Staphylocloccus aureus virulence genes identified by bursa aurealis mutagenesis and nematode killing

被引:241
作者
Bae, T
Banger, AK
Wallace, A
Glass, EM
Åslund, F
Schneewind, O
Missiakas, DM
机构
[1] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[3] Univ Chicago, Comm Microbiol, Chicago, IL 60637 USA
[4] Argonne Natl Lab, Math & Comp Sci Div, Argonne, IL 60439 USA
[5] Karolinska Inst, Ctr Genom & Bioinformat, S-17177 Stockholm, Sweden
关键词
D O I
10.1073/pnas.0404728101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Staphylococcus aureus is the leading cause of wound and hospital-acquired infections worldwide. The emergence of S. aureus strains with resistance to multiple antibiotics requires the identification of bacterial virulence genes and the development of novel therapeutic strategies. Herein, bursa aurealis, a mariner-based transposon, was used for random mutagenesis and for the isolation of 10,325 S. aureus variants with defined insertion sites. By screening for loss-of-function mutants in a Caenorhabditis elegans killing assay, 71 S. aureus virulence genes were identified. Some of these genes are also required for S. aureus abscess formation in a murine infection model.
引用
收藏
页码:12312 / 12317
页数:6
相关论文
共 56 条
[1]
VIRULENCE OF STAPHYLOCOCCUS-AUREUS MUTANTS ALTERED IN TYPE-5 CAPSULE PRODUCTION [J].
ALBUS, A ;
ARBEIT, RD ;
LEE, JC .
INFECTION AND IMMUNITY, 1991, 59 (03) :1008-1014
[2]
Bacterial virulence as a target for antimicrobial chemotherapy [J].
Alksne, LE ;
Projan, SJ .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (06) :625-636
[3]
Staphylococcus aureus:: A well-armed pathogen [J].
Archer, GL .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (05) :1179-1181
[4]
Staphylococcus aureus bacteremia -: Consider the source. [J].
Archer, GL ;
Climo, MW .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (01) :55-56
[5]
Genome and virulence determinants of high virulence community-acquired MRSA [J].
Baba, T ;
Takeuchi, F ;
Kuroda, M ;
Yuzawa, H ;
Aoki, K ;
Oguchi, A ;
Nagai, Y ;
Iwama, N ;
Asano, K ;
Naimi, T ;
Kuroda, H ;
Cui, L ;
Yamamoto, K ;
Hiramatsu, K .
LANCET, 2002, 359 (9320) :1819-1827
[6]
Inactivation of a novel three-cistronic operon tcaR-tcaA-tcaB increases teicoplanin resistance in Staphylococcus aureus [J].
Brandenberger, M ;
Tschierske, M ;
Giachino, P ;
Wada, A ;
Berger-Bächi, B .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2000, 1523 (2-3) :135-139
[7]
METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
BRUMFITT, W ;
HAMILTONMILLER, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (18) :1188-1196
[8]
Infection with vancomycin-resistant Staphylococcus aureus containing the vanA resistance gene [J].
Chang, S ;
Sievert, DM ;
Hageman, JC ;
Boulton, ML ;
Tenover, FC ;
Downes, FP ;
Shah, S ;
Rudrik, JT ;
Pupp, GR ;
Brown, WJ ;
Cardo, D ;
Fridkin, SK .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (14) :1342-1347
[9]
The genomic aspect of virulence, sepsis, and resistance to killing mechanisms in Staphylococcus aureus [J].
Cheung A.L. ;
Projan S.J. ;
Gresham H. .
Current Infectious Disease Reports, 2002, 4 (5) :400-410
[10]
Staphylococcus aureus genetic loci impacting growth and survival in multiple infection environments [J].
Coulter, SN ;
Schwan, WR ;
Ng, EYW ;
Langhorne, MH ;
Ritchie, HD ;
Westbrock-Wadman, S ;
Hufnagle, WO ;
Folger, KR ;
Bayer, AS ;
Stover, CK .
MOLECULAR MICROBIOLOGY, 1998, 30 (02) :393-404