TY - JOUR
T1 - A Potent Anti-SpuE Antibody Allosterically Inhibits Type III Secretion System and Attenuates Virulence of Pseudomonas Aeruginosa
AU - Zhang, Yang
AU - Sun, Xiaodan
AU - Qian, Yangyang
AU - Yi, Hongfei
AU - Song, Ke
AU - Zhu, Huanhu
AU - Zonta, Francesco
AU - Chen, Weizhong
AU - Ji, Quanjiang
AU - Miersch, Shane
AU - Sidhu, Sachdev S.
AU - Wu, Donghui
N1 - Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/12/6
Y1 - 2019/12/6
N2 - Multidrug-resistant gram-negative bacteria infection is particularly severe within the designated ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species), which underscores the urgent need to explore alternative therapeutic strategies. The type III secretion system (T3SS) is considered to be a key virulence factor in many gram-negative bacteria, and T3SS is in turn regulated by SpuE in P. aeruginosa, which is a spermidine binding protein from an ATP-binding cassette transporter family and highly conserved within ESKAPE pathogens. Here, we identified a potent anti-SpuE antagonistic antibody that allosterically inhibits the expression of T3SS and attenuates virulence of P. aeruginosa. X-ray crystallography and molecular dynamics simulations revealed that binding of antibody to SpuE induces a change in the dynamics of SpuE, which in turn may reduce spermidine uptake by P. aeruginosa. The antibody could serve as a template for developing novel biologics to target a broad spectrum of gram-negative bacteria.
AB - Multidrug-resistant gram-negative bacteria infection is particularly severe within the designated ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species), which underscores the urgent need to explore alternative therapeutic strategies. The type III secretion system (T3SS) is considered to be a key virulence factor in many gram-negative bacteria, and T3SS is in turn regulated by SpuE in P. aeruginosa, which is a spermidine binding protein from an ATP-binding cassette transporter family and highly conserved within ESKAPE pathogens. Here, we identified a potent anti-SpuE antagonistic antibody that allosterically inhibits the expression of T3SS and attenuates virulence of P. aeruginosa. X-ray crystallography and molecular dynamics simulations revealed that binding of antibody to SpuE induces a change in the dynamics of SpuE, which in turn may reduce spermidine uptake by P. aeruginosa. The antibody could serve as a template for developing novel biologics to target a broad spectrum of gram-negative bacteria.
KW - Pseudomonas aeruginosa
KW - SpuE
KW - antibody phage display
KW - multidrug resistant
KW - spermidine importer
KW - type III secretion system
UR - http://www.scopus.com/inward/record.url?scp=85076281710&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2019.10.026
DO - 10.1016/j.jmb.2019.10.026
M3 - Article
C2 - 31682834
AN - SCOPUS:85076281710
SN - 0022-2836
VL - 431
SP - 4882
EP - 4896
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 24
ER -