J. Christopherhennings et al., PERSISTENCE OF PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS INSERUM AND SEMEN OF ADULT BOARS, Journal of veterinary diagnostic investigation, 7(4), 1995, pp. 456-464
Four seronegative-adult boars were intranasally inoculated with porcin
e reproductive and respiratory syndrome virus (PRRSV) isolate VR-2332.
Serum and semen were collected 2-3 times weekly for over 100 days pos
tinoculation (DPI). Serum samples were assayed for PRRSV by virus isol
ation (VI) and a polymerase chain reaction (PCR) and screened for anti
bodies to PRRSV using the indirect fluorescent antibody (IFA) and viru
s neutralization (VN) tests. Semen was assayed for PRRSV RNA by PCR. V
irus or viral RNA was detected in the serum of all boars within 1 DPI
by VI and/or PCR. However, VI results indicated that viremia was trans
ient and occurred from 1 to 9 DPI. Viral RNA was detected in serum fro
m 1 to 31 DPI. In the acute stage of the infection, PRRSV RNA was dete
cted in serum by PCR prior to the presence of viral RNA in semen. The
PRRSV RNA was detected in semen as early as 3 DPI and persisted for 25
DPI in 2 of the boars and 56 and 92 DPI in the remaining 2 boars. Det
ection of PRRSV RNA in semen occurred 2-8 and 28-35 days prior to the
detection of antibodies by IFA and VN, respectively. PRRSV was isolate
d from the bulbourethral gland of the boar that shed viral RNA in seme
n for 92 DPI. These results suggest that PRRSV RNA can be detected by
PCR in boar serum and semen, and may persist for variable periods of t
ime; Viremia and the serologic status of the boar are not adequate ind
icators of when PRRSV or PRRSV RNA is being shed in the semen. Prelimi
nary findings also indicated that neither shipping stress nor reinocul
ation with homologous PRRSV resulted in viremia or viral RNA shedding
in semen.