caa a22 4500 60615812X CHVBK 20210128100617.0 cr unu---uuuuu 210128e20151101xx s 000 0 eng 10.1007/s10096-015-2481-z doi (NATIONALLICENCE)springer-10.1007/s10096-015-2481-z Contribution of IL6 −174 G>C and IL1B +3954 C>T polymorphisms to congenital infection with Toxoplasma gondii [Elektronische Daten] [W. Wujcicka, Z. Gaj, J. Wilczyński, D. Nowakowska] The purpose of this investigation was the determination of the distribution of genotypes and alleles, residing within interleukin 6 (IL6) and interleukin 1 (IL1) polymorphisms, among fetuses and neonates, congenitally infected with Toxoplasma gondii, and among uninfected control cases. The study included 22 fetuses and newborns infected with T. gondii and 49 control cases. Screening for IgG and IgM antibodies against the parasite and IgG avidity was performed by enzyme-linked fluorescent assay (ELFA) tests. Quantitation of T. gondii DNA in amniotic fluids was assayed by the real-time Q PCR technique for the parasitic B1 gene. Genotypes at IL6 and IL1 single nucleotide polymorphisms (SNPs) were determined by a self-designed, nested polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. Representative genotypes at the studied loci were confirmed by sequencing. All the genotypes were estimated for Hardy-Weinberg equilibrium and IL1 genotypes were tested for linkage disequilibrium. Genotypes and haplotypes at the studied SNPs were investigated for their possible association with the occurrence of congenital T. gondii infection, using a logistic regression model. GC heterozygotes at the IL6 −174 G>C SNP were significantly associated with toxoplasmosis and increased the risk of T. gondii infection [odds ratio (OR) 4.24, 95% confidence interval (CI) 1.24-14.50 in the codominant model, p ≤ 0.050]. In case of IL1 SNPs, similar prevalence rates were observed between T. gondii-infected and -uninfected offspring. Regarding allelic variability, the C alleles at both IL6 and IL1B SNPs were significantly more frequent in the infected than in the uninfected cases (p ≤ 0.050). It is concluded that IL6 −174 G>C and IL1B +3954 C>T SNPs might be involved in the development of congenital T. gondii infection. The Author(s), 2015 Wujcicka W. Scientific Laboratory of the Center of Medical Laboratory Diagnostics, Polish Mother's Memorial Hospital—Research Institute, 281/289 Rzgowska Street, 93-338, Lodz, Poland aut Gaj Z. Scientific Laboratory of the Center of Medical Laboratory Diagnostics, Polish Mother's Memorial Hospital—Research Institute, 281/289 Rzgowska Street, 93-338, Lodz, Poland aut Wilczyński J. Department of Perinatology and Gynecology, Polish Mother's Memorial Hospital—Research Institute, Lodz, Poland aut Nowakowska D. Department of Perinatology and Gynecology, Polish Mother's Memorial Hospital—Research Institute, Lodz, Poland aut European Journal of Clinical Microbiology & Infectious Diseases Springer Berlin Heidelberg 34/11(2015-11-01), 2287-2294 0934-9723 34:11<2287 2015 34 10096 https://doi.org/10.1007/s10096-015-2481-z text/html Onlinezugriff via DOI BK010053 XK010053 XK010000 Metadata rights reserved Springer special CC-BY-NC licence nationallicence 1 research-article jats NATIONALLICENCE NATIONALLICENCE NL-springer NATIONALLICENCE 856 40 https://doi.org/10.1007/s10096-015-2481-z text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Wujcicka W. Scientific Laboratory of the Center of Medical Laboratory Diagnostics, Polish Mother's Memorial Hospital—Research Institute, 281/289 Rzgowska Street, 93-338, Lodz, Poland aut NATIONALLICENCE 700 1- Gaj Z. Scientific Laboratory of the Center of Medical Laboratory Diagnostics, Polish Mother's Memorial Hospital—Research Institute, 281/289 Rzgowska Street, 93-338, Lodz, Poland aut NATIONALLICENCE 700 1- Wilczyński J. Department of Perinatology and Gynecology, Polish Mother's Memorial Hospital—Research Institute, Lodz, Poland aut NATIONALLICENCE 700 1- Nowakowska D. Department of Perinatology and Gynecology, Polish Mother's Memorial Hospital—Research Institute, Lodz, Poland aut NATIONALLICENCE 773 0- European Journal of Clinical Microbiology & Infectious Diseases Springer Berlin Heidelberg 34/11(2015-11-01), 2287-2294 0934-9723 34:11<2287 2015 34 10096