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Published on: October 15, 2013
Cepacia-like syndrome caused by Burkholderia multivorans
George Zahariadis1, Michelle H Levy, Jane L Burns
1Department of Medicine, Division of Infectious Diseases, University of Washington and Fred Hutchinson Cancer Research Center, Seattle.
Abstract:
The variable severity of Burkholderia cepacia complex infections in cystic fibrosis (CF) has recently been ascribed to differences in the virulence between genomovars. Specifically, genomovar III isolates have been associated with higher transmission rates and adverse outcomes compared to other B cepacia genomovars, and consequently further segregation between genomovar III and non-genomovar III B cepacia infected patients is advocated in some centres. The important role of non-genomovar III isolates is presented in the context of a clinical case whereby a patient with long-standing pulmonary infection with B multiovorans developed bacteremic infection reminiscent of the fatal 'cepacia syndrome'.
Insights
Burkholderia cepacia complex infections in cystic fibrosis (CF) vary in severity due to genomovar differences. Non-genomovar III isolates, like B. multivorans, can cause severe disease, challenging segregation strategies.
Area of Science:
- Microbiology
- Infectious Diseases
- Genomics
Background:
- The Burkholderia cepacia complex (BCC) comprises several genomovars causing opportunistic infections, particularly in individuals with cystic fibrosis (CF).
- Genomovar III BCC isolates are often linked to increased transmissibility and poorer clinical outcomes in CF patients.
- Current clinical management strategies sometimes advocate for patient segregation based on BCC genomovar, specifically separating genomovar III from non-genomovar III infections.
Observation:
- A clinical case highlights the potential for severe, life-threatening infections caused by non-genomovar III BCC isolates.
- A patient with a chronic pulmonary infection due to B. multivorans (a non-genomovar III BCC species) experienced a sudden deterioration.
- This deterioration manifested as a bacteremic infection resembling the severe 'cepacia syndrome'.
Findings:
- Virulence and clinical impact of BCC infections are not solely determined by genomovar III.
- Non-genomovar III BCC species, such as B. multivorans, possess the potential to cause severe, invasive disease.
- Clinical presentation of severe BCC infection can be similar regardless of the specific genomovar involved.
Implications:
- The findings challenge the strict segregation of CF patients based solely on BCC genomovar III status.
- Clinical vigilance for severe BCC infections is crucial, irrespective of the isolate's genomovar.
- Further research is needed to understand the factors contributing to severe disease caused by non-genomovar III BCC isolates.
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