|
Topic Name: BEST WAY TO DETECT AIRBORNE PATHOGENS
Category: Biomedical
Research persons: Timothy J. Buckley, PhD, CIH
Location: Division of Environmental Health Sciences ,College of Public Health,The Ohio State University 320 West 10th Avenue A333-C Starling Loving Hall,Columbus, Ohio 43210, United States
Details
Current methods used to sniff out dangerous
airborne pathogens may wrongly suggest that there is no threat to health when,
in reality, there may be.
But researchers have found a better method for
collecting and analyzing these germs that could give a more accurate assessment
of their actual threat. For example, the findings may make it easier to detect
airborne pathogens in low concentrations
“Our results suggest that commonly used
sampling methods detect only a small fraction of what is actually in the air,”
said Timothy
Buckley, the study's senior author and an associate professor of
public health at Ohio State.
“And what they detect is often so damaged – due
to the collection method – that the pathogens no longer possess the same
infectious potential as they did while in the air.”
Such damage can make it nearly impossible for
public health workers to determine if a pathogen is viable – that is, whether or
not it has the potential to infect.
Buckley and his colleagues found that a
relatively new device called the BioSampler caused the least amount of damage to
the non-infectious microorganisms used in this study. The
BioSampler was developed
in the late 1990s by a team of researchers from the University of Cincinnati .
Although it's not yet a commonly used method for detecting airborne pathogens,
it gave Buckley and his team the most accurate reading of the degree of the
microorganism's viability, its ability to grow in the human body.
The results currently appear online at the
website of the journal
Environmental Science & Technology. Ana Rule, a postdoctoral researcher
at the Johns Hopkins University Bloomberg School
of Public Health, led the study.
In a series of experiments, the researchers
tested the BioSampler along with two traditional methods used to sample air – a
simple membrane filter, which traps microorganisms on a tightly-woven mesh
screen, and the AGI-30 (All-Glass Impinger-30), which collects organisms in a
fluid-filled glass chamber. While the BioSampler also collects microorganisms in
a glass chamber, its design is slightly different. That difference may result in
less damage as the organism is trapped, Buckley said
The researchers used Pantoea agglomerans,
a non-pathogenic bacterium that is a distant relative to E. coli and to
Yersenia pestis, the bacterium that causes plague. Y. pestis
is among the pathogens listed by the Centers for Disease Control and Prevention
as a Category A
bioterrorism agent, meaning that it is easily transmitted from person to
person and may cause high mortality rates. E. coli can contaminate food
and water and also pose an air hazard, Buckley said.
The researchers loaded a sample of P.
agglomerans onto each device to determine how efficient the device was in
retaining the microorganism in its original state and which sampling method
damaged P. agglomerans the least. They collected the bacterial samples
from each device after a predetermined amount of time, and then tested the
microorganisms' viability – that is, whether or not the organism's cellular
membrane was intact. They also tried to grow each sample in a laboratory dish, a
trait the researchers call the pathogen's “culturability,” which reflects
whether or not the organism can replicate and grow.
“From a health standpoint, the current gold
standard is to determine if a pathogen can be grown in the lab,” Rule said. “In
reality, its viability may be a more accurate assessment of its potential threat
to human health.
“Even when damaged by the sampling process,
pathogens have repair mechanisms that with time in the right medium – for
example, the human body – would allow them to replicate and grow,” she
continued. “Growing the cells in a medium immediately after sampling may not
truly represent what happens biologically.”
The researchers used a technique called flow
cytometry to assess the viability of the P. agglomerans organisms
collected by each sampling method. In flow cytometry, cells are stained with a
fluorescent dye and passed through a beam of laser light. The resulting color,
which scientists see as the organisms pass through this light, tells them
whether the cells are live (viable) or dead.
“Just because we can't grow something in medium
in the lab doesn't mean it won't grow in a human,” Buckley said.
Flow cytometry also tells researchers how many
total cells there are in a given sample, which allows them to determine if any
cells were lost by the sampling method (they had determined the exact counts in
each bacteria sample prior to using each method.)
For each sampling method, the researchers
evaluated the number of total, viable and culturable bacteria.
They found that three to six times more cells
were viable than culturable after using the filtering method and the AGI-30,
suggesting that most of the P. agglomerans had been damaged in the
collection process. But P. agglomerans samples taken from the
BioSampler showed extremely close agreement between the numbers of viable and
culturable bacteria. It was also the sampler with the fewest cell losses.
“Based on these results, it's fair to conclude
that what conventional analysis methods measure may not always represent the
actual presence and composition of a microorganism,” Buckley said.
“Understanding what effects a sampling method has on a pathogen is important for
designing better sampling strategies.”
Buckley and Rule conducted the work with
Kellogg Schwab, an associate professor with the Johns Hopkins School of Public
Health, and Jana Kesavan, who is with the Aerosol Sciences Team, RDECOM, at the
Edgewood Chemical and Biological Center in Edgewood, Md.
About researcher:
Timothy
J. Buckley, PhD, CIH
Associate Professor and Chair, Division of Environmental Health Sciences
Mailing Address:
Division of Environmental Health Sciences
College of Public Health
The Ohio State University
320 West 10th Avenue
A333-C Starling Loving Hall
Columbus, Ohio 43210
Contact Info:
Phone: (614) 293-7161
Fax: (614) 293-7710
Send
me an email
Education:
Ph.D., Environmental Science, Rutgers
University, 1991
M.H.S., Industrial Hygiene, Johns Hopkins University, 1986
B.S., Chemistry, St. Johns University, 1981
Background:
Dr. Buckley’s professional activities have
focused on the link between the environment and public health. He started his
career as an environmental scientist with the United States Environmental
Protection Agency in 1991. He worked in the National Exposure Research
Laboratory where he conceived, designed, and conducted human exposures and
biomarker validation studies to support the agency’s risk assessment and
regulatory research needs. In 1996, he joined the Department of Environmental
Health Sciences at the Johns Hopkins Bloomberg School of Public Health. There,
his exposure assessment research became more health oriented-investigating the
effects of air pollution in susceptible subpopulations including children with
asthma, elderly with chronic obstructive pulmonary disease, and exercising
adults. He is a certified industrial hygienist with research interests in
occupational exposure assessment with a particular interest in dermal hazards.
While at Hopkins he was promoted to associate professor and had adjunct
appointments in Epidemiology and Oncology.
Research:
Impact of traffic on community air pollution
Dermal Hazards in the Workplace: Assessment of Protection
Air Pollutants, Allergens and Asthma Morbidity in Inner City Children
Development and validation of exposure biomarkers
Interventions to control emissions from concentrated animal feeding operations
Development of a Questionnaire to Assess Worker Knowledge, Attitudes, and
Perceptions Underlying Dermal Exposure
Manager Dermal KAP Survey
Worker Dermal KAP Survey
Funding:
Funding for the work was provided by the
U.S. Army Edgewood Chemical and Biological
Center through a Scientific Services Agreement with Battelle.
| Related research: |
450 new terms for describing gene products involved in microbe-host interactions., Advancing Knowledge Of Little 'Nano-machines' In Our Body, Biomarker, or biological indicator, for early diagnosis of neurological disorders, Detect cancer and neurological diseases by identifying certain molecules present in human blood or urine, Developed simple bladder cancer test, Different biomolecules (DNA, proteins, etc.) in a single sample, FINDING SURVIVORS, PROTECTING DRIVERS, Human Virus may Prove useful in Attacking the Deadliest form of Brain Tumors, MIT radar technology fights breast cancer using microwave heat treatments, Molecular devices’ remarkably precise scans of cellular activity could revolutionize medicine, Removing Indoor Mould Improves The Symptoms Of People With Asthma, Researcher develops real scientific evidence about the effectiveness of magnetic therapy, Researchers apply neuroimaging to study ESP to resolve the century-old debate over its existence, Researchers can identify tumors under the skin of a living animal using Gold nanoparticle, Researchers proved severely restricted diet linked to physical fitness into old age, Researchers studying bat's communication to better treatments for human speech disorders, Taming Stem Cells, The mechanisms of heredity reveal their secrets, Tool to measure Physical, Emotional and Psychological functioning in Children may fail to accurately gauge these Quality-of-Life
|
|