Antibacterial Activity of a Modified Choline Binding Peptide Against Streptococcus pneumoniae with Corresponding Antibody

被引:0
|
作者
Ji, Hongsheng [2 ]
Zhou, Guomin [1 ]
Xiao, Qifeng [1 ]
Tian, Jie [1 ]
Liu, Qi [1 ]
Liu, Jinhua [1 ]
Zhang, Zhikun [1 ]
机构
[1] Sch Basic Med, Dept Pathogen Biol, Chengdu, Sichuan, Peoples R China
[2] Southwest Med Univ, Sch Publ Hlth, Chengdu, Sichuan, Peoples R China
关键词
S; pneumoniae; Choline binding peptide; Influenza a virus; Secondary infection; SEROTYPE DISTRIBUTION; CHILDREN; COLONIZATION; YOUNGER; DISEASE;
D O I
10.1007/s10989-021-10300-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Streptococcus pneumoniae is an important human pathogen that colonizes the upper respiratory tract. The infection of influenza A virus (IAV) is associated with an increase in susceptibility to pneumococcal pneumonia. In the present study, we analyzed the antibacterial activity of ChBp-I2 with N-terminal choline binding peptide and C-terminal IAV epitope to S. pneumoniae. Three ChBp-Is with different IAV epitope were applied in pneumococcal binding test. Among which ChBp-I2 of 50 mu g/ml mediate a similar binding capacity of IAV antibody to capsular polysaccharide antibody. In the following tests, no inhibitory effect of ChBp-I2 was detected to pneumococcal cells alone. However, high concentrations of ChBp-I2 influence the synthesis of pneumococcal cell wall. Meanwhile, the growth rate, adhesion and the autolysis of pneumococcal cells are both decreased with the existence of ChBp-I2 and IAV antibodies. In vivo, the treatment of ChBp-I2 decrease the number of pneumococcal cells in lung and blood in IAV immunized mice. In conclusion, the distinctive activities of ChBp-I2 to S. pneumoniae indicate it could be a candidate for preventing secondary S. pneumoniae infection post IAV infection.
引用
收藏
页码:2923 / 2929
页数:7
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