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Author Spotlight: Advancing Therapeutics to Treat Vibriosis in Humans and Aquatic Organisms
Published on: May 31, 2024
Lrp, a global regulator, regulates the virulence of Vibrio vulnificus
Yu-Chi Ho1, Feng-Ru Hung1, Chao-Hui Weng1
1Department of Microbiology and Immunology, College of Medicine, Tainan, 70101, Taiwan.
Background:
An attenuated mutant (designated NY303) of Vibrio vulnificus, which causes serious wound infection and septicemia in humans, was isolated fortuitously from a clinical strain YJ016. This mutant was defective in cytotoxicity, migration on soft agar and virulence in the mouse. The purpose of this study was to map the mutation in this attenuated mutant and further explore how the gene thus identified is involved in virulence.
Methods:
The whole genome sequence of mutant NY303 determined by next-generation sequencing was compared with that of strain YJ016 to map the mutations. By isolating and characterizing the specific gene-knockout mutants, the gene associated with the phenotype of mutant NY303 was identified. This gene encodes a global regulator, Lrp. A mutant, YH01, deficient in Lrp was isolated and examined in vitro, in vivo and ex vivo to find the affected virulence mechanisms. The target genes of Lrp were further identified by comparing the transcriptomes, which were determined by RNA-seq, of strain YJ016 and mutant YH01. The promoters bound by Lrp were identified by genome footprinting-sequencing, and those related with virulence were further examined by electrophoretic mobility shift assay.
Results:
A mutation in lrp was shown to be associated with the reduced cytotoxicity, chemotaxis and virulence of mutant NY303. Mutant YH01 exhibited a phenotype resembling that of mutant NY303, and was defective in colonization in the mouse and growth in mouse serum, but not the antiphagocytosis ability. 596 and 95 genes were down- and up-regulated, respectively, in mutant YH01. Many of the genes involved in secretion of the MARTX cytotoxin, chemotaxis and iron-acquisition were down-regulated in mutant YH01. The lrp gene, which was shown to be negatively autoregulated, and 7 down-regulated virulence-associated genes were bound by Lrp in their promoters. A 14-bp consensus sequence, mkCrTTkwAyTsTG, putatively recognized by Lrp was identified in the promoters of these genes.
Conclusions:
Lrp is a global regulator involved in regulation of cytotoxicity, chemotaxis and iron-acquisition in V. vulnificus. Down-regulation of many of the genes associated with these properties may be responsible, at least partly, for loss of virulence in mutant NY303.
Insights
A mutation in the Lrp global regulator significantly reduced Vibrio vulnificus virulence by down-regulating key genes. This finding offers insights into V. vulnificus pathogenesis and potential therapeutic targets.
Area of Science:
- Microbiology
- Genetics
- Pathogenesis
Background:
- Vibrio vulnificus causes severe human infections, including wound infections and septicemia.
- An attenuated mutant, NY303, exhibited reduced cytotoxicity, migration, and virulence.
- The study aimed to identify the genetic basis of this attenuation and its impact on virulence.
Purpose of the Study:
- To map the mutation responsible for the attenuated phenotype of V. vulnificus NY303.
- To elucidate the role of the identified gene, Lrp, in V. vulnificus virulence mechanisms.
- To identify Lrp-regulated genes and understand its global regulatory function.
Main Methods:
- Whole genome sequencing of mutant NY303 compared to wild-type YJ016.
- Gene knockout analysis to confirm the role of Lrp.
- Transcriptome analysis (RNA-seq) to identify Lrp target genes.
- Genome footprinting-sequencing and electrophoretic mobility shift assays to identify Lrp binding sites.
Main Results:
- A mutation in the lrp gene was identified as the cause of reduced cytotoxicity, chemotaxis, and virulence.
- Lrp regulates genes involved in MARTX cytotoxin secretion, chemotaxis, and iron acquisition.
- Lrp is a negatively autoregulated global regulator, binding to a consensus sequence (mkCrTTkwAyTsTG) in target gene promoters.
- Mutant YH01 (Lrp-deficient) showed impaired colonization and serum growth but retained antiphagocytic ability.
Conclusions:
- Lrp is a critical global regulator in V. vulnificus, controlling cytotoxicity, chemotaxis, and iron acquisition.
- Down-regulation of virulence-associated genes by Lrp contributes significantly to the loss of V. vulnificus virulence.
- Understanding Lrp's regulatory network provides insights into V. vulnificus pathogenesis.
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