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Novelty Search Promotes Antigenic Diversity in Microbial Pathogens

Driven by host–pathogen coevolution, cell surface antigens are often the fastest evolving parts of a microbial pathogen. The persistent evolutionary impetus for novel antigen variants suggests the utility of novelty-seeking algorithms in predicting antigen diversification in microbial pathogens. In...

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Detalles Bibliográficos
Autores principales: Ely, Brandon, Koh, Winston, Ho, Eamen, Hassan, Tasmina M., Pham, Anh V., Qiu, Weigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053453/
https://www.ncbi.nlm.nih.gov/pubmed/36986310
http://dx.doi.org/10.3390/pathogens12030388
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author Ely, Brandon
Koh, Winston
Ho, Eamen
Hassan, Tasmina M.
Pham, Anh V.
Qiu, Weigang
author_facet Ely, Brandon
Koh, Winston
Ho, Eamen
Hassan, Tasmina M.
Pham, Anh V.
Qiu, Weigang
author_sort Ely, Brandon
collection PubMed
description Driven by host–pathogen coevolution, cell surface antigens are often the fastest evolving parts of a microbial pathogen. The persistent evolutionary impetus for novel antigen variants suggests the utility of novelty-seeking algorithms in predicting antigen diversification in microbial pathogens. In contrast to traditional genetic algorithms maximizing variant fitness, novelty-seeking algorithms optimize variant novelty. Here, we designed and implemented three evolutionary algorithms (fitness-seeking, novelty-seeking, and hybrid) and evaluated their performances in 10 simulated and 2 empirically derived antigen fitness landscapes. The hybrid walks combining fitness- and novelty-seeking strategies overcame the limitations of each algorithm alone, and consistently reached global fitness peaks. Thus, hybrid walks provide a model for microbial pathogens escaping host immunity without compromising variant fitness. Biological processes facilitating novelty-seeking evolution in natural pathogen populations include hypermutability, recombination, wide dispersal, and immune-compromised hosts. The high efficiency of the hybrid algorithm improves the evolutionary predictability of novel antigen variants. We propose the design of escape-proof vaccines based on high-fitness variants covering a majority of the basins of attraction on the fitness landscape representing all potential variants of a microbial antigen.
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spelling pubmed-100534532023-03-30 Novelty Search Promotes Antigenic Diversity in Microbial Pathogens Ely, Brandon Koh, Winston Ho, Eamen Hassan, Tasmina M. Pham, Anh V. Qiu, Weigang Pathogens Article Driven by host–pathogen coevolution, cell surface antigens are often the fastest evolving parts of a microbial pathogen. The persistent evolutionary impetus for novel antigen variants suggests the utility of novelty-seeking algorithms in predicting antigen diversification in microbial pathogens. In contrast to traditional genetic algorithms maximizing variant fitness, novelty-seeking algorithms optimize variant novelty. Here, we designed and implemented three evolutionary algorithms (fitness-seeking, novelty-seeking, and hybrid) and evaluated their performances in 10 simulated and 2 empirically derived antigen fitness landscapes. The hybrid walks combining fitness- and novelty-seeking strategies overcame the limitations of each algorithm alone, and consistently reached global fitness peaks. Thus, hybrid walks provide a model for microbial pathogens escaping host immunity without compromising variant fitness. Biological processes facilitating novelty-seeking evolution in natural pathogen populations include hypermutability, recombination, wide dispersal, and immune-compromised hosts. The high efficiency of the hybrid algorithm improves the evolutionary predictability of novel antigen variants. We propose the design of escape-proof vaccines based on high-fitness variants covering a majority of the basins of attraction on the fitness landscape representing all potential variants of a microbial antigen. MDPI 2023-02-28 /pmc/articles/PMC10053453/ /pubmed/36986310 http://dx.doi.org/10.3390/pathogens12030388 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ely, Brandon
Koh, Winston
Ho, Eamen
Hassan, Tasmina M.
Pham, Anh V.
Qiu, Weigang
Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title_full Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title_fullStr Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title_full_unstemmed Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title_short Novelty Search Promotes Antigenic Diversity in Microbial Pathogens
title_sort novelty search promotes antigenic diversity in microbial pathogens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053453/
https://www.ncbi.nlm.nih.gov/pubmed/36986310
http://dx.doi.org/10.3390/pathogens12030388
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