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1.
Dev Comp Immunol ; 53(1): 265-9, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26164198

RESUMO

The relation between gut symbiosis and immunity has been reported in various animal model studies. Here, we corroborate the effect of gut symbiont to host immunity using the bean bug model. The bean bug, Riptortus pedestris, is a useful gut symbiosis model due to the monospecific gut symbiont, genus Burkholderia. To examine the effect of gut symbiosis to host immunity, we generated the gut symbiont-harboring (symbiotic) insect line and the gut symbiont-lacking (aposymbiotic) insect line. Upon bacterial challenges, the symbiotic Riptortus exhibited better survival than aposymbiotic Riptortus. When cellular immunity was inhibited, the symbiotic Riptortus still survived better than aposymbioic Riptortus, suggesting stronger humoral immunity. The molecular basis of the strong humoral immunity was further confirmed by the increase of hemolymph antimicrobial activity and antimicrobial peptide expression in the symbiotic insects. Taken together, our data clearly demonstrate that Burkhoderia gut symbiont positively affect the Riptortus systemic immunity.


Assuntos
Burkholderia/imunologia , Microbioma Gastrointestinal/imunologia , Heterópteros/imunologia , Heterópteros/microbiologia , Simbiose , Animais , Escherichia coli K12/imunologia , Trato Gastrointestinal/imunologia , Trato Gastrointestinal/microbiologia , Hemolinfa/imunologia , Imunidade Celular/imunologia , Imunidade Humoral/genética , Imunidade Humoral/imunologia , Imunidade Inata/imunologia , Fagocitose/imunologia , Staphylococcus aureus/imunologia
2.
J Biol Chem ; 290(34): 21042-21053, 2015 Aug 21.
Artigo em Inglês | MEDLINE | ID: mdl-26116716

RESUMO

The molecular characterization of symbionts is pivotal for understanding the cross-talk between symbionts and hosts. In addition to valuable knowledge obtained from symbiont genomic studies, the biochemical characterization of symbionts is important to fully understand symbiotic interactions. The bean bug (Riptortus pedestris) has been recognized as a useful experimental insect gut symbiosis model system because of its cultivatable Burkholderia symbionts. This system is greatly advantageous because it allows the acquisition of a large quantity of homogeneous symbionts from the host midgut. Using these naïve gut symbionts, it is possible to directly compare in vivo symbiotic cells with in vitro cultured cells using biochemical approaches. With the goal of understanding molecular changes that occur in Burkholderia cells as they adapt to the Riptortus gut environment, we first elucidated that symbiotic Burkholderia cells are highly susceptible to purified Riptortus antimicrobial peptides. In search of the mechanisms of the increased immunosusceptibility of symbionts, we found striking differences in cell envelope structures between cultured and symbiotic Burkholderia cells. The bacterial lipopolysaccharide O antigen was absent from symbiotic cells examined by gel electrophoretic and mass spectrometric analyses, and their membranes were more sensitive to detergent lysis. These changes in the cell envelope were responsible for the increased susceptibility of the Burkholderia symbionts to host innate immunity. Our results suggest that the symbiotic interactions between the Riptortus host and Burkholderia gut symbionts induce bacterial cell envelope changes to achieve successful gut symbiosis.


Assuntos
Burkholderia/química , Parede Celular/química , Heterópteros/microbiologia , Antígenos O/química , Simbiose , Animais , Peptídeos Catiônicos Antimicrobianos/farmacologia , Burkholderia/efeitos dos fármacos , Burkholderia/metabolismo , Burkholderia/fisiologia , Membrana Celular/química , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Parede Celular/efeitos dos fármacos , Parede Celular/metabolismo , Trato Gastrointestinal/efeitos dos fármacos , Trato Gastrointestinal/imunologia , Trato Gastrointestinal/metabolismo , Trato Gastrointestinal/microbiologia , Heterópteros/imunologia , Heterópteros/metabolismo , Antígenos O/metabolismo
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