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Molecular basis for post-transcriptional regulation on type 3 secretion system 1 in Vibrio parahaemolyticus

研究課題

研究課題/領域番号 23K14521
研究種目

若手研究

配分区分基金
審査区分 小区分49050:細菌学関連
研究機関大阪大学

研究代表者

Pratama Andre  大阪大学, 微生物病研究所, 特任研究員(常勤) (30972319)

研究期間 (年度) 2023-04-01 – 2025-03-31
研究課題ステータス 交付 (2023年度)
配分額 *注記
4,680千円 (直接経費: 3,600千円、間接経費: 1,080千円)
2024年度: 2,340千円 (直接経費: 1,800千円、間接経費: 540千円)
2023年度: 2,340千円 (直接経費: 1,800千円、間接経費: 540千円)
キーワードVibrio parahaemolyticus / T3SS / gene regulation / virulence
研究開始時の研究の概要

The major seafood-borne pathogen Vibrio parahaemolyticus senses bile as a chemical cue in the intestine to activate the T3SS2, which is responsible for its enterotoxicity but represses the T3SS1 activity. In this study, the applicant tries to understand how bile affects T3SS1 repression. To this end, the responsible molecule will be identified and characterized using biochemistry and molecular biology techniques to understand this regulatory mechanism.

研究実績の概要

Pathogenic Vibrio parahaemolyticus causes septicemia and acute gastroenteritis in humans, by utilizing nano weapons called Type 3 Secretion Systems (T3SSs). This bacterium encoded two T3SSs called T3SS1 and T3SS2, whose expression is dictated by certain signals from the surrounding environment. It has been reported that bile, a compound found in the human intestine, acts as a chemical cue to trigger T3SS2 expression while also shutting off T3SS1 expression. In this study, the applicant tries to understand how bile affects T3SS1 repression.
During the first year, the applicant identified conjugated secondary bile acids, which are human metabolites found within bile, as a signal that represses T3SS1. The applicant investigated potential regulators that could serve as a signal for these molecules by examining the gene and protein expression of those regulator mutants in the context of T3SS1. As a result, one regulator (regulator X) is a key factor in this phenomenon. Furthermore, using the transcriptomic analysis, many genes were differentially expressed by regulator X besides T3SS1 downregulation. However, careful examination revealed that regulator X indirectly repressed the T3SS1. To find the direct repressor, the applicant created an expression library of genes activated by regulator X for screening and found genes A, B, and C linked to T3SS1 activity.

現在までの達成度 (区分)
現在までの達成度 (区分)

2: おおむね順調に進展している

理由

According to the research timeline for the first year, the applicant's objective was to identify the responsible molecules for T3SS1 repression. The results showed that three responsible molecules were identified and validated.

今後の研究の推進方策

Following the applicant’s plan, the next step involves characterizing and elucidating the identified molecules, aiming to understand how these molecules cause T3SS1 repression in the hope of revealing the molecular mechanism behind this phenomenon.

報告書

(1件)
  • 2023 実施状況報告書
  • 研究成果

    (1件)

すべて 2024

すべて 雑誌論文 (1件) (うち査読あり 1件、 オープンアクセス 1件)

  • [雑誌論文] The read-through transcription-mediated autoactivation circuit for virulence regulator expression drives robust type III secretion system 2 expression in Vibrio parahaemolyticus2024

    • 著者名/発表者名
      Anggramukti Dhira Saraswati、Ishii Eiji、Pratama Andre、Al Kadi Mohamad、Iida Tetsuya、Kodama Toshio、Matsuda Shigeaki
    • 雑誌名

      PLOS Pathogens

      巻: 20 号: 3 ページ: e1012094-e1012094

    • DOI

      10.1371/journal.ppat.1012094

    • 関連する報告書
      2023 実施状況報告書
    • 査読あり / オープンアクセス

URL: 

公開日: 2023-04-13   更新日: 2024-12-25  

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