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PMID: 15632420 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Gene expression diversity among Mycobacterium tuberculosis clinical isolates.

Microbiology (Reading, England) ·Vol. 151 ·No. Pt 1 ·2005-01-00 ·Pages 5-14

Gao Q, Kripke KE, Saldanha AJ, Yan W, Holmes S, Small PM

Abstract

Intraspecies genetic diversity has been demonstrated to be important in the pathogenesis and epidemiology of several pathogens, such as HIV, influenza, Helicobacter and Salmonella. It is also important to consider strain-to-strain variation when identifying drug targets and vaccine antigens and developing tools for molecular diagnostics. Here, the authors present a description of the variability in gene expression patterns among ten clinical isolates of Mycobacterium tuberculosis, plus the laboratory strains H37Rv and H37Ra, growing in liquid culture. They identified 527 genes (15 % of those tested) that are variably expressed among the isolates studied. The remaining genes were divided into three categories based on their expression levels: unexpressed (38 %), low to undetectable expression (31 %) and consistently expressed (16 %). The expression categories were compared with functional categories and three biologically interesting gene lists: genes that are deleted among clinical isolates, T-cell antigens and essential genes. There were significant associations between expression variability and the classification of genes as T-cell antigens, involved in lipid metabolism, PE/PPE, insertion sequences and phages, and deleted among clinical isolates. This survey of mRNA expression among clinical isolates of M. tuberculosis demonstrates that genes with important functions can vary in their expression levels between strains grown under identical conditions.

MeSH Terms
Bacterial Proteins/genetics,metabolism Gene Deletion Gene Expression Genes, Essential Genetic Variation Humans Mycobacterium tuberculosis/classification,genetics,growth & development,pathogenicity Oligonucleotide Array Sequence Analysis/methods Receptors, Antigen, T-Cell/genetics,metabolism Tuberculosis, Pulmonary/microbiology
Chemicals
Bacterial Proteins Receptors, Antigen, T-Cell
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Gao Qian
Department of Medicine, Division of Infectious Disease and Geographic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5107, USA.
Kripke Katharine E
Department of Medicine, Division of Infectious Disease and Geographic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5107, USA.
Saldanha Alok J
Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305-5307, USA.
Yan Weihong
Department of Medicine, Division of Infectious Disease and Geographic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5107, USA.
Holmes Susan
Statistics Department, Sequoia Hall, Stanford, CA 94305, USA.
Small Peter M
Department of Medicine, Division of Infectious Disease and Geographic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5107, USA.
Article Info
Journal
Microbiology (Reading, England)
Abbr.
Microbiology (Reading)
ISSN
1350-0872
Published
2005-01-00
Pages
5-14
Language
English
Region
England
NLM ID
9430468
Subset
IM
Grants
NHLBI NIH HHS · HL68537 · United States
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