α2-macroglobulin function of thioester-containing proteins guards <i>Drosophila</i> from a bacterial protease via two immune-induced peptides

C Chuping Cai (Sino-French Hoffmann Institute, Guangzhou Medical University) A Adrian Acker (Faculté des Sciences de la Vie, Université de Strasbourg) J Jianqiong Huang (Sino-French Hoffmann Institute, Guangzhou Medical University) Y Yingying Liu (Institute of Intelligent Machines, Hefei Institutes of Physical Science) M 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) J 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) E 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) P Philippe Bulet P Philippe Hammann (Plateforme Protéomique Strasbourg-Esplanade, CNRS UAR1589, Institut de Biologie Moléculaire et Cellulaire, Université de Strasbourg) J Johana Chicher (Strasbourg-Esplanade Proteomics Facility, Institut de Biologie Moléculaire et Cellulaire, UAR1589 du CNRS, Université de Strasbourg) S Samuel Liegeois (Sino-French Hoffmann Institute, Guangzhou Medical University) Z Zi Li (Sino-French Hoffmann Institute, Guangzhou Medical University) J Jules A. Hoffmann (Sino-French Hoffmann Institute, School of Basic Medical Science, Guangzhou Medical University) N Nicolas Matt (Faculté des Sciences de la Vie, Université de Strasbourg) D Dominique Ferrandon (Sino-French Hoffmann Institute, Guangzhou Medical University)

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

Volume / Issue Vol. 123, Issue 4
Published January 27, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (15)

C

Chuping Cai

Sino-French Hoffmann Institute, Guangzhou Medical University

A

Adrian Acker

Faculté des Sciences de la Vie, Université de Strasbourg

J

Jianqiong Huang

Sino-French Hoffmann Institute, Guangzhou Medical University

Y

Yingying Liu

Institute of Intelligent Machines, Hefei Institutes of Physical Science

M

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

J

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

E

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

P

Philippe Bulet

P

Philippe Hammann

Plateforme Protéomique Strasbourg-Esplanade, CNRS UAR1589, Institut de Biologie Moléculaire et Cellulaire, Université de Strasbourg

J

Johana Chicher

Strasbourg-Esplanade Proteomics Facility, Institut de Biologie Moléculaire et Cellulaire, UAR1589 du CNRS, Université de Strasbourg

S

Samuel Liegeois

Sino-French Hoffmann Institute, Guangzhou Medical University

Z

Zi Li

Sino-French Hoffmann Institute, Guangzhou Medical University

J

Jules A. Hoffmann

Sino-French Hoffmann Institute, School of Basic Medical Science, Guangzhou Medical University

N

Nicolas Matt

Faculté des Sciences de la Vie, Université de Strasbourg

D

Dominique Ferrandon

Sino-French Hoffmann Institute, Guangzhou Medical University