BBS Faculty Member - Stephen Lory

Stephen Lory

Department of Microbiology and Immunobiology

Harvard Medical School
Warren Alpert Building, Room 363
200 Longwood Avenue
Boston, MA 02115
Tel: 617-432-5099
Fax: 617-738-7664
Email: stephen_lory@hms.harvard.edu
Lab Members: 6 postdoctoral fellows, 1 graduate student



The research efforts in the laboratory are directed towards understanding the molecular basis of pathogenesis of human infections caused by opportunistic gram-negative bacteria. We have used Pseudomonas aeruginosa as a model opportunistic pathogen, because of its importance in infections of individuals with cystic fibrosis, neutropenia, and as complications of burns and wounds. In each of these environments, the unique host-parasite relationship allows us to examine a variety of bacterial factors that lead to colonization, persistence and resistance to host defenses as well as antibiotics.

The focus of the current work in the area of regulation is a broad attempt to define the complex signaling pathways and genetic regulatory networks, controlling virulence determinants. The areas investigated include the analyses of the functions of the various phosphorylation-based signaling pathways in assimilating and transmitting environmental cues leading to selective and controlled transcription specific genes encoding virulence factors. Recently discovered small regulatory RNAs, responsible for the post-transciptional control of genes are also investigated in the lab. The lab has a major effort in determining the role of cyclic nucleotides in coordinating expression and function of factors involved in the formation of different polysaccharide matrices and secreted toxins that are major virulence determinants expressed by P. aeruginosa during chronic infections.

Another area of research in the laboratory focuses on studying the evolution of virulence traits in P. aeruginosa. We have identified several mobile elements, arranged in blocks of genes (so called genomic islands) that can move between bacteria, resulting in re-shaping of the genetic repertoire of individual recipient strains. The mechanisms and the consequences of this type of horizontal gene transfer will be analyzed in several infection models.



Last Update: 8/22/2013



Publications

For a complete listing of publications click here.

 


 

Qiu, X. Gurkar, A.U. and Lory, S. (2006) Inter-strain transfer of the large pathogenicity island (PAPI-1) of Pseudomonas aeruginosa. Proc. Natl. Acad. Sci. USA. 103:19830-5.

Merighi M., Lee V.T., Hyodo M., Hayakawa Y. and Lory S. (2007) The second messenger bis-(3’- 5’)-cyclic-GMP and its PilZ domain-containing receptor Alg44 are required for alginate biosynthesis in Pseudomonas aeruginosa. Mol. Microbiol 65:876-9.

Goodman AL., Merighi M., M Hyodo M., Ventre I., Filloux A., and Lory S. (2009). Direct interaction between sensor kinase proteins mediates acute and chronic disease phenotypes in a bacterial pathogen. Genes and Development 23:249-59.

Brencic, A. McFarland, C, McManus, H.R., Castang, S., Mogno, I., Dove, S.L. and Lory, S. (2009). The GacS/GacA signal transduction system of Pseudomonas aeruginosa acts exclusively through its control over the transcription of the RsmY and RsmZ regulatory small RNAs. Mol. Microbiol. In press.



© 2013 by the President and Fellows of Harvard College