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Infection and Immunity, September 1999, p. 4376-4382, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Truncated Surface Protective Antigen (SpaA) of Erysipelothrix rhusiopathiae Serotype 1a Elicits Protection against Challenge with Serotypes 1a and 2b in Pigs

Yumiko Imada,* Noriko Goji, Hitoshi Ishikawa, Masato Kishima, and Tsutomu Sekizaki

National Institute of Animal Health, Tsukuba, Ibaraki 305-0856, Japan

Received 4 March 1999/Returned for modification 14 May 1999/Accepted 1 June 1999

Erysipelothrix rhusiopathiae is a causal agent of swine erysipelas, which is of economic importance in the swine industry by virtue of causing acute septicemia, chronic arthritis, and endocarditis. However, little is known about the genetic properties of its protective antigens. Recently, a surface protective antigen (SpaA) gene was identified from serotype 2 in a mouse model. We cloned spaA from virulent strain Fujisawa (serotype 1a) and determined that the N-terminal 342 amino acids without C-terminal repeats of 20 amino acids have the ability to elicit protection in mice. Fusions of 342 amino acids of Fujisawa SpaA and histidine hexamer (HisSpa1.0) protected pigs against challenge with both serotype 1 and serotype 2, the most important serotypes in the swine industry. Pigs immunized with HisSpa1.0 reacted well with both HisSpa1.0 and intact SpaA by enzyme-linked immunosorbent assay and immunoblotting. Serum collected at the time of challenge from a pig immunized with HisSpa1.0 markedly enhanced the in vitro phagocytic and killing activity of pig neutrophils against the bacteria. DNA sequences of protective regions of spaA genes from five strains of serotypes 1 and 2 were almost identical. The full DNA sequences also seemed to be conserved among strains of all 12 serotype reference strains harboring the spaA gene by restriction fragment length polymorphism analysis of PCR products. These results indicates that SpaA is a common protective antigen of serotypes 1 and 2 of E. rhusiopathiae in swine and will be a useful tool for development of new types of vaccines and diagnostic tools for effective control of the disease.


* Corresponding author. Mailing address: National Institute of Animal Health, Kannondai 3-1-1, Tsukuba, Ibaraki 305-0856, Japan. Phone: 0298-38-7873. Fax: 0298-38-7854. E-mail: yumima{at}niah.affrc.go.jp.


Infection and Immunity, September 1999, p. 4376-4382, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Nagai, S., To, H., Kanda, A. (2008). Differentiation of Erysipelothrix rhusiopathiae strains by nucleotide sequence analysis of a hypervariable region in the spaA gene: discrimination of a live vaccine strain from field isolates. jvdi 20: 336-342 [Abstract] [Full Text]  
  • To, H., Nagai, S. (2007). Genetic and Antigenic Diversity of the Surface Protective Antigen Proteins of Erysipelothrix rhusiopathiae. CVI 14: 813-820 [Abstract] [Full Text]  
  • Imada, Y., Mori, Y., Daizoh, M., Kudoh, K., Sakano, T. (2003). Enzyme-Linked Immunosorbent Assay Employing a Recombinant Antigen for Detection of Protective Antibody against Swine Erysipelas. J. Clin. Microbiol. 41: 5015-5021 [Abstract] [Full Text]