424 McGuire Life Sciences Building
PO Box: AC# 2237
Alexandra E. Purdy
Assistant Professor of Biology
(On Leave 1/1/2016 - 6/30/2016)
InterestsHost-microbe interactions; bacterial pathogenesis; marine microbiology; bacterial diversity and evolution; bacterial geneticsAmherst College
Courses in Fall 2012
Courses in Spring 2013
Courses in Fall 2013
Courses in Spring 2014
Courses in Fall 2014
Courses in Spring 2015
Courses in Spring 2016
- Alexandra E. Purdy is on leave during the Spring 2016 semester.
Professional and Biographical Information
Postdoctoral fellowship, Division of Infectious Diseases, Children’s Hospital Boston, Harvard Medical School (2008 – 2012)
Ph.D., Scripps Institution of Oceanography, University of California, San Diego, Marine Biology (2007)
B.S., College of William and Mary, Biology and Chemistry (2000)
Many bacterial species use carefully regulated attachment and virulence mechanisms to colonize and sometimes sicken their eukaryotic hosts. My laboratory aims to understand the complex molecular ‘conversations’ that underlie these interactions by studying Vibrio cholerae, the Gram-negative bacterium that causes cholera, an acute diarrheal disease that affects hundreds of thousands of people each year.
Vibrio cholerae is naturally found in aquatic environments, often attached to phytoplankton, aquatic arthropods such as copepods, and larger organisms. V. cholerae also can be carried by terrestrial arthropods such as houseflies. Our laboratory explores interactions between V. cholerae and arthropods using Drosophila melanogaster, the common fruit fly, as a model system. In the course of our work, we have discovered specific V. cholerae genes that are required for virulence and colonization in Drosophila. These include genes that likely initiate signal transduction cascades that regulate expression of V. cholerae genes in the fly. Our lab is interested in understanding how these regulatory cascades work; that is, what genes do they regulate? What environmental signals do they sense? How are they turned on and off?
Ultimately, this project will reveal the genetic mechanisms that allow V. cholerae to associate with arthropods in order to survive and spread in the rivers, lakes, ponds, and oceans that let the disease persist in areas where it is endemic, and spread to distant locales. Our ultimate goal is to better understand the ecology and evolution of a pathogen of major public health importance by integrating genomic, genetic, molecular and environmental approaches.
For more information about our lab, please take a look at our laboratory website.
At Amherst, I teach Biol-271 Microbiology, a course that invites students to explore the world from a microbial point of view. We seek to understand the diversity of ways in which microbes acquire energy, skirt immune responses, cause disease, rapidly adapt to change, and colonize almost every imaginable niche on the planet. In the laboratory, we use classical and molecular microbiological techniques to explore this remarkable microbial diversity, and in the classroom we incorporate readings from the primary literature that highlight the most exciting recent findings in many areas of microbiology, including microbial genetics, genomics, pathogenesis, cell structure, ecology and diversity.
I am also excited to be teaching a class for non-majors, Biol-110 Contagion, that focuses on mechanisms of bacterial and viral infectious disease and disease transmission. We discuss the molecular biology of pathogenesis, but we also explore larger societal issues related to the burden of infectious disease today.
I have also taught a specialized seminar course, Biol-414 Seminar in Microbiology: Host-Microbe Interactions and I have co-taught Biol-191 Molecules, Genes and Cells.
My hope is that my students leave my classes with a deep appreciation and understanding for the critical roles that these unseen bacteria, archaea, and viruses play throughout their own lives, the lives of their fellow humans around the world, and the life of the planet.
Hang S, AE Purdy, Z Wang, S Chang, WP Robins, JJ Mekalanos and PI Watnick. 2014. A bacterial acetate switch directs host metabolism from within the intestinal lumen. Cell Host & Microbe 16:592-604. **Highlighted in Nature Reviews Microbiology January 2015.
Wang Z, S Hang, AE Purdy and PI Watnick. 2013. Mutations in the IMD pathway and Mustard counter Vibrio cholerae suppression of intestinal stem cell division in Drosophila. mBio. 4(3) e00337-13.
Purdy AE and PI Watnick. 2011. Spatially-selective colonization of the arthropod intestine through activation of Vibrio cholerae biofilm formation. Proc Natl Acad Sci USA 108:19737-19742.
Purdy AE, D Balch, ML Lizarraga-Partida, MS Islam, J Martinez-Urtaza, A Huq, RR Colwell and DH Bartlett. 2010. Diversity and distribution of cholix toxin, a novel ADP-ribosylating factor from Vibrio cholerae. Environ Microbiol Rep. 2(1):198–207.
Jorgensen* R, AE Purdy*, R Fieldhouse, M Kimber, DH Bartlett and AR Merrill. 2008. Cholix toxin, a novel ADP-ribosylating factor from Vibrio cholerae. J Biol Chem 283:10671-10678. *These authors contributed equally.
Makri S, AE Purdy, D Bartlett and J Fierer. 2007. Pathogenicity of environmental isolates of V. cholerae in mice. Microb Infect 9:1351-1358.
Purdy A, F Rohwer, R Edwards, F Azam and DH Bartlett. 2005. A glimpse into the genome content of the Vibrio cholerae species through identification of genes present in environmental strains. J Bacteriol 187:2992-3001.
Awards and Honors
NIH Ruth L. Kirschstein NRSA Individual Fellowship (2009 - 2011)
Peterson Fellowship, Scripps Institution of Oceanography (2007)
Howard Hughes Medical Institute Predoctoral Fellowship (2001 - 2006)
Claude ZoBell Fellowship, Scripps Institution of Oceanography (2001)
Highest Honors in Biology, William & Mary (2000)
Charlotte P. Mangum Prize in Biology, William & Mary (2000)
Phi Beta Kappa, William & Mary (1999)
Scholarly and Professional Activities
American Society for Microbiology, member
Association for Women in Science, member