Identification of biomarkers for the accurate and sensitive diagnosis of three bacterial pneumonia pathogens using in silico approaches
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Date
2020
Journal Title
Journal ISSN
Volume Title
Publisher
Springer Nature
Abstract
: Pneumonia ranks as one of the main infectious sources of mortality among kids under 5 years of age,
killing 2500 a day; late research has additionally demonstrated that mortality is higher in the elderly. A few biomarkers,
which up to this point have been distinguished for its determination lack specificity, as these biomarkers fail to build
up a differentiation between pneumonia and other related diseases, for example, pulmonary tuberculosis and Human
Immunodeficiency Infection (HIV). There is an inclusive global consensus of an improved comprehension of the
utilization of new biomarkers, which are delivered in light of pneumonia infection for precision identification to defeat
these previously mentioned constraints. Antimicrobial peptides (AMPs) have been demonstrated to be promising
remedial specialists against numerous illnesses. This research work sought to identify AMPs as biomarkers for three
bacterial pneumonia pathogens such as Streptococcus pneumoniae, Klebsiella pneumoniae, Acinetobacter baumannii
using in silico technology. Hidden Markov Models (HMMER) was used to identify putative anti-bacterial pneumonia
AMPs against the identified receptor proteins of Streptococcus pneumoniae, Klebsiella pneumoniae, and Acinetobacter
baumannii. The physicochemical parameters of these putative AMPs were computed and their 3-D structures were
predicted using I-TASSER. These AMPs were subsequently subjected to docking interaction analysis against the
identified bacterial pneumonia pathogen proteins using PATCHDOCK.
Description
Keywords
Antimicrobial peptides, Bacteria, Algorithms, Pathogens, Protein and ligands
Citation
Bakare, O. O. et al. (2020). Identification of biomarkers for the accurate and sensitive diagnosis of three bacterial pneumonia pathogens using in silico approaches. BMC Molecular and Cell Biology, 21(1),82