Cloning and transposon insertion mutagenesis of virulence genes of the 100-kilobase plasmid of Salmonella typhimurium
- 1 December 1988
- journal article
- research article
- Published by American Society for Microbiology in Infection and Immunity
- Vol. 56 (12) , 3262-3271
- https://doi.org/10.1128/iai.56.12.3262-3271.1988
Abstract
We have cloned regions of the 100-kilobase (kb) plasmid, pStSR100, of Salmonella typhimurium SR-11 that confer virulence to plasmid-cured S. typhimurium. Cells carrying recombinant plasmids that conferred virulence were selected by inoculating mice orally with recombinant libraries in virulence plasmid-cured S. typhimurium and harvesting isolates that infected spleens. Three plasmids, pYA401, pYA402, and pYA403, constructed with the cosmid vector pCVD305 conferred wild-type levels of virulence to plasmid-cured S. typhimurium and had a common 14-kb DNA insert sequence. Another recombinant plasmid, pYA422, constructed with the vector pACYC184, conferred to plasmid-cured S. typhimurium a wild-type 50% lethal dose (LD50) level, but mice died more slowly than when infected with wild-type S. typhimurium. Furthermore, pYA422 conferred the ability to cause a higher, but not a wild-type, level of splenic infection on plasmid-cured S. typhimurium. pYA422 had a 3.2-kb insert sequence which mapped to the center of the 14-kb common sequence of the cosmid clones. Transposon Tn5 insertion mutations in pYA403 inhibited virulence to various degrees, and when transduced into the native virulence plasmid of S. typhimurium, these Tn5 insertions decreased virulence to degrees similar to those observed when the Tn5 insertions were present in pYA403. vir-22::Tn5 in pStSR100 greatly lowered infection of spleens relative to unmutagenized virulence plasmid, while vir-26::Tn5 and vir-27::Tn5 lowered splenic infection to lesser degrees. At least three proteins were encoded by pYA403 containing 23 kb of insert sequence and subclone pYA420, containing the 14-kb common insert sequence present in all of the cosmid clones. One of these proteins, with an apparent molecular weight of 28,000, was also encoded by pYA422. The Tn5 insertion that most attenuated virulence, vir-22::Tn5, inhibited synthesis of the 28,000-molecular-weight protein. The vir-22::Tn5 insertion was complemented by recombinant plasmids encoding only the 28,000-molecular-weight protein, suggesting a role of this protein in virulence. However, recombinant plasmids, exemplified by pYA422, that encoded only the 28,000-molecular-weight protein did not confer full virulence.This publication has 28 references indexed in Scilit:
- Physical and genetic mapping of the Salmonella dublin virulence plasmid pSDL2. Relationship to plasmids from other Salmonella strains.Journal of Clinical Investigation, 1988
- A new method for the physical and genetic mapping of large plasmids: application to the localisation of the virulence determinants on the 90 kb plasmid of Salmonella typhimuriumMicrobial Pathogenesis, 1987
- Mediation of Serum Resistance in Salmonella typhimurium by an 11-Kilodalton Polypeptide Encoded by the Cryptic PlasmidThe Journal of Infectious Diseases, 1987
- The Colonization of Peyer's Patches by a Strain of Salmonella typhimurium Cured of the Cryptic PlasmidThe Journal of Infectious Diseases, 1986
- A single genetic locus encoded by Yersinia pseudotuberculosis permits invasion of cultured animal cells by Escherichia coli K-12Nature, 1985
- Evidence for Related Virulence Sequences in Plasmids of Salmonella dublin and Salmonella typhimuriumMicrobiology, 1985
- Nucleotide sequence and exact localization of the neomycin phosphotransferase gene from transposon Tn5Gene, 1982
- Identification of a Sex-factor-affinity Site in E. coli asCold Spring Harbor Symposia on Quantitative Biology, 1981
- A colony bank containing synthetic CoI EI hybrid plasmids representative of the entire E. coli genomeCell, 1976
- A simple method for the large‐scale preparation of sucrose gradientsFEBS Letters, 1972