2012 Environmental Microbiology Research Abstracts

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    AIHA

    The viewpoints, opinions, and conclusions expressed in the presentations, sessions, and discussions at AIHce havenot necessarily been approved or endorsed by AIHAor ACGIHand do not necessarily reflect those of AIHAor ACGIH.

    NIOSH The findings and conclusions in the National Institute for Occupational Safety and Health presentations have not

    been formally disseminated by the National Institute for Occupational Safety and Health and should not be construed to

    represent any agency determination or policy.

    2012 Abstracts

    Ju ne 16-21: In di an ap olis, In di ana

    Podium Session 5

    Environmental Microbiology Research

    Wednesday, June 20, 2012, 10:00 AM 12:00

    PM

    Papers SR-115-01SR-115-06

    SR-115-01WITHDRAWNUsing New Parameters for

    Correlation between Concentration of Carbon

    Dioxide and Bacterial Bioaerosols in Indoor

    Workplaces

    T. Lin, J. Liu, L. Yang, China Medical University,

    Taichung, Taiwan; P. Hung, C. Chen, Institute of

    Occupational Safety and Health, CLA, Taipei, Taiwan.

    SR-115-02

    Detection and Identification of

    Stachybotrys chartarumMicrobial Volatile

    Organic Compounds (MVOCs) On-SiteUsing Person-Portable Gas

    Chromatography/Mass Spectrometry (GC-

    MS) Using a Thermal Desorption

    AccessoryA. Gifford, INFICON, Inc., East Syracuse, NY.

    Objective

    Water damage in residential and

    commercial buildings provides optimal conditions

    for toxigenic mold and fungal growth, potentially

    leading to severe health problems. A concern

    since the 1980s has been Sick Building

    Syndrome (SBS) and Damp Building-RelatedIllnesses (DBRI) which include neurological,

    immunological and pulmonary diseases. SBS and

    DBRI have been etiologically linked to toxic mold

    and fungal growth in water-damaged structures.

    Unique Microbial Volatile Organic Compounds

    (MVOCs) produced by these molds and fungi can

    be detected and identified to establish the extent

    and severity of a water-damaged area.

    Stachybotrys chartarum, one of the more toxic

    molds associated with SBS and DBRI, can be

    identified by its characteristic MVOCs (Gao et al.

    2002). These are easily detectable, on-site, using

    person-portable gas chromatography/mass

    spectrometry (GC-MS) with a thermal desorption

    accessory. Most MVOCs produced by S.chartarumare medium-dependent. However,

    anisole is one found to be common on several

    different media.

    Methods

    A custom mixture of selected S.

    chartarum MVOCs (including anisole) was

    injected into a 1 L polytetrafluoroethylene bag

    containing high-purity nitrogen for a target

    concentration of ~200 g/m3. The gaseous

    mixture was sampled onto a carbon-based

    thermal desorption tube and then desorbed using

    the thermal desorption accessory attached to theperson-portable GC-MS. A 20-minute analysis was

    used to seperate and identify each chemicals

    utilizing spectral libraries.

    Results

    The person-portable GC-MS used to

    analyze detected these MVOCs in the mid-to-low

    ppb range with no inhibitions. Further studies in

    to lower concentrations are in-process.

    Conclusions

    The ability to locate the source of

    MVOCs allows for the complete removal of water-

    damaged materials, ostensibly reducing or

    eliminating occupant exposure to the associated

    toxins. Usage of a person-portable GC-MS with

    thermal desorber accessory enables industrial

    hygienists or environmental consultants to

    perform these tasks on-site, taking only minutes

    instead of days.

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    SR-115-03

    A Building Performance Model for Evaluating

    Bioaerosol Data

    R. Spicer, H. Gangloff, WCD Group, Pennington, NJ.

    Objective

    This studys objective was to

    mathematically evaluate the common heuristic

    approach for interpreting environmental fungal

    using professional judgment and arbitrary

    numerical criteria that are anchored in industrialhygiene/public health models.

    Methods

    The experimental method involved

    collecting spore trap data (Air-O-CellTM ; 60 liters

    sample volume) at a northeast metropolitan

    school following post flood dry down and mold

    remediation. Samples were collected in the

    outdoor air, impact zone, and indoor control zone

    (N=17, 15, and 14 respectively) from 8:30 AM

    3:30 PM of the same day. Differences in

    numerical spore levels and the probability of

    observed differences in detection frequency

    greater than the combined median (fd) between

    the indoor and outdoor zones were calculated for

    each fungal type and total spores. The error rates

    of the criteria were then generated by

    bootstrapping the data to generate the frequency

    (random probability) of values for the respective

    criterion greater than actually observed from the

    data.

    Results

    Results

    were consistent with earlier

    studies indicating erratic performance of criteria

    based on numerical indices such as fungal

    levels, or ratios/proportions. As one example,data reported herein exhibited mean

    Basidiospore levels approximately four times

    greater in the (remediated) impact zone

    compared to the indoor control zone. However

    bootstrapping revealed a 0.30 probability for

    control zone numerical concentrations to be

    greater than in the impact zone for typical sample

    sizes. By contrast, fdindicated a 0.68 probability

    of Basidiospore being greater in the impact

    zone, a probability valued confirmed by

    bootstrapping.Conclusions

    The

    conclusion from this study is fdas a mathematically validated criterion,

    quantifies differences between comparative

    fungal populations for building evaluation

    purposes and is best viewed as a building

    performance indicator. This is to be differentiated

    from the industrial hygiene/public health model

    of relating numerical fungal levels to potential

    health effects.

    SR-115-04

    Evaluation of Bioaerosol and Antibiotic-

    resistant Characteristics in a Broiler Farm

    C. Lai, T. Fan, C. Chen, Y. Chen, J. Lee, Chung Shan

    Medical University, Taichung, Taiwan; Y. Lin, Chung

    Shan Medical University Hospital, Taichung, Taiwan.

    Objective

    This study aimed to study possibly

    bioaerosol exposure of employees in a broiler

    building in central-southern Taiwan.Methods

    An Anderson six-stage bioaerosol

    sampler, Anderson single-stage bioaerosol

    sampler, AGI-30, Biosampler, as well as TSA patri

    dish were used to sample bioaerosols. The

    identification and antibiotic-resistant

    characteristics of bacteria were studied by using

    Phoenix.

    Results

    The results showed that the relative

    humidity was between 46.3% and 80.9% and the

    temperature was between 17.5C and

    32.1Cduring the sampling. The bioaerosolconcentration in the coop for chicks was 3.2104

    to 5.8105cfu/m3and that in the coop for

    chickens was about 1.0 to 2.0106 cfu/m3.

    Based on the bacteria identification, it was

    concluded that Staphylococcusspp. belongs to

    superior strains; moreover, Staphylococcus

    lentus dominated the number concentration of

    bacteria identification results. However,

    Staphylococcus aureus was the most dangerous

    bacteria belonging to the biological safety level II

    in the study.

    Conclusions

    The Staphylococcus lentusrevealed

    antibiotic-resistant characteristics, for instance,

    Ampicillin (AM), Chloramphenicol (C), Clindamycin

    (CC), Gentamicin-Syn (GMS), Penicillin (P),

    Streptomycin-Syn (STS) cannot use to stop the

    growth of Staphylococcus lentus. In general, from

    the study, Staphylococcus spp.resisted to

    Ampicillin (AM), Streptomycin-Syn (STS),

    Gentamicin-Syn (GMS), Penicillin (P),

    Chloramphenicol (C).

    SR-115-05Effect of Relative Humidity on Impactor

    Sampling among Four Airborne Viruses

    P. Raynor, J. Appert, T. Kuehn, S. Ge, Z. Zuo, University

    of Minnesota, Minneapolis, MN; S. Goyal, M. Abin, Y.

    Chander, University of Minnesota, St. Paul, MN.

    Objective People in a wide spectrum of occupations

    are exposed to viruses present in the air. This

    research investigated the influence of humidity on the

    viability of live virus aerosols and the particle sizes

    test viruses were associated with.

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    Methods Four viruses bacteriophage MS2, human

    adenovirus, transmissible gastroenteritis virus of pigs,

    and avian influenza virus were aerosolized

    separately into an apparatus from suspensions using

    a nebulizer. The relative humidity in the apparatus

    was conditioned to 15, 50, and 85% at room

    temperature. An 8-stage Andersen impactor with

    aluminum plates was used to sample the test

    aerosols. Collected material was eluted from each

    impaction surface, and the amounts of live viruspresent were determined using standard virology

    techniques. By comparing the amount of live virus

    collected versus the concentration in the nebulizer

    suspension against the recovery of a fluorescent dye

    versus its concentration in the suspension, the

    relative recovery (R) of live virus was measured, with

    R=1 equivalent to 100% recovery.

    Results Relative recovery varied widely by virus,

    ranging from a minimum R=0.02 to a maximum of

    R=1. On average, MS2 aerosols yielded the highest

    values of R and avian influenza virus had the lowest

    relative recovery. All test viruses were affected byrelative humidity. Compared to other conditions, MS2

    recovery was highest at 50% relative humidity

    although transmissible gastroenteritis virus recovery

    was lowest. Recovery of human adenovirus was

    highest at 85% relative humidity (p=0.0002). Versus

    15 and 50% relative humidity (R=0.02 to R=0.06),

    recovery of live avian influenza virus was markedly

    higher at 85% relative humidity (R=0.59, p