ability of adenoviral vectors to transfer DNA into boar spermatozoa and to
offspring was tested. Exposure of spermatozoa to adenovirus bearing the E.
coli lacZ gene resulted in the transfer of the gene to the head of the sper
matozoa. Treatment did not affect either viability or acrosomal integrity o
f boar sperm. Of the 2- to 8-cell embryos obtained after in vitro fertiliza
tion with adenovirus-exposed sperm, 21.7% expressed the LacZ product. Four
out of 56 piglets (about 7%) obtained after artificial insemination with ad
enovirus-exposed spermatozoa were positive in PCR analyses, even though non
e of the piglets showed the LacZ gene after southern blot analysis. RT-PCR
analysis performed in tissues from two positive stillborn piglets showed th
e presence of the LacZ mRNA in all of the tissues tested. The offspring obt
ained after mating two positive animals did not show LacZ gene presence. Ou
r results indicate that adenovirus could be a feasible mechanism for the de
livery of DNA into spermatozoa, even though the transfer of the transgene m
ay be limited to the first generation. Mol. Reprod. Dev. 53:149-158, 1999.
(C) 1999 Wiley-Liss, Inc.