Municipal Environmental Research EPA-600 2-79-131
                    Laboratory         August 1979
                    Cincinnati OH 45268
&ER&
Analysis of
Airborne Viable
Bacteria at Solid
Waste Processing
    ilities

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                RESEARCH REPORTING SERIES

Research reports of the Office of Research and Development, U.S. Environmental
Protection Agency, have been grouped into nine series. These nine broad cate-
gories were established to facilitate further development and application of en-
vironmental technology.  Elimination of traditional  grouping was consciously
planned to foster technology transfer and a maximum interface in related fields.
The nine series are:

      1.  Environmental  Health  Effects Research
      2  Environmental  Protection Technology
      3.  Ecological Research
      4.  Environmental  Monitoring
      5.  Socioeconomic Environmental Studies
      6.  Scientific and Technical Assessment Reports (STAR)
      7  Interagency Energy-Environment Research and Development
      8.  "Special" Reports
      9.  Miscellaneous Reports

This report has been assigned  to the  ENVIRONMENTAL PROTECTION TECH-
NOLOGY series. This series describes research performed to develop and dem-
onstrate instrumentation, equipment, and methodology to repair or prevent en-
vironmental degradation from point and non-point sources of pollution. This work
provides the new or improved technology required for the control and treatment
of pollution sources to meet environmental quality standards.
This document is available to the public through the National Technical Informa-
tion Service, Springfield, Virginia 22161.

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                                      EPA-600/2-79-131
                                      August 1979
  ANALYSIS OF AIRBORNE VIABLE BACTERIA AT
     SOLID WASTE PROCESSING FACILITIES
                    by
      M. W. Fletcher and D. E. Fiscus
        Midwest Research Institute
       Kansas City, Missouri  64110
          Contract No. 68-02-1871
              Project Officer

              Carlton C. Wiles
Solid and Hazardous Waste Research Division
Municipal Environmental Research Laboratory
          Cincinnati, Ohio  45268
MUNICIPAL ENVIRONMENTAL RESEARCH LABORATORY
    OFFICE OF RESEARCH AND DEVELOPMENT
   U.S. ENVIRONMENTAL PROTECTION AGENCY
          CINCINNATI, OHIO  45268

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                              DISCLAIMER
     This report has been reviewed by the Municipal Environmental  Research
Laboratory,  U.  S. Environmental Protection Agency,  and approved for  publi-
cation.   Approval does not signify that the contents necessarily reflect
the views and policies of the U. S. Environmental Protection Agency, nor
does mention of trade names or commercial products  constitute endorsement
or recommendations for use.
                                    ii

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                                   FOREWORD
     The Environmental Protection Agency was created because of increasing
public and government concern about the dangers of pollution to the health and
welfare of the American people. Noxious air, foul water, and spoiled land are
tragic testimony to the deterioration of our natural environment. The complex-
ity of that environment and the interplay between its components require a
concentrated and integrated attack on the problem.

     Research and development is a necessary first step in problem solution,
and it involves defining the problem, measuring its impact, and searching for
solutions. The Municipal Environmental Research Laboratory develops new and
improved systems technology to minimize the adverse economic, social, health,
and aesthetic effects of pollution. This publication is one of the products of
that research.

     The St. Louis-Union Electric-Environmental Protection Agency refuse fuel
project was the first use demonstration of solid waste as a supplementary fuel
in power plant boilers for generating electricity. In addition to the fuel
demonstration, research tasks were conducted to evaluate the relative levels
of airborne bacteria and viruses at the St. Louis Refuse Processing Plant and
other waste handling facilities for purposes of hazard assessment.

     This report was prepared as an evaluation of the analytical methodologies
used to determine airborne microbiological emissions. The total research pro-
gram is fully discussed in the report, "Assessment of Bacteria and Virus Emis-
sions at a Refuse Derived Fuel Plant and Other Waste Handling Facilities,"
EPA-600/2-78-152, U.S. Environmental Protection Agency, August 1978.
                                          Francis T. Mayo, Director
                                          Municipal Environmental Research
                                            Laboratory
                                     iii

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                                   ABSTRACT
     This report presents a synopsis of aerobiological testing methodologies
used by Midwest Research Institute during studies conducted for the Environmen-
tal Protection Agency. The purpose of the programs was to determine relative
levels of airborne bacteria and virus aerosols within and around waste handling
facilities. The facilities tested were the St. Louis Refuse Processing Plant,
the Browning Ferris/Raytheon Service Company Resource Recovery Plant  (Houston),
and three other types of waste handling facilities:  an incinerator,  a waste
treatment plant, and a landfill. The report presents microbiological  air sam-
pling methodologies, sample handling procedures, and laboratory analysis meth-
odologies. It also includes a general discussion of pertinent considerations
with recommendations for future research, and an extensive bibliography.

     This report is of interest to those involved in measuring airborne micro-
organisms at waste handling and processing facilities. A complete discussion
of the entire research program is contained in the report entitled "Assessment
of Bacteria and Virus Emissions at a Refuse Derived Fuel Plant and Other Waste
Handling Facilities," EPA-600/2-78-152, U.S. Environmental Protection Agency,
August 1978.

     This report was submitted as part of Contract No. 68-02-1871, by Midwest
Research Institute under the sponsorship of the U.S. Environmental Protection
Agency and covers work done during the period 1975 through 1978.
                                      IV

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                                 CONTENTS

Foreword	
Abstract	    iv
Figures	•	•  •    vi
Tables	    vi
Acknowledgment	   vii

     1.  Summary of Recommendations.	      1
     2.  Introduction	      3
     3.  Aerosol Sampling Devices and Field Methodology	      5
              St. Louis program.	      5
              Houston program	      6
     4.  Aerosol Sample Handling Procedures	      7
              St. Louis program	      7
              Houston program. ............ 	      8
     5.  Sample Preparation and Microbiological Analysis .......    10
              Sample preparation 	    10
              Microbiological analysis procedures	    14
     6.  Discussion	    24
              General considerations 	    24
              Aerosol sampling devices 	    25
              Microbiological analysis of aerosol samples. . 	    27
              Bacteriological analysis 	 ..........    28
              Virus analysis	    29
              Future work	    31

References	    32
Bibliography 	    38
                                      v

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                                    FIGURES
Number
Page
   1     Microbiology sample processing procedure - St. Louis
           program	    11

   2     Bacterial analysis spectrum - St. Louis program 	    12

   3     Microbiology sample handling procedure - Houston program. . .    13

   4     Bacterial analysis spectrum - Houston program 	    15



                                    TABLES

Number                                                                   Page

   1     Flow Sheet for Viral Concentration Procedures of Aerosol
           Samples on Filter Media (Phase Separation Method) 	    21

   2     Monolayer Plaque Assay Technique	    22

   3     Recommended Bacterial Assay Methods for RDF Facility
           Aerosol Samples 	    30
                                      vi

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                              ACKNOWLEDGMENT
     This report was prepared by Midwest Research Institute for the Municipal
Environmental Research Laboratory, U.S. Environmental Protection Agency,
Cincinnati, Ohio, under EPA Contract No. 68-02-1871. The project officer for
the Environmental Protection Agency was Carlton C. Wiles.

     This report was written by Messrs. M. W. Fletcher and D. E. Fiscus.
However, many of Midwest Research Institute's personnel contributed to the
programs which resulted in this publication. Foremost among the contributors
are Dr. F. Wells, Dr. W. Spangler, Mr. R. Flippin, Mr. P. Gorman, Mr. M.
Golembiewski, and Dr. K. P. Ananth. Other contributors were Mr. B. DaRos,
Mr. T. Merrifield, Mr. R. White, Mr. M. P. Schrag, and Dr. L. J. Shannon.
The assistance and support of these scientists are gratefully acknowledged.

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                                  SECTION 1

                          SUMMARY OF RECOMMENDATIONS

     Airborne microorganism emissions from refuse-derived fuel (RDF) and other
waste handling facilities are not well characterized. Further research should
be conducted to better define their qualitative and quantitative nature. The
following summary of recommendations will aid future research attempts to
characterize microbial aerosol emissions.

        Hi-Vol air samplers are not recommended to sample for airborne micro-
        organisms because of the deleterious effects on microbial viability
        due to desiccation.

        AGI-30 impingers with gelatin-milk impinger fluid (or other suitable
        collection menstruum) are recommended for quantitative sampling for
        airborne bacteria and virus both in and around waste handling facili-
        ties.
     .  AGI-30 impingers should not be operated for periods greater than 10 to
        30 min.

     .  Sampling for airborne microorganisms with an AGI-30 in the presence of
        large particulates may necessitate the addition of a dry modified
        Greenburg-Smith impinger preceding the AGI-30 impinger. The contents
        of both impingers should be analyzed if quantitative microbiological
        results are desired.

        The Andersen impactor is recommended only for microorganism counts by
        particle size. The Andersen impactor is not recommended for quantita-
        tive airborne microorganism concentrations because airborne particu-
        lates may contain more than one microbial cell. Multiple microbial
        cells per particle may result in only one colony count and the true
        count may thereby be underestimated.

        The Andersen impactor should not be operated for periods exceeding
        30 min.

        AGI-30 impinger and Andersen impactor sampling devices should always
        be included as reference sampling devices if another sampler is to be
        principally used.

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Although not tested in these studies, the Litton  large-volume air  sam-
pler  (LVS) may be used to sample for specific airborne microorganisms,
i.e., Salmonella, Staphylococcus, and Klebsiella, and viruses. These
microorganisms may occur at threshold detection levels with the AGI-30
impinger, but still may be present at epidemiologically significant
levels.

Bacterial analysis of aerosol samples should be initiated within 4 hr
of collection.

Virus analysis of aerosol samples should be initiated as soon as possi-
ble.  If delays are unavoidable, the samples should be quick-frozen and
stored at -70°C.

Only  optimum media and/or methods which have undergone rigorous compar-
isons under identical conditions, preferably with aerosol samples,
should be used to analyze aerosol samples for microorganisms.

Monolayer plaque assay methods, with sensitive cell lines, are recom-
mended for titration of viruses. HeLa or KB cell  lines are recommended
for titration of adenoviruses. Primary rhesus monkey kidney cells  or
the continuous monkey kidney cell lines BGM or LLC-MIO? are recommended
for enterovirus titration.

Direct sample incorporation onto cell monolayers without prior sample
concentration is recommended for virus assays of samples containing
sufficiently large concentrations of viruses.

The phase separation method of virus concentration is one technique
recommended for samples containing low concentrations of viruses.  Con-
centration efficiency controls should be conducted with a known virus
strain.

Use of microbial indicators of sanitary significance such as total
coliforms, fecal coliforms, and fecal streptococci in determining  rela-
tive levels of air hazard should be avoided. The significance of these
indicators in the atmospheric environment has not been thoroughly  es-
tablished.

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                                  SECTION 2

                                 INTRODUCTION
     Concern that aerosol emissions might contain pathogenic microorganisms
from industrial and public utility facilities has prompted new interest in
aerobiological testing. Emissions assessments for airborne microorganisms
have recently been conducted at sewage treatment facilities (1-8), food pro-
cessing waste spray fields (9), cooling towers (10-12), and more recently
solid waste handling facilities with associated refuse derived fuel plants
(13,14).

     Difficulties in quantitatively determining aerosolized microorganisms in
controlled laboratory systems are well known. The problem of accurately as-
sessing airborne microorganism concentrations under field conditions presents
even greater difficulties due to the increased number of uncontrollable envi-
ronmental variables. Additional quantitation variables arise from individual
choices of aerosol sampling devices and laboratory analysis procedures.

     Midwest Research Institute (MRI) recently conducted aerosol emission
tests for bacteria and virus at the St. Louis-Union Electric Facility  (14)
(hereafter referred to as the St. Louis program) and at the Houston/Browning
Ferris Industries (15) (hereafter referred to as the Houston program). Nu-
merous problems were encountered during these programs, primarily concerning
the nature of the particulate emissions at the refuse facilities tested and
the microbial viability variables of the sampling methods employed.

     The purpose of this report is to present the aerosol sampling and micro-
biological assay procedures used during the St. Louis and Houston programs.
The report covers the air sampling devices, sample handling procedures in the
field, and microbiological analysis procedures used during the programs. Prob-
lems encountered with the methods are discussed and recommendations are made
with regard to future research. A bibliography is included to assist in future
research efforts.

     This report is primarily concerned with procedures and methodologies.
Further information concerning the results obtained during the St. Louis and
Houston programs may be found in the following reports:

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   Assessment of Bacteria and Virus  Emissions  at  a Refuse  Derived  Fuel
   Plant and Other Waste Handling Facilities  (14).

   Evaluation of Fabric Filter Performance at  Browning Ferris  Industries/
   Raytheon Service Company Resource Recovery  Plant,  Houston,  Texas  -
   Draft Report (15).

.   Executive Summary - Assessment of Bacteria  and Virus Emissions  at a
   Refuse Derived Fuel Plant and Other Waste Handling Facilities (16).

   Dust and Airborne Bacteria at Solid Waste  Processing Plants (17).

   Comparative Assessment of Bacterial and Viral  Field Sampling Methods
   Used at Solid Waste Handling and Processing Facilities  (18).

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                                  SECTION 3

                AEROSOL SAMPLING DEVICES AND FIELD METHODOLOGY
ST. LOUIS PROGRAM

     The major aerosol sampling device for airborne microorganisms during the
St. Louis program was the Model GMWL-2000 Hi-Vol sampler.£' It was chosen as
the primary sampling device because it could simultaneously sample aerosols
for three parameters:  microorganisms, physiochemical particulate morphology,
and trace metals. Hi-Vol samplers placed at upwind and downwind locations were
standard units. The Hi-Vol samplers used for in-plant sampling were standard
units equipped with a Model 230 CP Cyclone Preseparatork'  to remove large par-
ticulates and eliminate filter overloading, which has been reported as one of
the Hi-Vol's major problems (19). All of the Hi-Vol samplers were operated at
a continuous sampling rate of 1,134 liters/min for 6 hr with Gelman Type AE
glass fiber filters—' serving as the collection medium.

     Counts of airborne microorganisms by particle size were conducted with an
Andersen Model 10-800 sampler—' coupled with a backup modified Greenburg-Smith
impinger£/ to remove any viruses passing the Andersen impactor. Plate count
agar (27 ml) served as the collection medium for the Andersen impactor. The
Greenburg-Smith impinger contained 100 ml Hanks' balanced  salt solution (BSS)
as the collection menstruum. The sampling train was operated at 27.96 liters/
min for 0.5 min at in-plant sites and 10 min at property line sites.

     Greenburg-Smith impingers were used alone during special sampling appli-
cations for airborne microorganisms. Again, the collection menstruum was 100 ml
Hanks' BSS in all instances. The sampling rate was held constant at 27.96 li-
ters/min for 6 hr at each sampling site.
aj  General Metal Works, Inc., 8368 Bridgetown Road, Cleaves, Ohio  45002.
b/  Sierra Instruments, P.O. Box 909, Carmel Valley, California  93924.
c/  Gelman Instrument Company, 600 South Wagner Road, Ann Arbor, Michigan
      48106.
d/  Andersen Samplers, Inc., 4215-L Wendell Drive, Atlanta, Georgia  30336.
e/  Ace Glass, Inc., P.O. Box 688, Vineland, New Jersey  08360.

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HOUSTON PROGRAM

     The sampling devices were modified somewhat for the Houston program be-
cause of the experience gained during the St. Louis testing. Only AGI-30 im-
pingers£/ and the Andersen Model 10-800 sampler were used as sampling devices.

     AGI-30 impingers were used to collect air samples for quantitative deter-
minations of airborne bacteria and virus. At the baghouse inlet, the sampling
train consisted of a 1.52 m  (5.0 ft) stainless steel probe with a 2.54-cm  ID
(1.0-in. ) probe tip, a dry modified Greenburg-Smith impinger, and an AGI-30
impinger containing 25.0 ml  gelatin-milk solution  (same as collection medium
ii of White (20), but with omission of spermidine  phosphate), a vacuum pump,
and a dry gas meter. The Greenburg-Smith impinger  served to trap large parti-
cles that might otherwise plug the AGI-30 orifice. For sampling at the bag-
house outlet, the Greenburg-Smith impinger was omitted. Samples were taken
for 30-min intervals at 4.8  liters/min (0.18 cfm)  for the baghouse inlet
and 3.6 liters/min (0.13 cfm) at the baghouse outlet. Samples at both sites
were taken from single points in the duct.

     Andersen microbial impactors were used to quantitate bacterial concentra-
tions by particle size. Plate count agar (27 ml) containing 50 units Myco-
statinSL' antifungal agent per milliliter agar served as the collection medium.
Samples were collected from  a single point in the  duct using the same probe as
was used with the AGI-30 impingers. The baghouse inlet was sampled for 20  sec
at a flow rate of 27.0 liters/min (0.951 cfm). Sampling times were increased
to 10 min at the baghouse outlet to compensate for the lower particulate con-
centrations.
f/  Ace Glass, Inc., P.O. Box 688, Vineland, New Jersey  08360.
£/  Grand Island Biological Company, 3175 Staley Road, Grand Island, New
      York  14072.

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                                  SECTION 4

                      AEROSOL SAMPLE HANDLING PROCEDURES
     The  sample handling methodology was dependent upon the  type of sampling
equipment used. The  following are procedure descriptions for each  type of
sampling  device used.

ST. LOUIS PROGRAM

Hi-Vol Samplers

     The Hi-Vol samplers were equipped with a filter support screen and an
open metal  frame with  a foam gasket to seal the filter edges in place. The
samplers were  field-cleaned by wiping down the filter screen, metal frame,
and surrounding area inside the Hi-Vol with lint-free chemical wipes saturated
with 70%  isopropyl alcohol. The residual alcohol was allowed to evaporate
prior to  installing  the sterile filter. All manipulations of the sterile fil-
ter during  installation and removal were made while wearing sterile vinyl
gloves. After  sampling, the filter was removed, placed in a sterile envelope,
labeled,  and stored  in a refrigerator until sample shipment.

Hi-Vol Sampler with  Precyclone

     Sample handling procedures for the Hi-Vol with precyclone sampler were
identical to the standard Hi-Vol with the exception of that used for the pre-
cyclone. The precyclone was cleaned of debris and cleaned with 70% isopropyl
alcohol prior  to installing a new filter and initiating sampling.

Andersen  Impactor with Backup Impinger

     Andersen impactors and Greenburg-Smith impingers were field-sterilized in
a high-frequency ultraviolet light cabinet due to the unavailability of an
autoclave and the necessity of equipment turnover. In addition, prior to ultra-
violoet irradiation, the impingers were supplementally cleaned with 70% iso-
propyl alcohol. After  the technicians discarded the alcohol, the impingers
were thoroughly rinsed twice with sterile Hanks' BSS prior to being filled with
100 ml fresh Hanks'  BSS collection menstruum.

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     Lids to the Andersen agar plates were stored in the ultraviolet cabinet
to prevent contamination during sampling. Following sampling, the Andersen
plates were individually removed, covered with their lids, labeled, and taped
together as a set. Impinger solutions were poured into labeled sterile-glass
bottles and sealed. Samples were stored in a refrigerator until shipment.

Impingers

     Procedures used for the special sampling Greenburg-Stnith impingers were
identical to those used for the Andersen backup impingers discussed in the pre-
ceding section.

Sample Shipment

     Packaged samples were placed in insulated shipping cartons with plastic
enclosed ice packages. Void spaces in the shipping containers were filled with
packing to prevent sample damage during shipping. Shipping containers were
strapped shut and sent by air express to MRI at the end of each sampling day.

HOUSTON PROGRAM

     During the Houston program all materials were pre-sterilized at MRI and
shipped by air to Houston. Sufficient equipment was available so that sampling
devices were used only once in the field. The only piece of equipment reused
in the field was the stainless-steel sampling probe. Prior to each use, the
interior of the probe was thoroughly rinsed with absolute ethanol and carefully
ignited for sterilization purposes. The ends were then covered with sterile
squares of aluminum foil before transfer to the sample site. Individually bot-
tled gelatin-milk impinger solution was aseptically added to the AGI-30 impin-
gers with the aid of a propane torch on the day of sampling.

     Upon completion of each sampling run, the volume of the AGI-30 was recon-
stituted with sterile distilled water and aseptically halved. One portion was
transferred to a sterile sample bottle, quickly frozen, and shipped by air to
MRI for viral analysis. The remaining portion was delivered in the impinger to
MBA Laboratories in Houston so that bacterial analysis could begin promptly.
Andersen impactor plates were packed in ice and sent to MRI on a daily basis.

     During the initial tests at Houston, only the AGI-30 impinger solutions
were analyzed at the baghouse inlet. This procedure produced erroneous quanti-
tative results (15). During subsequent testing, two fractions at the baghouse
inlet were collected and analyzed. The first fraction consisted of pooled ster-
ile distilled water rinsings of:  the probe tip to the Greenburg-Smith impinger;
the connector tubing between the Greenburg-Smith impingers and AGI-30; and the
Greenburg-Smith impinger interior. The second fraction consisted of the asep-
tically reconstituted volume of the AGI-30 impinger solution.

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     All impingers were kept in an ice bath during sampling, but the samplers
were not shielded from direct sunlight during sampling.

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                                  SECTION 5

               SAMPLE PREPARATION AND MICROBIOLOGICAL ANALYSIS
     Microbiological samples obtained during the St. Louis program were ana-
lyzed exclusively at MRI's microbiology labs. During the Houston program,
however, only the bacteria count by size  (Andersen agar plates) and virus
assays were completed at MRI's labs. Analysis of total bacteria and bacteria
by species was conducted at MBA Laboratories, Houston, Texas. The analyses
were split during the Houston program because it was desirable to start the
bacterial assays within 4 to 6 hr of collection.

SAMPLE PREPARATION

St. Louis Program

     The previous day's samples generally arrived in the lab shortly after
8:00 AM. The immediate sample processing procedure for the St. Louis samples
is depicted in Figure 1. The Andersen agar plates were unpacked and placed
inverted in a 35°C incubator. The Andersen backup impingers, one-half of the
Air Density Separator (ADS) samples, and one-half of the Hi-Vol filters were
unpacked and frozen at -70°C in a Revco Ultra-low Freezer for later viral
analysis. The remaining halves of the ADS samples and Hi-Vol filters, along
with the refuse samples and mobile filter impinger solutions, were processed
immediately for bacterial analysis.

     Fluid samples such as the mobile filter impingers were prepared by vig-
orous shaking and distributed in appropriate 1:100 dilutions. Solid samples
such as the refuse samples, Hi-Vol filters, and ADS samples were diluted either
1:100 or 1:200 (w/w) with sterile distilled water and blended for 30 sec in a
sterile Waring blender. The resulting homogenates were used directly or after
subsequent 1:100 dilutions for inoculating the various media. The bacterial
analysis spectrum is depicted in Figure 2.

Houston Program

     During the Houston program, samples were shipped as soon as possible
after collection either to MRI or to MBA Laboratories in Houston.  The micro-
biology sample handling procedure is shown in Figure 3.


                                      10

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                           MICROBIOLOGY SAMPLE PROCESSING PROCEDURE
                                          ST. LOUIS PROGRAM
                                               Receipt of
                                               Iced Samples
 Andersen
 Plates
Mobile Filter
Impinger
Solutions
Placed in
Incubator
@35°Cfor
24-48hrs.
  Refuse
  Samples
       Hi-Vol Filters
       (Aseptically
       Halved)
       ADS Samples
       (Aseptically
       Halved)
 Processed
 Immediately
 for Bacterial
 Analysis
Processed
Immediately
for Bacterial
Analysis
1/2 Sample
Processed
Immediately
for Bacterial
Analysis
1/2 Sample
Frozen for
Later Viral
Analysis
@-70° C
                    Andersen
                    Back-up
                    Impingers
1/2 Sample
Processed
Immediately
for Bacterial
Analysis
Frozen (a) -70° C
for Later Viral
Analysis
                                                Figure 1

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                                                         BACTERIAL ANALYSIS  SPECTRUM
                                                              ST. LOUIS  PROGRAM
                                                                          Sample
                                                               Homogenate or Dilution Thereof
Total Plate Count
                         Total Coliform
Fecal Coliform           Fecal Streptococci         Salmonella, sp.         Klebsiella sp.    Stophylococcus aureus
Method:
Media:


Incub. Time:
Incub. Temp:
Level 2 Tests:






Pour Plate
PCA


48 hn.
35»C
(Proposed)
None





MPN(5-10. 5-1, 4 5-0. 1ml)
Lauryl Tryptose Broth &
Brilliant Green Lactose
Bile Broth
24 - 48 hrs.
35i0.5°C

None





MPN
Lauryl Tryptose Broth &
EC Broth

24 hrs.
44.5tO.2-C

Enteropathogenic
Serotypes
Isolation of Rep.
Colonies on EMB -
Nutrient Agor Slants
E. coli OK Polyantiserum
Pour Plate
KF Streptococci Agar
+ TTC

48 hrs.
3510. 5"C

None





Spread Plate & Enrichment
MacConkey Agar &
Brilliant Green Agar
Selenite Broth
24 - 48 hrs.
35'C

Serotyping





Spread Plate
MacConkey Agar


24 - 48 hrs.
35°C

Serotyping





Spread Plate
Staphylococcus
110 Medium

24 -48 hrs.
37°C

Coagulase
Production




                                                  Slide Agglutination
                                                                 Figure   2

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               MICROBIOLOGY SAMPLE HANDLING PROCEDURE
                             HOUSTON PROGRAM
                               Field Samples
Andersen Plates
AGI-30 Impinger
Solutions
Greenberg Smith
Impinger Solutions
Baghouse Hopper
Discharge
    Shipped     1/2 Sample   1/2 Sample    Shipped to    One Sample  One Sample
    to MRI      Shipped      Shipped to     MBA Labs     Shipped to   Shipped to

Placed in
Incubator
@28-30°C
for 48 hrs.
to MRI
1
1
Frozen @
-70°C for
Later Viral
Analysis
MBA Labs
i i
Processed
Immediately
for Bacterial
Analysis

\
Processed
Immediately
for Bacterial
Analysis
MRI
Frozen @
-70° C for
Later Viral
Analysis
MBA Labs
I
1
Processed
Immediately
for Bacterial
Analysis
                                   Figure 3
                                      13

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One-half of the AGI-30 impinger samples for virus analysis, Andersen  impactor
plates, and baghouse hopper discharge samples was shipped  to MRI for  analysis.
The AGI-30 impinger and baghouse hopper discharge samples  were stored frozen
at -70°C until virus analysis could be initiated. Andersen plates were  unpacked
and placed inverted in a 28 to 30°G incubator.

     The remaining halves of AGI-30 impinger, Greenburg-Smith impinger,  and
baghouse hopper discharge samples were hand-carried  to MBA Laboratories  within
2 to 3 hr of sampling. Bacterial analysis by MBA Laboratories was initiated
immediately upon receipt of the samples.

     Fluid samples such as the impinger solutions were used to inoculate media
as received or after a 1:6 dilution. Solid samples such  as the baghouse  hopper
discharge were diluted 1:90 (w/w) and vigorously shaken. The bacterial  analysis
spectrum for the Houston samples is depicted in Figure 4.

MICROBIOLOGICAL ANALYSIS PROCEDURES

     Aerosol samples obtained during the St. Louis and Houston programs  were
analyzed for general and specific microorganism content  (see Figures  2  and 4).
The following section presents the analytical methods used during analysis.

Bacteria Count by Size (Andersen Agar Plates)

St. Louis —

     Plate count agar (Difco) in polystyrene petri plates  (Falcon) served as
the collection medium for the Andersen aerosol samples. The plates were  poured
to a depth of 27 ml with the aid of a sterile Cornwall syringe and allowed to
solidify. After solidification, excess moisture on the agar surface was  evap-
orated by placing the plates in a sanitized laminar  flow unit for approximately
20 min with the lids partially removed. The plates were then repacked in their
original packing sleeve and sealed with tape for shipment  to the field.

     Upon receipt of the inoculated Andersen agar plate samples at the  lab, the
plates were unpacked and incubated in an inverted position  at 35°C for 24 to
48 hr depending upon the degree of mold contamination. After this period,
bacterial counts were made on the basis of colonial morphology with the  aid of
a Quebec colony counter. Select representative colonies were picked at random
from some of the Andersen plates and saved on typticase soy agar slants. These
cultures were then used for determination of morphology using gram staining
techniques.
                                      14

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                                                 BACTERIAL ANALYSIS SPECTRUM
                                                       HOUSTON PROGRAM
                                                           Sample or Dilution Thereof
Total Plate Count       Total Coliform         Fecal Coliform   Fecal Streptococci         Salmonella. sp_.         Klebsiella sp.        Staphylococcus aureus
Method:
Media:
Incub. Time:
Incub. Temp:
Spread Plate
Plate Count Agar
24 hrs.
35°C
MPN (3-10.0, 3-1.0,
& 3-0. 1 ml)
Lactose Broth & Brilliant
Green Lactose Broth
24 - 48 hrs.
35"C
MPN
EC Broth
24 hrs.
44.5°C
Spread Plate
KF Streptococcal Agar
^ TTC
48 hrs.
35°C
Modified MPN
Lactose Broth
Selenite Cysline Broth
Salmonella-Sliigella Agar
Bismuth Sulfite Agar
24 - 48 his.
35°C
Enrichment MPN
Lactose Biolli
£MB Agar
24 - 48 hrs.
35°C
MPN (3-1.0, 3-0.
3-0.001, & 3-0
Trypticase Soy Brol
10% NaCI,
Baird Parker Agar,
48 hrs.
35°C
1,
.0001,
h with
Etc.


                                                           Figure  4

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Houston--

     The Andersen aerosol plate count methods used on the Houston program were
the same as the St. Louis program with only a few modifications. In an effort
to control molds from overgrowing and masking the bacterial count, the anti-
fungal agent Mycostatin  (nystatin)  (21) was incorporated in the plate count
agar at 50 units/ml agar. The agar  plates were incubated at 28 to 30°C for
48 hr prior to determining the following microbial counts:  total count, bac-
teria, yeast, mold, and  antinomycetes. The categorical microbial counts were
separated from the total count on the basis of colony morphological character-
istics. It should be noted that the categorical counts can be used as a guide
only to the relative population number. To obtain more absolute values, spe-
cial sampling and assay  considerations would have to be implemented for each
microbial type. Isolates were not saved for morphology or gram-reaction deter-
minations.

Total Plate Count
St. Louis—

     Total plate counts were determined according to Standard Methods (22).
Analyses of the filter pad slurry were determined in duplicate by the pour-
plate method with plate count agar. The solidified plates were incubated aero-
bically at 35°C for 48 hr. Longer incubation times at a lower temperature might
have given slightly higher counts but because mold spores were present in large
numbers, it was not possible to extend the incubation time beyond 48 hr without
overgrowth by fungi.

     Isolated colonies were picked from representative plates and transferred
to trypticase soy agar slants. The cultures were then used for determination
of morphology and gram reaction.

Houston--

     Total plate counts were conducted according to procedures detailed in
Standard Methods (22). The impinger samples were not diluted. Solid samples
were diluted 1:90 (w/w) and then homogenized. The samples were then analyzed
by the spread-plate method, using plate count agar. Plates were incubated
aerobically at 35°C for 24 hr prior to determining colony counts.

Standard Total Coliform MPN Tests

     All coliform tests were conducted according to Standard Methods (22),
using most-probable-number (MPN) techniques.
                                       16

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St. Louis —

     Presumptive coliform tests during the St. Louis program were conducted
using lauryl tryptose broth  (LST) as the enrichment medium. Five fermentation
tubes each of 10,  1, and 0.1 ml of the filter pad slurry were  prepared  and in-
cubated at 35°C. At the end  of 24 hr, each tube was examined,  and those  showing
gas were recorded. Tubes showing no gas at 24 hr were reincubated for an addi-
tional 24 hr for a total of  48 hr. Formation of gas within 48  hr constituted
a positive presumptive test.

     Confirmation  of total coliforms was conducted by subculturing to brilliant
green lactose bile broth (BGLB) all LST tubes showing gas in 24 or 48 hr in the
presumptive test. The BGLB tubes were then incubated at 35°C for 48 hr.  Forma-
tion of gas within 48 hr constituted a positive confirmed test.

     Total coliform completion tests were conducted by streaking aliquots of
each BGLB tube showing gas onto eosin-methylene-blue (EMB) agar plates.  The
EMB plates were incubated at 35°C for 24 hr and then observed  for typical col-
onies (nucleated with or without metallic sheen). Typical colonies were  sub-
cultured on nutrient agar slants and examined after 24 hr by use of the  gram-
stain technique. Gram-negative cultures were considered to be  coliform.

Houston—

     Total coliform counts during the Houston program were also determined by
the MPN technique. Solid samples were diluted 1:90 (w/w) and the impinger sam-
ples 1:6. A lactose broth three-tube/three-dilution series of  10, 1.0, and
0.1 ml was used for both liquid and solid samples. After incubation at 35°C
for 48 hr, all tubes showing gas were transferred to BGLB for  confirmation of
positive reaction. Coliform  tests were not completed.

Fecal Coliform MPN Tests

St. Louis —

     Fecal coliform tests (22) during the St. Louis program were conducted on
all LST tubes showing gas in the presumptive coliform test. The LST tubes were
used to inoculate tubes of EC medium. The EC tubes were then incubated in a
water bath at 44.5°C for 24 hr. Gas production in 24 hr constituted a positive
test and indicated the presence of coliform microorganisms of  fecal origin.
Most probable number tables were used to determine probable fecal coliform
densities in the original sample.

     Subcultures were made from positive EC tubes to EMB agar, and typical
colonies on the solid medium were then transferred to nutrient agar slants
and saved for serological typing for enteropathogenic Escherichia coli.

                                      17

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Houston--

     Fecal coliform counts were determined by the MPN technique  (22). All lac-
tose tubes from the total coliform tests which showed gas production (positive
reaction) were used for fecal coliform analysis. EC media were inoculated from
each positive lactose tube and incubated at 44.5°C for 24 hr. Gas production
within 24 hr represented a positive test. Coliform densities were determined
from standard MPN tables.

Serological Typing of Escherichia coli

St. Louis—

     Subcultures from nutrient agar slants were made  to brain-heart infusion
agar (BHIA) of typical fecal coliform (EC) isolates.  The BHIA cultures were
incubated overnight, and on the following day portions of each culture were
serologically tested against E. coli OK antiserum (poly) by  the  slide agglu-
tination technique as described by Difco Laboratories (23).

Fecal Streptococci

St. Louis —

     Fecal streptococci were enumerated by a pour-plate technique utilizing KF
streptococci agar containing 0.01% 2,3,5-triphenyltetrazolium chloride (TTC).
Colonies appearing dark red or pink were counted as fecal streptococci.

Houston--

     Fecal streptococci were enumerated by the spread-plate  technique used
with KF streptococcal agar and TTC. Plates were incubated at 35°C for 48 hr.
All suspected colonies were examined microscopically  for confirming morphol-
ogy.

Salmonella

St. Louis—

     Salmonella tests were conducted on filter-pad slurry by direct-spread
plate and enrichment broth-spread plate techniques.  Slurry-sample and 24 to
48 hr selenite broth enrichment aliquots were transferred to both MacConkey
and brilliant green agars. Typical colonies appearing colorless  on MacConkey
agar and red or pink to nearly white on brilliant green agar were transferred
to triple sugar iron (TSI) agar slants. Cultures giving typical  reactions for
Salmonella on TSI agar were transferred to trypticase soy agar slants and re-
tained for serological testing.

                                      18

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     Salmonella isolates were serologically tested using the slide agglutina-
tion technique (23) with salmonella polyvalent antisera. Positive reactors
were then tested using salmonella group specific antisera.

Houston--

     One-miHi liter lactose broth aliquots from the coliform analysis procedure
were inoculated into selenite cystine broth (SCB) medium. After 24 hr incuba-
tion, inocula from SCB tubes were streaked onto salmonella-shigella  (SS) agar
and incubated at 35°C for 48 hr. Typical salmonella colonies on SS agar were
picked and transferred to TSI slants. Following incubation, slants showing
typical salmonella reactions were tested for confirming biochemical  reactions
in the following media:  lysine decarboxylase, dulcitol, sucrose, lactose,
malonate, citrate, indole, and motility.

Klebsiella

St. Louis—

     Tests for Klebsiella were conducted on filter pad slurry dilutions. The
spread-plate technique was used on MacConkey's agar. Typical red, mucoid-
appearing colonies were picked and transferred to additional MacConkey and EMB
agar plates for purity. Typical appearing colonies were transferred  to BHIA to
serve as stocks to determine their respective biochemical reactions  using the
API 20E system.—'  Isolates possessing biochemical characteristics similar to
those reported for Klebsiella sp. were serologically tested with polyvalent
klebsiella antiserum.

Houston--

     Positive lactose tubes from the coliform analysis procedure were streaked
onto EMB agar plates and incubated at 35°C for 24 hr. All colonies morphologi-
cally identified as typical Klebsiella were inoculated onto TSI slants. The
TSI slants exhibiting an acid slant with an acid butt, with or without gas,
were further tested for ornithine decarboxylase, indole, motility, and urease.
Only those isolates exhibiting typical klebsiella reactions were reported as
Klebsiella sp.

Staphylococcus aureus

St. Louis—

     The presence of Staphylococcus aureus was determined by spread-plate
technique on Staphylococcus 110 agar plates. These plates were incubated at
37°C for 24 and 48 hr; all typical appearing colonies (light yellow  to orange
h/  Analytical Products, 200 Express Street, Plainview, New York  11803.
                                      19

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pigment) were transferred to brain-heart infusion slants. After overnight
growth, the isolates were tested for production of coagulase by the rabbit
serum EDTA coagulase tube test.

Houston—

     S. aureus was determined by the MPN procedure detailed in the A.O.A.C.
Manual (24)  A four-dilution/three-tube series of trypticase soy broth with
10% sodium chloride was inoculated and incubated at 35°C  for 48 hr. Tubes
showing growth were streaked onto Baird Parker agar plates and incubated for
another 48 hr at 35°C. Plates were then examined for  suspect colonies which
were transferred to brain-heart infusion broth (BHIB). The BHIB tubes were
incubated at 35°C for 24 hr, after which aliquots were subjected to the rabbit
serum EDTA coagulase tube test. Tubes showing a positive  reaction after 4 hr
were reported as S_._ aureus.

Virus Methodology

St. Louis Program--

     Samples for virus analysis were concentrated prior to virus titration.
Initially, samples were concentrated by the hydroxyapatite method. This con-
centration method was replaced early in the research  by the more efficient
dextran sulfate-polyethylene glycol phase separation  method of Shuvall (25)
(see Table 1). Most of the samples were concentrated  by the phase separation
method.

     Concentrated samples were analyzed for virus content by the monolayer
plaque assay technique of Schmidt (26) with minor modifications (see Table 2).
In all samples, 5- to 7-day old confluent 75 cm  monolayers of heteroploid
monkey kidney cells, LLC-MK2 (GIBCO) were used. The monolayers were grown at
35°C in Earles' M-199 containing glutamine and supplemented with 10% fetal
calf serum, 0.22% NaHC03 for stoppered incubation, GIBCO1s antibiotic-
antimycotic amendment (penicillin, streptomycin, and  fungizone) and GIBCO's
anti-PPLO amendment (tylocine).

     Because of severe mold contaminations, samples for virus titration were
diluted 1:10 in Earles' BSS. One milliliter of the 1:10 sample dilution was
distributed over the monolayer after pouring off the  growth medium. The flask
was incubated for 30 min at 37°C to allow virus attachment. The inoculum was
poured off and, in a darkened room, replaced with 10.0 ml of molten overlay
medium at 45 to 47°C consisting of the growth medium  supplemented with 1.7 x
10'3% neutral red and 1.5% ion agar No. 2. The overlay was quickly distributed
over the monolayer and placed on a flat surface for 30 min to allow solidifica-
tion of the agar. The flasks were firmly sealed and incubated in the dark at
36 to 37°C. The tissue cultures were checked for plaque formation at 4, 7, and

                                      20

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    TABLE 1.  FLOW SHEET FOR VIRAL CONCENTRATION PROCEDURES OF AEROSOL
                SAMPLES ON FILTER MEDIA^/  (Phase Separation Method)
Homogenize weighed sample after diluting 1:100  (w/w) with distilled water.

Centrifuge at 1,080 x g for  15 min at 4°C.

    	^   Discard Ppt.
   V
Neutralize supernatant to pH 7.2.
   I
Add each of the following sequentially after each is thoroughly dissolved:

     1.75% (w/w)  (0.3 M) Dry sodium chloride
     0.2% (w/w) Sodium dextran sulfate 2000
     6.43% (w/w)  Polyethylene glycol 4000

Allow to mix 1 hr using a magnetic stirrer.

Transfer mixture  to separatory funnel and store at 4 C for 18 to 24 hr.
Collect bottom and interphase portions.
   I
Follow the method below:   (after Shuvall, H. I. et al., 1969)

          To bottom and interphase portions, add KCl to 5.22%  (w/w)  (0.7 M)
            to ppt. dextran sulfate.
          Centrifuge at 2,500 g for 10 min at 4°C.
          To supernatant,  add 1.0 ml anesthetic grade diethyl  ether  per 4 ml
            reconcentrate.
          Shake mixture and hold at 4 C for 18 hr to kill contaminating
            bacteria and molds.
          Tissue culture assay for viruses.
ja/  This procedure may be modified to process impinger samples by elimi-
      nating  the initial homogenization and centrifugation steps.
                                     21

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                TABLE 2.  MONOLAYER PLAQUE ASSAY TECHNIQUE^
1.  Remove growth medium from 5- to 7-day old monolayers in 75 cm  surface
    area flasks and rinse with three 8 ml portions of Earles' balanced
    salt solution.

2.  Check monolayer for confluency.

3.  Pipet 1.0 x 10   ml dilution of sample onto monolayer. Distribute the
    inoculum over the monolayer and incubate for 30 min at 37°C.

4.  Pour off inoculum.

5.  Pipet and evenly distribute 10.0 ml of the following nutrient overlay
    solution held at 45 to 47°G.

                                                    ml     Final cone.

    10X Earles1  M-199 + Glutamine (GIBGO)          10.0       IX
    Fetal Calf Serum (inactivated at 56°C for      10.0       10%
      30 min)
    7.5% NaHC03                                     3.0       0.22%
    Neutral Red (1:300)                             0.5       1.7 x !Q-3%
    10X Antibiotic-Antimycotic (penicillin,         1.0       IX
      streptomycin, fungizone, GIBCO)
    10X Anti-PPLO (tylocine, GIBCO)                 1.0       IX
    2% lonagar No. 2 in double distilled water     74.5       1.5%

6.  Place bottles on a flat surface in a darkened room for 30 min to permit
    the agar to solidify then firmly seal flasks.

7.  Incubate the flasks in the dark at 36 to 37°C.

8.  Check flasks for plaque formation at 4, 7,  and  10 days.


a/  After:   Reference 26.
                                    22

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10 days. Suspected plaques were picked and transferred to fresh monolayers  for
determining plaque reproducibility. Only reproducible plaques were considered
to be of viral origin.

Houston Program--

     Samples for virus analysis during the Houston program were handled simi-
lar to those during the St. Louis program. Only differences will be stressed
here.

     Houston samples were concentrated exclusively by the phase separation
method of Shuvall (25). The concentrated samples were analyzed by the mono-
layer plaque assay technique with confluent 75 cm  monolayers of three cell
lines:  7-day cultures of heteroploid monkey kidney cells (LLC-MK2 )» 3-day
cultures of a neoplastic nasopharnyx cell line (KB), 3-day cultures of a pri-
mary human fetal lung fibroblast line (similar to WI-38). Both positive and
negative controls were run with field samples using the same concentration and
analysis procedure. Negative controls consisted of Earles1 BSS and a sterile
impinger blank. Positive controls were prepared by seeding an Earles' BSS
blank and a sterile impinger blank with attentuated polio type 1 virus.
                                      23

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                                  SECTION 6

                                  DISCUSSION
GENERAL CONSIDERATIONS

     The accurate assessment of microbiological air quality in ambient and
confined air has proven difficult in the past. Part of the assessment problem
is due to the diversity and variance in the number of:  (a) microbiological
forms found in air, (b) particulate matter of unknown size and composition,
and (c) chemical composition of the air. In addition, evaluation of test data
is further complicated by the diversity of sampling methods and analytical
procedures employed by investigators in a variety of applications.

     An accurate assessment of airborne microorganisms depends upon method
sensitivity and reproducibility; these important quantitative considerations
are influenced by many factors, including:

        The air sampling device employed;

     .  Ability to obtain large statistically valid sample volumes (this may
        necessitate large air volumes to be sampled by one sampler or an in-
        crease in the number of sampling devices at a given point);

        Maintenance of viable conditions for vegetative microorganisms during
        and following sampling;

        Disruption of the microbial particulate and microbial microcolonies
        so that an accurate estimation of the absolute population can be made;

     .  A minimum of sample storage time prior to assay;

        Proper choice of general,  differential, or selective growth media for
        the microorganism of concern; and

     .  Proper choice of environmental growth variables for the organism of
        concern.
                                     24

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AEROSOL SAMPLING DEVICES

     Currently, a variety of sampling devices are being used to sample for
airborne microorganisms. Chief among those used today are:  all glass impingers
(AGI-30), Andersen multistage impactors, cascade impactors, and Litton Large
Volume Samplers (LVS). These devices and other sampling considerations are
described elsewhere in more detail  (27-33).

     Biological collection efficiencies of airborne microorganisms sampling
devices vary greatly because of complex interactions of many variables. Some
of these variables are:

        Physiological stage of the microorganisms, i.e., vegetative cells or
        spores;

        Physiological and structural state of the microorganisms, i.e., normal
        or sublethally stress-damaged cells;

        Method of collection by the sampling device, i.e., impaction, impinge-
        ment, filtration, etc.;

     .  Volume of air sampled; and

     .  Environmental conditions during sampling.

Biological efficiencies may be altered because of the sampling device's effect
on microbial viability both during and following sampling. Complex and often
deleterious stressing effects such as desiccation, rehydration, oxidation,
radiation, osmotic shock, impaction shock, length of sampling time, collection
menstruum, sample retention time, etc., contribute to decreases in biological
efficiencies during aerosol sampling. Also, collection efficiencies and stress-
ing effects vary both between and within diverse microbiological groups that
may be assayed, i.e., bacteria, yeasts, molds, actinomycetes, or viruses which
require different considerations altogether.

     Standard reference samplers for microbial aerosols have been recommended.
General agreement was reached at the First International Symposium on Aero-
biology (34) that the AGI-30 and the Andersen samplers be used as standard
reference samplers. In both cases, it was emphasized that methodology, i.e.,
techniques and materials, be rigorously and completely specified when report-
ing the results. The use of reference sampling devices with complete specifi-
cation of methodology has been a problem in the past. Unfortunately, the prob-
lem remains today. Defense of altered methodologies may rest on the undebatable
premise that environmental variables, type of information sought, or research
cost often necessitate individual alteration of published methodologies. How-
ever, it must be stressed that if altered methodologies are used by different
                                     25

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investigators, this can and often does prevent meaningful comparisons  of re-
sults even if the same type of sampling device is used.

     During the St. Louis program, the Hi-Vol air sampler was chosen as the
primary aerosol sampling device for several reasons. First, the Hi-Vol sam-
pler could sample large volumes of air (1,000 to 1,200 liters/min), which
theoretically would increase the representativeness of the samples obtained
without increasing the number of samples taken at a single location. Second,
the samples obtained by the Hi-Vol sampler would be used simultaneously for
three separate parameters to be measured, i.e., microorganisms, physiochemi-
cal particulate morphology, and trace metals. Both of these features made  the
Hi-Vol sampler attractive in terms of the time and manpower savings. Unfortu-
nately, the Hi-Vol air sampler was run for 6 hr as a compromise for the non-
microbiological parameters to be assessed. As a result, the microbiological
samples suffered severe exposure to desiccation and oxidation factors. Unfor-
tunately, AGI-30 impingers were not run concurrently as references at St.  Louis.
The experience gained, however, was applied on the Houston program.

     The AGI-30 impinger and Andersen impactor should always be used as ref-
erence airborne microorganism sampling devices during aerosol emission research
(34). Quantitative airborne bacteria and virus concentrations should be as-
sessed with the AGI-30 impinger containing a collection menstruum compatible
with the microorganism(s ) sought. Gelatin-milk or one-half strength tryptic
soy broth should be used as the collection menstruum for bacteria. Gelatin-
milk or tissue culture medium with serum should be used for viruses. In all
instances, menstruum compatibility tests should be conducted with a suitable
test microorganism prior to use in order to determine effects on microbial
viability.

     Sampling times for microbial aerosols should be closely monitored. Sam-
pling times with the AGI-30 impinger should be for 10 min or less. Absolute
maximum sampling times with an AGI-30 should be 30 min. Prolonged sampling
may cause significant microbial die-off as a result of complex sampling ef-
fects.   Regardless  of sampling time, it is advisable to set up control sam-
pling devices inoculated with an appropriate test microorganism to ascertain
the effects of sampling under field test conditions. In sampling areas contain-
ing large particulates, it may be necessary to add a dry Greenburg-Smith im-
pinger prior to the AGI-30 (as was done at Houston) to prevent clogging of the
AGI-30 orifices.  Rinsings  of both impingers and their connector tubing should
be included for quantitative analysis.

     The Andersen sampler  is recommended only for sizing aerosol particles
containing microorganisms.  The Andersen sampler should not be used for quanti-
tative microbial  aerosol concentrations because a colony resulting from one
aerosol particle  may have  contained more than one microbial cell.  Sampling
times with the Andersen impactor should not exceed 30 min. Prolonged sampling
at waste handling facilities may result in excessive build-up of sample on the

                                     26

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sieve  plates  thereby  altering  particle  sizing  efficiency.  In addition,  pro-
longed sampling may cause  desiccation of  the microbiological medium employed
leading to  altered concentrations  of the  medium's  components.  Increased con-
centration  of media components  over the recommended  level  may lead to  toxic
levels especially if  selective  media are  used.  As  with  the AGI-30,  it  is
recommended that control sampling  devices be set up with appropriate test
microorganisms to determine  the effects on microbial viability of  sampling
under  field test conditions.

     The Andersen sampler  might also be considered as a quantitative sampling
device for  airborne viruses. Andersen samplers  have been modified  and  used  as
samplers for  airborne  viruses  (39-42).

     It is  recommended that  both Andersen and  AGI-30 sampling  devices be
shielded from direct  exposure  to sunlight. Research by  Fedorak (35)  has shown
that significant microbial losses  are encountered  from  exposure of sampling
devices to  direct sunlight during  sampling.

     Although not specifically  tested during the St. Louis  or  Houston programs,
results indicate that  the  Litton LVS may  be included especially in sampling
for specific  low concentration  microorganisms  such as Salmonella sp., Klebsiella
sp., Staphylococcus aureus,  and viruses.  The LVS Model M is  capable  of sampling
at 1,000 liters/min, which is 35 times  greater  than the Andersen sampler (28.3
liters/min) and 80 times greater than the AGI-30 (12.5  liters/min).  The signif-
icance of using the LVS to detect  viruses at epidemiologically significant low
concentration has been demonstrated (36-38). The LVS is currently marketed by
Sci-Med Environmental  Systems,  Inc.i/

     It is  urged that  extreme diligence be shown in reporting  all aspects of
the sampling  procedure. It is also important to specify what the final sample
constitutes,  i.e., the collection  medium  only,  the collection medium plus
rinsings  of the connector  tubing (if applicable),  etc.

MICROBIOLOGICAL ANALYSIS OF  AEROSOL SAMPLES

     Microbiological  analysis of aerosol  samples should be  initiated as soon
as possible after collection. It is desirable  that sample  analysis begin with-
in the upper  limit of  4 to 6 hr to avoid  alteration of microorganism concentra-
tion due  to growth (increase in number) or die-off. Sample  analysis  delays
were encountered during the  St. Louis program because of logistical  problems.
During the  Houston program,  these  problems were alleviated  by  contracting a
qualified local laboratory to conduct the assays.  The alternatives would be
to maintain a field laboratory  or  rent  space at a  local hospital or  school.
i/  2411 Pilot Knob Road, St. Paul, Minnesota  55120.
                                      27

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If delays are unavoidable, bacteriological samples can be stored in ice up to
4 hr; however, die-off needs to be considered. Samples for virus analysis
should be quickly frozen in dry ice or liquid nitrogen and stored at -70 C
until analysis.

     Standardized analytical procedures have been established for the micro-
biological analysis of food (24,43,44); water (22); solid waste (45); and
clinical specimens (46-50). However, standard analytical procedures for micro-
bial aerosol samples have not been established. The unique stresses to which
aerosolized microorganisms are exposed present difficulties in choosing an
optimal medium for their recovery. General growth media would provide, perhaps,
a greater recovery of aerosol-stressed microorganisms than would differential
or selective media. However, the advantages of general media are often lost
by overgrowth of the desired vegetative microbial forms by the more resistant
and perhaps less important spore-formers.

BACTERIOLOGICAL ANALYSIS

     Numerous differential and selective media have been developed for assess-
ment of genera or classes of microorganisms. Yet, even with optimal samples,
qualitative accuracy and quantitative recovery will vary with media type. Com-
parisons of media for recovery of specific microorganisms are relatively com-
mon in the literature for clinical, food, and water samples, etc. Although
these comparisons may be used as guidelines for media selections for assay of
microbial aerosol samples, they cannot be applied with certainty because of
the unique stresses exerted on aerosolized microorganisms. The comparison of
media for the enumeration of Staphylococcus aureus in aerosol samples by Smith
(51) is one of the few such studies applied to aerosol samples. Clearly this
is an area of aerobiological research that needs further amplification.

     Indicator microorganisms such as total coliforms, fecal coliforms, and
fecal streptococci have been used for a number of years for assessing microbial
quality of food and water. Indicators are particularly cost-effective where
the pathogenic species, whose presence are used to indicate, are present at
low levels and the cost of sensitive methods are prohibitive. In the absence
of microbial air standards or thorough research methods needed to establish
them, indicator species may be of value in determining relative levels of air
hazard subject to further research.

     Microbiological indicator systems such as total coliforms, fecal coli-
forms, and fecal streptococci are currently being used to assess ambient and
confined air quality levels (13,14). Since these indicators possess real prob-
lems in assessing quality of the aqueous systems for which they were developed,
use of such indicators in air quality assessments is open to conjecture.  Coli-
form organisms have been found associated with a wide variety of nonfecal en-
vironmental sources including vegetation (53), soils (54), and insects (53,55).
                                     28

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Aerosols from these common sources may be  generated  easily  and may  cause
erroneously high background counts.  In addition,  solid waste  retention  times
may alter the original ratio of coliforms  to  pathogens.  Further  research  is
essential to clarify  the meaning  of  conventional  microbial  indicators in  the
atmospheric environment and to establish their  relationship to pathogens  in
that medium, if the indicators are to be of value in assessing microbial  air
hazard.

     Research should  be conducted to ascertain  optimal media-methodology  com-
binations for quantitation of aerosol-stressed  microorganisms. During the
St. Louis and Houston programs, reliance was  placed  on standard  microbiological
procedures. Until research is conducted comparing the various media of  choice,
under identical conditions with field aerosol samples, it is  recommended  that
several types of media/methods be used concurrently.  If  this  is  not possible,
emphasis should be placed on media/methods which  have undergone  rigorous  com-
parisons under identical conditions  for optimal differential, selective,  and
quantitative abilities. The research programs of  Gabis (56),  Raymond (57), and
Niskanen (58) are good examples of studies of this nature,  even  though  the
studies are not concerned with aerosol samples.

     At the present time, MRI recommends the  bacteriological methods outlined
in Table 3 for analysis of aerosol emission samples  obtained  at  waste handling
facilities. It should be noted that  some of the procedures  represent modifi-
cations of the ones used during the  St. Louis and Houston programs.

VIRUS ANALYSIS

     Previous research during the earlier  1975  St. Louis test program (unpub-
lished) established that virus concentration  procedures were  necessary  for
virus-containing aerosol samples  obtained  at  solid waste-type facilities.
Initial samples for virus analysis during  the St. Louis  program  were concen-
trated according to the hydroxyapatite method as  conducted  during the 1975
program. Concern over concentration  efficiency  of the hydroxyapatite method
led to comparisons between the hydroxyapatite and dextran sulfate-polyethylene
glycol phase separation method (25)  with both T-l bacteriophage  and attenuated
polio virus type 1. With bacteriophage T-4, percent  recovery  of  the phase
separation method was 18.2% as compared to 0.1% for  the hydroxyapatite  method.
The phase separation  method gave  23.9% recovery with polio  virus type 1 as
compared to 0.1% for  the hydroxyapatite method. These tests  proved  the  phase
separation method to  be significantly more efficient. As a  result,  the  phase
separation method was used to concentrate  the remainder  of  the samples.

     A large number of virus concentration procedures have  been  described in
the literature. These concentration  procedures  can be divided into  seven  main
groups (59):  sample  incorporation,  ultrafiltration,  freezing, two-phase  sep-
aration, ultracentrifugation, electrophoresis,  and adsorption and elution.
The phase separation  method was chosen over the other methods for several

                                     29

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TABLE 3.   RECOMMENDED BACTERIAL ASSAY METHODS FOR RDF FACILITY AEROSOL SAMPLES

A^say Mi thud
Total pi jte count or Pour or spread platej
(count by particle t Lze ) Ajidert.cn pi a tea

Total colitorm MHN


Fecal colUunm. MPN


Salmon^ 11 a iip» iiuri ctuiieiit


Spread plate
9t.ai>hvlticoccub duruui) Spread plate


t-U.-iii.j
Tr y p 1 1 c b L> y agar "•"
5U uiiitb/nil Myi:osLdtin
(Nyst.aLin)
Lauryl Lry[jtose broth +
bri 1 1 iant green bi LG
2Z broLh
Lauryi. tryptuse broth +
KC medium
0.017= TTC
I^vinu EMb agar
Lactose broth +

Bismutli sulfiLe agar
Bismuth sulf ite ^gar
Bdird Parker agar

lncub.it J on InciibdLi on
t.'inp. (° C.) Linu; (hr)
2ti - J5 48


J5 48


35 48
44.5 + 0.2 J4
J5 4d
'15 24
J5 24

35 48
J5 4b
J5 - 37 48

Verii icatious

Unpublished data and
1'arkiuson (21)

Re^onanended Standard Mucliodb Standard Mcttmds (22)
(22)

Standard Methods (22)

(22)
Recommended Swing (50) tuing (50)
Recojimended Ewing (50) Gabis (56)

Dtfco (23)
-
Kdcoiimitinded Kaynian (57 ) Rayman ( *j 1 )
Niskanen (58)

-------
reasons. The method is recommended for concentrating  samples  containing
viruses associated with particulates  (22)  as would be expected with  aerosols.
The method was the most promising to  use with  samples collected  on filter
media. Large or small volumes of sample can be concentrated by means  of  the
phase separation method. The procedure is  not  difficult  and time-consuming,
and is thus conducive to processing large  numbers of  samples.

     Many problems exist in the concentration  of viruses at low  levels from
samples. To eliminate these problems, it is recommended  that  direct  incorpora-
tion incorporation be the method of choice. If concentration  of  samples  is un-
avoidable because of low virus content, the phase separation  method  is recom-
mended for concentration of virus-containing samples.

     Contamination of tissue culture  monolayers by molds contained in the sam-
ples was a problem during the St. Louis and Houston programs. If severe mold
or other microbiological contamination problems exist, they may  be controlled
to a limited extent by higher concentrations of antibiotics providing cell
toxicity does not occur. Controls should be run to ensure that the antibiotic
levels do not interfere with cell line viability and  sensitivity.

     Monolayer plaque assay methods according  to Schmidt (26) are recommended
for virus analysis of aerosol samples. Particular attention should be focused
on virus sensitivity in the choice of cell lines for virus titration. For
adenovirus titrations, HeLa or KB cell lines are recommended  (15,60). Monkey
kidney cell lines, e.g., BGM or LLC-MK2, are recommended for  titration of
enteroviruses (14,61).

FUTURE WORK

     Currently, ASTM Committee E-38.07 (62) is developing microbial  air  sam-
pling and analysis standards for resource  recovery plants. Development of
standards for particular applications may well be the correct approach. How-
ever, general standards, included in  all research studies at  least as a  ref-
erence so that studies may be validly compared, need  also to  be  established.
                                      31

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                                      37

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                                   TECHNICAL REPORT DATA
                            (Please read Instructions on the reverse before completing)
1. REPORT NO.
 EPA-600/2-79-131
                                                           3. RECIPIENT'S ACCESSION NO.
4. TITLE AND SUBTITLE

 ANALYSIS OF AIRBORNE VIABLE BACTERIA AT  SOLID  WASTE
 PROCESSING FACILITIES
             5. REPORT DATE
              August 1979  (Issuing Date)
             6. PERFORMING ORGANIZATION CODE
7. AUTHOR(S)

 M. W. Fletcher  and  D.  E. Fiscus
             8. PERFORMING ORGANIZATION REPORT NO.

              MRI Project No.  4033-L
9. PERFORMING ORGANIZATION NAME AND ADDRESS
 Midwest Research Institute
 425 Volker Boulevard
 Kansas City, Missouri   64110
             10. PROGRAM ELEMENT NO.
              1NE624,  SOS WF, Task 6.1
             11. CONTRACT/GRANT NO.
              68-02-1871
12. SPONSORING AGENCY NAME AND ADDRESS
 Municipal Environmental Research Laboratory—Gin.,OH
 Office of Research and Development
 U.S. Environmental Protection Agency
 Cincinnati,  Ohio  45268
             13. TYPE OF REPORT AND PERIOD COVERED
              Analytical Methods
             14. SPONSORING AGENCY CODE
              EPA/600/14
15. SUPPLEMENTARY NOTES
 See also EPA-600/2-78-152 and EPA-600/2-79-090.
 Project Officer:   Carlton C. Wiles     513/684-7881.
16. ABSTRACT

      This report presents a synopsis of aerobiological testing methodologies used by
 Midwest Research Institute during studies  conducted for the Environmental Protection
 Agency.  The  purpose of the programs was to  determine relative levels  of  airborne
 bacteria and  virus aerosols within and around  waste handling facilities.   The
 facilities  tested were the St. Louis Refuse  Processing Plant, the Browning Ferris/
 Raytheon Service Company Resource Recovery Plant (Houston), and at  three  other types
 of waste handling facilities, i.e., an incinerator, a waste treatment  plant, and a
 landfill.   The  report presents microbiological air sampling methodologies, field
 sample handling procedures, and laboratory analysis methodologies.   It also includes
 a general discussion of pertinent considerations,  recommendations for  future research,
 and an extensive bibliography.
17.
                                KEY WORDS AND DOCUMENT ANALYSIS
                  DESCRIPTORS
                                              b.IDENTIFIERS/OPEN ENDED TERMS
                           c. COS AT I Field/Group
 Bacteria
 Viruses
 Microorganisms
 Wastes
 Refuse disposal
 Air pollution
 Laboratory methods
 Air  emissions
 Ambient  air
 Refuse derived fuel
13B
 8. DISTRIBUTION STATEMENT
 Release to Public
                                              19. SECURITY CLASS (ThisReport)
                                                  Unclassified
                           21. NO. OF PAGES
                                   90
20. SECURITY CLASS (This page)
   Unclassified
                                                                         22. PRICE
EPA Form 2220-1 (Rev. 4-77)
                                             82
                                                                    U.S. GOVERNMENT PRINTING OFFICE' 1979 -657-060/5418

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