Transcriptional profiling of the Bacillus anthracis life cycle in vitro and an implied model for regulation of spore formation

被引:81
作者
Bergman, Nicholas H.
Anderson, Erica C.
Swenson, Ellen E.
Niemeyer, Matthew M.
Miyoshi, Amy D.
Hanna, Philip C.
机构
[1] Univ Michigan, Sch Med, Bioinformat Program, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1128/JB.00723-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The life cycle of Bacillus anthracis includes both vegetative and endospore morphologies which alternate based on nutrient availability, and there is considerable evidence indicating that the ability of this organism to cause anthrax depends on its ability to progress through this life cycle in a regulated manner. Here we report the use of a custom B. anthracis GeneChip in defining the gene expression patterns that occur throughout the entire life cycle in vitro. Nearly 5,000 genes were expressed in five distinct waves of transcription as the bacteria progressed from germination through sporulation, and we identified a specific set of functions represented within each wave. We also used these data to define the temporal expression of the spore proteome, and in doing so we have demonstrated that much of the spore's protein content is not synthesized de novo during sporulation but rather is packaged from preexisting stocks. We explored several potential mechanisms by which the cell could control which proteins are packaged into the developing spore, and our analyses were most consistent with a model in which B. anthracis regulates the composition of the spore proteome based on protein stability. This study is by far the most comprehensive survey yet of the B. anthracis life cycle and serves as a useful resource in defining the growth-phase-dependent expression patterns of each gene. Additionally, the data and accompanying bioinformatics analyses suggest a model for sporulation that has broad implications. for B. anthracis biology and offer new possibilities for microbial forensics and detection.
引用
收藏
页码:6092 / 6100
页数:9
相关论文
共 41 条
[1]   INVIVO HALF-LIFE OF A PROTEIN IS A FUNCTION OF ITS AMINO-TERMINAL RESIDUE [J].
BACHMAIR, A ;
FINLEY, D ;
VARSHAVSKY, A .
SCIENCE, 1986, 234 (4773) :179-186
[2]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[3]   Rap phosphatase of virulence plasmid pXO1 inhibits Bacillus anthracis sporulation [J].
Bongiorni, C ;
Stoessel, R ;
Shoemaker, D ;
Perego, M .
JOURNAL OF BACTERIOLOGY, 2006, 188 (02) :487-498
[4]   Global effects of virulence gene regulators in a Bacillus anthracis strain with both virulence plasmids [J].
Bourgogne, A ;
Drysdale, M ;
Hilsenbeck, SG ;
Peterson, SN ;
Koehler, TM .
INFECTION AND IMMUNITY, 2003, 71 (05) :2736-2743
[5]   N-terminal processing:: the methionine aminopeptidase and Nα-acetyl transferase families [J].
Bradshaw, RA ;
Brickey, WW ;
Walker, KW .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (07) :263-267
[6]   Characterization of sporulation histidine kinases of Bacillus anthracis [J].
Brunsing, RL ;
La Clair, C ;
Tang, S ;
Chiang, C ;
Hancock, LE ;
Perego, M ;
Hoch, JA .
JOURNAL OF BACTERIOLOGY, 2005, 187 (20) :6972-6981
[7]   Codon adaptation index as a measure of dominating codon bias [J].
Carbone, A ;
Zinovyev, A ;
Képès, F .
BIOINFORMATICS, 2003, 19 (16) :2005-2015
[8]   Anthrax [J].
Dixon, TC ;
Meselson, M ;
Guillemin, J ;
Hanna, PC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (11) :815-826
[9]   Early Bacillus anthracis macrophage interactions:: intracellular survival and escape [J].
Dixon, TC ;
Fadl, AA ;
Koehler, TM ;
Swanson, JA ;
Hanna, PC .
CELLULAR MICROBIOLOGY, 2000, 2 (06) :453-463
[10]   Developmental commitment in a bacterium [J].
Dworkin, J ;
Losick, R .
CELL, 2005, 121 (03) :401-409