Student Author(s)

Jennifer E. Griffin

GSBS Program

Molecular Genetics & Microbiology

UMMS Affiliation

Department of Microbiology and Physiological Systems

Date

9-29-2011

Document Type

Article

Medical Subject Headings

Animals; Cholesterol; Gene Expression Profiling; Gene Expression Regulation, Bacterial; Genes, Bacterial; Mice; Mutagenesis; Mycobacterium tuberculosis; Tuberculosis; Virulence

Disciplines

Cellular and Molecular Physiology | Life Sciences | Medicine and Health Sciences | Microbiology

Abstract

The pathways that comprise cellular metabolism are highly interconnected, and alterations in individual enzymes can have far-reaching effects. As a result, global profiling methods that measure gene expression are of limited value in predicting how the loss of an individual function will affect the cell. In this work, we employed a new method of global phenotypic profiling to directly define the genes required for the growth of Mycobacterium tuberculosis. A combination of high-density mutagenesis and deep-sequencing was used to characterize the composition of complex mutant libraries exposed to different conditions. This allowed the unambiguous identification of the genes that are essential for Mtb to grow in vitro, and proved to be a significant improvement over previous approaches. To further explore functions that are required for persistence in the host, we defined the pathways necessary for the utilization of cholesterol, a critical carbon source during infection. Few of the genes we identified had previously been implicated in this adaptation by transcriptional profiling, and only a fraction were encoded in the chromosomal region known to encode sterol catabolic functions. These genes comprise an unexpectedly large percentage of those previously shown to be required for bacterial growth in mouse tissue. Thus, this single nutritional change accounts for a significant fraction of the adaption to the host. This work provides the most comprehensive genetic characterization of a sterol catabolic pathway to date, suggests putative roles for uncharacterized virulence genes, and precisely maps genes encoding potential drug targets.

Rights and Permissions

Citation: Griffin JE, Gawronski JD, DeJesus MA, Ioerger TR, Akerley BJ, et al. (2011) High-Resolution Phenotypic Profiling Defines Genes Essential for Mycobacterial Growth and Cholesterol Catabolism. PLoS Pathog 7(9): e1002251. doi:10.1371/journal.ppat.1002251. Link to article on publisher's website

Comments

Copyright: © 2011 Griffin et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Related Resources

Link to article in PubMed