Evaluation of phoP and rpoS mutants of Salmonella enterica serovar Typhi as attenuated typhoid vaccine candidates: virulence and protective immune responses in intranasally immunized mice

Abstract The attenuation and immunoenhancing effects of rpoS and phoPSalmonella enterica serovar strain Typhi (Salmonella typhi) mutants have not been compared. Here, three S. typhi deletion mutants (phoP, rpoS, and rpoS–phoP double mutant) are constructed and these mutants are characterized with re...

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Veröffentlicht in:FEMS immunology and medical microbiology 2007-11, Vol.51 (2), p.310-318
Hauptverfasser: Lee, Hui-Young, Cho, Sun-A., Lee, In-Soo, Park, Jong-Hwan, Seok, Seung-Hyeok, Baek, Min-Won, Kim, Dong-Jae, Lee, Seok-Ho, Hur, Sook-Ji, Ban, Sang-Ja, Lee, Yoo-Kyoung, Han, Yang-Keum, Cho, Young-Keun, Park, Jae-Hak
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Sprache:eng
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Zusammenfassung:Abstract The attenuation and immunoenhancing effects of rpoS and phoPSalmonella enterica serovar strain Typhi (Salmonella typhi) mutants have not been compared. Here, three S. typhi deletion mutants (phoP, rpoS, and rpoS–phoP double mutant) are constructed and these mutants are characterized with respect to invasiveness, virulence, and protective immune response compared with wild-type Ty2. It was found that phoP and phoP–rpoS deletion mutants are less invasive to HT-29 cells than the wild-type Ty2 and the rpoS single-deleted strain. The LD50 of immunized mice was higher for phoP than for rpoS mutants, and the highest for the phoP–rpoS double mutant. In addition, all S. typhi mutants showed an increase in the specific serum IgG levels and T-cell-mediated immunity, and showed equal protection abilities against a wild-type Ty2 challenge after two rounds of immunization in BALB/c mice. It is concluded that phoP genes appear to play a more important role than rpoS genes in both cellular invasion and virulence of S. typhi, but not in immunogenicity in mice. Furthermore, the data indicate that the phoP–rpoS double mutant may show promise as a candidate for an attenuated typhoid vaccine.
ISSN:0928-8244
1574-695X
2049-632X
DOI:10.1111/j.1574-695X.2007.00307.x