Skip to main content
  • Research article
  • Open access
  • Published:

Seroprevalence of Toxoplasma gondii infection in water buffaloes (Bubalus bubalis) in Veracruz State, Mexico and its association with climatic factors

Abstract

Background

Infection with Toxoplasma gondii in water buffaloes (Bubalus bubalis) is of epidemiological importance because of the risk for transmission to humans. We sought to determine the seroprevalence of T. gondii infection in 339 water buffaloes in Veracruz State, Mexico using the modified agglutination test (MAT, cut off 1:25). Seroprevalence association with general characteristics of buffaloes and their environment was also investigated.

Results

Antibodies to T. gondii were found in 165 (48.7%) of the 339 buffaloes with MAT titers of 1:25 in 104, 1:50 in 52, and 1:100 in 9. Bivariate analysis showed that seroprevalence of T. gondii infection was similar in buffaloes regardless of their general characteristics i.e., age, sex, and breed. In contrast, the seroprevalence in buffaloes varied significantly with environmental characteristics including altitude, mean annual temperature, and mean annual rainfall of the municipalities studied. Multivariate analysis showed that T. gondii seropositivity in buffaloes was associated with a mean annual rainfall between 1266–1650 mm (OR = 1.84; 95% CI: 1.15-2.94; P = 0.01).

Conclusions

Results indicate that environmental characteristics may influence the seroprevalence of T. gondii infection in buffaloes. This is the first report on the seroprevalence of T. gondii infection in buffaloes in Mexico. Further research is needed to assess the risk for infection in humans associated with the ingestion of raw or undercooked meat from buffaloes infected with T. gondii.

Background

Toxoplasma gondii is a widely distributed parasite infecting warm-blooded animals including the water buffalo (Bubalus bubalis) [1]. Toxoplasmosis in humans may be a severe disease affecting the lymph nodes, eyes, and central nervous system and can be life-threatening mostly in immunocompromised patients. Water buffaloes are important to the economy of many countries and in Mexico they represent an emerging alternative for diversified livestock production [2]. In Asia, water buffaloes are the major source of milk and milk products, and their meat is consumed by humans in several countries. In general, buffaloes, like cattle, are considered resistant to clinical toxoplasmosis and there is no valid report of isolation of viable T. gondii from buffalo meat [1],[3]. Recently, Dehkordi et al. [4] reported isolation of viable T. gondii from milk of 7 of 164 buffaloes in Iran, but the validity of these results has been questioned [5]. This report has raised concerns regarding transmission of T. gondii by consuming raw products from buffaloes.

We are not aware of any report of T. gondii infection in water buffaloes from Mexico. The objective of this study was to determine the seroprevalence and correlates of T. gondii infection in water buffaloes raised in several municipalities in Veracruz, Mexico.

Methods

Water buffaloes surveyed

Water buffaloes (Bubalus bubalis) (n = 339) from 2 geographical regions (Olmeca and Papaloapan) of Veracruz, Mexico were sampled from September 2012 to August 2013. These water buffaloes ranged freely and grazed on natural pastures. Sampling was based on accessibility to ranches raising buffaloes in the Mexican state of Veracruz that shares its eastern border with the Gulf of Mexico. Water buffaloes were located in 6 ranches throughout these 4 municipalities: Isla (18°02’N 95°32’W), Juan Rodriguez Clara (18°00’N 95°24’W), Las Choapas (17°55’N 94°06’W), and Sayula de Alemán (17°53’N 94°57’W). A questionnaire was used to obtain the general characteristics of the buffalo herds including age, sex, weight, breed, and obstetric history. Additionally, environmental data were recorded including presence of common water source shared with other animals in the ranch, cohabitation with other animals (cats, dogs, cattle), and climatic conditions. The age of the buffaloes ranged from 0.2 to 11 years old, 32 were males, and 307 females. Three water buffalo breeds were represented: Murrah, Carabao, and Jafarabadi.

Ethics statement

This project was approved by the Bioethics and Animal Welfare Commission of the Facultad de Medicina Veterinaria y Zootecnia of Universidad Veracruzana. Consent was obtained from the owners of the Buffaloes.

Serological examination for T. gondii antibodies

Serum samples were obtained and stored at −20°C until tested. Testing for T. gondii antibodies in the buffaloes’ sera was performed using 2-fold serial dilutions from 1:25 to 1:3200 with the modified agglutination test (MAT) as described by Dubey and Desmonts [6]. A titer of 1:25 was used as cut off for seropositivity in the MAT.

Statistical analysis

Statistical analysis was performed with the aid of Epi Info version 3.5.4. (Centers for Disease Control and Prevention: http://wwwn.cdc.gov/epiinfo/ and SPSS version 15.0 (SPSS Inc. Chicago, Illinois) software. The Pearson’s chi-squared test was used for comparison of the frequencies among groups. The association between the buffaloes’ characteristics and T. gondii seropositivity was assessed by multivariable analysis. The dependent variable was seropositivity to T. gondii by MAT for an individual animal. Independent variables included in the multivariable analysis were those with a P value ≤0.10 in the bivariate analysis: region, municipality, altitude, mean annual temperature, mean annual rainfall, and common water source. Odds ratio (OR) and 95% confidence interval (CI) were calculated by multivariate analysis using backward stepwise logistic regression analysis. The Hosmer-Lemeshow goodness of fit test was used to assess the fitness of the regression model. Statistical significance was set at a P value of < 0.05.

Results

Antibodies to T. gondii were found in 165 (48.7%) of the 339 buffaloes with MAT titers of 1:25 in 104, 1:50 in 52, and 1:100 in 9; none of the samples had a higher titer. Seroprevalence of T. gondii infection was significantly (P = 0.02) higher in buffaloes in the Olmeca region (53.3%) than in the Papaloapan region (40.8%). All ranches had seropositive buffaloes, and seroprevalence in buffaloes varied significantly (P = 0.009) among ranches (36.2%-63.8%).

A correlation of T. gondii seropositivity rates and environmental characteristics is shown in Table 1. The seroprevalence varied among municipalities (P = 0.002). The seroprevalence of T. gondii infection was significantly (P = 0.003) higher in buffaloes at 80-95 meters above sea level (121/222, 54.5%) than those at 10-60 meters above sea level (44/117, 37.6%). The seroprevalence in warm climate (142/280, 50.7%) was similar to the one in warm-humid climate (23/59, 39.0%) (P = 0.10). In contrast, the seroprevalence was significantly higher in municipalities with 27°C of mean annual temperature (114/214, 53.3%) than in those with 24.9-25°C mean annual temperature (51/125, 40.8%) (P = 0.02). In addition, seroprevalence varied among mean annual rainfall, the seroprevalence was significantly (P = 0.003) higher in municipalities with 1266-1650 mm of mean annual rainfall (121/222, 54.5%) than those with 2316-2900 mm of mean annual rainfall (44/117, 37.6%).

Table 1 Seroprevalence of T. gondii infection in water buffaloes in Veracruz, Mexico

Table 2 shows the correlation of T. gondii seropositivity rates and the general characteristics of the buffaloes. Seroprevalence of T. gondii infection did not vary with age, sex, breed, weight, and type of buffaloes, and with sharing of water, or contact with cattle. The seroprevalence of T. gondii infection was similar in female buffaloes with abortion history than in female buffaloes without abortion history. All buffaloes had contact with cats and dogs.

Table 2 Correlation of general characteristics of the 339 buffaloes and seroprevalence of T. gondii infection

Environmental and buffaloes characteristics with a P value equal to or less than 0.10 in the bivariate analysis included region (P = 0.02), municipality (P = 0.002), altitude (P = 0.002), a mean annual temperature of 27°C (P = 0.02), mean annual rainfall (P = 0.002), and water sharing (P = 0.10). Multivariate analysis of such characteristics showed that T. gondii seropositivity in buffaloes was associated only with a mean annual rainfall between 1266-1650 mm (OR = 1.84; 95% CI: 1.15-2.94; P = 0.01). The result of the Hosmer-Lemeshow test was 2 (P = 0.24) which indicates an acceptable fit of our regression model.

Discussion

Our results indicate that water buffaloes in Veracruz, Mexico have a relatively high seroprevalence of T. gondii infection. The worldwide prevalence of T. gondii infection in water buffaloes until 2010 was reviewed previously [1],[3], and seroprevalences varied from 0% to 100% by using MAT. Since then, a few additional papers were published on this subject. Antibodies to T. gondii were found in 1715 (35.5%) of 4796 water buffaloes from northern Brazil. They used an in-house ELISA and the cut-off titer for IFAT was 1:40 [7]. In a report from southern Brazil, antibodies were found in 46 (27.2%) of 169 water buffaloes by IFAT; sera were run at 1:64 and 1:256 dilutions and the seropositivity results were based on a titer of 1:64 [8]. In a study in Argentina, researchers found T. gondii antibodies in 127 (25.4%) of 500 buffaloes by IFAT using a 1:100 cut off titer [9]. Using the same MAT that we used, T. gondii antibodies were found in 53 (14.3%) of 300 water buffaloes in Iran; most of the buffaloes had low titers (1:25 in 21, 1:50 in 12, 1:100 in 6, 1:200 in 2 and 1:400 in 2) [10].

In most parts of the world water buffaloes are domesticated and probably acquire T. gondii by ingesting food or water contaminated with oocysts shed by infected domestic cats. Water buffaloes in the present report ranged freely and had contact with domestic and wild cats. Further research is needed to understand the dynamics of feline-buffalo transmission under free-ranging conditions in Veracruz, Mexico.

In the present study water buffaloes living in municipalities with a mean annual rainfall of 1266-1650 mm had a higher seroprevalence than those living in municipalities with higher mean annual rainfall (2316-2900 mm). It is not clear why a lower mean annual rainfall is associated with higher seroprevalence of T. gondii infection. It is possible that a higher mean annual rainfall might be accompanied with higher erosion of contaminated soil. In addition, copious rainfalls may dilute oocysts in contaminated water that might in turn lower the risk for T. gondii infection. Although we are unable to explain why other environmental factors (climate, altitude, and mean annual temperature) were associated with T. gondii infection, it has been postulated that shifts in environmental conditions can increase the prevalence of toxoplasmosis in susceptible hosts [11]. Environmental factors influencing the degree of oocysts exposure may also cause the difference in seropositivity among ranches as noted in water buffaloes from Trinidad [12]. There are no data regarding seroprevalence of T. gondii infection in cats among municipalities in Veracruz State. It would be of interest to test domestic and wild cats in the region for T. gondii infection.

Nothing is known of the validity of different serological tests used for the diagnosis of toxoplasmosis in buffaloes. We are not aware of any serious attempts at isolation of viable T. gondii from tissues of naturally exposed buffaloes. Buffaloes, like cattle, are considered resistant to clinical toxoplasmosis and we are not aware of any report of clinical toxoplasmosis in buffaloes [1]. Based on studies with naturally and experimentally infected cattle, the MAT gave the best results for determining antibodies to T. gondii in cattle [13],[14], and titers < 1:100 were considered nonspecific. A comparison of serological and bioassay data on naturally infected buffaloes is required to determine if the same criteria apply for MAT diagnosis of T. gondii infection in water buffaloes. The reported high excretion of viable T. gondii in milk of naturally infected buffaloes from Iran by Dehkordi et al. [4] needs confirmation. Further research should be conducted to determine the role of consumption of raw or undercooked meat from buffaloes in the transmission of T. gondii infection to humans.

Conclusion

Results of the present study indicate that buffaloes in Veracruz State have a high T. gondii exposure. Further research is needed to determine the risk of ingestion of raw or undercook buffalo meat for T. gondii infection in humans.

Authors’ contributions

CAE performed the laboratory tests, data analysis, and wrote the manuscript. DRS designed the study protocol, obtained the blood samples and general data of the buffaloes, analyzed the results, and helped in the writing of the manuscript. ZGV analyzed the results. ACR, APC, NIP, and MAD obtained the blood samples and general data of the buffaloes, and analyzed the results. AAPL performed the data analysis and helped in the writing of the manuscript. JPD analyzed the results and wrote the manuscript. All authors read and approved the final version of the manuscript.

References

  1. Dubey JP: Toxoplasmosis of Animals and Humans. 2nd edition. Boca Raton, Florida: CRC Press; 2010.

    Google Scholar 

  2. Suazo-Cortez R, Romero-Salas D, Villagómez-Cortés JA, Martínez-Herrera DI: First notification on the presence of brucellosis in water buffalo (Bubalus bubalis) in Mexico by serological tests. Afr J Microbiol Res. 2012, 6: 3242-3247.

    Google Scholar 

  3. Dubey JP, Beattie CP: Toxoplasmosis of Animals and Man. Boca Raton, Florida: CRC Press; 1988.

    Google Scholar 

  4. Dehkordi FS, Borujeni MR, Rahimi E, Abdizadeh R: Detection of Toxoplasma gondii in raw caprine, ovine, buffalo, bovine, and camel milk using cell cultivation, cat bioassay, capture ELISA, and PCR methods in Iran. Foodborne Pathog Dis. 2013, 10: 120-125. 10.1089/fpd.2012.1311.

    Article  CAS  PubMed  Google Scholar 

  5. Dubey JP, Jones JL: Comments on “detection of Toxoplasma gondii in raw caprine, ovine, buffalo, bovine, and camel milk using cell cultivation, cat bioassay, capture ELISA, and PCR methods in Iran”. Foodborne Pathog Dis. 2014, 11: 500-501. 10.1089/fpd.2014.1786.

    Article  PubMed  Google Scholar 

  6. Dubey JP, Desmonts G: Serological responses of equids fed Toxoplasma gondii oocysts. Equine Vet J. 1987, 19: 337-339. 10.1111/j.2042-3306.1987.tb01426.x.

    Article  CAS  PubMed  Google Scholar 

  7. da Silva JB, Dos Santos PN, de Santana-Castro GN, da Fonseca AH, Barbosa JD: Prevalence survey of selected bovine pathogens in water buffaloes in the north region of Brazil. J Parasitol Res. 2014, 2014: 603484-10.1155/2014/603484.

    Article  PubMed Central  PubMed  Google Scholar 

  8. Santos LM, Damé MC, Cademartori BG, da Cunha-Filho NA, Farias NA, Ruas JL: Occurrence of antibodies to Toxoplasma gondii in water buffaloes and meat cattle in Rio Grande do Sul State, southern Brazil. Acta Parasitol. 2013, 58: 334-336. 10.2478/s11686-013-0148-4.

    CAS  PubMed  Google Scholar 

  9. Konrad JL, Campero LM, Caspe GS, Brihuega B, Draghi G, Moore DP, Crudeli GA, Venturini MC, Campero CM: Detection of antibodies against Brucella abortus, Leptospira spp., and Apicomplexa protozoa in water buffaloes in the Northeast of Argentina. Tropl Anim Health Prod. 2013, 45: 1751-1756. 10.1007/s11250-013-0427-y.

    Article  Google Scholar 

  10. Hamidinejat H, Ghorbanpour M, Nabavi L, Haji Hajikolaie MR, Razi Jalali MH: Seroprevalence of Toxoplasma gondii in water buffaloes (Bubalus bubalis) in South-West of Iran. Trop Biomed. 2010, 27: 275-279.

    PubMed  Google Scholar 

  11. Meerburg BG, Kijlstra A: Changing climate-changing pathogens: Toxoplasma gondii in North-Western Europe. Parasitol Res. 2009, 105: 17-24. 10.1007/s00436-009-1447-4.

    Article  PubMed Central  PubMed  Google Scholar 

  12. Persad A, Charles R, Adesiyun AA: Frequency of Toxoplasmosis in Water Buffalo (Bubalus bubalis) in Trinidad. Vet Med Int. 2011, 2011: 705358-10.4061/2011/705358.

    Article  PubMed Central  PubMed  Google Scholar 

  13. Dubey JP, Desmonts G, McDonald C, Walls KW: Serologic evaluation of cattle inoculated with Toxoplasma gondii: comparison of Sabin-Feldman dye test and other agglutination tests. Am J Vet Res. 1985, 46: 1085-1088.

    CAS  PubMed  Google Scholar 

  14. Dubey JP, Thulliez P: Persistence of tissue cysts in edible tissues of cattle fed Toxoplasma gondii oocysts. Am J Vet Res. 1993, 54: 270-273.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

USDA is an equal opportunity provider and employer. This study was financed in part by Juárez University of Durango State.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Cosme Alvarado-Esquivel.

Additional information

Competing interests

The authors declare that they have no competing interests.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Alvarado-Esquivel, C., Romero-Salas, D., García-Vázquez, Z. et al. Seroprevalence of Toxoplasma gondii infection in water buffaloes (Bubalus bubalis) in Veracruz State, Mexico and its association with climatic factors. BMC Vet Res 10, 232 (2014). https://doi.org/10.1186/s12917-014-0232-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12917-014-0232-5

Keywords