DUKE BACTERIOLOGY
RESEARCH UNIT
Faculty and Research
Alejandro Aballay, PhD
Assistant Professor
Department of Molecular Genetics and Microbiology
lab members
alumni publications website
Biography:
Alejandro Aballay earned his bachelor's degree in Pharmacy from Juan A. Maza
University, in Mendoza, Argentina, in 1994. During this time, he worked as an
undergraduate student at Nacional de Cuyo University, in Mendoza, Argentina, where
he studied soil bioremediation. He finished his M.S. equivalent studies in 1995
and started exploring the machinery that governs early steps in endocytosis at
Nacional de Cuyo University. During this period, he received a World Bank fellowship
to complement his studies in endocytosis by working as a summer student for two
consecutive years at Washington University, in St. Louis, Missouri. In 1998, he
earned his Ph.D. at Nacional de Cuyo University and received a Pew Fellowship to
move to St. Louis, where he continued his studies in endocytosis at Washington
University. In 1999, following an interest in bacterial pathogenesis he developed
while studying the intracellular transport of Brucella abortus when he was a
graduate student, he moved to Boston to join the Ausubel laboratory at Harvard Medical
School. Dr. Aballay moved to Durham in 2002 to join the Department of Molecular Genetics
and Microbiology, where his studies focus on what makes bacteria pathogenic and hosts
resistant.
In the Ausubel laboratory, Dr. Aballay developed a novel pathogenesis system
utilizing the simple well-studied nematode Caenorhabditis elegans and the
common human bacterial pathogen Salmonella enterica. Salmonella is well
known for its ability to cause food poisoning. Nematodes like C. elegans eat
bacteria and surprisingly, C. elegans is killed when it is provided S. enterica
as a food source. This killing is accompanied by a persistent infection of S. enterica
in the C. elegans intestine. Importantly, Dr. Aballay has shown that several
well-studied S. enterica virulence factors required for causing disease in
mammalian hosts are also required for C. elegans killing. This validates the use
of C. elegans as a host to model Salmonella infection in mammals, including
humans.
Dr. Aballay's laboratory takes advantage of the compromise between complexity and
tractability of the C. elegans-S. enterica pathogenesis model. The focus
of the laboratory is to use C. elegans as a host to screen thousands of bacterial
clones from mutagenized libraries to identify novel Salmonella virulence factors and to
address how they alter host signaling pathways. Since several components of innate immunity
are conserved among different organisms throughout evolution, his group is also exploiting
the genetic and genomic resources available for C. elegans to study the basis of the
immune response.