Literature DB >> 12061643

Location of increased serum survival gene and selected virulence traits on a conjugative R plasmid in an avian Escherichia coli isolate.

Timothy J Johnson1, Catherine W Giddings, Shelley M Horne, Penelope S Gibbs, Richard E Wooley, Jerod Skyberg, Pam Olah, Ronda Kercher, Julie S Sherwood, Steven L Foley, Lisa K Nolan.   

Abstract

Avian colibacillosis is a costly disease for the poultry industry. The mechanisms of virulence employed by the etiologic agent of this disease remain ill defined. However, accumulated evidence suggests that complement resistance and the presence of the increased serum survival gene (iss) in an avian Escherichia coli isolate may be indicative of its ability to cause disease. This association of iss with the E. coli implicated in avian disease may mean that iss and/or, perhaps, the genes associated with it are important contributors to avian E. coli virulence. For this reason, we have begun a search for iss's location in the bacterial genome. Thus far, iss in an avian E coli isolate has been localized to a conjugative R plasmid and estimated to be about 100 kilobase (kb) in size, encoding resistance to tetracycline and ampicillin. Hybridization studies have revealed that this plasmid contains sequences with homology to tsh, a gene associated with virulence of avian E coli; intI 1, a gene encoding the integrase of Class 1 integrons; and certain genes of the aerobactin- and CoIV-encoding operons. Sequences homologous to merA, a gene of the mercury resistance operon, were not identified on this R plasmid. This plasmid, when transferred into an avirulent, recipient strain by conjugation, enhanced the transconjugant's resistance to complement but not its virulence, in spite of the plasmid's possession of several putative virulence genes and traits. Such results may reflect the multifactorial nature of virulence, the degree of the recipient's impairment for virulence, or an inability of the embryo assay used here to detect this plasmid's contribution to virulence. Additionally, this plasmid contains genes encoding antimicrobial resistances, which may provide a selective advantage to virulent E. coli in the production environment. Further study will be needed to determine whether this plasmid is widespread among virulent E. coli and to ascertain the implications that this link between virulence and antimicrobial resistance genes may have for poultry management.

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Year:  2002        PMID: 12061643     DOI: 10.1637/0005-2086(2002)046[0342:LOISSG]2.0.CO;2

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  23 in total

1.  Plasmid replicon typing of commensal and pathogenic Escherichia coli isolates.

Authors:  Timothy J Johnson; Yvonne M Wannemuehler; Sara J Johnson; Catherine M Logue; David G White; Curt Doetkott; Lisa K Nolan
Journal:  Appl Environ Microbiol       Date:  2007-02-02       Impact factor: 4.792

2.  DNA sequence and comparative genomics of pAPEC-O2-R, an avian pathogenic Escherichia coli transmissible R plasmid.

Authors:  Timothy J Johnson; Kylie E Siek; Sara J Johnson; Lisa K Nolan
Journal:  Antimicrob Agents Chemother       Date:  2005-11       Impact factor: 5.191

3.  Complete DNA sequence of a ColBM plasmid from avian pathogenic Escherichia coli suggests that it evolved from closely related ColV virulence plasmids.

Authors:  Timothy J Johnson; Sara J Johnson; Lisa K Nolan
Journal:  J Bacteriol       Date:  2006-08       Impact factor: 3.490

4.  In Vivo Transmission of an IncA/C Plasmid in Escherichia coli Depends on Tetracycline Concentration, and Acquisition of the Plasmid Results in a Variable Cost of Fitness.

Authors:  Timothy J Johnson; Randall S Singer; Richard E Isaacson; Jessica L Danzeisen; Kevin Lang; Kristi Kobluk; Bernadette Rivet; Klaudyna Borewicz; Jonathan G Frye; Mark Englen; Janet Anderson; Peter R Davies
Journal:  Appl Environ Microbiol       Date:  2015-03-13       Impact factor: 4.792

5.  Characterization of the contribution to virulence of three large plasmids of avian pathogenic Escherichia coli chi7122 (O78:K80:H9).

Authors:  Melha Mellata; Keith Ameiss; Hua Mo; Roy Curtiss
Journal:  Infect Immun       Date:  2010-01-19       Impact factor: 3.441

Review 6.  Role of antimicrobial selective pressure and secondary factors on antimicrobial resistance prevalence in Escherichia coli from food-producing animals in Japan.

Authors:  Kazuki Harada; Tetsuo Asai
Journal:  J Biomed Biotechnol       Date:  2010-06-02

Review 7.  Pathogenomics of the virulence plasmids of Escherichia coli.

Authors:  Timothy J Johnson; Lisa K Nolan
Journal:  Microbiol Mol Biol Rev       Date:  2009-12       Impact factor: 11.056

8.  Characterization of Escherichia coli isolates incriminated in colisepticaemia in mink.

Authors:  R J Tibbetts; D G White; N W Dyer; C W Giddings; L K Nolan
Journal:  Vet Res Commun       Date:  2003-07       Impact factor: 2.459

9.  Conjugal transfer of a virulence plasmid in the opportunistic intracellular actinomycete Rhodococcus equi.

Authors:  V N Tripathi; W C Harding; J M Willingham-Lane; M K Hondalus
Journal:  J Bacteriol       Date:  2012-10-05       Impact factor: 3.490

10.  Insights into the environmental resistance gene pool from the genome sequence of the multidrug-resistant environmental isolate Escherichia coli SMS-3-5.

Authors:  W Florian Fricke; Meredith S Wright; Angela H Lindell; Derek M Harkins; Craig Baker-Austin; Jacques Ravel; Ramunas Stepanauskas
Journal:  J Bacteriol       Date:  2008-08-15       Impact factor: 3.490

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