J Med Microbiol NEW Faster Access
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published online ahead of print on 3 September 2009 as doi:10.1099/jmm.0.012500-0
J Med Microbiol (2009), DOI: 10.1099/jmm.0.012500-0
© 2009 Society for General Microbiology
This Article
Right arrow Full Text (Papers in Press[PDF])
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by AuCoin, D. P
Right arrow Articles by Kozel, T.
PubMed
Right arrow PubMed Citation
Right arrow Articles by AuCoin, D. P
Right arrow Articles by Kozel, T.
Agricola
Right arrow Articles by AuCoin, D. P
Right arrow Articles by Kozel, T.

Identification of Burkholderia cepacia complex (Bcc) bacteria with a lipopolysaccharide specific monoclonal antibody

David P AuCoin1,3, Reva Crump1, Peter Thorkildson1, Dana Nuti1, John LiPuma2 and Thomas Kozel1

1 University of Nevada Reno;

2 Universtiy of Michigan Medical School

3 E-mail: daucoin{at}medicine.nevada.edu

Received April 29, 2009
Accepted September 1, 2009

The genus Burkholderia includes many bacteria that cause serious human infections. As is the case with other Gram-negative bacteria, Burkholderia species produce lipopolysaccharides (LPS) which is an abundant component of the bacterial cell surface. Burkholderia cepacia complex (Bcc) bacteria (including at least 17 separate species) produce LPS structures that are quite different. In an attempt to determine the degree of LPS epitope variation among Bcc species, we produced a monoclonal antibody (mAb), designated 5D8, specific for the LPS of B. cepacia. Western blot analysis determined that mAb 5D8 was able to produce the classic 'ladder pattern' when used to probe B. cepacia and B. anthina lysates, although 5D8 did not produce this pattern with the other seven Bcc species tested. mAb 5D8 reacted with varying intensity to most but not all of the additional B. cepacia and B. anthina strains tested. Therefore, there seems to be significant epitope variation among Bcc LPS both between and within species. Additionally, mAb 5D8 reacted with a proteinase K-sensitive 22 kD antigen in all Bcc strains and also in a strain of Burkholderia pseudomallei.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2009 Society for General Microbiology.