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Author
- Di Lorenzo, Flaviana2
- Molinaro, Antonio2
- Bragonzi, Alessandra1
- Cho, Jae Hyun1
- Cigana, Cristina1
- de Soyza, Anthony1
- Hamad, Mohamad A1
- Jang, Ho Am1
- Jerala, Roman1
- Kim, Jiyeun Kate1
- Kim, Min Seon1
- Kubik, Łukasz1
- Lanzetta, Rosa1
- Lee, Bok Luel1
- Lee, Junbeom1
- Lorè, Nicola Ivan1
- Martín-Santamaría, Sonsoles1
- Oblak, Alja1
- Parrilli, Michelangelo1
- Sturiale, Luisa1
- Valvano, Miguel A1
Immunology
2 Results
- MicrobiologyOpen Access
The lipopolysaccharide core oligosaccharide of Burkholderia plays a critical role in maintaining a proper gut symbiosis with the bean bug Riptortus pedestris
Journal of Biological ChemistryVol. 292Issue 47p19226–19237Published online: September 25, 2017- Jiyeun Kate Kim
- Ho Am Jang
- Min Seon Kim
- Jae Hyun Cho
- Junbeom Lee
- Flaviana Di Lorenzo
- and others
Cited in Scopus: 17Lipopolysaccharide, the outer cell-wall component of Gram-negative bacteria, has been shown to be important for symbiotic associations. We recently reported that the lipopolysaccharide O-antigen of Burkholderia enhances the initial colonization of the midgut of the bean bug, Riptortus pedestris. However, the midgut-colonizing Burkholderia symbionts lack the O-antigen but display the core oligosaccharide on the cell surface. In this study, we investigated the role of the core oligosaccharide, which directly interacts with the host midgut, in the Riptortus–Burkholderia symbiosis. - Glycobiology and Extracellular MatricesOpen Access
Activation of Human Toll-like Receptor 4 (TLR4)·Myeloid Differentiation Factor 2 (MD-2) by Hypoacylated Lipopolysaccharide from a Clinical Isolate of Burkholderia cenocepacia
Journal of Biological ChemistryVol. 290Issue 35p21305–21319Published online: July 9, 2015- Flaviana Di Lorenzo
- Łukasz Kubik
- Alja Oblak
- Nicola Ivan Lorè
- Cristina Cigana
- Rosa Lanzetta
- and others
Cited in Scopus: 41Background: The Burkholderia cenocepacia lipid A is hypoacylated.Results: Aminoarabinose residues in lipid A contribute to Burkholderia lipid A binding to the TLR4·MD-2 complex.Conclusion: A novel mode of Burkholderia lipopolysaccharide-TLR4·MD-2 interactions promotes inflammation.Significance: Modifications of the lipid A structure enhance proinflammatory responses of hypoacylated lipopolysaccharide.