Monoclonal antibodies to the GP(5) of porcine reproductive and respiratorysyndrome virus are more effective in virus neutralization than monoclonal antibodies to the GP(4)
E. Weiand et al., Monoclonal antibodies to the GP(5) of porcine reproductive and respiratorysyndrome virus are more effective in virus neutralization than monoclonal antibodies to the GP(4), VET MICROB, 66(3), 1999, pp. 171-186
The arterivirus porcine reproductive and respiratory syndrome virus (PRRSV)
contains six structural proteins the roles of which are not completely und
erstood. In a preceding study, immunization with the dutch isolate I10 of P
RRSV had led to the development of MAbs against four structural proteins [W
ieczorek-Krohmer, M., 1994. Herstellung und Charakterisierung von monoklona
len Antikorpern gegen das Virus des Porzinen Reproduktiven und Respiratoris
chen Syndroms (PRRSV). Inaugural-Dissertation, Ludwig-Maximilians-Universit
y, Munchen] here finally identified by reaction with individual plasmid-exp
ressed PRRSV proteins as products of ORFs 3 (GP(3)), 4 (GP(4)), 5 (GP(5)) a
nd 7 (N). Surprisingly, the MAbs against GP(5) revealed the presence of two
antigenically distinct virus populations in the isolate I10, the populatio
n PRRSV-'PPV', isolated from plaques and the PRRSV-'EPV', gained by end poi
nt dilution. MAbs against GP3, GP4 and N reacted with both I10 populations
as well as with natural PRRSV isolates. However, the anti-GP(5) MAbs exclus
ively recognized PRRSV-'PPV'. In this study immunization of mice with both
separated I10 populations confirmed that solely PRRSV-'PPV' possesses the p
roperty to induce an immune response ultimately leading to the establishmen
t of MAbs against GP(5). Whereas the 15 anti-GP(5) MAbs (derived from four
independent fusions) reacted exclusively with PRRSV-'PPV' of the isolate I1
0, anti-GP(4) MAbs detected their target antigen on various isolates of Eur
opean origin and were able to neutralize them. As indicated by competition
assays and selection of neutralization-resistant virus mutants, all GP(5) M
Abs are directed against a single antigenic site on the ORF 5 protein. Both
groups of neutralizing antibodies bound to the surface of purified virions
demonstrating that the recognized epitopes represent surface structures of
the virion envelope. However, anti-GP(5) MAbs mediated the binding of more
gold granules than anti-GP(4) MAbs. Comparison of the neutralizing effect
of anti-GP(4) and anti-GP(5) MAbs revealed the anti-GP(5) MAbs as the more
efficient antibodies. For the complete neutralization of about 100 ID50 of
PRRSV-'PPV' anti-GP(5) culture supernatant was effective up to a dilution o
f 1 : 1280 whereas the most effective anti-GP4 antibodies exhibited a compa
rable effect only up to 1 : 64. These results indicate that PRRSV GP(5) in
principle is a major target for neutralizing antibodies, as is found for ot
her arteriviruses, but that in nature 'ORF 5 escape mutants' may develop as
easily as in vitro. (C) 1999 Elsevier Science B.V. All rights reserved.