Phenol-soluble modulins and staphylococcal infection

被引:323
作者
Peschel, Andreas [1 ]
Otto, Michael [2 ]
机构
[1] Univ Tubingen, Cellular & Mol Microbiol Div, Interfac Inst Microbiol & Infect Med, D-72076 Tubingen, Germany
[2] NIAID, Pathogen Mol Genet Sect, Lab Human Bacterial Pathogenesis, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
QUORUM-SENSING SYSTEM; AMINO-ACID-SEQUENCE; HUMAN NEUTROPHILS; VIRULENCE DETERMINANTS; REGULATOR AGR; AUREUS; EPIDERMIDIS; PEPTIDES; BIOFILMS; IDENTIFICATION;
D O I
10.1038/nrmicro3110
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus is an important human pathogen and a leading cause of death worldwide. Phenol-soluble modulins (PSMs) have recently emerged as a novel toxin family defining the virulence potential of highly aggressive S. aureus isolates. PSMs have multiple roles in staphylococcal pathogenesis, causing lysis of red and white blood cells, stimulating inflammatory responses and contributing to biofilm development and the dissemination of biofilm-associated infections. Moreover, the pronounced capacity of PSMs to kill human neutrophils after phagocytosis might explain failures in the development of anti-staphylococcal vaccines. Here, we discuss recent progress made in our understanding of the biochemical and genetic properties of PSMs and their role in S. aureus pathogenesis, and suggest potential avenues to target PSMs for the development of anti-staphylococcal drugs.
引用
收藏
页码:667 / 673
页数:7
相关论文
共 65 条
[1]   Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis [J].
Anderson, Annaliesa S. ;
Scully, Ingrid L. ;
Timofeyeva, Yekaterina ;
Murphy, Ellen ;
McNeil, Lisa K. ;
Mininni, Terri ;
Nunez, Lorna ;
Carriere, Marjolaine ;
Singer, Christine ;
Dilts, Deborah A. ;
Jansen, Kathrin U. .
JOURNAL OF INFECTIOUS DISEASES, 2012, 205 (11) :1688-1696
[2]   Enterococcus faecium Stimulates Human Neutrophils via the Formyl-Peptide Receptor 2 [J].
Bloes, Dominik Alexander ;
Otto, Michael ;
Peschel, Andreas ;
Kretschmer, Dorothee .
PLOS ONE, 2012, 7 (06)
[3]   Identification of an immunodominant ABC transporter in methicillin-resistant Staphylococcus aureus infections [J].
Burnie, JP ;
Matthews, RC ;
Carter, T ;
Beaulieu, E ;
Donohoe, M ;
Chapman, C ;
Williamson, P ;
Hodgetts, SJ .
INFECTION AND IMMUNITY, 2000, 68 (06) :3200-3209
[4]  
Carnes EC, 2010, NAT CHEM BIOL, V6, P41, DOI [10.1038/NCHEMBIO.264, 10.1038/nchembio.264]
[5]  
Chatterjee S. S., 2013, NAT MED, V19, P346
[6]   Distribution and Regulation of the Mobile Genetic Element-Encoded Phenol-Soluble Modulin PSM-mec in Methicillin-Resistant Staphylococcus aureus [J].
Chatterjee, Som S. ;
Chen, Liang ;
Joo, Hwang-Soo ;
Cheung, Gordon Y. C. ;
Kreiswirth, Barry N. ;
Otto, Michael .
PLOS ONE, 2011, 6 (12)
[7]   Direct and synergistic hemolysis caused by Staphylococcus phenol-soluble modulins: implications for diagnosis and pathogenesis [J].
Cheung, Gordon Y. C. ;
Duong, Anthony C. ;
Otto, Michael .
MICROBES AND INFECTION, 2012, 14 (04) :380-386
[8]   Role of the Accessory Gene Regulator agr in Community-Associated Methicillin-Resistant Staphylococcus aureus Pathogenesis [J].
Cheung, Gordon Y. C. ;
Wang, Rong ;
Khan, Burhan A. ;
Sturdevant, Daniel E. ;
Otto, Michael .
INFECTION AND IMMUNITY, 2011, 79 (05) :1927-1935
[9]   Staphylococcus epidermidis Strategies to Avoid Killing by Human Neutrophils [J].
Cheung, Gordon Y. C. ;
Rigby, Kevin ;
Wang, Rong ;
Queck, Shu Y. ;
Braughton, Kevin R. ;
Whitney, Adeline R. ;
Teintze, Martin ;
DeLeo, Frank R. ;
Otto, Michael .
PLOS PATHOGENS, 2010, 6 (10)
[10]   Selective Antimicrobial Action Is Provided by Phenol-Soluble Modulins Derived from Staphylococcus epidermidis, a Normal Resident of the Skin [J].
Cogen, Anna L. ;
Yamasaki, Kenshi ;
Sanchez, Katheryn M. ;
Dorschner, Robert A. ;
Lai, Yuping ;
MacLeod, Daniel T. ;
Torpey, Justin W. ;
Otto, Michael ;
Nizet, Victor ;
Kim, Judy E. ;
Gallo, Richard L. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2010, 130 (01) :192-200