FAB1 Actinomycetes plus ERMI

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Description

Quantitative detection of the microbial content of Actinomycetes using (NGS) Next-Generation Sequencing and ERMI test.

Turnaround Time: 7 Days for Actinomycetes, ERMI options are 7 days, 3 days and 1 day.  

Sample Limitations:  Dust by Swiffer cloth sampling – we require a minimum of 10 mg dust – if you can see plenty of dust on the Swiffer it will be fine.

 

  1. Avoid sampling surfaces that have been hot.
  2. Avoid surfaces that have been exposed to biocides, e.g. Chlorine containing chemicals
  3. Don’t sample from surfaces where there is Drywall dust or clay-like powder present.

 

Actinomycetes

The most frequent bacteria species found on Water-Damaged Building are Actinomycetes (which includes Actinomyces and Mycobacteria) this is the kind of bacteria that produce biotoxins similar to mold mycotoxin.  As a whole, biotoxins from bacteria by weight and by mass are far more important than say, mycotoxins. “This test is based on Next Generation DNA sequencing, also known as 16S metagenomics.  The test is based on microbial I.D of all the bacteria in the sample.  The Actinomycetes test was developed by selecting the top 40 Actinomycetes species in the sample to create a score of actinomycetes in a situation of Building-Related Illness (BRI).

 

Species included in the score have been reported in multiple studies linking them with BRI.

 

    

Score system:

Score Score RangeInterpretation
Q19 or belowIndicative of a Healthy Building
Q2Between 10 to 15Further investigation needed
Q3Greater than 15Suggestive of Building-Related Illness

 

 

ERMI Background

The US Environmental Protection Authority developed ERMI to provide a straightforward, objective, sensitive and standardized way to assess mold and indoor air quality investigations. The USEPA developed the ERMI as a ranking system based on dust samples collected from homes, the ERMI will help predict the moldiness of homes.

Based on widely published data from EPA researchers and the 2006 HUD American Healthy Home Survey, the test has been developed as a tool to evaluate the potential risk of indoor mold growth and associated health effects to occupants.

In order to most effectively use this tool, the ERMI obtained needs to be compared to a national database. Indices were determined using this method for 1,096 homes across the U.S. as part of the 2006 HUD American Healthy Home Survey. Individual indices ranked from lowest to highest were used to create a national Relative Moldiness Index (RMI) Scale.

In initial studies by the USEPA, the concentrations of different mold species in “moldy homes” (homes with visible mold growth or a history of water damage) and “reference homes” (homes with no visible mold) were compared. Based on those results, mold species were selected and grouped into those with higher concentrations in moldy homes (group 1) and those with lower concentrations (group 2). To calculate the ERMI the individual concentrations of the mold species detected are log-transformed and the sum of group 2 logs is subtracted from the sum of group 1 logs.

 

ERMI =|  Sum of Log10 Group I|  minus|  Sum of Log10 Group II

 

Below is a list of the mold species included in an ERMI report:

Group 1: Water Damage MoldsGroup 2: Common Indoor Molds
1) Aspergillus flavus/oryzae,27. Acremonium strictum
2) Aspergillus fumigatus28. Alternaria alternata
3) Aspergillus niger29. Aspergillus ustus
4) Aspergillus ochraceus30. Cladosporium cladosporioides1
5) Aspergillus penicillioides31. Cladosporium cladosporioides2
6) Aspergillus restrictus32. Cladosporium herbarum
7) Aspergillus sclerotiorum33. Epicoccum nigrum
8) Aspergillus sydowii34. Mucor amphibiorum
9) Aspergillus unguis35. Penicillium chrysogenum
10) Aspergillus versicolor36. Rhizopus stolonifer
11) Aureobasidium pullulans
12) Chaetomium globosum
13) Cladosporiumsphaerospermum
14) Eurotium (Asp.) amstelodami
15) Paecilomyces variotii
16) Penicillium brevicompactum
17) Penicillium corylophilum
18) Penicillium crustosum
19) Penicillium purpurogenum
20) Penicillium Spinulosum
21) Penicillium variabile
22) Scopulariopsis brevicaulis/fusca
23) Scopulariopsis chartarum
24) Stachybotrys chartarum
25) Trichodermaviride
26) Wallemia sebi

 

 

ERMI Graph

This table assists in interpreting the graph

 

QuartileZonePercentageERMI ValueRelative Mouldiness
Q1Green25% of housesBetween -10 to -4Low Relative Mouldiness
Q2Amber25% of housesBetween -4 to 0Low to Medium
Q3Amber25% of housesBetween 0 to 5Medium to High
Q4Red25% of housesBetween 5 to 20High
RedGreater than 20Very High

 

 

Vacuum Sampling

EBI offers two methods for collecting dust samples. The original ERMI process used vacuum dust sampling where a special nozzle is fitted to a vacuum cleaner and allowed a sample of dust to be taken by masking off a 900 x 1800mm rectangle in the occupants living room and a similar area in the master bedroom. They are each vacuumed for 5 minutes to obtain a composite sample. One clear advantage of this test is that the carpet acts as a repository for the mold spores to collect over time. An issue that also occurs is that when a home has been water damaged the carpet may have been removed. We have included a video on the product page that outlines the steps for vacuum sampling.

 

Swiffer Cloth Sampling

One clear limitation of ERMI vacuum sampling is that many homes do not have carpet, and many people who are susceptible to mold-related illness have chosen to have wooden or tiled floors. As a result, the “Swiffer Cloth Method” was developed. The important issue when sampling is that the procedure needs to collect dust that is representative of the area sampled, providing a sufficient quantity of dust so that the lab analysis can be successful.

Additional information

WeightN/A
DimensionsN/A
Item Type

Swiffer Kit, Vacuum Kit

Turn Around Time

1 Day, 3 Days, 7 Days