Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments

ABSTRACT: Introduction: Aerobiological studies have found an increasing number of fungal taxa in the intrahospital environments, including Aspergillus species. There is a gap in knowledge on drug-susceptibility in spores circulating in intrahospital environ- ments. In this work, we evaluated the CYP...

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Autores:
Rúa Giraldo, Alvaro León
López García, Angela María
Torres Morales, Susana
Zuleta González, María Camila
Aristizabal Quintero, Mariana
Jiménez Zapata, Liliana
Gómez Guzmán, Oscar Mauricio
Hernández Ruiz, Orville
Tipo de recurso:
http://purl.org/coar/resource_type/c_6670
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/31227
Acceso en línea:
https://hdl.handle.net/10495/31227
Palabra clave:
Aspergillus
Hongos
Fungi
Antifúngicos
Antifungal Agents
Familia 51 del Citocromo P450
Cytochrome P450 Family 51
Farmacorresistencia Fúngica
Drug Resistance, Fungal
Aspergillus fumigatus
Mutación
Mutation
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-sa/2.5/co/
id UDEA2_cae47c9cd130b8e5883c65619f647d25
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/31227
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
title Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
spellingShingle Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
Aspergillus
Hongos
Fungi
Antifúngicos
Antifungal Agents
Familia 51 del Citocromo P450
Cytochrome P450 Family 51
Farmacorresistencia Fúngica
Drug Resistance, Fungal
Aspergillus fumigatus
Mutación
Mutation
title_short Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
title_full Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
title_fullStr Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
title_full_unstemmed Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
title_sort Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environments
dc.creator.fl_str_mv Rúa Giraldo, Alvaro León
López García, Angela María
Torres Morales, Susana
Zuleta González, María Camila
Aristizabal Quintero, Mariana
Jiménez Zapata, Liliana
Gómez Guzmán, Oscar Mauricio
Hernández Ruiz, Orville
dc.contributor.author.none.fl_str_mv Rúa Giraldo, Alvaro León
López García, Angela María
Torres Morales, Susana
Zuleta González, María Camila
Aristizabal Quintero, Mariana
Jiménez Zapata, Liliana
Gómez Guzmán, Oscar Mauricio
Hernández Ruiz, Orville
dc.contributor.conferencename.spa.fl_str_mv Congress of the International Society for Human and Animal Mycology (ISHAM) (21 : 21 de septiembre de 2022 : New Delhi, India)
dc.subject.decs.none.fl_str_mv Aspergillus
Hongos
Fungi
Antifúngicos
Antifungal Agents
Familia 51 del Citocromo P450
Cytochrome P450 Family 51
Farmacorresistencia Fúngica
Drug Resistance, Fungal
Aspergillus fumigatus
Mutación
Mutation
topic Aspergillus
Hongos
Fungi
Antifúngicos
Antifungal Agents
Familia 51 del Citocromo P450
Cytochrome P450 Family 51
Farmacorresistencia Fúngica
Drug Resistance, Fungal
Aspergillus fumigatus
Mutación
Mutation
description ABSTRACT: Introduction: Aerobiological studies have found an increasing number of fungal taxa in the intrahospital environments, including Aspergillus species. There is a gap in knowledge on drug-susceptibility in spores circulating in intrahospital environ- ments. In this work, we evaluated the CYP51A genome alterations and Aspergillus spore susceptibility to antifungal drugs. Objectives: To determine the sequence of CYP51A gene in clinical and environmental Aspergillus spp. isolates from in- trahospital environments in Medellín, Colombia II. To evaluate the phenotypical response of Aspergillus isolates harboring mutations in CYP51 gene from intrahospital environments. Methods: We used Aspergillus spp. collected from air and surfaces from intrahospital environments, as well clinical sam- ples. We performed Whole Genome Sequencing ( WGS ) using HiSeqXten Illumina platform for species identification. Genomes were assembled de novo using the SPADES algorithm.Genome annotation by ab initio prediction was done using the Augustus program. We extracted the sequences from the CYP51A gene and its promoter using OrthoFinder workflow. To identify previ- ously described mutations related with drug-resistance, we performed SNPs search in Geneious software using Clustal Omega. For the determination of broth dilution minimum inhibitory concentrations ( MIC ) of antifungal agents, we used the Eucast method 9.4. Results: We identified 26 Aspergillus from Fumitagi section using morphological characteristics. Three were isolates from clinical samples and twenty-three were obtained from intrahospital environments. We performed whole genome sequence for identification to species level. We identified 26 Aspergillus fumigatus using an in-house script base in BLASTn algorithm for 4 genes: internal transcribed spacer, b-tubulin, calmodulin, and RNA polymerase II. OrthoFinder workflow was performed to obtain CYP51A sequence. Clustal-Omega analysis showed two SNPs A1147G and T11167A, which constituted two non- synonymous mutations N248K and I242V respectively. A total of 8 and 3 isolates presented the changes in the CYP51A gene respectively. To determine their role in antifungal resistance, the strains were tested against 10 concentrations ( 0.03-8 mg/l ) of voriconazole antifungal agent. We used one clinical isolate without genomic changes in the CYP51A gene as control. The MIC was 0.5 mg/l for all the tested isolates. This value suggests isolates are susceptible to voriconazole. Conclusions: -Identification of Aspergillus fumigatus to species level was achieved through whole genome sequence. -Described mutations had been related to resistance to voriconazole, itraconazole and had not been tested for posaconazole. In this work, isolates presenting non-synonymous mutations were susceptible to voriconazole with breakpoints > 1 mg/l. It is necessary to evaluate the antifungal susceptibility to other antifungal agents. -The mutation N248K was previously described only in isolates from clinical samples.Mutation I242V was found in clinical and environmental samples from agricultural lands. Here we described SNPs in isolates from intrahospital environments. This work is the first one describing mutations and elucidating their role in the drug-resistance of airborne A. fumigatus in Medellín, Colombia.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-10-10T19:32:14Z
dc.date.available.none.fl_str_mv 2022-10-10T19:32:14Z
dc.date.issued.none.fl_str_mv 2022-09-21
dc.type.spa.fl_str_mv info:eu-repo/semantics/conferenceObject
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/31227
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dc.language.iso.spa.fl_str_mv eng
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dc.publisher.group.spa.fl_str_mv Biología Celular y Molecular CIB U. de A. U. del Rosario
Micología Médica y Experimental
dc.publisher.place.spa.fl_str_mv Nueva Delhi, India
institution Universidad de Antioquia
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spelling Rúa Giraldo, Alvaro LeónLópez García, Angela MaríaTorres Morales, SusanaZuleta González, María CamilaAristizabal Quintero, MarianaJiménez Zapata, LilianaGómez Guzmán, Oscar MauricioHernández Ruiz, OrvilleCongress of the International Society for Human and Animal Mycology (ISHAM) (21 : 21 de septiembre de 2022 : New Delhi, India)2022-10-10T19:32:14Z2022-10-10T19:32:14Z2022-09-21https://hdl.handle.net/10495/31227ABSTRACT: Introduction: Aerobiological studies have found an increasing number of fungal taxa in the intrahospital environments, including Aspergillus species. There is a gap in knowledge on drug-susceptibility in spores circulating in intrahospital environ- ments. In this work, we evaluated the CYP51A genome alterations and Aspergillus spore susceptibility to antifungal drugs. Objectives: To determine the sequence of CYP51A gene in clinical and environmental Aspergillus spp. isolates from in- trahospital environments in Medellín, Colombia II. To evaluate the phenotypical response of Aspergillus isolates harboring mutations in CYP51 gene from intrahospital environments. Methods: We used Aspergillus spp. collected from air and surfaces from intrahospital environments, as well clinical sam- ples. We performed Whole Genome Sequencing ( WGS ) using HiSeqXten Illumina platform for species identification. Genomes were assembled de novo using the SPADES algorithm.Genome annotation by ab initio prediction was done using the Augustus program. We extracted the sequences from the CYP51A gene and its promoter using OrthoFinder workflow. To identify previ- ously described mutations related with drug-resistance, we performed SNPs search in Geneious software using Clustal Omega. For the determination of broth dilution minimum inhibitory concentrations ( MIC ) of antifungal agents, we used the Eucast method 9.4. Results: We identified 26 Aspergillus from Fumitagi section using morphological characteristics. Three were isolates from clinical samples and twenty-three were obtained from intrahospital environments. We performed whole genome sequence for identification to species level. We identified 26 Aspergillus fumigatus using an in-house script base in BLASTn algorithm for 4 genes: internal transcribed spacer, b-tubulin, calmodulin, and RNA polymerase II. OrthoFinder workflow was performed to obtain CYP51A sequence. Clustal-Omega analysis showed two SNPs A1147G and T11167A, which constituted two non- synonymous mutations N248K and I242V respectively. A total of 8 and 3 isolates presented the changes in the CYP51A gene respectively. To determine their role in antifungal resistance, the strains were tested against 10 concentrations ( 0.03-8 mg/l ) of voriconazole antifungal agent. We used one clinical isolate without genomic changes in the CYP51A gene as control. The MIC was 0.5 mg/l for all the tested isolates. This value suggests isolates are susceptible to voriconazole. Conclusions: -Identification of Aspergillus fumigatus to species level was achieved through whole genome sequence. -Described mutations had been related to resistance to voriconazole, itraconazole and had not been tested for posaconazole. In this work, isolates presenting non-synonymous mutations were susceptible to voriconazole with breakpoints > 1 mg/l. It is necessary to evaluate the antifungal susceptibility to other antifungal agents. -The mutation N248K was previously described only in isolates from clinical samples.Mutation I242V was found in clinical and environmental samples from agricultural lands. Here we described SNPs in isolates from intrahospital environments. This work is the first one describing mutations and elucidating their role in the drug-resistance of airborne A. fumigatus in Medellín, Colombia.COL0000962COL0013709application/pdfenginfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjecthttp://purl.org/coar/resource_type/c_6670http://purl.org/coar/resource_type/c_c94fhttps://purl.org/redcol/resource_type/ECPóster de conferenciahttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by-nc-sa/4.0/Detection of CYP51A mutations in airborne Aspergillus spp isolates from intrahospital environmentsBiología Celular y Molecular CIB U. de A. U. del RosarioMicología Médica y ExperimentalNueva Delhi, IndiaAspergillusHongosFungiAntifúngicosAntifungal AgentsFamilia 51 del Citocromo P450Cytochrome P450 Family 51Farmacorresistencia FúngicaDrug Resistance, FungalAspergillus fumigatusMutaciónMutation21th Congress of the International Society for Human and Animal Mycology (ISHAM)2022-09-20/2022-09-24CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-81051https://bibliotecadigital.udea.edu.co/bitstream/10495/31227/3/license_rdfe2060682c9c70d4d30c83c51448f4eedMD53ORIGINALRuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus-Abstract.pdfRuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus-Abstract.pdfResumenapplication/pdf275398https://bibliotecadigital.udea.edu.co/bitstream/10495/31227/1/RuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus-Abstract.pdf7fb827453afbd83ce5ba4a7f8048a0d4MD51Poster_RuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus.pdfPoster_RuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus.pdfPóster de conferenciaapplication/pdf4485069https://bibliotecadigital.udea.edu.co/bitstream/10495/31227/2/Poster_RuaAlvaro_2022_DetectionCYP51A-MutationsAspergillus.pdfd9e9a609373b6a8bb5023a1c1546809aMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstream/10495/31227/4/license.txt8a4605be74aa9ea9d79846c1fba20a33MD5410495/31227oai:bibliotecadigital.udea.edu.co:10495/312272022-11-29 13:52:23.625Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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