α2-macroglobulin function of thioester-containing proteins guards <i>Drosophila</i> from a bacterial protease via two immune-induced peptides
Abstract
RNAseq analysis of the Drosophila genome has revealed further immune-induced genes. Two genes initially annotated as lncRNAs, CG44404 ( yulü ) and CG45045 ( shenshu ), are strongly induced. We report here that these two genes actually encode highly related secreted peptides found in the Sophophora subgenus of Drosophila species. We have generated single and double null mutants of these loci and found that the double mutant line did not display any enhanced susceptibility to an immune challenge with a panel of bacterial and fungal pathogens, except for Pseudomonas aeruginosa . We did not observe any increased P. aeruginosa burden in yulü-shenshu mutants, suggesting that the two peptides may not be required for resistance to infection. Rather, we find that they provide a level of protection against Outer Membrane Vesicles (OMVs) purified from either P. aeruginosa or Serratia marcescens culture supernatants. We have recently reported that S. marcescens OMVs induce the paralysis of flies through the induction of apoptosis in at least some neurons. Much of the virulence of these OMVs is mediated by the metalloprotease PrtA. While Yulü/Shenshu do not display any protease inhibition activity, the detection of an association between Yulü and the Drosophila complement thioester-containing protein 2 (Tep2) led to the finding that both Tep2 and Tep4 mutants are sensitive to the injection of PrtA while their overexpression significantly protects wild-type flies from the effects of this protease. Both Tep2 and Tep4 are able to inhibit the activity of PrtA in a thioester- and yulü/shenshu -dependent manner. Thus, these Teps may also function as α2-macroglobulins.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (15)
Chuping Cai
Sino-French Hoffmann Institute, Guangzhou Medical University
Adrian Acker
Faculté des Sciences de la Vie, Université de Strasbourg
Jianqiong Huang
Sino-French Hoffmann Institute, Guangzhou Medical University
Yingying Liu
Institute of Intelligent Machines, Hefei Institutes of Physical Science
Maria Victoria Molino
Laboratorio de Patogénesis Bacteriana, Instituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario
Javier F. Mariscotti
Laboratorio de Patogénesis Bacteriana, Instituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario
Eleonora Garcia-Véscovi
Laboratorio de Patogénesis Bacteriana, Instituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario
Philippe Bulet
Philippe Hammann
Plateforme Protéomique Strasbourg-Esplanade, CNRS UAR1589, Institut de Biologie Moléculaire et Cellulaire, Université de Strasbourg
Johana Chicher
Strasbourg-Esplanade Proteomics Facility, Institut de Biologie Moléculaire et Cellulaire, UAR1589 du CNRS, Université de Strasbourg
Samuel Liegeois
Sino-French Hoffmann Institute, Guangzhou Medical University
Zi Li
Sino-French Hoffmann Institute, Guangzhou Medical University
Jules A. Hoffmann
Sino-French Hoffmann Institute, School of Basic Medical Science, Guangzhou Medical University
Nicolas Matt
Faculté des Sciences de la Vie, Université de Strasbourg
Dominique Ferrandon
Sino-French Hoffmann Institute, Guangzhou Medical University