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. 2010 Aug 30;78(11):4779–4791. doi: 10.1128/IAI.00678-10

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Description Reference or source
H. ducreyi strains
    35000HP Human-passaged H. ducreyi strain 57
    35000HPΔcpxA 35000HP ΔcpxA::Cmr This study
    35000HPΔcpxR 35000HP ΔcpxR::Cmr 35
E. coli strains
    DH5α F φ80lacZΔM15 Δ(lacZYA-argF)U169recA1endA1hsdR17(rK mK+) phoAsupE44 λthi-1gyrA96relA1 Invitrogen
    TOP10 FmcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74recA1araD139Δ(ara-leu)7697galUgalKrpsLendA1nupG Invitrogen
    HB101 Fthi-1hsdS20(rB mB) supE44recA13ara-14leuB6proA2lacY1galK2rpsL20 (Strr) xyl-5mtl-1 Promega
Plasmids
    pCR2.1 E. coli cloning vector; Ampr Invitrogen
    pML117 pCR2.1 containing a 35000HP cpxA gene with a 1.15-kb deletion This study
    pML118C pML117 with a cat cartridge in the deletion site in cpxA This study
    pLS88 H. ducreyi shuttle vector; Kmr 66
    pML141 pLS88 containing the wild-type 35000HP cpxA gene This study
    pML153 pL141 with the H253Q substitution in CpxA This study
    pML125 pLS88 containing the wild-type 35000HP cpxR gene 35
    pML154 pML125 with the D52A substitution in CpxR This study