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  3. Peptide occurring in Enterobacteriaceae triggers Streptococcus pneumoniae cell death
 

Peptide occurring in Enterobacteriaceae triggers Streptococcus pneumoniae cell death

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BORIS DOI
10.7892/boris.133297
Publisher DOI
10.3389/fcimb.2019.00320
PubMed ID
31552200
Description
Nonencapsulated Streptococcus pneumoniae often possess two genes, aliB-like ORF 1 and aliB-like ORF 2, in place of capsule genes. AliB-like ORF 1 is thought to encode a substrate binding protein of an ABC transporter which binds peptide SETTFGRDFN, found in 50S ribosomal subunit protein L4 of Enterobacteriaceae.
Here, we investigated the effect of binding of AliB-like ORF 1 peptide on the transcriptome and proteome of nonencapsulated pneumococci. We found upregulation of gene expression of a metacaspase and a gene encoding N-acetylmuramoyl-L-alanine amidase, both of which are proposed to be involved in programmed cell death in prokaryotic cells. Proteome profiling indicated upregulation of transcriptional regulators and downregulation of metabolism-associated genes. Exposure to the peptide specifically triggered death in pneumococci which express AliB-like ORF 1, with the bacteria having an apoptotic appearance by electron microscopy. We propose that binding of the AliB-like ORF 1 peptide ligand by the pneumococcus signals a challenging environment with hostile bacterial species leading to death of a proportion of the pneumococcal population.
Date of Publication
2019-09-10
Publication Type
Article
Subject(s)
500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health
Language(s)
en
Contributor(s)
Nasher, Fauzy Negiub Ali
Institut für Infektionskrankheiten
Kwun, Min Jung
Croucher, Nicholas J
Heller, Manfredorcid-logo
Department for BioMedical Research (DBMR)
Hathaway, Lucy Janeorcid-logo
Institut für Infektionskrankheiten
Additional Credits
Institut für Infektionskrankheiten
Department for BioMedical Research (DBMR)
Series
Frontiers in cellular and infection microbiology
Publisher
Frontiers
ISSN
2235-2988
Access(Rights)
open.access
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