Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>

ABSTRACT Through coevolution with host cells, microorganisms have acquired mechanisms to avoid the detection by the host surveillance system and to use the cell’s supplies to establish themselves. Indeed, certain pathogens have evolved proteins that imitate specific eukaryotic cell proteins, allowin...

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Autores principales: Sonia Mondino, Silke Schmidt, Carmen Buchrieser
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:6d1b5ad0e1714d00a1c8fbe23676a0da2021-11-15T16:19:10ZMolecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>10.1128/mBio.01201-202150-7511https://doaj.org/article/6d1b5ad0e1714d00a1c8fbe23676a0da2020-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01201-20https://doaj.org/toc/2150-7511ABSTRACT Through coevolution with host cells, microorganisms have acquired mechanisms to avoid the detection by the host surveillance system and to use the cell’s supplies to establish themselves. Indeed, certain pathogens have evolved proteins that imitate specific eukaryotic cell proteins, allowing them to manipulate host pathways, a phenomenon termed molecular mimicry. Bacterial “eukaryotic-like proteins” are a remarkable example of molecular mimicry. They are defined as proteins that strongly resemble eukaryotic proteins or that carry domains that are predominantly present in eukaryotes and that are generally absent from prokaryotes. The widest diversity of eukaryotic-like proteins known to date can be found in members of the bacterial genus Legionella, some of which cause a severe pneumonia in humans. The characterization of a number of these proteins shed light on their importance during infection. The subsequent identification of eukaryotic-like genes in the genomes of other amoeba-associated bacteria and bacterial symbionts suggested that eukaryotic-like proteins are a common means of bacterial evasion and communication, shaped by the continuous interactions between bacteria and their protozoan hosts. In this review, we discuss the concept of molecular mimicry using Legionella as an example and show that eukaryotic-like proteins effectively manipulate host cell pathways. The study of the function and evolution of such proteins is an exciting field of research that is leading us toward a better understanding of the complex world of bacterium-host interactions. Ultimately, this knowledge will teach us how host pathways are manipulated and how infections may possibly be tackled.Sonia MondinoSilke SchmidtCarmen BuchrieserAmerican Society for Microbiologyarticlemolecular mimicryeukaryotic-like proteinsLegionellaamoeba-resistant bacteriahost-pathogen interactionsLegionella pneumophilaMicrobiologyQR1-502ENmBio, Vol 11, Iss 5 (2020)
institution DOAJ
collection DOAJ
language EN
topic molecular mimicry
eukaryotic-like proteins
Legionella
amoeba-resistant bacteria
host-pathogen interactions
Legionella pneumophila
Microbiology
QR1-502
spellingShingle molecular mimicry
eukaryotic-like proteins
Legionella
amoeba-resistant bacteria
host-pathogen interactions
Legionella pneumophila
Microbiology
QR1-502
Sonia Mondino
Silke Schmidt
Carmen Buchrieser
Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
description ABSTRACT Through coevolution with host cells, microorganisms have acquired mechanisms to avoid the detection by the host surveillance system and to use the cell’s supplies to establish themselves. Indeed, certain pathogens have evolved proteins that imitate specific eukaryotic cell proteins, allowing them to manipulate host pathways, a phenomenon termed molecular mimicry. Bacterial “eukaryotic-like proteins” are a remarkable example of molecular mimicry. They are defined as proteins that strongly resemble eukaryotic proteins or that carry domains that are predominantly present in eukaryotes and that are generally absent from prokaryotes. The widest diversity of eukaryotic-like proteins known to date can be found in members of the bacterial genus Legionella, some of which cause a severe pneumonia in humans. The characterization of a number of these proteins shed light on their importance during infection. The subsequent identification of eukaryotic-like genes in the genomes of other amoeba-associated bacteria and bacterial symbionts suggested that eukaryotic-like proteins are a common means of bacterial evasion and communication, shaped by the continuous interactions between bacteria and their protozoan hosts. In this review, we discuss the concept of molecular mimicry using Legionella as an example and show that eukaryotic-like proteins effectively manipulate host cell pathways. The study of the function and evolution of such proteins is an exciting field of research that is leading us toward a better understanding of the complex world of bacterium-host interactions. Ultimately, this knowledge will teach us how host pathways are manipulated and how infections may possibly be tackled.
format article
author Sonia Mondino
Silke Schmidt
Carmen Buchrieser
author_facet Sonia Mondino
Silke Schmidt
Carmen Buchrieser
author_sort Sonia Mondino
title Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
title_short Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
title_full Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
title_fullStr Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
title_full_unstemmed Molecular Mimicry: a Paradigm of Host-Microbe Coevolution Illustrated by <italic toggle="yes">Legionella</italic>
title_sort molecular mimicry: a paradigm of host-microbe coevolution illustrated by <italic toggle="yes">legionella</italic>
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/6d1b5ad0e1714d00a1c8fbe23676a0da
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