Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution

For a profound understanding of antagonistic coevolution, it is necessary to identify the coevolving genes. The bacterium Pasteuria and its host, the microcrustacean Daphnia, are a well-characterized paradigm for co-evolution, but the underlying genes remain largely unknown. A genome-wide associatio...

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Main Authors: Benjamin Huessy, Dirk Bumann, Dieter Ebert
Format: Article
Language:English
Published: The Royal Society 2024-04-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/10.1098/rsos.231441
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author Benjamin Huessy
Dirk Bumann
Dieter Ebert
author_facet Benjamin Huessy
Dirk Bumann
Dieter Ebert
author_sort Benjamin Huessy
collection DOAJ
description For a profound understanding of antagonistic coevolution, it is necessary to identify the coevolving genes. The bacterium Pasteuria and its host, the microcrustacean Daphnia, are a well-characterized paradigm for co-evolution, but the underlying genes remain largely unknown. A genome-wide association study suggested a Pasteuria collagen-like protein 7 (Pcl7) as a candidate mediating parasite attachment and driving its coevolution with the host. Since Pasteuria ramosa cannot currently be genetically manipulated, we used Bacillus thuringiensis to express a fusion protein of a Pcl7 carboxy-terminus from P. ramosa and the amino-terminal domain of a B. thuringiensis collagen-like protein (CLP). Mutant B. thuringiensis (Pcl7-Bt) spores but not wild-type B. thuringiensis (WT-Bt) spores attached to the same site of susceptible hosts as P. ramosa. Furthermore, Pcl7-Bt spores attached readily to susceptible host genotypes, but only slightly to resistant host genotypes. These findings indicated that the fusion protein was properly expressed and folded and demonstrated that indeed the C-terminus of Pcl7 mediates attachment in a host genotype-specific manner. These results provide strong evidence for the involvement of a CLP in the coevolution of Daphnia and P. ramosa and open new avenues for genetic epidemiological studies of host–parasite interactions.
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spelling doaj.art-a73beef178884947b7e9bae913fc5d8e2024-04-03T14:45:40ZengThe Royal SocietyRoyal Society Open Science2054-57032024-04-0111410.1098/rsos.231441Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolutionBenjamin Huessy0Dirk Bumann1Dieter Ebert2Department of Environmental Sciences, Zoology, University of Basel , Basel 4051, SwitzerlandUniversity of Basel , Basel 4056, SwitzerlandDepartment of Environmental Sciences, Zoology, University of Basel , Basel 4051, SwitzerlandFor a profound understanding of antagonistic coevolution, it is necessary to identify the coevolving genes. The bacterium Pasteuria and its host, the microcrustacean Daphnia, are a well-characterized paradigm for co-evolution, but the underlying genes remain largely unknown. A genome-wide association study suggested a Pasteuria collagen-like protein 7 (Pcl7) as a candidate mediating parasite attachment and driving its coevolution with the host. Since Pasteuria ramosa cannot currently be genetically manipulated, we used Bacillus thuringiensis to express a fusion protein of a Pcl7 carboxy-terminus from P. ramosa and the amino-terminal domain of a B. thuringiensis collagen-like protein (CLP). Mutant B. thuringiensis (Pcl7-Bt) spores but not wild-type B. thuringiensis (WT-Bt) spores attached to the same site of susceptible hosts as P. ramosa. Furthermore, Pcl7-Bt spores attached readily to susceptible host genotypes, but only slightly to resistant host genotypes. These findings indicated that the fusion protein was properly expressed and folded and demonstrated that indeed the C-terminus of Pcl7 mediates attachment in a host genotype-specific manner. These results provide strong evidence for the involvement of a CLP in the coevolution of Daphnia and P. ramosa and open new avenues for genetic epidemiological studies of host–parasite interactions.https://royalsocietypublishing.org/doi/10.1098/rsos.231441Daphnia magnaPasteuria ramosaBacillus thuringiensiscollagen-like proteinshost–parasite interactionsfusion protein
spellingShingle Benjamin Huessy
Dirk Bumann
Dieter Ebert
Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
Royal Society Open Science
Daphnia magna
Pasteuria ramosa
Bacillus thuringiensis
collagen-like proteins
host–parasite interactions
fusion protein
title Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
title_full Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
title_fullStr Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
title_full_unstemmed Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
title_short Ectopical expression of bacterial collagen-like protein supports its role as adhesin in host–parasite coevolution
title_sort ectopical expression of bacterial collagen like protein supports its role as adhesin in host parasite coevolution
topic Daphnia magna
Pasteuria ramosa
Bacillus thuringiensis
collagen-like proteins
host–parasite interactions
fusion protein
url https://royalsocietypublishing.org/doi/10.1098/rsos.231441
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