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Role of Bordetella bronchiseptica Fimbriae in Tracheal Colonization and Development of a Humoral Immune Response
Author(s) -
Seema Mattoo,
Jeff F. Miller,
Peggy A. Cotter
Publication year - 2000
Publication title -
infection and immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.508
H-Index - 220
eISSN - 1070-6313
pISSN - 0019-9567
DOI - 10.1128/iai.68.4.2024-2033.2000
Subject(s) - bordetella bronchiseptica , fimbria , biology , microbiology and biotechnology , bordetella , bacterial adhesin , filamentous haemagglutinin adhesin , mutant , pertactin , pilus , gene , bordetella pertussis , escherichia coli , bacteria , genetics , pertussis toxin , receptor , g protein
Fimbriae are filamentous, cell surface structures which have been proposed to mediate attachment ofBordetella species to respiratory epithelium.Bordetella bronchiseptica has four known fimbrial genes:fim2 ,fim3 ,fimX , andfimA . While these genes are unlinked on the chromosome, their protein products are assembled and secreted by a single apparatus encoded by thefimBCD locus. ThefimBCD locus is embedded within thefha operon, whose genes encode another putative adhesin, filamentous hemagglutinin (FHA). We have constructed a Fim− B. bronchiseptica strain, RB63, by introducing an in-frame deletion extending fromfimB throughfimD . Western blot analysis showed that RB63 is unable to synthesize fimbriae but is unaffected for FHA expression. Using this mutant, we assessed the role of fimbriae in pathogenesis in vitro and in vivo in natural animal hosts. Although RB63 was not significantly defective in its ability to adhere to various tissue culture cell lines, including human laryngeal HEp-2 cells, it was considerably altered in its ability to cause respiratory tract infections in rats. The number of ΔfimBCD bacteria recovered from the rat trachea at 10 days postinoculation was significantly decreased compared to that of wild-typeB. bronchiseptica and was below the limit of detection at 30 and 60 days postinoculation. The number of bacteria recovered from the nasal cavity and larynx was not significantly different between RB63 and the wild-type strain at any time point. The ability of fimbriae to mediate initial attachment to tracheal tissue was tested in an intratracheal inoculation assay. Significantly fewer RB63 than wild-type bacteria were recovered from the tracheas at 24 h after intratracheal inoculation. These results demonstrate that fimbriae are involved in enhancing the ability ofB. bronchiseptica to establish tracheal colonization and are essential for persistent colonization at this site. Interestingly, anti-Bordetella serum immunoglobulin M (IgM) levels were significantly lower in animals infected with RB63 than in animals infected with wild-typeB. bronchiseptica at 10 days postinoculation. Even at 30 days postinoculation, RB63-infected animals had lower serum anti-Bordetella antibody titers in general. This disparity in antibody profiles suggests that fimbriae are also important for the induction of a humoral immune response.

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