Comparative Transcriptomic Analysis of Staphylococcus aureus Associated with Periprosthetic Joint Infection under in Vivo and in Vitro Conditions

被引:8
作者
Le Masters, Thao [1 ]
Johnson, Stephen [2 ]
Jeraldo, Patricio R. [2 ,3 ]
Greenwood-Quaintance, Kerryl E. [1 ]
Cunningham, Scott A. [1 ]
Abdel, Matthew P. [4 ]
Chia, Nicholas [2 ,3 ]
Patel, Robin [1 ,5 ]
机构
[1] Mayo Clin, Div Clin Microbiol, Dept Med, Rochester, MN USA
[2] Mayo Clin, Dept Lab Med & Pathol, Ctr Individualized Med, Dept Med, Rochester, MN USA
[3] Mayo Clin, Dept Surg, Dept Med, Rochester, MN USA
[4] Mayo Clin, Dept Orthoped Surg, Dept Med, Rochester, MN USA
[5] Mayo Clin, Div Infect Dis, Dept Med, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
FIBRONECTIN-BINDING PROTEINS; METHICILLIN-RESISTANT; RNA-SEQ; BIOFILM DEVELOPMENT; NASAL COLONIZATION; VIRULENCE FACTORS; SURFACE PROTEIN; GENE-EXPRESSION; FIBRINOGEN; IDENTIFICATION;
D O I
10.1016/j.jmoldx.2021.05.011
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Transcriptomic analysis can provide insight as to how Staphylococcus aureus adapts to the environmental niche of periprosthetic joint infection (PJI), a challenging clinical infection. Here, in vivo RNA expression of eight S. aureus PJIs was compared with expression of the corresponding isolates in planktonic culture using a total RNA-sequencing approach. Expression varied among isolates, with a common trend showing increased expression of several ica-independent biofilm formation genes, including sdr, fnb, ebpS, and aaa; genes encoding enzymes and toxins, including coa, nuc, hlb, and hlgA/B/C; and genes facilitating acquisition of iron via the iron-binding molecule siderophore B (snb) and heme consumption protein (isd) pathways in PJI. Several antimicrobial resistance determinants were detected; although their presence correlated with phenotypic susceptibility of the associated isolates, no difference in expression between in vivo and in vitro conditions was identified.
引用
收藏
页码:986 / 999
页数:14
相关论文
共 107 条
[1]   Scalable metagenomic taxonomy classification using a reference genome database [J].
Ames, Sasha K. ;
Hysom, David A. ;
Gardner, Shea N. ;
Lloyd, G. Scott ;
Gokhale, Maya B. ;
Allen, Jonathan E. .
BIOINFORMATICS, 2013, 29 (18) :2253-2260
[2]   Staphylococcus aureus biofilms Properties, regulation and roles in human disease [J].
Archer, Nathan K. ;
Mazaitis, Mark J. ;
Costerton, J. William ;
Leid, Jeff G. ;
Powers, Mary Elizabeth ;
Shirtliff, Mark E. .
VIRULENCE, 2011, 2 (05) :445-459
[3]   Redefining the Role of the β-Lactamase Locus in Methicillin-Resistant Staphylococcus aureus: β-Lactamase Regulators Disrupt the MecI-Mediated Strong Repression on mecA and Optimize the Phenotypic Expression of Resistance in Strains with Constitutive mecA Expression [J].
Arede, Pedro ;
Ministro, Joana ;
Oliveira, Duarte C. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (07) :3037-3045
[4]   PSM Peptides of Staphylococcus aureus Activate the p38-CREB Pathway in Dendritic Cells, Thereby Modulating Cytokine Production and T Cell Priming [J].
Armbruster, Nicole S. ;
Richardson, Jennifer R. ;
Schreiner, Jens ;
Klenk, Juliane ;
Guenter, Manina ;
Kretschmer, Dorothee ;
Poeschel, Simone ;
Schenke-Layland, Katja ;
Kalbacher, Hubert ;
Clark, Kristopher ;
Autenrieth, Stella E. .
JOURNAL OF IMMUNOLOGY, 2016, 196 (03) :1284-1292
[5]   Staphylococcus aureus Exploits a Non-ribosomal Cyclic Dipeptide to Modulate Survival within Epithelial Cells and Phagocytes [J].
Blaettner, Sebastian ;
Das, Sudip ;
Paprotka, Kerstin ;
Eilers, Ursula ;
Krischke, Markus ;
Kretschmer, Dorothee ;
Remmele, Christian W. ;
Dittrich, Marcus ;
Mueller, Tobias ;
Schuelein-Voelk, Christina ;
Hertlein, Tobias ;
Mueller, Martin J. ;
Huettel, Bruno ;
Reinhardt, Richard ;
Ohlsen, Knut ;
Rudel, Thomas ;
Fraunholz, Martin J. .
PLOS PATHOGENS, 2016, 12 (09)
[6]   Near-optimal probabilistic RNA-seq quantification [J].
Bray, Nicolas L. ;
Pimentel, Harold ;
Melsted, Pall ;
Pachter, Lior .
NATURE BIOTECHNOLOGY, 2016, 34 (05) :525-527
[7]  
Bumgarner R., 2013, CURR PROTOC MOL BIOL, V206, P1, DOI DOI 10.1002/0471142727.MB2201S101
[8]   Description of a new group of variants of the Staphylococcus aureus elastin-binding protein that lacks an entire DNA segment of 180 bp [J].
Campoccia, Davide ;
Montanaro, Lucio ;
Ravaioli, Stefano ;
Cangini, Ilaria ;
Speziale, Pietro ;
Arciola, Carla Renata .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2009, 32 (09) :621-629
[9]   The Healthy Human Blood Microbiome: Fact or Fiction? [J].
Castillo, Diego J. ;
Rifkin, Riaan F. ;
Cowan, Don A. ;
Potgieter, Marnie .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2019, 9
[10]   Changes in the Staphylococcus aureus Transcriptome during Early Adaptation to the Lung [J].
Chaffin, Donald O. ;
Taylor, Destry ;
Skerrett, Shawn J. ;
Rubens, Craig E. .
PLOS ONE, 2012, 7 (08)