Literature DB >> 3036772

Facilitated transfer of IncP beta R751 derivatives from the chromosome of Bacteroides uniformis to Escherichia coli recipients by a conjugative Bacteroides tetracycline resistance element.

N B Shoemaker, A A Salyers.   

Abstract

The broad-host-range IncP beta plasmid R751 can mobilize itself from Escherichia coli to Bacteroides spp, but it is not maintained in Bacteroides spp. If R751 carries the Bacteroides transposon Tn4351, it can be integrated into the Bacteroides chromosome. Previously we showed that R751, integrated in the chromosome of Bacteroides uniformis, cannot mobilize itself out of B. uniformis into E. coli or isogenic B. uniformis strains. In this report, we showed that if the Bacteroides conjugative tetracycline resistance element Tcr ERL was coresident with the R751 insertion in B. uniformis, derivatives of R751 were transferred to E. coli, where they were recovered as plasmids. The most common derivatives were R751::Tn4351 and R751::IS4351, but some strains transferred R751 derivatives, containing additional DNA segments ranging in size from 10 to 23 kilobases. These DNA inserts cross-hybridized with chromosomal DNA from B. uniformis which did not carry the Tcr ERL element. Therefore, the inserts appeared to be segments of the wild-type B. uniformis chromosome and were not associated with the Tcr ERL element. The transfer of integrated R751 from B. uniformis was independent of the RecA phenotype of the E. coli recipients and did not appear to be due to transfer of B. uniformis chromosomal DNA, followed by RecA-dependent recombination between homologous IS4351 sequences to form the resultant R751 plasmid derivatives. Consistent with this, no transfer of Tn4351 (associated with the cointegrated R751) from B. uniformis donors to isogenic B. uniformis recipients was detected (< 10(-8)). Our data support the hypothesis that R751 excises from the B. uniformis chromosome by recombination involving flanking Tn4351 or IS4351 sequences and forms nonreplicating circles. The mobilization of these circular forms out of B. uniformis to E.coli is then facilitated by the Tcr ERL element.

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Year:  1987        PMID: 3036772      PMCID: PMC212365          DOI: 10.1128/jb.169.7.3160-3167.1987

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  14 in total

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Authors:  N B Shoemaker; E P Guthrie; A A Salyers; J F Gardner
Journal:  J Bacteriol       Date:  1985-05       Impact factor: 3.490

3.  Expression in Escherichia coli of cryptic tetracycline resistance genes from bacteroides R plasmids.

Authors:  D G Guiney; P Hasegawa; C E Davis
Journal:  Plasmid       Date:  1984-05       Impact factor: 3.466

4.  Homology between clindamycin resistance plasmids in Bacteroides.

Authors:  D G Guiney; P Hasegawa; C E Davis
Journal:  Plasmid       Date:  1984-05       Impact factor: 3.466

5.  Hybridization studies reveal homologies between pBF4 and pBFTM10, Two clindamycin-erythromycin resistance transfer plasmids of Bacteroides fragilis.

Authors:  M J Shimell; C J Smith; F P Tally; F L Macrina; M H Malamy
Journal:  J Bacteriol       Date:  1982-11       Impact factor: 3.490

6.  Genetic organization of the broad-host-range IncP-1 plasmid R751.

Authors:  R J Meyer; J A Shapiro
Journal:  J Bacteriol       Date:  1980-09       Impact factor: 3.490

7.  Natural relationship between bacteroides and flavobacteria.

Authors:  W G Weisburg; Y Oyaizu; H Oyaizu; C R Woese
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

8.  Specific-purpose plasmid cloning vectors. II. Broad host range, high copy number, RSF1010-derived vectors, and a host-vector system for gene cloning in Pseudomonas.

Authors:  M Bagdasarian; R Lurz; B Rückert; F C Franklin; M M Bagdasarian; J Frey; K N Timmis
Journal:  Gene       Date:  1981-12       Impact factor: 3.688

9.  Tn4400, a compound transposon isolated from Bacteroides fragilis, functions in Escherichia coli.

Authors:  N J Robillard; F P Tally; M H Malamy
Journal:  J Bacteriol       Date:  1985-12       Impact factor: 3.490

10.  Construction and characterization of new cloning vehicles. V. Mobilization and coding properties of pBR322 and several deletion derivatives including pBR327 and pBR328.

Authors:  L Covarrubias; L Cervantes; A Covarrubias; X Soberón; I Vichido; A Blanco; Y M Kupersztoch-Portnoy; F Bolivar
Journal:  Gene       Date:  1981 Jan-Feb       Impact factor: 3.688

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  15 in total

1.  A newly discovered Bacteroides conjugative transposon, CTnGERM1, contains genes also found in gram-positive bacteria.

Authors:  Yanping Wang; Gui-Rong Wang; Aikiesha Shelby; Nadja B Shoemaker; Abigail A Salyers
Journal:  Appl Environ Microbiol       Date:  2003-08       Impact factor: 4.792

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

3.  Translational control of tetracycline resistance and conjugation in the Bacteroides conjugative transposon CTnDOT.

Authors:  Yanping Wang; Ella R Rotman; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2005-04       Impact factor: 3.490

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.  The small RNA RteR inhibits transfer of the Bacteroides conjugative transposon CTnDOT.

Authors:  Jillian L Waters; Abigail A Salyers
Journal:  J Bacteriol       Date:  2012-07-20       Impact factor: 3.490

6.  Tetracycline-related transcriptional regulation of the CTnDOT mobilization region.

Authors:  Jillian L Waters; Gui-Rong Wang; Abigail A Salyers
Journal:  J Bacteriol       Date:  2013-09-27       Impact factor: 3.490

7.  Community signalling between Streptococcus gordonii and Porphyromonas gingivalis is controlled by the transcriptional regulator CdhR.

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8.  Characterization of the mobilization region of a Bacteroides insertion element (NBU1) that is excised and transferred by Bacteroides conjugative transposons.

Authors:  L Y Li; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

9.  Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element.

Authors:  N B Shoemaker; G R Wang; A M Stevens; A A Salyers
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

10.  Regulation of a Bacteroides operon that controls excision and transfer of the conjugative transposon CTnDOT.

Authors:  Yanping Wang; Nadja B Shoemaker; Abigail A Salyers
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

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