Molecular study of Toxoplasma gondii B1 Gene in Quails Birds (Coturnix Japonica) in Baghdad City, Iraq
Keywords:
toxoplasma, B1gene, Nested-PCR, tissue, quail BirdAbstract
Toxoplasmosis is a common zoonotic parasitic disease of medical and veterinary importance worldwide, caused by an obligate intracellular protozoan parasite Toxoplasma gondii. The study was conducted to investigate the infection rate of Toxoplasma gondii in 100 tissues samples of (25/150) seropositive quail bird organs (25 brain, 25 liver, 25 heart and 25 pectoral muscles) of both sex by Nested Polymerase Chain Reaction (N-PCR) based on B1 gene in some areas of Baghdad city during the period from the 1st January 2021, up to 30th September 2021. The total infection rate was 24% (24/100) and the highest percentage was recorded in pectoral muscles 28% (7/25) and the lowest percentage was recorded in the heart 20% (5/25) without significant difference. Regarding the sex the results revealed that the total infection rate of T. gondii in hens was 30.76% (16/52) more than cocks tissues samples 16.66% (8/48) with highly significant (P≤0.01) differences between organs type. In cock quail, the highest percentage was recorded in brain 33.33% (4/12) and the lowest percentage was recorded in the pectoral muscles and heart 8.33% (1/12).
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Albert, J. and Fenyö, E.M. (1990). Simple, sensitive, and specific detection of human immunodeficiency virus type 1 in clinical specimens by polymerase chain reaction with nested primers. J. Clin. Microbiol. 28(7):1560–1564.
Al-Khaled, M.J.A. (2012). Serological and molecular study of toxoplasmosis in chickens and ducks in some regions of middle Euphrates. Ph.D. thesis, College of Veterinary Medicine, University of Baghdad, Iraq.
Al-khanak, M. N. and Salman, S. S. (2021). Genotyping and DNA Sequencing of Toxoplasma gondii from Women and Domestic Chickens in the Wasit Province Iraq. Indian Journal of Forensic Medicine & Toxicology, July-September, 15(3).
Al-Sanjary, R.A. and Hussien, T.H. (2012). Using species-specific PCR technique to detect Toxoplasma gondii in broiler chickens. Iraqi J. Vet .Med. Sci. 26 (2): 53-56.
Ayinmode, A.B. and Dubey, J.P. (2012). Toxoplasma gondii infection in free-range chicken: mini-review and seroprevalence study in Oyo state, Nigeria. African Journal Biomedical Research; 15(3):145–148.
Burg, J.L., Grover, C.M., Pouletty, P. and Boothroyd, J. (1989). Direct and sensitive detection of a pathogenic protozoan, Toxoplasma gondii, by polymerase chain reaction. J. Clin. Microbiol., 27(8): 1787-1792.
Cong, W., Chi, W.B., Sun, W.W., Shan, X.F., Kang, Y.H., Meng, Q.F and Qian, A.D. (2017). First report of Toxoplasma gondii infection in common quails (Coturnix coturnix) intended for human consumption in three provinces of northeastern China. Vector-Borne and Zoonotic Diseases 17, 351–353.
Contini, C., Seraceni, S., Cultrera, R., Incorvaia, C., Sebastiani, A. and Picot, S. (2005). Evaluation of a Realtime PCR-based assay using the lightcycler system for detection of T. gondii bradyzoite genes in blood specimens from patients with toxoplasmic retinochoroiditis. Int. J. Parasitol. 35: 275–283.
Dubey J.P., Ruff, M.D., Kwok,O.C., Shen, S.K., Wilkins, G.C. and Thulliez, P.
a. (1993). Experimental toxoplasmosis in bobwhit quail (Golinus virginianus). J. Parasitol., 79(6): 935 – 939.
Dubey J.P., Ruff, M.D., Wilkins, G.C., Shen, S.K. and Kwok, O.C. (1994). Experimental toxoplasmosis in pheasants. J. Wildl. Dis. 30(1): 40 – 45.
Dubey, J.P. (2010). Toxoplasmosis of animals and humans. CRC Press, Taylor & Francis Group, Boca. Raton., FL.
Dubey, J.P., Murata, F.H.A., Cerqueira-Cézar, C.K., Kwok, O.C.H.; Su, C. (2020). Epidemiologic significance of Toxoplasma gondii infections in turkeys, ducks, ratites and other wild birds: 2009–2020. Parasitology. 148, 1–30.
Halleyantoro, R., Andriyani, Y., Sari, I.P., Kurniawan, A. (2019). Nested PCR method for detection Toxoplasma gondii B1 gene in Cerebrospinal Fluid of HIV patients. Journal of Biomedicine and Translational Research, 5 (2): 62-66.
Hassan, A.K., Naeem, E.V. and Soliman, M.A. (2020). Investigation the Prevalence of Common Parasitic Infections in Farmed Quails in Upper Egypt. SVU-IJVS, 3(2): 38-50.
Hussein, A., Taher, D., Ghaly, S., Hassanien, A. and Abd-Elgaffar LGAFFAR, S. (2018). Epidemiological Study on the Role of Quails in Transmitting of T. gondii to Man. Assiut Veterinary Medical Journal Article 1, 64(156): 1-7.
Ivovic, V., Vujanic, M., Zivkovic, T., Klun, I. and Djurkovic-Djakovic, O. (2012). Molecular detection and genotyping of Toxoplasma gondii from clinical samples, toxoplasmosis-recent advances, intech open.
Jones, J.L., Kruszon-Moran, D., Wilson, M., McQuillan, G., Navin, T. & McAuley, J.B. (2001). Toxoplasma gondii infection in the United States: seroprevalence and risk factors. American Journal of Epidemiology 154: 357-365.
Khan, M.B., Khan, S., Rafiq, K., Khan, S.N., Attaullah, S. and Ali, I. (2020). Molecular identification of Toxoplasma gondii in domesticated and broiler chickens (Gallus domesticus) that possibly augment the pool of human toxoplasmosis. Plos One. Apr 22; 15(4):1-12. DOI: 10.1371/journal.pone.0232026.
Lorencova, A., Lamka, J. and Slany, M. (2015). T.gondii in wild ruminant bred in game preserves and farms with production destined for human consumption in the Czech Republic. Potravinarstvo, Sci. J. Food Ind. 9 (1): 288-292.
Mahami-Oskouei, M., Morad, M., Fallah, E., Hamidi, F. and Akbari NAR. (2017). Molecular Detection and Genotyping of Toxoplasma gondii in Chicken, Beef, and Lamb Meat Consumed in Northwestern Iran. Iran J Parasitol. 12(1): 38–45.
Mikaeel, F.B. and Al-Saeed, A.T. (2020). Molecular detection and seroprevalence of Toxoplasmosis in free range local chickens (Gallus domesticus) in Duhok province, Iraq. Iraqi Journal of Veterinary Sciences. 34(2): 247-252.
Mose, J.M., Kagira, J.M., Karanja, S.M., Ngotho, M., Kamau, D.M., Njuguna A.N., and Maina, N.W. (2016). Detection of Natural Toxoplasma gondii Infection in Chicken in Thika Region of Kenya Using Nested Polymerase Chain
a. Reaction. BioMed Res Int.1–5.
Nazir, M.M., Ayaz, M.M., Ahmed, A.N., Maqbool, A., Ashraf, K., Oneeb, M., Yasin, G., Subhani, A., Ali, M.A., Nazir, N., Sajid, M.A. (2018). Prevalence of Toxoplasma gondii, Neospora caninum, and Sarcocystis Species DNA in the Heart and Breast Muscles of Rock Pigeons (Columbia livia). J Parasitol Res.
Rajendran, C., Keerthana, C.M., Anilakumar, K.R., Satbige, A.S. and Gopal, S. (2018). Development of B1 Nested PCR for Assessing the Prevalence of Zoonotic Protozoan Disease Agent Toxoplasma Gondii among Food Animals from Karnataka State, Southern India. J Microbiol Lab Sci,1:101.
SAS. Statistical Analysis System. (2012). User's Guide. Statistical. Version 9.1th ed. SAS. Inst. Inc. Cary. N.C. USA.
Tenter, A. M, Heckerroth, A. R and Weiss, L. M. (2000). Toxoplasma gondii: from animals to human. Int. J. Parasitol. 30: 1217–1258.
Vitale M. (2013). A High Sensitive Nested PCR for Toxoplasma gondii Detection in Animal and Food Samples. J Microb Biochem Technol. 05(02):39–41.
Azimpour-Ardakan, T., Fotouhi-Ardakani, R., Hoghooghi-Rad, N., Rokni, N., Motallebi, A. (2021). Phylogenetic Analysis and Genetics Polymorphisms Evaluation of ROP8 and B1 Genes of T.gondii in Livestock and Poultry Hosts of Yazd, Qom and Golestan Provinces of Iran. Iran J Parasitol. 16(4):576-586.
Suwija, N., Suarta, M., Suparsa, N., Alit Geria, A.A.G., Suryasa, W. (2019). Balinese speech system towards speaker social behavior. Humanities & Social Sciences Reviews, 7(5), 32-40. https://doi.org/10.18510/hssr.2019.754
Widana, I.K., Dewi, G.A.O.C., Suryasa, W. (2020). Ergonomics approach to improve student concentration on learning process of professional ethics. Journal of Advanced Research in Dynamical and Control Systems, 12(7), 429-445.
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