Comparison Between Nested-PCR and ELISA for the Detection of Toxoplasma gondii in Blood and Milk and its Genotyping in Lactating Goats and Aborted Women in Iraq
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Abstract
The present study aimed to assess enzyme-linked immunosorbent assay (ELISA) and nested-polymerase chain reaction (n-PCR) methods based on B1 gene for the detection of Toxoplasma (T.) gondii in the blood and milk of local Iraqi goats. The SAG3 gene was also used to identify the genotyping of T. gondii in goats and aborted women in Iraq. A total of 240 (80 blood, 80 sera, 80 milk) lactating goats and 30 blood samples from aborted women were included in this study. A total of 17 (21.2%) infected goats were found in blood samples and 23 (28.7%) in milk samples when using n-PCR, while the numbers were 23 (28.7%) and 17 (21.2%) when using ELISA. Aborted women had an overall infection rate of 50% when using ELISA and 33% when using n-PCR. The degree of agreement between n-PCR in milk and blood was almost perfect (Kappa=0.801), with a sensitivity of 100 and a specificity of 90.5, while there was a slight degree of agreement (Kappa=0.14) between n-PCR and ELISA in blood, with 58.8 sensitivity and 74.6 specificity. The results of the comparison between n-PCR in blood and ELISA in milk showed positive samples of 17 (21.2%) for each, with 82.4 sensitivity and 22.2 specificity, and no agreement (Kappa=–0.046). Sequencing of the SAG3 gene of T. gondii from goat and human isolates showed that the similarity ranged from 98.65–99.90% for genotypes I and III. In conclusion, n-PCR may be more accurate than ELISA for detecting T. gondii in blood and milk. In addition, the phylogenetic tree's evidence of a high degree of similarity between human and goat isolates provides further evidence that goats are an important reservoir of T. gondii and that public awareness is necessary.
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Dubey JP, Murata FH, Cerqueira-Cézar CK, Kwok OC. Public health and economic importance of Toxoplasma gondii infections in goats: the last decade. Res Vet Sci. 2020;1: 132:292-307.
Djurković-Djaković O, Dupouy-Camet J, Van der Giessen J, Dubey JP. Toxoplasmosis: an overview from a one health perspective. Food Waterborne Parasitol. 2019; 1:15: e00054.
Freppel W, Ferguson DJ, Shapiro K, Dubey JP, Puech PH, Dumètre A. Structure, composition, and roles of the Toxoplasma gondii oocyst and sporocyst walls. Cell Surf. 2019; 1: 5:100016.
Mancianti F, Nardoni S, D'Ascenzi C, Pedonese F, Mugnaini L, Franco F, et al. Seroprevalence, detection of DNA in blood and milk, and genotyping of Toxoplasma gondii in a goat population in Italy. Biomed Res Int. 2013; 2013: 905326.
Camossi LG, Greca-Júnior H, Corrêa AP, Richini-Pereira VB, Silva RC, Da Silva AV, et al. Detection of Toxoplasma gondii DNA in the milk of naturally infected ewes. Vet Parasitol. 2011; 177(3-4):256-261.
Abu-Dalbouh MA, Ababneh MM, Giadinis ND, Lafi SQ. Ovine and caprine toxoplasmosis (Toxoplasma gondii) in aborted animals in Jordanian goat and sheep flocks. Trop Anim Health Prod. 2012; 44(1):49-54.
Manuel L, Santos-Gomes G, Noormahomed EV. Human toxoplasmosis in Mozambique: gaps in knowledge and research opportunities. Parasitol Vectors. 2020;13(1):1-0.
Dubey JP. Toxoplasmosis–a waterborne zoonosis. Vet Parasitol. 2004; 126(1-2):57-72.
Spišák F, Turčeková Ľ, Reiterová K, Špilovská S, Dubinský P. Prevalence estimation and genotypization of Toxoplasma gondii in goats. Biologia. 2010; 65(4):670-674.
Bezerra MJ, Kim PC, Moraes ÉP, Sá SG, Albuquerque PP, Silva JG, et al. Detection of Toxoplasma gondii in the milk of naturally infected goats in the Northeast of Brazil. Transbound Emerg Dis. 2015; 62(4):421-424.
Dubey JP, Verma SK, Ferreira LR, Oliveira S, Cassinelli AB, Ying Y, et al. Detection and survival of Toxoplasma gondii in milk and cheese from experimentally infected goats. J Food Prot. 2014; 77(10):1747-1753.
Switaj K, Master A, Skrzypczak M, Zaborowski P. Recent trends in molecular diagnostics for Toxoplasma gondii infections. Clin Microbiol Infect. 2005; 11(3):170-176.
Liu Q, Wang ZD, Huang SY, Zhu XQ. Diagnosis of toxoplasmosis and typing of Toxoplasma gondii. Parasite Vector. 2015; 8(1):1-4.
Bretagne S. Molecular diagnostics in clinical parasitology and mycology: limits of the current polymerase chain reaction (PCR) assays and interest of the real-time PCR assays. Clin Microbiol Infect. 2003; 9(6):505-511.
Cong H, Mui EJ, Witola WH, Sidney J, Alexander J, Sette A, et al. Toxoplasma gondii HLA-B*0702-restricted GRA7(20-28) peptide with adjuvants and a universal helper T cell epitope elicits CD8(+) T cells producing interferon-γ and reduces parasite burden in HLA-B*0702 mice. Hum Immunol. 2012; 73(1):1-10.
Halleyantoro R, Andriyani Y, Sari IP, Kurniawan A. Nested PCR methods for detection Toxoplasma gondii B1 gene in cerebrospinal fluid of HIV patients. J Biomed Transl Res. 2019; 5(2):62-66.
Vitale DC, Armenakis AA, Feild HS. Integrating qualitative and quantitative methods for organizational diagnosis: Possible priming effects? J Mix Meth Res. 2008; 2(1):87-105.
Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics, 1977; 33(1):159-174.
Luptakova L, Benova K, Rencko A, Petrovova E. DNA detection of Toxoplasma gondii in sheep milk and blood samples in relation to phase of infection. Vet Parasitol. 2015; 208(3-4):250-253.
Saki J, Zamanpour M, Najafian M, Mohammadpour N, Foroutan M. Detection of acute and chronic Toxoplasma gondii infection among women with history of abortion in the Southwest of Iran. J Parasitol Res. 2021; 2:2021.
Ibrahim HM, Mohamed AH, El-Sharaawy AA, El-Shqanqery HE. Molecular and serological prevalence of Toxoplasma gondii in pregnant women and sheep in Egypt. Asian Pac J Trop Med. 2017; 10(10):996-1001.
Mason S, Quinnell RJ, Smith JE. Detection of Toxoplasma gondii in lambs via PCR screening and serological follow-up. Vet Parasitol 2010; 169(3-4):258-63.
Duncanson P, Terry RS, Smith JE, Hide G. High levels of congenital transmission of Toxoplasma gondii in a commercial sheep flock. Int J Parasitol. 2001; 31(14):1699-703.
Kijlstra A, Jongert E. Toxoplasma-safe meat: close to reality? Trends in Parasitol.2009; 25(1):18-22.
Silva RC da, Silva AV, da and Langoni H. Recrudescence of Toxoplasma gondii infection in chronically infected rats (Rattus norvegicus).
Exp Parasitol. 2010;125(4): 409-412.
de Santana Rocha D, de Sousa Moura RL, Maciel BM, Guimarães LA, O’dwyer HN, Munhoz AD, et al. Detection of Toxoplasma gondii DNA in naturally infected sheep’s milk. Genet Mol Res. 2015; 14(3):8658-8662.
Montoya JG. Laboratory diagnosis of Toxoplasma gondii infection and toxoplasmosis. J Infect Dis. 2002; 185(Supplement_1): S73-82.
Amairia S, Rouatbi M, Rjeibi MR, Nouasri H, Sassi L, Mhadhbi M, Gharbi M. Molecular prevalence of Toxoplasma gondii DNA in goats’ milk and seroprevalence in Northwest Tunisia. Vet Medicine Sci. 2016;2(3):154-160.
Saad NM, Hussein AA, Ewida RM. Occurrence of Toxoplasma gondii in raw goat, sheep, and camel milk in Upper Egypt. Vet World. 2018; 11(9):1262.
Mahmood AS, Al-Sarray SA, Al-Kazaz A. PCR detection of Toxoplasma gondii B1 gene in women suffering from abortion. J Biotech Res Cen. 2019; 13(1):12-5.