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The Neisseria Meningitidis ADP-Ribosyltransferase NarE Enters Human Epithelial Cells and Disrupts Epithelial Monolayer Integrity

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Journal PLoS One
Date 2015 May 22
PMID 25996923
Citations 2
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Abstract

Many pathogenic bacteria utilize ADP-ribosylating toxins to modify and impair essential functions of eukaryotic cells. It has been previously reported that Neisseria meningitidis possesses an ADP-ribosyltransferase enzyme, NarE, retaining the capacity to hydrolyse NAD and to transfer ADP-ribose moiety to arginine residues in target acceptor proteins. Here we show that upon internalization into human epithelial cells, NarE gains access to the cytoplasm and, through its ADP-ribosylating activity, targets host cell proteins. Notably, we observed that these events trigger the disruption of the epithelial monolayer integrity and the activation of the apoptotic pathway. Overall, our findings provide, for the first time, evidence for a biological activity of NarE on host cells, suggesting its possible involvement in Neisseria pathogenesis.

Citing Articles

Targeting ADP-ribosylation as an antimicrobial strategy.

Catara G, Corteggio A, Valente C, Grimaldi G, Palazzo L Biochem Pharmacol. 2019; 167:13-26.

PMID: 31176616 PMC: 7172630. DOI: 10.1016/j.bcp.2019.06.001.


The NarE protein of Neisseria gonorrhoeae catalyzes ADP-ribosylation of several ADP-ribose acceptors despite an N-terminal deletion.

Rodas P, Alamos-Musre A, Alvarez F, Escobar A, Tapia C, Osorio E FEMS Microbiol Lett. 2016; 363(17).

PMID: 27465490 PMC: 5812539. DOI: 10.1093/femsle/fnw181.

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