PHENOTYPIC VARIABILITY OF X-PROTEIN EXPRESSION BY MASTITIS-CAUSING STREPTOCOCCUS-AGALACTIAE OF SEROTYPE NT X AND OPSONIC ACTIVITIES OF SPECIFIC ANTIBODIES/
P. Rainard et al., PHENOTYPIC VARIABILITY OF X-PROTEIN EXPRESSION BY MASTITIS-CAUSING STREPTOCOCCUS-AGALACTIAE OF SEROTYPE NT X AND OPSONIC ACTIVITIES OF SPECIFIC ANTIBODIES/, Microbial pathogenesis, 16(5), 1994, pp. 359-372
This study examined the role of antibodies against the X-protein, a su
rface-localized antigen frequently associated with streptococci causin
g mastitis in cattle, in the opsonization and phagocytosis of unencaps
ulated Streptococcus agalactiae. The analysis of various strains of se
rotype NT/X by flow cytometry, after labeling with a monoclonal antibo
dy to X-protein, revealed that they consisted of a mixture of unstaine
d and stained bacteria. Cloning of mother strains yielded clones of un
stained bacteria but not homogeneous clones of stained bacteria. Analy
sis by ELISA of an unstained clone (4.1) derived from the reference NT
/X strain 24/60 indicated that it expressed low amount of X-protein at
its surface, about 25 times less than the stained clone 24/60 5.6. Co
lloidal gold immunolabeling showed the X-protein at the periphery of b
acteria (of clone 5.6 and in lower amount of clone 4.1), at a distance
from the cell wall. Bovine antibodies (essentially IgG) to X-protein
behaved like the monoclonal antibody in the cytometric assay. They act
ivated the classical pathway of complement as shown by the deposition
of Clq and C4 on bacteria. Deposition of C4 also occurred on the low-s
urface-producing clone 4.1 in the presence of antibodies to X-protein,
although less efficiently than on the high-surface-producing clone 5.
6. When used alone, antibodies promoted the ingestion of bacteria and
heat-inactivated immune serum promoted the chemiluminescence activity
and the killing by polymorphonuclear cells. In conclusion, antibodies
to X-protein induced the deposition of C3 by the classical pathway and
were also able to stimulate opsonophagocytic killing of X-bearing S.
agalactiae in the absence of deposited C3.