Induction of the Staphylococcal Proteolytic Cascade by Antimicrobial Fatty Acids in Community Acquired Methicillin Resistant Staphylococcus aureus

被引:37
作者
Arsic, Benjamin [1 ]
Zhu, Yue [1 ]
Heinrichs, David E. [1 ,2 ]
McGavin, Martin J. [1 ,2 ]
机构
[1] Univ Western Ontario, Dept Microbiol & Immunol, London, ON, Canada
[2] Univ Western Ontario, Ctr Human Immunol, London, ON, Canada
来源
PLOS ONE | 2012年 / 7卷 / 09期
基金
加拿大自然科学与工程研究理事会;
关键词
CATABOLIC MOBILE ELEMENT; GRAM-POSITIVE BACTERIA; PEPTIDE-SENSING SYSTEM; METALLOPROTEASE AUREOLYSIN; NASAL CARRIAGE; ANALYSIS REVEALS; SERINE-PROTEASE; GENOME SEQUENCE; IMMUNE EVASION; SKIN SURFACE;
D O I
10.1371/journal.pone.0045952
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 ; 0710 ; 09 ;
摘要
Community acquired methicillin resistant Staphylococcus aureus (CA-MRSA), and the USA300 strain of CA-MRSA in particular, are known for their rapid community transmission, and propensity to cause aggressive skin and soft tissue infections. To assess factors that contribute to these hallmark traits of CA-MRSA, we evaluated how growth of USA300 and production of secreted virulence factors was influenced on exposure to physiologic levels of unsaturated free fatty acids that would be encountered on the skin or anterior nares, which represent the first sites of contact with healthy human hosts. There was a sharp threshold between sub-inhibitory and inhibitory concentrations, such that 100 mu M sapienic acid (C16:1) and linoleic acid (C18:1) were sufficient to prevent growth after 24 h incubation, while 25 mM allowed unrestricted growth, and 50 mM caused an approximate 10-12 h lag, followed by unimpeded exponential growth. Conversely, saturated palmitic or stearic acids did not affect growth at 100 mu M. Although growth was not affected by 25 mM sapienic or linoleic acid, these and other unsaturated C16 and C18 fatty acids, but not their saturated counterparts, promoted robust production of secreted proteases comprising the Staphylococcal proteolytic cascade. This trait was also manifested to varying degrees in other CA-MRSA, and in genetically diverse methicillin susceptible S. aureus strains. Therefore, induction of the Staphylococcal proteolytic cascade by unsaturated fatty acids is another feature that should now be evaluated as a potential contributing factor in the aggressive nature of skin and soft tissue infections caused by USA300, and as a general virulence mechanism of S. aureus.
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共 85 条
[1]  
[Anonymous], [No title captured]
[2]   Staphylococcus aureus:: A well-armed pathogen [J].
Archer, GL .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (05) :1179-1181
[3]   New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria [J].
Arnaud, M ;
Chastanet, A ;
Débarbouillé, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (11) :6887-6891
[4]   BIOCHEMICAL-PROPERTIES OF A NOVEL METALLOPROTEASE FROM STAPHYLOCOCCUS-HYICUS SUBSP HYICUS INVOLVED IN EXTRACELLULAR LIPASE PROCESSING [J].
AYORA, S ;
LINDGREN, PE ;
GOTZ, F .
JOURNAL OF BACTERIOLOGY, 1994, 176 (11) :3218-3223
[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]   Genome sequence of Staphylococcus aureus strain newman and comparative analysis of staphylococcal genomes:: Polymorphism and evolution of two major pathogenicity islands [J].
Baba, Tadashi ;
Bae, Taeok ;
Schneewind, Olaf ;
Takeuchi, Fumihiko ;
Hiramatsu, Keiichi .
JOURNAL OF BACTERIOLOGY, 2008, 190 (01) :300-310
[7]   The human fibrinolytic system is a target for the staphylococcal metalloprotease aureolysin [J].
Beaufort, Nathalie ;
Wojciechowski, Piotr ;
Sommerhoff, Christian P. ;
Szmyd, Grzegorz ;
Dubin, Grzegorz ;
Eick, Sigrun ;
Kellermann, Josef ;
Schmitt, Manfred ;
Potempa, Jan ;
Magdolen, Viktor .
BIOCHEMICAL JOURNAL, 2008, 410 (157-165) :157-165
[8]   Epistatic Relationships between sarA and agr in Staphylococcus aureus Biofilm Formation [J].
Beenken, Karen E. ;
Mrak, Lara N. ;
Griffin, Linda M. ;
Zielinska, Agnieszka K. ;
Shaw, Lindsey N. ;
Rice, Kelly C. ;
Horswill, Alexander R. ;
Bayles, Kenneth W. ;
Smeltzer, Mark S. .
PLOS ONE, 2010, 5 (05)
[9]   agr-mediated dispersal of Staphylococcus aureus biofilms [J].
Boles, Blaise R. ;
Horswill, Alexander R. .
PLOS PATHOGENS, 2008, 4 (04)
[10]   Staphylococcal biofilm disassembly [J].
Boles, Blaise R. ;
Horswill, Alexander R. .
TRENDS IN MICROBIOLOGY, 2011, 19 (09) :449-455