Abstract

Recent years have seen a rising incidence of male infertility, mostly caused by the decline of sperm quality. The ratio of infertile males to infertile females has escalated from 3:7 in 2013 to current 5:5, which turns male infertility into the research focus of reproductive medicine. This study aimed to clarify the effect of reproductive tract infection by ureaplasma urealyticum (UU) and chlamydia trachomatis (CT) on the DNA integrity and routine semen parameters of infertile males. A retrospective study was performed. A total of 259 infertile males who were treated at the Andrological Laboratory Examination and Reproductive Medicine Center in our hospital were analyzed. qRT-PCR was used to examine the infection status of CT and UU. According to the eligibility criteria, we evaluated the semen parameters and biochemical data of 253 men. Based on the results of PCR, the subjects were divided into four groups: Group I (CT positive, 63 cases), Group II (UU positive, 60 cases), Group III (CT positive and UU positive, 62 cases), and Group IV (no infection, 68 cases). DNA fragmentation index (DFI), sperm count, vitality and morphology, elastase level, seminal plasma malondialdehyde (MDA), and total antioxidant capacity (TAC) were assessed. Compared to Group IV, three groups (Group I, Group II and Group III) showed difference in semen volume, proportion of sperm with normal morphology, sperm motility, progressive motility, and vitality (P < 0.05). Compared to Group IV, Group II and Group III showed difference in DFI (P < 0.05). Compared to Group IV, Group II and Group III showed difference in elastase level (P < 0.05). VCL, VSL, VAP, WOB, ROS, TM, HDS showed differences between groups of abnormal/normal WBC (*P < 0.01).UU infection significantly increased the level of seminal leukocytes only in Group II, but not in the other three groups, indicating that UU is a factor to increase the level of seminal leukocytes. Compared with the normal leukocyte group, there were significant differences in total motility, forward motility and normal sperm ratio between the two groups. The proportion of sperm with abnormal morphology (mostly in the head) showed obvious difference between groups of high and normal seminal leukocytic levels. At the same time, in this study, SCGE and SCD verified that leukocytes could damage sperm DNA by increasing ROS, which ultimately affects male fertility.

Highlights

  • Human sperm quality can be affected by various factors, including physical injury, psychological stress, or environmental pollutants [1]

  • The effects of different groups of reproductive tract infections on sperm DNA fragmentation, seminal elastase level and oxidative stress parameters We detected the infection among 63 patients in Group I (CT Positive), 60 patients in Group II (UU Positive), 62 patients in Group III (CT Positive and UU Positive) and 68 patients in Group IV (Control)

  • We compared the DNA fragmentation index (DFI) and other routine seminal parameters in 253 patients. We found that these parameters showed significant difference between the three groups (I, II, III) and the control group, which demonstrated that chlamydia trachomatis (CT) and UU infection can affect seminal quality

Read more

Summary

Introduction

Human sperm quality can be affected by various factors, including physical injury, psychological stress, or environmental pollutants [1]. Gonococcal urethritis caused by these two types of organism is more likely to invade male’s genital tract, epididymides, prostate gland, and testes, exerting bad effect on semen quality, spermatogenesis, sperm-egg binding, and pregnancy outcomes [4]. UU, a pathogenic microorganism, can adhere to the enitourinary tract and evoke urinary tract infections It can affect male fertility in several ways, such as interfering with spermatogenesis, distorting sperm metabolism and sperm-egg binding, as well as triggering immune responses in the genital tract [6]. It has been reported that reproductive tract infection can increase the ROS level in semen, cause lipid peroxidation of sperm membrane and sperm nuclear damage, and the mechanism may involve the increase of white blood cells in semen [7] MDA is one of the degradation products of lipid peroxidation. TAC represents the overall level of antioxidant capacity in the body, and the antioxidant capacity can be reflected by measuring the content of TAC in the seminal plasma [8, 9]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call