EAL domain protein YdiV acts as an anti-FlhD4C2 factor responsible for nutritional control of the flagellar regulon in Salmonella enterica serovar typhimurium

Takeo Wada, Tomoe Morizane, Tatsuhiko Abo, Akira Tominaga, Kanako Inoue-Tanaka, Kazuhiro Kutsukake

Research output: Contribution to journalArticle

57 Citations (Scopus)


Flagellar operons are divided into three classes with respect to their transcriptional hierarchy in Salmonella enterica serovar Typhimurium. The class 1 gene products FlhD and FlhC act together in an FlhD4C2 heterohexamer, which binds upstream of the class 2 promoters to facilitate binding of RNA polymerase. In this study, we showed that flagellar expression was much reduced in the cells grown in poor medium compared to those grown in rich medium. This nutritional control was shown to be executed at a step after class 1 transcription. We isolated five Tn5 insertion mutants in which the class 2 expression was derepressed in poor medium. These insertions were located in the ydiV (cdgR) gene or a gene just upstream of ydiV. The ydiV gene is known to encode an EAL domain protein and to act as a negative regulator of flagellar expression. Gene disruption and complementation analyses revealed that the ydiV gene is responsible for nutritional control. Expression analysis of the ydiV gene showed that its translation, but not transcription, was enhanced by growth in poor medium. The ydiV mutation did not have a significant effect on either the steady-state level of flhDC mRNA or that of FlhC protein. Purified YdiV protein was shown in vitro to bind to FlhD4C2 through interaction with FlhD subunit and to inhibit its binding to the class 2 promoter, resulting in inhibition of FlhD4C2-dependent transcription. Taking these data together, we conclude that YdiV is a novel anti-FlhD4C2 factor responsible for nutritional control of the flagellar regulon.

Original languageEnglish
Pages (from-to)1600-1611
Number of pages12
JournalJournal of bacteriology
Issue number7
Publication statusPublished - Apr 1 2011


ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology

Cite this