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2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico
BACKGROUND: Invasive aspergillosis (IA) is a leading cause of morbidity and mortality in immunocompromised hosts. Triazole resistance in Aspergillus fumigatus is emerging globally. We performed antifungal susceptibility testing (AST) in Aspergillus isolates from Mexico and evaluated risk factors ass...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809092/ http://dx.doi.org/10.1093/ofid/ofz360.1798 |
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author | Gonzalez-Lara, María F Valenzuela-Almada, Maria O Marina Román-Montes, Carla Piñon-Hernandez, Viridiana Rodriguez, Jose Ponce de Leon, Alfredo Sifuentes-Osornio, José Martinez-Gamboa, Areli Ostrosky-Zeichner, Luis |
author_facet | Gonzalez-Lara, María F Valenzuela-Almada, Maria O Marina Román-Montes, Carla Piñon-Hernandez, Viridiana Rodriguez, Jose Ponce de Leon, Alfredo Sifuentes-Osornio, José Martinez-Gamboa, Areli Ostrosky-Zeichner, Luis |
author_sort | Gonzalez-Lara, María F |
collection | PubMed |
description | BACKGROUND: Invasive aspergillosis (IA) is a leading cause of morbidity and mortality in immunocompromised hosts. Triazole resistance in Aspergillus fumigatus is emerging globally. We performed antifungal susceptibility testing (AST) in Aspergillus isolates from Mexico and evaluated risk factors associated with 6 week mortality, including the MICs. METHODS: Aspergillus isolates from clinical samples were collected in a tertiary care center from 2014 to 2018. Species-level identification and broth microdilution following the CLSI M38 method were performed. MICs were interpreted according to epidemiological cutoff values. PCR and cyp51A gene sequencing were performed in A. fumigatus isolates with voriconazole (VRC) MIC >1 µg/mL. Data from the medical record were obtained to classify patients according to the MSG/EORTC criteria. The relationship between the MICs and 6-week mortality was described. Multivariate analysis of factors associated with six week mortality was performed. RESULTS: AST was performed on 85 Aspergillus isolates: 60/85 from patients with IA, 15/85 from patients with Aspergillus colonization, 2 patients with Aspergilloma, 1 with chronic otitis media and 1 with endophtalmitis. Information from 6 patients was unavailable. VRC MIC > 1 µg/mL was found in 3/38 (7.8%) A. fumigatus, from two patients with IA. Both had a TR34/L98H mutation in the cyp51A gene. Amphotericin B (AmB) MICs ≥ 2 were found in 16/49 (32%) A. fumigatus, 10/15 (66%) A. flavus and 1/14 (8%) A. niger. Forty-one patients with IA were treated: 29/41 (71%) with VRC or posaconazole, 7/41 (17%) with AmB and 5 with combination therapy. Overall, 6-week mortality was 30/49 (61.2%) among patients with IA; 2/2 (100%) when VRC MIC >1 µg/mL and 12/19 (63%) when AmB > 2 µg/mL, of which only 4 patients received initial treatment with AmB. Age older than 65 years (OR 11.8; 95% CI 1.14–123) and hepatic failure (OR 7.9; 95% CI 1.22–50.9) were independently associated with 6-week mortality in multivariate analysis. CONCLUSION: We found a VRC MIC >1 µg/mL prevalence of 7.8% among A. fumigatus and a high prevalence of AmB MIC ≥ 2 among clinical isolates of Aspergillus in Mexico. Elevated mortality was seen in IA among older patients with hepatic failure. Larger epidemiological studies are warranted. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6809092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68090922019-10-28 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico Gonzalez-Lara, María F Valenzuela-Almada, Maria O Marina Román-Montes, Carla Piñon-Hernandez, Viridiana Rodriguez, Jose Ponce de Leon, Alfredo Sifuentes-Osornio, José Martinez-Gamboa, Areli Ostrosky-Zeichner, Luis Open Forum Infect Dis Abstracts BACKGROUND: Invasive aspergillosis (IA) is a leading cause of morbidity and mortality in immunocompromised hosts. Triazole resistance in Aspergillus fumigatus is emerging globally. We performed antifungal susceptibility testing (AST) in Aspergillus isolates from Mexico and evaluated risk factors associated with 6 week mortality, including the MICs. METHODS: Aspergillus isolates from clinical samples were collected in a tertiary care center from 2014 to 2018. Species-level identification and broth microdilution following the CLSI M38 method were performed. MICs were interpreted according to epidemiological cutoff values. PCR and cyp51A gene sequencing were performed in A. fumigatus isolates with voriconazole (VRC) MIC >1 µg/mL. Data from the medical record were obtained to classify patients according to the MSG/EORTC criteria. The relationship between the MICs and 6-week mortality was described. Multivariate analysis of factors associated with six week mortality was performed. RESULTS: AST was performed on 85 Aspergillus isolates: 60/85 from patients with IA, 15/85 from patients with Aspergillus colonization, 2 patients with Aspergilloma, 1 with chronic otitis media and 1 with endophtalmitis. Information from 6 patients was unavailable. VRC MIC > 1 µg/mL was found in 3/38 (7.8%) A. fumigatus, from two patients with IA. Both had a TR34/L98H mutation in the cyp51A gene. Amphotericin B (AmB) MICs ≥ 2 were found in 16/49 (32%) A. fumigatus, 10/15 (66%) A. flavus and 1/14 (8%) A. niger. Forty-one patients with IA were treated: 29/41 (71%) with VRC or posaconazole, 7/41 (17%) with AmB and 5 with combination therapy. Overall, 6-week mortality was 30/49 (61.2%) among patients with IA; 2/2 (100%) when VRC MIC >1 µg/mL and 12/19 (63%) when AmB > 2 µg/mL, of which only 4 patients received initial treatment with AmB. Age older than 65 years (OR 11.8; 95% CI 1.14–123) and hepatic failure (OR 7.9; 95% CI 1.22–50.9) were independently associated with 6-week mortality in multivariate analysis. CONCLUSION: We found a VRC MIC >1 µg/mL prevalence of 7.8% among A. fumigatus and a high prevalence of AmB MIC ≥ 2 among clinical isolates of Aspergillus in Mexico. Elevated mortality was seen in IA among older patients with hepatic failure. Larger epidemiological studies are warranted. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6809092/ http://dx.doi.org/10.1093/ofid/ofz360.1798 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Gonzalez-Lara, María F Valenzuela-Almada, Maria O Marina Román-Montes, Carla Piñon-Hernandez, Viridiana Rodriguez, Jose Ponce de Leon, Alfredo Sifuentes-Osornio, José Martinez-Gamboa, Areli Ostrosky-Zeichner, Luis 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title | 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title_full | 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title_fullStr | 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title_full_unstemmed | 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title_short | 2118. Antifungal Susceptibility Testing of Clinical Isolates of Aspergillus in Mexico |
title_sort | 2118. antifungal susceptibility testing of clinical isolates of aspergillus in mexico |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6809092/ http://dx.doi.org/10.1093/ofid/ofz360.1798 |
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