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Environmental Microbiology

Hemolytic Porcine Intestinal Escherichia coli without Virulence-Associated Genes Typical of Intestinal Pathogenic E. coli

Peter Schierack, Joerg Weinreich, Christa Ewers, Babila Tachu, Bryon Nicholson, Stefanie Barth
Peter Schierack
1Fachbereich Bio-, Chemie- und Verfahrenstechnik, Hochschule Lausitz, Senftenberg, Germany
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  • For correspondence: peter.schierack@hs-lausitz.de
Joerg Weinreich
1Fachbereich Bio-, Chemie- und Verfahrenstechnik, Hochschule Lausitz, Senftenberg, Germany
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Christa Ewers
2Institut f�r Mikrobiologie und Tierseuchen, Fachbereich Veterin�rmedizin, Freie Universit�t Berlin, Berlin, Germany
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Babila Tachu
3Abteilung Neuroproteomics, Max-Delbr�ck-Centrum f�r Molekulare Medizin, Berlin, Germany
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Bryon Nicholson
4Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa
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Stefanie Barth
5Institut f�r Hygiene und Infektionskrankheiten der Tiere, Justus-Liebig-Universit�t Giessen, Giessen, Germany
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DOI: 10.1128/AEM.05289-11
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    Fig. 1.

    Flowchart of sampling and characterization of E. coli isolates in this study. Clinically healthy pigs were from production units in Berlin, Brandenburg, Lower Saxony, Saxony, Thuringia, and Schleswig-Holstein, Germany. Diseased pigs were from production units in North Rhine-Westphalia, Hesse, Schleswig-Holstein, Bavaria, Lower Saxony, and Baden-Wuerttemberg, Germany, and Styria and Lower Austria, Austria. Asterisks indicate that the remaining 59 (out of 121) hemolytic E. coli isolates were not available as cultures and therefore could not be included in further analysis.

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    Fig. 2.

    Presence or absences of eVAGs in 99 porcine intestinal hemolytic E. coli isolates in this study. n, number of isolates per pattern. Solid squares indicate the presence of the respective gene, and open squares indicate its absence.

Tables

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  • Table 1.

    Occurrence of eVAGs in porcine intestinal hemolytic E. coli and comparison to data from an already published study on porcine intestinal nonhemolytic E. colia,b

    Gene(s) or operonDescription% of positive isolatesc
    Hemolytic E. colidNonhemolytic E. coli from healthy pigs (n = 65)b
    Diseased pigs (n = 62)Healthy pigs (n = 37)Total (n = 99)
    Adhesins
        afa/draBAfimbrial/Dr antigen-specific adhesin05.42.00
        fimCType 1 fimbriae (d-mannose-specific adhesin)98.497.398.080.0
        hraHeat-resistant agglutinin25.8*54.1*36.410.8
        ihaIron-regulated-gene homologue adhesin0000
        papCPilus associated with pyelonephritis21.037.827.30
        sfa/focCDS fimbriae (sialic acid-specific) and F1C fimbriae17.732.423.20
        tshbTemp-sensitive hemagglutinin53.2*18.9*40.46.2
        csgACurli fiber-encoding gene90.391.990.0NT
        matMeningitis-associated and temp-regulated fimbriae88.589.588.976.9
    Iron acquisition
        chuAHeme receptor gene (E. coli heme utilization)16.1*40.5*25.310.8
        fyuAFerric Yersinia uptake (yersiniabactin receptor)17.7*48.6*30.016.9
        ireAIron-responsive element (putative catecholate siderophore receptor)6.58.17.10
        iroNbCatecholate siderophore (salmochelin) receptor19.4*51.4*31.310.8
        irp2Iron-repressible protein (yersiniabactin synthesis)14.5*40.5*24.216.9
        iucDAerobactin synthesis9.724.315.210.8
        sitD (chromosomal)Salmonella iron transport system gene9.721.614.11.5
        sitD (episomal)Salmonella iron transport system gene9.724.315.29.2
        iutAAerobactin receptor25.827.026.3NT
    Protectins/serum resistance
        issIncreased serum survival22.616.220.210.8
        neuCK1 capsular polysaccharide3.202.00
        kpsMTIIGroup II capsule antigens32.335.133.39.2
        ompAOuter membrane protein10010010098.5
        traTTransfer protein85.5*64.9*77.860.0
    Toxins
        astAEAST-1 (heat-stable cytotoxin associated with enteroaggregative E. coli)1.6*18.9*8.112.3
        satSecreted autotransporter toxin0000
        hlyAHemolysin A98.410099.00
        cnf1/2Cytotoxic necrotizing factor16.124.319.2NT
    Invasins
        gimBGenetic island associated with newborn meningitis3.22.73.00
        ibeAInvasion of brain endothelium3.2*18.9*9.14.6
        tiaToxigenic invasion locus in ETECe isolates02.71.00
    Miscellaneous
        cvi/cvaStructural genes of colicin V operon (microcin ColV)8.110.89.110.8
        picSerine protease autotransporter11.316.213.11.5
        malXPathogenicity-associated island marker CFT07314.527.019.20
    • ↵a Primer references are cited in the study by Ewers et al. (4).

    • ↵b Schierack et al. (10).

    • ↵c *, differences between hemolytic isolates from diseased pigs and hemolytic isolates from clinically healthy pigs are statistically significant (P < 0.05). NT, not tested.

    • ↵d This study.

    • ↵e ETEC, enterotoxigenic E. coli.

Additional Files

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    Files in this Data Supplement:

    • Supplemental file 1 - Pig production units with clinically healthy pigs and occurrence of hemolytic E. coli (Table S1); eVAGs in porcine intestinal hemolytic E. coli without iVAGs according to their phylogenetic affiliation (Table S2).
      MS Word document, 127K.
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Hemolytic Porcine Intestinal Escherichia coli without Virulence-Associated Genes Typical of Intestinal Pathogenic E. coli
Peter Schierack, Joerg Weinreich, Christa Ewers, Babila Tachu, Bryon Nicholson, Stefanie Barth
Applied and Environmental Microbiology Nov 2011, 77 (23) 8451-8455; DOI: 10.1128/AEM.05289-11

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Hemolytic Porcine Intestinal Escherichia coli without Virulence-Associated Genes Typical of Intestinal Pathogenic E. coli
Peter Schierack, Joerg Weinreich, Christa Ewers, Babila Tachu, Bryon Nicholson, Stefanie Barth
Applied and Environmental Microbiology Nov 2011, 77 (23) 8451-8455; DOI: 10.1128/AEM.05289-11
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