Elongation factor P restricts Salmonella's growth by controlling translation of a Mg2+ transporter gene during infection

Eunna Choi, Soomin Choi, Daesil Nam, Shinae Park, Yoontak Han, Jung Shin Lee, Eun Jin Lee

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

When a ribosome translates mRNA sequences, the ribosome often stalls at certain codons because it is hard to translate. Consecutive proline codons are such examples that induce ribosome stalling and elongation factor P (EF-P) is required for the stalled ribosome to continue translation at those consecutive proline codons. We found that EF-P is required for translation of the mgtB gene encoding a Mg2+ transporter in the mgtCBR virulence operon from the intracellular pathogen Salmonella enterica serovar Typhimurium. Salmonella lacking EF-P decreases MgtB protein levels in a manner dependent on consecutive proline codons located in the mgtB coding region despite increasing transcription of the mgtCBR operon via the mgtP open reading frame in the leader RNA, resulting in an altered ratio between MgtC and MgtB proteins within the operon. Substitution of the consecutive proline codons to alanine codons eliminates EF-P-mediated control of the mgtB gene during infection and thus contributes to Salmonella's survival inside macrophages where Salmonella experiences low levels of EF-P. This suggests that this pathogen utilizes a strategy to coordinate expression of virulence genes by an evolutionarily conserved translation factor.

Original languageEnglish
Article number42098
JournalScientific reports
Volume7
DOIs
Publication statusPublished - 2017 Feb 9
Externally publishedYes

Bibliographical note

Funding Information:
We thank Dongwoo Shin for providing strains. This work was supported, in part, by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF-2013R1A1A2074505 and NRF-2016R1A2B2012424) to E.-J.L. and NRF- 2015R1A4A1041105 to J.-S.L. The authors declare no conflict of interest.

Publisher Copyright:
© 2017 The Author(s).

ASJC Scopus subject areas

  • General

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