availability of animals, staff, and materials, a total of 229 goat samples were collected (106 in Sousa and 123 in Patos), along with 205 sheep samples (105 in Sousa and 100 in Patos). The samples were collected from June 2019 to November 2020. The animals came from 10 municipalities in the semi-arid region of the state of Paraíba (Figure 1).

Figure 1
Geographical data pertaining to the source municipalities of goats and sheep, as well as the visited slaughterhouses for sample collection in the state of Paraíba, Brazil.

Blood samples were collected during the slaughter of the animals, at the bleeding, in glass tubes previously identifies and without anticoagulant, to obtain serum. They were stored frozen at -20°C at the Laboratório de Imunologia e Doenças Infectocontagiosas (LIDIC), do Hospital Veterinário do Instituto Federal da Paraíba-IFPB, campus Sousa.

Serological diagnosis

For the detection of anti-N. caninum, the samples were submitted to the Indirect Immunofluorescence Reaction (IFAT) using the 1:50 cutoff point (Lima et al., 2008Lima JTR, Ahid SMM, Barrêto RA Jr, Pena HFJ, Dias RA, Gennari SM. Prevalência de anticorpos anti-Toxoplasma gondii e anti-Neospora caninum em rebanhos caprinos do município de Mossoró, Rio Grande do Norte. Braz J Vet Res Anim Sci 2008; 45(2): 81-86. http://dx.doi.org/10.11606/issn.1678-4456.bjvras.2008.26703.
http://dx.doi.org/10.11606/issn.1678-445...
), following the method described by Camargo (1974)Camargo ME. Introdução às técnicas de imunofluorescência. Rev Bras Patol Clín 1974; 10(3): 143-171., with the Nc-1 tachyzoite strain fixed on a slide as antigen. Serum was diluted using 3μL added to 147μL of PBS pH 7.2. Diluted samples were distributed on slide and incubated in an oven (37°C for 30 minutes). Then, they were submitted to three immersion washes of five minutes each, with PBS pH 7.2. After drying, the slides were covered with 20μL of anti-goat or ovine IgG antibodies conjugated to fluorescein isothiocynate (whole molecule, SIGMA, St. Louis, Mo, USA). Subsequently, they were incubated for 30 minutes at 37°C and washed again with PBS pH 7.2. After drying, buffered glycerin was added to the slides and readings were performed in a fluorescence microscope with ultraviolet light emission, 400x magnification. Samples that showed total peripheral fluorescence of tachyzoites were considered positive, with positive samples submitted to sequential dilutions in base two until negative.

Epidemiological questionnaire

During the collections, epidemiological questionnaires were applied to the owners. The variables analyzed and their respective categories were: gender (male or female), breed (pure or crossbred), age (< 1 year, 1-2 years, >2 years), rearing system (semi-intensive or extensive), rearing aptitude (meat, dairy or mixed), access to water (treated or untreated), contact with wild animals (yes or no), contact with other domestic animals (cattle, horses, pigs, sheep, goats, dogs, cats or birds), vaccination history (yes- which ones?; or no) and history of abortions (yes or no).

Statistical analysis

Descriptive statistical analysis was used to calculate the frequencies of the results obtained in the IFAT. To identify the factors associated with the prevalence of anti-N. caninum, data from the epidemiological questionnaires were used in two stages, univariate and multivariate analyses. In the univariate analysis, each independent variable was correlated with the dependent variable (seropositivity), and those with a p-value ≤ 0.2, according to the Chi-square test (Zar, 1999Zar JH. Biostatistical analysis. Upper Saddle River: Prentice Hall; 1999.), were selected for the multivariate analysis using multiple logistic regression (Hosmer & Lemeshow, 2000Hosmer DW, Lemeshow S. Applied logistic regression. Danvers: John Wiley & Sons; 2000. http://dx.doi.org/10.1002/0471722146.
http://dx.doi.org/10.1002/0471722146...
), with a significance level of 5%. To verify any possible collinearity between the data, a correlation test was applied and, if the correlation coefficient was greater than 0.9, one of the variables was eliminated using the criterion of biological plausibility. To verify the fit of the model, the Chi-square parameters and the Omnibus test were used. The results were analyzed using GraphPad Prism 8.0.1 Software.

Results

Among the 229 evaluated goats, 65 (28.4%; 95% CI: 22.6-34.2) were positive for anti-N. caninum; in sheep, 12.7% (26/205; 95% CI: 8.2-17.2%) were seropositive. For both species, antibody titers ranged from 1:50 to 1:12,800, with 1:200 being the most frequent titer (Table 1).

Table 1
Distribution of anti-Neospora caninum antibodies by Indirect Immunofluorescence Reaction (IFAT) in goats and sheep slaughtered in the semi-arid region of the state of Paraíba, Brazil.

In the univariate analysis, the variables that showed a statistically significant difference (p ≤ 20) and were selected for the multivariate analysis for goats were age, contact with dogs, contact with cattle and history of abortions. For sheep, they were rearing system, contact with dogs, contact with cattle and history of abortion (Table 2).

Table 2
Univariate analysis of factors associated with Neospora caninum infections in goats and sheep slaughtered in the semi-arid region of the state of Paraíba, Brazil.

The risk factors identified through multivariate analysis for goats were contact with dogs (OR. 4.81; IC 2.07-8.87; p = 0.041) and contact with cattle (OR. 1.87; IC 1.13- 2.67; p = 0.002) and for sheep the variables identified were contact with dogs (OR. 2.32; IC 1.58-3.14; p = 0.026) and history of abortions (OR. 1.94; IC 1.28-2.90; p = 0.001) (Table 3).

Table 3
Multivariate analysis of risk factors associated with Neospora caninum infections in goas and sheep slaughtered in the semi-arid region of the state of Paraíba, Brazil.

Discussion

The seroprevalence above 28% for anti-N. caninum antibodies in goats found in this study was the highest reported in goats in Brazil until this date, the previously described seroprevalence ranges from 1.05% (Lima et al., 2008Lima JTR, Ahid SMM, Barrêto RA Jr, Pena HFJ, Dias RA, Gennari SM. Prevalência de anticorpos anti-Toxoplasma gondii e anti-Neospora caninum em rebanhos caprinos do município de Mossoró, Rio Grande do Norte. Braz J Vet Res Anim Sci 2008; 45(2): 81-86. http://dx.doi.org/10.11606/issn.1678-4456.bjvras.2008.26703.
http://dx.doi.org/10.11606/issn.1678-445...
) to 26.10% (Braz et al., 2018Braz BMA, Valente JDM, Villalobos EMC, Lara MCCSH, Machado CAL, Barbosa IC, et al. Seroepidemiology of Neospora caninum among goats (Capra hircus) in the state of Paraíba, northeastern, Brazil. Arq Bras Med Vet Zootec 2018; 70(1): 147-152. http://dx.doi.org/10.1590/1678-4162-9453.
http://dx.doi.org/10.1590/1678-4162-9453...
). In the Northeast region, seroprevalences were found that corroborate with was presented in this study. In the state of Pernambuco, 20.37% (Galvão et al., 2023Galvão CMMQ, Oliveira PRF, Cavalcanti ALA, Nogueira DB, Azevedo SS, Ramos RAN, et al. Occurrence of IgG antibodies against Toxoplasma gondii, Neospora caninum and Leptospira spp. in goats and sheep from an indigenous village in Pernambuco, Brazil. Rev Bras Parasitol Vet 2023; 32(2): e000423. http://dx.doi.org/10.1590/s1984-29612023022. PMid:37132735.
http://dx.doi.org/10.1590/s1984-29612023...
) and 26.6% (Tembue et al., 2011Tembue AASM, Ramos RAN, Sousa TR, Albuquerque AR, Costa AJ, Meunier IMJ, et al. Serological survey of Neospora caninum in small ruminants from Pernambuco State, Brazil. Rev Bras Parasitol Vet 2011; 20(3): 246-248. http://dx.doi.org/10.1590/S1984-29612011000300013. PMid:21961757.
http://dx.doi.org/10.1590/S1984-29612011...
) of seropositivity were fescribed. In the state of Bahia was identified 15% of seropositivity in goats (Uzêda et al., 2007Uzêda RS, Pinheiro AM, Fernández SY, Ayres MCC, Gondim LFP, Almeida MAO. Seroprevalence of Neospora caninum in dairy goats from Bahia, Brazil. Small Rumin Res 2007; 70(2-3): 257-259. http://dx.doi.org/10.1016/j.smallrumres.2006.04.003.
http://dx.doi.org/10.1016/j.smallrumres....
), and in Paraíba 26.10% (Braz et al., 2018Braz BMA, Valente JDM, Villalobos EMC, Lara MCCSH, Machado CAL, Barbosa IC, et al. Seroepidemiology of Neospora caninum among goats (Capra hircus) in the state of Paraíba, northeastern, Brazil. Arq Bras Med Vet Zootec 2018; 70(1): 147-152. http://dx.doi.org/10.1590/1678-4162-9453.
http://dx.doi.org/10.1590/1678-4162-9453...
), which demonstrates uniformity in the occurrence of N. caninum in goats from different states of this region, due to the similarity in climate and herd management practices. The disparity between the seroprevalence rates reported in a study conducted by Faria et al. (2007)Faria EB, Gennari SM, Pena HFJ, Athayde ACR, Silva MLCR, Azevedo SS. Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in goats slaughtered in the public slaughterhouse of Patos city, Paraíba State, Northeast region of Brazil. Vet Parasitol 2007; 149(1-2): 126-129. http://dx.doi.org/10.1016/j.vetpar.2007.07.009. PMid:17706359.
http://dx.doi.org/10.1016/j.vetpar.2007....
(3.3% - 10/306) in Patos, Paraíba, and the findings of our study is quite substantial. Notably, both studies involved sample collections at the Patos slaughterhouse. However, the temporal gap of over a decade between these studies may imply an upward trend in the prevalence of neosporosis within herds in that particular region.

In other regions of Brazil has been demonstrate the same uniformity between the studies in goats from a same region. In Southeast region Figliuolo et al. (2004a) have identified 6.4% of seroprevalence in the state of São Paulo; Varaschin et al. (2011)Varaschin MS, Guimarães AM, Hirsch C, Mesquita LP, Abreu CC, Rocha CMBM, et al. Fatores associados a soroprevalência de Neospora caninum e Toxoplasma gondii em rebanhos caprinos na região sul de Minas Gerais. Pesq Vet Bras 2011; 31(1): 53-58. http://dx.doi.org/10.1590/S0100-736X2011000100008.
http://dx.doi.org/10.1590/S0100-736X2011...
and Andrade et al (2013)Andrade GS, Bruhn FRP, Rocha CMBM, Guimarães AS, Gouveia AMG, Guimarães AM. Seroprevalence for Neospora caninum in goats of Minas Gerais state, Brazil. Res Vet Sci 2013; 94(3): 584-586. http://dx.doi.org/10.1016/j.rvsc.2012.09.026. PMid:23200513.
http://dx.doi.org/10.1016/j.rvsc.2012.09...
have identified 10.7% state of Minas Gerais. In South region Topazio et al. (2014)Topazio JP, Weber A, Camillo G, Vogel FF, Machado G, Ribeiro A, et al. Seroprevalence and risk factors for Neospora caninum in goats in Santa Catarina state, Brazil. Rev Bras Parasitol Vet 2014; 23(3): 360-366. http://dx.doi.org/10.1590/S1984-29612014062. PMid:25271457.
http://dx.doi.org/10.1590/S1984-29612014...
has described 4.58% of seropositivity in Santa Catarina and Romanelli et al. (2020)Romanelli PR, Matos AMRN, Pinto-Ferreira F, Caldart ET, Oliveira JS, Anteveli G, et al. Toxoplasma gondii and Neospora caninum infections and factors associated in goats in the Parana state, Southern Brazil. Rev Bras Parasitol Vet 2020; 29(4): e003620. http://dx.doi.org/10.1590/s1984-29612020076. PMid:33053053.
http://dx.doi.org/10.1590/s1984-29612020...
6.3% in Paraná. The North region is the only with the highest lack of information about the seroprevalence in goats, the scarcity of data on the occurrence of N. caninum in goats from different regions of Brazil is a factor that makes it difficult to compare the distribution of the parasite in the country’s herds (Moraes et al., 2011Moraes LMB, Raimundo JM, Guimarães A, Santos HA, Macedo GL Jr, Masssard CL, et al. Occurrence of anti-Neospora caninum and anti-Toxoplasma gondii IgG antibodies in goats and sheep in western Maranhão, Brazil. Rev Bras Parasitol Vet 2011; 20(4): 312-317. http://dx.doi.org/10.1590/S1984-29612011000400010. PMid:22166386.
http://dx.doi.org/10.1590/S1984-29612011...
).

In sheep, the seroprevalence found in this study was above 12%, remaining within the seroprevalence range described in studies from different states and regions of Brazil, ranging from 1.8% (Soares et al., 2009Soares HS, Ahid SMM, Bezerra ACDS, Pena HFJ, Dias RA, Gennari SM. Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in sheep from Mossoró, Rio Grande do Norte, Brazil. Vet Parasitol 2009; 160(3-4): 211-214. http://dx.doi.org/10.1016/j.vetpar.2008.10.102. PMid:19091473.
http://dx.doi.org/10.1016/j.vetpar.2008....
) to 64.2% (Tembue et al., 2011Tembue AASM, Ramos RAN, Sousa TR, Albuquerque AR, Costa AJ, Meunier IMJ, et al. Serological survey of Neospora caninum in small ruminants from Pernambuco State, Brazil. Rev Bras Parasitol Vet 2011; 20(3): 246-248. http://dx.doi.org/10.1590/S1984-29612011000300013. PMid:21961757.
http://dx.doi.org/10.1590/S1984-29612011...
). The result of the present study corroborates the data found by Mendonça et al. (2019)Mendonça CED, Munhoz AD, Rocha DS, Guimarães LA, Bezerra RA, Albuquerque GR, et al. Factors associated with seroprevalence of Neospora caninum (Apicomplexa: Toxoplasmatinae) in sheep from the State of Sergipe, Brazil. Braz J Vet Med 2019; 41(1): e002819. http://dx.doi.org/10.29374/2527-2179.bjvm002819.
http://dx.doi.org/10.29374/2527-2179.bjv...
in the state of Sergipe, who obtained seropositivity of 12.4% and by Nunes et al. (2020)Nunes ACBT, Silva EMV, Oliveira JÁ, Kim PCP, Almeida JC, Nunes KB, et al. Detection of anti-Neospora caninum antibodies in slaughteed sheep. Med Vet 2020; 14(4): 283-286. http://dx.doi.org/10.26605/medvet-v14n4-2371.
http://dx.doi.org/10.26605/medvet-v14n4-...
with 13% seroprevalence in the state of Alagoas, both in the Northeast region. Despite the similarity of these seroprevalences, Moraes et al. (2011)Moraes LMB, Raimundo JM, Guimarães A, Santos HA, Macedo GL Jr, Masssard CL, et al. Occurrence of anti-Neospora caninum and anti-Toxoplasma gondii IgG antibodies in goats and sheep in western Maranhão, Brazil. Rev Bras Parasitol Vet 2011; 20(4): 312-317. http://dx.doi.org/10.1590/S1984-29612011000400010. PMid:22166386.
http://dx.doi.org/10.1590/S1984-29612011...
in the state of Maranhão found seroprevalence of 4.69% in sheep and Tembue et al. (2011)Tembue AASM, Ramos RAN, Sousa TR, Albuquerque AR, Costa AJ, Meunier IMJ, et al. Serological survey of Neospora caninum in small ruminants from Pernambuco State, Brazil. Rev Bras Parasitol Vet 2011; 20(3): 246-248. http://dx.doi.org/10.1590/S1984-29612011000300013. PMid:21961757.
http://dx.doi.org/10.1590/S1984-29612011...
found a seroprevalence of 64.2% in sheep from the state of Pernambuco, both in Northeast region which demonstrate a high divergence in states from the same region where the climatic conditions are similar.

Such variations are also observed in different regions of Brazil. In the Southeastern region, there appears to be consistency in the distribution of the parasite, with seroprevalence rates ranging from 9.2% to 12.8% in the state of São Paulo (Figliuolo et al., 2004bFigliuolo LPC, Kasai N, Ragozo AMA, Paula VSO, Dias RA, Souza SLP, et al. Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in ovine from São Paulo State, Brazil. Vet Parasitol 2004b; 123(3-4): 161-166. http://dx.doi.org/10.1016/j.vetpar.2004.06.006. PMid:15325042.
http://dx.doi.org/10.1016/j.vetpar.2004....
; Langoni et al., 2011Langoni H, Greca H Jr, Guimarães FF, Ullmann LS, Gaio FC, Uehara RS, et al. Serological profile of Toxoplasma gondii and Neospora caninum infection in commercial sheep from São Paulo State, Brazil. Vet Parasitol 2011; 177(1-2): 50-54. http://dx.doi.org/10.1016/j.vetpar.2010.11.024. PMid:21256676.
http://dx.doi.org/10.1016/j.vetpar.2010....
; Machado et al., 2011Machado GP, Kikuti M, Langoni H, Paes AC. Seroprevalence and risk factors associated with neosporosis in sheep and dogs from farms. Vet Parasitol 2011; 182(2-4): 356-358. http://dx.doi.org/10.1016/j.vetpar.2011.05.021. PMid:21676548.
http://dx.doi.org/10.1016/j.vetpar.2011....
; Cosendey et al., 2018Cosendey RIJ, Oliveira FCR, Frazão-Teixeira E, Souza GN, Brandão FZ, Ferreira AMR, et al. Seroprevalence of anti-Neospora caninum antibodies in sheep from the rapidly expanding flock of Rio de Janeiro, Brazil. Vet Parasitol Reg Stud Rep 2018; 14: 59-62. http://dx.doi.org/10.1016/j.vprsr.2018.09.001. PMid:31014738.
http://dx.doi.org/10.1016/j.vprsr.2018.0...
), from 8.1% to 13.1% in the state of Minas Gerais (Salaberry et al., 2010Salaberry SRS, Okuda LH, Nassar AFC, Castro JR, Lima-Ribeiro AMC. Prevalence of Neospora caninum antibodies in sheep flocks of Uberlândia county, MG. Rev Bras Parasitol Vet 2010; 19(3): 148-151. http://dx.doi.org/10.1590/S1984-29612010000300004. PMid:20943017.
http://dx.doi.org/10.1590/S1984-29612010...
; Andrade et al., 2012Andrade GS, Bruhn FRP, Rocha CMBM, Guimarães AS, Gouveia AMG, Guimarães AM. Seroprevalence and risk factors for Neospora caninum in sheep in the state Minas Gerais, southeastern Brazil. Vet Parasitol 2012; 188(1-2): 168-171. http://dx.doi.org/10.1016/j.vetpar.2012.03.006. PMid:22475416.
http://dx.doi.org/10.1016/j.vetpar.2012....
), and a reported 6.2% in the state of Rio de Janeiro (Cosendey et al., 2018Cosendey RIJ, Oliveira FCR, Frazão-Teixeira E, Souza GN, Brandão FZ, Ferreira AMR, et al. Seroprevalence of anti-Neospora caninum antibodies in sheep from the rapidly expanding flock of Rio de Janeiro, Brazil. Vet Parasitol Reg Stud Rep 2018; 14: 59-62. http://dx.doi.org/10.1016/j.vprsr.2018.09.001. PMid:31014738.
http://dx.doi.org/10.1016/j.vprsr.2018.0...
). In the South region, seroprevalence rates range from 9.5% to 17.6% (Romanelli et al., 2007Romanelli PR, Freire RL, Vidotto O, Marana ERM, Ogawa L, Paula VSO, et al. Prevalence of Neospora caninum and Toxoplasma gondii in sheep and dogs from Guarapuava farms, Paraná State, Brazil. Res Vet Sci 2007; 82(2): 202-207. http://dx.doi.org/10.1016/j.rvsc.2006.04.001. PMid:17266999.
http://dx.doi.org/10.1016/j.rvsc.2006.04...
, 2021Romanelli PR, Matos AMRN, Pinto-Ferreira F, Caldart ET, Carmo JLM, Santos NG, et al. Anti-Toxoplasma gondii and anti-Neospora caninum antibodies in sheep from Paraná state, South Brazil: prevalence and associated factors. Rev Bras Parasitol Vet 2021; 30(1): e023220. http://dx.doi.org/10.1590/s1984-29612021021. PMid:33909837.
http://dx.doi.org/10.1590/s1984-29612021...
), suggesting a possible increasing trend in seropositivity. In the North region, seroprevalence rates range from 13.74% to 60.6% (Guimarães et al., 2015Guimarães A, Raimundo JM, Moraes LMB, Silva AT, Santos HA, Pires MS, et al. Occurrences of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in sheep from four districts of Tocantins state, Brazilian Legal Amazon Region. Pesq Vet Bras 2015; 35(2): 110-114. http://dx.doi.org/10.1590/S0100-736X2015000200002.
http://dx.doi.org/10.1590/S0100-736X2015...
; Maia et al., 2021Maia MO, Maia MO, Silva ARS, Gomes AAD, Aguiar DM, Pacheco RC, et al. Seroprevalence of Toxoplasma gondii and Neospora caninum in sheep intended for human consumption in the Rondônia state, Western Brazilian Amazon. Comp Immunol Microbiol Infect Dis 2021; 74: 101599. http://dx.doi.org/10.1016/j.cimid.2020.101599. PMid:33260021.
http://dx.doi.org/10.1016/j.cimid.2020.1...
), a range similar to that observed in the Northeast. These data illustrate a significant divergence from the findings presented in this study and others conducted in Brazil. It is important to acknowledge that variations between epidemiological studies can be attributed to several factors, including the inherent climatic conditions of the studied regions, the age of animals, the size of herds, the types of management practices, and variations in laboratory procedures such as evaluation methods, cutoff points used, the experience of the evaluator, and equipment maintenance (Dubey et al., 2007Dubey JP, Schares G, Ortega-mora LM. Epidemiology and control of Neosporosis and Neospora caninum. Clin Microbiol Rev 2007; 20(2): 323-367. http://dx.doi.org/10.1128/CMR.00031-06. PMid:17428888.
http://dx.doi.org/10.1128/CMR.00031-06...
; Nunes et al., 2020Nunes ACBT, Silva EMV, Oliveira JÁ, Kim PCP, Almeida JC, Nunes KB, et al. Detection of anti-Neospora caninum antibodies in slaughteed sheep. Med Vet 2020; 14(4): 283-286. http://dx.doi.org/10.26605/medvet-v14n4-2371.
http://dx.doi.org/10.26605/medvet-v14n4-...
).

The risk factors identified in the multivariate analysis for goats were contact with dogs and contact with cattle. Contact with dogs increased the chances of infection by 4.81 time according to the odds ratio. In according to the systematic review and meta-analysis performed by Rodrigues et al. (2020)Rodrigues AA, Reis SS, Sousa ML, Moraes ES, Garcia JL, Nascimento TVC, et al. A systematic literature review and meta-analysis of risk factors for Neospora caninum seroprevalence in goats. Prev Vet Med 2020; 185: 105176. http://dx.doi.org/10.1016/j.prevetmed.2020.105176. PMid:33129022.
http://dx.doi.org/10.1016/j.prevetmed.20...
, contact with dogs is the most frequently reported risk factors associated with N. caninum infection in goats. Dogs are the definitive hosts and their presence on the properties allows the occurrence of horizontal transmission associated with vertical transmission, which facilitates the propagations and perpetuation of the parasite in the herd (Nunes et al., 2017Nunes ACBT, Yamasaki EM, Kim PCP, Melo RPB, Ribeiro-Andrade M, Porto WJN, et al. Transplacental transmission of Neospora caninum in naturally infected small ruminants from northeastern Brazil. Pesq Vet Bras 2017; 37(9): 921-925. http://dx.doi.org/10.1590/s0100-736x2017000900004.
http://dx.doi.org/10.1590/s0100-736x2017...
; Pereira et al., 2021Pereira KAG, Sousa RS, Varaschin MS, Becker APBB, Monteiro ALG, Koch MO, et al. Transplacental transmission of Neospora caninum to lambs in successive pregnancies of naturally infected sheep in Southern Brazil. Vet Parasitol Reg Stud Rep 2021; 23: 100537. http://dx.doi.org/10.1016/j.vprsr.2021.100537. PMid:33678390.
http://dx.doi.org/10.1016/j.vprsr.2021.1...
).

Contact with cattle increased the chances of infection by 1.87 times according to the Odds ratio, probably because the parasite is an important cause of abortion for cattle, which favors the transmission of the disease to the definitive hosts, due to the ingestion of placental remains and allows the occurrence of the two main forms of transmission and the transmission to goats on properties that carry out goat and cattle farming concomitantly (Dubey et al., 2007Dubey JP, Schares G, Ortega-mora LM. Epidemiology and control of Neosporosis and Neospora caninum. Clin Microbiol Rev 2007; 20(2): 323-367. http://dx.doi.org/10.1128/CMR.00031-06. PMid:17428888.
http://dx.doi.org/10.1128/CMR.00031-06...
; Robbe et al., 2016Robbe D, Passarelli A, Gloria A, Di Cesare A, Capelli G, Lorio R, et al. Neospora caninum seropositivity and reproductive risk factors in dogs. Exp Parasitol 2016; 164: 31-35. http://dx.doi.org/10.1016/j.exppara.2016.02.003. PMid:26873272.
http://dx.doi.org/10.1016/j.exppara.2016...
).

In sheep, contact with dogs and history of abortion were considered risk factors. The contact of sheep with dogs increased the chances of infection by N. caninum by 2.32 times. Despite the presence of the definitive host enabling the occurrence of horizontal and vertical transmission, few studies have identified contact with dogs as a risk factor for sheep in Brazil (Machado et al., 2011Machado GP, Kikuti M, Langoni H, Paes AC. Seroprevalence and risk factors associated with neosporosis in sheep and dogs from farms. Vet Parasitol 2011; 182(2-4): 356-358. http://dx.doi.org/10.1016/j.vetpar.2011.05.021. PMid:21676548.
http://dx.doi.org/10.1016/j.vetpar.2011....
; Gheller et al., 2016Gheller JM, Carniel R, Carrasco AOT, Seki MC. Occurrence and risk factors for Toxoplasma gondii and Neospora caninum in sheep of the Guarapuava region, Paraná, Brazil. Braz J Vet Res Anim Sci 2016; 53(2): 177-181. http://dx.doi.org/10.11606/issn.1678-4456.v53i2p177-181.
http://dx.doi.org/10.11606/issn.1678-445...
;). Furthermore, Mendonça et al. (2019)Mendonça CED, Munhoz AD, Rocha DS, Guimarães LA, Bezerra RA, Albuquerque GR, et al. Factors associated with seroprevalence of Neospora caninum (Apicomplexa: Toxoplasmatinae) in sheep from the State of Sergipe, Brazil. Braz J Vet Med 2019; 41(1): e002819. http://dx.doi.org/10.29374/2527-2179.bjvm002819.
http://dx.doi.org/10.29374/2527-2179.bjv...
considered the presence of dogs on the property as protective factor for sheep, since the presence of dogs can limit the access of other canids and reduce pasture contamination. This divergence between studies of risk factors may occur due to the lack of standardization of epidemiological questionnaires, as well as the methodologies applied in epidemiological surveys (Dubey et al., 2007Dubey JP, Schares G, Ortega-mora LM. Epidemiology and control of Neosporosis and Neospora caninum. Clin Microbiol Rev 2007; 20(2): 323-367. http://dx.doi.org/10.1128/CMR.00031-06. PMid:17428888.
http://dx.doi.org/10.1128/CMR.00031-06...
).

The presence of a history of abortion on the property increased the chances of infection by 1.94 times. The history of abortion was also identified as a risk factor in other studies (Machado et al., 2011Machado GP, Kikuti M, Langoni H, Paes AC. Seroprevalence and risk factors associated with neosporosis in sheep and dogs from farms. Vet Parasitol 2011; 182(2-4): 356-358. http://dx.doi.org/10.1016/j.vetpar.2011.05.021. PMid:21676548.
http://dx.doi.org/10.1016/j.vetpar.2011....
; Gheller et al., 2016Gheller JM, Carniel R, Carrasco AOT, Seki MC. Occurrence and risk factors for Toxoplasma gondii and Neospora caninum in sheep of the Guarapuava region, Paraná, Brazil. Braz J Vet Res Anim Sci 2016; 53(2): 177-181. http://dx.doi.org/10.11606/issn.1678-4456.v53i2p177-181.
http://dx.doi.org/10.11606/issn.1678-445...
). Abortion in pastures or open areas facilitates ingestion of the placenta by dogs, which favors horizontal transmission through contamination of pastures with dog feces and may increase the occurrence of neosporosis in the herd (Romanelli et al., 2021Romanelli PR, Matos AMRN, Pinto-Ferreira F, Caldart ET, Carmo JLM, Santos NG, et al. Anti-Toxoplasma gondii and anti-Neospora caninum antibodies in sheep from Paraná state, South Brazil: prevalence and associated factors. Rev Bras Parasitol Vet 2021; 30(1): e023220. http://dx.doi.org/10.1590/s1984-29612021021. PMid:33909837.
http://dx.doi.org/10.1590/s1984-29612021...
). In addition, females are usually slaughtered older than males, which leads to a longer exposure time to the possibility of infection by N. caninum and allows the occurrence of congenital transmission more than once in a breeding female leading to contamination of several generations and greater probability of occurrence of abortions, for this reason N. caninum must be considered whenever there are cases of abortions, stillbirths and weak fetuses in the herd (Nunes et al., 2017Nunes ACBT, Yamasaki EM, Kim PCP, Melo RPB, Ribeiro-Andrade M, Porto WJN, et al. Transplacental transmission of Neospora caninum in naturally infected small ruminants from northeastern Brazil. Pesq Vet Bras 2017; 37(9): 921-925. http://dx.doi.org/10.1590/s0100-736x2017000900004.
http://dx.doi.org/10.1590/s0100-736x2017...
; Pereira et al., 2021Pereira KAG, Sousa RS, Varaschin MS, Becker APBB, Monteiro ALG, Koch MO, et al. Transplacental transmission of Neospora caninum to lambs in successive pregnancies of naturally infected sheep in Southern Brazil. Vet Parasitol Reg Stud Rep 2021; 23: 100537. http://dx.doi.org/10.1016/j.vprsr.2021.100537. PMid:33678390.
http://dx.doi.org/10.1016/j.vprsr.2021.1...
).

Conclusion

The seroprevalence of N. caninum found in this study in goats was the highest ever recorded in Brazil so far and indicates an increase in cases of infection by the parasite in the state of Paraíba. Contact between goats and dogs and cattle has been identified as a risk factor and should be avoided. In sheep, seroprevalence was considered high and contact between sheep and dogs was considered a risk factor. As well as the history of abortion in sheep, which should be considered and indicator of the disease in the herd. Understanding the epidemiology of the disease is essential to establish effective control and prophylaxis measures and minimize economic losses resulting from reproductive problems.

Acknowledgements

The authors would like to thank the Coordination for the Improvement of Higher Education Personnel (CAPES) - Scholarship grant to S.P.B and the National Council for Scientific and Technological Development (CNPq) for providing a scholarship to RAM, TFF and VLRV.

  • How to cite: Batista SP, Silva SS, Sarmento WF, Mota RA, Feitosa TF, Vilela VLR. Seroprevalence and associated factors with Neospora caninum infection in sheep and goats slaughtered in the state of Paraíba, Brazil. Braz J Vet Parasitol 2023; 32(4): e012423. https://doi.org/10.1590/S1984-29612023068

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Publication Dates

  • Publication in this collection
    27 Nov 2023
  • Date of issue
    2023

History

  • Received
    04 Aug 2023
  • Accepted
    04 Oct 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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