Association of Actinobacillus pleuropneumoniae Capsular Polysaccharide with Virulence in Pigs

ABSTRACT The capsular polysaccharide (CP) of Actinobacillus pleuropneumoniae is required for virulence of the bacteria in swine. However, a molecular investigation of whether the type or quantity of CP affects A. pleuropneumoniae virulence has not been reported. To initiate this investigation, a DNA region downstream of conserved genes required for CP export in A. pleuropneumoniae serotype 1 was cloned and sequenced. Three open reading frames, designated cps1A, cps1B, and cps1C, were identified that had amino acid homology to bacterial carbohydrate biosynthesis genes. A kanamycin resistance cassette (Kanr) was inserted into a 750-bp deletion spanning cps1AB or into a 512-bp deletion in cps1B only, and the constructs were cloned in a suicide vector. The Kanr gene was then transferred into the chromosome of strain 4074 by homologous recombination to produce strain 4074Δcps1N and strain 4074Δcps1B, respectively. Strain 4074Δcps1N produced no detectable CP, but strain 4074Δcps1B made 15% of the serotype 1 CP made by the parent strain, 4074, as determined by enzyme-linked immunosorbent assay and precipitation of free CP. The cps1ABC genes of strain 4074 and the cps5ABC and cps5ABCDE genes of serotype 5a strain J45 were cloned into the shuttle vector pLS88 and electroporated into 4074Δcps1N to produce 4074Δcps1N(pABcps101), 4074Δcps1N(pJMLcps53), and 4074Δcps1N(pABcps55), respectively. Strain 4074Δcps1N(pABcps101) produced about 33% of the serotype 1 CP produced by strain 4074. Strains 4074Δcps1N(pJMLcps53) and 4074Δcps1N(pABcps55) produced serotype 5a CP in similar quantity or in fourfold excess, respectively, to that produced by strain 4074. With intratracheal challenge in pigs at similar dosages, the order of virulence of strains producing serotype 1 CP (assessed by mortality, lung consolidation, hemorrhage, and fibrinous pleuritis) was the following: strain 4074 > strain 4074Δcps1N(pABcps101) ≥ strain 4074Δcps1N > strain 4074Δcps1B. Strain 4074Δcps1N(pJMLcps53) was less virulent than strain 4074Δcps1N(pABcps55). However, both strains produced serotype 5a CP in similar or greater quantities than was observed for production of serotype 1 CP by the parent strain, 4074, but were less virulent than the parent strain. Therefore, the amount of serotype 1 or 5a CP produced by isogenic strains of A. pleuropneumoniae correlated with the virulence of the bacteria in pigs. However, virulence was also influenced by the type of CP produced or by its mechanism of expression.

[1]  J. Harel,et al.  Isolation and characterization of a capsule-deficient mutant of Actinobacillus pleuropneumoniae serotype 1. , 2000, Microbial pathogenesis.

[2]  A. Rycroft,et al.  Complement resistance in Actinobacillus (Haemophilus) pleuropneumoniae infection of swine. , 1990, American journal of veterinary research.

[3]  P. Kuhnert,et al.  Characterization of apxIVA, a new RTX determinant of Actinobacillus pleuropneumoniae. , 1999, Microbiology.

[4]  T. Meyer,et al.  Molecular characterization and expression in Escherichia coli of the gene complex encoding the polysaccharide capsule of Neisseria meningitidis group B. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[5]  P. Anderson,et al.  Virulence properties and protective efficacy of the capsular polymer of Haemophilus (Actinobacillus) pleuropneumoniae serotype 5 , 1988, Infection and immunity.

[6]  B. Barrell,et al.  Massive gene decay in the leprosy bacillus , 2001, Nature.

[7]  The kdsA gene coding for 3-deoxy-D-manno-octulosonic acid 8-phosphate synthetase is part of an operon in Escherichia coli , 1987, Molecular and General Genetics MGG.

[8]  M. Gottschalk,et al.  Detection of Actinobacillus pleuropneumoniae in the porcine upper respiratory tract as a complement to serological tests. , 1993, Canadian journal of veterinary research = Revue canadienne de recherche veterinaire.

[9]  D. Williams,et al.  Experimental reproduction of acute lesions of porcine pleuropneumonia with a haemolysin-deficient mutant of Actinobacillus pleuropneumoniae , 1991, Veterinary Record.

[10]  J R Saunders,et al.  Haemophilus pleuropneumoniae infection in swine: a review. , 1983, Journal of the American Veterinary Medical Association.

[11]  P. Willson,et al.  Characterization of a multiple antibiotic resistance plasmid from Haemophilus ducreyi , 1989, Antimicrobial Agents and Chemotherapy.

[12]  D. K. Hawley,et al.  Compilation and analysis of Escherichia coli promoter DNA sequences. , 1983, Nucleic acids research.

[13]  T. Inzana,et al.  Detection and Identification ofActinobacillus pleuropneumoniae Serotype 5 by Multiplex PCR , 1998, Journal of Clinical Microbiology.

[14]  J. Harel,et al.  Isolation and characterization of mini-Tn10 lipopolysaccharide mutants of Actinobacillus pleuropneumoniae serotype 1. , 1999, Canadian journal of microbiology.

[15]  J. Brisson,et al.  Structural characteristics of the antigenic capsular polysaccharides and lipopolysaccharides involved in the serological classification of Actinobacillus (Haemophilus) pleuropneumoniae strains , 1990 .

[16]  J. Boyce,et al.  Role of Capsule in the Pathogenesis of Fowl Cholera Caused by Pasteurella multocida Serogroup A , 2001, Infection and Immunity.

[17]  P. Langford,et al.  Actinobacillus pleuropneumoniae: pathobiology and pathogenesis of infection. , 2002, Microbes and infection.

[18]  M. Jacques,et al.  Electron microscopic examination of capsular material from various serotypes of Actinobacillus pleuropneumoniae , 1988, Journal of bacteriology.

[19]  H. van den Bosch,et al.  Proposal of a new serovar of Actinobacillus pleuropneumoniae: serovar 15. , 2002, Veterinary microbiology.

[20]  E. Moxon,et al.  The Haemophilus influenzae capsulation gene cluster: a compound transposon , 1991, Molecular microbiology.

[21]  T. Inzana,et al.  Identification and Characterization of a DNA Region Involved in the Export of Capsular Polysaccharide by Actinobacillus pleuropneumoniae Serotype 5 a , 1997 .

[22]  T. Inzana,et al.  Characterization of a non-hemolytic mutant of Actinobacillus pleuropneumoniae serotype 5: role of the 110 kilodalton hemolysin in virulence and immunoprotection. , 1991, Microbial pathogenesis.

[23]  W. J. Dower,et al.  High efficiency transformation of E. coli by high voltage electroporation , 1988, Nucleic Acids Res..

[24]  P. Berche,et al.  Transposon mutagenesis in Actinobacillus pleuropneumoniae with a Tn10 derivative , 1993, Journal of bacteriology.

[25]  K. Mittal,et al.  Grouping of Actinobacillus pleuropneumoniae strains of serotypes 1 through 12 on the basis of their virulence in mice. , 1990, Veterinary microbiology.

[26]  福安 嗣昭,et al.  豚胸膜肺炎由来 Actinobacillus pleuropneumoniae の血清型と薬剤感受性 , 1996 .

[27]  T. Inzana,et al.  Identification and characterization of a DNA region involved in the export of capsular polysaccharide by Actinobacillus pleuropneumoniae serotype 5a , 1997, Infection and immunity.

[28]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[29]  W. L. Steffens,et al.  Identification and localization of surface sialylated glycoconjugates in Actinobacillus pleuropneumoniae by direct enzyme-colloidal gold cytochemistry. , 1990, Veterinary microbiology.

[30]  D. Reimer,et al.  Molecular investigation of the role of ApxI and ApxII in the virulence of Actinobacillus pleuropneumoniae serotype 5. , 1995, Microbial pathogenesis.

[31]  Inzana Tj Capsules and virulence in the HAP group of bacteria. , 1990 .

[32]  B. Barrell,et al.  Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.

[33]  T. Inzana Simplified procedure for preparation of sensitized latex particles to detect capsular polysaccharides: application to typing and diagnosis of Actinobacillus pleuropneumoniae , 1995, Journal of clinical microbiology.

[34]  T. Inzana,et al.  Safety, stability, and efficacy of noncapsulated mutants of Actinobacillus pleuropneumoniae for use in live vaccines , 1993, Infection and immunity.

[35]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[36]  T. Inzana Capsules and virulence in the HAP group of bacteria. , 1990, Canadian journal of veterinary research = Revue canadienne de recherche veterinaire.

[37]  M. Kostrzynska,et al.  Analysis of the Capsule Biosynthetic Locus ofMannheimia (Pasteurella)haemolytica A1 and Proposal of a Nomenclature System , 2001, Infection and Immunity.

[38]  J. Vázquez-Boland,et al.  The RTX haemolysins ApxI and ApxII are major virulence factors of the swine pathogen Actinobacillus pleuropneumoniae: evidence from mutational analysis , 1994, Molecular microbiology.

[39]  F. Haesebrouck,et al.  Actinobacillus pleuropneumoniae RTX-toxins: uniform designation of haemolysins, cytolysins, pleurotoxin and their genes. , 1993, Journal of general microbiology.

[40]  J. MacInnes,et al.  Characterization of an attenuated strain of Actinobacillus pleuropneumoniae, serotype 1. , 1990, American journal of veterinary research.

[41]  D. Boyd,et al.  Comparative virulence of porcine Haemophilus bacteria. , 1985, Canadian journal of comparative medicine : Revue canadienne de medecine comparee.

[42]  A. J. Barr,et al.  SAS user's guide , 1979 .

[43]  E. Moxon,et al.  Region II of the Haemophilus influenzae Type b capsulation locus as involved in serotype‐specific polysaccharide synthesis , 1995, Molecular microbiology.

[44]  A. Jensen,et al.  Morphological and biochemical comparison of virulent and avirulent isolates of Haemophilus pleuropneumoniae serotype 5 , 1986, Infection and immunity.

[45]  T. Inzana,et al.  Cloning and Mutagenesis of a Serotype-Specific DNA Region Involved in Encapsulation and Virulence of Actinobacillus pleuropneumoniae Serotype 5a: Concomitant Expression of Serotype 5a and 1 Capsular Polysaccharides in Recombinant A. pleuropneumoniae Serotype 1 , 1998, Infection and Immunity.

[46]  E. Southern Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.

[47]  T. Inzana,et al.  Resistance of Actinobacillus pleuropneumoniae to bactericidal antibody and complement is mediated by capsular polysaccharide and blocking antibody specific for lipopolysaccharide. , 1994, Journal of immunology.

[48]  S. Hammerschmidt,et al.  Molecular analysis of the biosynthesis pathway of the α‐2,8 polysialic acid capsule by Neisseria meningitidls serogroup B , 1994, Molecular microbiology.

[49]  G. Boulnois,et al.  Common organization of gene clusters for production of different capsular polysaccharides (K antigens) in Escherichia coli , 1988, Journal of bacteriology.

[50]  T. Inzana,et al.  Serotype specificity and immunogenicity of the capsular polymer of Haemophilus pleuropneumoniae serotype 5 , 1987, Infection and immunity.

[51]  J. Shine,et al.  The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[52]  K. Bousset,et al.  Evidence for a common molecular origin of the capsule gene loci in Gram‐negative bacteria expressing group II capsular polysaccharides , 1991, Molecular microbiology.

[53]  A. Collmer,et al.  An nptI-sacB-sacR cartridge for constructing directed, unmarked mutations in gram-negative bacteria by marker exchange-eviction mutagenesis. , 1987, Gene.

[54]  A. Rycroft,et al.  Phagocytosis by pig alveolar macrophages of Actinobacillus pleuropneumoniae serotype 2 mutant strains defective in haemolysin II (ApxII) and pleurotoxin (ApxIII). , 1994, Microbiology.

[55]  W. Vann,et al.  Genetic and molecular analyses of Escherichia coli K1 antigen genes , 1984, Journal of bacteriology.