Detection of Indoor Fungi: Part II

A special issue of Pathogens (ISSN 2076-0817). This special issue belongs to the section "Fungal Pathogens".

Deadline for manuscript submissions: 31 May 2024 | Viewed by 3495

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National Center for Public Health and Pharmacy, Albert Flórián út 2-6, H-1097 Budapest, Hungary
Interests: aerobiology; fungal spore dispersal; fungal diversity
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Dear Colleagues,

Building dampness or mold has been shown to be associated quite consistently with a variety of adverse health effects according to reviews carried out on a long list of studies from different geographic areas by scientific bodies, including the WHO. The most relevant diseases that molds can cause are allergies, hypersensitivity pneumonitis, and infection. The prevalence of mold allergy is approximately 5% to 30% of patients with atopy. However, there are still many questions and uncertainties around other symptoms, as well as the severity of health risk represented by mold contamination. These precautions stem from many factors, e.g., the fact that the metabolism of fungi (production of mycotoxins, MVOCs, and antigens) depends on many factors; that standardized fungal extracts are not available for clinical studies; and that questionnaire-based studies assessing dampness or mold most often rely on answers from the building occupants that may underestimate the real level of fungal contamination. Finally, common mold detection methods seem to be insufficient (e.g., low volume and frequency of air samples). Detection of indoor mold growth is challenging, even for trained professionals, and modern architecture does not make the situation any easier, as building materials widely used in modern buildings (e.g., drywall, dropped ceiling, fibrous insulation materials), once wetted, offer an appropriate environment for fungal growth, which often remains unobserved by residents or even professionals.

There are many points of view from which mold problems can be discussed; our focus will be on the detection of fungi in the indoor environment. For this Special Issue of the journal Pathogens, we invite you to submit innovative research papers and review articles as well as brief communications presenting recent advances related to our knowledge of fungi in enclosed spaces, including homes, office buildings, schools, healthcare and industrial settings and extreme indoor environments (HVAC, household devices), etc. Research papers and reviews can cover any aspect of detection methods and related issues of biodiversity, substrate preference, interaction with modern building materials, (chemo)taxonomic and phylogenetic studies, metabolism, pathogenicity, and strategies for mold remediation. We look forward to your contribution.

Dr. Donát Magyar
Guest Editor

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Keywords

  • molds
  • fungi
  • indoor environment
  • indoor air quality and molds
  • mycotoxins
  • fungal MVOCs
  • fungal allergens
  • pathogenic fungi in the indoor environment
  • biodeterioration by fungi in the indoor environment
  • aeromycology
  • fungal diversity

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Published Papers (3 papers)

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Research

18 pages, 288 KiB  
Article
Analysis of Mycotoxins and Cytotoxicity of Airborne Molds Isolated from the Zoological Garden—Screening Research
by Kinga Plewa-Tutaj, Magdalena Twarużek, Robert Kosicki and Ewelina Soszczyńska
Pathogens 2024, 13(4), 294; https://doi.org/10.3390/pathogens13040294 - 30 Mar 2024
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Abstract
Objective: The objective of this paper was to assess the airborne mold contamination, secondary metabolite profiles, and cytotoxicity of the dominant fungal species isolated from the air in selected rooms at a Zoological Garden. Materials and methods: Fungal concentrations were measured with MAS-100 [...] Read more.
Objective: The objective of this paper was to assess the airborne mold contamination, secondary metabolite profiles, and cytotoxicity of the dominant fungal species isolated from the air in selected rooms at a Zoological Garden. Materials and methods: Fungal concentrations were measured with MAS-100 air samplers. The collected airborne fungi were identified using a combination of morphological and molecular methods. The cytotoxicity of 84 strains belonging to two Penicillium and Aspergillus genera was determined using the quantitative colorimetric MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium salt) assay. The mycotoxins were detected using high-performance liquid chromatography (HPLC) with a mass spectrometry detector. Results: The ITS gene was amplified and sequenced to identify the 132 species. For mycotoxicological and cytotoxicity analyses, 52 Penicillium isolates and 32 Aspergillus representatives were selected. Cytotoxicity was confirmed in 97.6% of cases analyzed. Using the LC-MS/MS method, 42 out of 84 strains produced at least one of the following toxins: ochratoxin A, ochratoxin B, patulin, gliotoxin, roquefortine C, griseofulvin, sterigmatocystin, fumonisin B2, moniliformin, and mycophenolic acid. Conclusions: Analytical methods for assessing the presence of mycotoxins in fungal isolates collected directly from the air have proven to be an effective tool. Our research provides new information on the occurrence of potentially toxin-producing molds within a zoo. Full article
(This article belongs to the Special Issue Detection of Indoor Fungi: Part II)
24 pages, 1622 KiB  
Article
Toxicity Screening of Fungal Extracts and Metabolites, Xenobiotic Chemicals, and Indoor Dusts with In Vitro and Ex Vivo Bioassay Methods
by Tuomas Hintikka, Maria A. Andersson, Taina Lundell, Tamás Marik, László Kredics, Raimo Mikkola, Magnus C. Andersson, Jarek Kurnitski and Heidi Salonen
Pathogens 2024, 13(3), 217; https://doi.org/10.3390/pathogens13030217 - 29 Feb 2024
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Abstract
It is controversial how useful bioassays are for identifying the in vivo toxicity of hazardous environmental exposures. In this study, fruiting bodies of forest mushrooms (n = 46), indoor mold colonies (n = 412), fungal secondary metabolites (n = 18), xenobiotic chemicals such [...] Read more.
It is controversial how useful bioassays are for identifying the in vivo toxicity of hazardous environmental exposures. In this study, fruiting bodies of forest mushrooms (n = 46), indoor mold colonies (n = 412), fungal secondary metabolites (n = 18), xenobiotic chemicals such as biocides and detergents (n = 6), and methanol extracts of indoor dusts from urban buildings (n = 26) were screened with two different bioactivity assays: boar sperm motility inhibition (BSMI) and inhibition of cell proliferation (ICP) tests. For the forest mushrooms, the toxicity testing result was positive for 100% of poisonous-classified species, 69% of non-edible-classified species, and 18% of edible-classified species. Colonies of 21 isolates of Ascomycota mold fungal species previously isolated from water-damaged buildings proved to be toxic in the tests. Out of the fungal metabolites and xenobiotic chemicals, 94% and 100% were toxic, respectively. Out of the indoor dusts from moldy-classified houses (n = 12) and from dry, mold-free houses (n = 14), 50% and 57% were toxic, respectively. The bioassay tests, however, could not differentiate the samples from indoor dusts of moldy-classified buildings from those from the mold-free buildings. Xenobiotic chemicals and indoor dusts were more toxic in the BSMI assay than in the ICP assay, whereas the opposite results were obtained with the Ascomycota mold colonies and fungal secondary metabolites. The tests recognized unknown methanol-soluble thermoresistant substances in indoor settled dusts. Toxic indoor dusts may indicate a harmful exposure, regardless of whether the toxicity is due to xenobiotic chemicals or microbial metabolites. Full article
(This article belongs to the Special Issue Detection of Indoor Fungi: Part II)
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15 pages, 1116 KiB  
Article
Characterization of Indoor Molds after Ajka Red Mud Spill, Hungary
by Donát Magyar, Zsófia Tischner, Bence Szabó, Ágnes Freiler-Nagy, Tamás Papp, Henrietta Allaga and László Kredics
Pathogens 2024, 13(1), 22; https://doi.org/10.3390/pathogens13010022 - 26 Dec 2023
Viewed by 899
Abstract
A red mud suspension of ~700,000 m3 was accidentally released from the alumina plant in Ajka, Hungary, on the 4th of October 2010, flooding several buildings in the nearby towns. As there is no information in the literature on the effects of [...] Read more.
A red mud suspension of ~700,000 m3 was accidentally released from the alumina plant in Ajka, Hungary, on the 4th of October 2010, flooding several buildings in the nearby towns. As there is no information in the literature on the effects of red mud on indoor mold growth, we conducted studies to answer the following question: does the heavy metal content of red mud inhibit fungal colonization in flooded houses? In order to gain knowledge on fungal spectra colonizing surfaces soaked with red mud and on the ability of fungi to grow on them, swabs, tape lifts, and air samples were collected from three case study buildings. A total of 43 fungal taxa were detected. The dominant species were Penicillium spp. on plaster/brick walls, but Aspergillus series Versicolores, Cladosporium, Acremonium, and Scopulariopsis spp. were also present. The level of airborne penicillia was high in all indoor samples. Selected fungal strains were subcultured on 2% MEA with 10−1 and 10−4 dilutions of red mud. The growth rate of most of the strains was not significantly reduced by red mud on the artificial media. The consequences of similar industrial flooding on indoor molds are also discussed in this paper. Full article
(This article belongs to the Special Issue Detection of Indoor Fungi: Part II)
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