PHENOTYPIC VARIABILITY OF X-PROTEIN EXPRESSION BY MASTITIS-CAUSING STREPTOCOCCUS-AGALACTIAE OF SEROTYPE NT X AND OPSONIC ACTIVITIES OF SPECIFIC ANTIBODIES/

Citation
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
Citations number
26
Categorie Soggetti
Immunology,Microbiology
Journal title
ISSN journal
08824010
Volume
16
Issue
5
Year of publication
1994
Pages
359 - 372
Database
ISI
SICI code
0882-4010(1994)16:5<359:PVOXEB>2.0.ZU;2-4
Abstract
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.