LitR, a new transcriptional activator in Vibrio fischeri, regulates luminescence and symbiotic light organ colonization

• Published in: Molecular microbiology 2002-07, Vol.45 (1), p.131-143
• Main Authors: Fidopiastis, Pat M., Miyamoto, Carol M., Jobling, Michael G., Meighen, Edward A., Ruby, Edward G.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Decapodiformes - anatomy & histology; Decapodiformes - microbiology; Gene Expression Regulation, Bacterial; Light; Luminescent Measurements; Marine; Molecular Sequence Data; Repressor Proteins - genetics; Repressor Proteins - metabolism; Sequence Analysis, DNA; Symbiosis; Trans-Activators - chemistry; Trans-Activators - genetics; Trans-Activators - metabolism; Vibrio - genetics; Vibrio - growth & development; Vibrio - metabolism; Vibrio - physiology
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1046/j.1365-2958.2002.02996.x

Summary Vibrio fischeri is the bacterial symbiont within the light‐emitting organ of the sepiolid squid Euprymna scolopes . Upon colonizing juvenile squids, bacterial symbionts grow on host‐supplied nutrients, while providing a bioluminescence that the host uses during its nocturnal activities. Mutant bacterial strains that are unable to emit light have been shown to be defective in normal colonization. A 606 bp open reading frame was cloned from V. fischeri that encoded a protein, which we named LitR, that had about 60% identity to four related regulator proteins: Vibrio cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vibrio vulnificus SmcR. When grown in culture, cells of V. fischeri strain PMF8, in which litR was insertionally inactivated, were delayed in the onset of luminescence induction and emitted only about 20% as much light per cell as its parent. Protein‐binding studies suggested that LitR enhances quorum sensing by regulating the transcription of the luxR gene. Interestingly, when competed against its parent in mixed inocula, PMF8 became the predominant symbiont present in 83% of light organs. Thus, the litR mutation appears to represent a novel class of mutations in which the loss of a regulatory gene function enhances the bacterium's competence in initiating a benign infection.