Publicação
Analysis of Aspergillus spp. burden by culture and molecular based methods in different occupational environments: what needs to be done?
| dc.contributor.author | Quintal Gomes, Anita | |
| dc.contributor.author | Faria, Tiago | |
| dc.contributor.author | Caetano, Liliana Aranha | |
| dc.contributor.author | Sabino, Raquel | |
| dc.contributor.author | Viegas, Carla | |
| dc.date.accessioned | 2019-02-19T11:06:02Z | |
| dc.date.available | 2019-02-19T11:06:02Z | |
| dc.date.issued | 2018-02 | |
| dc.description.abstract | Fungal burden have traditionally being detected by conventional culture analysis, which despite its limitations, is widely used by the scientific community. Alternatively, quantitative real-time PCR (qPCR), based on the amplification of genomic regions specific to certain fungal species, has been associated with increased sensivity, allowing the detection of dormant forms of fungi, such as spores. We present several studies where both methods were used to detect the presence of toxigenic fungi, namely Aspergillus, particularly from the Fumigati, Flavi and Circumdati sections | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/5886 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.subject | Aspergillus | pt_PT |
| dc.subject | Fungal Exposure | pt_PT |
| dc.subject | Environment | pt_PT |
| dc.subject | Occupational Exposure | pt_PT |
| dc.subject | PCR | pt_PT |
| dc.subject | Infecções Sistémicas e Zoonoses | pt_PT |
| dc.title | Analysis of Aspergillus spp. burden by culture and molecular based methods in different occupational environments: what needs to be done? | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Lisboa, Portugal | pt_PT |
| oaire.citation.title | 8th Advances Against Aspergillosis Conference, 1-3 February 2018 | pt_PT |
| rcaap.rights | restrictedAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |