A novel lux operon in the cryptically bioluminescent fish pathogen Vibrio salmonicida is associated with virulence

Molecular and Microbiology Department, Tufts University School of Medicine, 136 Harrison Ave., Boston, MA 02111, USA; Department of Food Hygiene and Infection Biology, Norwegian School of Veterinary Science, PB 8146 Dep., 0033 Oslo, Norway; Biological Sciences Department, California Polytechnic University, San Luis Obispo, CA, 93407; Department of Medical Microbiology and Immunology, 1300 University Ave., University of Wisconsin, Madison, WI, 53706

^* To whom correspondence should be addressed. Email: egruby{at}wisc.edu.

	Abstract

The cold-water fish pathogen, Vibrio salmonicida, expresses a functional bacterial luciferase, but produces insufficient levels of its aliphatic-aldehyde substrate to be detectably luminous in culture. Our goals were to (i) better explain this cryptic bioluminescent phenotype through molecular characterization of the lux operon, as well as (ii) test whether the bioluminescence gene cluster is associated with virulence. Cloning and sequencing of the V. salmonicida lux operon revealed that homologs of all of the genes required for luminescence are present: luxAB (luciferase) and luxCDE (aliphatic-aldehyde synthesis; AAS). The arrangement and sequence of these structural lux genes are conserved when compared to related species of luminous bacteria. However, V. salmonicida strains have a novel arrangement and number of homologs for the luxR and luxI quorum-sensing regulatory genes. RT-PCR analysis suggests that this novel arrangement of quorum-sensing genes generates anti-sense transcripts that may be responsible for the reduced production of bioluminescence. In addition, infection with a strain in which the luxA gene was mutated resulted in a marked delay in Atlantic salmon mortality relative to the wild-type parent in single-strain challenge experiments. In mixed-strain competition between the luxA mutant and wild type, the mutant was attenuated up to 50-fold. It remains unclear whether the attenuation results from a direct loss of luciferase or a polar disturbance elsewhere in the lux operon. Nevertheless, these findings document for the first time an association between a mutation in a structural lux gene and virulence, as well as provide a new molecular system to study Vibrio pathogenesis in a natural host.