Journal
CELL REPORTS
Volume 31, Issue 12, Pages -Publisher
CELL PRESS
DOI: 10.1016/j.celrep.2020.107813
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Funding
- Sao Paulo Research Foundation (FAPESP) [2017/02178-2, 2016/09047-8, 2017/17303-7, 2019/00195-2]
- FAPESP [2018/13819-1, 2018/25316-4, 2016/00458-5, 2018/04553-8]
- CAPES fellowship
- Biotechnology and Biological Sciences Research Council (BBSRC) studentship [BB/M011151/1]
- BBSRC [2058718] Funding Source: UKRI
- MRC [MR/S009272/1] Funding Source: UKRI
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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.
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