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  • MAE4, an eLtaS monoclonal antibody, blocks Staphylococcus aureus virulence.

MAE4, an eLtaS monoclonal antibody, blocks Staphylococcus aureus virulence.

Scientific reports (2015-11-26)
Yu Liu, Jiannan Feng, Qiang Lu, Xin Zhang, Yaping Gao, Jun Yan, Chunhua Mu, Yan Hei, Ming Lv, Gencheng Han, Guojiang Chen, Peng Jin, Weiguo Hu, Beifen Shen, Guang Yang
ABSTRACT

Staphylococcus aureus causes a wide range of infectious diseases. Treatment of these infections has become increasingly difficult due to the widespread emergence of antibiotic-resistant strains; therefore, it is essential to explore effective alternatives to antibiotics. A secreted protein of S. aureus, known as eLtaS, is an extracellular protein released from the bacterial membrane protein, LtaS. However, the role of eLtaS in S. aureus pathogenesis remains largely unknown. Here we show eLtaS dramatically aggravates S. aureus infection by binding to C3b and then inhibiting the phagocytosis of C3b-deposited S. aureus. Furthermore, we developed a monoclonal antibody against eLtaS, MAE4, which neutralizes the activity of eLtaS and blocks staphylococcal evasion of phagocytosis. Consequently, MAE4 is capable of protecting mice from lethal S. aureus infection. Our findings reveal that targeting of eLtaS by MAE4 is a potential therapeutic strategy for the treatment of infectious diseases caused by S. aureus.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Mannan from Saccharomyces cerevisiae, prepared by alkaline extraction
Sigma-Aldrich
Anti-C3 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
Sigma-Aldrich
Fibrinogen from human plasma, 50-70% protein (≥80% of protein is clottable)
Sigma-Aldrich
Lipopolysaccharides from Salmonella typhosa, purified by phenol extraction