Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples
ABSTRACT: Histoplasmosis, one of the most frequent endemic mycoses in the Americas, is caused by the inhalation of airborne conidia of Histoplasma capsulatum. Better understanding of the distribution of this fungus in the environment is important for the development of appropriate public health meas...
- Autores:
-
McEwen Ochoa, Juan Guillermo
Gómez Lonndoño, Luisa Fernanda
Peláez Jaramillo, Carlos Alberto
Arango Arteaga, Myrtha
Jiménez Alzate, María del Pilar
Gade, Lalitha
Litvintseva, Anastasia P.
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2022
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/42105
- Acceso en línea:
- https://hdl.handle.net/10495/42105
- Palabra clave:
- Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Técnicas de Diagnóstico Molecular
Molecular Diagnostic Techniques
Reacción en Cadena en Tiempo Real de la Polimerasa
Real-Time Polymerase Chain Reaction
Histoplasma
Histoplasmosis
Vigilancia Sanitaria Ambiental
Environmental Health Surveillance
https://id.nlm.nih.gov/mesh/D016133
https://id.nlm.nih.gov/mesh/D025202
https://id.nlm.nih.gov/mesh/D060888
https://id.nlm.nih.gov/mesh/D006658
https://id.nlm.nih.gov/mesh/D006660
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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| dc.title.spa.fl_str_mv |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| title |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| spellingShingle |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples Reacción en Cadena de la Polimerasa Polymerase Chain Reaction Técnicas de Diagnóstico Molecular Molecular Diagnostic Techniques Reacción en Cadena en Tiempo Real de la Polimerasa Real-Time Polymerase Chain Reaction Histoplasma Histoplasmosis Vigilancia Sanitaria Ambiental Environmental Health Surveillance https://id.nlm.nih.gov/mesh/D016133 https://id.nlm.nih.gov/mesh/D025202 https://id.nlm.nih.gov/mesh/D060888 https://id.nlm.nih.gov/mesh/D006658 https://id.nlm.nih.gov/mesh/D006660 |
| title_short |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| title_full |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| title_fullStr |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| title_full_unstemmed |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| title_sort |
Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples |
| dc.creator.fl_str_mv |
McEwen Ochoa, Juan Guillermo Gómez Lonndoño, Luisa Fernanda Peláez Jaramillo, Carlos Alberto Arango Arteaga, Myrtha Jiménez Alzate, María del Pilar Gade, Lalitha Litvintseva, Anastasia P. |
| dc.contributor.author.none.fl_str_mv |
McEwen Ochoa, Juan Guillermo Gómez Lonndoño, Luisa Fernanda Peláez Jaramillo, Carlos Alberto Arango Arteaga, Myrtha Jiménez Alzate, María del Pilar Gade, Lalitha Litvintseva, Anastasia P. |
| dc.contributor.researchgroup.spa.fl_str_mv |
Biología Celular y Molecular CIB U. de A. U. del Rosario Grupo Interdisciplinario de Estudios Moleculares Micología Médica |
| dc.subject.decs.none.fl_str_mv |
Reacción en Cadena de la Polimerasa Polymerase Chain Reaction Técnicas de Diagnóstico Molecular Molecular Diagnostic Techniques Reacción en Cadena en Tiempo Real de la Polimerasa Real-Time Polymerase Chain Reaction Histoplasma Histoplasmosis Vigilancia Sanitaria Ambiental Environmental Health Surveillance |
| topic |
Reacción en Cadena de la Polimerasa Polymerase Chain Reaction Técnicas de Diagnóstico Molecular Molecular Diagnostic Techniques Reacción en Cadena en Tiempo Real de la Polimerasa Real-Time Polymerase Chain Reaction Histoplasma Histoplasmosis Vigilancia Sanitaria Ambiental Environmental Health Surveillance https://id.nlm.nih.gov/mesh/D016133 https://id.nlm.nih.gov/mesh/D025202 https://id.nlm.nih.gov/mesh/D060888 https://id.nlm.nih.gov/mesh/D006658 https://id.nlm.nih.gov/mesh/D006660 |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D016133 https://id.nlm.nih.gov/mesh/D025202 https://id.nlm.nih.gov/mesh/D060888 https://id.nlm.nih.gov/mesh/D006658 https://id.nlm.nih.gov/mesh/D006660 |
| description |
ABSTRACT: Histoplasmosis, one of the most frequent endemic mycoses in the Americas, is caused by the inhalation of airborne conidia of Histoplasma capsulatum. Better understanding of the distribution of this fungus in the environment is important for the development of appropriate public health measures to prevent human infections. Previously, we used Hc100 nested polymerase chain reaction (PCR) to identify H. capsulatum DNA in 10% of environmental samples in Colombia. Here, we validate a 100-kDa real-time PCR assay for the detection of this fungus in the environment. Using this method, we identified H. capsulatum DNA in 80% of samples of raw organic materials, such as chicken manure, soil from caves, and bird and bat guano, as well as in 62% of samples of organic fertilizer that underwent the composting process. We demonstrated that 100-KDa real-time PCR is a useful tool for environmental surveillance that can be used to identify the potential reservoirs of H. capsulatum and to prevent outbreaks, especially in people with the higher risk of exposure, such as spelunkers, farmers, poultry manure collectors, and anyone who handle organic fertilizers or bat and bird excreta. |
| publishDate |
2022 |
| dc.date.issued.none.fl_str_mv |
2022 |
| dc.date.accessioned.none.fl_str_mv |
2024-09-14T15:24:56Z |
| dc.date.available.none.fl_str_mv |
2024-09-14T15:24:56Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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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 |
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Gómez LF, Gade L, Litvintseva AP, McEwen JG, Peláez CA, Arango M, Jiménez MDP. Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples. Am J Trop Med Hyg. 2022 Mar 14;106(5):1329–32. doi: 10.4269/ajtmh.20-1396. |
| dc.identifier.issn.none.fl_str_mv |
0002-9637 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/42105 |
| dc.identifier.doi.none.fl_str_mv |
10.4269/ajtmh.20-1396 |
| dc.identifier.eissn.none.fl_str_mv |
1476-1645 |
| identifier_str_mv |
Gómez LF, Gade L, Litvintseva AP, McEwen JG, Peláez CA, Arango M, Jiménez MDP. Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples. Am J Trop Med Hyg. 2022 Mar 14;106(5):1329–32. doi: 10.4269/ajtmh.20-1396. 0002-9637 10.4269/ajtmh.20-1396 1476-1645 |
| url |
https://hdl.handle.net/10495/42105 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Am. J. Trop. Med. Hyg. |
| dc.relation.citationendpage.spa.fl_str_mv |
1332 |
| dc.relation.citationissue.spa.fl_str_mv |
5 |
| dc.relation.citationstartpage.spa.fl_str_mv |
1329 |
| dc.relation.citationvolume.spa.fl_str_mv |
106 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
American Journal of Tropical Medicine and Hygiene |
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http://creativecommons.org/licenses/by/2.5/co/ |
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openAccess |
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4 páginas |
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American Society of Tropical Medicine and Hygiene |
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McEwen Ochoa, Juan GuillermoGómez Lonndoño, Luisa FernandaPeláez Jaramillo, Carlos AlbertoArango Arteaga, MyrthaJiménez Alzate, María del PilarGade, LalithaLitvintseva, Anastasia P.Biología Celular y Molecular CIB U. de A. U. del RosarioGrupo Interdisciplinario de Estudios MolecularesMicología Médica2024-09-14T15:24:56Z2024-09-14T15:24:56Z2022Gómez LF, Gade L, Litvintseva AP, McEwen JG, Peláez CA, Arango M, Jiménez MDP. Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental Samples. Am J Trop Med Hyg. 2022 Mar 14;106(5):1329–32. doi: 10.4269/ajtmh.20-1396.0002-9637https://hdl.handle.net/10495/4210510.4269/ajtmh.20-13961476-1645ABSTRACT: Histoplasmosis, one of the most frequent endemic mycoses in the Americas, is caused by the inhalation of airborne conidia of Histoplasma capsulatum. Better understanding of the distribution of this fungus in the environment is important for the development of appropriate public health measures to prevent human infections. Previously, we used Hc100 nested polymerase chain reaction (PCR) to identify H. capsulatum DNA in 10% of environmental samples in Colombia. Here, we validate a 100-kDa real-time PCR assay for the detection of this fungus in the environment. Using this method, we identified H. capsulatum DNA in 80% of samples of raw organic materials, such as chicken manure, soil from caves, and bird and bat guano, as well as in 62% of samples of organic fertilizer that underwent the composting process. We demonstrated that 100-KDa real-time PCR is a useful tool for environmental surveillance that can be used to identify the potential reservoirs of H. capsulatum and to prevent outbreaks, especially in people with the higher risk of exposure, such as spelunkers, farmers, poultry manure collectors, and anyone who handle organic fertilizers or bat and bird excreta.Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIColombia. Ministerio de Ciencia, Tecnología e Innovación - MiniCienciasCOL0000963COL0042069COL00074624 páginasapplication/pdfengAmerican Society of Tropical Medicine and HygieneBaltimore, 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_abf2Comparison between Two Molecular Techniques: Nested and Real-Time Polymerase Chain Reaction Targeting 100-kDa Hc Protein for Detection of Histoplasma capsulatum in Environmental SamplesArtículo 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/publishedVersionReacción en Cadena de la PolimerasaPolymerase Chain ReactionTécnicas de Diagnóstico MolecularMolecular Diagnostic TechniquesReacción en Cadena en Tiempo Real de la PolimerasaReal-Time Polymerase Chain ReactionHistoplasmaHistoplasmosisVigilancia Sanitaria AmbientalEnvironmental Health Surveillancehttps://id.nlm.nih.gov/mesh/D016133https://id.nlm.nih.gov/mesh/D025202https://id.nlm.nih.gov/mesh/D060888https://id.nlm.nih.gov/mesh/D006658https://id.nlm.nih.gov/mesh/D006660Am. J. Trop. Med. 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