Transcriptomic Analysis of Streptococcus pyogenes Colonizing the Vaginal Mucosa Identifies hupY , an MtsR-Regulated Adhesin Involved in Heme Utilization

Author:

Cook Laura C. C.1,Chatterjee Nilanjana2,Li Yan3,Andrade Jorge4,Federle Michael J.5,Eichenbaum Zehava2

Affiliation:

1. Binghamton Biofilm Research Center, Department of Biology, Binghamton University, Binghamton, New York, USA

2. Department of Biology, Georgia State University, Atlanta, Georgia, USA

3. Center for Research Informatics, The University of Chicago, Chicago, Illinois, USA

4. Center for Research Informatics and Department of Pediatrics, Biological Sciences Division, The University of Chicago, Chicago, Illinois, USA

5. Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, Illinois, USA

Abstract

Colonization of the host requires the ability to adapt to an environment that is often low in essential nutrients such as iron. Here we present data showing that the transcriptome of the important human pathogen Streptococcus pyogenes shows extensive remodeling during in vivo growth, resulting in, among many other differentially expressed genes and pathways, a significant increase in genes involved in acquiring iron from host heme. Data show that HupY, previously characterized as an adhesin in both S. pyogenes and the related pathogen Streptococcus agalactiae , binds heme and affects intracellular iron concentrations. HupY, a protein with no known heme binding domains, represents a novel heme binding protein playing an important role in bacterial iron homeostasis as well as vaginal colonization.

Funder

HHS | National Institutes of Health

American Heart Association

Burroughs Wellcome Fund

SUNY | Binghamton University

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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