Evidence map›Paper›PMID 28858343›Full record

ArticleEnvironmental science. Processes & impacts2017

Comparison of indoor air sampling and dust collection methods for fungal exposure assessment using quantitative PCR.

Jennie Cox, Reshmi Indugula, Stephen Vesper, Zheng Zhu, Roman Jandarov, Tiina Reponen

Abstract read
In one paragraph

Article in Environmental science. Processes & impacts, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. The Indoor Microbiome: Sampling, Analysis and Emerging Trends.Environmental microbiology reports · 2026
    Pooled it
  2. Mold in Paradise: A Review of Fungi Found in Libraries.Journal of fungi (Basel, Switzerland) · 2023
    Review
  3. Article
  4. HEPA filtration intervention in classrooms may improve some students' asthma.The Journal of asthma : official journal of the Association for the Care of Asthma · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Direct-Read Fluorescence-Based Measurements of Bioaerosol Exposure in Home Healthcare.International journal of environmental research and public health · 2022
    Article
  11. Review
  12. Article
  13. Asthma Prevalence and Mold Levels in US Northeastern Schools.The journal of allergy and clinical immunology. In practice · 2021
    Article
  14. Article
  15. Field sampling of indoor bioaerosols.Aerosol science and technology : the journal of the American Association for Aerosol Research · 2020
    Article
  16. Bioaerosol Sampling: Classical Approaches, Advances, and Perspectives.Aerosol science and technology : the journal of the American Association for Aerosol Research · 2020
    Article
  17. Article
  18. Article
  19. Sampling Devices for Indoor Allergen Exposure: Pros and Cons.Current allergy and asthma reports · 2019
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jennie CoxDepartment of Environmental Health University of Cincinnati, P.O. Box 670056, Cincinnati, OH 45267-0056, USA. reponeta@ucmail.uc.edu.
Reshmi Indugula
Stephen Vesper
Zheng Zhu
Roman Jandarov
Tiina Reponen

Funding

University of Cincinnati Education and Research CenterT42OH008432 · OH · UNIVERSITY OF CINCINNATI · PI DAVIS, KERMIT G. · 2005 to 2025
$32.7M
Intramural EPA EPA999999NIOSH CDC HHS T42 OH008432
6 · The paper itself

Abstract

Evaluating fungal contamination indoors is complicated because of the many different sampling methods utilized. In this study, fungal contamination was evaluated using five sampling methods and four matrices for results. The five sampling methods were a 48 hour indoor air sample collected with a Button™ inhalable aerosol sampler and four types of dust samples: a vacuumed floor dust sample, newly settled dust collected for four weeks onto two types of electrostatic dust cloths (EDCs) in trays, and a wipe sample of dust from above floor surfaces. The samples were obtained in the bedrooms of asthmatic children (n = 14). Quantitative polymerase chain reaction (qPCR) was used to analyze the dust and air samples for the 36 fungal species that make up the Environmental Relative Moldiness Index (ERMI). The results from the samples were compared by four matrices: total concentration of fungal cells, concentration of fungal species associated with indoor environments, concentration of fungal species associated with outdoor environments, and ERMI values (or ERMI-like values for air samples). The ERMI values for the dust samples and the ERMI-like values for the 48 hour air samples were not significantly different. The total cell concentrations of the 36 species obtained with the four dust collection methods correlated significantly (r = 0.64-0.79, p < 0.05), with the exception of the vacuumed floor dust and newly settled dust. In addition, fungal cell concentrations of indoor associated species correlated well between all four dust sampling methods (r = 0.68-0.86, p < 0.01). No correlation was found between the fungal concentrations in the air and dust samples primarily because of differences in concentrations of Cladosporium cladosporioides Type 1 and Epicoccum nigrum. A representative type of dust sample and a 48 hour air sample might both provide useful information about fungal exposures.

Indexed as

Air MicrobiologyAir Pollution, IndoorAnalysis of VarianceAsthmaChildDustEnvironmental MonitoringFungiHousingHumansOhioPolymerase Chain ReactionDust

Identifiers

PMID28858343
PMCPMC5884110

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.