Putative Antimicrobial Peptides Within Bacterial Proteomes Affect Bacterial Predominance: A Network Analysis Perspective

被引:4
|
作者
Oulas, Anastasis [1 ,2 ]
Zachariou, Margarita [1 ,2 ]
Chasapis, Christos T. [3 ]
Tomazou, Marios [1 ,2 ]
Ijaz, Umer Z. [4 ]
Schmartz, Georges Pierre [5 ]
Spyrou, George M. [1 ,2 ]
Vlamis-Gardikas, Alexios [6 ]
机构
[1] Cyprus Inst Neurol & Genet, Bioinformat Dept, Nicosia, Cyprus
[2] Cyprus Sch Mol Med, Nicosia, Cyprus
[3] Univ Patras, Sch Nat Sci, Instrumental Anal Lab, NMR Ctr, Patras, Greece
[4] Univ Glasgow, Sch Engn, Glasgow, Lanark, Scotland
[5] Saarland Univ, Chair Clin Bioinformat, Saarbrucken, Germany
[6] Univ Patras, Dept Chem, Div Organ Chem Biochem & Nat Prod, Patras, Greece
关键词
putative antimicrobial peptides; interbacterial antagonism; network analysis; bioinformatics analysis; bacterial competition; GUT MICROBIOTA; CD-HIT; GENERATION; PREDICTION; PROTEIN; GAME;
D O I
10.3389/fmicb.2021.752674
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The predominance of bacterial taxa in the gut, was examined in view of the putative antimicrobial peptide sequences (AMPs) within their proteomes. The working assumption was that compatible bacteria would share homology and thus immunity to their putative AMPs, while competing taxa would have dissimilarities in their proteome-hidden AMPs. A network-based method ("Bacterial Wars") was developed to handle sequence similarities of predicted AMPs among UniProt-derived protein sequences from different bacterial taxa, while a resulting parameter ("Die" score) suggested which taxa would prevail in a defined microbiome. T he working hypothesis was examined by correlating the calculated Die scores, to the abundance of bacterial taxa from gut microbiomes from different states of health and disease. Eleven publicly available 16S rRNA datasets and a dataset from a full shotgun metagenomics served for the analysis. The overall conclusion was that AMPs encrypted within bacterial proteomes affected the predominance of bacterial taxa in chemospheres.
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页数:14
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