Seroprevalence of Toxoplasma gondii infection in arthritis patients in eastern China
Infectious Diseases of Poverty volume 6, Article number: 153 (2017)
There is accumulating evidence for an increased susceptibility to infection in patients with arthritis. We sought to understand the epidemiology of Toxoplasma gondii infection in arthritis patients in eastern China, given the paucity of data on the magnitude of T. gondii infection in these patients.
Seroprevalence of T. gondii infection was assessed by enzyme-linked immunosorbent assay using a crude antigen of the parasite in 820 arthritic patients, and an equal number of healthy controls, from Qingdao and Weihai cities, eastern China. Sociodemographic, clinical and lifestyle information on the study participants were also obtained.
The prevalence of anti-T. gondii IgG was significantly higher in arthritic patients (18.8%) compared with 12% in healthy controls (P < 0.001). Twelve patients with arthritis had anti-T. gondii IgM antibodies – comparable with 10 control patients (1.5% vs 1.2%). Demographic factors did not significantly influence these seroprevalence frequencies. The highest T. gondii infection seropositivity rate was detected in patients with rheumatoid arthritis (24.8%), followed by reactive arthritis (23.8%), osteoarthritis (19%), infectious arthritis (18.4%) and gouty arthritis (14.8%). Seroprevalence rates of rheumatoid arthritis and reactive arthritis were significantly higher when compared with controls (P < 0.001 and P = 0.002, respectively). A significant association was detected between T. gondii infection and cats being present in the home in arthritic patients (odds ratio [OR], 1.68; 95% confidence interval [CI]: 1.24 – 2.28; P = 0.001).
These findings are consistent with and extend previous results, providing further evidence to support a link between contact with cats and an increased risk of T. gondii infection. Our study is also the first to confirm an association between T. gondii infection and arthritis patients in China. Implications for better prevention and control of T. gondii infection in arthritis patients are discussed.
This is an epidemiological survey, therefore trial registration was not required.
Please see Additional file 1 for translation of the abtract into the five official working languages of the United Nations.
Toxoplasmosis is a parasitic disease caused by infection with the obligate intracellular apicomplexan protozoan Toxoplasma gondii. This parasite is able to infect all warm-blooded animals and chronically infects approximately one-third of the world’s human population . In immunocompetent individuals, T. gondii infection induces no apparent morbidity. In immunocompromised individuals however, or patients undergoing immunosuppressive treatments or during pregnancy, infection with T. gondii can cause serious clinical consequences and even death [2,3,4,5]. Many of the clinical manifestations of acute toxoplasmosis are partially mediated by an overproduction of the patient’s pro-inflammatory cytokines, e.g. tumor necrosis factor alpha (TNF-α), interleukin-1 (IL-1) and interferon gamma (IFN-γ) , all of which are important in limiting the parasite’s growth [7,8,9].
There is growing interest in exploring the link between infection with this parasite and autoimmune diseases, given the propensity of T. gondii infection to occur in immunocompromised patients [10,11,12,13,14]. Opportunistic infection with T. gondii is an increasing problem in association with inflammatory rheumatoid arthritis (RA) [15,16,17]. A heightened risk of T. gondii infection in patients with rheumatic diseases can be attributed to alterations in innate and adaptive immune responses . Patients with RA were found to be highly susceptible to T. gondii infection - particularly during periods of immunosuppression that followed treatment with TNF-α inhibitors . Contrasting data, however, suggest that T. gondii infection may ameriolate the severity of arthritis - delaying its onset in IL-1 receptor antagonist-deficient mice via T. gondii-derived Th1 immune response against Th17 cell-mediated arthritis .
Any reduction in the body’s defences against infection places arthritis patients at risk. Recognising the early symptoms of infection, while knowing the factors that increase susceptibility to T. gondii infection in patients with arthritis, will enable medical professionals to better assess patients’ needs, plan preventative therapy and initiate supportive measures. Several questions remain unanswered: Firstly, it is not clear whether there is an association between T. gondii infection and an increased risk of all forms of arthritis, or if the risk is limited to specific forms of arthritis. Secondly, it is unclear whether demographic or lifestyle variables increase the risk of T. gondii infection in arthritis patients. Thirdly, the prevalence of T. gondii infection in arthritis patients in China is still unknown. The present study was designed to investigate any possible association between T. gondii infection and arthritis by assessing the seroprevalence of, and risk factors associated with, T. gondii infection in patients with defined clinical forms of arthritis in eastern China.
The study was conducted in two cities, Qingdao and Weihai, in Shandong Province, eastern China (Fig. 1). Qingdao is located at the south-eastern tip of Shandong Province (35°35′ – 37°09′N, 119°30′ – 121°00′E) and Weihai is located at the eastern tip of Shandong province (36°41′ – 37°35′N, 121°11′ – 122°42′E).
Study design and data collection
A case-control study was conducted in order to identify the prevalence of, and risk factors associated with, T. gondii seropositivity in patients with arthritis. The study was undertaken between December 2014 and November 2015, and included 820 inpatients hospitalized with the diagnosis or for treatment of arthritis. The clinical cases included patients with rheumatoid arthritis (n = 238), reactive arthritis (n = 122), osteoarthritis (n = 142), infectious arthritis (n = 109) and gouty arthritis (n = 209). An equivalent number of healthy control subjects (n = 820), of similar age and gender and from the same geographic region, were included in the study. We included only those individuals who had no history or current evidence of infection or comorbidities. Information on demographics; such as age, gender and area of residence, was obtained from the computerized inpatient registry of cases, or by asking the control individuals. A questionnaire was distributed to adult individuals, and to the parents/guardians of children, in order to obtain information about their lifestyle and feeding habits - including any history of contact with cats in the home (Yes/No), contact with pigs (Yes/No), the consumption of raw vegetables (Yes/No), consumption of raw/undercooked meat (Yes/No) and exposure to soil (Yes/No). All personal information was anonymized and treated as strictly confidential.
Serum collection and serological testing
Approximately 5 ml of venous blood was drawn from each participant. Blood samples were stored overnight at ambient temperature, in order to allow blood clot formation, and then centrifuged at 1000×g for 10 min. The sera were collected in 2-ml Eppendorf tubes and kept at 4 °C for 24 – 48 h, until they were transported in an icebox to the State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Gansu Province. Samples were stored (−20 °C) at the State Key Labs until analysis. Serum samples were analyzed for the presence of anti-T. gondii IgG and IgM antibodies using commercially available ELISA kits (Demeditec Diagnostics GmbH, Germany), according to the manufacturer’s instructions. Positive and negative serum controls were included in each plate. There was a concern that sera from RA patients might contain Rheumatoid factor (RF) autoantibody, which could potentially cross react non-specifically with IgM, leading to a false-positive result in the T. gondii IgM ELISA test . Future work should consider using RF Neutralization Reagents (RFNR) to remove the RF from positive IgM specimens, then retesting these specimens. Samples would not be interpreted as positive for the specific IgM antibodies, unless they remained positive following adsorption with the RFNR.
Statistical analysis was performed using the statistical software SPSS v19.0. For the univariate analysis, Chi-square test or Fisher’s exact test provided a comparison of the categorical variables. The Mantel-Haenszel test was used to probe any differences between patient and control groups. Multivariate logistic regression models were used to adjust for potential confounders. Variables associated with T. gondii infection in univariate analysis (P ≤ 0.10) were included in a multivariate logistic regression analysis. Odds ratios (ORs) and the corresponding 95% confidence interval (CI) were calculated, in order to identify independent risk factors for T. gondii infection. Results with a P-value <0.05 were considered as statistically significant.
Epidemiology of arthritic patients with T. gondii infection
A total of 1640 individuals (820 arthritis patients and 820 health controls) were examined between December 2014 to November 2015. A significant difference (P < 0.001) was detected in the level of anti-T. gondii IgG antibodies in 154 arthritis patients (18.8%) vs. 98 control subjects (12%). Twelve patients tested positive for T. gondii IgM antibodies (prevalence, 1.5%), compared with 10 controls (1.2%) (P = 0.66). The details of arthritis patients and control subjects, including age distribution, gender, geographic region and area of residence are shown in Table 1. There was no evidence of a statistically significant association between being T. gondii seropositive and any of the tested variables, except for the ≤30-year-old age group (26.5%) and the >70-year-old age group (28.9%), which recorded the highest prevalence (Table 1). Our analysis revealed no significant differences between female (21.2%) and male (18.8%) arthritis patients (P = 0.414). T. gondii infection seroprevalence was not significantly different between urban and rural areas (17.9% vs. 22.2%; P = 0.128).
Seropositivity among patients with arthritis
Seroprevalence is presented in Table 2, by each clinical form of arthritis. The highest seropositivity rate of T. gondii infection was detected in patients with rheumatoid arthritis (24.8%), followed by reactive arthritis (23.8%), osteoarthritis (19%), infectious arthritis (18.4%) and gouty arthritis (14.8%). Patients with rheumatoid arthritis and reactive arthritis had significantly higher seroprevalence when compared with control subjects (P < 0.001 and P < 0.002, respectively).
Domestic risk factors associated with T. gondii infection
Univariate analysis showed some lifestyle variables with a P value ≤0.25, including: contact with cats in the home, contact with pigs, the consumption of raw vegetables or raw/undercooked meat, and exposure to soil. In our multivariate analysis, only contact with cats in the home (OR, 1.68; 95% CI, 1.24 to 2.28; P = 0.001) was associated with significantly increased odds of T. gondii infection in arthritis patients (Table 3). There was no evidence of a significant association between patients’ T. gondii status and the other variables (i.e., contact with pigs, consumption of raw vegetables or raw/undercooked meat, or exposure to soil).
Toxoplasma gondii infection is increasingly being reported in arthritis patients [15,16,17]; however, both the epidemiology and impact of this have been unclear. We assessed the risk of T. gondii infection among 820 arthritis patients from Shandong province, eastern China, during the period from December 2014 to November 2015; and determined the seroprevalence of anti-T. gondii antibodies in arthritis patients versus an equal number of healthy controls. Patients with arthritis were more likely to be infected with T. gondii (18.8% compared to 12% of healthy controls, P < 0.001), based on IgG seropositivity. Correlation between T. gondii infection and RA has been reported in other geographical areas, for example Iraq (54.0%) , Tunisia (58.4%) , Europe (63.0%) , and Egypt (54.0%  and 76.7% ). The higher seroprevalence of anti-T. gondii IgG antibodies among RA patients versus control patients reflects an association between latent T. gondii infection and RA. Contrastingly, there was no signficant difference between RA patients and controls with regard to the level of IgM antibodies, which was found to be consistent with a previous study reporting no anti-T. gondii IgM in RA patients . Among the various clinical forms of arthritis, seroprevalence rates of only rheumatoid arthritis (24.8%; P < 0.001) and reactive arthritis (23.8%; P = 0.002) were significantly raised when compared with controls.
An increased risk of T. gondii infection in RA patients may be anticipated due to the disease-related immunological changes that compromise adaptive cellular immunity - crucial for the control of an intracellular pathogen such as T. gondii. RA is associated with alterations in the T cell repertoire , a reduction in clonal expansion of naïve T cells in response to a previously unknown antigen  and a reduction in newly generated naïve T cells migrating from the thymus into the periphery . The lack of clinical information on the treatment history of study participants has precluded establishing corroborative evidence for any link between the use of immunosuppressive treatment and the frequency of T. gondii seropositivity in RA patients. Immunosuppressive therapies frequently used in the treatment of RA (especially TNF-α inhibitors) have been known to induce reactivation of latent T. gondii infection in arthritis patients, and may increase their propensity to acquire new opportunistic infections such as T. gondii or tuberculosis . Clinical cases of cerebral toxoplasmosis and chorioretinitis have been reported in RA patients undergoing treatment with TNF-α antagonists [29,30,31,32]. Given the important role of TNF-α in controlling the growth of T. gondii, infection with opportunistic pathogens such as T. gondii can be a major safety concern in patients receiving this therapy. Measures should therefore be taken to prevent such opportunistic infections.
Physicians who prescribe TNF-α inhibitor drugs must understand the therapeutic implications on patients’ immunity and the potential risks of infection, in order to maximize therapeutic benefits and minimize adverse effects. In rheumatology practice, it is common practice to screen for tuberculosis, HBV, HCV, HIV and varicella zoster virus antibodies prior to the initiation of anti-TNF-α therapy in patients. Patients with arthritis should be monitored for early signs of opportunistic infection and, if confirmed, it may be necessary to withdraw anti-TNF-α therapy until the infection is properly treated. One study, based on a small sample of only 30 individuals, reported no difference in the level of anti-T. gondii IgG antibodies among RA patients undergoing treatment with traditional disease-modifying antirheumatic drugs or biological TNF inhibitors .
Our results showed the highest seroprevalence in individuals within the ≤30-year-old age and >70-year-old age groups. Young and elderly individuals may have less efficient immunity to control opportunistic infections, or be more likely to interact with cats than those within other age groups. Previous studies have also shown an association between age and seropositivity of T. gondii [5, 33,34,35]; with higher T. gondii seroprevalence reported in older RA patients . In our study, no significant difference in the seropositive rates was observed between males and females (P = 0.414). However, we detected a significant association between contact with cats in the home and T. gondii seropositivity (OR, 1.68; 95% CI, 1.24 to 2.28; P = 0.001), contributing to the body of evidence suggesting that contact with cats is associated with an increased risk of T. gondii infection [5, 35, 36]. Felines are the primary host of T. gondii, whose oocytes pass with the animal’s stool and cause toxoplasmosis if ingested by humans or any other intermediate host. Although cats are popular as domestic pets in China, little attention has been paid to their role in environmental contamination with T. gondii oocysts [37, 38]. It is important to inform the general public and medical professionals about the risk factors of T. gondii infection - in particular the important role cats can play in transmitting T. gondii infection to arthritis patients.
Although the association between contact with pigs and T. gondii seropositivity was not statistically significant (P = 0.184), it deserves some attention. The identification of contact with cats and with pigs as the two most important risk factors, is of interest and to be expected. Human infection can occur via cat-to-pig and pig-to-human transmission . T. gondii will always be a risk while cats are maintained in the swine environment; cats shed millions of oocysts which can survive in the environment for months or even years, with a single oocyst having the potential to cause full-blown infection in a pig. Pork has been implicated as the meat most commonly associated with food-borne toxoplasmosis . People who handle pigs, or consume food within pig facilities, may be less likely to wash their hands before eating or after handling raw meat, leaving them at higher risk of infection [40, 41].
This study has demonstrated a high correlation between anti-T. gondii antibodies and arthritis for the first time in a population from eastern China, suggesting an increased susceptibility to opportunistic T. gondii infection in arthritic patients. It remains to be elucidated if chronic T. gondii infection was a trigger for the development of arthritis; whether disease-related immunosuppression promoted the reactivation of a latent infection; or if arthritis patients were idopathically predisposed to novel infections. TNF-α inhibitors used for the treatment of rheumatic diseases can increase the risk of frank toxoplasmosis; therefore, screening for latent T. gondii infection is strongly recommended before initiating such therapy. Our study adds to the body of evidence that contact with cats is associated with an increased risk of T. gondii infection. These findings should inform Public Health policy on the risk of opportunistic infections in arthritis patients.
Enzyme-linked immunosorbent assay
Hepatitis B virus
Hepatitis C virus
Human immunodeficiency virus
Statistical Packages for Social Sciences
Tumor necrosis factor-alpha
Dubey JP. Toxoplasmosis of animals and humans. 2nd ed. Florida: CRC Press; 2010. p. 313.
McLeod R, Kieffer F, Sautter M, Hosten T, Pelloux H. Why prevent, diagnose and treat congenital toxoplasmosis? Mem Inst Oswaldo Cruz. 2009;104:320–44.
Choi WY, Nam HW, Kwak NH, Huh W, Kim YR, Kang MW, et al. Foodborne outbreaks of human toxoplasmosis. J Infect Dis. 1997;175:1280–2.
Phan L, Kaszab K, Jalbrzikowski J, Noblea AG, Latkany P, Kuo A, et al. Longitudinal study of new eye lesions in children with toxoplasmosis who were not treated during the first year of life. Am J Ophthalmol. 2008;146:375–84.
Elsheikha HM. Congenital toxoplasmosis: priorities for further health promotion action. Public Health. 2008;122:335–53.
Donahoe SL, Phalen DN, McAllan BM, O'Meally D, McAllister MM, Ellis J, et al. Differential gamma interferon- and tumor necrosis factor alpha-driven cytokine response distinguishes acute infection of a metatherian host with Toxoplasma gondii and Neospora caninum. Infect Immun. 2017;85:e00173–17.
Gazzinelli RT, Eltoum I, Wynn TA, Sher A. Acute cerebral toxoplasmosis is induced by in vivo neutralization of TNF-alpha and correlates with the down-regulated expression of inducible nitric oxide synthase and other markers of macrophage activation. J Immunol. 1993;151:3672–81.
Giese A, Stuhlsatz S, Däubener W, MacKenzie CR. Inhibition of the growth of Toxoplasma gondii in immature human dendritic cells is dependent on the expression of TNF-alpha receptor 2. J Immunol. 2004;173:3366–74.
Derouich-Guergour D, Aldebert D, Vigan I, Jouvin-Marche E, Marche PN, Aubert D, et al. Toxoplasma gondii infection can regulate the expression of tumour necrosis factor-alpha receptors on human cells in vitro. Parasite Immunol. 2002;24:271–9.
Radon K, Dressel H, Windstetter D, Reichert J, Schmid M, Nowak D. Toxoplasma gondii infection, atopy and autoimmune disease. Eur J Med Res. 2003;8:147–53.
Chen M, Aosai F, Norose K, Mun HS, Ishikura H, Hirose S, et al. Toxoplasma gondii infection inhibits the development of lupus-like syndrome in autoimmune (New Zealand black x New Zealand white) F1 mice. Int Immunol. 2004;16:937–46.
Sagi L, Baum S, Agmon-Levin N, Sherer Y, Katz BS, Barzilai O, et al. Autoimmune bullous diseases the spectrum of infectious agent antibodies and review of the literature. Autoimmun Rev. 2011;10:527–35.
Shapira Y, Agmon-Levin N, Selmi C, Petríková J, Barzilai O, Ram M, et al. Prevalence of anti-Toxoplasma antibodies in patients with autoimmune diseases. J Autoimmun. 2012;39:112–6.
Balleari E, Cutolo M, Accardo S. Adult-onset Still’s disease associated to Toxoplasma gondii infection. Clin Rheumatol. 1991;10:326–7.
Mousa MA, Soliman HE, el Shafie MS, Abdel-Baky MS, Aly MM. Toxoplasma seropositivity in patients with rheumatoid arthritis. J Egypt Soc Parasitol. 1988;18:345–51.
Tomairek HA, Saeid MS, Morsy TA, Michael SA. Toxoplasma gondii as a cause of rheumatoid arthritis. J Egypt Soc Parasitol. 1982;12:17–23.
Fischer S, Agmon-Levin N, Shapira Y, Porat Katz BS, Graell E, Cervera R, et al. Toxoplasma gondii: bystander or cofactor in rheumatoid arthritis. Immunol Res. 2013;56:287–92.
Listing J, Gerhold K, Zink A. The risk of infections associated with rheumatoid arthritis, with its comorbidity and treatment. Rheumatology (Oxford). 2013;52:53–61.
Germano V, Cattaruzza MS, Osborn J, Tarantino A, Di Rosa R, Salemi S, et al. Infection risk in rheumatoid arthritis and spondyloarthropathy patients under treatment with DMARDs, corticosteroids and TNF-α antagonists. J Transl Med. 2014;12:77.
Washino T, Moroda M, Iwakura Y, Aosai F. Toxoplasma gondii infection inhibits Th17-mediated spontaneous development of arthritis in interleukin-1 receptor antagonist-deficient mice. Infect Immun. 2012;80:1437–44.
Araujo FG, Handman E, Remington JS. Use of monoclonal antibodies to detect antigens of Toxoplasma gondii in serum and other body fluids. Infect Immun. 1980;30:12–6.
Salman YJ, Mohammed KA. Relationship between Toxoplasma gondii and arthritis among patients in Kirkuk city. Int J Curr Res Aca Rev. 2015;3:175–87.
Bouratbine A, Siala E, Chahand MK, Aoun K, Ben Ismail R. Sero-epidimiological profile of toxoplasmosis in Northren Tunisia. Parasite. 2001;8:61–6.
El-Sayed NM, Kishik SG, Fawzy RM. The current status of Toxoplasma gondii infection among Egyptian rheumatoid arthritis patients. Asian Pacific. J Trop Med. 2016;6:797–801.
El-Henawy AA, Hafez EAR, Nabih N, Shalaby NM, Mashaly M. Anti-Toxoplasma antibodies in Egyptian rheumatoid arthritis patients. Rheumatol Int. 2017;37:785–90.
Wagner UG, Koetz K, Weyand CM, Goronzy JJ. Perturbation of the T cell repertoire in rheumatoid arthritis. Proc Natl Acad Sci U S A. 1998;95:14447–52.
Koetz K, Bryl E, Spickschen K, O'Fallon WM, Goronzy JJ, Weyand CM. T cell homeostasis in patients with rheumatoid arthritis. Proc Natl Acad Sci U S A. 2000;97:9203–8.
Acevedo-Vásquez E, Ponce de León D, Gamboa-Cárdenas R. Latent infection and tuberculosis disease in rheumatoid arthritis patients. Rheum Dis Clin N Am. 2009;35:163–81.
Young JD, McGwire BS. Infliximab and reactivation of cerebral toxoplasmosis. N Engl J Med. 2005;353:1530–1.
Nardone R, Zuccoli G, Brigo F, Trinka E, Golaszewski S. Cerebral toxoplasmosis following adalimumab treatment in rheumatoid arthritis. Rheumatology (Oxford). 2014;53:284.
Lassoued S, Zabraniecki L, Marin F, Billey T. Toxoplasmic chorioretinitis and antitumor necrosis factor treatment in rheumatoid arthritis. Semin Arthritis Rheum. 2007;36:262–3.
Cren JB, Bouvard B, Crochette N. Cerebral toxoplasmosis and anti-TNFα: a case report. IDCases. 2016;5:40–2.
Nowakowska D, Wujcicka W, Sobala W, Spiewak E, Gaj Z, Wilczyñski J. Age-associated prevalence of Toxoplasma gondii in 8281 pregnant women in Poland between 2004 and 2012. Epidemiol Infect. 2014;142:656–61.
Falusi O, French AL, Seaberg EC, Tien PC, Watts DH, Minkoff H, et al. Prevalence and predictors of Toxoplasma seropositivity in women with and at risk for human immunodeficiency virus infection. Clin Infect Dis. 2002;35:1414–7.
Wilking H, Thamm M, Stark K, Aebischer T, Seeber F. Prevalence, incidence estimations, and risk factors of Toxoplasma gondii infection in Germany: a representative, cross-sectional, serological study. Sci Rep. 2016;6:22551.
Chiang TY, Kuo MC, Chen CH, Yang JY, Kao CF, Ji DD, et al. Risk factors for acute Toxoplasma gondii diseases in Taiwan: a population-based case-control study. PLoS One. 2014;9:e90880.
Torrey EF, Yolken RH. Toxoplasma oocysts as a public health problem. Trends Parasitol. 2013;29:380–4.
Du F, Feng HL, Nie H, Tu P, Zhang QL, Hu M, et al. Survey on the contamination of Toxoplasma gondii oocysts in the soil of public parks of Wuhan, China. Vet Parasitol. 2012;184:141–6.
Edelhofer R, Prossinger H. Infection with Toxoplasma gondii during pregnancy: seroepidemiological studies in Austria. Zoonoses Public Health. 2010;57:18–26.
Seuri M, Koskela P. Contact with pigs and cats associated with high prevalence of Toxoplasma antibodies among farmers. Br J Ind Med. 1992;49:845–9.
Weigel RM, Dubey JP, Dyer D, Siegel AM. Risk factors for infection with Toxoplasma gondii for residents and workers on swine farms in Illinois. Am J Trop Med Hyg. 1999;60:793–8.
The authors would like to thank all study participants and medical staff who took part in the study. We also thank Drs Kevin Webb and Paul Goodwin from The University of Nottingham, United Kingdom for improving the English language of the manuscript.
Project support was provided by Fundamental Research Funds of Chinese Academy of Agricultural Sciences (Grant Nos. Y2016JC05 and 1610312017004) and by the Agricultural Science and Technology Innovation Program (ASTIP) (Grant No. CAAS-ASTIP-2014-LVRI-03).
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article.
Ethics approval and consent to participate
The study protocol was reviewed and approved by the Ethics Committee of the Medical College of Qingdao University and Wenhaiwei People’s Hospital. Patients were made aware of the aim of the study. Each individual provided written consent for their participation in the study. Informed consent was obtained from parents or guardians of children before enrolment in the study. Control sera were collected from volunteers.
Consent for publication
The authors declare that they have no competing interests.
About this article
Cite this article
Tian, AL., Gu, YL., Zhou, N. et al. Seroprevalence of Toxoplasma gondii infection in arthritis patients in eastern China. Infect Dis Poverty 6, 153 (2017). https://doi.org/10.1186/s40249-017-0367-2