Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in

causes a common sexually transmitted infection with a marked propensity to develop antimicrobial resistance. As few treatment options exist, this poses significant challenges to clinicians. Recent diagnostic advances have resulted in tests that report the simultaneous detection of and any resistance...

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Autores: Fernández-Huerta, Miguel|||0000-0002-1733-0925, Bodiyabadu, Kaveesha, Esperalba, Juliana|||0000-0003-1326-1341, Bradshaw, Catriona S., Serra-Pladevall, Judit|||0000-0002-4798-2385, Garland, Suzanne M., Fernandez-Naval, Candela|||0000-0002-5584-3537, Jensen, Jorgen S.|||0000-0002-7464-7435, Pumarola Suñé, Tomàs|||0000-0002-5171-7461, Ebeyan, Samantha, Lundgren, Marie, Tan, Lit Yeen, Espasa, Mateu|||0000-0003-4822-1024, Murray, Gerald L.
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:226588
Acceso en línea:https://ddd.uab.cat/record/226588
https://dx.doi.org/urn:doi:10.1128/JCM.00886-19
Access Level:acceso abierto
Palabra clave:Mycoplasma genitalium
Fluoroquinolone resistance
Multiplex qPCR assay
Multicenter evaluation
Antibiotic resistance
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spelling Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance inFernández-Huerta, Miguel|||0000-0002-1733-0925Bodiyabadu, KaveeshaEsperalba, Juliana|||0000-0003-1326-1341Bradshaw, Catriona S.Serra-Pladevall, Judit|||0000-0002-4798-2385Garland, Suzanne M.Fernandez-Naval, Candela|||0000-0002-5584-3537Jensen, Jorgen S.|||0000-0002-7464-7435Pumarola Suñé, Tomàs|||0000-0002-5171-7461Ebeyan, SamanthaLundgren, MarieTan, Lit YeenEspasa, Mateu|||0000-0003-4822-1024Murray, Gerald L.Mycoplasma genitaliumFluoroquinolone resistanceMultiplex qPCR assayMulticenter evaluationAntibiotic resistancecauses a common sexually transmitted infection with a marked propensity to develop antimicrobial resistance. As few treatment options exist, this poses significant challenges to clinicians. Recent diagnostic advances have resulted in tests that report the simultaneous detection of and any resistance to macrolides, the first-line treatment. This allows for therapy to be tailored to the individual, thereby optimizing treatment outcomes. causes a common sexually transmitted infection with a marked propensity to develop antimicrobial resistance. As few treatment options exist, this poses significant challenges to clinicians. Recent diagnostic advances have resulted in tests that report the simultaneous detection of and any resistance to macrolides, the first-line treatment. This allows for therapy to be tailored to the individual, thereby optimizing treatment outcomes. However, resistance to fluoroquinolones, the second-line treatment, is increasing in . In this study, we describe a new assay, MG+parC (beta), which simultaneously reports the detection of and five parC mutations that have been associated with resistance to fluoroquinolones. These mutations affect the amino acid sequence of ParC at residues S83R (A247C), S83I (G248T), D87N (G259A), D87Y (G259T), and D87H (G259C). The study tested the MG+parC (beta) assay with 202 -positive clinical samples from Australia (n = 141) and Spain (n = 61). Compared to Sanger sequencing, the assay performed with a kappa value of 0.985 (95% confidence interval [CI], 0.955 to 1.000), with a mutation detection sensitivity of 97.6% (95% CI, 87.4 to 99.9), and specificity of 100.0% (95% CI, 97.7 to 100.0). Fluoroquinolone resistance-associated mutations in parC targeted by the assay were more prevalent among the Australian cohort (23.4% [95% CI,16.3 to 31.8]) compared to the Spanish population (8.8% [95% CI, 2.9% to 19.3%]) (P = 0.019). The MG+parC (beta) kit is a simple and reliable method for simultaneous detection of and fluoroquinolone resistance-associated mutations in clinical settings. This novel diagnostic tool may extend the utility of the second line of antimicrobial therapies in infection.Universitat Autònoma de Barcelona 22019-01-0120192019-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/226588https://dx.doi.org/urn:doi:10.1128/JCM.00886-19reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:2265882026-06-06T12:50:31Z
dc.title.none.fl_str_mv Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
title Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
spellingShingle Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
Fernández-Huerta, Miguel|||0000-0002-1733-0925
Mycoplasma genitalium
Fluoroquinolone resistance
Multiplex qPCR assay
Multicenter evaluation
Antibiotic resistance
title_short Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
title_full Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
title_fullStr Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
title_full_unstemmed Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
title_sort Multicenter Clinical Evaluation of a Novel Multiplex Real-Time PCR (qPCR) Assay for Detection of Fluoroquinolone Resistance in
dc.creator.none.fl_str_mv Fernández-Huerta, Miguel|||0000-0002-1733-0925
Bodiyabadu, Kaveesha
Esperalba, Juliana|||0000-0003-1326-1341
Bradshaw, Catriona S.
Serra-Pladevall, Judit|||0000-0002-4798-2385
Garland, Suzanne M.
Fernandez-Naval, Candela|||0000-0002-5584-3537
Jensen, Jorgen S.|||0000-0002-7464-7435
Pumarola Suñé, Tomàs|||0000-0002-5171-7461
Ebeyan, Samantha
Lundgren, Marie
Tan, Lit Yeen
Espasa, Mateu|||0000-0003-4822-1024
Murray, Gerald L.
author Fernández-Huerta, Miguel|||0000-0002-1733-0925
author_facet Fernández-Huerta, Miguel|||0000-0002-1733-0925
Bodiyabadu, Kaveesha
Esperalba, Juliana|||0000-0003-1326-1341
Bradshaw, Catriona S.
Serra-Pladevall, Judit|||0000-0002-4798-2385
Garland, Suzanne M.
Fernandez-Naval, Candela|||0000-0002-5584-3537
Jensen, Jorgen S.|||0000-0002-7464-7435
Pumarola Suñé, Tomàs|||0000-0002-5171-7461
Ebeyan, Samantha
Lundgren, Marie
Tan, Lit Yeen
Espasa, Mateu|||0000-0003-4822-1024
Murray, Gerald L.
author_role author
author2 Bodiyabadu, Kaveesha
Esperalba, Juliana|||0000-0003-1326-1341
Bradshaw, Catriona S.
Serra-Pladevall, Judit|||0000-0002-4798-2385
Garland, Suzanne M.
Fernandez-Naval, Candela|||0000-0002-5584-3537
Jensen, Jorgen S.|||0000-0002-7464-7435
Pumarola Suñé, Tomàs|||0000-0002-5171-7461
Ebeyan, Samantha
Lundgren, Marie
Tan, Lit Yeen
Espasa, Mateu|||0000-0003-4822-1024
Murray, Gerald L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universitat Autònoma de Barcelona
dc.subject.none.fl_str_mv Mycoplasma genitalium
Fluoroquinolone resistance
Multiplex qPCR assay
Multicenter evaluation
Antibiotic resistance
topic Mycoplasma genitalium
Fluoroquinolone resistance
Multiplex qPCR assay
Multicenter evaluation
Antibiotic resistance
description causes a common sexually transmitted infection with a marked propensity to develop antimicrobial resistance. As few treatment options exist, this poses significant challenges to clinicians. Recent diagnostic advances have resulted in tests that report the simultaneous detection of and any resistance to macrolides, the first-line treatment. This allows for therapy to be tailored to the individual, thereby optimizing treatment outcomes. causes a common sexually transmitted infection with a marked propensity to develop antimicrobial resistance. As few treatment options exist, this poses significant challenges to clinicians. Recent diagnostic advances have resulted in tests that report the simultaneous detection of and any resistance to macrolides, the first-line treatment. This allows for therapy to be tailored to the individual, thereby optimizing treatment outcomes. However, resistance to fluoroquinolones, the second-line treatment, is increasing in . In this study, we describe a new assay, MG+parC (beta), which simultaneously reports the detection of and five parC mutations that have been associated with resistance to fluoroquinolones. These mutations affect the amino acid sequence of ParC at residues S83R (A247C), S83I (G248T), D87N (G259A), D87Y (G259T), and D87H (G259C). The study tested the MG+parC (beta) assay with 202 -positive clinical samples from Australia (n = 141) and Spain (n = 61). Compared to Sanger sequencing, the assay performed with a kappa value of 0.985 (95% confidence interval [CI], 0.955 to 1.000), with a mutation detection sensitivity of 97.6% (95% CI, 87.4 to 99.9), and specificity of 100.0% (95% CI, 97.7 to 100.0). Fluoroquinolone resistance-associated mutations in parC targeted by the assay were more prevalent among the Australian cohort (23.4% [95% CI,16.3 to 31.8]) compared to the Spanish population (8.8% [95% CI, 2.9% to 19.3%]) (P = 0.019). The MG+parC (beta) kit is a simple and reliable method for simultaneous detection of and fluoroquinolone resistance-associated mutations in clinical settings. This novel diagnostic tool may extend the utility of the second line of antimicrobial therapies in infection.
publishDate 2019
dc.date.none.fl_str_mv 2
2019-01-01
2019
2019-01-01
dc.type.none.fl_str_mv Article
http://purl.org/coar/resource_type/c_6501
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://ddd.uab.cat/record/226588
https://dx.doi.org/urn:doi:10.1128/JCM.00886-19
url https://ddd.uab.cat/record/226588
https://dx.doi.org/urn:doi:10.1128/JCM.00886-19
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
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dc.source.none.fl_str_mv reponame:Dipòsit Digital de Documents de la UAB
instname:Universitat Autònoma de Barcelona
instname_str Universitat Autònoma de Barcelona
reponame_str Dipòsit Digital de Documents de la UAB
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