This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schuchert, J. A.
Right arrow Articles by Jessing, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schuchert, J. A.
Right arrow Articles by Jessing, S.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, September 2004, p. 4344-4348, Vol. 42, No. 9
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.9.4344-4348.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Detection and Identification of Actinobacillus pleuropneumoniae Serotypes 1, 2, and 8 by Multiplex PCR

Jennifer A. Schuchert,1 T. J. Inzana,1* Ø. Angen,2 and S. Jessing2

Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia,1 Danish Veterinary Institute, Copenhagen, Denmark2

Received 8 October 2003/ Returned for modification 16 February 2004/ Accepted 20 May 2004

Multiplex PCR assays were developed to identify Actinobacillus pleuropneumoniae serotypes 1, 2, and 8. Primers designed for the conserved capsular polysaccharide (CP) export region amplified a 489-bp DNA fragment from all serotypes. Primers specific to the CP biosynthesis regions of serotypes 1, 2, and 8 amplified fragments of 1.6 kb, 1.7 kb, and 970 bp from only their respective serotypes.


* Corresponding author. Mailing address: Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, 1410 Prices Fork Rd., Virginia Polytechnic Institute and State University, Blacksburg, VA 24061-0342. Phone: (540) 231-4692. Fax: (540) 231-3426. E-mail: tinzana{at}vt.edu.


Journal of Clinical Microbiology, September 2004, p. 4344-4348, Vol. 42, No. 9
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.9.4344-4348.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Angen, O., Andreasen, M., Nielsen, E. O., Stockmarr, A., Baekbo, P. (2008). Effect of tulathromycin on the carrier status of Actinobacillus pleuropneumoniae serotype 2 in the tonsils of pigs. Vet Rec. 163: 445-447 [Abstract] [Full Text]  
  • Zhou, L., Jones, S. C. P., Angen, O., Bosse, J. T., Nash, J. H. E., Frey, J., Zhou, R., Chen, H. C., Kroll, J. S., Rycroft, A. N., Langford, P. R. (2008). PCR specific for Actinobacillus pleuropneumoniae serotype 3. Vet Rec. 162: 648-652 [Abstract] [Full Text]  
  • Zhou, L., Jones, S. C. P., Angen, O., Bosse, J. T., Nash, J. H. E., Frey, J., Zhou, R., Chen, H. C., Kroll, J. S., Rycroft, A. N., Langford, P. R. (2008). Multiplex PCR That Can Distinguish between Immunologically Cross- Reactive Serovar 3, 6, and 8 Actinobacillus pleuropneumoniae Strains. J. Clin. Microbiol. 46: 800-803 [Abstract] [Full Text]  
  • Kokotovic, B., Angen, O. (2007). Genetic Diversity of Actinobacillus pleuropneumoniae Assessed by Amplified Fragment Length Polymorphism Analysis. J. Clin. Microbiol. 45: 3921-3929 [Abstract] [Full Text]  
  • Anjum, M. F., Tucker, J. D., Sprigings, K. A., Woodward, M. J., Ehricht, R. (2006). Use of Miniaturized Protein Arrays for Escherichia coli O Serotyping.. CVI 13: 561-567 [Abstract] [Full Text]