Molecular analysis of the accessory gene regulator (agr) locus and balance of virulence factor expression in epidemic methicillin-resistant Staphylococcus aureus

被引:72
作者
Papakyriacou, H
Vaz, D
Simor, A
Louie, M
McGavin, MJ
机构
[1] Sunnybrook & Womens Coll, Hlth Sci Ctr, Dept Microbiol, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Lab Med & Pathol, Toronto, ON, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1086/315342
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Potential relationships between virulence factor expression and transmissibility were assessed in epidemic methicillin-resistant Staphylococcus aureus (MRSA) clones CMRSA-1 and CMRSA-3, A major subtype of CMRSA-1 exhibited normal transcription of RNAIII, which facilitates the induction of secreted virulence factors and repression of colonization factor expression at high cell density. However, these isolates characteristically did not express alpha-toxin or protease and displayed a limited profile of secreted proteins. CMRSA-1 also expressed a novel cell surface glycoprotein and exhibited a unique polymorphism within the accessory gene regulator (agr) locus, CMRSA-3 displayed attenuated activation of RNAIII transcription, which was consistent with its higher fibronectin-binding and coagulase activity relative to sporadic MRSA or CMRSA-1 (P = .05), low protease activity, and limited profile of secreted proteins. Thus, the balance of virulence factor expression in CMRSA-1 and CMRSA-3 favors the colonization phase of infection, and CMRSA-1 possesses unique genotypic and phenotypic traits.
引用
收藏
页码:990 / 1000
页数:11
相关论文
共 60 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
Altschul Stephen F., J MOL BIOL, V215, P403, DOI [10.1016/S0022-2836(05)80360-2, DOI 10.1016/S0022-2836(05)80360-2]
[3]  
[Anonymous], [No title captured]
[4]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[6]   PULSED-FIELD GEL-ELECTROPHORESIS AS A REPLACEMENT FOR BACTERIOPHAGE-TYPING OF STAPHYLOCOCCUS-AUREUS [J].
BANNERMAN, TL ;
HANCOCK, GA ;
TENOVER, FC ;
MILLER, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :551-555
[7]   STREPTOCOCCAL CYSTEINE PROTEINASE RELEASES BIOLOGICALLY-ACTIVE FRAGMENTS OF STREPTOCOCCAL SURFACE-PROTEINS [J].
BERGE, A ;
BJORCK, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (17) :9862-9867
[8]  
BOYCE JM, 1997, STAPHYLOCOCCI HUMAN, P309, DOI DOI 10.1002/9781444308464.CH15
[9]   Genetic inactivation of the extracellular cysteine protease enhances in vitro internalization of group A Streptococci by human epithelial and endothelial cells [J].
Burns, EH ;
Lukomski, S ;
Rurangirwa, J ;
Podbielski, A ;
Musser, JM .
MICROBIAL PATHOGENESIS, 1998, 24 (06) :333-339
[10]   Spread of a methicillin-resistant and multiresistant epidemic clone of Staphylococcus aureus in Argentina [J].
Corso, A ;
Sanches, IS ;
de Sousa, MA ;
Rossi, A ;
de Lencastre, H .
MICROBIAL DRUG RESISTANCE, 1998, 4 (04) :277-288