P-41: Association Study of MICA*008 Gene Polymorphism with Chlamydia Trachomatis Infection in Infertile Men Reffer to Royan Institute

Authors

  • Asadpor U
  • Gourabi H
  • Haghighat S
  • Mohseni Meybodi A
  • Sadighi Gilani MA
  • Totonchi M
Abstract:

Background: Chlamydia trachomatis(CT) is an obligate intracellular bacteria, requires living cells to replicate itself. CT infection can remain up to 4 years in the couple and affect their fertility. The relationship between CT and infertility is very important because most patients are asymptomatic and untreated. After infection with CT, NK activation signals begin through interactions of its receptors with molecules like MHC class I(MICA/B). Materials and Methods: Seven hundred patients with poor sperm parameters were selected for primary screening and detecting the presence of Chlamydia. ELISA test was performed for the presence of anti- CT IgA in these patients&#039; semen plasma. The Sperm&#039;s DNA was extracted in order to confirm the presence of Chlamydia. Chlamydia genome amplification was performed using specific primers. Among these samples, 62 patients were diagnosed with Chlamydia infection, in which 32 samples were symptomatic while the others were asymptomatic. Moreover 34 fertile men with normal spermogram and without any past history of CT infection were selected as controls. PCR-SSP method by eight primers were used to detect MICA*008 alleles. Results: The results indicate that the frequency of MICA*008 allele was significantly higher in control group than that of infected patients with CT (p<0.05). Although there were no significant difference between the allele frequency of control and symptomatic patients (p=0.193), it was higher in control group than in idiopathic group (p<0.05). Moreover, the frequency of this polymorphism was significantly higher in asymptomatic patients than in symptomatic patients (p=0.010). Conclusion: These results show that the presence of MICA*008 allele product may reduce the susceptibility of the host to be infected with CT and those with its protein have more resistant to Chlamydia infection. According to these results, MICA gene can be considered as a good candidate gene to determine the host potential genetic predisposition toward resistance against pathogens.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

P-194: SEPT12-G800A Polymorphism in Azoospermic Infertile Men Referred to Royan Institute

Background: SEPTINS belong to a family of polymerizing GTP-binding proteins that are required for many cellular functions, such as vesicular trafficking, mitosis, membrane compartmentalization and cytoskeletal remodeling. Among all SEPTIN genes, SEPT12 is dominantly expressed in testis tissue of adults, known as an essential annulus component of mature sperm. Therefore, it is hypothesized that ...

full text

P-123: Genetic Variation of AKAP3 Gene in Infertile Men with Abnormal Spermogram Referred to Royan Institute

Background One kind of sperm abnormality that leads to men infertility is short flagella sperms. In this defect, fibrous sheath and axoneme are disorganized, the sperms tail is short, the numbers of sperms in the semen fluid reduce and the sperms are immotile. There are also other kinds of oligoasthenoteratozospermia (OAT) disorder that causes infertility in men. A kinas anchoring protein 3 (AK...

full text

P-208: Analysis of H2BFWT Gene Alterations in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Telomeres play a dramatic role in sperm pronuclei formation and subsequently successful fertilization. The H2B family, member W, testis specific (H2BFWT) gene encodes a testis specific histone that colocalized with telomeric sequences and interfere in the dynamic rearrangement of telomeres at late stages of spermatogenesis. H2BFWT is essential for transmission of the telomeric chrom...

full text

P-202: Reduced Expression of JMJD1A Histone Demethylase Gene in Testis Tissues of Infertile Men Referred to Royan Institute

Background: Epigenetic modifications are involved in different cellular processes through regulating chromatin dynamics. histone methylation is an important modification that can be dynamically regulated by histone methyltransferase and histone demethylase enzymes. JMJD1A (also known as JHDM2A and KDM3A) is a histone demethylase specific for H3K9me2/me1. JMJD1A is a key epigenetic regulator tha...

full text

P-236: Haplotype Analysis of The H2B.W Gene in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Recent studies demonstrated the multifactorial and chronic nature of male infertility, including mutations of some known spermatogenesis-related genes. The H2B family, member W (H2B.W) gene is one of the testis specific histone variant genes that encodes a sperm telomere-binding protein, required for reorganization and integration of sperm chromosomes. The objective of the present s...

full text

the study of aaag repeat polymorphism in promoter of errg gene and its association with the risk of breast cancer in isfahan region

چکیده: سرطان پستان دومین عامل مرگ مرتبط با سرطان در خانم ها است. از آنجا که سرطان پستان یک تومور وابسته به هورمون است، می تواند توسط وضعیت هورمون های استروئیدی شامل استروژن و پروژسترون تنظیم شود. استروژن نقش مهمی در توسعه و پیشرفت سرطان پستان ایفا می کند و تاثیر خود را روی بیان ژن های هدف از طریق گیرنده های استروژن اعمال می کند. اما گروه دیگری از گیرنده های هسته ای به نام گیرنده های مرتبط به ا...

15 صفحه اول

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 7  issue 3

pages  52- 52

publication date 2013-09-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023