c-di-AMP Is a New Second Messenger in Staphylococcus aureus with a Role in Controlling Cell Size and Envelope Stress

被引:359
作者
Corrigan, Rebecca M. [1 ]
Abbott, James C. [2 ]
Burhenne, Heike [3 ]
Kaever, Volkhard [3 ]
Gruendling, Angelika [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Microbiol Sect, London, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Life Sci, London, England
[3] Hannover Med Sch, Inst Pharmacol, D-3000 Hannover, Germany
基金
英国惠康基金; 欧洲研究理事会; 英国医学研究理事会;
关键词
WALL TEICHOIC-ACID; LIPOTEICHOIC ACID; BACILLUS-SUBTILIS; CHECKPOINT PROTEIN; ESSENTIAL GENES; GMP; IDENTIFICATION; BIOSYNTHESIS; RESISTANCE; VIRULENCE;
D O I
10.1371/journal.ppat.1002217
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The cell wall is a vital and multi-functional part of bacterial cells. For Staphylococcus aureus, an important human bacterial pathogen, surface proteins and cell wall polymers are essential for adhesion, colonization and during the infection process. One such cell wall polymer, lipoteichoic acid (LTA), is crucial for normal bacterial growth and cell division. Upon depletion of this polymer bacteria increase in size and a misplacement of division septa and eventual cell lysis is observed. In this work, we describe the isolation and characterization of LTA-deficient S. aureus suppressor strains that regained the ability to grow almost normally in the absence of this cell wall polymer. Using a whole genome sequencing approach, compensatory mutations were identified and revealed that mutations within one gene, gdpP (GGDEF domain protein containing phosphodiesterase), allow both laboratory and clinical isolates of S. aureus to grow without LTA. It was determined that GdpP has phosphodiesterase activity in vitro and uses the cyclic dinucleotide c-di-AMP as a substrate. Furthermore, we show for the first time that c-di-AMP is produced in S. aureus presumably by the S. aureus DacA protein, which has diadenylate cyclase activity. We also demonstrate that GdpP functions in vivo as a c-di-AMP-specific phosphodiesterase, as intracellular c-di-AMP levels increase drastically in gdpP deletion strains and in an LTA-deficient suppressor strain. An increased amount of cross-linked peptidoglycan was observed in the gdpP mutant strain, a cell wall alteration that could help bacteria compensate for the lack of LTA. Lastly, microscopic analysis of wild-type and gdpP mutant strains revealed a 13-22% reduction in the cell size of bacteria with increased c-di-AMP levels. Taken together, these data suggest a function for this novel secondary messenger in controlling cell size of S. aureus and in helping bacteria to cope with extreme membrane and cell wall stress.
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页数:16
相关论文
共 66 条
[51]   Fibronectin-binding protein acts as Staphylococcus aureus invasin via fibronectin bridging to integrin α5β1 [J].
Sinha, B ;
François, PP ;
Nusse, O ;
Foti, M ;
Hartford, OM ;
Vaudaux, P ;
Foster, TJ ;
Lew, DP ;
Herrmann, M ;
Krause, KH .
CELLULAR MICROBIOLOGY, 1999, 1 (02) :101-117
[52]  
Song JH, 2005, MOL CELLS, V19, P365
[53]   A liquid chromatography-coupled tandem mass spectrometry method for quantitation of cyclic di-guanosine monophosphate [J].
Spangler, Christian ;
Boehm, Alex ;
Jenal, Urs ;
Seifert, Roland ;
Kaever, Volkhard .
JOURNAL OF MICROBIOLOGICAL METHODS, 2010, 81 (03) :226-231
[54]   Riboswitches in eubacteria sense the second messenger cyclic di-GMP [J].
Sudarsan, N. ;
Lee, E. R. ;
Weinberg, Z. ;
Moy, R. H. ;
Kim, J. N. ;
Link, K. H. ;
Breaker, R. R. .
SCIENCE, 2008, 321 (5887) :411-413
[55]   Wall Teichoic Acid Function, Biosynthesis, and Inhibition [J].
Swoboda, Jonathan G. ;
Campbell, Jennifer ;
Meredith, Timothy C. ;
Walker, Suzanne .
CHEMBIOCHEM, 2010, 11 (01) :35-45
[56]   Three cdg operons control cellular turnover of cyclic di-GMP in Acetobacter xylinum:: Genetic organization and occurrence of conserved domains in isoenzymes [J].
Tal, R ;
Wong, HC ;
Calhoon, R ;
Gelfand, D ;
Fear, AL ;
Volman, G ;
Mayer, R ;
Ross, P ;
Amikam, D ;
Weinhouse, H ;
Cohen, A ;
Sapir, S ;
Ohana, P ;
Benziman, M .
JOURNAL OF BACTERIOLOGY, 1998, 180 (17) :4416-4425
[57]   PAS domains: Internal sensors of oxygen, redox potential, and light [J].
Taylor, BL ;
Zhulin, IB .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1999, 63 (02) :479-+
[58]   Protection from lethal gram-positive infection by macrophage scavenger receptor-dependent phagocytosis [J].
Thomas, CA ;
Li, YM ;
Kodama, T ;
Suzuki, H ;
Silverstein, SC ;
El Khoury, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (01) :147-155
[59]   Imaging peptidoglycan biosynthesis in Bacillus subtilis with fluorescent antibiotics [J].
Tiyanont, Kittichoat ;
Doan, Thierry ;
Lazarus, Michael B. ;
Fang, Xiao ;
Rudner, David Z. ;
Walker, Suzanne .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (29) :11033-11038
[60]   A slipped-mispairing mutation in AgrA of laboratory strains and clinical isolates results in delayed activation of agr and failure to translate δ- and α-haemolysins [J].
Traber, K ;
Novick, R .
MOLECULAR MICROBIOLOGY, 2006, 59 (05) :1519-1530