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Airborne DNA: State of the art - Established methods and missing pieces in the molecular genetic detection of airborne microorganisms, viruses and plant particles.

dc.contributor.authorPogner, C-E
dc.contributor.authorAntunes, C
dc.contributor.authorApangu, G P
dc.contributor.authorBruffaerts, N
dc.contributor.authorCristofori, A
dc.contributor.authorGonzález Roldán, N
dc.contributor.authorGrinn-Gofroń, A
dc.contributor.authorLara, B
dc.contributor.authorLika, M
dc.contributor.authorMagyar, D
dc.contributor.authorMartinez-Bracero, M
dc.contributor.authorMuggia, L
dc.contributor.authorMuyshondt, B
dc.contributor.authorO'Connor, D
dc.contributor.authorPallavicini, A
dc.contributor.authorMarchã Penha, M A
dc.contributor.authorPérez-Badia, R
dc.contributor.authorRibeiro, H
dc.contributor.authorRodrigues Costa, A
dc.contributor.authorTischner, Z
dc.contributor.authorXhetani, M
dc.contributor.authorAmbelas Skjøth, C
dc.contributor.buuauthorÇELENK, SEVCAN
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentBiyoloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-4925-8902
dc.contributor.scopusid24170598000
dc.date.accessioned2025-12-11T10:21:41Z
dc.date.issued2024-12-20
dc.description.abstractBioaerosol is composed of different particles, originating from organisms, or their fragments with different origin, shape, and size. Sampling, analysing, identification and describing this airborne diversity has been carried out for over 100 years, and more recently the use of molecular genetic tools has been implemented. However, up to now there are no established protocols or standards for detecting airborne diversity of bacteria, fungi, viruses, pollen, and plant particles. In this review we evaluated commonalities of methods used in molecular genetic based studies in the last 23 years, to give an overview of applicable methods as well as knowledge gaps in diversity assessment. Various sampling techniques show different levels of effectiveness in detecting airborne particles based on their DNA. The storage and processing of samples, as well as DNA processing, influences the outcome of sampling campaigns. Moreover, the decisions on barcode selection, method of analysis, reference database as well as negative and positive controls may severely impact the results obtained. To date, the chain of decisions, methodological biases and error propagation have hindered DNA based molecular sequencing from offering a holistic picture of the airborne biodiversity. Reviewing the available studies, revealed a great diversity in used methodology and many publications didn't state all used methods in detail, making comparisons with other studies difficult or impossible. To overcome these limitations and ensure genuine comparability across studies, it is crucial to standardize protocols. Publications need to include all necessary information to enable comparison among different studies and to evaluate how methodological choices can impacts the results. Besides standardization, implementing of automatic tools and combining of different analytical techniques, such as real-time evaluation combined with sampling and molecular genetic analysis, could assist in achieving the goal of accurately assessing the actual airborne biodiversity.
dc.identifier.doi10.1016/j.scitotenv.2024.177439
dc.identifier.pubmed39549753
dc.identifier.scopus2-s2.0-85210275058
dc.identifier.urihttps://hdl.handle.net/11452/57327
dc.language.isoen
dc.relation.journalScience of The Total Environment
dc.subjectAerobiology
dc.subjectBacteria
dc.subjectBioaerosols
dc.subjectDNA sequencing
dc.subjectFungi
dc.subjectMolecular genetic analysis
dc.subjectPollen
dc.subjectVirus
dc.titleAirborne DNA: State of the art - Established methods and missing pieces in the molecular genetic detection of airborne microorganisms, viruses and plant particles.
dc.typeArticle
dspace.entity.typePublication
local.indexed.atScopus
local.indexed.atPubMed
relation.isAuthorOfPublication287f5285-8e64-402e-a481-36aff1c24232
relation.isAuthorOfPublication.latestForDiscovery287f5285-8e64-402e-a481-36aff1c24232

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