Exploring the microbiome of the built environment: A primer on four biological methods available to building professionals

Building professionals are increasingly being called upon to conduct indoor microbial investigations as they remediate moisture-damaged buildings and design new, healthy, sustainable buildings. Characterizing the indoor microbial community present in the built environment is challenging and complicated by the vast array of biological methods available to building professionals. Furthermore, the particular biological technique employed to study an indoor environment can have a significant impact on the results obtained. This study evaluates the advantages and disadvantages of four biological methods suitable for indoor microbial investigations: culturing, quantitative polymerase chain reaction (qPCR), Sanger sequencing, and pyrosequencing. The results obtained from a study of four buildings are used to evaluate the merits of each bioanalytical approach. In each of the four study sites, the microbial-laden dust recovered on HVAC filters was used to provide a passive, long-term sample of the indoor air. Culturing of the microorganisms recovered from the dust was the least expensive method tested but provided a limited characterization of the microbial community present. qPCR provided the most specific information about the presence and quantity of target microorganisms but this method requires a priori knowledge of the species of interest and specifically designed primers that may not enumerate unanticipated species. Sanger sequencing provided microbial identification at the species level but lacked coverage to fully describe the microbial community present. Pyrosequencing provided in-depth sequence coverage of the microbial community present (to the genus level) but the vast dataset generated required increased computational analysis and data storage. Nevertheless, pyrosequencing when coupled with qPCR for target species quantification represents a viable approach that should become more accessible to building professionals as user-friendly software for analyzing sequencing results becomes available and more commercial laboratories offer these services.

[1]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[2]  A. Chao Estimating the population size for capture-recapture data with unequal catchability. , 1987, Biometrics.

[3]  A Hedge,et al.  Sick building syndrome: a study of 4373 office workers. , 1987, The Annals of occupational hygiene.

[4]  E. Faragher,et al.  An investigation of the relationship between microbial and particulate indoor air pollution and the sick building syndrome. , 1992, Respiratory medicine.

[5]  K. Schleifer,et al.  Phylogenetic identification and in situ detection of individual microbial cells without cultivation. , 1995, Microbiological reviews.

[6]  S. Giovannoni,et al.  Bias caused by template annealing in the amplification of mixtures of 16S rRNA genes by PCR , 1996, Applied and environmental microbiology.

[7]  M. T. Hampton Atlas of Clinical Fungi , 1997 .

[8]  A. Verhoeff,et al.  Health risk assessment of fungi in home environments. , 1997, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[9]  F. Martinez,et al.  Alternaria as a major allergen for asthma in children raised in a desert environment. , 1997, American journal of respiratory and critical care medicine.

[10]  J. Badge DNA sequencing. , 1998, Methods in molecular biology.

[11]  M. Möritz,et al.  Investigations on the survival time of outdoor microorganisms on air filters. , 1998, Zentralblatt fur Hygiene und Umweltmedizin = International journal of hygiene and environmental medicine.

[12]  H. Wichmann,et al.  Indoor viable mold spores – a comparison between two cities, Erfurt (eastern Germany) and Hamburg (western Germany) , 2000, Allergy.

[13]  G. S. Hoog,et al.  Atlas of clinical fungi . ..[et al.] , 2000 .

[14]  P. C. Kemp,et al.  Survival and growth of micro-organisms on air filtration media during initial loading , 2001 .

[15]  M. Ronaghi Pyrosequencing sheds light on DNA sequencing. , 2001, Genome research.

[16]  M. Möritz,et al.  Capability of air filters to retain airborne bacteria and molds in heating, ventilating and air-conditioning (HVAC) systems. , 2001, International journal of hygiene and environmental health.

[17]  R. Maus,et al.  Survival of bacterial and mold spores in air filter media , 2001 .

[18]  A. Nevalainen,et al.  Personal exposures and microenvironmental concentrations of particles and bioaerosols. , 2002, Journal of environmental monitoring : JEM.

[19]  D. Milton,et al.  Risk of indoor airborne infection transmission estimated from carbon dioxide concentration. , 2003, Indoor air.

[20]  H. Vijay,et al.  Fungal allergens. , 2020, Clinical allergy and immunology.

[21]  M. Lebuhn,et al.  Evaluating real-time PCR for the quantification of distinct pathogens and indicator organisms in environmental samples. , 2004, Water science and technology : a journal of the International Association on Water Pollution Research.

[22]  L. T. Angenent,et al.  Molecular identification of potential pathogens in water and air of a hospital therapy pool. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Neil J. Zimmerman,et al.  Evaluation of Culturable Particle Load on HVAC Filters Before and After Remediation: A Pilot Study , 2006 .

[24]  T. Sterling,et al.  Transmission of Mycobacterium tuberculosis from health care workers. , 2006, The New England journal of medicine.

[25]  Peter C Raynor,et al.  Development of a method for bacteria and virus recovery from heating, ventilation, and air conditioning (HVAC) filters. , 2006, Journal of environmental monitoring : JEM.

[26]  Miia Pitkäranta,et al.  Diversity and seasonal dynamics of bacterial community in indoor environment , 2008, BMC Microbiology.

[27]  P. Auvinen,et al.  Analysis of Fungal Flora in Indoor Dust by Ribosomal DNA Sequence Analysis, Quantitative PCR, and Culture , 2007, Applied and Environmental Microbiology.

[28]  Rob Knight,et al.  Short-Term Temporal Variability in Airborne Bacterial and Fungal Populations , 2007, Applied and Environmental Microbiology.

[29]  W J Fisk,et al.  Public health and economic impact of dampness and mold. , 2007, Indoor air.

[30]  D. Denning,et al.  Aspergillus flavus: human pathogen, allergen and mycotoxin producer. , 2007, Microbiology.

[31]  M. Deloge-Abarkan,et al.  Detection of airborne Legionella while showering using liquid impingement and fluorescent in situ hybridization (FISH). , 2007, Journal of environmental monitoring : JEM.

[32]  Warren Friedman,et al.  Development of an Environmental Relative Moldiness Index for US Homes , 2007, Journal of occupational and environmental medicine.

[33]  Peter C Raynor,et al.  Background culturable bacteria aerosol in two large public buildings using HVAC filters as long term, passive, high-volume air samplers. , 2008, Journal of environmental monitoring : JEM.

[34]  T. Haahtela,et al.  Predominance of Gram-positive bacteria in house dust in the low-allergy risk Russian Karelia. , 2008, Environmental microbiology.

[35]  Philip Hugenholtz,et al.  A renaissance for the pioneering 16S rRNA gene. , 2008, Current opinion in microbiology.

[36]  S. Vesper,et al.  Quantifying fungal viability in air and water samples using quantitative PCR after treatment with propidium monoazide (PMA). , 2008, Journal of microbiological methods.

[37]  Anne Hyvärinen,et al.  Quantitative PCR analysis of fungi and bacteria in building materials and comparison to culture-based analysis. , 2008, Journal of environmental monitoring : JEM.

[38]  Tao Zhang,et al.  The Airborne Metagenome in an Indoor Urban Environment , 2008, PloS one.

[39]  R. Knight,et al.  Accurate taxonomy assignments from 16S rRNA sequences produced by highly parallel pyrosequencers , 2008, Nucleic acids research.

[40]  M. Bracken,et al.  Association of pediatric asthma severity with exposure to common household dust allergens. , 2009, Environmental research.

[41]  C. Blackwood,et al.  Assessment of Bias Associated with Incomplete Extraction of Microbial DNA from Soil , 2009, Applied and Environmental Microbiology.

[42]  Martin Täubel,et al.  The occupant as a source of house dust bacteria. , 2009, The Journal of allergy and clinical immunology.

[43]  Robert Samson,et al.  Indoor fungal composition is geographically patterned and more diverse in temperate zones than in the tropics , 2010, Proceedings of the National Academy of Sciences.

[44]  L. Tedersoo,et al.  454 Pyrosequencing and Sanger sequencing of tropical mycorrhizal fungi provide similar results but reveal substantial methodological biases. , 2010, The New phytologist.

[45]  Jordan Peccia,et al.  Accuracy, Precision, and Method Detection Limits of Quantitative PCR for Airborne Bacteria and Fungi , 2010, Applied and Environmental Microbiology.

[46]  R. Knight,et al.  Sources of Bacteria in Outdoor Air across Cities in the Midwestern United States , 2011, Applied and Environmental Microbiology.

[47]  C. Chang,et al.  Methodologies for quantifying culturable, viable, and total Legionella pneumophila in indoor air. , 2011, Indoor air.

[48]  Kuan-Liang Liu,et al.  Accurate, Rapid Taxonomic Classification of Fungal Large-Subunit rRNA Genes , 2011, Applied and Environmental Microbiology.

[49]  Mark J. Mendell,et al.  Respiratory and Allergic Health Effects of Dampness, Mold, and Dampness-Related Agents: A Review of the Epidemiologic Evidence , 2011, Environmental health perspectives.

[50]  C. Gostinčar,et al.  Evolution of fungal pathogens in domestic environments? , 2011, Fungal biology.

[51]  Federico Noris,et al.  Evaluation of HVAC filters as a sampling mechanism for indoor microbial communities , 2011 .

[52]  K. Bibby,et al.  New Directions: A revolution in DNA sequencing now allows for the meaningful integration of biology with aerosol science , 2011 .

[53]  Jeff Kline,et al.  Architectural design influences the diversity and structure of the built environment microbiome , 2012, The ISME Journal.

[54]  Andrew R. McFarland,et al.  Bioaerosol Sampling with a Wetted Wall Cyclone: Cell Culturability and DNA Integrity of Escherichia coli Bacteria , 2012 .