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. 2004 May;186(10):2909–2920. doi: 10.1128/JB.186.10.2909-2920.2004

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Description Reference
Serovar Typhi strains
    IMSS-1 Mexican clinical isolate; 9,12, d:-, Vi 42
    81 Serovar Typhi ΔompB::km isogenic IMSS-1 derivative 31
    IMSS-40 Serovar Typhi ΔompR::km isogenic IMSS-1 derivative This study
    IMSSTN103 Serovar Typhi isogenic IMSS-1 derivative containing a Tn10::Cm insertion 160 bp upstream of the first ATG and 60 bp downstream of the promoter for the leuO gene This study
Plasmids
    pFM413S2 pBR322-derived plasmid, containing the whole structural ompS2 gene plus its 5′ regulatory region, up to 413 bp upstream of the transcriptional start point This study
    pFM97S2 pBR322-derivative, containing the ompS2 gene plus the regulatory region up to position −97 This study
    pFM413 to 34 series pMC1871-derived plasmids containing translational fusions of the ompS2 5′ regulatory region, up to 413 to 34 bp upstream of the transcriptional start point, to the lacZ reporter gene This study
    pMPM-A3 p15A-derived vector (Apr), with a multiple cloning site 32
    pFM800TL pMPMA-3-derived plasmid containing the serovar Typhi leuO gene together with Tn10 inserted in the upstream region This study
    pFMTrcleuO pFMTrc12 (p15A1 lacI trcp Apr)-derived plasmid containing serovar Typhi leuO This study
    pKD46 Red recombinase expression plasmid (Apr) 10
    pKD4 Template plasmid for gene inactivation with Kmr 10