Association of Typing HLA with Toxoplasmosis in Iraqi Women Patients
[1]
Yassir Dakheel Kremsh Alasadiy, Department of Biology, College of Science, University of Al - Muthanna, Ministry of Higher Education & Scientific Research, AL-Samawa city (Southern Iraq), Iraq.
[2]
Hawraa Hamza Abbas, Department of Biology, College of Science, University of Al - Muthanna, Ministry of Higher Education & Scientific Research, AL-Samawa city (Southern Iraq), Iraq.
Toxoplasma gondii is an obligate intracellular protozoan responsible for common parasitic infections throughout the world. It can invade and multiply in the nucleated cells of virtually all worm blooded animals including humans, domestic mammals, and birds, with members of the cat family being the only known hosts for the sexual stages of T. gondii infection, it is a world - wide disease results in serious health and financial loss. Iraq considered as an endemic region for this disease. One hundred fifty women were included in this study with a history of single or repeated abortion that was referred by physicians to detect anti-Toxoplasma antibodies. The study included one hundred women with spontaneous abortion and 25 women with normal pregnancy and 25 healthy women were used as a control. Blood samples were collected for extraction of DNA and amplification by Real-Time PCR technique and HLA typing of injured and healthy control groups, our work studying the associations between Human Leukocyte Antigen (HLA) (i.e. human major histocompatibility complex (MHC) genes and susceptibility to infections with toxoplasmosis have been described. The present study showed the percentage of the HLA-DQA1 and HLA-DQB1 alleles between the groups, there were decreased percentage of the HLA-DQA1*0302 and HLA-DQB1 *0501 alleles in the patient group compared to the control group (37.5% v 62.5%), (16.7% vs 70.8%) respectively, but the precentage of the HLA-DRB1*1302 explained increased in patients with compared to the with control (66.7 % vs 37.5%) respectively.
[1]
Alexander DL, Mital J, Ward GE, Bradley P, Boothroyd JC (2005) Identification of the Moving Junction Complex of Toxoplasma gondii: A Collaboration between Distinct Secretory Organelles. PLoS Pathog 1(2): e17.doi: 10.1371/journal.ppat.0010017.
[2]
Asgari, Q.; Motazedian, M. H.; Esmaeelzadeh, B.; Kalantari, M. and Hatam, Gh. R. (2009). The Prevalence of Toxoplasma Infection among Free-Ranging Chickens in Southern Iran Using IFA and Nested-PCR. Iranian J. Parasitol., 4(4): 29-36.
[3]
Remington, J. S., R. McLeod, and G. Desmonts. (1995). Toxoplasmosis, p. 4124 LIN ET AL. J. CLIN. MICROBIOL.140–267. In J. S. Remington and J. O. Klein (ed.), Infectious diseases of the fetus and newborn infant, 4th ed. The W. B. Saunders Co., Philadelphia, Pa.
[4]
Montoya JG and Remington JS. (2008). Management of Toxoplasma gondii infection during pregnancy .Clinical practice. Cyto. Incl. Dis. 47: 554-566.
[5]
Jenum PA, Holberg-Petersen M, Melby KK, Stray Pedersen B. (1998). Diagnosis of Congenital Toxoplasma gondii infection by polymerase chain Reaction (PCR) on amniotic fluid samples. The Norwegian experience. APMIS; 106: 680-6.
[6]
Cingolani A, De Luca A, Ammassari A, et al.(1996). PCR detection of Toxoplasma gondii DNA in CSF for the differential diagnosis of AIDS-related focal brain lesions. J Med Microbiol; 45: 472-6.
[7]
Held TK, Krüger D, Switala AR, et al. (2000). Diagnosis of toxoplasmosis in bone marrow transplant recipients: comparison of PCRbased results and immunohisto chemistry. Bone Marrow Transplant; 25:1257-62.
[8]
Mahalakshmi B, Therese KL, Madhavan HN, Biswas J. (2006). Diagnostic value of specific local antibody production and nucleic acid amplification technique-nested polymerase chain reaction (nPCR) in clinically suspected ocular toxoplasmosis. Ocul Immunol Inflamm; 14: 105-12.
[9]
Kompalic-Cristo A, FrottaC, Suárez-Mutis M, Fernandes O, Britto C. (2007). Evaluation of a real-time PCR assay based on the repetitive B1 gene for the detection of Toxoplasma gondii in human peripheral blood. Parasitol Res; 101: 619-25.
[10]
Barret J.T., (2000). The MHC In; Bricher S’ The text book of immmunology 9th Ed. The C.V. Mosby company chapter 4, pp 76-83.
[11]
Fernandes A., Maciel L., Foss M., Donadi E.A. (2003). Como entender a associação entre o sistema HLA e as doenças auto-imunes endócrinas. Arq Bras Endocrinol Metab; 47(5):601-11.
[12]
Klein J., Sato A. (2000). The HLA System - First of two parts. N Engl J Med; 343(11): 702-9.
[13]
Zhiburt EB, Ionova AI, Danil’chenko VV, Serebrianaia NB, Bel’gesov NV, Trofimenko EV. (1997). The spread of antibodies to cytomegalovirus and Toxoplasma among donors of blood components. Zh Mikrobiol Epidemiol Immunobiol; 1: 59–61.
[14]
Lee, P. Y. C., J. Mangan, R. E. Holliman, and P. D. Butcher. )1999(. Quantitation of Toxoplasma gondii DNA in a competitive nested polymerase chain reaction. J. Clin. Pathol. 52: 61–64.
[15]
Fisher PR, Boone P. (1998). Short report: severe malaria associated with blood group. Am J Trop Med Hyg; 58: 122–123.
[16]
Hakomori S. (1999). Antigen structure and genetic basis of histoblood groups A, B and O: their changes associated with human cancer. Biochim Biophys Acta; 1473: 247–266.
[17]
Midtvedt T, and Vaage L. (1989). Relationship between Toxoplasma gondii antibodies and blood group. Eur J Clin Microbiol Infec Dis; 8: 575-6.
[18]
Kolbekova P, Kourbatova E, Novotna M, Kodym P, Flegr J.(2007). New and old risk factors for Toxoplasma gondii infection: prospective cross-sectional study among military personnel in the Czech Republic. Clin Microbiol Infect; 13: 1012-7.
[19]
Gill HS. (1985). Occurrence of Toxoplasma gondii ntibodies in Tanzanian blood donors. East Afr Med J.; 62(8):585-8.
[20]
Lecolier B, Grynberg H, Freund M. (1990). Absence of relationship between Toxoplasma gondii antibodies and blood group in pregnant women in France. Eur J Clin Microbiol Infect Dis. 1990; 9(2): 152-3.
[21]
Howard J C. (1991). Disease and evolution. Nature; 352:565-7.
[22]
Nussenblatt RB, Mittal KK, Fuhrman S, Sharma SD, Palestine AG. (1989). Lymphocyte proliferative responses of patients with ocular toxoplasmosis to parasite and retinal antigens. Am J Ophthalmol; 107: 632-41.
[23]
Rothova A, van Knapen F, Baarsma GS, Kruit PJ, Loewer-Sieger DH, Kijlstra A. (1994). Serology in ocular toxoplasmosis. BrJ Ophthalmol 1986; 70: 615-22.
[24]
Desmonts, G., and J. Couvreur. (1974). Congenital toxoplasmosis: a prospective study of 378 pregnancies. N. Engl. J. Med. 290: 1110–1116.
[25]
Hohlfeld, P., F. Daffos, J.-M. Costa, P. Thulliez, F. Forestier, and M. Vidaud. (1994). Prenatal diagnosis of congenital toxoplasmosis with a polymerase chain reaction test on amniotic fluid. N. Engl. J. Med. 331: 695–699.
[26]
Balakrishnan V (2003). A preliminary study of genetic distance among some populations of the Indian subcontinent, J. Hum. Immunol. Erol., 7: 67-75.
[27]
Stephent M, Donnely P (2003). A comparison of Bayesian methods for haplotype reconstruction from population genotype data. Am. J. Hum. Genet., 73: 1162.
[28]
Aljenaidi FA, Ghorayedb SFW, Abbasi AA, Arekat MR, Hakine NI, Najm P, Ola KA (2005). Contribution of selective HLA – DRB1 / DQBI alleles and hoplotypes to the genetic susceptibility of Type I diabetes among labanese and Baheaini Aeabs, J. Chin. Endocrinol. Metah., 90: 5104- 5109.