Antigenic Characterization of Haemophilus somnus Lipooligosaccharide
dc.contributor.author | Howard, Michael D. | en |
dc.contributor.committeechair | Inzana, Thomas J. | en |
dc.contributor.committeemember | Schurig, Gerhardt G. | en |
dc.contributor.committeemember | Nagarkatti, Mitzi | en |
dc.contributor.department | Veterinary Medical Sciences | en |
dc.date.accessioned | 2014-03-14T20:46:39Z | en |
dc.date.adate | 1998-11-16 | en |
dc.date.available | 2014-03-14T20:46:39Z | en |
dc.date.issued | 1998-10-23 | en |
dc.date.rdate | 1999-11-16 | en |
dc.date.sdate | 1998-10-14 | en |
dc.description.abstract | Lipooligosaccharide (LOS) is the major outer membrane component of many Gram-negative bacteria inhabiting the mucosal membranes, including pathogenic species of <I>Haemophilus</I> and <I>Neisseria</I>. LOS phase variation is one mechanism by which some of these bacteria avoid the host immune response. To better understand LOS phase variation as a virulence mechanism of <I>H. somnus</I>, knowledge of the antigenic diversity of LOS epitopes must be increased. Monoclonal antibodies (MAbs) to <I>H. somnus</I> LOS were produced and used with cross-reacting MAbs to <I>H. aegyptius</I> LOS (MAb 5F5) and <I>Neisseria</I> <I>gonorrhoeae</I> LOS (MAb 3F11) in an ELISA to investigate LOS heterogeneity among forty-five strains of <I>H. somnus</I>. Using three MAbs, thirty-nine of these <I>H. somnus</I> strains were grouped into six antigenic types. Three groups, associated solely with the cross-reacting MAbs 5F5 and 3F11, included the majority (76%) of <I>H. somnus</I> strains. The anti-<I>H. somnus</I> LOS MAb 5D7 recognized a low frequency epitope associated with each of the remaining three groups, which included 11% of the <I>H. somnus</I> strains. Six strains (13%) were not recognized by any of these MAbs. Inhibition ELISA experiments showed that the MAb 5F5 epitope contained phosphocholine (PCho) and this epitope was present in 56% of the strains tested. The MAb 5F5 epitope is phase variable in <I>H. somnus</I> LOS. How PCho negative variants could allow for systemic infection after initial colonization of the mucosa by PCho positive variants is discussed. | en |
dc.description.degree | Master of Science | en |
dc.identifier.other | etd-101398-081516 | en |
dc.identifier.sourceurl | http://scholar.lib.vt.edu/theses/available/etd-101398-081516/ | en |
dc.identifier.uri | http://hdl.handle.net/10919/35378 | en |
dc.publisher | Virginia Tech | en |
dc.relation.haspart | etd.pdf | en |
dc.rights | In Copyright | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
dc.subject | LOS | en |
dc.subject | phase variation | en |
dc.subject | typing scheme | en |
dc.subject | epitope | en |
dc.subject | monoclonal antibody | en |
dc.title | Antigenic Characterization of <I>Haemophilus somnus</I> Lipooligosaccharide | en |
dc.type | Thesis | en |
thesis.degree.discipline | Veterinary Medical Sciences | en |
thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
thesis.degree.level | masters | en |
thesis.degree.name | Master of Science | en |
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