Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood
Objective: Histoplasmosis is a fungal infection that causes significant morbidity and mortality in persons living with HIV/AIDS, especially in countries with limited resources. Currently used diagnostic tests rely on culture and serology, lack sensitivity and often require weeks to obtain results ca...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2018
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/28458
- Acceso en línea:
- https://doi.org/10.1093/mmy/myy036
https://repository.urosario.edu.co/handle/10336/28458
- Palabra clave:
- Histoplasmosis
HIV/AIDS
Histoplasma capsulatum
- Rights
- License
- Abierto (Texto Completo)
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EDOCUR2_e60093ab735ee9b02a2790f4809517ba |
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oai_identifier_str |
oai:repository.urosario.edu.co:10336/28458 |
network_acronym_str |
EDOCUR2 |
network_name_str |
Repositorio EdocUR - U. Rosario |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
dc.title.TranslatedTitle.spa.fl_str_mv |
Aplicación de ensayos de PCR en tiempo real para el diagnóstico de histoplasmosis utilizando tres dianas moleculares en tejidos FFPE humanos y sangre completa |
title |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
spellingShingle |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood Histoplasmosis HIV/AIDS Histoplasma capsulatum |
title_short |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
title_full |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
title_fullStr |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
title_full_unstemmed |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
title_sort |
Application of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-blood |
dc.subject.keyword.spa.fl_str_mv |
Histoplasmosis HIV/AIDS Histoplasma capsulatum |
topic |
Histoplasmosis HIV/AIDS Histoplasma capsulatum |
description |
Objective: Histoplasmosis is a fungal infection that causes significant morbidity and mortality in persons living with HIV/AIDS, especially in countries with limited resources. Currently used diagnostic tests rely on culture and serology, lack sensitivity and often require weeks to obtain results causing significant diagnosis delays; molecular assays are not commercially available. Methods: we aimed to apply quantitative real-time PCR (qPCR) targeting three protein-coding genes of Histoplasma capsulatum (100-kDa, H and M antigens) for detection of H. capsulatum infection in formalin-fixed paraffin-embedded (FFPE) and whole blood (WB) samples from patients with proven histoplasmosis. Results: For FFPE samples, the sensitivity of 100-kDa, H and M qPCR assays were 93.9%, 91% and 57%, respectively; however, the same qPCR assays showed only 23%, 19% and 11.5% of sensitivity for 100-kDa, H y M qPCR assays when used with the WB samples. The specificity of qPCR was determined by testing samples from patients with other clinical infections and healthy controls and was 93%-100% depending upon the assay and the specimen type. Conclusion: we applied three qPCR assays for detecting H. capsulatum DNA in human samples, and demonstrated that the molecular protocols based on amplification of 100-kDa and H antigen can be successfully used for diagnosing this mycosis when using FFPE samples; however, we do not recommend WB for routine diagnosis of histoplasmosis by qPCR in patients with progressive disseminated histoplasmosis. |
publishDate |
2018 |
dc.date.created.spa.fl_str_mv |
2018-06-05 |
dc.date.accessioned.none.fl_str_mv |
2020-08-28T15:48:15Z |
dc.date.available.none.fl_str_mv |
2020-08-28T15:48:15Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1093/mmy/myy036 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 1369-3786 EISSN: 1460-2709 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/28458 |
url |
https://doi.org/10.1093/mmy/myy036 https://repository.urosario.edu.co/handle/10336/28458 |
identifier_str_mv |
ISSN: 1369-3786 EISSN: 1460-2709 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
S159 |
dc.relation.citationIssue.none.fl_str_mv |
No. S2 |
dc.relation.citationStartPage.none.fl_str_mv |
S1 |
dc.relation.citationTitle.none.fl_str_mv |
Medical Mycology |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 56 |
dc.relation.ispartof.spa.fl_str_mv |
Medical Mycology, ISSN: 1369-3786;EISSN: 1460-2709, Vol. 56, No. S2, (1 June 2018); pp. S1–S159 |
dc.relation.uri.spa.fl_str_mv |
https://watermark.silverchair.com/myy036.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAqUwggKhBgkqhkiG9w0BBwagggKSMIICjgIBADCCAocGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMaclXdCt4kS7kNIOpAgEQgIICWKwQY0oC1E6pBFBZoQul3vKK0SQTRjQ6nlttuAHYG3eAuqz1hGjDb_YSblSdbjL5qsfp2JUzO3unwuZMI7-LUFcDWvciHug2ljzaxm21V8JBrj8P_F_6H-EvBRUQMhkbClLqdgwTdq8r80oD3aGAjoGSoHk1-hCy0pXbs1QCQxOc2RJ-OcTqbwHtL8n8xLyY9cPBl8ZW4St751HZQ8mlhORnJBRciSYcXrH8SNmfJFyTZsTi4idJugSEP7wmFWLKKaX-10oOg7Wav2a6dYJOplT1KSguxlaAnzBylqsgUPRulNaBczD8YclQ-QcyEb4LuJPJnuavpUm4ZYXuw1R65-WrLJrY-w9iLNEFj60EUbPzgDHfrBD277cuiLFz1-81S6LCVl8kWGbo8A-7fq91UOgQX1-bfwqK3bMMgYVh0bIsNBcz8kVbEo9ukZkjKbHRNofDIgaLvht8_eP3wMVREp4bwT1CyPBLpHfqVTrmc53U254DD9k44di4BWW0g8ZNlZHbGmd5cOwgW1MafI1Ck04mRnzDdDppaUezk2TIEc1sKqZtxbFmcLFDqMB0kWW01jqYqtaKEs70xOVFTskd7BBxr2eI1gQ_GLaYjORtIeMzX4lIWXxq8-jAYG8fWWW_xmo5ZUCLp_Mp_f-AwFI2pnkkEkSRfHP1lkC_87BupsEWFDlMzqsyCyeUZ9zMGex383huNwkAtnO1xVRv351OZUIIksE60GG_AwmkVicnpqTjKDzU-Y8pJ_RTGgMz6EHoNlP-nFNftSWVGtHy_4HpB4YWezimocBOjQ |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
International Society for Human and Animal Mycology Oxford University Press |
dc.source.spa.fl_str_mv |
Medical Mycology |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1814167683494576128 |
spelling |
fa336fc9-6784-499b-a7d2-2e7792a10079-1caec4fce-a394-4a7c-bf0b-17e55cab6377-193df6263-238b-4edb-9a67-9b0c94447d0d-1487b60dc-6389-4081-b3b9-39a3c8d7eec1-18cf0b725-c81a-4683-9a32-9c94aaa516aa-1fc293067-3402-4a18-bd71-3e71b9b0fde9-1d46eb564-3d91-44b6-8678-260eac36679e-16b4798fc-f008-40bf-bb96-42e420164447-1c4ce06d5-5043-49fe-9135-9448e880cc39-1fe654d66-a85a-4468-8af4-4b90f3378421-1acf56719-6777-4ead-8ee6-2efd46de562a-12020-08-28T15:48:15Z2020-08-28T15:48:15Z2018-06-05Objective: Histoplasmosis is a fungal infection that causes significant morbidity and mortality in persons living with HIV/AIDS, especially in countries with limited resources. Currently used diagnostic tests rely on culture and serology, lack sensitivity and often require weeks to obtain results causing significant diagnosis delays; molecular assays are not commercially available. Methods: we aimed to apply quantitative real-time PCR (qPCR) targeting three protein-coding genes of Histoplasma capsulatum (100-kDa, H and M antigens) for detection of H. capsulatum infection in formalin-fixed paraffin-embedded (FFPE) and whole blood (WB) samples from patients with proven histoplasmosis. Results: For FFPE samples, the sensitivity of 100-kDa, H and M qPCR assays were 93.9%, 91% and 57%, respectively; however, the same qPCR assays showed only 23%, 19% and 11.5% of sensitivity for 100-kDa, H y M qPCR assays when used with the WB samples. The specificity of qPCR was determined by testing samples from patients with other clinical infections and healthy controls and was 93%-100% depending upon the assay and the specimen type. Conclusion: we applied three qPCR assays for detecting H. capsulatum DNA in human samples, and demonstrated that the molecular protocols based on amplification of 100-kDa and H antigen can be successfully used for diagnosing this mycosis when using FFPE samples; however, we do not recommend WB for routine diagnosis of histoplasmosis by qPCR in patients with progressive disseminated histoplasmosis.application/pdfhttps://doi.org/10.1093/mmy/myy036ISSN: 1369-3786EISSN: 1460-2709https://repository.urosario.edu.co/handle/10336/28458engInternational Society for Human and Animal MycologyOxford University PressS159 No. S2S1Medical MycologyVol. 56Medical Mycology, ISSN: 1369-3786;EISSN: 1460-2709, Vol. 56, No. S2, (1 June 2018); pp. S1–S159https://watermark.silverchair.com/myy036.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAqUwggKhBgkqhkiG9w0BBwagggKSMIICjgIBADCCAocGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMaclXdCt4kS7kNIOpAgEQgIICWKwQY0oC1E6pBFBZoQul3vKK0SQTRjQ6nlttuAHYG3eAuqz1hGjDb_YSblSdbjL5qsfp2JUzO3unwuZMI7-LUFcDWvciHug2ljzaxm21V8JBrj8P_F_6H-EvBRUQMhkbClLqdgwTdq8r80oD3aGAjoGSoHk1-hCy0pXbs1QCQxOc2RJ-OcTqbwHtL8n8xLyY9cPBl8ZW4St751HZQ8mlhORnJBRciSYcXrH8SNmfJFyTZsTi4idJugSEP7wmFWLKKaX-10oOg7Wav2a6dYJOplT1KSguxlaAnzBylqsgUPRulNaBczD8YclQ-QcyEb4LuJPJnuavpUm4ZYXuw1R65-WrLJrY-w9iLNEFj60EUbPzgDHfrBD277cuiLFz1-81S6LCVl8kWGbo8A-7fq91UOgQX1-bfwqK3bMMgYVh0bIsNBcz8kVbEo9ukZkjKbHRNofDIgaLvht8_eP3wMVREp4bwT1CyPBLpHfqVTrmc53U254DD9k44di4BWW0g8ZNlZHbGmd5cOwgW1MafI1Ck04mRnzDdDppaUezk2TIEc1sKqZtxbFmcLFDqMB0kWW01jqYqtaKEs70xOVFTskd7BBxr2eI1gQ_GLaYjORtIeMzX4lIWXxq8-jAYG8fWWW_xmo5ZUCLp_Mp_f-AwFI2pnkkEkSRfHP1lkC_87BupsEWFDlMzqsyCyeUZ9zMGex383huNwkAtnO1xVRv351OZUIIksE60GG_AwmkVicnpqTjKDzU-Y8pJ_RTGgMz6EHoNlP-nFNftSWVGtHy_4HpB4YWezimocBOjQAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Medical Mycologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURHistoplasmosisHIV/AIDSHistoplasma capsulatumApplication of real-time PCR assays for the diagnosis of histoplasmosis using three molecular targets in human FFPE tissues and whole-bloodAplicación de ensayos de PCR en tiempo real para el diagnóstico de histoplasmosis utilizando tres dianas moleculares en tejidos FFPE humanos y sangre completaarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Lopez, L. F.Munoz, C.O.Tobon, A.Caceres, D.H.Loparev, V.Clay, O.Chiller, T.M.Litvintseva, A.P.Gade, L.Gonzalez, A.Gomez, B.L.10336/28458oai:repository.urosario.edu.co:10336/284582021-06-03 00:49:49.606https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |