| Literature DB >> 33643301 |
Smadar Hada-Neeman1, Yael Weiss-Ottolenghi1, Naama Wagner1, Oren Avram1, Haim Ashkenazy2, Yaakov Maor3, Ella H Sklan4, Dmitry Shcherbakov5, Tal Pupko1, Jonathan M Gershoni1.
Abstract
The presence of pathogen-specific antibodies in an individual's blood-sample is used as an indication of previous exposure and infection to that specific pathogen (e.g., virus or bacterium). Measurement of the diagnostic antibodies is routinely achieved using solid phase immuno-assays such as ELISA tests and western blots. Here, we describe a sero-diagnostic approach based on phage-display of epitope arrays we term "Domain-Scan". We harness Next-generation sequencing (NGS) to measure the serum binding to dozens of epitopes derived from HIV-1 and HCV simultaneously. The distinction of healthy individuals from those infected with either HIV-1 or HCV, is modeled as a machine-learning classification problem, in which each determinant ("domain") is considered as a feature, and its NGS read-out provides values that correspond to the level of determinant-specific antibodies in the sample. We show that following training of a machine-learning model on labeled examples, we can very accurately classify unlabeled samples and pinpoint the domains that contribute most to the classification. Our experimental/computational Domain-Scan approach is general and can be adapted to other pathogens as long as sufficient training samples are provided.Entities:
Keywords: DNA barcodes; machine learning; next-generation sequencing; phage-display; sero-diagnostics
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Year: 2021 PMID: 33643301 PMCID: PMC7902724 DOI: 10.3389/fimmu.2020.619896
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561