Association of toll-like receptors polymorphism and intrauterine transmission of cytomegalovirus

PLoS One. 2017 Dec 21;12(12):e0189921. doi: 10.1371/journal.pone.0189921. eCollection 2017.

Abstract

Background: Congenital Cytomegalovirus (CMV) is a very common intrauterine infection which can cause severe developmental disabilities. Transmission of the virus to the fetus occurs in only 40% of primarily infected women. The probability of intrauterine transmission is higher when infection occurs during the second trimester of pregnancy than in the first trimester. The Toll-like receptors (TLRs) protein family plays a key role in both innate immune response to CMV infections and in normal pregnancy. Specific single nucleotide polymorphisms (SNPs) in TLRs can affect CMV infections and maternal-fetal interface expression. Therefore, TLR SNPs could be involved in intrauterine transmission determination.

Study aim: To establish a correlation between TLR2 (rs4696480, rs3804100, rs1898830), TLR3 (rs3775291) and TLR7(rs179008) SNPs with CMV intrauterine transmission during the first and second trimester.

Methods: SNPs of 83 pregnant women with primary CMV were analyzed by Real-Time PCR and PCR-RFLP assay and compared to intrauterine transmission state.

Results: Women bearing the GG genotype in the rs1898830 TLR2 SNP who were infected with CMV during the second trimester did not transmit the virus to the fetus. Likewise, in the co-dominant or recessive models of this SNP, a significant association was found between the genotypes and CMV intrauterine transmission. In all cohort women or in women infected during the first trimester, no such associations were found between the tested SNPs and intrauterine transmission of the virus.

Conclusion: Women bearing the GG genotype in the rs1898830 SNP, who are infected with CMV during the second trimester of pregnancy, have a low likelihood of transmitting the virus to the fetus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytomegalovirus Infections / complications
  • Cytomegalovirus Infections / transmission*
  • Female
  • Humans
  • Polymorphism, Genetic*
  • Pregnancy
  • Pregnancy Complications, Infectious*
  • Toll-Like Receptors / genetics*

Substances

  • Toll-Like Receptors

Grants and funding

This study was funded by internal research grants of the Hospital. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.