The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates

ABSTRACT: We compared the prevalence of levofloxacin (LVX) resistance with that of ofloxacin (OFX) and moxifloxacin (MFX) among multidrug resistant (MDR) MTB clinical isolates collected in Medellin, Colombia, between 2004 and 2009 and aimed at unraveling the underlying molecular mechanisms that expl...

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Autores:
Peláez Jaramillo, Carlos Alberto
Álvarez Zuluaga, Nataly
Zapata, E.
Mejía, G.I
Realpe, T.
Araque Marín, Predonel
Rouzaud, F.
Robledo, J.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2014
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/35210
Acceso en línea:
https://hdl.handle.net/10495/35210
Palabra clave:
Sustitución de Aminoácidos
Amino Acid Substitution
Antibacterianos
Anti-Bacterial Agents
Proteínas Bacterianas
Bacterial Proteins
Dominio Catalítico
Catalytic Domain
Farmacorresistencia Bacteriana Múltiple
Drug Resistance, Multiple, Bacterial
Levofloxacino
Levofloxacin
Mycobacterium tuberculosis
Tuberculosis Resistente a Múltiples Medicamentos
Tuberculosis, Multidrug-Resistant
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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network_acronym_str UDEA2
network_name_str Repositorio UdeA
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dc.title.spa.fl_str_mv The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
title The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
spellingShingle The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
Sustitución de Aminoácidos
Amino Acid Substitution
Antibacterianos
Anti-Bacterial Agents
Proteínas Bacterianas
Bacterial Proteins
Dominio Catalítico
Catalytic Domain
Farmacorresistencia Bacteriana Múltiple
Drug Resistance, Multiple, Bacterial
Levofloxacino
Levofloxacin
Mycobacterium tuberculosis
Tuberculosis Resistente a Múltiples Medicamentos
Tuberculosis, Multidrug-Resistant
title_short The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
title_full The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
title_fullStr The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
title_full_unstemmed The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
title_sort The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical Isolates
dc.creator.fl_str_mv Peláez Jaramillo, Carlos Alberto
Álvarez Zuluaga, Nataly
Zapata, E.
Mejía, G.I
Realpe, T.
Araque Marín, Predonel
Rouzaud, F.
Robledo, J.
dc.contributor.author.none.fl_str_mv Peláez Jaramillo, Carlos Alberto
Álvarez Zuluaga, Nataly
Zapata, E.
Mejía, G.I
Realpe, T.
Araque Marín, Predonel
Rouzaud, F.
Robledo, J.
dc.contributor.researchgroup.spa.fl_str_mv Grupo Interdisciplinario de Estudios Moleculares
dc.subject.decs.none.fl_str_mv Sustitución de Aminoácidos
Amino Acid Substitution
Antibacterianos
Anti-Bacterial Agents
Proteínas Bacterianas
Bacterial Proteins
Dominio Catalítico
Catalytic Domain
Farmacorresistencia Bacteriana Múltiple
Drug Resistance, Multiple, Bacterial
Levofloxacino
Levofloxacin
Mycobacterium tuberculosis
Tuberculosis Resistente a Múltiples Medicamentos
Tuberculosis, Multidrug-Resistant
topic Sustitución de Aminoácidos
Amino Acid Substitution
Antibacterianos
Anti-Bacterial Agents
Proteínas Bacterianas
Bacterial Proteins
Dominio Catalítico
Catalytic Domain
Farmacorresistencia Bacteriana Múltiple
Drug Resistance, Multiple, Bacterial
Levofloxacino
Levofloxacin
Mycobacterium tuberculosis
Tuberculosis Resistente a Múltiples Medicamentos
Tuberculosis, Multidrug-Resistant
description ABSTRACT: We compared the prevalence of levofloxacin (LVX) resistance with that of ofloxacin (OFX) and moxifloxacin (MFX) among multidrug resistant (MDR) MTB clinical isolates collected in Medellin, Colombia, between 2004 and 2009 and aimed at unraveling the underlying molecular mechanisms that explain the correlation between QRDR-A mutations and LVX resistance phenotype. We tested 104 MDR isolates for their susceptibility to OFX, MFX, and LVX. Resistance to OFX was encountered in 10 (9.6%) of the isolates among which 8 (7.7%) were also resistant to LVX and 6 (5.7%) to MFX. Four isolates resistant to the 3 FQ were harboring the Asp94Gly substitution, whilst 2 other isolates resistant to OFX and LVX presented the Ala90Val mutation. No mutations were found in the QRDR-B region.The molecular modeling of the interaction between LVX and the DNA-DNA gyrase complex indicates that the loss of an acetyl group in the Asp94Gly mutation removes the acid base interaction with LVX necessary for the quinolone activity. The Ala90Val mutation that substitutes a methyl for an isopropyl group induces a steric modification that blocks the LVX access to the gyrase catalytic site.
publishDate 2014
dc.date.issued.none.fl_str_mv 2014
dc.date.accessioned.none.fl_str_mv 2023-06-01T11:28:10Z
dc.date.available.none.fl_str_mv 2023-06-01T11:28:10Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.citation.spa.fl_str_mv Álvarez N, Zapata E, Mejía GI, Realpe T, Araque P, Peláez C, Rouzaud F, Robledo J. The structural modeling of the interaction between levofloxacin and the Mycobacterium tuberculosis gyrase catalytic site sheds light on the mechanisms of fluoroquinolones resistant tuberculosis in Colombian clinical isolates. Biomed Res Int. 2014;2014:367268. doi: 10.1155/2014/367268.
dc.identifier.issn.none.fl_str_mv 2314-6133
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/35210
dc.identifier.doi.none.fl_str_mv 10.1155/2014/367268
dc.identifier.eissn.none.fl_str_mv 2314-6141
identifier_str_mv Álvarez N, Zapata E, Mejía GI, Realpe T, Araque P, Peláez C, Rouzaud F, Robledo J. The structural modeling of the interaction between levofloxacin and the Mycobacterium tuberculosis gyrase catalytic site sheds light on the mechanisms of fluoroquinolones resistant tuberculosis in Colombian clinical isolates. Biomed Res Int. 2014;2014:367268. doi: 10.1155/2014/367268.
2314-6133
10.1155/2014/367268
2314-6141
url https://hdl.handle.net/10495/35210
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Biomed. Res. Int.
dc.relation.citationendpage.spa.fl_str_mv 9
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 2014
dc.relation.ispartofjournal.spa.fl_str_mv BioMed Research International
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dc.publisher.spa.fl_str_mv Hindawi
dc.publisher.place.spa.fl_str_mv Nueva York, Estados Unidos
institution Universidad de Antioquia
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spelling Peláez Jaramillo, Carlos AlbertoÁlvarez Zuluaga, NatalyZapata, E.Mejía, G.IRealpe, T.Araque Marín, PredonelRouzaud, F.Robledo, J.Grupo Interdisciplinario de Estudios Moleculares2023-06-01T11:28:10Z2023-06-01T11:28:10Z2014Álvarez N, Zapata E, Mejía GI, Realpe T, Araque P, Peláez C, Rouzaud F, Robledo J. The structural modeling of the interaction between levofloxacin and the Mycobacterium tuberculosis gyrase catalytic site sheds light on the mechanisms of fluoroquinolones resistant tuberculosis in Colombian clinical isolates. Biomed Res Int. 2014;2014:367268. doi: 10.1155/2014/367268.2314-6133https://hdl.handle.net/10495/3521010.1155/2014/3672682314-6141ABSTRACT: We compared the prevalence of levofloxacin (LVX) resistance with that of ofloxacin (OFX) and moxifloxacin (MFX) among multidrug resistant (MDR) MTB clinical isolates collected in Medellin, Colombia, between 2004 and 2009 and aimed at unraveling the underlying molecular mechanisms that explain the correlation between QRDR-A mutations and LVX resistance phenotype. We tested 104 MDR isolates for their susceptibility to OFX, MFX, and LVX. Resistance to OFX was encountered in 10 (9.6%) of the isolates among which 8 (7.7%) were also resistant to LVX and 6 (5.7%) to MFX. Four isolates resistant to the 3 FQ were harboring the Asp94Gly substitution, whilst 2 other isolates resistant to OFX and LVX presented the Ala90Val mutation. No mutations were found in the QRDR-B region.The molecular modeling of the interaction between LVX and the DNA-DNA gyrase complex indicates that the loss of an acetyl group in the Asp94Gly mutation removes the acid base interaction with LVX necessary for the quinolone activity. The Ala90Val mutation that substitutes a methyl for an isopropyl group induces a steric modification that blocks the LVX access to the gyrase catalytic site.COL00074629application/pdfengHindawiNueva York, Estados Unidoshttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2The Structural Modeling of the Interaction between Levofloxacin and the Mycobacterium tuberculosis Gyrase Catalytic Site Sheds Light on the Mechanisms of Fluoroquinolones Resistant Tuberculosis in Colombian Clinical IsolatesArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionSustitución de AminoácidosAmino Acid SubstitutionAntibacterianosAnti-Bacterial AgentsProteínas BacterianasBacterial ProteinsDominio CatalíticoCatalytic DomainFarmacorresistencia Bacteriana MúltipleDrug Resistance, Multiple, BacterialLevofloxacinoLevofloxacinMycobacterium tuberculosisTuberculosis Resistente a Múltiples MedicamentosTuberculosis, Multidrug-ResistantBiomed. Res. 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