Detection of Toxoplasma gondii-specific immunoglobulin (IgG) antibodies in meat juice of beef
Iraqi Journal of Veterinary Sciences,
2021, Volume 35, Issue 2, Pages 319-324
AbstractToxoplasmosis is an important worldwide foodborne zoonotic disease. Infected cattle meats is considered a serous cause of human toxoplasmosis. Here, this study assesses the infection with Toxoplasma gonddi (T. gondii) in cattle using meat juice samples from diaphragmatic muscles collected at the slaughter. An in house indirect enzyme linked immunosorbent assay (ELISA), and commercial latex agglutination test (LAT) followed by immunoblotting were developed on the meat juice (fluids) using tachyzoites of locally isolated T. gondii strain. The comparative analysis of the results of the tested juice samples showed an excellent agreement between the in-house indirect ELISA and LAT test in the positive and negative of meat juice. Relative sensitivity was higher for ELISA on diaphragms fluids random samples 80.39%, for the LAT test was 68.6%. Immune-reactive bands of T. gondii local strain Ag with naturally infected meat juice were 116, 83, 65, 30 and 23 KDa. The obtained results concluded that the development of an effective ELISA test to be used in for detection of toxoplasmosis infection of slaughtered cattle in large-scale would be exactly valuable, since the important role that beef plays in epidemiology of T. gondii, in particular the hazard of transmission to human and food safety.
Detection of Toxoplasma gondii-specific immunoglobulin (IgG) antibodies in meat juice of beef
Raafat M. Shaapan 1*,Nagwa I. Toaleb2 and Eman H. Abdel-Rahman 2
2 Department of Parasitology and Animal Diseases, Veterinary Research Division, National Research Centre, Giza, Egypt
Toxoplasmosis is an important worldwide foodborne zoonotic disease. Infected cattle meats is considered a serous cause of human toxoplasmosis. Here, this study assesses the infection with Toxoplasma gonddi (T. gondii) in cattle using meat juice samples from diaphragmatic muscles collected at the slaughter. An in house indirect enzyme linked immunosorbent assay (ELISA), and commercial latex agglutination test (LAT) followed by immunoblotting were developed on the meat juice (fluids) using tachyzoites of locally isolated T. gondii strain. The comparative analysis of the results of the tested juice samples showed an excellent agreement between the in-house indirect ELISA and LAT test in the positive and negative of meat juice. Relative sensitivity was higher for ELISA on diaphragms fluids random samples 80.39%, for the LAT test was 68.6%. Immune-reactive bands of T. gondii local strain Ag with naturally infected meat juice were 116, 83, 65, 30 and 23 KDa. The obtained results concluded that the development of an effective ELISA test to be used in for detection of toxoplasmosis infection of slaughtered cattle in large-scale would be exactly valuable, since the important role that beef plays in epidemiology of T. gondii, in particular the hazard of transmission to human and food safety.
Keywords: Toxoplasma gondii, Beef, Meat juice, ELISA, LAT.
الکشف عن الأجسام المضادة للجلوبیولین المناعی النوعی ج لطفیل المقوسة الکوندیة فی عصیر لحوم الأبقار
رأفت محمد شعبان1، نجوى إبراهیم تعیلب2 إیمان حسبن عبد الرحمن2
1قسم الأمراض المشترکة، 2قسم الطفیلیات وأمراض الحیوان، شعبة البحوث البیطریة، المرکز القومی للبحوث، الدقی، الجیزة، مصر
المقوسة الکوندیةهو طفیل اولی ینتقل عن طریق الأغذیة وینتشر فی جمیع أنحاء العالم. وتعتبر لحوم الأبقار المصابة به سببًا لمرض خطیرًا هو داء المقوسات الغندیه الذی ینتقل للبشر. وفى هذه الدراسة تم تقیم معدل انتشار الإصابة بالمقوسات الکوندیة فی الأبقار باستخدام عینات عصیر اللحم من عضلات الحجاب الحاجز التی تم جمعها عند ذبح هذه الأبقار. تم تطویر اختبار الممتص المناعی المرتبط بالإنزیم غیر المباشر المجهز محلیا واختبار تراص اللاتکس التجاری متبوعاً باختبار الطبع المناعی على عصیر اللحوم (السوائل) باستخدام مستضدات محضره من الأطوار المعدیة للطفیل من سلالة المقوسة الکوندیة المعزولة محلیاً. وقد أظهر التحلیل المقارن لنتائج اختبار عینات عصیر اللحوم توافقًا ممتازًا بین اختبار الممتص المناعی المرتبط بالإنزیم غیر المباشر واختبار تراص اللاتکس التجاری فی الإیجابیة والسلبیة لعصیر اللحوم. وکانت الحساسیة النسبیة أعلى فی اختبار الممتص المناعی المرتبط بالإنزیم غیر المباشر فی عینات عشوائیة من سوائل الأنسجة اللحوم المختبرة 80.39٪، ولکن اختبار تراص اللاتکس التجاری أعطى حساسیه أقل 68.6% وکانت الأوزان الجزیئیة للأشرطة البروتینیة المرتبطة والمتفاعلة مناعیا من المستضد المحضر من سلالة المقوسة الکوندیة المعزولة محلیًا مع عصیر اللحم المصاب طبیعیا هی 116 و 83 و 65 و 30 و 23 کیلو دالتون. وخلصت النتائج التی تم الحصول علیها إلى أن بتطویر اختبار اختبار الممتص المناعی المرتبط بالإنزیم غیر المباشر یکون فعال وذو قیمة کبیرة لاستخدامه على نطاق واسع للکشف عن عدوى داء المقوسات الکوندیة فی عصیر اللحوم للماشیة المذبوحة، ونبهت الدراسة للدور الهام الذی یلعبه لحم البقر فی وبائیات طفیل المقوسات الکوندیة وعلى وجه الخصوص خطر انتقاله إلى الإنسان مع الحفاظ على سلامة الغذاء للمستهلک.
Toxoplasmosis is a world-wide distributed infection is due the infection by the zoonotic Toxoplasma gondii (T. gondii)) protozoal parasite which can be transmitted to humans and other animals; including cattle and it is an important foodborne zoonosis (1,2). Human and most of warm-blooded mammals become infected through ingestion of environmentally resist sporulated T. gondii oocysts from final host (cat) or ingest the infected intermediate host tissues containing T. gondii tissue cysts (3). The diagnosis of T. gondii infection in livestock animals and its originated food products is obstructed by the deficient of well effective procedures that can investigate viable T. gondii parasite infective stages in meat and tissues that make food dangerous for consumers (4).
Previously, studies in our laboratory used purified fractions to minimize or avoid the cross reactivity and increasing the sensitivity of available techniques to detect low levels of antibodies of toxoplasmosis in cattle and camel sera (5). Also, to diagnosis of ovine toxoplasmosis isolated cross reactive fraction was used as antigen in ELISA assay (6). Moreover, the isolation fraction from Fasciola worm at molecular weight 65 kDa used as diagnostic potency of toxoplasmosis in experimentally infected sheep serum using immunoblot method (7). Different degrees of specificity were found in sheep naturally and or experimentally infected when comparing ELISA dependent on crude or recombinant antigens (8) Whereas Mikaee et al. (9) used serological (ELISA) and molecular tools (PCR), to diagnose toxoplasmosis in sheep, showed that the PCR results were essential in the diagnosis of the infected animals more than ELISA techniques. Although Dong et al. (10) showed that the detection of antibodies against T. gondii in dairy cattle was low prevalence. In Egypt, the antibodies against T. gondii prevalence in goat and sheep was high and may refers to the important role of mutton and other meat as transmissible media of human toxoplasmosis due to the habit of eating undercooked grilled meat (11). Recently, some alternative methods, based on antibody found in meat juice and multiple diagnostic assays are applied for serological investigation for toxoplasmosis, which is commonly made for the meat of different food animals (12). Fluids from muscle (meat juice) give an interesting alternative matrix because it can be easily collected than blood drawing and serum preparation (13). Several studies that have been done to examine antibodies against. T. gondii infection on meat juice, in domestic animals; pigs (14), rabbit (15), meat from wild boars (16), chickens (17), sheep (18). While livestock in particular cattle are one of the major meat sources in the world, people who eat infected T. gondii undercooked meat or raw cow milk can be expose to the infection (19).
In spite of the wide range of serologically available diagnostic tests routinely applied to investigate toxoplasmainfection in animal groups of different species (20), there are no documented standard serological tests available at this time that accurate the relationship between sero-positivity and the parasitic infective stages existence in animal tissues and meat (21). The accuracy of diagnosis of varies methods of serological assays is commonly evaluated by comparing its findings with those of biological tests like bioassays in cats or mice as a standard gold test (22), or another different serological investigation with the high sensitivity and good specificity expected tests such as the Sabin Feldman (dye test), ELISA and modified agglutination test (MAT) (23). The using of different crude, fractionated, or recombinant antigen in ELISA procedures have been has been adapted d to find out the T. gondii antibodies in meat juice (18,24).
Due to suitable muscle fluid production from meat pieces and may be automated as a large-scale analysis, also offer the opportunity for parasitological evidence. The aim of this study was to estimate the potential of cattle meat juice infection with T. gondii serologically, using indirect home ELISA and compared to commercial LAT, to assess the feasibility of such a strategy to control toxoplasmosis.
Materials and methods
Diaphragmatic meat samples of 51 cattle carcasses were collected in Cairo slaughterhouses unidentified age. Diaphragms samples were individual cut into small pieces (about 25 gm) and kept in plastic bags at -20◦C until examined (25).
Meat juice (fluid) collection
Meat juice from each frozen diaphragm sample were obtained individually, thawing at room temperature, then fluids were collected with a pipette into a small tubes and labeled, as the previously described technique by Nockler et al. (13).
Preparation of T. gondii tachyzoites antigen
T. gondii infective stages had been isolated from the pooled meat sample (heart and diaphragm) obtained from slaughtered sheep as the method carried out by Shaapan and Ghazy (26). Virulent strain of T. gondii was obtained by feeding of pooled meat samples of sheep to cats according of Davis and Dubey (27) method and then isolated parasite maintained in our laboratory through the serial passage in mice peritoneum. T. gondii tachyzoites antigen was prepared and assayed for protein content (28).
Enzyme Linked Immunosorbent Assay (ELISA)
Indirect ELISA was adopted to detect the T. gondii IgG in meat juice toxoplasmosis infected diaphragms, using tachyzoites antigens of virulent local strain of T. gondii. The assay was conducted as described by method of Shaapan et al. (29) with some modifications. Optical density was recorded at 405 nm with automated ELISA reader (BIOTEC, LX800, USA). The cutoff was determined as the two times of the standard deviation plus mean of negative fluid and the optimal concentration of antigen, antibody and conjugate were estimated after the checker- board titrations (30).
Toxoplasma IgG Latex agglutination test (LAT)
Commercial LAT (Nova Test), is one step Diagnostic Rapid Test, depending on the Gold Immuno-Chromatography Assay (BEIJING) was used for anti T. gondii IgG detection in diaphragms fluids samples.
Protein components of the prepared virulent local strain of T. gondii electrophoretically separated on 10% slab SDS-PAGE according to the procedures mentioned by Laemmli (31). The separated gel was fixed in 50% methyl alcohol, stained with silver nitrate (32).
Proteins of T. gondii antigen was fractionated by SDS-PAGE transferred to nitrocellulose membrane (33). After washing and blocking, apply the incubation of the membrane with infected meat juice diluted at 1:10. Whereas, anti-bovine IgG horse radish peroxidase-conjugate (sigma, USA) was used at dilution 1:1000.
T. gondii IgG in meat juice using ELISA
ELISA was performed to evaluate the success of tachyzoites of local strain of T. gondii antigen to detected toxoplasmosis antibodies IgG in diaphragms meat juice. Sensitivity was 80.39% (Figure 1).
Figure 1: Diagnostic potential of tachyzoites of local T. gondii strain antigen in diaphragms meat juice toxoplasmosis
T. gondii IgG in meat juice using LAT
Toxoplasmosis antibodies IgG detected by recombinant Toxoplasma antigen in Colloidal Gold Chromatography (Cassette), commercial Rapid test (LAT). Positive and negative fluid (meat juice) samples were observed (Figure 2).
Figure 2: Diagnosis of meat juice toxoplasmosis by commercial diagnostic LAT test (Cassette); two colored bands in positive meat juice sample (A) and one band in negative meat juice sample (B).
Comparing of ELISA with LAT
Out of 51 fluids diaphragms analyzed random samples 41(80.39%) and 35(68.6%) fluid samples were positive by local strain T. gondii antigen using ELISA and LAT assays respectively. Of 35 positive meat fluid samples with LAT 31(60.79%) were positive by local strain T. gondii antigen ELISA (Table 1).
Table 1:Immunodiagnosis of toxoplasmosis in diaphragms meat juice by ELISA compared with commercial LAT
T. gondii antigen SDS
Electrophoretic profile of T. gondii tachyzoites Ag showed 10 bands were detected at 165, 116, 97, 83, 76, 65, 53, 30, 27and 23 kDa (Figure -1 Lane A) (Figure 3).
Figure 3: electrophoretic profiles of T. gondii local strain Ag (Lane A). Molecular weight standards (Lane Mr.)
Identified immune-reactive bands of T. gondii local strain Ag with naturally infected meat juice were 116, 83, 65, 30 and 23 KDa (Fig. 4).
Figure 4: Immune-reactive bands identified by positive meat juice against local of T. gondii strain (Lane: Ag). Standard molecular weight (lane: St).
In this study the in-house indirect ELISA using tachyzoites antigen of local isolated T. gondii is effective and specific test compared with a commercial LAT as the main standard were used for T. gondii antibodies standard in cattle meat. These tests have been described elsewhere to detect infection in meat and tissues that are commonly diagnosed by examining other zoonotic diseases such as trichinella in experimentally infected porcine tissues (13), and has been widely accepted, suitable, sensitive and may be used confidentially for screening animals against toxoplasmosis regardless of the host species (34).
The detection anti-Toxoplasma IgG antibodies in samples of tested meat juice obtained from 51 previously infected cattle diaphragm tissues revealed high sensitivity 80.39% using ELISA than the commercial LAT Rapid kit 68.63%. Similar values of results 87.4% in sheep have been documented by Verhelst et al (35). In addition, these results agreement with Hill et al. (36), when reported the sensitivity values for tissue fluid ELISA was 79.9% in swine and was lower values using PCR method. Moreover, Ahmed et al. (37) revealed that the prevalence of infection among the examine camels blood samples in Egypt by indirect ELISA was 52.5% and by using PCR was 24%. In addition, this high sensitivity of meat juice ELISA than the commercial LAT rapid test for determining infection was reported by other authors before (38,39). Moreover, Vismarra et al. (18) showed that the T. gondii identification in sheep using molecular investigation in tissue or meat samples was less sensitive 45.4% than serological one 100% for assess the infection status. Various previous researches have reported that the infection rats of T. gondii in small ruminants range from 66% to 97% (40-42).
The prevalence of human toxoplasmosis associated with foodborne infection was about 50%, corresponding to raw or undercooked meat consumption (43). In addition to that the local cattle meat are riskier than the imported due to the higher rate of infection with T. gondii, the parasite can infect all examined organs (heart, muscles, tongue), and the infection rate effected by season not by age of animals (44). Moreover, Mikaeel and Al-Saeed (45) found that high infection rate of T. gondii in free range local chickens in Duhok Province and chickens of older age showed higher infection rates than younger chickens, this due to the number of times to exposure which increased with age. So it must be follow strict hygienic measures in order to minimize the transmission of infection to human.
During slaughter inspection, there is no method to differentiate the infected T. gondii from the uninfected animal carcasses and the parasite tissue cysts remain viable for the lifetime of the animal; thus, all edible parts were seropositive for T. gondii (46). Our results devised a possible alternative protocol through using diaphragm meat juice for determination toxoplasmosis in cattle without need for experimental infection and the bioassay of parasite in laboratory animals to confirm the a live or viable parasite stages of infection presence and without needing to additional equipment other than that required for ELISA and also this study explain the comparative results of ELISA with that of commercial LAT. Furthermore, the immunoblotting proved immune-reactivity of samples of meat juice. In fact, sensitivity of toxoplasmosis in meat juice affected by the amount or concentration of blood in the tissue and not a local detection of the specific antibodies (24). Looking at the overall ELISA results on tissue and meat samples can be useful to conduct a serological and epidemiological survey. It may give an acceptable sensitivity in relation to the simplicity of use (4).
The study results provide a basic information on the toxoplasmosis in cattle meat juice and indicate the significant human health and hygiene risks corresponding with consuming raw and undercooked beef. The indirect ELISA was a simple, rapid, inexpensive and more sensitive for diagnosis T. gondii in meat juice and it can be considered as a promising test for monitoring Toxoplasmosis in meat and meat products of cattle. The meat juice (fluid) was helpful as an acceptable sample for detecting antibodies to T. gondii using ELISA and diaphragmatic tissues are a potential matrix for parallel seropositive diagnosis.
Author wish to thank knowledge his colleges in the Department of Zoonotic Diseases, NRC for supporting and providing facilities.
Conflict of interest
The authors of the current work declare that they have no conflicts of interest in this work.
- The meat juice (fluid) was helpful as a reasonable sample for detecting antibodies to T. gondii.
- ELISA is a simple, rapid, inexpensive and more sensitive test for diagnosis T. gondii in meat juice.
- ELISA can be considered as a promising test for monitoring Toxoplasmosis in meat or meat products of cattle in large-scale.
- The study results refer to the potential risks to human health associated with consuming raw and undercooked beef.
- Dubey JP. Toxoplasmosis of animals and humans. 2nd ed. USA: CRC Press;2010. 313 p. DOI: 10.1186/1756-3305-3-112
- EFSA. The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2015. EFSA J. 2016;14(12):4634. DOI: 10.2903/j.efsa.2015.4329
- Shaapan RM. The common zoonotic protozoal diseases causing abortion. J Parasit Dis.2016;40(4):1116-1129. DOI: 10.1007%2Fs12639-015-0661-5
- Ranucci D, Veronesi F, Di Matteo I, Branciari R, Miraglia D, Marini C, Fioretti DP. Comparison of serum and meat juice for detection of anti-Toxoplasma gondii antibodies in hunted wild boars (Sus scrofa). Trend Vet Sci. 2013:79-83. DOI: 10.1007/978-3-642-36488-4_15
- Toaleb NI, Shaapan RM, Hassan SE, El Moghazy E. High diagnostic efficiency of affinity isolated fraction in camel and cattle toxoplasmosis. World J Med Sci. 2013;8(1):61-66. DOI: 10.5829/idosi.wjms.2013.8.1.72161
- Toaleb NI, Shaapan RM, Abdel-Rahman EH. Adoption of immuno-affinity isolated fasciola gigantica fraction for diagnosis of ovine toxoplasmosis. Global Vet. 2014;12(1):140-145. DOI: 10.5829/idosi.gv.2014.12.01.8240
- Shaapan RM, Toaleb NI, Abdel-Rahman EH. Significance of a common 65 kDa antigen in the experimental fasciolosis and toxoplasmosis. J Parasit Dis. 2015;39(3):550-556. DOI: 10.1007/s12639-013-0394-2
- Caballero-Ortega H, Palma J, García-Márquez L, Gildo-Cárdenas A, Correa D. Frequency and risk factors for toxoplasmosis in ovines of various regions of the State of Colima, Mexico. Parasitol. 2008;135:1385-1389. DOI: 10.1017/S0031182008004873
- Mikaeel FB, Abdo J, Omer LT. Diagnosis of toxoplasmosis in sheep using serological (ELISA) and molecular technique in Duhok governorate. J Univ Zakho. 2015;3(A):32-38. [available here]
- Dong H, Lu YY, Su RJ, Wang YH, Wang MY, Jiang YB, Yang YR. Low prevalence of antibodies against Toxoplasma gondii in dairy cattle from China’s central region. BMC Vet Res. 2018;14:315. DOI: 10.1186/s12917-018-1629-3
- Al-Kappany YM, Abbas IE, Devleesschauwer B, Dorny P, Jennes M, Cox E. Seroprevalence of anti-Toxoplasma gondii antibodies in Egyptian sheep and goats. BMC Vet Res. 2018;14:120. DOI: 10.1186/s12917-018-1440-1
- Halos L, Thébault A, Aubert D, Thomas M, Perret C, Geers R, Alliot A, Escotte-Binet S, Ajzenberg D, Dardé ML, Durand B. An innovative survey underlining the significant level of contamination by Toxoplasma gondii of ovine meat consumed in France. Int J Parasitol. 2010;40(2):193-200. DOI: 10.1016/j.ijpara.2009.06.009
- Nockler K, Serrano FJ, Boireau P, Kapel CM, Pozio E. Experimental studies in pigs on Trichinella detection in different diagnostic matrices. Vet Parasitol. 2005;132:85-90. DOI: 10.1016/j.vetpar.2005.05.033
- Berger-Schoch AE, Bernet D, Doherr MG, Gottstein B, Frey CF. Toxoplama gondii in Switzerland. A serosurvey based on meat juice analysis of slaughtered pigs, wild boar, sheep and cattle. Zoonoses Public Hlth. 2011;58:472-478. DOI: 10.1111/j.1863-2378.2011.01395.x
- Mecca JN, Meireles LR, de Andrade Jr HF. Quality control of Toxoplasma gondii in meat packages: Standardization of an ELISA test and its use for detection in rabbit meat cuts. Meat Sci. 2011;88(3):584-589. DOI: 10.1016/j.meatsci.2011.01.016
- Racka K, Bártová E, Budíková M, Vodrazka P. Survey of Toxoplasma gondii antibodies in meat juice of wild boar (Sus scrofa) in several districts of the Czech Republic. An Agr Env Med. 2015;22(2):1-4. 10.5604/12321966.1152071
- Vismarra A, Mangia C, Barilli E, Brindani F, Bacci C, Kramer L. Meat juice serology for Toxoplasma gondii infection in chickens. Ital J Food Saf. 2016;5:5586. DOI: 10.4081/ijfs.2016.5586
- Vismarra A, Barilli E, Miceli M, Mangia C, Genchi M, Brindani F, Kramer L, Bacci C. Toxoplasma gondii in the Cornigliese sheep breed in Italy: Meat juice serology, in vitro isolation and genotyping. Vet Parasitol. 2017;243:125-129. DOI: 10.1016/j.vetpar.2017.06.013
- Dubey JP. Toxoplasmosis- a waterborne zoonosis. Vet Parasitol. 2004;126:57-72. DOI: 10.1016/j.vetpar.2004.09.005
- Dubey JP, Thulliez P, Weigel RM, Andrews CD, Lind P, Powell EC. Sensitivity and specificity of various serologic tests for detection of Toxoplasma gondii infection in naturally infected sows. Am J Vet Res. 1995;56:1030-1036. [available here]
- Kijlstra A, Jongert E. Control of the risk of human toxoplasmosis transmitted by meat. Int J Parasitol. 2008;38(12):1359-1370. DOI: 10.1016/j.ijpara.2008.06.002
- Wingstrand A, Lind PJ, Haugegaard J, Henriksen SA, Bille-hansen V, Sorensen V. Clinical observations, pathology, bioassay in mice and serological response at slaughter in pigs experimentally infected with Toxoplasma gondii. Vet Parasitol. 1997;72:129-140. DOI: 10.1016/S0304-4017(97)00034-4
- Dubey JP, Jones JL. Toxoplasma gondii infection in humans and animals in the United States. Int J Parasitol. 2008;11:1257-1278. DOI: 10.1016/j.ijpara.2008.03.007
- Villena I, Durand B, Aubert D, Blaga R, Geers R, Thomas M, Perret C, Alliot A, Escotte-Binet S, Thebault A, Boireau P. New strategy for the survey of Toxoplasma gondii in meat for human consumption. Vet Parasitol. 2012;183(3-4):203-208. DOI: 10.1016/j.vetpar.2011.08.001
- El-Nawawi FA, Tawfik MA, Shaapan RM. Methods for inactivation of Toxoplasma gondii cysts in meat and tissues of experimentally infected sheep. Foodborne Path Dis. 2008;5:687-690. DOI: 10.1089/fpd.2007.0060
- Shaapan RM, Ghazy AA. Isolation of Toxoplasma gondii from horse meat in Egypt PJBS. 2007;10(1):174-177. DOI: 10.3923/pjbs.2007.174.177
- Davis SW, Dubey JP. Mediation of immunity to Toxoplasma gondii oocysts shedding cats. J Parasitol. 1995;81:882-886. DOI: 10.2307/3284034jstor.org/stable/3284034
- Elfadaly HA, Hassanain NA, Hassanain MA, Barakat AM, Shaapan RM. Evaluation of primitive ground water supplies as a risk factor for the development of major waterborne zoonosis in Egyptian children living in rural areas. J Inf Public Hlth. 2018;11(2):203-208. DOI: 10.1016/j.jiph.2017.07.025
- Shaapan RM, El-Nawawi FA, Tawfik MA. Sensitivity and specificity of various serological tests for the detection of Toxoplasma gondii infection in naturally infected sheep. Vet Parasitol. 2008;153(3-4):359-362. DOI: 10.1016/j.vetpar.2008.02.016
- Elfadaly HA, Hassanain MA, Shaapan RM, Barakat AM, Toaleb NI. Serological and hormonal assays of murine materno-fetal Toxoplasma gondii infection with emphasis on virulent strains. World J Med Sci. 2012;7(4):248-254. DOI: 10.5829/idosi.wjms.2012.7.4.6559
- Laemmli UK. Cleavage of structural protein during the assembly of the head of bacteriophage T4. Nature 1970;227:680-685. DOI: 10.1038/227680a0
- Wray W, Boulikas T, Wray VP, Hancock R. Silver staining of proteins in polyacrylamide gels. Anal Biochem. 1981;118:197-203. DOI: 10.1016/0003-2697(81)90179-2
- Towbin H, Stachelin T, Gordon J. Electrophoretic transfer of proteins from polacrylamide gels to nitrocellulose sheets: Procedure and some application. Proc Nat Acad Sci. 1979;179:4350-4354. DOI: 10.1073/pnas.76.9.4350
- Beck R, Gaspar A, Mihaljević Z, Marinculić A, Stojcević D, Brstilo M. Evaluation of ELISA for detection of Trichinella antibodies in muscle juice samples of naturally infected pigs. Vet Parasitol. 2005;132(1-2):91-95. DOI: 10.1016/j.vetpar.2005.05.034.
- Verhelst D, De Craeye S, Vanrobaeys M, Czaplicki G, Dorny P, Cox E. Seroprevalence of Toxoplasma gondii in domestic sheep in Belgium. Vet Parasitol. 2014;205(1-2):57-61. DOI: 10.1016/j.vetpar.2014.07.001.
- Hill DE, Chirukandoth S, Dubey JP, Lunney JK, Gamble HR. Comparison of detection methods for Toxoplasma gondii in naturally and experimentally infected swine. Vet Parasitol. 2006;141:9-17. DOI: 10.1016/j.vetpar.2006.05.008
- Ahmed NE, Al-Akabway LM, Ramadan MY, Abd El-Gawad SM, Moustafa MMA. Serological and PCR-sequencing assays for diagnosis of Toxoplasma gondii and Neospora caninum infecting camels in Egypt. BVMJ. 2017;33(2):200-210. DOI: 10.21608/BVMJ.2017.30466
- Forbes LB, Parker S, Gajadhar AA. Performance of commercial ELISA and agglutination test kits for the detection of Toxoplasma gondii antibodies in serum and muscle fluid of swine infected with 100, 300, 500 or 1000 oocysts. Vet Parasitol. 2012;190:362-367. DOI: 10.1016/j.vetpar.2012.06.040
- Al-Adhami BH, Gajadhar AA. A new multi-host species indirect ELISA using protein A/G conjugate for detection of anti-Toxoplasma gondii IgG antibodies with comparison to ELISA-IgG, agglutination assay and Western blot. Vet Parasitol. 2014;200:66-73. DOI: 10.1016/j.vetpar.2013.11.004
- Zedda MT, Rolesu S, Pau S, Rosati I, Ledda S, Satta G, Patta C, Masala G. Epidemiological study of Toxoplasma gondii infection in ovine breeding. Zoonoses Public Hlth. 2010;57(7-8):102-108. DOI: 10.1111/j.1863-2378.2009.01292.x
- Chessa G, Chisu V, Porcu R, Masala G. Molecular characterization of Toxoplasma gondii type II in sheep abortion in Sardinia. Italy Parasite. 2014;21:6-10. DOI: 10.1051/parasite/2014007
- Gazzonis AL, Veronesi F, Di Cerbo AR, Zanzani SA, Molineri G, Moretta I, Moretti A, Piergili FD, Invernizzi A, Manfredi MT. Toxoplasma gondii in small ruminants in Northern Italy - prevalence and risk factors. Ann Agr Env Med. 2015;24:62-68. DOI: 10.5604/12321966.1141370.
- Tenter AM, Heckeroth AR, Weiss LM. Toxoplasma gondii: From animals to humans. Int J Parasitol. 2000;30:1217-1258. DOI: 10.1016/S0020-7519(00)00124-7
- 44. Sakban FM, A’aiz NN. Investigate the Toxoplasma gondii infection in the consumed beef in Al-Diwaniyah province. Iraqi J Vet Sci. 2020;34(1):95-99. DOI: 10.33899/ijvs.2020.164336
- 45. Mikaeel FB, Al-Saeed AT. Molecular detection and seroprevalence of Toxoplasmosis in free range local chickens (Gallus domesticus) in Duhok province, Iraq. Iraqi J Vet Sci. 2020;34(2):247-252. DOI: 10.33899/ijvs.2019.125885.1173
- Halos L, Thébault A, Aubert D, Thomas M, Perret C, Geers R, Alliot A, Escotte- Binet S, Ajzenberg D, Dardé ML, Durand B, Boireau P, Villena I. An innovative survey underlining the significant level of contamination by Toxoplasma gondii of ovine meat consumed in France. Int J Parasitol. 2009;40:193-200. DOI: 10.1016/j.ijpara.2009.06.009
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