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Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles
Theoretically, Aspergillus spp. grow in culture media, but frequently, blood cultures of patients with invasive Aspergillosis are negative, even if until now, the reasons are not clear. This aspect underlines the lack of a good strategy for the cultivation and isolation of Aspergillus spp. In order...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608713/ https://www.ncbi.nlm.nih.gov/pubmed/36296302 http://dx.doi.org/10.3390/microorganisms10102026 |
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author | Pasqua, Salvatore Monaco, Francesco Cardinale, Francesca Bonelli, Simone Conaldi, Pier Giulio D’Apolito, Danilo |
author_facet | Pasqua, Salvatore Monaco, Francesco Cardinale, Francesca Bonelli, Simone Conaldi, Pier Giulio D’Apolito, Danilo |
author_sort | Pasqua, Salvatore |
collection | PubMed |
description | Theoretically, Aspergillus spp. grow in culture media, but frequently, blood cultures of patients with invasive Aspergillosis are negative, even if until now, the reasons are not clear. This aspect underlines the lack of a good strategy for the cultivation and isolation of Aspergillus spp. In order to develop a complete analytical method to detect Aspergillus in clinical and pharmaceutical samples, we investigated the growth performance of two blood culture systems versus the pharmacopeia standard method. At <72 h, all test systems showed comparable sensitivity, about 1–2 conidia. However, the subculture analysis showed a suboptimal recovery for the methods, despite the positive growth and the visualization of the “Aspergillus balls” in the culture media. To investigate this issue, we studied three different subculture approaches: (i) the use of a sterile subculture unit, (ii) the use of a sterile subculture unit and the collection of a larger aliquot (100 µL), following vigorous agitation of the vials, and (iii) to decapsulate the bottle, withdrawing and centrifuging the sample, and aliquot the pellet onto SDA plates. Our results showed that only the third procedure recovered Aspergillus from all positive culture bottles. This work confirmed that our strategy is a valid and faster method to culture and isolate Aspergillus spp. from blood culture bottles. |
format | Online Article Text |
id | pubmed-9608713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96087132022-10-28 Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles Pasqua, Salvatore Monaco, Francesco Cardinale, Francesca Bonelli, Simone Conaldi, Pier Giulio D’Apolito, Danilo Microorganisms Article Theoretically, Aspergillus spp. grow in culture media, but frequently, blood cultures of patients with invasive Aspergillosis are negative, even if until now, the reasons are not clear. This aspect underlines the lack of a good strategy for the cultivation and isolation of Aspergillus spp. In order to develop a complete analytical method to detect Aspergillus in clinical and pharmaceutical samples, we investigated the growth performance of two blood culture systems versus the pharmacopeia standard method. At <72 h, all test systems showed comparable sensitivity, about 1–2 conidia. However, the subculture analysis showed a suboptimal recovery for the methods, despite the positive growth and the visualization of the “Aspergillus balls” in the culture media. To investigate this issue, we studied three different subculture approaches: (i) the use of a sterile subculture unit, (ii) the use of a sterile subculture unit and the collection of a larger aliquot (100 µL), following vigorous agitation of the vials, and (iii) to decapsulate the bottle, withdrawing and centrifuging the sample, and aliquot the pellet onto SDA plates. Our results showed that only the third procedure recovered Aspergillus from all positive culture bottles. This work confirmed that our strategy is a valid and faster method to culture and isolate Aspergillus spp. from blood culture bottles. MDPI 2022-10-13 /pmc/articles/PMC9608713/ /pubmed/36296302 http://dx.doi.org/10.3390/microorganisms10102026 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pasqua, Salvatore Monaco, Francesco Cardinale, Francesca Bonelli, Simone Conaldi, Pier Giulio D’Apolito, Danilo Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title | Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title_full | Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title_fullStr | Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title_full_unstemmed | Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title_short | Growth Performance and Recovery of Nosocomial Aspergillus spp. in Blood Culture Bottles |
title_sort | growth performance and recovery of nosocomial aspergillus spp. in blood culture bottles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608713/ https://www.ncbi.nlm.nih.gov/pubmed/36296302 http://dx.doi.org/10.3390/microorganisms10102026 |
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