S. Hosseinzadeh et al., Co-incubation of human spermatozoa with Chlamydia trachomatis serovar E causes premature sperm death, HUM REPR, 16(2), 2001, pp. 293-299
The aim of this work was to investigate the effect of elementary bodies (EB
) of Chlamydia trachomatis serovars E and LGV on sperm motility, viability
and acrosomal status. Highly motile preparations of spermatozoa from normoz
oospermic patients were co-incubated for 6 h with 0.54x10(6) EB per ml. At
1, 3 and 6 h of incubation, sperm motility was determined by computer-assis
ted semen analysis (CASA) and the proportion of dead cells determined by th
e hypo-osmotic swelling (HOS) test. Acrosomal status was also examined usin
g a standard monoclonal antibody assay. In the absence of EB, the percentag
e of motile spermatozoa remained >69% over the 6 h incubation and the propo
rtion of dead spermatozoa at <12%. However, during the incubation with EB o
f serovar E there was a significant decline in the percentage of motile spe
rmatozoa (P < 0.05), and a corresponding increase in the proportion of dead
spermatozoa (P < 0.05) at all time-points. However, following incubation w
ith serovar LGV, only the percentage of dead spermatozoa after 6 h incubati
on was significantly different from the control (P < 0.05). The amount of a
crosome-reacted spermatozoa remained unchanged (<16%) in all incubations at
all time-points. Dose-response experiments indicated that increasing the c
oncentration of EB to 2.5x10(6) per ml did not significantly alter the resu
lts. Furthermore, co-incubation of spermatozoa with dead EB (killed by heat
treatment) abolished the chlamydia-mediated response, indicating that the
effect is a result of the live organism and not soluble components or membr
ane elements. These data suggest that a detrimental effect on sperm functio
n by some serovars may be an as yet unrecognized component of infertility p
roblems.