Role of the Omp25/Omp31 Family in Outer Membrane Properties and Virulence of Brucella ovis

Author:

Caro-Hernández Paola1,Fernández-Lago Luis1,de Miguel María-Jesús2,Martín-Martín Ana I.1,Cloeckaert Axel3,Grilló María-Jesús24,Vizcaíno Nieves1

Affiliation:

1. Departamento de Microbiología y Genética, Edificio Departamental, Universidad de Salamanca, Plaza Doctores de la Reina s/n, 37007 Salamanca, Spain

2. Centro de Investigación y Tecnología Agroalimentaria del Gobierno de Aragón, Unidad de Sanidad Animal, Carretera de Montañana 930, 50059 Zaragoza, Spain

3. INRA, UR1282, Infectiologie Animale et Santé Publique, IASP, Nouzilly F-37380, France

4. Instituto de Agrobiotecnología y Recursos Naturales, CSIC-UPNA, Ctra. Mutilva Baja, 31192 Pamplona, Spain

Abstract

ABSTRACT The genes coding for the five outer membrane proteins (OMPs) of the Omp25/Omp31 family expected to be located in the outer membrane (OM) of rough virulent Brucella ovis PA were inactivated to evaluate their role in virulence and OM properties. The OM properties of the mutant strains and of the mutants complemented with the corresponding wild-type genes were analyzed, in comparison with the parental strain and rough B. abortus RB51, in several tests: (i) binding of anti-Omp25 and anti-Omp31 monoclonal antibodies, (ii) autoagglutination of bacterial suspensions, and (iii) assessment of susceptibility to polymyxin B, sodium deoxycholate, hydrogen peroxide, and nonimmune ram serum. A tight balance of the members of the Omp25/Omp31 family was seen to be essential for the stability of the B. ovis OM, and important differences between the OMs of B. ovis PA and B. abortus RB51 rough strains were observed. Regarding virulence, the absence of Omp25d and Omp22 from the OM of B. ovis PA led to a drastic reduction in spleen colonization in mice. While the greater susceptibility of the Δ omp22 mutant to nonimmune serum and its difficulty in surviving in the stationary phase might be on the basis of its dramatic attenuation, no defects in the OM able to explain the attenuation of the Δ omp25d mutant were found, especially considering that the fully virulent Δ omp25c mutant displayed more important OM defects. Accordingly, Omp25d, and perhaps Omp22, could be directly involved in the penetration and/or survival of B. ovis inside host cells. This aspect, together with the role of Omp25d and Omp22 in the virulence both of B. ovis in rams and of other Brucella species, should be thoroughly evaluated in future studies.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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