Multilingual abstracts

Please see Additional file 1 for translations of the abstract into the six official working languages of the United Nations.

Background

Hand, foot and mouth disease (HFMD) is a common viral illness mainly caused by coxsackievirus A16 (Cox A16) and enterovirus 71 (EV71) [1, 2] infections. Children under five years of age are more susceptible to HFMD, as over 50 % of children in this age bracket lack the neutralizing antibodies that protect against EV71 and Cox A16 infections [1, 3, 4].

Symptoms of HFMD include fever, headache and poor appetite, followed by an intensely sore throat and a rash with very small blisters on the hands, feet and diaper area. A small number of children suffer complications such as myocarditis, pulmonary edema and aseptic meningoencephalitis, which can be fatal [5–7]. Occasionally, adults can contract HFMD [1, 8].

Since the 1980s, a number of severe HFMD outbreaks have been documented and HFMD remains a significant public health challenge, especially in the Asia-Pacific region [9–13]. Since the initiation of the national surveillance for HFMD in China in 2008, the incidence of reported cases has sharply increased, with more than seven million cases reported, including approximately 2,500 deaths [11]. From 1 January 2008 to 31 December 2013, a total of 400,264 HFMD cases have been reported in the Henan province alone, including 22,309 severe and 141 fatal cases [11].

According to the guidelines of the National Health and Family Planning Commission (NHFPC) of the People’s Republic of China for diagnosis and treatment of HFMD (2010 edition, http://www.nhfpc.gov.cn/), HFMD cases are classified as mild, severe or critical. In mild cases, a skin rash appears on the hands, feet, mouth or buttocks of the patient, with or without fever. In severe cases, in addition to the above, patients can experience deflated moods or lethargy; become easily frightened or delirious; develop headaches; suffer from vomiting, limb shaking, myoclonus, nystagmus, ataxia, eye movement disorders, weakness or acute flaccid paralysis; and/or experience convulsions. There are also visible signs of meningeal irritation, and tendon reflexes are diminished or absent. In critical cases, at least one of the following has to occur: frequent convulsions, coma and brain herniation; dyspnea, cyanosis, bloody foam sputum, pulmonary rales, etc.; or shock and other signs of circulatory insufficiency.

Toxoplasma gondii (T. gondii) is a protozoan parasite that can infect virtually all warm-blooded animals, including humans. It has been estimated that one-third of the world’s population has been infected with this parasite [14, 15]. The prevalence of infection with T. gondii in humans has been increasing in China due to the growing number of cats in the country [16]. Although in immunocompetent individuals, most T. gondii infections are asymptomatic, the infection can lead to serious diseases among immunocompromised patients such as HIV-positive and cancer patients, and transplant recipients [17–19].

Hand, foot and mouth disease is a serious public health issue in China and still one of the leading causes of child mortality. Numerous studies have shown that Th1/Th2 and Th17/Treg imbalances exist in HFMD patients [20]. Children with HFMD caused by the EV71 infection can suffer from functional disorders of cell, humoral and innate immunity [21]. Any of these functional disorders can increase the chance of infection with opportunistic pathogens such as T. gondii [22]. Yet, epidemiological knowledge about the prevalence of T. gondii infection among HFMD patients is unavailable in China. The present study is the first to estimate the prevalence of T. gondii infection among HFMD patients in China.

Methods

Sample collection

A total of 281 clinically diagnosed HFMD patients (24 mild cases, 226 severe cases and 31 critical cases) from the First People’s Hospital of Pingdingshan in Pingdingshan city, Henan province, central China, were enrolled in the study from March to April 2014. The HFMD patients were classified into mild, severe or critical cases, according to the guidelines of the NHFPC of the People’s Republic of China for diagnosis and treatment of HFMD (2010 edition, http://www.nhfpc.gov.cn/). Demographic data such as gender and age were obtained. Two hundred and twenty-two control subjects, matched with HFMD patients by age, gender and residence, were also included in the study. They were clinically healthy children without EV71, CoxA16 or other enterovirus infections, all from Pingdingshan city.

Samples of approximately 4 ml of venous blood were taken from each patient and the control subjects with informed consent. All blood samples were labelled individually and cooled using ice packs to maintain the temperature at 4 °C during transportation to the laboratory.

Serum sample preparation

Blood samples were centrifuged and sera were recovered and transferred to 1.5 ml Eppendorf Tubes™. The serum samples were stored at − 80 °C until tested for T. gondii antibodies.

Toxoplasma-IgG assessment

Immunoglobulin G (IgG) antibodies of T. gondii were detected using a commercially manufactured enzyme-linked immunosorbent assay (ELISA) kit (Zhuhai S.E.Z. Haitai Biological Pharmaceuticals Co., Ltd, Zhuhai, China). The manufacturer’s instructions were followed to conduct the procedure. In brief, test serum (1:100 dilution) was added to each well in the coated plate and incubated for 30 minutes at 37 °C. After additional washing with a washing solution (PBS containing 0.05 % Tween20, PBST), 50 μL of peroxidase-conjugated anti-human IgG was added to the wells and incubated at 37 °C for 30 minutes. This was followed by three washes using the washing solution. The colour reactions were developed by adding 50 μL “A” solution (H2O2) and 50 μL “B” solution (3,3′,5,5′-Tetramethylbenzidine) at 37 °C for 10 minutes, and then the reaction was stopped by adding 50 μL of stopping solution (0.5 ml/L H2SO4). Microplates were read at an optical density (OD) of 450nm in the Model 550 microplate ELISA reader (Bio-Rad, Hercules, CA, USA), and ratios (OD450 nm value of serum sample/OD450 nm value of negative control) were calculated after correcting for the OD450 nm value of the blank control (without serum and peroxidase-conjugated anti-human IgG). Test serum samples were considered positive when the ratio was ≥2.1.

Statistical analysis

Statistical analysis was performed using the SPSS version 20 software for Windows (SPSS Inc., Chicago, Illinois, USA). The chi-square test was used to perform statistical analyses of T. gondii prevalence using different variables. Differences were considered statistically significant if p < 0.05.

Ethical statement

The study was reviewed and approved by the Ethical Review Committee of the Xinxiang Medical University (reference no. 2013008). Written informed consent was obtained from all participants.

Results

As shown in Table 1, anti-T. gondii IgG antibodies were detectable in the sera of 35 HFMD cases (35/281), with an overall seroprevalence of 12.46 %. For clinically healthy children, a total of four (1.80 %) of the 222 samples were positive for anti-T. gondii IgG antibodies. The seropositive rate of the former was significantly higher than that of the latter (X 2 = 19.681, p <0.001).

Table 1 Seroprevalence of Toxoplasma gondii infection in the study populations in China
Full size table

In HFMD cases, the seroprevalence of T. gondii in males was 12.30 % (23/187) and 12.77 % (12/94) in females. No significant difference between genders was observed (X 2 = 0.012, p = 0.911). The highest seroprevalence of T. gondii infection was found among children in the age group of one to two years (16.09 %, 14/87) and the lowest was found among children in the age group of < one year (8.87 %, 11/124). However, the difference between age groups was not significantly significant (p >0.05) (see Table 1).

Table 2 shows the clinical diagnosis data of HFMD patients based on the severity of their disease. The seroprevalence of T. gondii infection was highest in critical cases (22.58 %, 7/31), followed by severe cases (11.50 %, 26/226), and was the lowest in mild cases (8.33 %, 2/24). However, no statistically significant differences were observed among the three groups (X 2 = 3.476, p = 0.176).

Table 2 Clinical diagnosis and seroprevalence of T. gondii in HFMD patients in China
Full size table

Discussion

Infection with T. gondii in humans is common all around the world, with prevalence rates varying depending on the environment, people’s eating habits and age [23]. The two nation-wide surveys carried out in 1995 and 2004 reported that the prevalence of T. gondii infection in the Chinese population was around 7 % [24]. In 2010, the infection rate of T. gondii in the Chinese population increased to 12.3 % [25].

In the present study, 12.46 % (35/281) of HFMD patients were seropositive for T. gondii. This is higher than that reported in HIV-positive patients (3.5–7.7 %) [26, 27], similar to the general infection rate of T. gondii (12.3 %) [25], and lower than that observed in female sterility patients (15.9 %) [28], patients in intensive care units (18.78 %) [23], psychiatric patients (17.30 %) [29], cancer patients (35.56 %) and dialysis patients (27.3 %) [30, 31] in China.

Additionally, the seropositive rate of T. gondii infection among HFMD patients was significantly higher than that of clinically healthy children (1.80 %). Children with HFMD caused by the EV71 infection can suffer from functional disorders of cell, humoral and innate immunity [20, 21], which can reduce the body’s resistance to opportunistic pathogens such as T. gondii and predispose them to develop secondary toxoplasmosis. Latent T. gondii infections could also be activated. However, whether the prevalence of T. gondii infection can increase the risk of contracting HFMD and affect the disease outcome of HFMD patients requires further study.

In the present study, female HFMD patients had a higher prevalence than male patients, although the difference was not significant (p > 0.05). Gender was thus not significantly associated with the presence of anti-T. gondii antibodies (P >0.05), which was consistent with other reports [32, 33].

Rates of T. gondii infection increased with age in this study, however, the difference between age groups was not significantly significant (p >0.05). A hypothesis would be that the increase is a reflection of increasing ‘exposure years’ as the children get older [32]. The results provided further evidence for the increased risk of T. gondii infection with acquisition of age. Seroprevalence of T. gondii infection was highest in critical HFMD cases, followed by severe cases, and the lowest was detected in mild cases, with percentages of CD4+, CD8+ T and CD16+56+ cells (natural killer cells) continuously decreasing as the disease worsens [21]. Additionally, CD4+ and CD8+ T cells and natural killer cells play important roles in the process of anti-T. gondii infection [34, 35]. These findings might explain why the probability of seroprevalence with T. gondii infection increases with the severity of the HFMD disease. With respect to the increased numbers of HFMD patients worldwide, toxoplasmosis should be considered as potentially associated with HFMD in humans.

Conclusion

The present study revealed for the first time the seroprevalence of T. gondii infection among HFMD patients in the Henan province, China. Further studies should be conducted to estimate the prevalence of T. gondii infection among HFMD patients in other provinces of China, with increased sample sizes.