Dp. Evenson et al., Characteristics of human sperm chromatin structure following an episode ofinfluenza and high fever: A case study, J ANDROLOGY, 21(5), 2000, pp. 739-746
Semen samples from a fertile patient presenting with influenza and a 1-day
fever of 39.9 degrees C were obtained and analyzed at 13-66 days postfever
(dpf) for sperm nuclear proteins, DNA stainability, free thiols (-SH), and
susceptibility to DNA denaturation in situ. At 18 dpf, 36% of sperm demonst
rated denatured DNA as measured by the sperm chromatin structure assay (SCS
A), and decreased to 23% by 39 dpf. Samples at 33 and 39 dpf contained 49%
and 30%, respectively, of cells with increased DNA stainability (HIGRN). A
unique sperm nuclear protein band migrating between histones and protamines
on acid-urea gels appeared at 33 and 39 dpf and nearly disappeared by 52 d
pf. Amino acid sequencing of the first 8 N-terminal residues identified thi
s protein as the precursor to protamine 2. The protamine P1 and P2 ratio re
mained normal, whereas the histone to protamine ratio increased slightly at
33 to 39 dpf. Flow cytometric measurements of nuclear -SH groups revealed
the greatest reduction in free nuclear thiols at 33 dpf, and returned to no
rmal by 45 dpf. The time of appearance of the unprocessed protamine 2 precu
rsor and the relative increase in histone suggest a fever-related disruptio
n of the synthesis of mRNA that codes for a P2 processing enzyme or enzymes
. increased DNA staining is likely due to the increased histone/protamine r
atio. This case study demonstrates that fever/influenza can have latent eff
ects on sperm chromatin structure and may result in transient release of ab
normal sperm.