Open Access
Vet. Res.
Volume 41, Number 3, May–June 2010
Number of page(s) 11
Published online 10 December 2009
How to cite this article Vet. Res. (2010) 41:26
  • Aebi C., Maciver I., Latimer J.L., Cope L.D., Stevens M.K., Thomas S.E., et al., A protective epitope of Moraxella catarrhalis is encoded by two different genes, Infect. Immun. (1997) 65:4367–4377. [PubMed] [Google Scholar]
  • Bambini S., Muzzi A., Olcen P., Rappuoli R., Pizza M., Comanducci M., Distribution and genetic variability of three vaccine components in a panel of strains representative of the diversity of serogroup B meningococcus, Vaccine (2009) 27:2794–2803. [CrossRef] [PubMed] [Google Scholar]
  • Blanco I., Galina-Pantoja L., Oliveira S., Pijoan C., Sanchez C., Canals A., Comparison between Haemophilus parasuis infection in colostrums-deprived and sow-reared piglets, Vet. Microbiol. (2004) 103:21–27. [CrossRef] [PubMed] [Google Scholar]
  • Carlone G.M., Thomas M.L., Rumschlag H.S., Sottnek F.O., Rapid microprocedure for isolating detergent-insoluble outer membrane proteins from Haemophilus species, J. Clin. Microbiol. (1986) 24:330–332. [PubMed] [Google Scholar]
  • Comanducci M., Bambini S., Brunelli B., Adu-Bobie J., Arico B., Capecchi B., et al., NadA, a novel vaccine candidate of Neisseria meningitidis, J. Exp. Med. (2002) 195:1445–1454. [CrossRef] [PubMed] [Google Scholar]
  • Cotter S.E., Surana N.K., St. Geme J.W. 3rd , Trimeric autotransporters: a distinct subfamily of autotransporter proteins, Trends Microbiol. (2005) 13:199–205. [CrossRef] [PubMed] [Google Scholar]
  • Del Rio M.L., Navas J., Martin A.J., Gutierrez C.B., Rodriguez-Barbosa J.I., Rodriguez Ferri E.F., Molecular characterization of Haemophilus parasuis ferric hydroxamate uptake (fhu) genes and constitutive expression of the FhuA receptor, Vet. Res. (2006) 37:49–59. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  • Forsgren A., Brant M., Riesbeck K., Immunization with the truncated adhesin Moraxella catarrhalis immunoglobulin D-binding protein (MID764-913) is protective against M. catarrhalis in a mouse model of pulmonary clearance, J. Infect. Dis. (2004) 190:352–355. [CrossRef] [PubMed] [Google Scholar]
  • Girard V., Mourez M., Adhesion mediated by autotransporters of Gram-negative bacteria: structural and functional features, Res. Microbiol. (2006) 157:407–416. [CrossRef] [PubMed] [Google Scholar]
  • Giuliani M.M., Adu-Bobie J., Comanducci M., Arico B., Savino S., Santini L., , A universal vaccine for serogroup B meningococcus, Proc. Natl. Acad. Sci. USA (2006) 103:10834–10839. [CrossRef] [Google Scholar]
  • Hill C.E., Metcalf D.S., MacInnes J.I., A search for virulence genes of Haemophilus parasuis using differential display RT-PCR, Vet. Microbiol. (2003) 96:189–202. [CrossRef] [PubMed] [Google Scholar]
  • Leduc I., Olsen B., Elkins C., Localization of the domains of the Haemophilus ducreyi trimeric autotransporter DsrA involved in serum resistance and binding to the extracellular matrix proteins fibronectin and vitronectin, Infect. Immun. (2009) 77:657–666. [CrossRef] [PubMed] [Google Scholar]
  • Litt D.J., Savino S., Beddek A., Comanducci M., Sandiford C., Stevens J., , Putative vaccine antigens from Neisseria meningitidis recognized by serum antibodies of young children convalescing after meningococcal disease, J. Infect. Dis. (2004) 190:1488–1497. [CrossRef] [PubMed] [Google Scholar]
  • Magagnoli C., Bardotti A., De Conciliis G., Galasso R., Tomei M., Campa C., et al., Structural organization of NadADelta(351–405), a recombinant MenB vaccine component, by its physico-chemical characterization at drug substance level, Vaccine (2009) 27:2156–2170. [CrossRef] [PubMed] [Google Scholar]
  • Martin de la Fuente A.J., Rodriguez-Ferri E.F., Frandoloso R., Martinez S., Tejerina F., Gutierrez-Martin C.B., Systemic antibody response in colostrum-deprived pigs experimentally infected with Haemophilus parasuis, Res. Vet. Sci. (2009) 86:248–253. [CrossRef] [PubMed] [Google Scholar]
  • Mason K.W., Zhu D., Scheuer C.A., McMichael J.C., Zlotnick G.W., Green B.A., Reduction of nasal colonization of nontypeable Haemophilus influenzae following intranasal immunization with rLP4/rLP6/UspA2 proteins combined with aqueous formulation of RC529, Vaccine (2004) 22:3449–3456. [CrossRef] [PubMed] [Google Scholar]
  • Meier P.S., Freiburghaus S., Martin A., Heiniger N., Troller R., Aebi C., Mucosal immune response to specific outer membrane proteins of Moraxella catarrhalis in young children, Pediatr. Infect. Dis. J. (2003) 22:256–262. [CrossRef] [PubMed] [Google Scholar]
  • Melnikow E., Dornan S., Sargent C., Duszenko M., Evans G., Gunkel N., , Microarray analysis of Haemophilus parasuis gene expression under in vitro growth conditions mimicking the in vivo environment, Vet. Microbiol. (2005) 110:255–263. [CrossRef] [PubMed] [Google Scholar]
  • Metcalf D.S., MacInnes J.I., Differential expression of Haemophilus parasuis genes in response to iron restriction and cerebrospinal fluid, Can. J. Vet. Res. (2007) 71:181–188. [PubMed] [Google Scholar]
  • Miniats O.P., Smart N.L., Ewert E., Vaccination of gnotobiotic primary specific pathogen-free pigs against Haemophilus parasuis, Can. J. Vet. Res. (1991) 55:33–36. [PubMed] [Google Scholar]
  • Miniats O.P., Smart N.L., Rosendal S., Cross protection among Haemophilus parasuis strains in immunized gnotobiotic pigs, Can. J. Vet. Res. (1991) 55:37–41. [PubMed] [Google Scholar]
  • Murphy T.F., Brauer A.L., Aebi C., Sethi S., Antigenic specificity of the mucosal antibody response to Moraxella catarrhalis in chronic obstructive pulmonary disease, Infect. Immun. (2005) 73:8161–8166. [CrossRef] [PubMed] [Google Scholar]
  • Murphy T.F., Brauer A.L., Aebi C., Sethi S., Identification of surface antigens of Moraxella catarrhalis as targets of human serum antibody responses in chronic obstructive pulmonary disease, Infect. Immun. (2005) 73:3471–3478. [CrossRef] [PubMed] [Google Scholar]
  • Nielsen R., Pathogenicity and immunity studies of Haemophilus parasuis serotypes, Acta Vet. Scand. (1993) 34:193–198. [PubMed] [Google Scholar]
  • Pina S., Olvera A., Barcelo A., Bensaid A., Trimeric autotransporters of Haemophilus parasuis: generation of an extensive passenger domain repertoire specific for pathogenic strains, J. Bacteriol. (2009) 191:576–587. [CrossRef] [PubMed] [Google Scholar]
  • Rapp-Gabrielson V., Oliveira S., Pijoan C., Haemophilus parasuis, in: Straw B.E., Zimmerman J.J., D’Allaire S., Taylor D.J. (Eds.), Diseases of swine, Iowa State University Press, Iowa, 2006, p. 1153. [Google Scholar]
  • Riising H.J., Prevention of Glässer’s disease through immunity to Haemophilus parasuis, Zentralbl. Veterinarmed. B (1981) 28:630–638. [CrossRef] [PubMed] [Google Scholar]
  • Scarselli M., Serruto D., Montanari P., Capecchi B., Adu-Bobie J., Veggi D., et al., Neisseria meningitidis NhhA is a multifunctional trimeric autotransporter adhesin, Mol. Microbiol. (2006) 61:631–644. [CrossRef] [PubMed] [Google Scholar]
  • Sjolinder H., Eriksson J., Maudsdotter L., Aro H., Jonsson A.B., Meningococcal outer membrane protein NhhA is essential for colonization and disease by preventing phagocytosis and complement attack, Infect. Immun. (2008) 76:5412–5420. [CrossRef] [PubMed] [Google Scholar]
  • Smart N.L., Miniats O.P., Preliminary assessment of a Haemophilus parasuis bacterin for use in specific pathogen free swine, Can. J. Vet. Res. (1989) 53:390–393. [PubMed] [Google Scholar]
  • Szczesny P., Lupas A., Domain annotation of trimeric autotransporter adhesins – daTAA, Bioinformatics (2008) 24:1251–1256. [CrossRef] [PubMed] [Google Scholar]
  • Vahle J.L., Haynes J.S., Andrews J.J., Experimental reproduction of Haemophilus parasuis infection in swine: clinical, bacteriological, and morphologic findings, J. Vet. Diagn. Invest. (1995) 7:476–480. [PubMed] [Google Scholar]
  • Zhang B., Tang C., Yang F.L., Yue H., Molecular cloning, sequencing and expression of the outer membrane protein A gene from Haemophilus parasuis, Vet. Microbiol. (2009) 136:408–410. [CrossRef] [PubMed] [Google Scholar]
  • Zhou M., Guo Y., Zhao J., Hu Q., Hu Y., Zhang A., et al., Identification and characterization of novel immunogenic outer membrane proteins of Haemophilus parasuis serovar 5, Vaccine (2009) 27:5271–5277. [CrossRef] [PubMed] [Google Scholar]
  • Zhou M., Zhang A., Guo Y., Liao Y., Chen H., Jin M., A comprehensive proteome map of the Haemophilus parasuis serovar 5, Proteomics (2009) 9:2722–2739. [CrossRef] [PubMed] [Google Scholar]