Skip to main content
Download PDF

Toxoplasma gondii infection in interstate truck drivers: a case–control seroprevalence study

Parasites & Vectors volume 8, Article number: 77 (2015) Cite this article

Abstract

Background

Infection with Toxoplasma gondii can be acquired via the ingestion of undercooked or raw meat containing tissue cysts, or via ingestion of water contaminated with oocysts. Professional long distance truck driving may have epidemiological importance for food-borne infections since drivers eat out of home and in places where hygiene and cooking practices are uncertain. We aimed to determine whether interstate truck drivers in Durango, Mexico have an increased risk of infection with T. gondii as indicated by seropositivity; and to determine the socio-demographic, work, clinical, and behavioral characteristics associated with T. gondii seropositivity in interstate truck drivers.

Methods

Through a case–control study design, 192 truck drivers and 192 controls from the general population of the same region matched by gender and age were examined with enzyme-linked immunoassays for the presence of anti-Toxoplasma IgG and IgM antibodies. Socio-demographic, work, clinical and behavioral characteristics from the truck drivers were obtained.

Results

Anti-T. gondii IgG antibodies were found in 23 (12.0%) of 192 truck drivers and in 13 (6.8%) of 192 controls (OR = 21.0; 95% CI: 1.23-358.38; P = 0.002). Anti-T. gondii IgM antibodies were found in 7 (3.6%) cases and in 7 (3.6%) controls (P = 1.00). The seroprevalence of T. gondii infection was higher in drivers with reflex impairment than in those without this impairment (4/13, 30.8% vs 19/179, 10.6%, respectively; P = 0.05), and in drivers with hearing impairment than in those without this impairment (3/7, 42.9% vs 20/185, 10.8%, respectively; P = 0.03). Multivariate analysis of work and behavioral characteristics of truck drives showed positive associations of T. gondii exposure with trips to the south of Mexico (OR = 3.11; 95% CI: 1.02-9.44; P = 0.04) and consumption of horse meat (OR = 5.18; 95% CI: 1.62-16.55; P = 0.005).

Conclusions

Results suggest that interstate truck drivers may have an increased risk for T. gondii infection, and that T. gondii exposure may be impacting neurological functions in truck drivers. Contributing factors for T. gondii exposure should be taken into account for the design of optimal prevention measures against T. gondii infection.

Background

The protozoan parasite Toxoplasma gondii (T. gondii) causes infections in humans all around the world [1]. Most infections with T. gondii are acquired by ingesting food or water contaminated with T. gondii oocysts shed by cats or by eating undercooked or raw meat containing T. gondii tissue cysts [2]. Infections with T. gondii are usually asymptomatic but in some individuals infections may lead to severe disease. Toxoplasmosis is characterized by affection of the host’s lymph nodes, eyes, central nervous system, and other organs [2-5]. Infections with T. gondii have been associated with schizophrenia [6,7], traffic accidents [8], work accidents [9], and suicide attempts [10,11].

Interstate truck drivers are a group of workers driving trucks for long distances from one state to the other within a country and some of them drive trucks abroad too. This condition may have epidemiological importance for food-borne infectious diseases because such workers eat out of home in places where hygiene and cooking practices are uncertain. Eating away of home has been associated with T. gondii exposure in Mexico [12]. In a previous study in patients with liver disease, we observed that patients with an occupation of truck driver had a higher seroprevalence of T. gondii infection than those without this occupation [13]. However, case–control studies to assess the association of T. gondii exposure and interstate truck driver occupation have not been performed. Therefore, we performed an age- and gender matched case–control study to determine the association of T. gondii seropositivity with interstate truck driver occupation in Durango, Mexico. Furthermore, we investigated the socio-demographic, work, clinical, and behavioral characteristics associated with T. gondii seropositivity in the interstate truck drivers studied.

Methods

Study design and study populations

Through a case–control study design, we studied the association of seropositivity to T. gondii with interstate truck drivers. The present study was performed in Durango City, Mexico from November 2013 to July 2014.

Interstate truck drivers: One hundred and ninety two interstate truck drivers were enrolled in the study. Inclusion criteria for the cases were current working as interstate truck drivers for at least one year, aged 18 years and older, any gender, and who accepted to participate in the study. As a strategy to enroll drivers, they were invited to participate in gas stations, small motels for truck drivers, and truck stops on the roads. One hundred and eighty seven of them were males and five were female. The mean age of the drivers was 43.40 ± 10.16 years (range: 20–71 years).

Control subjects: One hundred and ninety two control subjects without truck driver occupation matched with drivers by age and gender were included in the study. Control subjects were randomly selected from the general population of Durango City, Mexico. The mean age in controls was 43.45 ± 10.21 (range: 20–71 years) and comparable with that in truck drivers (P = 0.96).

Socio-demographic, clinical, work and behavioral data

We obtained the socio-demographic, work, clinical and behavioral characteristics of the participants with the aid of a standardized questionnaire. Socio-demographic items included age, gender, birthplace, residence area, educational level, and socio-economic level. Work characteristics assessed in truck drivers included number of years in the activity, type of materials transported, frequency and duration of trips, regions and number of states visited within Mexico, work abroad, traffic accidents, type of places of getting meals out of home, transportation of animals, and washing the truck by themselves. Clinical data in truck drivers included presence of any disease, presence or history of lymphadenopathy, frequent headache, dizziness, impairments in memory, reflexes, hearing and vision, and history of blood transfusion, transplant or surgery. Behavioral items included contact with animals or cat feces, type of meat consumed, consumption of raw or undercooked meat, unpasteurized milk, dried or cured meat, consumption of unwashed raw vegetables, fruits, or untreated water, frequency of eating away from home (in restaurants or fast food outlets), washing hands before eating, contact with soil, and type of flooring at home.

Laboratory tests

A blood sample from each participant was obtained. Blood samples were centrifuged and sera were obtained and kept frozen at −20°C until analyzed. Sera were analyzed by qualitative and quantitative methods for anti-T. gondii IgG antibodies with the commercially available enzyme immunoassay kit “Toxoplasma IgG” (Diagnostic Automation Inc., Calabasas, CA, USA). Anti-T. gondii IgG antibody levels were expressed as International Units (IU)/ml, and a result equal to or greater than 8 IU/ml was considered positive. In addition, sera positive for anti-T. gondii IgG antibodies were further analyzed for anti-T. gondii IgM antibodies by the commercially available enzyme immunoassay “Toxoplasma IgM” kit (Diagnostic Automation Inc., Calabasas, CA, USA). All tests were performed following the instructions of the manufacturer.

Statistical analysis

We performed the statistical analysis with the aid of Epi Info version 7 and SPSS 15.0 (SPSS Inc. Chicago, Illinois). For calculation of the sample size, we used a 95% confidence level, a power of 80%, a 1:1 proportion of cases and controls, a reference seroprevalence of 6.1% [14] as the expected frequency of exposure in controls, and an odds ratio of 2.8. The result of the sample size calculation was 175 cases and 175 controls. Age among the groups was compared by the student’s t test. For comparison of the seroprevalences of T. gondii infection between truck drivers and control subjects, the McNemar’s test was used. We used the Pearson’s chi-squared test and the two-tailed Fisher’s exact test (when values were less than 5) to determine the association of T. gondii seropositivity and the characteristics of the drivers studied. Odds ratio (OR) and 95% confidence interval (CI) were calculated by multivariate analysis using logistic regression with the Enter method. Variables were included in the multivariate analysis if they had a P value less than 0.05 in the bivariate analysis. The Hosmer-Lemeshow goodness of fit test was used to assess the fitness of our regression model. Statistical significance was set at a P value less than 0.05.

Ethical aspects

This study was approved by the Institutional Ethical Committee of the General Hospital of the Secretary of Health in Durango City. The purpose and procedures of the study were explained to all participants, and a written informed consent was obtained from each participant. Participants did not receive financial compensation.

Results

Anti-T. gondii IgG antibodies were found in 23 (12.0%) of 192 interstate truck drivers and in 13 (6.8%) of 192 controls. The difference between the seroprevalences in cases and controls was statistically significant according to the McNemar’s pair test (OR = 21.0; 95% CI: 1.23-358.38; P = 0.002). Of the 23 anti-T. gondii IgG positive drivers, 11 (5.7%) had IgG levels higher than 150 IU/ml, 1 (0.5%) between 100 to 150 IU/ml, and 11 (5.7%) between 8 to 99 IU/ml. In contrast, of the 13 anti-T. gondii IgG positive controls, 8 (4.2%) had IgG levels higher than 150 IU/ml, 1 (0.5%) between 100 to 150 IU/ml, and 4 (2.1%) between 8 to 99 IU/ml. Prevalence of high (>150 IU/ml) anti-T. gondii IgG levels was comparable among drivers and controls (P = 0.48). Anti-T. gondii IgM antibodies were found in 7 (3.6%) cases and in 7 (3.6%) controls (P = 1.00).

The socio-demographic characteristics among Toxoplasma-positive and Toxoplasma-negative drivers were not significantly different (Table 1). Of the work characteristics, only two variables showed potential association with seropositivity by bivariate analysis: “trips to the south of Mexico” (P = 0.007) and “number of eating places during trips” (P = 0.01). Concerning clinical characteristics of drivers, the seroprevalence of T. gondii infection was higher in drivers with reflex impairment than in those without this impairment (4/13, 30.8% vs 19/179, 10.6%, respectively; P = 0.05), and in drivers with hearing impairment than in those without this impairment (3/7, 42.9% vs 20/185, 10.8%, respectively; P = 0.03). In the subset of 62 drivers with traffic accidents, the frequency of T. gondii infection was significantly higher in drivers with reflexes impairment than in those without this impairment (3/5, 60% vs 7/57, 12.3%, respectively; P = 0.02). In the same subset of drivers with traffic accidents, the frequency of T. gondii infection was similar in drivers with hearing impairment than in those without this impairment (0/1, 0% vs 10/61, 16.4%, respectively; P = 1.0). Other clinical characteristics assessed were not associated with T. gondii seropositivity.

Table 1 Socio-demographic characteristics of truck drivers and seroprevalence of T. gondii infection
Full size table

Of the behavioral characteristics, only seven variables showed potential association with T. gondii seropositivity by bivariate analysis (P values <0.05): consumption of meat from goat, rabbit, horse, armadillo, iguana, snake and type of flooring at home. Multivariate analysis of work and behavioral characteristics of truck drives with P value <0.05 obtained in bivariate analysis showed two positive associations of T. gondii exposure including trips to the south of Mexico (OR = 3.11; 95% CI: 1.02-9.44; P = 0.04) and consumption of horsemeat (OR = 5.18; 95% CI: 1.62-16.55; P = 0.005) (Table 2). The result of the Hosmer-Lemeshow test (P = 0.47) indicated an acceptable fit of our regression model.

Table 2 Multivariate analysis of selected characteristics of truck drivers and their association with T. gondii infection
Full size table

Discussion

Toxoplasmosis is a food-borne [15] and a water-borne disease [16]. The seroprevalence of infection with T. gondii differs from state to state or region in the general population dependent on the presence or absence of risk factors for the infection. People living in low seroprevalence areas therefore have an increased risk for infection when visiting high seroprevalence states. The frequent traveling to different regions could therefore represent a risk factor for infection with T. gondii in interstate truck drivers. In the present study, the seroprevalence of T. gondii infection (12%) was significantly higher in interstate truck drivers than in control subjects of the general population of Durango City. This two-fold increase points towards an association of T. gondii infection with an occupation of interstate truck driver. To the best of our knowledge, this is the first age- and gender matched case control study that demonstrates this association.

We attempted to identify contributing factors for infection in the truck drivers. The number of variables assessed in the present study was large. However, the number of variables was reduced by performing firstly bivariate analysis of all variables followed by multivariate analysis of a small number of selected variables with potential association (P < 0.05) with T. gondii seropositivity. None of the socio-demographic characteristics of the drivers was associated with T. gondii seropositivity. Multivariate analysis of work and behavioral characteristics of drivers showed that T. gondii infection was associated with work trips to the south of Mexico and with consumption of horsemeat. The seroprevalence of T. gondii infection in the general population is higher in southern Mexican states than in northern Mexican states. Seroprevalences higher than 50% have been found in southern Mexican states [17]. In contrast, a 6.1% seroprevalence of T. gondii infection in the general population in the northern Mexican city of Durango was found [14]. Differences in climatic conditions may contribute to a higher seroprevalence of T. gondii infection in southern Mexican states. Seroprevalence of T. gondii infection is higher in humid than in dry climates [18-20]. Durango has a dry climate while southern Mexican states have a more humid climate. Regarding the association of T. gondii infection with consumption of horsemeat, this is the first time we found such association in a Mexican population. Our result strengthens the epidemiological role of horsemeat as a source of T. gondii infection. A 6.1% seroprevalence of T. gondii infection in horses in Durango State was reported recently [21]. We are not aware of further studies on the seroprevalence of T. gondii infection in equids in other Mexican states. Viable T. gondii has been recovered from tissues of equids experimentally infected with parasite oocysts [22]. In addition, several cases of clinical toxoplasmosis due to consumption of horsemeat have been described [23,24]. None of the drivers studied referred to eat raw meat. Nevertheless, there is no certainty that tissue cysts, if present in the horsemeat consumed, were all inactivated by cooking. Several factors including temperature and time of cooking, and thickness of meat should be consider for inactivation of tissue cysts. In a study using infectivity bioassays in cats and mice, inactivation of tissue cysts in sheep meat was reached by cooking meat at 60°C or 100°C for 10 minutes [25]. Further research to determine the heating parameters for inactivation of tissue cysts in horsemeat is needed.

Infection with T. gondii has been associated with traffic accidents [8] and reflex impairment [26]. In the present study, drivers with traffic accidents had a higher, but not statistically significant, seroprevalence of T. gondii infection than drivers without traffic accidents. The lack of association of T. gondii infection and traffic accidents may be due to a small sample size of our study population. However, since reflexes impairment showed a borderline (P = 0.05) association with T. gondii exposure in the present study we further assess whether seropositivity to T. gondii in the subset of drivers with traffic accidents differ between drivers with reflexes impairment and those without this impairment. Remarkably, seroprevalence of T. gondii infection in the subset of drivers with traffic accidents was significantly higher in drivers with reflex impairment than in those without this impairment. Results thus suggest that infection with T. gondii might lead to reflexes impairment that in turn may contribute for traffic accidents. Chronic infection with T. gondii has been associated with slowing of neural processing speed [27], reduced psychomotor performance and changes in behavior [28]. In the present study, we also found that T. gondii infection was associated with hearing impairment. This impairment might also contribute for traffic accidents. Infection with T. gondii has been associated with hearing loss in congenital toxoplasmosis. This hearing loss is likely caused by inflammation induced by tachyzoites of T. gondii [29]. Congenital hearing loss has not always been associated with primary infection during pregnancy [30], and very little is known about hearing loss caused by T. gondii in adults. In a previous study in an ethnic group (Tepehuanos) in Durango, Mexico, we found a significantly higher seroprevalence of IgM antibodies against T. gondii in subjects suffering from hearing impairment than those without this impairment [31]. It is unclear whether infection with T. gondii may affect the inner ear. However, dizziness -a symptom that may reflect disease in the inner ear- has been associated with T. gondii infection in the ethnic group of Huicholes [32] and in migrant agricultural workers in Durango, Mexico [33]. Further research to elucidate the role of T. gondii infection in inner ear disease is needed.

Conclusions

Results of this first case–control study suggest that interstate truck drivers in Mexico are at increased risk for T. gondii infection, and that T. gondii exposure may impact the health of truck drivers. Contributing factors for T. gondii exposure such as horsemeat should be taken into account for the design of optimal prevention measures against T. gondii infection.

References

  1. Dubey JP. Toxoplasmosis of Animals and Humans. 2nd ed. Boca Raton, Florida: CRC Press; 2009.

    Book  Google Scholar 

  2. Montoya JG, Liesenfeld O. Toxoplasmosis. Lancet. 2004;363:1965–76.

    Article  CAS  PubMed  Google Scholar 

  3. Walker M, Zunt JR. Parasitic central nervous system infections in immunocompromised hosts. Clin Infect Dis. 2005;40:1005–15.

    Article  PubMed Central  PubMed  Google Scholar 

  4. Balasundaram MB, Andavar R, Palaniswamy M, Venkatapathy N. Outbreak of acquired ocular toxoplasmosis involving 248 patients. Arch Ophthal. 2010;128:28–32.

    Article  PubMed  Google Scholar 

  5. Karasawa T, Shikata T, Takizawa I, Morita K, Komukai M. Localized hepatic necrosis related to cytomegalovirus and Toxoplasma gondii. Acta Pathol Jpn. 1981;31:527–34.

    CAS  PubMed  Google Scholar 

  6. Torrey EF, Bartko JJ, Yolken RH. Toxoplasma gondii and other risk factors for schizophrenia: an update. Schizophr Bull. 2012;38:642–7.

    Article  PubMed Central  PubMed  Google Scholar 

  7. Alvarado-Esquivel C, Urbina-Álvarez JD, Estrada-Martínez S, Torres-Castorena A, Molotla-de-León G, Liesenfeld O, et al. Toxoplasma gondii infection and schizophrenia: a case control study in a low Toxoplasma seroprevalence Mexican population. Parasitol Int. 2011;60:151–5.

    Article  PubMed  Google Scholar 

  8. Flegr J, Havlícek J, Kodym P, Malý M, Smahel Z. Increased risk of traffic accidents in subjects with latent toxoplasmosis: a retrospective case–control study. BMC Infect Dis. 2002;2:11.

    Article  PubMed Central  PubMed  Google Scholar 

  9. Alvarado-Esquivel C, Torres-Castorena A, Liesenfeld O, Estrada-Martínez S, Urbina-Álvarez JD. High seroprevalence of Toxoplasma gondii infection in a subset of Mexican patients with work accidents and low socioeconomic status. Parasit Vectors. 2012;5:13.

    Article  PubMed Central  PubMed  Google Scholar 

  10. Arling TA, Yolken RH, Lapidus M, Langenberg P, Dickerson FB, Zimmerman SA, et al. Toxoplasma gondii antibody titers and history of suicide attempts in patients with recurrent mood disorders. J Nerv Ment Dis. 2009;197:905–8.

    Article  PubMed  Google Scholar 

  11. Alvarado-Esquivel C, Sánchez-Anguiano LF, Arnaud-Gil CA, López-Longoria JC, Molina-Espinoza LF, Estrada-Martínez S, et al. Toxoplasma gondii infection and suicide attempts: a case–control study in psychiatric outpatients. J Nerv Ment Dis. 2013;201:948–52.

    Article  PubMed  Google Scholar 

  12. Alvarado-Esquivel C, Liesenfeld O, Torres-Castorena A, Estrada-Martínez S, Urbina-Alvarez JD, Ramos-de la Rocha M, et al. Seroepidemiology of Toxoplasma gondii infection in patients with vision and hearing impairments, cancer, HIV, or undergoing hemodialysis in Durango, Mexico. J Parasitol. 2010;96:505–8.

    Article  CAS  PubMed  Google Scholar 

  13. Alvarado-Esquivel C, Torres-Berumen JL, Estrada-Martínez S, Liesenfeld O, Mercado-Suarez MF. Toxoplasma gondii infection and liver disease: a case–control study in a northern Mexican population. Parasit Vectors. 2011;4:75.

    Article  PubMed Central  PubMed  Google Scholar 

  14. Alvarado-Esquivel C, Estrada-Martínez S, Pizarro-Villalobos H, Arce-Quiñones M, Liesenfeld O, Dubey JP. Seroepidemiology of Toxoplasma gondii infection in general population in a northern Mexican city. J Parasitol. 2011;97:40–3.

    Article  CAS  PubMed  Google Scholar 

  15. Tenter AM. Toxoplasma gondii in animals used for human consumption. Mem Inst Oswaldo Cruz. 2009;104:364–9.

    Article  PubMed  Google Scholar 

  16. Dubey JP. Toxoplasmosis - a waterborne zoonosis. Vet Parasitol. 2004;126:57–72.

    Article  CAS  PubMed  Google Scholar 

  17. Velasco-Castrejón O, Salvatierra-Izaba B, Valdespino JL, Sedano-Lara AM, Galindo-Virgen S, Magos C, et al. Seroepidemiology of toxoplasmosis in Mexico. Salud Publica Mex. 1992;34:222–9.

    Article  PubMed  Google Scholar 

  18. Julvez J, Magnaval JF, Meynard D, Perie C, Baixench MT. Seroepidemiology of toxoplasmosis in Niamey, Niger. Med Trop (Mars). 1996;56:48–50.

    CAS  Google Scholar 

  19. Assmar M, Amirkhani A, Piazak N, Hovanesian A, Kooloobandi A, Etessami R. Toxoplasmosis in Iran. Results of a seroepidemiological study. Bull Soc Pathol Exot. 1997;90:19–21.

    CAS  PubMed  Google Scholar 

  20. Markovich MP, Shohat T, Riklis I, Avni R, Yujelevski-Rozenblit D, Bassal R, et al. Seroepidemiology of Toxoplasma gondii infection in the Israeli population. Epidemiol Infect. 2014;142:149–55. doi:10.1017/S0950268813000903.

    CAS  PubMed  Google Scholar 

  21. Alvarado-Esquivel C, Rodríguez-Peña S, Villena I, Dubey JP. Seroprevalence of Toxoplasma gondii infection in domestic horses in Durango State, Mexico. J Parasitol. 2012;98:944–5. doi:10.1645/GE-3174.1.

    Article  CAS  PubMed  Google Scholar 

  22. Dubey JP. Persistence of encysted Toxoplasma gondii in tissues of equids fed oocysts. Am J Vet Res. 1985;46:1753–4.

    CAS  PubMed  Google Scholar 

  23. Pomares C, Ajzenberg D, Bornard L, Bernardin G, Hasseine L, Darde ML, et al. Toxoplasmosis and horse meat, France. Emerg Infect Dis. 2011;17:1327–8. doi:10.3201/eid1707.101642.

    Article  PubMed Central  PubMed  Google Scholar 

  24. Sobanski V, Ajzenberg D, Delhaes L, Bautin N, Just N. Severe toxoplasmosis in immunocompetent hosts: be aware of atypical strains. Am J Respir Crit Care Med. 2013;187:1143–5. doi:10.1164/rccm.201209-1635LE.

    Article  PubMed  Google Scholar 

  25. El-Nawawi FA, Tawfik MA, Shaapan RM. Methods for inactivation of Toxoplasma gondii cysts in meat and tissues of experimentally infected sheep. Foodborne Pathog Dis. 2008;5:687–90. doi:10.1089/fpd.2007.0060.

    Article  PubMed  Google Scholar 

  26. Alvarado-Esquivel C, Estrada-Martínez S, Liesenfeld O. Toxoplasma gondii infection in workers occupationally exposed to unwashed raw fruits and vegetables: a case control seroprevalence study. Parasit Vectors. 2011;4:235. doi:10.1186/1756-3305-4-235.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  27. Pearce BD, Hubbard S, Rivera HN, Wilkins PP, Fisch MC, Hopkins MH, et al. Toxoplasma gondii exposure affects neural processing speed as measured by acoustic startle latency in schizophrenia and controls. Schizophr Res. 2013;150:258–61. doi:10.1016/j.schres.2013.07.028.

    Article  PubMed Central  PubMed  Google Scholar 

  28. Flegr J. Effects of Toxoplasma on human behavior. Schizophr Bull. 2007;33:757–60.

    Article  PubMed Central  PubMed  Google Scholar 

  29. Salviz M, Montoya JG, Nadol JB, Santos F. Otopathology in congenital toxoplasmosis. Otol Neurotol. 2013;34:1165–9. doi:10.1097/MAO.0b013e31828297b6.

    Article  PubMed Central  PubMed  Google Scholar 

  30. Austeng ME, Eskild A, Jacobsen M, Jenum PA, Whitelaw A, Engdahl B. Maternal infection with Toxoplasma gondii in pregnancy and the risk of hearing loss in the offspring. Int J Audiol. 2010;49:65–8. doi:10.3109/14992020903214053.

    Article  PubMed  Google Scholar 

  31. Alvarado-Esquivel C, Estrada-Martínez S, García-López CR, Rojas-Rivera A, Sifuentes-Álvarez A, Liesenfeld O. Seroepidemiology of Toxoplasma gondii infection in Tepehuanos in Durango, Mexico. Vector Borne Zoonotic Dis. 2012;12:138–42. doi:10.1089/vbz.2011.0747.

    Article  PubMed  Google Scholar 

  32. Alvarado-Esquivel C, Pacheco-Vega SJ, Hernández-Tinoco J, Sánchez-Anguiano LF, Berumen-Segovia LO, Rodríguez-Acevedo FJ, et al. Seroprevalence of Toxoplasma gondii infection and associated risk factors in Huicholes in Mexico. Parasit Vectors. 2014;7:301. doi:10.1186/1756-3305-7-301.

    Article  PubMed Central  PubMed  Google Scholar 

  33. Alvarado-Esquivel C, Campillo-Ruiz F, Liesenfeld O. Seroepidemiology of infection with Toxoplasma gondii in migrant agricultural workers living in poverty in Durango, Mexico. Parasit Vectors. 2013;6:113. doi:10.1186/1756-3305-6-113.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgements

This study was supported by Juarez University of Durango State, Mexico.

Author information

Authors and Affiliations

  1. Faculty of Medicine and Nutrition, Juárez University of Durango State, Avenida Universidad S/N, 34000, Durango, Dgo, Mexico

    Cosme Alvarado-Esquivel, Sandy Janet Pacheco-Vega, Misael Salcedo-Jáquez, Luis Omar Berumen-Segovia & Elizabeth Rábago-Sánchez

  2. Institute for Scientific Research “Dr. Roberto Rivera Damm”, Juárez University of Durango State, Avenida Universidad S/N, 34000, Durango, Durango, Mexico

    Jesús Hernández-Tinoco & Luis Francisco Sánchez-Anguiano

  3. General Hospital, Secretary of Health, Avenida 5 de febrero 220, 34000, Durango, Mexico

    Elizabeth Rábago-Sánchez

  4. Institute for Microbiology and Hygiene, Campus Benjamin Franklin, Charité Medical School, Hindenburgdamm 27, D-12203, Berlin, Germany

    Oliver Liesenfeld

  5. Current address: Medical and Scientific Affairs, Roche Molecular Systems, Pleasanton, CA, 94588, USA

    Oliver Liesenfeld

Authors
  1. Cosme Alvarado-Esquivel
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Sandy Janet Pacheco-Vega
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Jesús Hernández-Tinoco
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Misael Salcedo-Jáquez
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Luis Francisco Sánchez-Anguiano
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Luis Omar Berumen-Segovia
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Elizabeth Rábago-Sánchez
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Oliver Liesenfeld
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Cosme Alvarado-Esquivel.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

CAE conceived and designed the study protocol, participated in the coordination and management of the study, performed the laboratory tests, data analysis, and wrote the manuscript. SJPV, MSJ, and LOBS obtained blood samples, applied questionnaires and performed the data analysis. JHT, LFSA, and ERS performed the data analysis. OL performed the data analysis, and wrote the manuscript. All authors read and approved the final manuscript.

Rights and permissions

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., Pacheco-Vega, S.J., Hernández-Tinoco, J. et al. Toxoplasma gondii infection in interstate truck drivers: a case–control seroprevalence study. Parasites Vectors 8, 77 (2015). https://doi.org/10.1186/s13071-015-0690-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13071-015-0690-z

Keywords

Parasites & Vectors

ISSN: 1756-3305

Contact us