Prediction of host - pathogen protein interactions between Mycobacterium tuberculosis and Homo sapiens using sequence motifs

被引:40
|
作者
Huo, Tong [1 ,2 ,4 ]
Liu, Wei [1 ,2 ,4 ]
Guo, Yu [1 ,3 ,4 ]
Yang, Cheng [1 ,3 ,4 ]
Lin, Jianping [1 ,3 ,4 ]
Rao, Zihe [1 ,2 ,4 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Nankai Univ, Coll Pharm, Tianjin 300071, Peoples R China
[4] Tianjin Int Joint Acad Biotechnol & Med, Tianjin 300457, Peoples R China
来源
BMC BIOINFORMATICS | 2015年 / 16卷
关键词
INTERACTION NETWORKS; IMMUNE-RESPONSES; IDENTIFICATION; DATABASE; CELLS; ANNOTATION; RESISTANCE; INFERENCE; SYSTEMS; TOOL;
D O I
10.1186/s12859-015-0535-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Emergence of multiple drug resistant strains of M. tuberculosis (MDR-TB) threatens to derail global efforts aimed at reigning in the pathogen. Co-infections of M. tuberculosis with HIV are difficult to treat. To counter these new challenges, it is essential to study the interactions between M. tuberculosis and the host to learn how these bacteria cause disease. Results: We report a systematic flow to predict the host pathogen interactions (HPIs) between M. tuberculosis and Homo sapiens based on sequence motifs. First, protein sequences were used as initial input for identifying the HPIs by 'interolog' method. HPIs were further filtered by prediction of domain-domain interactions (DDIs). Functional annotations of protein and publicly available experimental results were applied to filter the remaining HPIs. Using such a strategy, 118 pairs of HPIs were identified, which involve 43 proteins from M. tuberculosis and 48 proteins from Homo sapiens. A biological interaction network between M. tuberculosis and Homo sapiens was then constructed using the predicted inter-and intra-species interactions based on the 118 pairs of HPIs. Finally, a web accessible database named PATH (Protein interactions of M. tuberculosis and Human) was constructed to store these predicted interactions and proteins. Conclusions: This interaction network will facilitate the research on host-pathogen protein-protein interactions, and may throw light on how M. tuberculosis interacts with its host.
引用
收藏
页数:9
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