Temperature Influences the Composition and Cytotoxicity of Extracellular Vesicles in Staphylococcus aureus

被引:28
作者
Briaud, Paul [1 ]
Frey, Andrew [2 ]
Marino, Emily C. [1 ]
Bastock, Raeven A. [1 ]
Zielinski, Riley E. [1 ]
Wiemels, Richard E. [1 ]
Keogh, Rebecca A. [1 ]
Murphy, Erin R. [3 ,4 ]
Shaw, Lindsey N. [2 ]
Carroll, Ronan K. [1 ,4 ]
机构
[1] Ohio Univ, Dept Biol Sci, Athens, OH 45701 USA
[2] Univ S Florida, Dept Cell Biol Microbiol & Mol Biol, Tampa, FL 33620 USA
[3] Ohio Univ, Heritage Coll Osteopath Med, Dept Biomed Sci, Athens, OH 45701 USA
[4] Ohio Univ, Infect & Trop Dis Inst, Athens, OH 45701 USA
关键词
Staphylococcus aureus; temperature; extracellular vesicle; membrane vesicle; proteomics; transcriptomics; GRAM-POSITIVE BACTERIA; MEMBRANE-VESICLES; INFLAMMATION; RESISTANCE; EXPRESSION; GENOME; WALL;
D O I
10.1128/mSphere.00676-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus is a pathogenic bacterium but also a commensal of skin and anterior nares in humans. As S. aureus transits from skins/nares to inside the human body, it experiences changes in temperature. The production and content of S. aureus extracellular vesicles (EVs) have been increasingly studied over the past few years, and EVs are increasingly being recognized as important to the infectious process. Nonetheless, the impact of temperature variation on S. aureus EVs has not been studied in detail, as most reports that investigate EV cargoes and host cell interactions are performed using vesicles produced at 37 degrees C. Here, we report that EVs in S. aureus differ in size and protein/RNA cargo depending on the growth temperature used. We demonstrate that the temperature-dependent regulation of vesicle production in S. aureus is mediated by the alpha phenol-soluble modulin peptides (aPSMs). Through proteomic analysis, we observed increased packaging of virulence factors at 40 degrees C, whereas the EV proteome has greater diversity at 34 degrees C. Similar to the protein content, we perform transcriptomic analysis and demonstrate that the RNA cargo also is impacted by temperature. Finally, we demonstrate greater aPSM- and alpha-toxin-mediated erythrocyte lysis with 40 degrees C EVs, but 34 degrees C EVs are more cytotoxic toward THP-1 cells. Together, our study demonstrates that small temperature variations have great impact on EV biogenesis and shape the interaction with host cells. IMPORTANCE Extracellular vesicles (EVs) are lipid bilayer spheres that contain proteins, nucleic acids, and lipids secreted by bacteria. They are involved in Staphylococcus oureus infections, as they package virulence factors and deliver their contents inside host cells. The impact of temperature variations experienced by S. aureus during the infectious process on EVs is unknown. Here, we demonstrate the importance of temperature in vesicle production and packaging. High temperatures promote packaging of virulence factors and increase the protein and lipid concentration but reduce the overall RNA abundance and protein diversity in EVs. The importance of temperature changes is highlighted by the fact that EVs produced at low temperature are more toxic toward macrophages, whereas EVs produced at high temperature display more hemolysis toward erythrocytes. Our research brings new insights into temperature-dependent vesiculation and interaction with the host during S. aureus transition from colonization to virulence.
引用
收藏
页数:16
相关论文
共 47 条
[1]   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
[2]   Staphylococcus aureus Responds to Physiologically Relevant Temperature Changes by Altering Its Global Transcript and Protein Profile [J].
Bastock, Raeven A. ;
Marino, Emily C. ;
Wiemels, Richard E. ;
Holzschu, Donald L. ;
Keogh, Rebecca A. ;
Zapf, Rachel L. ;
Murphy, Erin R. ;
Carroll, Ronan K. .
MSPHERE, 2021, 6 (02)
[3]   Identification of Genes Involved in Polysaccharide-Independent Staphylococcus aureus Biofilm Formation [J].
Boles, Blaise R. ;
Thoendel, Matthew ;
Roth, Aleeza J. ;
Horswill, Alexander R. .
PLOS ONE, 2010, 5 (04)
[4]   Extracellular Vesicle Biogenesis and Functions in Gram-Positive Bacteria [J].
Briaud, Paul ;
Carroll, Ronan K. .
INFECTION AND IMMUNITY, 2020, 88 (12)
[5]   Through the wall: extracellular vesicles in Gram-positive bacteria, mycobacteria and fungi [J].
Brown, Lisa ;
Wolf, Julie M. ;
Prados-Rosales, Rafael ;
Casadevall, Arturo .
NATURE REVIEWS MICROBIOLOGY, 2015, 13 (10) :620-630
[6]  
Carroll RK, 2016, METHODS MOL BIOL, V1373, P131, DOI 10.1007/7651_2014_192
[7]   The lone S41 family C-terminal processing protease in Staphylococcus aureus is localized to the cell wall and contributes to virulence [J].
Carroll, Ronan K. ;
Rivera, Frances E. ;
Cavaco, Courtney K. ;
Johnson, Grant M. ;
Martin, David ;
Shaw, Lindsey N. .
MICROBIOLOGY-SGM, 2014, 160 :1737-1748
[8]   Macrophages recognize streptococci through bacterial single-stranded RNA [J].
Deshmukh, Sachin D. ;
Kremer, Bernhard ;
Freudenberg, Marina ;
Bauer, Stefan ;
Golenbock, Douglas T. ;
Henneke, Philipp .
EMBO REPORTS, 2011, 12 (01) :71-76
[9]   STAPHYLOCOCCAL COAGULASE - MODE OF ACTION AND ANTIGENICITY [J].
DUTHIE, ES ;
LORENZ, LL .
JOURNAL OF GENERAL MICROBIOLOGY, 1952, 6 (1-2) :95-107
[10]   A Genetic Resource for Rapid and Comprehensive Phenotype Screening of Nonessential Staphylococcus aureus Genes [J].
Fey, Paul D. ;
Endres, Jennifer L. ;
Yajjala, Vijaya Kumar ;
Widhelm, Todd J. ;
Boissy, Robert J. ;
Bose, Jeffrey L. ;
Bayles, Kenneth W. .
MBIO, 2013, 4 (01)