Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B

An E. coli and K. pneumoniae phenotype resistant to piperacillin/tazobactam has recently emerged. Here, the authors show that hyperproduction of the β-lactamase driving this resistance occurs due to excision and reinsertion of a translocatable unit containing bla TEM-1B, creating a tandem array.

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Autores principales: Alasdair T. M. Hubbard, Jenifer Mason, Paul Roberts, Christopher M. Parry, Caroline Corless, Jon van Aartsen, Alex Howard, Issra Bulgasim, Alice J. Fraser, Emily R. Adams, Adam P. Roberts, Thomas Edwards
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/49781534e05f4b11946b910dc6606509
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spelling oai:doaj.org-article:49781534e05f4b11946b910dc66065092021-12-02T18:51:09ZPiperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B10.1038/s41467-020-18668-22041-1723https://doaj.org/article/49781534e05f4b11946b910dc66065092020-10-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18668-2https://doaj.org/toc/2041-1723An E. coli and K. pneumoniae phenotype resistant to piperacillin/tazobactam has recently emerged. Here, the authors show that hyperproduction of the β-lactamase driving this resistance occurs due to excision and reinsertion of a translocatable unit containing bla TEM-1B, creating a tandem array.Alasdair T. M. HubbardJenifer MasonPaul RobertsChristopher M. ParryCaroline CorlessJon van AartsenAlex HowardIssra BulgasimAlice J. FraserEmily R. AdamsAdam P. RobertsThomas EdwardsNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Alasdair T. M. Hubbard
Jenifer Mason
Paul Roberts
Christopher M. Parry
Caroline Corless
Jon van Aartsen
Alex Howard
Issra Bulgasim
Alice J. Fraser
Emily R. Adams
Adam P. Roberts
Thomas Edwards
Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
description An E. coli and K. pneumoniae phenotype resistant to piperacillin/tazobactam has recently emerged. Here, the authors show that hyperproduction of the β-lactamase driving this resistance occurs due to excision and reinsertion of a translocatable unit containing bla TEM-1B, creating a tandem array.
format article
author Alasdair T. M. Hubbard
Jenifer Mason
Paul Roberts
Christopher M. Parry
Caroline Corless
Jon van Aartsen
Alex Howard
Issra Bulgasim
Alice J. Fraser
Emily R. Adams
Adam P. Roberts
Thomas Edwards
author_facet Alasdair T. M. Hubbard
Jenifer Mason
Paul Roberts
Christopher M. Parry
Caroline Corless
Jon van Aartsen
Alex Howard
Issra Bulgasim
Alice J. Fraser
Emily R. Adams
Adam P. Roberts
Thomas Edwards
author_sort Alasdair T. M. Hubbard
title Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
title_short Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
title_full Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
title_fullStr Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
title_full_unstemmed Piperacillin/tazobactam resistance in a clinical isolate of Escherichia coli due to IS26-mediated amplification of bla TEM-1B
title_sort piperacillin/tazobactam resistance in a clinical isolate of escherichia coli due to is26-mediated amplification of bla tem-1b
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/49781534e05f4b11946b910dc6606509
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