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You are here: Home / Archives for Indoor Air Quality

Moulds commonly found in carpet and mattress dust

Jackson Kung'u

A number of moulds are frequently found in carpet and mattress dust. Eurotium repens is the most frequently detected mould in mattress dust. Others include Aureobasidium pullulans, Alternaria alternata, Penicillium chrysogenum, Aspergillus penicilloides and Aspergillus restrictus.

More than 100 species of moulds have been recorded from carpet dust. As with mattress dust, the most frequently isolated mould in carpet dust is Eurotium repens. The others are Penicillium chrysogenum, Alternaria alternata, Aureobasidium pullulans and Phoma herbarum.

Concentrations of these moulds in carpet and mattress dust can be as high as 70 million colony forming units per gram of dust. Such high concentrations of moulds are likely to cause respiratory allergy or irritating symptoms. Therefore, it is import to regularly HEPA vacuum the carpets, mattresses and upholstered furniture to reduce the dust and spore concentration. If people are suffering from reoccurring respiratory allergy or irritating symptoms in a building where there is no visible mould, it is suggested that dust be tested for the types and concentrations of mould present.

Filed Under: Fungi, Microbial Sampling Tagged With: allergy, Alternaria, Aureobasidium, carpet, dust, eurotium, mould, Penicillium chrysogenum, Phoma herbarum

Legionella: Health Effects, Occurrence and Sampling

Jackson Kung'u

Health effects of Legionella

In 1976, in Philadelphia, USA, over 200 attendees of the US-American Legion, developed pneumonia. The disease was later called “Legionnaires’ disease”. The causative agent, a Gram-negative bacterium, was named Legionella pneumophila. Legionella pneumophila causes 85-90% of all cases of Legionella infections (legionellosis). There are over 40 species of Legionella.

Legionella pneumophila can cause very severe infection of the respiratory system. However, Legionnaires’ disease epidemics are rare but the disease is fatal if untreated. The disease may develop within 2 to 13 days (average 5-6 days).

Another form of legionellosis is Pontiac fever, named after an outbreak in 1968 in Pontiac, USA. This form of disease, caused by a number of Legionella species, is milder than Legionnaires’ disease. Pontiac fever develops within 48 to 72 hours and the illness may clear in 2-5 days. No fatal cases have been reported in relation to Pontiac fever. This disease mainly appears as epidemics. Pontiac fever is believed to be a reaction to inhaled Legionella antigens rather than an infection.

Disease transmission

There is no evidence for transmission of legionellosis from person to person or by ingestion. Legionella infection occurs when people inhale the bacterium via fine water droplets as aerosols from the environment. Indoor transmission of legionellosis has been reported via contaminated hot water supplies in hospitals, hotels and other public buildings, respiratory therapy equipment, jacuzzis, spas and air-humidifiers.

Occurrence

Legionella bacteria are part of the natural aquatic bacterial population of lakes and rivers. They are present in all types of fresh water, including tap water. Legionella multiply in water, using other microorganisms like bacteria, algae and protozoa. Their concentration in fresh water is influenced mainly by the temperature. They are isolated more frequently and in higher concentrations from warm water (30 to 50 °C.). However, Legionella also survive at much lower temperatures indoors as well as outdoors. At temperatures above 60 °C Legionella can’t survive.

Sampling Of Legionella

Sampling of Legionella in indoor air or water on a routine basis is not recommended. However, sampling is recommended to:

  • determine the source of outbreaks of legionellosis
  • check the effectiveness of maintenance practices and control measures for hot water supplies and humidified ventilation systems
  • guarantee the safe use of hot water supplies and humidified ventilation systems.

When investigating the water services within a building for Legionella, the condition of pipes, the joining methods used, the presence of lagging, sources of heat, and the standard of protection afforded tanks should be noted, as well as disconnected fittings, ‘dead-ends’, and cross-connections with other services.Water Sampling
Water samples should be collected in sterile autoclavable plastic containers. The samples should be taken from:

  • the incoming supply;
  • tanks;
  • an outlet close to, but downstream of, each tank;
  • the distant point of each service;
  • the water entering and leaving any fitting under particular suspicion.

Surface Sampling
Using swabs, surface samples should be taken from shower heads, pipes and taps. Also, sludge, slime or sediments within building water services or humidifiers can also be collected, particularly where accumulation occurs.

Sample Handling and Storage
Samples should be stored at room temperature (20 ± 5 °C.) in the dark and should be processed within 2 days. That means the samples should be sent to the laboratory within 24 hours. It is also important to confirm with the lab that they have the necessary media before sampling is done.

Air sampling
The presence of Legionella in indoor air can be investigated using Reuter Centrifugal Sampler (RCS) or the Andersen sampler. Regardless of the sampler used, the recommended sampling agar at present is BCYE-agar.

References

  1. Flannigan, B., R.A. Samson, and J.D. Miller (Editors). Microorganisms in home and indoor work environments: diversity, health impacts, investigation and control. 2001. London, UK: Taylor & Francis (ISBN: 0-415-26800-1).
  2. Wanner, H-U, AP Verhoeff, A Colombi, B Flannigan, S Gravesen, A Mouilleseux, A Nevalainen, J Papadakis, and K Seidel. 1993. Biological Particles in Indoor Environments. Indoor Air Quality and Its Impact On Man. Brussels: Commission of the European Communities. Report No. 12.

For more information on indoor bacteria, please visit http://www.moldbacteria.com/ or call 905-290-101.

Filed Under: Bacteria, Microbial Sampling, Water Testing Tagged With: algae, Bacteria, health risks, Legionella, legionellosis, legionnaires disease, pontiac fever, protozoa, sampling

Mould Exposure

Jackson Kung'u

The best strategy to determine if building occupants are exposed to hazardous mould is to take air samples. It is important to note that even in rooms with visible mould growth air sampling may give very low spore counts. Two methods are widely used in sampling air for mould.

  1. Impacting air on some growth media. This method is used when one is interested in determining the concentration of viable mould spores/fragments in the air.
  2. Impacting air on some inert sticky surface. In this case the mould spores and other particulate are directly counted under a microscope regardless of whether the spores are viable or not.

Both methods have limitations. Therefore, whether to use the first, second or both methods depends on the type of data required, which in turn depends on the objective of the investigation.

Filed Under: Fungi, Microbial Sampling Tagged With: air sampling, mould exposure, visible mould

Mold Removal: when to use a mold removal company

Jackson Kung'u

When to call a professional mold removal company

Mold removal is the process of removing  all moldy or contaminated material from a building. Generally material that can be cleaned are cleaned and dried. Although it’s tempting to remove any mold you see, it’s not always practical or safe to remove it yourself. Removing mold before you know whether it’s toxic can make your family feel ill. And sometimes there’s simply too much mold for you to remove safely yourself.

What mold removal guidelines say

You may clean small areas of mold (less than 1 square meter or 3 square feet) yourself. If you do choose to clean small areas of mold yourself, please follow mold guidelines for your safety and that of your family.

Mold growth covering an area less than 10 square feet is categorised as level 1 mold growth. Level 1 mold growth can be one single area of mold or it can include several patches of mold which together would be less than 10 square feet. Remember! Cleaning the mold without fixing the moisture problem, doesn’t solve the mold problem.

If visible mold growth in your house covers more than 10 square feet or if you are not sure how to clean the mold safely, it is recommended you seek professional advice. Cleaning large areas of mold growth releases high concentrations of mold spores into the air, which could make your family feel sick.

Therefore, extensive areas of mold growth should be cleaned by a professional. Heavy concentrations of mold spores can cause or worsen health problems.

Molds don’t have to be toxic to cause health problems. Even a common, usually harmless mold can be a health issue if there is a lot of it. However, always consult a professional if your house mold is a toxigenic mold, or if you even suspect a toxigenic mold.

How Do You Tell If A Mold is Toxigenic?

If you need to know whether your house mold is toxic or not, you may want to send a sample to our lab for testing. To send a sample, download the Order Form, complete it and send it together with your samples.

Remember! – please call a mold remediation professional when:

    • You the area covered by mold growth is greater than 10 square feet
    • You’re not sure of the extent of your mold problem
    • Mold comes back after repeated cleaning
    • The home is very damp
    • A family member suffers from allergies or asthma
    • You think the mold may be a toxic mold because a family member is suffering from unexplained symptoms that may be related to exposure to toxic mold

 

If you need a professional mold removal company, please visit this mold remediation professionals directory for a comprehensive list of mold remediation specialists listed by province. We also work closely with some mold removal companies and we may be able to direct you to the right people. Give us a call at 905-290-9101.

Filed Under: Fungi, Microbial Sampling, Mold Tagged With: allergy, asthma, mold growth, mold guidelines, mold removal, toxic mold

Mold Sampling: How To Select Agar Media

Jackson Kung'u

Why selecting the right type of mold sampling agar media is critical

There are several types of agar media used in a microbiology laboratory for culturing molds. These media may differ in their water activity, pH, nutrient content or composition. Molds differ in their growth requirements. Therefore, no single medium is suitable for each and every mold out there. It’s therefore important to select mold sampling agar media wisely.

 

How would one select mold sampling media to use then?

 It is easy to select the mold sampling media to use if one is looking for a specific type of mold. However, in most mold investigation projects, one is interested in knowing the kinds of viable molds present in the air and their concentrations. Penicillium chrysogenum growing on DG18The problem of using a single type of media is that some molds may not grow well (or may not grow at all) in the selected media. Hence, although such molds may be the dominant contaminants in the air, they may end up being missed or underestimated. The solution, therefore, is to use more than one type of mold sampling media or select one that is known to support a wide range of environmental molds. A good example is Malt Extract Agar (MEA). The problem with this media is that it also supports the growth of bacteria to some extent. Picture of Penicillium Chrysogenum and Stachybotrys chartarum on MEAIf the environment sampled is contaminated with bacteria, the bacteria grow faster than molds and interfere with mold growth. This problem can be overcome by incorporating a suitable antibiotic or other suitable compounds (e.g., Rose Bengal) into MEA to suppress bacterial growth. Rose Bengal not only suppresses the growth of bacteria but also restricts the spread of fast growing molds thus making it easy for colony counting.

 

What about culturing of bulk samples?

 

The same applies to culturing of bulk samples such as pieces of building material or dust. Direct culturing of such material in a single type of media could give erroneous results. If a single media is to be used to culture these types of samples, it is recommended that a lab performs a direct microscopic examination of the samples before culturing. Stachybotrys on MEADirect microscopy allows identification of the dominant contaminant (at least to genus level) regardless of whether the mold is dead or cannot grow on media used.

 

Demonstrating the effect of media on mold growth

 

To demonstrate how results from a single media can be misleading, examine the 4 petridishes. Two bulk samples were cultured onto 2 different media (DG18 and MEA) after serial dilution. Sample 1 was cultured in petridishes marked “A”. Direct micrsocopic examination of sample 1, indicated it had Stachybotrys as the dominant mold and some slight growth of Penicillium. After incubation, Stachybotrys did not show up at all in DG18 but both Stachybotrys (cream colonies with dark centres) and Penicillium (blue colonies) appeared on MEA. The second sample had Stachybotrys only. Stachybotrys on MEAAfter plating onto DG18 and MEA and incubation (see petridishes marked “B”), Stachybotrys appeared on MEA but not on DG18. These observations clearly indicate how wrong conclusions can be made if the right type of media is not used either in air sampling or culturing of bulk samples.

 

If you would like more information on mold sampling media, give us a call at 905-290-9101.

 

References

Microorganisms in home and indoor work environments: diversity, health impacts, investigation and control. Flanning Brian, Samson, Robert A., and Miller, David J (Ed.), Taylor and Francis, 2001.

For more information on sampling media,
please visit http://www.moldbacteria.com/prices.html or
call 905-290-101.

Filed Under: Fungi, Microbial Sampling Tagged With: agar media, culture media, mold growth, mold sampling

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