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Bacteriophages, Transposons, and Plasmids

Evolution of Microcin V and Colicin Ia Plasmids in Escherichia coli

Anne Jeziorowski, David M. Gordon
Anne Jeziorowski
School of Botany & Zoology, The Australian National University, Canberra, ACT 0200, Australia
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David M. Gordon
School of Botany & Zoology, The Australian National University, Canberra, ACT 0200, Australia
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  • For correspondence: David.Gordon@anu.edu.au
DOI: 10.1128/JB.00243-07
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  • FIG. 1.
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    FIG. 1.

    Maximum-likelihood tree of the 36 Ia nucleotide sequence types detected in E. coli isolates from human and nonhuman vertebrates living in Australia. In each label, the first number is the ST and the number in parentheses is the number of times the ST was observed, followed by the genetic groups of E. coli in which the ST was detected and finally if the ST co-occurred with the microcin V operon in the same strain. Bootstrap values are based on 500 replicates.

Tables

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  • TABLE 1.

    Frequency of E. coli strains encoding colicin Ia, microcin V, or both bacteriocins, together with the predicted fraction of strains encoding both bacteriocins assuming that they randomly associatea

    Source and groupNo. of isolates% Observed % Predicted, colicin Ia and microcin VP > χ2
    Colicin IaMicrocin VColicin Ia and microcin V
    Human
        A904.43.36.61.1<0.001
        B1519.87.82.01.10.575
        B23503.72.37.11.0<0.001
        D1284.72.73.10.4<0.001
    Animal
        A932.21.10<0.10.834
        B12726.21.81.1<0.1<0.001
        B221317.80.12.3<0.1<0.001
        D1126.200
    • ↵ a Data presented are for strains isolated from humans and nonhuman vertebrates living in Australia with respect to the genetic group membership of the strains.

  • TABLE 2.

    Phenotypic and genotypic characteristics of plasmids encoding the bacteriocins colicin Ia and microcin V

    StrainColicin IaMicrocin VfinO STTraY typeIncFIItraTiroNisssitAiutAResistance profilea
    AE008+−10−−−−−−−TMP SXT AM
    CE015+−14R−+−+−−TMP SXT AM S
    PE006+−6−−−−−−−TE
    SE016+−7−−−−−−−AM TE C
    SE017+−20−−−−−−−AM TE C
    AE013+−4F++−−−−TMP SXT S SPT
    CE003+−18F++−−−−TMP AM TE
    AE011−+5F+++++−TMP SXT AM S TE
    CE014−+3F++++++TMP STX
    PE007−+5F+++++−TMP STX S
    SE010−+5F+++++−TMP STX
    H772−+15F++++++TE
    AE016++8F−+++−−TMP STX
    CE004++8−−+++++TMP STX AM S TE K
    CE010++12−−+++++TMP STX AM S TE K
    PE001++8F−+++++TMP STX AM S
    PE002++8F−+++++AM TE
    PE004++5F−++++−TMP
    PE009++19F−+++++TMP STX AM S TE
    H053++8F−+++++TMP SXT AM S
    H070++8F−+++++TMP A S TE
    H073++8F−+++++TMP A S TE
    H111++8F−+++++SXT AM
    H112++8F−+++++AM TE
    H127++11F−+++++AM S TE
    H188++8F−+++++TMP SXT AM S TE K
    H190++8F−+++++TMP AM S TE K
    H461++8F−+++++AM S
    H549++8F−+++++TMP SXT AM S
    H098++13R++++−−S
    H100++9R++++−−TMP STX AM
    H314++1−++++−−AM S
    AE009++17R++++++TMP STX
    AE010++17R++++++TMP STX TE
    SE018++5F+++++−TE C
    • ↵ a AM, ampicillin; C, chloramphenicol; K, kanamycin; S, streptomycin; SXT, sulfisoxazole; TE, tetracycline; TMP, trimethoprim.

  • TABLE 3.

    Nucleotide variation in a 527-bp fragment of the microcin V operon found in this study compared to previously published results (26)a

    VariantbNucleotide at position:
    21442515576105109110111112113114115116117118119120121122131134142143144145146147148149150151152153154155156294295323459
    AF062847 (1)CGTTATGTAATGGGATAGAAAGA---------------GCTA
    H030 (1)GATTATGTAATGGGATAGAAAAA---------------GCTG
    AF062845 (1)GGGCCGATAATGGGATAGAAAAA---------------ATTA
    AF062849 (1)GGGCCGGTAATGGGATAGAAAAA---------------ATTA
    H368 (1)GGGTATGTAATGGGATAGAAAAA---------------GCTG
    H781 (1)GGTTATG--------------AA---------------GCCG
    AF062844 (1)GGTTATGTAATGGGATAGAAAAA---------------GCCG
    ECCVAC (52)GGTTATGTAATGGGATAGAAAAA---------------GCTG
    B177 (1)GGTTATGTAATGGGATAGAAAAG---------------GCTG
    H244 (2)GGTTATGTAATGGGATAGAAAAGTGGGATAAAAAGTAAGCTG
    AF062848 (1)GGTTATGTAATGGGATAGAAAGA---------------GCTA
    • ↵ a Positions 2 to 156 correspond to the 5′ flanking region, positions 294 to 323 correspond to the immunity gene, and position 459 corresponds to the toxin gene.

    • ↵ b The number in parentheses is the number of times the variant was observed.

  • TABLE 4.

    Population differentiation estimates (PhiPT) to determine the extent to which colicin Ia nucleotide sequence variation depended on the host group from which the strains were isolated or whether the strains also encoded microcin V

    ComparisonaPhiPTProbabilityb
    Ia animal vs Ia human0.1010.040
    Ia animal vs IaV animal0.4800.001
    Ia human vs IaV animal0.3860.002
    Ia animal vs IaV human0.2920.001
    Ia human vs IaV human0.1270.014
    IaV animal vs IaV human0.1290.081
    • ↵ a Ia, colicin Ia; V, microcin V; IaV, colicin Ia plus microcin V.

    • ↵ b The probability that a greater PhiPT value could have arisen by chance.

  • TABLE 5.

    Amino acid sequences of the colicin Ia variants detected in this study together with the human or nonhuman vertebrate sources from which the strains were isolated and whether the strains also encode microcin V

    StrainSourceMicrocin VVariantaNucleotide at position:
    4608892109130141169206238241247275284295340346367
    H190Human+3 (1)RGTIGRRHAAVANALATE
    B439Animal+6 (1)RGTMARRHAAVANAPATE
    B313Animal+14 (1)SGTMARRHAAVANALATE
    TA311Animal+16 (1)SGTMARRHAAVANAPATE
    M550Animal+17 (2)SGTMARRYAAVANALATE
    AE016Human+4 (1)RGTMARRHAAVANALATE
    H098Human+5 (1)RGTMARRHAAVANAPASE
    H314Human+6 (7)RGTMARRHAAVANAPATE
    H151Human+14 (12)SGTMARRHAAVANALATE
    H244Human+15 (1)SGTMARRHAAVANAPASE
    PE002Human+16 (1)SGTMARRHAAVANAPATE
    AE008Human−13 (1)SGTMARRHAAVAKAPATE
    CE015Human−15 (1)SGTMARRHAAVANAPASE
    SE017Human−2 (2)RGANGRRHAAVANAPASE
    H730Human−10 (2)RGTNGRRHAAVANAPATE
    H591Human−11 (1)RGTNGRRHAAVANAPVSE
    H556Human−18 (1)SGTNGRQHTAVANAPATE
    H468Human−19 (1)SGTNGRRHAAVANAPASE
    H422Human−21 (1)SGTNGRRHTAVANAPATE
    PE001Human+7 (2)RGTNGRRHAAVANALATE
    H331Human+8 (2)RGTNGRRHAAVANAPASE
    PE004Human+9 (1)RGTNGRRHAAVANAPASK
    TA060Animal−1 (2)RGANGHRHAAVANAPATE
    M411Animal−8 (1)RGTNGRRHAAVANAPASE
    TA026Animal−10 (3)RGTNGRRHAAVANAPATE
    R148Animal−12 (1)RGTNGRRHTAVANAPATE
    R529Animal−20 (1)SGTNGRRHTAIANAPATE
    TA261Animal−21 (3)SGTNGRRHTAVANAPATE
    B564Animal−22 (1)SGTNGRRHTAVANTPATE
    M008Animal−23 (1)SGTNGRRHTAVSNAPATE
    M318Animal−24 (1)SGTNGRRHTVVANAPATE
    M028Animal−25 (1)SVTNGRRHTVVANAPATE
    • ↵ a The number in parentheses is the number of times the variant was observed in that source population and in the presence or absence of microcin V.

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Evolution of Microcin V and Colicin Ia Plasmids in Escherichia coli
Anne Jeziorowski, David M. Gordon
Journal of Bacteriology Sep 2007, 189 (19) 7045-7052; DOI: 10.1128/JB.00243-07

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Evolution of Microcin V and Colicin Ia Plasmids in Escherichia coli
Anne Jeziorowski, David M. Gordon
Journal of Bacteriology Sep 2007, 189 (19) 7045-7052; DOI: 10.1128/JB.00243-07
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KEYWORDS

bacteriocins
colicins
Escherichia coli
Evolution, Molecular
plasmids

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