Cite this asSukthana Y, Udonsom R, Chaichan P, Mahittikorn A, Vignoles P, et al. (2017) Toxoplasma Serostatus in Thai Free-Range Chickens: Prevalence and Two Diagnostic Methods. Open J Trop Med 1(1): 018-023. DOI: 10.17352/ojtm.000004
Toxoplasma seroprevalence in free-range chicken, which directly feed from ground, is a good indicator for detecting an environment contamination by T. gondii oocysts. Many serological methods have been used for diagnosing Toxoplasma infection in animals including chicken. Selection of appropriate methods primarily depend on their sensitivity and specificity as well as laboratory techniques, special reagent or tool requirements and regional prevalence status. The aims of this study were to determine the prevalence of T. gondii antibody in free-range chickens in Thailand and to compare two serodiagnostic methods, indirect fluorescent antibody test (IFAT) and Modified Agglutination Test (MAT). Six hundred free-range chicken sera were collected from 2 villages in Kanchanaburi Province, Thailand, 300 in 2014 and 300 in 2015. The age of chickens was between 3-6 mo, of which chickens of 2015 were older than of 2014. Collected sera were test for T. gondii IgG antibody by both methods. Over all Toxoplasma seroprevalence were 33.0% and 17.7% by IFAT and MAT, respectively. There was poor agreement between the two serological methods (kappa=0.09). IFAT in this study revealed higher positive percentage than MAT. Even though the way of living and environment in the present study was suitable for Toxoplasma transmission, the seroprevalence in Thai free-range chickens was low compared to other tropical regions such as Africa or South America. A low Toxoplasma prevalence was also found in humans, cats and other intermediate hosts in Thailand. Toxoplasmosis in Thailand causes low burden compare to other infectious diseases, however, consume well-cooked free-range chicken meat and proper practice during handling raw meat when cooking should be advocated to prevent and reduce this infection.
Toxoplasmosis is a food and water-borne parasitic zoonosis caused by an intracellular protozoan, namely Toxoplasma gondii. The disease is mainly asymptomatic or causes benign clinical manifestations in healthy infected persons, but can have severe consequences in immunocompromised patients or produce congenital toxoplasmosis once primary acquired infection occurs during pregnancy. Cat and other felids are the only definitive hosts, while human, warm-blooded animals, bird and rodent are intermediate host. The infection is transmitted to human by three important routes i.e. 1) ingesting oocysts contaminated in food or water; 2) consuming raw or under-cooked meat containing tissues cysts and 3) vertical transmission from primarily infected mother to fetus.
Due to the asymptomatic character or non-specific signs of this infection in human as well as in other animals, identifying infected hosts to deliver effective prevention measures needs an indirect way such as detection of antibodies. Acting as an intermediate host, free-range chickens mainly feed from bare ground of which T. gondii oocysts, from cat and other felids, are laid. Toxoplasma antibody in chickens, thus, represents a good indicator for T. gondii oocyst contamination in an environment . Evaluation of previously Toxoplasma infection requires accurate diagnostic tools that can rapidly and precisely identify infected hosts, in both definitive and intermediate .
Many serological tests are available for Toxoplasma antibody detection, mainly immunoglobulin G (IgG), indicating previous infection. The Sabin-Feldman dye test is the gold-standard method for detecting T. gondii antibody in human, and according to Dubey, it works on many animal species but not on chicken sera since this may be related to fixation of the first component of the complement [3,4]. To date, agglutination tests either direct or modified methods are commonly used for T. gondii antibody detection in animals  including free-range chickens . Modified agglutination test (MAT) was recently validated by using cat and mouse bioassays . Toxo-screen DA (Biomérieux®) is one of modified agglutination methods using commercial suspension of T. gondii as antigen . Indirect fluorescent antibody test (IFAT), another highly specific test utilizing species-specific conjugated fluorescein is the gold-standard test for T. gondii detection in pigs [8,9].
Despite the agreement of agglutination tests and IFAT in terms of sensitivity and specificity in pigs  and cats , the comparison between these two methods is unclear for chickens. Moreover, the seroprevalence of T. gondii in Thai free-range chickens indicating the situation of contaminated environment is not well established. Therefore, this study aims for detecting the prevalence of Toxoplasma serostatus in free-range chickens in Thailand and to evaluate the performance of the two serological diagnostic methods, IFAT and a commercially available MAT (Toxo-screen DA®, Biomérieux).
The project was carried out in the westernmost province of Thailand, Kanchanaburi, located at Thai-Myanmar border (Figure 1). Our studied site included 2 villages from Saiyok district, Kangpralom (14°01’ 28.76’’ N, 99°13’ 19.26’’ E) and Wangpow (14°21’ 44.53’’ N, 98°53’ 59.46’’ E). They are situated in the valley of the Kwai River, in a well-preserved rural environment, surrounded by forests with a high biodiversity. Cats and dogs are widely present and freely roam in people’s houses and outside. In Thailand, the majority of chicken husbandry is run by closed-system but there are some areas where naturally free-range chickens still prevail, which our studied sites are among those. Those chickens were free to roam and feed themselves on bare ground around houses together with dogs and cats (Figure 2).
From April to August 2014, approximately of 1-2 ml of blood samples of 300 free-range chickens, aged 2-5 months, were collected by puncture of the axillary vein. Blood from another batch of 300 chickens, aged 3-6 months, were collected from May to September 2015. Collected samples were kept in a 4°C container and brought to laboratory at the Department of Protozoology, Faculty of Tropical medicine, Mahidol University for T. gondii IgG antibody.
All experiments with animals were carried out in strict and correct conditions in order to ensure to meet the criteria for approving by animal welfare according to the Animal Ethics Procedures of Faculty of Tropical Medicine–Animal Care and Use Committee (FTM-ACUC), Mahidol University, Bangkok, Thailand (Permit No. FTM-ACUC 007/2014).
Positive Toxoplasma of chicken serum is needed for the prevalence study. Therefore, 10 free-range chickens from the study sites (6-8 weeks old) were obtained and initially examined by MAT and IFAT to confirm the absence of T. gondii antibody before allocating each 5 chickens into group 1 and group 2. Four chickens from both groups were intraperitoneally inoculated with T. gondii RH strain tachyzoites; 10,000 cells and 40,000 cells, for group 1 and 2, respectively. One chicken from both groups were injected with normal saline as a negative control. All chickens were observed daily and recorded for any clinical sign and symptom of toxoplasmosis. Approximately 1-2 ml of blood samples were collected by puncture of the axillary vein of infected chickens at day 1, 3, 5, 7, 14 and 30 post-inoculation; MAT and IFAT were performed on those collected sera to determine whether these experimental chickens develop T. gondii IgG antibodies.
The suspension of antigen used for MAT technique in this study was an in- house antigen. The test was performed as previously described . Briefly, the sera samples were diluted in a stock of 2-mercaptoethanol performed in U-shaped well microtiter plate by two-fold dilutions starting at 1:10. Killed T. gondii (RH strain) tachyzoites suspension was diluted with BABS buffer and was added to the wells as antigen. The wells were then incubated for at least 7 hr or overnight at room temperature in the absence of light. The diffuse opacity of the Toxoplasma agglutinated form was regarded as a positive result, whereas a central white opaque dot at the well bottom was regarded as a negative result. Positive and negative controls were also analyzed alongside each batch testing. Titers ≥ 10 were defined as positive.
The suspension of antigen used for MAT serology is a commercial antigen (Toxo-Screen DA®, BioMérieux, Marcy l’Etoile, France) . Chicken sera were diluted in 2-mercaptoethanol (1:10, 1:20, 1:100 and 1:800). Twenty-five µL of antigen suspension were added in each well for the final volume of 50 µl, the antigen was diluted in 1:5 in colored BAB’s albumin buffer (red) pH 8.95. After 5 hours of incubation, sedimentation or agglutination of Toxoplasma was observed. Titers ≥ 10 were defined as positive. Positive and negative controls used were provided in the Toxo-screen DA kit.
IFAT was conducted following the protocol of the Animal Health Laboratories, Division of Agriculture, and Western Australia . Killed T. gondii (RH strain) tachyzoites were fixed on a Teflon printed slides and were incubated with 20 μl of the two-fold diluted sera starting at 1:8, for 1 hour at 37 ºC in moist chamber. Goat anti-chicken IgG conjugated to fluorescein isothiocyanate (FITC) (Southern Biotech, USA) was then added to the slides, and incubated for a further 1 hr. Following a rinse, the slides were interpreted under fluorescent microscope at 400x magnification. Positive and negative control were included with each slides, and a titer of ≥ 1:16 is defined as positive result.
Statistical analyses were conducted using Fisher’s exact test and Chi Square Test (χ2). The alpha level was set at a standard level of 5% for statistical tests. Results were considered significant when p<0.05. Statistical analyses were performed using the R x 22.214.171.124 software with one or two-tailed significance level of 5%. Furthermore, Kappa coefficient was used to estimate the agreement between serological techniques for the detection of T. gondii antibodies. Binomial model was used to calculate the 95% confidence interval.
Following T. gondii inoculation, no chickens showed any clinical sign and symptom specific or suggestive to toxoplasmosis, however, one chicken in group 2 (higher dose of inoculation) died before day 30. The earliest detection of T. gondii antibodies was at 7 days post-inoculation in one chicken (C4) in group 1 with titer of 1:32 and another (C9) in group 2 with titer of 1:64 by IFAT. Although, MAT could not detect any positive chicken in group 1 within 7 days post inoculation, one (C9) in group 2 showed seropositive titer at 1:100 (Table 1). Antibodies were detected in all infected chickens by day 14 showing titers ranging from 1:64 to 1:1024 by IFAT and from 1:100 to 1:400 by MAT. At day 30, more than half of seropositive showed stable or lower titer by both IFAT and MAT. All control chicken sera were found negative by both serological methods.
Table 2 showed the number of Toxoplasma seropositive in free-range chickens from two villages, Kangpralom and Wangpow for the two sampling years, 2014 and 2015. Over the 2 periods of sampling, the overall prevalence was 17.7% with MAT vs 33.0% with IFAT. The positive results in the year of 2014 were 11.3% (95% CI=8.0-15.5) and 23.7% (95% CI=19.0-28.9) by MAT and IFAT, respectively. In 2015, the positive results were approximately double, respectively 24.0% (19.2-28.8) and 42.3% (36.7-47.9) by both methods. This may due to older chickens tested in the later than the former year. Toxoplasma IgG antibody prevalence in Wangpow village in 2015 was significantly higher than in Kangprolom (29.0% v.s. 18.1%; p-value = 0.03) by MAT (Table 2). There is poor agreement between the two assays with k = 0.09 (Table 3).
The overall prevalence of T. gondii in Thai free-range chickens determined by IFAT and MAT in this study were 33.0% and 17.7%, respectively. The results of the year 2014 revealed approximately 2 times higher than the 2015’s by both methods. This may be because of the older chickens in later year were examined. Our results showed much lower than the previous study in Thailand that reported the prevalence by IFAT of 64% by IFAT in 1-year chickens from Bangkok . A study from Kenya  also reported high prevalence as 79.0% in 2-years chickens. These results support the hypothesis that the longer the chickens are exposed to their bare ground environment, the higher Toxoplasma antibody was found.
The 33.0%-42.3% prevalence by IFAT observed in this study were similar to the 40.5% prevalence reported in Costa Rica , but lower than in Brazil (53.6%)  and in Kenya (79%) . The difference might be due to higher cat density in those areas, or suitable temperature for T. gondii oocysts survival. Toxoplasma seropositive in human and other warm-blooded animals in those regions were high compared to Thailand, suggesting a higher level of soil contamination by oocysts and in a general way a more important circulation of the parasite in the environment from these areas. Actually, a higher prevalence was expected in the present study as the study sites were suitable for T. gondii transmission among its definitive and intermediate hosts including cats, dogs, chickens and human, which shared the same bare-ground environment. However, in Thailand in general Toxoplasma seroprevalence was about 30% in human  and very low as 7.3% in stray cats . Sukthana  suggested that may be because of the high temperature and strong sunlight which inactivate oocysts. Furthermore, even though Thai domestic and stray cats are kept outdoors, they are fed on rice and well cooked fish.
When using MAT, T. gondii antibody were found 11.3% in 2014 and 24.0% in 2015. This was relatively similar to other countries where the seropositivity of T. gondii in free-range chickens determined by MAT were 17.9% in India , 18.8% in Northeastern China , 24.2% in Vietnam, 24.4% in Indonesia . For comparison, seroprevalence in chickens seems higher in Africa and South America with 30.5% in Central Ethiopia , 40.4% in Nigeria , 38.8% in Brazil as well as 50.3% and 51.1% in rural and urban environments from Gabon .
There are several serological methods that are commonly used in Toxoplasma laboratories; the Sabin-Feldman dye test is recommended for human toxoplasmosis diagnosis, whereas indirect immunofluorescent test (IFAT) and modified agglutination test (MAT) are amongst the preferably used methods for T. gondii antibodies detection in various animal species. Those techniques are, however, present with some limitations for diagnosing toxoplasma infection . Such as IFAT requires special equipment or appropriate anti-species serum. MAT is simple, easy to perform and does not require those , however, some articles seems to call into question the fact that this technique can be applied to all animal species . In this study, both IFAT and MAT were used and able to detect T. gondii antibodies in all inoculated chickens. IFAT detected Toxoplasma IgG antibody with the titer of 1:32 at the earliest on day 7 in one chicken even in the group inoculated with lower concentration (Group 1 = 10,000 tachyzoites/ml), while MAT was unable to detect any. One chicken, inoculated with the higher concentration at 400,000 tachyzoites/ml, was seropositive at the titer of 1:64 by IFAT and 1:100 by MAT at day 7. This might be due to storage and travel conditions that affected in-house MAT antigen. Thus, we designed to use Toxo-Screen DA (BioMérieux®) instead of MAT to detect Toxoplasma prevalence in naturally free-range chickens. The principle of Toxo-Screen DA (BioMérieux®) is identical to MAT technique, but the condition of storage of this commercially available antigen was better than that of in-house MAT. The results from the present study bear some resemblance to other experimental chicken studies, who demonstrated that IFAT was able to detect T. gondii antibodies in chickens at first to second week post-inoculation, when infected with 1.5 x 107 T. gondii tachyzoites (RH strain) injected muscularly , or fed with 103 or 105 T. gondii oocysts K7 (avirulent) strains . Similarly, after chickens was fed with 103 or 105 of ME49 oocysts, MAT was able to detect antibody at 1:100 serum dilutions at day 15 post-inoculation .
Although IFAT was defined as the gold standard test for T. gondii antibody detection in cow and pig [9,31], this technique however has not been validated in chicken. The higher seroprevalence in free-range chickens detected by IFAT than MAT in this study might be due to some explanations: firstly, false positives IFAT reactions due to non-specific fluorescent labelling with limited number of T. gondii tachyzoite or to variations in the brightness of fluorescein [31,32]. Secondly, agglutination test is less sensitive than IFAT, as shown by our experimental chickens results, therefore, MAT may have detected less positive cases in naturally chickens , comparing the sensitivity and specificity of serological tests with bioassay in mice, found 48.0% of false positive rate for IFAT and 32.0% of false positive rate by MAT. This suggests that there is no reliable serological technique as shown by the low kappa coefficient found in our study.
Most conventional serological tests require whole-cell of T. gondii tachyzoites from mice or cell culture, which lacks of standardization between laboratories, therefore, may give inaccurate and non-specific results . Recently, the recombinant antigens of secretory microneme proteins (MIC3), rhoptry proteins (ROPs), rhoptry neck proteins (RONs), and dense granule antigens (GRA) were developed as an alternative method for Toxoplasma sero-diagnosis for both humans and animals, and demonstrated to be more sensitive and specific at detecting T. gondii antibodies in multiple animal species compared to MAT and IFAT [33-38]. Specifically, Sun and colleagues reported >90% agreement between recombinant GRA1, GRA7 and Toxoplasma soluble antigens (TSA) for T. gondii antibody detection in chickens, with GRA7 showed higher sensitivity and specificity than GRA1 and TSA . To establish good epidemiological data of toxoplasmosis, additional other serological tests such as ELISA or recombinant antigen based diagnostic technique, bioassays and polymerase PCR based assays was recommended. Some reports found that using ELISA to detect T. gondii antibody in free-range chickens is seemingly more specific and sensitive than IFAT and MAT [30,41].
In the present study, both IFAT and MAT were able to detect T. gondii antibody in chickens as an indicator for contamination in environment. Despite comparatively different prevalence determined by the two diagnostic methods, the data indicates contamination of T. gondii in chickens and ultimately in the environment in rural area of Thailand. Even though chicken meat is normally consumed well-cooked in Thailand, care should be taken when handling undercooked meat to reduce the spreading of T. gondii infection to other animal hosts.
This study was partially supported by the ICTM grant of the Faculty of Tropical Medicine, Mahidol University. The authors are grateful to the veterinarian assistant staff of the Faculty of Veterinary Science, Kanchanaburi Campus, Mahidol University for their help taking care of the chickens.
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