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Transcriptome Analysis Reveals the Effect of PdhR in Plesiomonas shigelloides
Junxiang Yan1,2,3, Bin Yang1,2,3, Xinke Xue1,2,3
1TEDA Institute of Biological Sciences and Biotechnology, Nankai University, Tianjin 300457, China.
Insights
The pyruvate dehydrogenase complex regulator (PdhR) in Plesiomonas shigelloides controls flagella, motility, and virulence. PdhR positively regulates Type III Secretion System (T3SS) genes, impacting bacterial infection.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- The pyruvate dehydrogenase complex regulator (PdhR) is known to control metabolic pathways in bacteria.
- Its specific function in *Plesiomonas shigelloides* pathogenesis remains largely uncharacterized.
Purpose of the Study:
- To elucidate the regulatory role of PdhR in *Plesiomonas shigelloides*.
- To identify PdhR-controlled genes and pathways, including those related to virulence and motility.
Main Methods:
- Comparative RNA sequencing (RNA-Seq) between wild-type and Δ*pdhR* mutant strains.
- Motility assays and Transmission Electron Microscopy (TEM) to assess flagellar function.
- Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) to validate gene expression.
Main Results:
- PdhR regulates approximately 7.38% of the *P. shigelloides* transcriptome.
- Deletion of *pdhR* abolished flagella formation and motility.
- PdhR positively regulates the Type III Secretion System (T3SS) cluster, enhancing *P. shigelloides* virulence in Caco-2 cells.
- PdhR directly represses the *pdhR-aceEF-lpd* operon, *metR*, and *nuoA* expression.
- ArcA was identified as a repressor of *pdhR* and *lpdA*.
Conclusions:
- PdhR is a key regulator of motility, flagella synthesis, and T3SS-mediated virulence in *P. shigelloides*.
- This study reveals novel regulatory targets of PdhR, including *metR* and *nuoA*.
- The findings provide insights into the complex regulatory network governing *P. shigelloides* pathogenicity.
Abstract:
The pyruvate dehydrogenase complex regulator (PdhR) was originally identified as a repressor of the pdhR-aceEF-lpd operon, which encodes the pyruvate dehydrogenase complex (PDHc) and PdhR itself. According to previous reports, PdhR plays a regulatory role in the physiological and metabolic pathways of bacteria. At present, the function of PdhR in Plesiomonas shigelloides is still poorly understood. In this study, RNA sequencing (RNA-Seq) of the wild-type strain and the ΔpdhR mutant strains was performed for comparison to identify the PdhR-controlled pathways, revealing that PdhR regulates ~7.38% of the P. shigelloides transcriptome. We found that the deletion of pdhR resulted in the downregulation of practically all polar and lateral flagella genes in P. shigelloides; meanwhile, motility assay and transmission electron microscopy (TEM) confirmed that the ΔpdhR mutant was non-motile and lacked flagella. Moreover, the results of RNA-seq and quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) showed that PdhR positively regulated the expression of the T3SS cluster, and the ΔpdhR mutant significantly reduced the ability of P. shigelloides to infect Caco-2 cells compared with the WT. Consistent with previous research, pyruvate-sensing PdhR directly binds to its promoter and inhibits pdhR-aceEF-lpd operon expression. In addition, we identified two additional downstream genes, metR and nuoA, that are directly negatively regulated by PdhR. Furthermore, we also demonstrated that ArcA was identified as being located upstream of pdhR and lpdA and directly negatively regulating their expression. Overall, we revealed the function and regulatory pathway of PdhR, which will allow for a more in-depth investigation into P. shigelloides pathogenicity as well as the complex regulatory network.
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