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. 2015 Jun 3;197(13):2171–2178. doi: 10.1128/JB.02455-14

TABLE 2.

Chloramphenicol selection pressure assaysa

Integron Cm concn (mg/liter) on day:
Level of gene cassette rearrangementsd
1 2 3 4 5
Integrons 1S (initial Cm MIC: 32 mg/liter)
    p1S (PcS, IntI1R32_N39) 50 75 100 300 400 +
    p1S + pBad-intI1*P32_H39 100 250 400 +
    p1S + pBad-intI1*R32_H39 100 300 400 +++
    p1S + pBad-intI1*R32_N39b 100 300 400 +
    p1SLc 100 150 400 +
    p1SintI1Y312F 50 75 100 150
Integrons 1W (initial Cm MIC: 8 mg/liter)
    p1W (PcW, IntI1R32_H39) 5 5 15 75 +
    p1W + pBad-intI1*P32_H39 ND ND ND ND ND ND
    p1W + pBad-intI1*R32_H39b 5 10 75 +++
    p1W + pBad-intI1*R32_N39 ND ND ND ND ND ND
    p1WLc 5 15 60 +
Integrons 1WTGN-10 (initial Cm MIC: 16 mg/liter)
    p1WTGN-10 (PcWTGN-10, IntI1P32_H39) 25 25 100 250 350 +
    p1WTGN-10 + pBad-intI1*P32_H39b 25 100 250 350 +
    p1WTGN-10 + pBad-intI1*R32_H39 50 150 350 +++
    p1WTGN-10 + pBad-intI1*R32_N39 ND ND ND ND ND ND
    p1WTGN-10Lc 25 50 300 +
a

Values indicate Cm concentrations reached in BHI broth each day of the protocol using DH5α strains. The native integron organization, without intI1 overexpression, and its corresponding values are presented in bold. Each experiment was performed at least 3 times. ND, not determined.

b

intI1 overexpression was obtained with the same integrase as those present in the synthetic integron.

c

“L” indicates a mutated LexA-binding site.

d

To locate the position of the catB9 gene cassette within the integron, 100 colonies were analyzed each day by PCR and sequencing. Symbols: +, single rearrangement with integron intI1-aac(6′)-Ib-catB9; +++, multiple rearrangements; −, no rearrangement.