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Demonstration of heterogeneity among the antigenic proteins of Mobiluncus species.

TitleDemonstration of heterogeneity among the antigenic proteins of Mobiluncus species.
Publication TypeJournal Article
Year of Publication1990
AuthorsSchwebke, JR, Hillier, SL, Fohn, MJ, Lukehart, SA
JournalJ Clin Microbiol
Volume28
Issue3
Pagination463-8
Date Published1990 Mar
ISSN0095-1137
KeywordsAnimals, Antibodies, Monoclonal, Antibody Specificity, Antigens, Bacterial, Bacteria, Anaerobic, Bacterial Infections, Bacterial Proteins, Cross Reactions, Electrophoresis, Polyacrylamide Gel, Epitopes, Female, Fluorescent Antibody Technique, Humans, Immune Sera, Immunoblotting, Male, Rabbits, Species Specificity, Vaginitis
Abstract

The protein and antigenic profiles of the American Type Culture Collection type strains of Mobiluncus species and those of 114 clinical isolates were determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis and immunoblotting with homologous polyvalent antisera. The majority of isolates (82%) possessed characteristic protein profiles and could be identified to the species level by sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. The major protein bands were also antigenic, and some antigenic cross-reactivity was noted between the two Mobiluncus species. All of the isolates were examined for reactivity with a panel of 12 monoclonal antibodies previously prepared against the type strains. While 56 of 60 clinical isolates of Mobiluncus curtisii (93%) reacted with one or more of the monoclonal antibodies, only 23 of 54 clinical isolates which were identified as Mobiluncus mulieris by biochemical methods (48%) reacted with one or more of the monoclonal antibodies. One of the 4 M. curtisii isolates (25%) and 11 of the 31 M. mulieris isolates (35%) which did not react with the monoclonal antibodies also had atypical protein profiles. These results demonstrate a high degree of heterogeneity in the protein and antigenic profiles of Mobiluncus isolates and suggest that further taxonomic division may be appropriate.

Alternate JournalJ. Clin. Microbiol.
PubMed ID1691207
PubMed Central IDPMC269645
Grant ListAI 07140-12 / AI / NIAID NIH HHS / United States
AI 12192 / AI / NIAID NIH HHS / United States