A Family of T6SS Antibacterial Effectors Related t... - BV FAPESP
Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A Family of T6SS Antibacterial Effectors Related to L,D-Transpeptidases Targets the Peptidoglycan

Full text
Author(s):
Sibinelli-Sousa, Stephanie [1] ; Hespanhol, Julia T. [1] ; Nicastro, Gianlucca G. [1] ; Matsuyama, Bruno Y. [2] ; Mesnage, Stephane [3] ; Patel, Ankur [3] ; de Souza, Robson F. [1] ; Guzzo, Cristiane R. [1] ; Bayer-Santos, Ethel [1]
Total Authors: 9
Affiliation:
[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, BR-05508900 Sao Paulo - Brazil
[2] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05508000 Sao Paulo - Brazil
[3] Univ Sheffield, Dept Mol Biol & Biotechnol, Sheffield S10 2TN, S Yorkshire - England
Total Affiliations: 3
Document type: Journal article
Source: CELL REPORTS; v. 31, n. 12 JUN 23 2020.
Web of Science Citations: 0
Abstract

Type VI secretion systems (T6SSs) are nanomachines used by bacteria to inject toxic effectors into competitors. The identity and mechanism of many effectors remain unknown. We characterized a Salmonella T6SS antibacterial effector called TIde1 that is toxic in target-cell periplasm and is neutralized by its cognate immunity protein (TIdi1), Microscopy analysis reveals that cells expressing TIde1 stop dividing and lose cell envelope integrity. Bioinformatic analysis uncovers similarities between TIde1 and the catalytic domain of L,D-transpeptidases. Point mutations on conserved catalytic residues abrogate toxicity. Biochemical assays reveal that TIde1 displays both L,D-carboxypeptidase activity by cleaving peptidoglycan tetrapeptides between meso-diaminopimelic acid(3) and D-alanine(4) and L,D-transpeptidase exchange activity by replacing D-alanine(4) by a non-canonical D-amino acid. Phylogenetic analysis shows that TIde1 homologs constitute a family of T6SS-associated effectors broadly distributed among Proteobacteria. This work expands our current knowledge about bacterial effectors used in interbacterial competition and reveals a different mechanism of bacterial antagonism. (AU)

FAPESP's process: 18/04553-8 - Function of type VI secretion systems of pathogenic bacteria in the interaction with eukaryotic cells
Grantee:Ethel Bayer Santos
Support Opportunities: Scholarships in Brazil - Young Researchers
FAPESP's process: 17/02178-2 - Function of type VI secretion systems of pathogenic bacteria in the interaction with eukaryotic cells
Grantee:Ethel Bayer Santos
Support Opportunities: Research Grants - Young Investigators Grants
FAPESP's process: 16/09047-8 - Comparative genomics of bacterial toxins associated with type IV secretion systems
Grantee:Robson Francisco de Souza
Support Opportunities: Regular Research Grants
FAPESP's process: 19/00195-2 - Understanding the c-di-GMP signaling networks and the Type II secretion system present into the human pathogen Leptospira interrogans Copenhageni
Grantee:Cristiane Rodrigues Guzzo Carvalho
Support Opportunities: Regular Research Grants
FAPESP's process: 17/17303-7 - Structure and function of bacterial secretion systems
Grantee:Shaker Chuck Farah
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 18/25316-4 - Function of SPI-6 T6SS and SPI-19 T6SS of Salmonella during competition with the gut microbiota
Grantee:Julia Takuno Hespanhol
Support Opportunities: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 16/00458-5 - Structural and functional characterization of Xanthomonas citri type IV secretion system.
Grantee:Bruno Yasui Matsuyama
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 18/13819-1 - Analysis of the activation dynamics of the type 6 secretion system of Salmonella during infection of eukaryotic cells
Grantee:Stephanie Sibinelli de Sousa
Support Opportunities: Scholarships in Brazil - Scientific Initiation