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...
- 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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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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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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publishedVersion |
| 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 |
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1 |
| dc.relation.citationvolume.spa.fl_str_mv |
2014 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
BioMed Research International |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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openAccess |
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9 |
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application/pdf |
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Hindawi |
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Nueva York, Estados Unidos |
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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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