Literature DB >> 2193699

Capsules and virulence in the HAP group of bacteria.

T J Inzana1.   

Abstract

Many species in the genera Haemophilus, Actinobacillus, and Pasteurella produce serotype-specific, negatively-charged, polysaccharide capsules. In pure form, these capsules are nontoxic, relatively inert biologically, and some are poorly immunogenic. The capsule forms the outer-most surface of the bacterium, and prior to the development of specific antibody, inhibits the bactericidal and opsonic activity of normal serum. In contrast, noncapsulated isogenic mutants are generally avirulent, and are quickly cleared by host defenses. In conjunction with the bacterial cell, or through covalent conjugation to a protein carrier, relatively high titers of antibody to capsule can be produced in immunocompetent hosts. For some pathogens (such as H. influenzae type b) antibody to capsule alone is bactericidal, opsonic, and adequate for complete protection against disease. For pathogens that produce potent exotoxins, however, (such as P. haemolytica and A. pleuropneumoniae) antibody to capsule alone may provide only partial protection. The composition or structure of the capsule may also influence the relative virulence of a particular organism. Molecular analysis of the interaction between capsules and host defenses will be required to understand more fully how capsules influence bacterial virulence.

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Year:  1990        PMID: 2193699

Source DB:  PubMed          Journal:  Can J Vet Res        ISSN: 0830-9000            Impact factor:   1.310


  9 in total

1.  Humoral antibody response and protective immunity in swine following immunization with the 104-kilodalton hemolysin of Actinobacillus pleuropneumoniae.

Authors:  J Devenish; S Rosendal; J T Bossé
Journal:  Infect Immun       Date:  1990-12       Impact factor: 3.441

2.  Interaction of Haemophilus parasuis with nasal and tracheal mucosa following intranasal inoculation of cesarean derived colostrum deprived (CDCD) swine.

Authors:  J L Vahle; J S Haynes; J J Andrews
Journal:  Can J Vet Res       Date:  1997-07       Impact factor: 1.310

3.  Influence of Actinobacillus pleuropneumoniae serotype 2 and its cytolysins on porcine neutrophil chemiluminescence.

Authors:  P Dom; F Haesebrouck; E M Kamp; M A Smits
Journal:  Infect Immun       Date:  1992-10       Impact factor: 3.441

4.  Association of Actinobacillus pleuropneumoniae capsular polysaccharide with virulence in pigs.

Authors:  Aloka B Bandara; Mark L Lawrence; Hugo P Veit; Thomas J Inzana
Journal:  Infect Immun       Date:  2003-06       Impact factor: 3.441

5.  Effects of sub-MICs of antibiotics on cell surface characteristics and virulence of Pasteurella multocida.

Authors:  A Lebrun; M Caya; M Jacques
Journal:  Antimicrob Agents Chemother       Date:  1992-10       Impact factor: 5.191

6.  Transcription analysis on response of porcine alveolar macrophages to Haemophilus parasuis.

Authors:  Yang Wang; Chong Liu; Ying Fang; Xiaoli Liu; Wentao Li; Shuqing Liu; Yingyu Liu; Yuxi Liu; Catherine Charreyre; Jean-Christophe Audonnet; Pin Chen; Qigai He
Journal:  BMC Genomics       Date:  2012-02-13       Impact factor: 3.969

Review 7.  Immunology of the porcine respiratory disease complex.

Authors:  E L Thacker
Journal:  Vet Clin North Am Food Anim Pract       Date:  2001-11       Impact factor: 3.357

8.  malT knockout mutation invokes a stringent type gene-expression profile in Actinobacillus pleuropneumoniae in bronchoalveolar fluid.

Authors:  Abdul G Lone; Vincent Deslandes; John H E Nash; Mario Jacques; Janet I MacInnes
Journal:  BMC Microbiol       Date:  2009-09-14       Impact factor: 3.605

9.  Differences in phagocytosis susceptibility in Haemophilus parasuis strains.

Authors:  Alexandre Olvera; Maria Ballester; Miquel Nofrarías; Marina Sibila; Virginia Aragon
Journal:  Vet Res       Date:  2009-02-26       Impact factor: 3.683

  9 in total

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