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Mold & Mycotoxin Building Profile

The Mold & Mycotoxin Building Profile analyses settled indoor dust to identify and quantify fungal spores — including Aspergillus, Penicillium, Stachybotrys, and Chaetomium — and detect mycotoxins such as ochratoxin A, aflatoxins, and trichothecenes.

7

Biomarkers

Dust

Sample

10–14 business days

Turnaround

N/A

Fasting

What is the Mold Building Profile test?

The Mold & Mycotoxin Building Profile analyses settled dust collected from indoor environments to identify and quantify viable fungal spores and mycotoxin residues. It is ordered to document the presence and extent of mould contamination when building occupants report symptoms consistent with mould-related illness — respiratory complaints, chronic sinusitis, fatigue, cognitive difficulties, or hypersensitivity reactions — and visible water damage or a musty odour suggests fungal growth. Unlike air sampling, which captures only airborne spores at a single moment, dust sampling integrates exposure over time and is more sensitive for detecting heavy, sticky spores such as those of Stachybotrys chartarum. Clinicians order this profile to objectively confirm an environmental hypothesis, to guide and verify remediation efforts, and to support discussions with patients about exposure reduction. The results are not diagnostic of illness — environmental testing documents hazard, not individual response — but they provide an evidence base for environmental intervention and help differentiate mould exposure from other indoor air quality concerns such as volatile organic compounds or particulate matter.

What does the Mold Building Profile test measure?

1
Aspergillus spp.(Aspergillus Species Spore Count)
Range: Laboratory provides comparative thresholds; no universal environmental limit exists.Optimal: Indoor spore counts should not substantially exceed outdoor levels; the absence of water-damaged materials is the true goal.spores/mg dust

Aspergillus species are ubiquitous saprophytic fungi that colonise damp building materials and produce airborne spores. Indoor spore counts that exceed outdoor ambient levels or reach concentrations associated with water damage suggest an amplification reservoir and potential for inhalation exposure. Certain Aspergillus species produce mycotoxins including aflatoxins and ochratoxin A under specific conditions.

Elevated indoor Aspergillus spore counts may correlate with respiratory symptoms in susceptible individuals and signal water intrusion or poor ventilation. For clinicians managing patients with suspected mould-related illness, documenting an environmental source strengthens the causal hypothesis and guides remediation.

2
Penicillium spp.(Penicillium Species Spore Count)
Range: Laboratory provides comparative thresholds; no universal environmental limit exists.Optimal: Indoor levels comparable to or below outdoor ambient; no active water damage.spores/mg dust

Penicillium species thrive on water-damaged cellulose and gypsum board, releasing spores that can remain airborne for extended periods. Some strains produce mycotoxins such as ochratoxin A and citrinin. Indoor amplification is a hallmark of chronic moisture intrusion.

Penicillium is commonly implicated in damp indoor environments; elevated indoor counts relative to outdoor baselines suggest an active moisture problem and potential for chronic low-level mycotoxin exposure.

3
Stachybotrys(Stachybotrys chartarum Spore Count)
Range: Detection at any quantifiable level is considered significant; Stachybotrys is not normally present indoors.Optimal: Not detected.spores/mg dust

Stachybotrys chartarum, often called 'black mould,' colonises chronically wet cellulose-rich materials and produces trichothecene mycotoxins. Spores are relatively heavy and sticky, so airborne counts may underestimate surface contamination; settled dust sampling is more sensitive for detecting this organism.

Any detection of Stachybotrys in indoor dust warrants environmental investigation and remediation. While the strength of epidemiological evidence linking it to specific clinical syndromes is debated, its presence confirms severe water damage and mycotoxin production potential.

4
Chaetomium spp.(Chaetomium Species Spore Count)
Range: Detection suggests water damage; not normally quantifiable indoors.Optimal: Not detected.spores/mg dust

Chaetomium species colonise chronically wet drywall, wood, and paper, often appearing alongside Stachybotrys. They produce cellulolytic enzymes and some mycotoxins. Detection indicates prolonged moisture exposure.

Presence of Chaetomium spores in settled dust signals chronic water intrusion and supports an environmental trigger in patients reporting building-related symptoms.

5
OTA(Ochratoxin A)
Range: Laboratory provides detection thresholds; presence at any quantifiable level is significant.Optimal: Not detected.ng/g dust

Ochratoxin A is a nephrotoxic mycotoxin produced by Aspergillus and Penicillium species under favourable moisture and temperature conditions. It persists in dust and can be inhaled or ingested via hand-to-mouth transfer.

Detection of ochratoxin A in building dust confirms that toxigenic fungi are not only present but actively producing toxins, strengthening the rationale for remediation and reducing occupant exposure.

6
Aflatoxins(Total Aflatoxins)
Range: Laboratory provides detection thresholds; any detection is significant.Optimal: Not detected.ng/g dust

Aflatoxins are potent hepatotoxic and carcinogenic mycotoxins produced by Aspergillus flavus and Aspergillus parasiticus. While foodborne exposure is more common, indoor contamination can occur in humid climates or agricultural settings.

Detection in building dust is uncommon outside agricultural or tropical environments but, when present, indicates a significant contamination requiring immediate remediation.

7
Trichothecenes(Trichothecene Mycotoxins)
Range: Laboratory provides detection thresholds; presence is significant.Optimal: Not detected.ng/g dust

Trichothecenes are a class of sesquiterpene mycotoxins produced by Stachybotrys, Fusarium, and other moulds. They inhibit protein synthesis and are potent irritants of mucous membranes and skin. Settled dust can harbour these toxins long after active growth has ceased.

Detection of trichothecenes in indoor dust supports the hypothesis of toxigenic mould exposure in symptomatic occupants and underscores the need for thorough remediation and dust removal.

Why is the Mold Building Profile test ordered?

  • Evaluation of patients with chronic respiratory symptoms, recurrent sinusitis, or asthma exacerbations when history or inspection suggests water-damaged buildings
  • Investigation of suspected mould-related hypersensitivity or allergic bronchopulmonary aspergillosis when environmental confirmation would guide allergen avoidance
  • Assessment of indoor environments for patients reporting building-related cognitive symptoms, fatigue, or mucosal irritation in the absence of other identified causes
  • Objective documentation of mould contamination to support remediation planning and verify that interventions have successfully reduced spore and mycotoxin loads
  • Occupational health evaluation when employees in a shared building report clustering of respiratory or constitutional symptoms
  • Paediatric cases where chronic rhinitis, cough, or wheeze correlate temporally with occupancy of a specific building
  • Pre- and post-remediation sampling to quantify the burden and confirm that professional cleaning has normalised the indoor environment
  • Situations where litigation, insurance claims, or lease disputes hinge on objective evidence of mould contamination

Sample collection and turnaround

Sample type

Dust

Fasting required

N/A

Collection method

At-home collection kit

Turnaround

10–14 business days

Collection notes

The laboratory provides a collection kit with detailed instructions, typically including a vacuum dust collection cassette or swabs and sterile containers. Patients or building occupants collect settled dust from high-traffic areas, carpets, HVAC filters, or visibly affected surfaces, following the protocol to ensure adequate sample volume and avoid cross-contamination. The sample is returned to the laboratory by courier or post in the provided packaging.

Specimen requirements

Minimum dust quantity as specified by the laboratory (typically 1–2 grams of settled dust or a representative swab). Samples should be collected from locations reflecting chronic exposure — bedroom, living areas, or air-handling systems — and labelled with collection site and date. Avoid collecting immediately after deep cleaning or HVAC filter replacement, which can transiently lower detectable levels.

What can affect Mold Building Profile results?

variableSampling technique and dust quantity

The amount and location of dust collected — carpet, HVAC filter, elevated surfaces — influence results. Inadequate sample volume or contamination during collection can yield false negatives or non-representative data.

variableOutdoor ambient mould levels

Outdoor spore concentrations vary by season, weather, and geography. Indoor counts must be interpreted relative to outdoor baselines; elevated outdoor levels can raise indoor counts through ventilation.

variableBuilding ventilation and occupancy patterns

High air exchange dilutes spore concentrations, while closed, stagnant spaces allow accumulation. Recent deep cleaning or HVAC filter changes can transiently lower detectable levels.

variableTime since water damage or remediation

Active growth produces higher spore counts; mycotoxins can persist in dust long after growth has stopped, so toxin detection may outlast viable spore elevations.

variableLaboratory culture versus molecular methods

Culture-based identification captures only viable, culturable organisms and may miss fastidious species; molecular or immunoassay-based mycotoxin detection is independent of viability but does not differentiate past from ongoing production.

What do Mold Building Profile results mean?

Elevated

Spore counts that exceed outdoor ambient levels or detection of toxigenic species (Stachybotrys, Chaetomium) indicate indoor amplification and support a mould exposure hypothesis. Mycotoxin detection confirms that toxigenic fungi have been metabolically active. Results should prompt environmental remediation — source removal, drying, cleaning, and ventilation improvement — and guide clinical decisions about allergen avoidance and exposure reduction.

Normal

A 'normal' or baseline result — indoor levels comparable to outdoor ambient, no detection of indicator toxigenic species or mycotoxins — does not exclude hypersensitivity in a particularly susceptible individual, but it makes ongoing environmental exposure unlikely. Negative results can also reflect sampling error or missed reservoirs.

Reduced

Spore counts at or below outdoor baselines and absence of mycotoxins suggest that the sampled environment is not a significant source of mould exposure. If clinical suspicion remains high, consider sampling additional locations, inspecting hidden reservoirs (wall cavities, under flooring), or investigating non-mould indoor air quality factors.

Note: Environmental testing documents contamination, not individual illness; clinical correlation is essential. Results are method- and laboratory-specific, and interpretation requires knowledge of regional outdoor mould ecology. A single sample may not represent the entire building; multiple samples and inspection by a qualified environmental professional strengthen conclusions. Mycotoxin detection does not establish causation of symptoms, and the clinical significance of low-level environmental mycotoxin exposure remains contested in the scientific literature.

Frequently asked questions

Air sampling captures spores that are airborne at a single moment and may miss heavy, sticky spores such as Stachybotrys. Dust sampling integrates exposure over time and is more sensitive for detecting settled contamination, making it the preferred method for documenting chronic indoor mould reservoirs.

How to access the Mold Building Profile test

The Mold Building Profile reference page is free and open to all practitioners. Create a free practitioner account to see pricing, save tests to your list, and generate requisition forms. Verification takes 1–2 business days.

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About this page

Published: October 7, 2026

Last reviewed: October 7, 2026

References:
  1. WHO guidelines for indoor air quality: dampness and mould. World Health Organization. (2009)
  2. Fisk WJ, et al. Meta-analyses of the associations of respiratory health effects with dampness and mold in homes. Indoor Air. (2007)
  3. Bush RK, et al. The medical effects of mold exposure. J Allergy Clin Immunol. (2006)
  4. Institute of Medicine (US) Committee on Damp Indoor Spaces and Health. Damp indoor spaces and health. National Academies Press. (2004)
  5. ACGIH Bioaerosols: Assessment and control. American Conference of Governmental Industrial Hygienists. (1999)

This content is for licensed healthcare practitioners only and does not constitute medical advice. Clinical decisions should be based on the full clinical picture and not on any single test result.