Mobile genetic elements of Staphylococcus aureus

被引:380
作者
Malachowa, Natalia [1 ]
DeLeo, Frank R. [1 ]
机构
[1] NIAID, Lab Human Bacterial Pathogenesis, Rocky Mt Labs, NIH, Hamilton, MT 59840 USA
基金
美国国家卫生研究院;
关键词
Mobile genetic elements; Staphylococcus aureus; Virulence; Antibiotic resistance; Horizontal gene transfer; PANTON-VALENTINE LEUKOCIDIN; COAGULASE-NEGATIVE STAPHYLOCOCCI; CADMIUM RESISTANCE DETERMINANTS; CHEMOTAXIS INHIBITORY PROTEIN; COMPLETE NUCLEOTIDE-SEQUENCE; STREPTOGRAMIN-B RESISTANCE; LEVEL MUPIROCIN RESISTANCE; METHICILLIN-RESISTANT; PATHOGENICITY ISLANDS; BETA-LACTAMASE;
D O I
10.1007/s00018-010-0389-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacteria such as Staphylococcus aureus are successful as commensal organisms or pathogens in part because they adapt rapidly to selective pressures imparted by the human host. Mobile genetic elements (MGEs) play a central role in this adaptation process and are a means to transfer genetic information (DNA) among and within bacterial species. Importantly, MGEs encode putative virulence factors and molecules that confer resistance to antibiotics, including the gene that confers resistance to beta-lactam antibiotics in methicillin-resistant S. aureus (MRSA). Inasmuch as MRSA infections are a significant problem worldwide and continue to emerge in epidemic waves, there has been significant effort to improve diagnostic assays and to develop new antimicrobial agents for treatment of disease. Our understanding of S. aureus MGEs and the molecules they encode has played an important role toward these ends and has provided detailed insight into the evolution of antimicrobial resistance mechanisms and virulence.
引用
收藏
页码:3057 / 3071
页数:15
相关论文
共 172 条
[11]   Complete nucleotide sequence of pSK41: Evolution of staphylococcal conjugative multiresistance plasmids [J].
Berg, T ;
Firth, N ;
Apisiridej, S ;
Hettiaratchi, A ;
Leelaporn, A ;
Skurray, RA .
JOURNAL OF BACTERIOLOGY, 1998, 180 (17) :4350-4359
[12]   GENE HETEROGENEITY FOR TETRACYCLINE RESISTANCE IN STAPHYLOCOCCUS SPP [J].
BISMUTH, R ;
ZILHAO, R ;
SAKAMOTO, H ;
GUESDON, JL ;
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (08) :1611-1614
[13]   Class II broad-spectrum mercury resistance transposons in Gram-positive bacteria from natural environments [J].
Bogdanova, E ;
Minakhin, L ;
Bass, I ;
Volodin, A ;
Hobman, JL ;
Nikiforov, V .
RESEARCH IN MICROBIOLOGY, 2001, 152 (05) :503-514
[14]   Human α-defensins neutralize fibrinolytic activity exerted by staphylokinase [J].
Bokarewa, M ;
Tarkowski, A .
THROMBOSIS AND HAEMOSTASIS, 2004, 91 (05) :991-999
[15]   ARSENIC EFFLUX GOVERNED BY THE ARSENIC RESISTANCE DETERMINANT OF STAPHYLOCOCCUS-AUREUS PLASMID PI258 [J].
BROER, S ;
JI, GY ;
BROER, A ;
SILVER, S .
JOURNAL OF BACTERIOLOGY, 1993, 175 (11) :3480-3485
[16]   Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion [J].
Brüssow, H ;
Canchaya, C ;
Hardt, WD .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :560-+
[17]   NUCLEOTIDE-SEQUENCE ANALYSIS OF IS256 FROM THE STAPHYLOCOCCUS-AUREUS GENTAMICIN-TOBRAMYCIN-KANAMYCIN-RESISTANCE TRANSPOSON TN4001 [J].
BYRNE, ME ;
ROUCH, DA ;
SKURRAY, RA .
GENE, 1989, 81 (02) :361-367
[18]   4',4'' ADENYLTRANSFERASE ACTIVITY ON CONJUGATIVE PLASMIDS ISOLATED FROM STAPHYLOCOCCUS-AUREUS IS ENCODED ON AN INTEGRATED COPY OF PUB110 [J].
BYRNE, ME ;
GILLESPIE, MT ;
SKURRAY, RA .
PLASMID, 1991, 25 (01) :70-75
[19]   Molecular characterization of the iron-hydroxamate uptake system in Staphylococcus aureus [J].
Cabrera, G ;
Xiong, AM ;
Uebel, M ;
Singh, VK ;
Jayaswal, RK .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (02) :1001-1003
[20]  
CARLES U, 2005, MOL MICROBIOL, V56, P836