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Infection and Immunity, August 2003, p. 4326-4332, Vol. 71, No. 8
0019-9567/03/$08.00+0 DOI: 10.1128/IAI.71.8.4326-4332.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Rose-Anne Boigegrain,1 Jan Machold,1,
Christoph Weise,2 Axel Cloeckaert,3 and Bruno Rouot1*
INSERM U431, Université de Montpellier 2, 34095 Montpellier Cedex 05,1 Unité BioAgresseurs, Santé et Environnement, INRA, 37380 Nouzilly, France,3 Institut für Chemie-Biochemie Freie Universität Berlin, D-14195 Berlin Germany2
Received 6 February 2003/ Returned for modification 25 March 2003/ Accepted 29 April 2003
Impairment of the omp25 gene in Brucella spp. leads to attenuated strains and confers protection to the host. Omp25 and Omp31, whose functions remain unknown, were the first characterized members of group 3 outer membrane proteins (Omps) (25 to 34 kDa). Recently, genomic and proteomic approaches identified five new putative members of this family, some of which are produced in B. melitensis or B. abortus. In the present study, using protein microsequencing, we identified new members of group 3 Omps proteins produced in B. suis. Since several monoclonal antibodies (MAbs) against Omp25 cross-reacted with other members of group 3 Omps, we also performed Western immunoblotting to compare wild-type B. suis with mutants systematically having B. suis omp25-related genes knocked out. We demonstrate the production of three paralogs of Omp31 and/or Omp25 in B. suis, and the existence of a common site of signal peptide cleavage (AXAAD), which is very similar to that present in the five homologous Omps of Bartonella quintana. The seven group 3 Omps were classified in four-subgroups on the basis of percentage amino acid sequence identities: Omp25 alone, the Omp25b-Omp25c-Omp25d cluster, the Omp31/31b subgroup, and the less related Omp22 protein (also called Omp3b). Together with previous data, our results demonstrate that all new members of group 3 Omps are produced in B. suis or in other Brucella species and we propose a nomenclature that integrates all of these proteins to facilitate the understanding of future Brucella interspecies study results.
Present address: INSERM, EMI 0227, CRLC Val d'Aurelle-Paul Lamarque, F-34298 Montpellier Cedex 5, France.
Present address: Amersham Pharmacia Biotech, D-79111 Freiburg, Germany.
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