Molecular basis of surface anchored protein A deficiency in the Staphylococcus aureus strain Wood 46

被引:6
作者
Balachandran, Manasi [1 ]
Giannone, Richard J. [2 ]
Bemis, David A. [1 ]
Kania, Stephen A. [1 ]
机构
[1] Univ Tennessee, Dept Biomed & Diagnost Sci, Knoxville, TN 37996 USA
[2] Oakridge Natl Labs, Div Chem Sci, Mass Spectrometry & Laser Spectrometry, Oakridge, TN USA
关键词
GRAM-POSITIVE BACTERIA; ENTEROTOXIN-D GENE; CELL-WALL ANCHOR; EXTRACELLULAR PROTEIN; IMMUNE EVASION; ALPHA-TOXIN; IMMUNOLOGICAL REAGENT; ANTIINFECTIVE THERAPY; REGULATORY ELEMENTS; BINDING PROTEINS;
D O I
10.1371/journal.pone.0183913
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
Protein A in Staphylococcus aureus is encoded by the spa (staphylococcal protein A) gene and binds to immunoglobulin (Ig). The S. aureus strain Wood 46 has been variously reported as protein A-deficient and/or spa negative and used as a control in animal models of staphylococcal infections. The results of this study indicate that Wood 46 has normal spa expression but transcribes very low levels of the srtA gene which encodes the sortase A (SrtA) enzyme. This is consistent with unique mutations in the srtA promoter. In this study, a low level of sortase A explains deficient anchoring of proteins with an LPXTG motif, such as protein A, fibrinogen-binding protein and fibronectin-binding proteins A and B on to the peptidoglycan cell wall. The activity of secreted protein A is an important consideration for use of Wood 46 in functional experiments and animal models.
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页数:14
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