An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state

The cyclic antimicrobial lipopeptide daptomycin (DAP) triggers the LiaFSR membrane stress response pathway in enterococci and many other Gram-positive organisms. LiaR is the response regulator that, upon phosphorylation, binds in a sequence-specific manner to DNA to regulate transcription in respons...

Full description

Autores:
Davlieva, Milya G.
Tovar-Yanez, Angel
DeBruler, Kimberly
Leonard, Paul G.
Zianni, Michael R.
Arias, César A.
Shamoo, Yousif
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/3526
Acceso en línea:
http://hdl.handle.net/20.500.12495/3526
https://doi.org/10.1016/j.jmb.2016.09.016
https://repositorio.unbosque.edu.co
Palabra clave:
Daptomicina
Diagnóstico por imagen
Enterococos resistentes a la vancomicina
LiaR
E. faecium
Response regulator
Rights
openAccess
License
Acceso abierto
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oai_identifier_str oai:repositorio.unbosque.edu.co:20.500.12495/3526
network_acronym_str UNBOSQUE2
network_name_str Repositorio U. El Bosque
repository_id_str
dc.title.spa.fl_str_mv An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
dc.title.translated.spa.fl_str_mv An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
title An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
spellingShingle An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
Daptomicina
Diagnóstico por imagen
Enterococos resistentes a la vancomicina
LiaR
E. faecium
Response regulator
title_short An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
title_full An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
title_fullStr An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
title_full_unstemmed An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
title_sort An adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated state
dc.creator.fl_str_mv Davlieva, Milya G.
Tovar-Yanez, Angel
DeBruler, Kimberly
Leonard, Paul G.
Zianni, Michael R.
Arias, César A.
Shamoo, Yousif
dc.contributor.author.none.fl_str_mv Davlieva, Milya G.
Tovar-Yanez, Angel
DeBruler, Kimberly
Leonard, Paul G.
Zianni, Michael R.
Arias, César A.
Shamoo, Yousif
dc.subject.decs.spa.fl_str_mv Daptomicina
Diagnóstico por imagen
Enterococos resistentes a la vancomicina
topic Daptomicina
Diagnóstico por imagen
Enterococos resistentes a la vancomicina
LiaR
E. faecium
Response regulator
dc.subject.keywords.spa.fl_str_mv LiaR
E. faecium
Response regulator
description The cyclic antimicrobial lipopeptide daptomycin (DAP) triggers the LiaFSR membrane stress response pathway in enterococci and many other Gram-positive organisms. LiaR is the response regulator that, upon phosphorylation, binds in a sequence-specific manner to DNA to regulate transcription in response to membrane stress. In clinical settings, non-susceptibility to DAP by Enterococcus faecium is correlated frequently with a mutation in LiaR of Trp73 to Cys (LiaRW73C). We have determined the structure of the activated E. faecium LiaR protein at 3.2 Å resolution and, in combination with solution studies, show that the activation of LiaR induces the formation of a LiaR dimer that increases LiaR affinity at least 40-fold for the extended regulatory regions upstream of the liaFSR and liaXYZ operons. In vitro, LiaRW73C induces phosphorylation-independent dimerization of LiaR and provides a biochemical basis for non-susceptibility to DAP by the upregulation of the LiaFSR regulon. A comparison of the E. faecalis LiaR, E. faecium LiaR, and the LiaR homolog from Staphylococcus aureus (VraR) and the mutations associated with DAP resistance suggests that physicochemical properties such as oligomerization state and DNA specificity, although tuned to the biology of each organism, share some features that could be targeted for new antimicrobials.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-07-16T15:27:39Z
dc.date.available.none.fl_str_mv 2020-07-16T15:27:39Z
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dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.local.none.fl_str_mv Artículo de revista
dc.type.coar.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.issn.none.fl_str_mv 1089-8638
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/3526
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.jmb.2016.09.016
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
dc.identifier.repourl.none.fl_str_mv https://repositorio.unbosque.edu.co
identifier_str_mv 1089-8638
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
url http://hdl.handle.net/20.500.12495/3526
https://doi.org/10.1016/j.jmb.2016.09.016
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Journal of molecular biology, 1089-8638, Vol. 428, Nro. 22, 2016, p. 4503-4519
dc.relation.uri.none.fl_str_mv https://www.sciencedirect.com/science/article/abs/pii/S0022283616303953?via%3Dihub
dc.rights.local.spa.fl_str_mv Acceso abierto
dc.rights.accessrights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
info:eu-repo/semantics/openAccess
Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2016-11-06
rights_invalid_str_mv Acceso abierto
http://purl.org/coar/access_right/c_abf2
2016-11-06
eu_rights_str_mv openAccess
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Elsevier
dc.publisher.journal.spa.fl_str_mv Journal of molecular biology
institution Universidad El Bosque
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spelling Davlieva, Milya G.Tovar-Yanez, AngelDeBruler, KimberlyLeonard, Paul G.Zianni, Michael R.Arias, César A.Shamoo, Yousif2020-07-16T15:27:39Z2020-07-16T15:27:39Z1089-8638http://hdl.handle.net/20.500.12495/3526https://doi.org/10.1016/j.jmb.2016.09.016instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengElsevierJournal of molecular biologyJournal of molecular biology, 1089-8638, Vol. 428, Nro. 22, 2016, p. 4503-4519https://www.sciencedirect.com/science/article/abs/pii/S0022283616303953?via%3DihubAn adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated stateAn adaptive mutation in enterococcus faecium LiaR associated with antimicrobial peptide resistance mimics phosphorylation and stabilizes LiaR in an activated stateArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85DaptomicinaDiagnóstico por imagenEnterococos resistentes a la vancomicinaLiaRE. faeciumResponse regulatorThe cyclic antimicrobial lipopeptide daptomycin (DAP) triggers the LiaFSR membrane stress response pathway in enterococci and many other Gram-positive organisms. LiaR is the response regulator that, upon phosphorylation, binds in a sequence-specific manner to DNA to regulate transcription in response to membrane stress. In clinical settings, non-susceptibility to DAP by Enterococcus faecium is correlated frequently with a mutation in LiaR of Trp73 to Cys (LiaRW73C). We have determined the structure of the activated E. faecium LiaR protein at 3.2 Å resolution and, in combination with solution studies, show that the activation of LiaR induces the formation of a LiaR dimer that increases LiaR affinity at least 40-fold for the extended regulatory regions upstream of the liaFSR and liaXYZ operons. In vitro, LiaRW73C induces phosphorylation-independent dimerization of LiaR and provides a biochemical basis for non-susceptibility to DAP by the upregulation of the LiaFSR regulon. A comparison of the E. faecalis LiaR, E. faecium LiaR, and the LiaR homolog from Staphylococcus aureus (VraR) and the mutations associated with DAP resistance suggests that physicochemical properties such as oligomerization state and DNA specificity, although tuned to the biology of each organism, share some features that could be targeted for new antimicrobials.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2016-11-06THUMBNAILMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.jpgMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.jpgimage/jpeg5775https://repositorio.unbosque.edu.co/bitstreams/a423de69-87cc-424e-afdd-e2383550b4a8/download7210a811635d1799e7c05fee5d259be7MD53Milya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.jpgMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.jpgIM Thumbnailimage/jpeg10663https://repositorio.unbosque.edu.co/bitstreams/9a61795e-2bb2-4c28-8da3-2fce7a4462a4/download0f8b3d0b3315501eeb75784f5996be22MD54ORIGINALMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdfMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdfapplication/pdf2118258https://repositorio.unbosque.edu.co/bitstreams/75a4a49a-a92b-40e7-9f87-5023818daec1/download847282b03b2fa0ba39617e08c78fe6f7MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.unbosque.edu.co/bitstreams/dfe5cc55-869b-417f-94e0-e9a10f31663d/download8a4605be74aa9ea9d79846c1fba20a33MD52TEXTMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.txtMilya Davlieva , Ángel Tovar-Yanez , Kimberly DeBruler_2016.pdf.txtExtracted texttext/plain87001https://repositorio.unbosque.edu.co/bitstreams/144d269d-053b-4f19-bbc9-74effdd7cecf/downloadb5ffa2170fb23b1f1dd862814a045876MD5520.500.12495/3526oai:repositorio.unbosque.edu.co:20.500.12495/35262024-02-07 05:42:58.001restrictedhttps://repositorio.unbosque.edu.coRepositorio Institucional Universidad El Bosquebibliotecas@biteca.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