
| Document Type: | Master's Thesis |
| Name: | Terry Lo |
| Email address: | tlo |
| URN: | 1997/00093 |
| Title: | Detection and Identification of Acinobacillus pleuropneumoniae serotype 5 by multiplex Polymerase Chain Reaction |
| Degree: | Master of Science |
| Department: | VMS |
| Committee Chair: | Dr. Inzana |
| Chair's email: | tinzana@vt.edu |
| Committee\ Members: | |
| Keywords: | PCR, multiplex, serotyping, Actinobacillus pleuropneumoniae |
| Date of defense: | July 31, 1997 |
| Availability: | Release the entire work for Virginia Tech access only.
After one year release worldwide only with written permission of the student and the advisory committee chair. |
Traditional serologic assays of Actinobacillus pleuropeumoniae often have problems with cross-reactivity. To avoid the complications of antibody-antigen reactions, a PCR assay was developed to detect Actinobacillus pleuropneumoniae and identify serotype 5 strains. Primers specific to the conserved capsular export region of A. pleuropneumoniae amplified a 0.7 kb DNA band in all strains with the exception of serotype 4. A second set of primers specific to the unique capsular biosynthesis region of serotype 5 amplified a unique 1.1 kb band for serotype 5 only. The sensitivity of this assay was determined to be less than 100 colony forming units. This PCR assay enables us to detect A. pleuronpeumoniae and definitively distinguishes serotype 5 strains from other serotyes.
List of Attached Files | ||
| At.pdf | vita.pdf | |
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At the author's request, all materials (PDF files, images, etc.) associated with this ETD are accessible from the Virginia Tech network only. |
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