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


     


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
Right arrow Citation Map
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 HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Whitby, P. W.
Right arrow Articles by Stull, T. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Whitby, P. W.
Right arrow Articles by Stull, T. L.
Agricola
Right arrow Articles by Whitby, P. W.
Right arrow Articles by Stull, T. L.
J Med Microbiol 55 (2006), 11-21; DOI: 10.1099/jmm.0.46138-0
© 2006 Society for General Microbiology
ISSN 0022-2615

Identification of an RTX determinant of Burkholderia cenocepacia J2315 by subtractive hybridization

Paul W. Whitby1, Timothy M. VanWagoner1, Ashlee A. Taylor1, Thomas W. Seale1, Daniel J. Morton1, John J. LiPuma2 and Terrence L. Stull1,3

1 ,3 Departments of Pediatrics1 and Microbiology/Immunology3 , University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA

2 Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI 48109, USA

Correspondence
Terrence L. Stull
tstull{at}ouhsc.edu

Received 26 April 2005
Accepted 31 August 2005


This study utilized suppressive subtractive hybridization between the clinical isolate Burkholderia cenocepacia J2315 and the closely related environmental isolate Burkholderia cepacia ATCC 25416T to isolate DNA fragments specific to B. cenocepacia J2315. Analysis of the resulting pools of B. cenocepacia-specific DNAs identified several fragments that may be part of putative virulence factors. Further in silico analysis of a single fragment indicated that it was internal to a gene of which the predicted product had characteristics of repeat in toxin (RTX)-like proteins and high similarity to proteins in other human or plant pathogens. In conjunction with this finding, phenotypic traits associated with known RTX proteins were assessed. A haemagglutinating activity of B. cenocepacia J2315 was identified that was absent in B. cepacia ATCC 25416T. The expression of this activity appeared to be growth phase-dependent. Analysis of the gene presence and haemagglutinating activity across the species of the B. cepacia complex showed that both were common to the ET12 lineage of B. cenocepacia, but were absent in the other species examined. Haemagglutinating activity was limited to isolates with the RTX-like gene. Expression studies utilizing quantitative PCR demonstrated an association between onset of haemagglutinating activity and increased expression of the gene, which suggests that the putative RTX determinant encodes a haemagglutinating activity.


Abbreviations: Bcc, Burkholderia cepacia complex; CF, cystic fibrosis; CRD, conserved repeat domain; HHRP, haemagglutinin/haemolysin-related protein; LRP, large repetitive protein; nr, non-redundant; Q-PCR, real-time quantitative PCR; RTX, repeat in toxin.




This article has been cited by other articles:


Home page
J Med MicrobiolHome page
P. W. Whitby, T. M. VanWagoner, J. M. Springer, D. J. Morton, T. W. Seale, and T. L. Stull
Burkholderia cenocepacia utilizes ferritin as an iron source
J. Med. Microbiol., June 1, 2006; 55(6): 661 - 668.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2006 Society for General Microbiology.