Increased Cell Wall Teichoic Acid Production and D-alanylation Are Common Phenotypes among Daptomycin-Resistant Methicillin-Resistant Staphylococcus aureus (MRSA) Clinical Isolates

被引:76
作者
Bertsche, Ute [1 ]
Yang, Soo-Jin [2 ,3 ]
Kuehner, Daniel [1 ,4 ]
Wanner, Stefanie [1 ]
Mishra, Nagendra N. [2 ]
Roth, Tobias [1 ]
Nega, Mulugeta [1 ]
Schneider, Alexander [1 ]
Mayer, Christoph [1 ]
Grau, Timo [1 ]
Bayer, Arnold S. [2 ,3 ]
Weidenmaier, Christopher [1 ]
机构
[1] Univ Tubingen, Interfak Inst Mikrobiol & Infektionsmed, Tubingen, Germany
[2] Harbor UCLA Med Ctr, Div Infect Dis, LA Biomed Res Inst, Torrance, CA 90509 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Cecolabs UG, Tubingen, Germany
基金
美国国家卫生研究院;
关键词
REDUCED VANCOMYCIN SUSCEPTIBILITY; ANTIMICROBIAL PEPTIDE RESISTANCE; INTERMEDIATE; STRAINS; MPRF; NONSUSCEPTIBILITY; PEPTIDOGLYCAN; BIOSYNTHESIS; MECHANISMS; EXPRESSION;
D O I
10.1371/journal.pone.0067398
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
Multiple mechanisms have been correlated with daptomycin-resistance (DAP-R) in Staphylococcus aureus. However, one common phenotype observed in many DAP-R S. Aureus strains is a thickened cell wall (CW). The first evidence for an impact of CW-linked glycopolymers on this phenotype was recently demonstrated in a single, well-characterized DAP-R methicillin-susceptible S. aureus (MSSA) strain. In this isolate the thickened CW phenotype was linked to an increased production and D-alanylation of wall teichoic acids (WTA). In the current report, we extended these observations to methicillin-resistant daptomycin-sensitive/daptomyin-resistant (DAP-S/DAP-R) strain-pairs. These pairs included methicillin-resistant S. aureus (MRSA) isolates with and without single nucleotide polymorphisms (SNPs) in mprF (a genetic locus linked to DAP-R phenotype). We found increased CW dry mass in all DAP-R vs DAP-S isolates. This correlated with an increased expression of the WTA biosynthesis gene tagA, as well as an increased amount of WTA in the DAP-R vs DAP-S isolates. In addition, all DAP-R isolates showed a higher proportion of WTA D-alanylation vs their corresponding DAP-S isolate. We also detected an increased positive surface charge amongst the DAP-R strains (presumably related to the enhanced D-alanylation). In comparing the detailed CW composition of all isolate pairs, substantive differences were only detected in one DAP-S/DAP-R pair. The thickened CW phenotype, together with an increased surface charge most likely contributes to either: i) a charge-dependent repulsion of calcium complexed-DAP; and/or ii) steric-limited access of DAP to the bacterial cell envelope target. Taken together well-defined perturbations of CW structural and functional metrics contribute to the DAP-R phenotype and are common phenotypes in DAP-R S. Aureus isolates, both MSSA and MRSA. Note: Although "daptomycin-nonsusceptibility" is the generally accepted terminology, we have utilized the term "daptomycin resistance" for ease of presentation in this manuscript
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