| Literature DB >> 28972189 |
Jiyeun Kate Kim1, Ho Am Jang2, Min Seon Kim2, Jae Hyun Cho2, Junbeom Lee2, Flaviana Di Lorenzo3, Luisa Sturiale4, Alba Silipo3, Antonio Molinaro3, Bok Luel Lee5.
Abstract
Lipopolysaccharide, 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. To this end, we generated the core oligosaccharide mutant strains, ΔwabS, ΔwabO, ΔwaaF, and ΔwaaC, and determined the chemical structures of their oligosaccharides, which exhibited different compositions. The symbiotic properties of these mutant strains were compared with those of the wild-type and O-antigen-deficient ΔwbiG strains. Upon introduction into Riptortus via the oral route, the core oligosaccharide mutant strains exhibited different rates of colonization of the insect midgut. The symbiont titers in fifth-instar insects revealed significantly reduced population sizes of the inner core oligosaccharide mutant strains ΔwaaF and ΔwaaC These two strains also negatively affected host growth rate and fitness. Furthermore, R. pedestris individuals colonized with the ΔwaaF and ΔwaaC strains were vulnerable to septic bacterial challenge, similar to insects without a Burkholderia symbiont. Taken together, these results suggest that the core oligosaccharide from Burkholderia symbionts plays a critical role in maintaining a proper symbiont population and in supporting the beneficial effects of the symbiont on its host in the Riptortus-Burkholderia symbiosis.Entities:
Keywords: biosynthesis; insect; lipopolysaccharide (LPS); oligosaccharide; symbiosis
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Year: 2017 PMID: 28972189 PMCID: PMC5702664 DOI: 10.1074/jbc.M117.813832
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157