Literature DB >> 12568330

The role of Bacteroides conjugative transposons in the dissemination of antibiotic resistance genes.

G Whittle1, N B Shoemaker, A A Salyers.   

Abstract

Investigations into the mechanisms of antibiotic resistance gene transfer utilized by Bacteroides species have led to a greater understanding of how bacteria transfer antibiotic resistance genes, and what environmental stimuli promote such horizontal transfer events. Although Bacteroides spp. harbor a variety of transmissible elements that are involved in the dissemination of antibiotic resistance genes, it is one particular class of elements, the conjugative transposons, that are responsible for most of the resistance gene transfer in Bacteroides. The potential for Bacteroides conjugative transposons to transfer antibiotic resistance genes extends beyond those genes carried by the conjugative transposon itself, because Bacteroides conjugative transposons are able to mobilize coresident plasmids in trans and in cis, and also stimulate the excision and transfer of unlinked integrated elements called mobilizable transposons. These characteristics of conjugative transposons alone have significant implications for the ecology and spread of antibiotic resistance genes, and in terms of biotechnology. A novel feature of the most widespread family of Bacteroides conjugative transposons, the CTnDOT/ERL family, is that their transfer is stimulated 100- to 1000-fold by low concentrations of tetracycline. This is significant because the use of antibiotics not only selects for resistant Bacteroides strains, but also stimulates their transfer. Other Bacteroides conjugative transposons do not require any induction to stimulate transfer, and hence appear to transfer constitutively. The constitutively transferring elements characterized so far appear to have a broader host range than the CTnDOT/ERL family of conjugative transposons, and the prevalence of these elements is on the increase. Since these constitutively transferring elements do not require induction by antibiotics to stimulate transfer, they have the potential to become as pervasive as the CTnDOT/ERL family of conjugative transposons.

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Year:  2002        PMID: 12568330     DOI: 10.1007/s000180200004

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  62 in total

1.  Formation of SXT tandem arrays and SXT-R391 hybrids.

Authors:  Vincent Burrus; Matthew K Waldor
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

2.  Characterization of the Bacteroides CTnDOT regulatory protein RteC.

Authors:  Jiyeon Park; Abigail A Salyers
Journal:  J Bacteriol       Date:  2010-10-29       Impact factor: 3.490

Review 3.  Integrative and conjugative elements: mosaic mobile genetic elements enabling dynamic lateral gene flow.

Authors:  Rachel A F Wozniak; Matthew K Waldor
Journal:  Nat Rev Microbiol       Date:  2010-07-05       Impact factor: 60.633

4.  Regulation of excision genes of the Bacteroides conjugative transposon CTnDOT.

Authors:  Kyung Moon; Nadja B Shoemaker; Jeffrey F Gardner; Abigail A Salyers
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

5.  Integration and excision of a newly discovered bacteroides conjugative transposon, CTnBST.

Authors:  Neil A Wesslund; Gui-Rong Wang; Bo Song; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2006-11-22       Impact factor: 3.490

6.  A bacteroides conjugative transposon, CTnERL, can transfer a portion of itself by conjugation without excising from the chromosome.

Authors:  Gabrielle Whittle; Nathan Hamburger; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

7.  Analysis of the zinc finger domain of TnpA, a DNA targeting protein encoded by mobilizable transposon Tn4555.

Authors:  Melissa K Bacic; Jinesh C Jain; Anita C Parker; C Jeffrey Smith
Journal:  Plasmid       Date:  2007-01-03       Impact factor: 3.466

8.  Regulation of a Bacillus subtilis mobile genetic element by intercellular signaling and the global DNA damage response.

Authors:  Jennifer M Auchtung; Catherine A Lee; Rita E Monson; Alisa P Lehman; Alan D Grossman
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-16       Impact factor: 11.205

9.  Interactions of NBU1 IntN1 and Orf2x proteins with attachment site DNA.

Authors:  Margaret M Wood; Lara Rajeev; Jeffrey F Gardner
Journal:  J Bacteriol       Date:  2013-10-04       Impact factor: 3.490

10.  Identification of a new ribosomal protection type of tetracycline resistance gene, tet(36), from swine manure pits.

Authors:  Gabrielle Whittle; Terence R Whitehead; Nathan Hamburger; Nadja B Shoemaker; Michael A Cotta; Abigail A Salyers
Journal:  Appl Environ Microbiol       Date:  2003-07       Impact factor: 4.792

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