scholarly journals A Comparison of the Costs and Benefits of Bacterial Gene Expression

2016 ◽  
Author(s):  
Morgan N. Price ◽  
Kelly M. Wetmore ◽  
Adam M. Deutschbauer ◽  
Adam P. Arkin

AbstractTo study how a bacterium allocates its resources, we compared the costs and benefits of most of the proteins inEscherichia coliK-12 during growth in minimal glucose medium. Proteins that are important for fitness are usually highly expressed, and 95% of these proteins are expressed at above 13 parts per million (ppm). Conversely, proteins that do not measurably benefit the host tend to be weakly expressed, with a median expression of 13 ppm. In aggregate, genes with no detectable benefit account for 31% of protein production, or about 22% if we correct for genetic redundancy. Although some of the apparently unnecessary expression could have subtle benefits in minimal glucose medium, the majority of the burden is due to genes that are important in other conditions. We propose that over 10% of the cell’s protein is “on standby” in case conditions change.

PLoS ONE ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. e0164314 ◽  
Author(s):  
Morgan N. Price ◽  
Kelly M. Wetmore ◽  
Adam M. Deutschbauer ◽  
Adam P. Arkin

2002 ◽  
Vol 56 (1) ◽  
pp. 599-624 ◽  
Author(s):  
Virgil Rhodius ◽  
Tina K. Van Dyk ◽  
Carol Gross ◽  
Robert A. LaRossa

2005 ◽  
Vol 54 (5) ◽  
pp. 497-504 ◽  
Author(s):  
Joseph Richardson ◽  
Justin Corey Craighead ◽  
Sam Linsen Cao ◽  
Martin Handfield

Actinobacillus actinomycetemcomitans is a facultatively intracellular pathogen and the aetiological agent of localized aggressive periodontitis. Screening of the genome of A. actinomycetemcomitans for in vivo-induced antigen determinants previously demonstrated that the proteome of this organism differs in laboratory culture compared with conditions found during active infection. The aim of the present study was to determine whether the bacterial gene expression pattern inferred with in vivo-induced antigen technology (IVIAT) in human infections was consistent with the gene expression pattern occurring upon epithelial cell association. To this end, a real-time PCR method was developed and used to quantify absolute and relative bacterial gene expression of A. actinomycetemcomitans grown extra- and intracellularly in two human epithelial cell lines (HeLa and IHGK). The amount of template used in the assay was normalized using the total count of viable bacteria (c.f.u.) as a reference point and performed in duplicate in at least two independent experiments. Controls for this experiment included 16S rRNA and gapdh. Transcription of all eight ORFs tested increased significantly (P < 0.05) in HeLa and IHGK cells compared with bacteria grown extracellularly. The concurrence of gene expression patterns found in the two models suggests that these epithelial cells are valid in vitro models of infection for the genes tested. IVIAT is an experimental platform that can be used as a validation tool to assess the reliability of animal and other models of infection and is applicable to most pathogens.


Author(s):  
Sofia Startceva ◽  
Vinodh K. Kandavalli ◽  
Ari Visa ◽  
Andre S. Ribeiro

2013 ◽  
Vol 163 (2-3) ◽  
pp. 171-179 ◽  
Author(s):  
Ji Young Jung ◽  
Se Hee Lee ◽  
Hyun Mi Jin ◽  
Yoonsoo Hahn ◽  
Eugene L. Madsen ◽  
...  

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