Vector-Borne
Disease Ecology and Epidemiology
| Paul
R. Grimstad
Associate
Professor
Ph.D. University of Wisconsin-Madison
Postdoctoral,
University of Wisconsin-Madison, University of Notre
Dame |
|
Some
of the world's most severe infectious diseases, such as
yellow fever, dengue hemorrhagic fever and a number of
encephalitides, result from arthropod-borne virus (arbovirus)
infection. Most arboviruses are mosquito-transmitted in
nature, often involving complex vector- virus-host relationships.
The focus of work in my laboratory has been the epidemiology
and ecology of mosquito-borne encephalitis diseases, especially
those found in the midwesternUnited States. Among these
viruses are Eastern equine encephalitis (EEE), St. Louis
encephalitis (SLE) and several members of the family Bunyaviridae,
especially La Crosse (LAC), Jamestown Canyon (JC) and
Cache Valley (CV) viruses. Work on LAC virus encephalitis
epidemiology and ecology and the biology of its primary
vector, Ochlerotatus triseriatus, has been conducted by
my students, and those of the late Dr. George B. Craig,
Jr., at Notre Dame since 1974. One of the first reports
of geographic variation in susceptibility to an arbovirus
in mosquitoes came from this early work. Following a major
equine epizootic of EEE in southwestern Michigan in 1980,
attention was focused also on this often fatal disease
of equines and humans. Basic studies have included evaluation
of vector status of suspect mosquito species, local field
biology of the primary enzootic vector, Culiseta melanura,
and surveillance for disease among Indiana and Michigan
equine populations. One of the largest serologic surveys
of a United States' human population for arboviral disease
was conducted by my group. In that survey, more than 10,200
residents, representing every county in the State of Indiana,
were serologically screened for evidence of past infection
with LAC, SLE, EEE and Western equine encephalitis viruses.
Our
group was the first to report severe human central nervous
system disease caused by JC, a bunyavirus distributed
over most of temperate North America. This virus is now
recognized as the cause of numerous clinical infections
that can result in severe disease and even death. The
natural cycle is quite complex involving white-tailed
deer as the primary vertebrate host and a variety of aedine
mosquito species, some of which harbor the virus over
winter in their eggs and thus serve as the reservoir tissue
for JC virus from which it "emerges" in the
spring with the hatch of the mosquito eggs. The same is
true of LAC virus. Work continues on the natural JC virus
cycle and the role of anopheline mosquito species in an
alternate late summer transmission cycle. Evidence of
transplacental virus transmission in deer has important
implications for human maternal infection that is being
explored by our group.
A
second bunyavirus, CV, has been identified recently as
the agent of an "emerging" human disease. Human
infection with CV virus can result in a fatal encephalitis
to more mild forms of central nervous system disease.
This virus has also been linked to neural tube defects
in infants born to mothers infected in the first trimester
of pregnancy. Our group has been investigating the epidemiology
and ecology of CV virus since the early 1990's and have
found evidence of widespread infection in the upper Midwestern
human population as well infection as of domestic animals
and wildlife. Laboratory studies have implicated several
mosquito species, and especially Anopheles quadrimaculatus,
as potential vectors. Laboratory studies using pregnant
mice have shown that early trimester infection results
in the loss of many mouse embryos. Of concern is the possibility
that CV virus infection may be a cause of first trimester
miscarriage in women. Indeed, recent serologic analysis
by one of my students of human cord bloods taken at birth
has suggested a possible link between infection and spontaneous
miscarriage or abortion in local residents.
Graduate
students in my laboratory work from the level of the viral
and/or vector mosquito genome to the natural disease cycle
in the field. Critical to our understanding of viral pathogenesis
for vertebrate hosts is the vector biology of the invertebrate
mosquito host. Thus, field studies supported by state-of-the-art
molecular laboratory studies are essential for the complete
characterization of these disease cycles. The overall
goal of these multiple studies is to better understand
the dynamics of arbovirus transmission in natural foci,
aid public health workers in case detection and surveillance
and to use this information to minimize human infection
and potentially improve means of vector control.
|
|
Biomodal period of onset
for human clinical Jamestown Canyon virus diease vs.
unimodal LaCross virus infections. |
 |
Immune profile of a
deer population from birth of fawns (and acquisition
of maternal antibody) through a primary infection
of the second spring of life. |
Selected
Publications:
Wallace
JR, Grimstad PR. (2002) A preliminary characterization
of the physiological ecology of overwintering Anopheles
mosquitoes in the midwestern USA. J Am Mosq Control Assoc.
18(2):126-7.
Anderson JR, Grimstad PR, Severson DW. (2001)
Chromosomal evolution among six mosquito species (Diptera:
Culicidae) based on shared restriction fragment length polymorphisms.
Mol Phylogenet Evol. 20:316-21.
Brockus CL, Grimstad PR. (2001) Comparative
analysis of G1 glycoprotein coding sequences of Cache Valley
virus (Bunyaviridae: Bunyavirus) isolates. Virus Genes.
2001 22:133-9.
Brockus CL, Grimstad PR. (1999) Sequence analysis
of the medium (M) segment of Cache Valley virus, with comparison
to other Bunyaviridae. Virus Genes. 19:73-83.
Blackmore CG, Grimstad PR. (1998) Cache Valley
and Potosi viruses (Bunyaviridae) in white-tailed deer (Odocoileus
virginianus): experimental infections and antibody prevalence
in natural populations. Am J Trop Med Hyg. 59(5):704-9.