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Faculty
Harald Beck, Ph.D.
Curator of TU Mammal
Collection
Smith 249
(410) 704-3125
hbeck@towson.edu
My current research focuses
on understanding how disturbances, either natural (i.e.
treefalls, ecosystem engineers) or anthropogenic (i.e.
habitat destruction, overhunting), affect population
dynamics and species richness of mammals and plants in the
Amazon. For instance, the dramatic impact of peccaries (a
pig-like creature) on forest ecology is apparent to anyone
who has watched a 300-strong herd of these animals thunder
through the understory (animal mediated disturbance). But
because of habitat destruction and hunting (anthropogenic
disturbance), the species has been driven to local
extinction and a new generation of trees is maturing without
the massive seed predation, dispersal (mammal-plant
interactions), soil disturbance, or physical damage wrought
by peccaries. To test some of
these hypotheses, I have set up several long-term
experiments in Cocha Cashu and Los Amigos, two sites within
the Peruvian Amazon. Furthermore, in collaboration with
colleagues from the IUCN Tapir Specialists Group, we are
currently testing the impact of tapir disturbances on the
seedling and sapling communities using hundreds of
exclosures across five Neotropical countries and in
Malaysia.
Another “hot topic” in my lab
is to quantify the role of ecosystem
engineers. These species physically modify and create new
habitats
and thereby
control the availability of resources to species. However,
unlike most mammalian ecosystem engineers (i.e.
beavers), I
posit that
peccaries have two distinct engineering mechanisms. First,
while foraging for below-ground resources they “bulldoze”
through the soil, creating germination sites for “leaf
litter-gap dependent” plant species, and thus potentially
increasing plant richness. Second, peccaries can function as
ecosystem engineers by creating and maintaining wallows that
may be critical habitats for aquatic species. Since 2003 I
have been studying the effects of peccaries as ecosystem
engineers.
Dr. Brian Fath
Smith Hall 273
(410) 704-2535
bfath@towson.edu
My research broadly focuses
on sustainability, which I address using three different
approaches: network environ analysis, integrated
environmental assessment, and information theory.
Sustainability is a critically important area that
encompasses a broad range of research interests including
ecosystem services, biodiversity, natural resources, human
cultures, and specific environments. I use network analysis
to investigate thermodynamic sustainability indicators.
These indicators are often referred to as ecosystem goal
functions because they determine holistic properties of the
ecosystem such as energy or exergy flow, biomass production,
and respiration. These metrics help understand the overall
behavior and health of that system and its response due to
perturbations. Integrated environmental assessment is an
application of multidisciplinary methods to human systems to
address specific place-based issues. I have used IEA to
study the watershed quality of a major metropolitan
reservoir and am interested in further applying this process
to local and international issues. Recently, I have begun
looking at using information theory, particularly, Fisher
Information, as a potential sustainability metric.
Dr. Don C.
Forester
Smith Hall 255
(410) 704-2385
dforester@towson.edu
Dr. Forester's research
focuses on the behavioral ecology of lower vertebrates,
especially amphibians. In recent years his interests have
diverged into three primary areas: (1) Kin recognition among
salamanders, (2) sexual selection and alternative mating
systems among frogs, (3) home range and activity patterns of
amphibians and reptiles using radio telemetry. Presently he
is investigating the importance of chemical signals in the
social structure of the seepage salamander (Desmognathus
wrighti), a miniaturized terrestrial salamander indigenous
to the southern Appalachian mountains of North Carolina and
Tennessee. The current thrust of the investigation involves
testing the ability of seepage salamanders to recognize
conspecifics based on substrate-bore chemical cues.
Dr. Gail Gasparich
Smith Hall 487
(410) 704 - 4515
ggasparich@towson.edu
Dr. Gasparich's current
research focuses on two main projects: 1) The development of
taxonomic and phylogenetic classification of the eubacterial
class Mollicutes whose members are all closely associated
with a variety of hosts including vertebrates (Mycoplasmas,
Ureaplasmas), arthropod hosts (Entomoplasmas, Spiroplasms,
Mesoplasmas) and plants (Phytoplasmas). A major long-term
project within Dr. Gasparich's laboratory is to characterize
the diversity and assess the relationships among the genera
using cladistic analyses based on serology, metabolic tests,
morphology, ecology, molecular and biogeographical
data. Graduate students have a wide range of opportunities
to conduct research on evolutionary relationships within and
among the different Mollicute genera. 2) The development of
a gene expression vector for use with the genera
Spiroplasmas for the basic examination of gene expression
and regulation is also a research focus in the
laboratory. Such a vector could also be used for the more
applied purpose of developing insect biocontrol by
expression of arthropod lethal toxins (i.e. Bt toxin and
scorpion toxin) by spiroplasmas in their arthropod hosts
(which include disease carrying mosquitoes and ticks).
Dr. Susan E. Gresens
Smith Hall 223
(410) 704-4368
sgresens@towson.edu
Dr. Gresens is interested
in the ecology of freshwater systems, particularly
streams. Her research focuses on communities of
macroinvertebrates and attached algae; the ecology of midge
larvae (Diptera: Chironomidae) is her specialty. Midge
larvae occur in a wide range of aquatic habitats, exhibit
high species diversity, and are often very numerous. The
potential importance of midges as primary consumers, which
transform algal and detrital material, and transfer it to
higher trophic levels has been largely overlooked, due to
their small size. Her previous research has demonstrated
interactive effects of food quality and thermal regime on
feeding and growth of larvae. Current research in her
laboratory is defining spatial patterns in the composition
of stream invertebrate communities, in response to watershed
urbanization. Her goals are to develop a mechanistic
understanding of the causes of low biological diversity in
urban streams, and to determine the value of midge larvae as
ecological indicators within urban areas.
Dr.
James C. Hull
Smith Hall 215C
(410) 704-4117
jhull@towson.edu
Dr. Hull’s interests are in
the interactions between plants and their physical-chemical
environment. His research utilizes physiological techniques
such as photosynthetic measurements or plant water
potentials to assess plant responses to environment. Typical
problems addressed in his laboratory are those associated
with transient light beneath forest canopies, plant
distribution along water availability gradients, and
nutrient limitations to growth. A current emphasis in his
laboratory is on an invasive plant, mile-a-minute weed (Polygonum
perfoliatum). Most studies are oriented towards field
situations in local habitats.
Dr. L. Scott
Johnson
Smith Hall 263
(410) 704-2587
sjohnson@towson.edu
Dr. Johnson
is broadly interested in the reproductive behavior and
ecology of small birds. More specifically, his interests
include the evolution of mating systems including extra-pair
mating behavior, sex ratio manipulation, factors affecting
nestling growth, the evolution of egg shape and size, the
function of song, the proximate and ultimate effects of
nestling ectoparasites on reproduction, the effect of
calcium availability and reproductive output, territorial
behavior, and parental behavior. Much of Dr. Johnson’s
research involves they House Wren as a study species but
research is also planned involving Tree Swallows and
Mountain Bluebirds. His primary research site is the Helen
Brinton Bird Reserve near Big Horn, Wyoming. Dr. Johnson
takes several students to this site each summer.
Dr. John Lapolla
Smith Hall 351
(410)-704-3121
jlapolla@towson.edu
1)
Coevolution of Acropyga ants and mealybugs
Acropyga ants display a fascinating
behavior I have termed trophophoresy. Trophophoresy is the
behavior of a queen ant taking with her on her mating flight
a mealybug from her birth nest (LaPolla, 2002). This
mealybug serves as a "seed" individual through which a new
colony of mealybugs will be created. The ants feed on the
sugary substances produced by the mealybugs. It is believed
the ants and mealybugs are mutually dependent on one another
for survival. Acropyga ants are, in a sense, the
dairy farmers of the ant world.
We know virtually nothing about the symbiosis
between Acropyga ants and their mealybug “cattle.”
Investigating the biological aspects of this complex
symbiosis has become a major component of my research
program. In collaboration with Drs. Ted Schultz & Sean
Brady (National Museum of Natural History) and Dr. Joseph
Bischoff (National Institutes of Health-GenBank), several
important studies are planned over the next several years.
2)
Biodiversity Studies
I have employed the replicable "ALL" (Ants of
the Leaf Litter) protocol to examine patterns of ant
diversity across South America. In collaboration with Dr.
Ted Schultz (NMNH) and doctoral student Jeffery Sosa-Calvo
(U Maryland-College Park), my research project will continue
gathering and examining leaf litter ant data from Guyana,
Suriname, French Guiana, Brazil and Peru. Over the next
three years, we will complete on-going studies comparing the
Guiana Shield fauna to the rest of South America to
extrapolate patterns of endemism and identify areas of
conservation concern.
I am also Lead Scientist for Conservation
International’s Tropical Ecology Assessment and Monitoring
in Suriname. This project involves periodic ant sampling at
Raleighvallen in the Central Suriname Nature Reserve.
3)
Revisionary Systematics
I am in the process of completing a world
revision of the ant genus Paratrechina, a large genus
of over 140 species, and a group that contains many invasive
species of agricultural and economic importance. With no
taxonomic monograph available, most Paratrechina
species are currently impossible to identify. Defining the
species will help efforts at using biological control
methods to control invasive species. The genus has never
been revised and there are undoubtedly many new species
awaiting discovery.
I am also currently beginning a world revision
of the genus Discothyrea with doctoral student Jeffery Sosa-Calvo
(U Maryland-College Park). These enigmatic ants are found
worldwide in subtropical and tropical localities. They are
thought to be specialist predators on arthropod eggs.
Dr. Barry Margulies
Smith Hall 251
(410) 704-5019
bmargulies@towson.edu
The Towson University Herpes Virus Laboratory
(TUHVL) is studying pathogenic mechanisms employed by three
different human herpesviruses, the virus’ interactions with
the host immune system, and means of antiviral intervention
for each infectious agent.
Herpes simplex virus type 1 (HSV-1) is the
etiologic agent for fever blisters and cold sores. We are
using a mouse model of infection to explore long-term
delivery of the useful anti-herpetic acyclovir. We have
already developed silicone-based controlled-release devices
that release acyclovir at a quantity and rate that
completely stops infection in vitro, and prevent
reoccurrences in vivo. We are currently
collaborating with multiple labs in the US to improve
efficacy and extend our studies to other viruses and model
systems, including HSV-2, the etiologic agent of genital
herpes.
We are also examining an odd molecular
phenomenon exhibited by the US27-encoded chemokine
receptor-like glycoprotein expressed by human
cytomegalovirus (CMV), a ubiquitous pathogen that tends to
cause solid organ damage, including but not limited to CMV
retinitis, a blindness caused by death of retinal cells in
the eye. Although there does not appear to be anything
special about the mRNA or protein sequences from this gene,
it is clear that a single transcript codes for two related
glycoproteins. Our favorite hypothesis, that alternative
initiation codons are being employed, is currently under
investigation.
It has
been hypothesized, through many lines of circumstantial
evidence, that human herpevirus-6 (HHV-6) is the indirect
cause of multiple sclerosis (MS), perhaps by tricking the
host immune system into attacking itself through a
phenomenon called molecular mimicry. We are developing a
mouse model for MS that employs expression of a single HHV-6
protein and whether it can be proved as a causative link to
MS. We believe such a system will give us an ideal small
animal model to definitively prove or disprove the currently
circulating theories of a viral origin for MS, and provide a
system to test many different antiviral drugs' ability to
combat MS.
Dr. Brian Masters
Smith Hall 489A
(410) 704-2035
bmasters@towson.edu
personal web site
Dr. Masters is interested
in the application of molecular techniques (such as DNA
fingerprinting) to the study of ecological
questions. Specifically, his interests include the study of
a number of behaviors such as migration, mate choice,
cooperation, kin recognition, and maternal behavior. Recent
research has also involved investigation of the impact of
genetic diversity on fitness, an area of study with clear
implications for species conservation. Most of his research
has involved various species of salamander, but Dr. Masters
is not a slave to taxa, and has worked on a variety of
organisms, including birds, insects, and plants.
Dr. Jay A. Nelson
Smith Hall 257
(410) 704-3945
jnelson@towson.edu
Dr. Nelson’s research
broadly focuses on trying to understand how the environment
controls life processes and how living organisms have
evolved to respond to environmental pressures in two (
thinking of growing to three) systems: 1) The main focus of
my research is the nutritional physiological ecology of
Loricariid catfish. Evidence suggests that loricariid
catfishes of the genus Panaque are capable of utilizing wood
in their diet. I am studying the ability of Panaque to
degrade carbon polymers like cellulose and hemi-cellulose.
In collaboration with Dr. Daniel Wubah of this department, I
am also investigating the enzymes produced by the microflora
of Panaque guts. In collaboration with Dr. Don Stewart of
the SUNY College of Environmental Sciences and Forestry and
Bill Patterson of Syracuse University, I am trying to take
this research to South America so that we may better
understand the unique biology of Panaque in situ. 2) I am
also collaborating with colleagues in Canada to investigate
factors that contribute to locomotor performance in Atlantic
cod. I have already shown that exercise physiology in these
fish varies on an individual and population level and that
environment (salinity and temperature) are important
limiting factors. We are currently trying to better
understand the inter-relationships of various locomotor
types in cod, their relationship to predatory ability, and
how other physiological factors like nutritional state
influence locomotor capacity and physiology. 3) I am in the
planning stages of starting a research project on the
locomotor capacity of local fishes. This may take the form
of a collaboration with Dr. Joel Snodgrass of this
department studying the effects of human developments on
local stream fish populations.
Dr. Roland Roberts
Smith Hall 205
(410) 704-3034
rroberts@towson.edu
My
laboratory is engaged in research on the systematics and
evolution of vascular plants. Taxonomic groups of current
interest are the Asteraceae and Euphorbiaceae. I am also
interested in the evolution of desert flora, particularly
population structure and the roll of hybridization in
speciation, and the biogeography and evolution of the flora
of the West Indies specifically that of the islands of the
Lesser Antilles. Methodologies employed for uncovering
evolutionary relationships include the use DNA sequences of
chloroplast and nuclear genes along with traditional
techniques.
Dr . Gerald D. Robinson
Smith Hall 349
(410) 704-2373
grobinson@towson.edu
Dr. Robinson is interested
in the comparative physiology of animals, especially the
regulation of salt and water exchanges between aquatic
species and their environments. Past studies completed have
focused on ion and fluid balance in crustaceans, fish,
amphibians, diamondback terrapins, and sea snakes. His
current research examines the cutaneous electrical
properties and modifications of sodium uptake in urodele
amphibians following exposure to low pH conditions. Dr.
Robinson is also interested in any physiological mechanisms
(respiratory, cardiovascular, metabolic, etc.) employed by
animals to permit survival in stressful environments.
Dr. Erik P. Scully
Smith Hall 261
(410) 704-3012
escully@towson.edu
My primary research
interests are the population biology of invertebrates,
especially crustaceans, and the population level
consequences of individual behavior. My current research
interests include: (1) Effects of chronic exposure to heavy
metals on life history patterns of terrestrial isopods
living in serpentine areas; (2) The dynamics of
aggregation formation in terrestrial isopods. I am also
engaged in collaborative research projects with other
faculty: (1) Laboratory and in vitro studies of disease and
bleaching in corals (with Gary K. Ostrander, Johns Hopkins
University); (2) Using Neural Network models to study the
evolution of simple behavioral responses (with Dr. John
Alexander, Computer and Information Sciences, Towson
University). I am willing to advise students in a variety of
research areas. For example, one of my current students is
investigating a model in theoretical systems ecology, and I
would be interested working with individuals who wish to
explore historical and philosophical questions in
evolutionary biology.
Dr. Richard Seigel
Smith Hall 345
(410) 704-3012
rseigel@towson.edu
My basic research
philosophy is that one cannot be a good conservation
biologist without first being a strong population ecologist,
and, conversely, that an interest in conservation biology is
a required interest of anyone calling themselves a
population ecologist. Thus, research in my lab is oriented
in two main directions; studies on the evolutionary ecology
of amphibians and reptiles (using both field and
experimental approaches) and studies on the conservation
biology of amphibians and reptiles, which is almost
exclusively field-oriented. My selection and recruitment of
graduate students follows these approaches; of the 16
students I have mentored to date, eight have focused on
evolutionary ecology and eight on conservation biology.
Naturally, students are strongly encouraged to work outside
of their specific area of expertise and to collaborate with
myself or with their fellow students.
Jack D. Shepard, Ph.D.
(410) 704-2394
Smith 259
jshepard@towson.edu
My
research program is directed toward determining the
biological and behavioral effects of stress. While
responses
to acute
stress are primarily adaptive, chronic stress can lead to
both somatic and psychiatric illness. A key feature of
stress-related disease is increased reactivity to stress
including excess secretion of stress hormones such as the
glucocorticoids and corticotropin releasing factor. My
research interests are centered around three areas of
investigation:
1.)
behavioral responses to stress and glucocorticoid excess
2.) neuroendocrine regulation during acute stress
3.)
functional plasticity in the stress axis in response to
chronic stress or exposure to psychostimulant drugs.I
welcome the participation of both undergraduate and graduate
students in my research program.
Dr. Vonnie Shields
Smith Hall 357
(410) 704-3130
vshields@towson.edu
Chemosensory cues, such as
odor and taste stimuli, play a pivotal role for insects in
selecting food sources, mates, and oviposition sites.
Research in the Dr. Shields’ laboratory concentrates on
olfactory and gustatory processing by the peripheral and
central nervous systems of both larval and adult insects
(Lepidoptera). One area of study focuses on (a) the sensory
mechanisms by which female moths detect hostplant-associated
odorants that allow them to assess hostplant availability
and suitability and the presence of potential competitors or
co-habitants and (b) how this neural information is conveyed
to the brain by antennal olfactory sensory organs. Other
avenues of research will be directed towards exploring the
importance of gustatory cues in the location of food sources
by larval insects and examining the structural organization
of gustatory organs. Work in this laboratory combines
anatomical, neurophysiological, and behavioral methods in a
multidisciplinary approach to seek answers to specific
questions such as: (i) which plant odors provide important
cues by which larvae and adults detect their hostplants? and
(ii) what role do phagostimulants (nutrients, sugars,
secondary plant compounds) and deterrents play in hostplant
selection and feeding behavior in larvae? Recent evidence
indicates that the basic processing of chemosensory
information is similar in invertebrates and vertebrates.
Consequently, using insects as model systems has
implications for chemosensory research on species in diverse
animal phyla and therefore, allows students to gain insights
into the fundamental processing of sensory information in
the brain. Also, students will acquire microscopic
techniques and learn methods associated with behavioral and
physiological assays.
Dr. Erik Silldorff
Smith Hall 249/367
(410) 704-3120
esilldorff@towson.edu
My laboratory focuses on
the study of vasoactive characteristics of the mammalian
renal microcirculation (rat model), specifically the
descending vasa recta, to determine the potential for
regulation of total and regional renal medullary blood flow.
Because of the unique vascular anatomy of the renal medulla,
medullary blood flow is derived exclusively from vasa recta
originating from efferent arterioles of juxtamedullary
glomeruli. Focus is on the effects and interactions of
vasoactive agents acting in a paracrine or autocrine (local)
manner within the renal medulla. This research may
ultimately be linked to such physiological phenomenon as
pressure natriuresis and the urine concentrating mechanism
as well as pathological conditions such as ischemic acute
renal failure. A recent project examined the ability of
adenosine to alter vascular tone in vasa recta as well as
the second messenger systems involved in this action. We are
currently examining the response to angiotensin II in these
vessels and their dependence upon arachidonic acid
metabolites for the generation of vasoconstriction. The
majority of our studies focus upon locally produced hormonal
or paracrine agents which alter vascular activity in an
autoregulatory fashion.
Dr. Colleen Schehl
Sinclair
Smith Hall 215A
(410) 704-3124
csinclair@towson.edu
Dr.
Sinclair's laboratory is involved in the study of genetic
diversity in populations of invertebrates and vertebrates.
Current projects include the evaluation of population
diversity in non-biting midges (Cricotopus sp.) from
Baltimore streams, an analysis of the genetic structure of
terrestrial snail populations in the Potomac River basin,
and an analysis of genetic influence on sea bass (Dicentrarchus
labrax) success.
Dr. Joel W. Snodgrass
Smith Hall 302
(410) 704-5033
jsnodgrass@towson.edu
Dr. Snodgrass is interested
in the dynamics of aquatic vertebrate populations,
particularly over larger temporal and spatial scales, and
the effects of human landscape alteration on their dynamics
and evolution. His past research has focused on the roles of
hydrological variability and aquatic habitat patch dynamics
in determining the distribution of amphibians and fishes in
southeastern streams and wetlands. Dr. Snodgrass also is
interested in the application of community ecology theory to
the development of biological monitoring programs focus on
amphibians and fishes, and the use of stochastic simulation
models in directing land planning activities. Recently he
has collaborated with ecotoxicologist and ornithologist to
investigate the role of wetland fish population dynamics in
controlling mercury-poisoning risk among fish-eating birds.
Michelle Snyder, Ph.D.
Smith 253
410-704-4817
msnyder@towson.edu
The immune
system is the body's line of defense against disease-causing
bacteria, viruses and fungi. In order to carry out its
function the immune system must be able to distinguish self
from non-self. If the immune system fails to detect foreign
invading pathogens, the body succumbs to infection and
possible death. On the other hand, if the system mounts an
attack against its own tissues, autoimmunity can develop.
It has
been recently appreciated that the crucial ability of the
immune system to quickly detect foreign invading pathogens
is a function of an evolutionarily ancient arm of the
system, termed the innate system. Cells of the innate
system have evolved to distinguish pathogens from self by
recognizing highly conserved pathogen-associated molecular
patterns (PAMPs) through a similarly-conserved array of
surface-associated pattern-recognition receptors (PRRs).
PRRs used by mammalian immune systems have been identified
in organisms as diverse as horseshoe crabs, tomatoes, worms
and fruitflies. In fact, some of the ground-breaking work
in identifying the PRRs by which innate immune systems
recognize invading pathogens was completed in fruitflies.
The slime
mold Dictyostelium discoideum is a unique model
organism that exists for part of its lifecycle as
unicellular amoebae but is induced to form a multicellular
sporulating body upon starvation. The amoeboid cells
phagocytose bacteria for nutrient uptake, and this process
is utilized in higher organisms by innate immune cells to
eliminate invading bacteria. Due to the ease with which
they can be cultured and genetically manipulated,
Dictyostelium amoebae have long been used to study the
process of phagocytosis. It has not been appreciated,
however, whether Dictyostelium detect bacteria using
the same types of PRRs as do innate immune cells.
The
research in our laboratory is aimed at studying
Dictyostelium responses to known PAMPs found in
bacteria, fungi and viruses. Our preliminary studies have
revealed that Dictyostelium amoebae can indeed
respond to known PAMPs, suggesting that elements of the
pattern-recognition machinery used by innate immune systems
in higher organisms are conserved. We are taking advantage
of the manipulability of the Dictyostelium genome to
identify and study particular gene products that may be
involved in the Dictyostelium response to PAMPs.
Characterization of such proteins in Dictyostelium
may allow for identification of novel players conserved in
the innate immune systems of mammals.
Although
the immune system has developed to recognize and eliminate
foreign organisms, various pathogens have evolved strategies
to evade immune responses. Some pathogens such as
Mycobacterium tuberculae have evolved strategies
to evade mammalian immune surveillance by acquiring the
ability to survive within phagosomes of innate immune
cells. Recent studies have shown that microbial pathogens
also can infect and survive within phagosomes of
Dictyostelium. We are working to develop a model system
using Dictyostelium and Mycobacterium bovis BCG
(a weakened Mycobacterium strain that is safely
administered as part of a vaccine for tuberculosis in much
of the developing world). We hope that such a system will
allow us to translate our findings related to pattern
recognition in Dictyostelium to host-pathogen
interactions in human diseases such as tuberculosis.
Dr. Joy Watts
Smith 489A
(410) 704-2623
jwatts@towson.edu
Environmental Microbiology
Dr. Larry Wimmers
Smith Hall 483
(410) 704-2766
lwimmers@towson.edu
Dr. Wimmers' laboratory
employs a combination of molecular genetic and classical
physiological tools to address three aspects of plant
function. He has long-term interests in the response of
plants to salt stress and the mechanisms of phloem
translocation. His approach to the salt stress response has
been to identify genes induced by sub-lethal levels of salt
stress, and to test their role in salt-stress resistance by
altering their expression in transgenic plants. His studies
of phloem translocation have concentrated on the mechanism
of phloem loading, and the control of that process. Recently
he has also investigated factors affecting the ability of
plants to accumulate heavy metals, the goal being to produce
plants with a high potential for accumulation of heavy
metals that can be used to remove such toxins from
contaminated soils and wetlands.
United States Army
Medical Research Institute of Chemical Defense Adjunct
Faculty
Dr. Steven Baskin
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-2378
Steven.Baskin@amedd.army.mil
personal web site
Dr. Baskin's research
focuses primarily on mechanisms of cyanide intoxication and
therapies for the treatment of this poison, he also devotes
studies to the cardiac actions of neuroactive agents such as
oximes and organophosphates as well as muscarinic and other
compounds that would antagonize a cholinergic-induced
cardiomyopathy.
Dr. Alan Brimfield
UNDER CONSTRUCTION
Dr. David Lenz
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-1311
david.lenz@amedd.army.mil
personal web site
Dr. Lenz' current research
is directed toward the development of human proteins capable
of being used as bioscavengers that would afford protection
against exposure to highly toxic organophosphorus
cholinesterase inhibitors which form the basis of some nerve
agents. Current research interests involve the generation,
purification and sequencing of mutants of several esterases
of human origin such as acetylcholinesterase,
butyrylcholinesterase, carboxylesterase and paraoxonase with
the goal of producing and characterizing enzymes with novel
binding or kinetic properties. The projects require skill in
the art of mutagenesis, both site-directed and random, as
well as the ability to develop kinetic assays and expression
systems. An interest in molecular biology is required and a
strong background in chemistry or biochemistry is helpful.
Dr. John McDonough
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-1942
john.mcdonough@amedd.army.mil
personal web site
Current research explores
the following subjects: (1) the mechanisms by which toxic
compounds – specifically organophosphate agents – affect the
central nervous system to produce changes in brain function;
(2) the mechanisms by which seizures develop following
exposure to organophosphates, the functional and
pathological consequences of these seizures, and how
different classes of drugs can block or terminate the
seizure activity; and (3) the short- and long-term
neurobehavioral consequences of exposure (acute high dose or
chronic low dose) to organophosphate agents. These projects
involve neuropharmacological studies involving
electrophysiological (quantitative EEG analysis),
behavioral, and neuropathological analysis of drugs in whole
animal preparations (rat, guinea pig, nonhuman primate).
Dr. John Petrali
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-2334
john.petrali@amedd.army.mil
personal web site
Dr. Petrali oversees the
daily activities of a state-of-the-art electron microscopy
facility that provides high resolution transmission electron
microscopy, scanning electron microscopy, x-ray
microanalysis, immunohistochemistry, immunoelectron
microscopy, cryomicroscopy and image analysis. The facility
is responsive to all mission directives of the United States
Medical Research Institute of Chemical Defense and is
considered a highly visible competitive functional
laboratory of the scientific community. As principal
investigator, Dr. Petrali develops and conducts primary
investigations to detect diagnostic and ultrastructural
mechanisms of action of chemical and biological threat
agents. Primary investigations included contributions toward
the development of a internationally recognized
immunohistochemical procedure, ultrastructural
identification of cells targeted by sulfur mustard toxicity
in skin, determining pathogenesis of microblister formation,
determining sulfur mustard effects on effects of the
microenvironment of the skin basement membrane, determining
sulfur mustard effects on the morphological integrity of
structural attachment mechanisms of epidermal – dermal
connections. Results of these published studies are now
driving the investigations of threat agents conducted by
other scientific disciplines in-house as well as
extramurally.
Dr. James Romano, Jr.
UNDER CONSTRUCTION
Dr. John Schlager
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
john.schlager@amedd.army.mil
personal web site
Molecular and cellular
biology research approaches are applied to characterize the
cytotoxicity, devise therapies for toxicities, and determine
specific biomarkers for quantitative analysis of chemical
warfare agent exposure. We are elucidating the specific
mechanism(s) of cell toxicity produced by alkylating
chemicals by identifying pathways for potential therapeutic
intervention and cytoprotection prior to or just following
chemical exposure. Laboratory research centers on the effect
of sulfur mustard on its disruption of normal gene
expression in in vivo exposure models such as animal skin
and lung and in vitro models including cultured human
keratinocyte and immortalized cells. Techniques used for
board transcript identification studies include subtraction
library construction, probing DNA arrays, differential
display-polymerase chain reaction (PCR), and quantitative
RT-PCR, and 2d gel/MS proteomics.
Dr. Alfred Sciuto
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-5115
alfred.sciuto@amedd.army.mil
personal web site
Studies in Dr. Sciuto's
laboratory are conducted to develop and test the efficacy of
therapeutic compounds against acute lung injury. Acute lung
injury, defined as the progression of injury to life
threatening pulmonary edema formation, is produced by using
either inhalation or system injection techniques. Areas of
investigation of acute lung injury and related mechanisms
include the following: (1) use of whole-body inhalation
exposure systems; (2) small animal isolated perfused lung
preparations; (3) investigations of the role of reactive
mediators, such as leukotrienes, prostaglandins, and
cytokines in the injury process; (4) investigation of both
tissue and bronchoalveolar lavage fluid for clues to the
injury processes; (5) the effect of toxic agents and
therapies on lung dynamics; (6) efficacy testing of
therapeutic compounds based on their capacity as anti-edemagens;
(7) survival analysis of effective drug interventions in in
vivo experiments; (8) assessment of the role of antioxidant
mechanisms and lipid peroxidation in lung injury processes;
(9) investigation of the role of glutathione (thiol groups)
in protection; and (10) assessment of histopathological
changes related to lung damage and treatment efficacy.
Studies will utilize spectrophotometric, high-performance
liquid chromatography; enzyme immunoassay analysis; gas
chromatography; and established biochemical assay techniques
of compounds of interest. Information will be gathered into
a data base for use in the treatment against chemical
agent-induced pulmonary injury.
Dr. Tsung-Ming Shih
U.S. Army Medical Research Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
tsung-ming.shih@amedd.army.mil
personal web page
Dr. Shih's laboratory
employs a combination of electrophysiological and
neurochemical tools to address the actions of
organophosphorus (OP) anti-cholinesterase agents and their
therapeutic compounds in whole animal models. He has
long-term interests in the relationship between central
neurotransmission and pathophysiological responses. Current
research interests involve a comparison of the effects of
various OP compounds on the neurotransmitter systems
subsequent to either acute toxic or chronic repeated
subtoxic exposure of these agents; the identification of
pharmacological classes of drugs that are most effective
against OP agents-induced electroencephalographic (EEG)
seizures in animals models; and the ability of therapeutic
drugs to reverse the alterations in brain neurotransmitter
systems induced by OP agents and the subsequent
neuropathology.
Dr. William Smith
U.S. Army Medical Research
Institute of Chemical Defense
3100 Ricketts Point Road
Aberdeen Proving Ground, Maryland 21010-5400
(410)436-4255
william.smith@amedd.army.mil
personal web site
Dr. Smith’s research
objective is to develop relevant cellular and tissue models
to evaluate biochemical changes initiated by sulfur mustard.
Cell biology research is conducted to establish flow
cytometric assays for the determination of alkylation
induced alterations in cultured human epithelial cells, and
develop therapeutic means to protect epithelium from
deleterious biochemical changes induced by sulfur mustard.
His laboratory’s goal is to identify approaches that will
intervene in the production of vesicant induced injury.
Research is conducted to: (1) determine which biochemical
mechanisms are likely to mediate vesicant injury, thereby
allowing meaningful research on intervention; (2) define
mechanisms of action of vesicating agents and their
antidotes to develop better methods of therapy and
prophylaxis; and (3) develop in vitro models for determining
the efficacy of prophylactic and therapeutic compounds for
mustard injury. |