Identification of Burkholderia cepacia complex pathogens by rapid-cycle PCR with fluorescent hybridization probes.
| dc.contributor.author | Vonberg, Ralf-Peter | |
| dc.contributor.author | Häussler, Susanne | |
| dc.contributor.author | Vandamme, Peter | |
| dc.contributor.author | Steinmetz, Ivo | |
| dc.date.accessioned | 2007-11-13T14:09:50Z | |
| dc.date.available | 2007-11-13T14:09:50Z | |
| dc.date.issued | 2006-06-01 | |
| dc.identifier.citation | J. Med. Microbiol. 2006, 55(Pt 6):721-7 | en |
| dc.identifier.issn | 0022-2615 | |
| dc.identifier.pmid | 16687590 | |
| dc.identifier.doi | 10.1099/jmm.0.46457-0 | |
| dc.identifier.uri | http://hdl.handle.net/10033/14554 | |
| dc.description.abstract | Members of the Burkholderia cepacia complex are important bacterial pathogens in cystic fibrosis (CF) patients. The B. cepacia complex currently consists of nine genetic subgroups (genomovars) of different epidemiological relevance and possibly of different pathogenic potential in humans. In this study, a new approach was developed for the rapid identification of B. cepacia genomovar I, Burkholderia multivorans (genomovar II), Burkholderia cenocepacia (lineage III-A and III-B), Burkholderia stabilis (genomovar IV) and Burkholderia vietnamiensis (genomovar V), which cause the large majority of infections in CF patients. The method was based on the detection of differences in the recA gene sequence by using rapid-cycle PCR and genomovar-specific fluorescence resonance energy transfer (FRET) probes. The genomovar status of all 39 B. cepacia complex strains tested (genomovars I-V) was identified by melting-curve analysis. Each FRET probe produced a specific fluorescence signal only with the respective genomovar, and not with other B. cepacia complex strains and Burkholderia spp. The identification system was easy to handle and revealed B. cepacia complex genomovar I-V status from culture isolates within about 1 h. | |
| dc.format.extent | 732544 bytes | |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | en |
| dc.title | Identification of Burkholderia cepacia complex pathogens by rapid-cycle PCR with fluorescent hybridization probes. | en |
| dc.type | Article | en |
| dc.format.dig | YES | |
| refterms.dateFOA | 2018-06-13T19:45:29Z | |
| html.description.abstract | Members of the Burkholderia cepacia complex are important bacterial pathogens in cystic fibrosis (CF) patients. The B. cepacia complex currently consists of nine genetic subgroups (genomovars) of different epidemiological relevance and possibly of different pathogenic potential in humans. In this study, a new approach was developed for the rapid identification of B. cepacia genomovar I, Burkholderia multivorans (genomovar II), Burkholderia cenocepacia (lineage III-A and III-B), Burkholderia stabilis (genomovar IV) and Burkholderia vietnamiensis (genomovar V), which cause the large majority of infections in CF patients. The method was based on the detection of differences in the recA gene sequence by using rapid-cycle PCR and genomovar-specific fluorescence resonance energy transfer (FRET) probes. The genomovar status of all 39 B. cepacia complex strains tested (genomovars I-V) was identified by melting-curve analysis. Each FRET probe produced a specific fluorescence signal only with the respective genomovar, and not with other B. cepacia complex strains and Burkholderia spp. The identification system was easy to handle and revealed B. cepacia complex genomovar I-V status from culture isolates within about 1 h. |
