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Published on: September 5, 2016
Burkholderia multivorans survival and trafficking within macrophages
Crystal L Schmerk1,2, Miguel A Valvano1,2
1Center for Human Immunology, University of Western Ontario, London, Ontario, N6A 5C1, Canada.
Abstract:
Cystic fibrosis (CF) patients are at great risk of opportunistic lung infection, particularly by members of the Burkholderia cepacia complex (Bcc). This group of bacteria can cause damage to the lung tissue of infected patients and are difficult to eradicate due to their high levels of antibiotic resistance. Although the highly virulent Burkholderia cenocepacia has been the focus of virulence research for the past decade, Burkholderia multivorans is emerging as the most prevalent Bcc species infecting CF patients in North America. Despite several studies detailing the intramacrophage trafficking and survival of B. cenocepacia, no such data exist for B. multivorans. The results of this study demonstrated that the clinical CF isolates C5568 and C0514 and an environmental B. multivorans isolate, ATCC 17616, were able to replicate and survive within murine macrophages in a manner similar to that of B. cenocepacia strain K56-2. These strains were also able to survive but were unable to replicate within human THP-1 macrophages. Differences in macrophage uptake were observed among all three B. multivorans strains; these variances were attributed to major differences in O-antigen production. Unlike B. cenocepacia-containing vacuoles, which delay phagosomal maturation in murine macrophages by 6 h, all B. multivorans-containing vacuoles co-localized with lysosome-associated membrane protein-1, a late endosome/lysosomal marker, and the lysosomal marker dextran within 2 h of uptake. Together, these results indicated that, whilst both Bcc species were able to survive and replicate within macrophages, they utilized different intramacrophage survival strategies. To observe differences in virulence, the strains were compared using the Galleria mellonella (wax worm) model. When compared with the B. multivorans strains tested, B. cenocepacia K56-2 was highly virulent in this model and killed all worms within 24 h when injected at 10(7) c.f.u. B. multivorans clinical isolates C5568 and C0514 were significantly more virulent than the soil isolate ATCC 17616, which was avirulent even when worms were injected with 10(7) c.f.u. These results suggest strain differences in the virulence of B. multivorans isolates.
Insights
Burkholderia multivorans, a prevalent bacteria in cystic fibrosis (CF) patients, can survive within macrophages using different strategies than Burkholderia cenocepacia. Strain virulence varies, with clinical isolates showing higher pathogenicity than environmental ones.
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Cystic fibrosis (CF) patients face high risk of opportunistic lung infections from Burkholderia cepacia complex (Bcc) bacteria.
- Burkholderia multivorans is increasingly prevalent in North American CF patients, yet its intramacrophage survival mechanisms are poorly understood.
- Previous research focused on the virulent Burkholderia cenocepacia, leaving a knowledge gap regarding B. multivorans virulence factors.
Purpose of the Study:
- To investigate the intramacrophage survival strategies of Burkholderia multivorans clinical and environmental isolates.
- To compare the virulence of different B. multivorans strains and B. cenocepacia in a model organism.
- To elucidate the differences in macrophage interaction and phagosomal trafficking between B. multivorans and B. cenocepacia.
Main Methods:
- Murine and human macrophage models (THP-1) were used to assess bacterial survival and replication.
- Macrophage uptake differences were analyzed, correlating with O-antigen production.
- Phagosomal maturation and co-localization with lysosomal markers were tracked.
- The Galleria mellonella (wax worm) model was employed to evaluate bacterial virulence.
Main Results:
- B. multivorans strains replicated and survived within murine macrophages similarly to B. cenocepacia, but only survived, not replicated, in human THP-1 macrophages.
- Differences in O-antigen production influenced macrophage uptake of B. multivorans.
- B. multivorans-containing vacuoles rapidly co-localized with lysosomal markers, unlike B. cenocepacia.
- B. cenocepacia was highly virulent in the G. mellonella model, while clinical B. multivorans isolates were more virulent than environmental isolates.
Conclusions:
- B. multivorans and B. cenocepacia exhibit distinct intramacrophage survival strategies despite both being able to survive and replicate within macrophages.
- Strain-dependent variations in virulence exist within B. multivorans, with clinical isolates demonstrating greater pathogenicity.
- Understanding these differences is crucial for managing Bcc infections in cystic fibrosis patients.
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