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Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs

Type IV pili are evolutionarily conserved cell surface filaments that promote surface adhesion and cell aggregation providing bacteria and archaea protection from a variety of stress conditions. In fact, prokaryotic genomes frequently contain several copies of the core biosynthesis genes, pilB and p...

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Autores principales: Legerme, Georgio, Pohlschroder, Mechthild
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491452/
https://www.ncbi.nlm.nih.gov/pubmed/31068907
http://dx.doi.org/10.3389/fmicb.2019.00700
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author Legerme, Georgio
Pohlschroder, Mechthild
author_facet Legerme, Georgio
Pohlschroder, Mechthild
author_sort Legerme, Georgio
collection PubMed
description Type IV pili are evolutionarily conserved cell surface filaments that promote surface adhesion and cell aggregation providing bacteria and archaea protection from a variety of stress conditions. In fact, prokaryotic genomes frequently contain several copies of the core biosynthesis genes, pilB and pilC, encoding an ATPase and membrane anchor, respectively. Recent phylogenetic analyses suggest that in haloarchaea, a subset of pilB-C paralogs, such as the Haloferax volcanii pilB1-C1, were gained via horizontal transfer from the crenarchaea, while the co-regulated type IV pilus subunits, the pilins, evolved by duplication, followed by diversification of the ancestral euryarchaeal pilins. Here, we report the identification of an H. volcanii pilB1 transposon mutant that exhibits an adhesion defect in defined media. A similar defect observed in an H. volcanii ∆pilB1-C1 strain can be rescued by expressing pilB1-C1 in trans. However, these proteins cannot rescue the severe adhesion defect of a previously reported ∆pilB3-C3 strain. Conversely, pilB3-C3, which are not predicted to have been laterally transferred, expressed in trans can rescue the adhesion defect of a ∆pilB1-C1 strain. This cross-complementation supports the proposed hybrid origin of the operon containing pilB1-C1 and shows that at least certain euryarchaeal PilB paralogs can work with different pilin sets. Efficient recognition of the euryarchaeal pilins by the crenarchaeal PilB1-C1 may have required some degree of pilin modification, but perhaps the modifications were minor enough that PilB3 recognition of these pilins was not precluded, resulting in modular evolution and an extensive combinatorial diversity that allows for adaptation to a variety of stress conditions and attachment to varied surfaces.
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spelling pubmed-64914522019-05-08 Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs Legerme, Georgio Pohlschroder, Mechthild Front Microbiol Microbiology Type IV pili are evolutionarily conserved cell surface filaments that promote surface adhesion and cell aggregation providing bacteria and archaea protection from a variety of stress conditions. In fact, prokaryotic genomes frequently contain several copies of the core biosynthesis genes, pilB and pilC, encoding an ATPase and membrane anchor, respectively. Recent phylogenetic analyses suggest that in haloarchaea, a subset of pilB-C paralogs, such as the Haloferax volcanii pilB1-C1, were gained via horizontal transfer from the crenarchaea, while the co-regulated type IV pilus subunits, the pilins, evolved by duplication, followed by diversification of the ancestral euryarchaeal pilins. Here, we report the identification of an H. volcanii pilB1 transposon mutant that exhibits an adhesion defect in defined media. A similar defect observed in an H. volcanii ∆pilB1-C1 strain can be rescued by expressing pilB1-C1 in trans. However, these proteins cannot rescue the severe adhesion defect of a previously reported ∆pilB3-C3 strain. Conversely, pilB3-C3, which are not predicted to have been laterally transferred, expressed in trans can rescue the adhesion defect of a ∆pilB1-C1 strain. This cross-complementation supports the proposed hybrid origin of the operon containing pilB1-C1 and shows that at least certain euryarchaeal PilB paralogs can work with different pilin sets. Efficient recognition of the euryarchaeal pilins by the crenarchaeal PilB1-C1 may have required some degree of pilin modification, but perhaps the modifications were minor enough that PilB3 recognition of these pilins was not precluded, resulting in modular evolution and an extensive combinatorial diversity that allows for adaptation to a variety of stress conditions and attachment to varied surfaces. Frontiers Media S.A. 2019-04-24 /pmc/articles/PMC6491452/ /pubmed/31068907 http://dx.doi.org/10.3389/fmicb.2019.00700 Text en Copyright © 2019 Legerme and Pohlschroder. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Legerme, Georgio
Pohlschroder, Mechthild
Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title_full Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title_fullStr Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title_full_unstemmed Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title_short Limited Cross-Complementation Between Haloferax volcanii PilB1-C1 and PilB3-C3 Paralogs
title_sort limited cross-complementation between haloferax volcanii pilb1-c1 and pilb3-c3 paralogs
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491452/
https://www.ncbi.nlm.nih.gov/pubmed/31068907
http://dx.doi.org/10.3389/fmicb.2019.00700
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