Brucella abortus ure2 region contains an acid-activated urea transporter and a nickel transport system

• Published in: BMC microbiology Vol. 10; no. 1; p. 107
• Main Authors: Sangari, Félix J, Cayón, Ana M, Seoane, Asunción, García-Lobo, Juan M
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 10.04.2010; BioMed Central; BMC
• Subjects: Acids - metabolism; Acids - toxicity; Anti-Bacterial Agents - metabolism; Anti-Bacterial Agents - toxicity; Bacteria; Bacterial genetics; Bacterial Proteins - genetics; Bacteriology; Biological transport, Active; Brucella abortus; Brucella abortus - drug effects; Brucella abortus - genetics; Brucella abortus - physiology; Enzymes; Gene clusters; Gene Knockout Techniques; Genes; Genes, Bacterial; Genetic aspects; Health aspects; Membrane Transport Proteins - genetics; Membrane Transport Proteins - metabolism; Microbial Viability; Multigene Family; Nickel; Nickel - metabolism; Operon; Operons; pH effects; Proteins; Research article; Stress, Physiological; Survival; Transcriptional Activation; Urea; Urea Transporters; Urease; Urease - metabolism; virulence factors; Spain
• ISSN: 1471-2180; 1471-2180
• DOI: 10.1186/1471-2180-10-107

Urease is a virulence factor that plays a role in the resistance of Brucella to low pH conditions, both in vivo and in vitro. Brucella contains two separate urease gene clusters, ure1 and ure2. Although only ure1 codes for an active urease, ure2 is also transcribed, but its contribution to Brucella biology is unknown. Re-examination of the ure2 locus showed that the operon includes five genes downstream of ureABCEFGDT that are orthologs to a nikKMLQO cluster encoding an ECF-type transport system for nickel. ureT and nikO mutants were constructed and analyzed for urease activity and acid resistance. A non-polar ureT mutant was unaffected in urease activity at neutral pH but showed a significantly decreased activity at acidic pH. It also showed a decreased survival rate to pH 2 at low concentration of urea when compared to the wild type. The nikO mutant had decreased urease activity and acid resistance at all urea concentrations tested, and this phenotype could be reverted by the addition of nickel to the growth medium. Based on these results, we concluded that the operon ure2 codes for an acid-activated urea transporter and a nickel transporter necessary for the maximal activity of the urease whose structural subunits are encoded exclusively by the genes in the ure1 operon.