Identification of Vibrio harveyi proteins involved in the specific immune response of Senegalese sole (Solea senegalensis, Kaup)

• Published in: Fish & shellfish immunology Vol. 47; no. 1; pp. 377 - 380
• Main Authors: Medina, A., Mancera, J.M., Martínez-Manzanares, E., Moriñigo, M.A., Arijo, S.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.11.2015
• Subjects: 2D-PAGE; Animals; Antibodies, Bacterial - blood; Antibody; Antigen identification; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacterial Vaccines - pharmacology; ELISA; Fish Diseases - immunology; Fish Diseases - microbiology; Flatfishes; Immunity, Innate; Immunization; Solea senegalensis; Vibrio - genetics; Vibrio - physiology; Vibrio harveyi; Vibrio Infections - immunology; Vibrio Infections - microbiology; Vibrio Infections - veterinary; Western Blot; Immunization; Western Blot; Antigen identification; Vibrio harveyi; Antibody; 2D-PAGE; Solea senegalensis; ELISA
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2015.09.031

Senegalese sole cultures are frequently affected by Vibrio harveyi disease outbreaks. Vaccines in aquaculture are one of the most successful methods of preventing fish pathologies; however, these vaccines are usually composed of inactivated whole cells containing a wide pool of antigens, and some do not induce any protection against pathogens. Thus, the aim of this study was to identify immunogenic proteins of V. harveyi involved in the specific antibody production by Senegalese sole. S. senegalensis specimens were immunized, by intraperitoneal injection, with V. harveyi bacterin supplemented with inactivated extracellular polymeric substances (ECP) and Freund incomplete adjuvant to obtain polyclonal antiserum. One month later, specimens were re-inoculated with the same antigens. Sera from immunized fish were collected two months post first immunization. Strong specific immune response to V. harveyi antigens was detected by ELISA using bacterin (limit dilutions of sera were 1:64000), ECP (1:4000) and outer membrane proteins (OMP) (1:4000) as antigens. Presence of immunogenic proteins in V. harveyi ECP and OMP were determined by 2D-PAGE. For Western Blot analysis some gels were transferred onto nitrocellulose membranes and incubated with sera from S. senegalensis specimens immunized against V. harveyi. 2D-PAGE and Western Blot showed at least five reactive proteins in the ECP and two in the OMP fraction. The spots that clearly reacted with the sole antiserum were excised from stained gel, and analyzed by mass spectrometry (MALDI/TOFTOF). A database search was then performed, using MASCOT as the search method. According to the results, the five ECP spots were identified as Maltoporine, protein homologous to Metal dependent phosphohydrolase, two porins isoforms of V. harveyi and a protein homologous to the cell division protein FtsH. Reactive proteins in the OMP fraction were identified as the protein 3-hydroxyisobutyrate dehydrogenase and a protein homologous to acid phosphatase. •Sole specimens were immunized with V. harveyi bacterin and ECP to obtain antiserum.•Specific immune response was detected by ELISA using V. harveyi antigens.•2D-PAGE and Western Blot showed five reactive proteins in ECP and two in OMP.•ECP proteins were identified as maltoporine, phosphohydrolase, two porins and FtsH.•OMP spots were identified as hydroxyisobutyrate dehydrogenase and acid phosphatase.