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“Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past

Downy mildews caused by obligate biotrophic oomycetes result in severe crop losses worldwide. Among these pathogens, Pseudoperonospora cubensis and P. humuli, two closely related oomycetes, adversely affect cucurbits and hop, respectively. Discordant hypotheses concerning their taxonomic relationshi...

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Autores principales: Nowicki, Marcin, Hadziabdic, Denita, Trigiano, Robert N., Boggess, Sarah L., Kanetis, Loukas, Wadl, Phillip A., Ojiambo, Peter S., Cubeta, Marc A., Spring, Otmar, Thines, Marco, Runge, Fabian, Scheffler, Brian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317435/
https://www.ncbi.nlm.nih.gov/pubmed/34335513
http://dx.doi.org/10.3389/fmicb.2021.686759
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author Nowicki, Marcin
Hadziabdic, Denita
Trigiano, Robert N.
Boggess, Sarah L.
Kanetis, Loukas
Wadl, Phillip A.
Ojiambo, Peter S.
Cubeta, Marc A.
Spring, Otmar
Thines, Marco
Runge, Fabian
Scheffler, Brian E.
author_facet Nowicki, Marcin
Hadziabdic, Denita
Trigiano, Robert N.
Boggess, Sarah L.
Kanetis, Loukas
Wadl, Phillip A.
Ojiambo, Peter S.
Cubeta, Marc A.
Spring, Otmar
Thines, Marco
Runge, Fabian
Scheffler, Brian E.
author_sort Nowicki, Marcin
collection PubMed
description Downy mildews caused by obligate biotrophic oomycetes result in severe crop losses worldwide. Among these pathogens, Pseudoperonospora cubensis and P. humuli, two closely related oomycetes, adversely affect cucurbits and hop, respectively. Discordant hypotheses concerning their taxonomic relationships have been proposed based on host–pathogen interactions and specificity evidence and gene sequences of a few individuals, but population genetics evidence supporting these scenarios is missing. Furthermore, nuclear and mitochondrial regions of both pathogens have been analyzed using microsatellites and phylogenetically informative molecular markers, but extensive comparative population genetics research has not been done. Here, we genotyped 138 current and historical herbarium specimens of those two taxa using microsatellites (SSRs). Our goals were to assess genetic diversity and spatial distribution, to infer the evolutionary history of P. cubensis and P. humuli, and to visualize genome-scale organizational relationship between both pathogens. High genetic diversity, modest gene flow, and presence of population structure, particularly in P. cubensis, were observed. When tested for cross-amplification, 20 out of 27 P. cubensis-derived gSSRs cross-amplified DNA of P. humuli individuals, but few amplified DNA of downy mildew pathogens from related genera. Collectively, our analyses provided a definite argument for the hypothesis that both pathogens are distinct species, and suggested further speciation in the P. cubensis complex.
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spelling pubmed-83174352021-07-29 “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past Nowicki, Marcin Hadziabdic, Denita Trigiano, Robert N. Boggess, Sarah L. Kanetis, Loukas Wadl, Phillip A. Ojiambo, Peter S. Cubeta, Marc A. Spring, Otmar Thines, Marco Runge, Fabian Scheffler, Brian E. Front Microbiol Microbiology Downy mildews caused by obligate biotrophic oomycetes result in severe crop losses worldwide. Among these pathogens, Pseudoperonospora cubensis and P. humuli, two closely related oomycetes, adversely affect cucurbits and hop, respectively. Discordant hypotheses concerning their taxonomic relationships have been proposed based on host–pathogen interactions and specificity evidence and gene sequences of a few individuals, but population genetics evidence supporting these scenarios is missing. Furthermore, nuclear and mitochondrial regions of both pathogens have been analyzed using microsatellites and phylogenetically informative molecular markers, but extensive comparative population genetics research has not been done. Here, we genotyped 138 current and historical herbarium specimens of those two taxa using microsatellites (SSRs). Our goals were to assess genetic diversity and spatial distribution, to infer the evolutionary history of P. cubensis and P. humuli, and to visualize genome-scale organizational relationship between both pathogens. High genetic diversity, modest gene flow, and presence of population structure, particularly in P. cubensis, were observed. When tested for cross-amplification, 20 out of 27 P. cubensis-derived gSSRs cross-amplified DNA of P. humuli individuals, but few amplified DNA of downy mildew pathogens from related genera. Collectively, our analyses provided a definite argument for the hypothesis that both pathogens are distinct species, and suggested further speciation in the P. cubensis complex. Frontiers Media S.A. 2021-07-14 /pmc/articles/PMC8317435/ /pubmed/34335513 http://dx.doi.org/10.3389/fmicb.2021.686759 Text en Copyright © 2021 Nowicki, Hadziabdic, Trigiano, Boggess, Kanetis, Wadl, Ojiambo, Cubeta, Spring, Thines, Runge and Scheffler. https://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
Nowicki, Marcin
Hadziabdic, Denita
Trigiano, Robert N.
Boggess, Sarah L.
Kanetis, Loukas
Wadl, Phillip A.
Ojiambo, Peter S.
Cubeta, Marc A.
Spring, Otmar
Thines, Marco
Runge, Fabian
Scheffler, Brian E.
“Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title_full “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title_fullStr “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title_full_unstemmed “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title_short “Jumping Jack”: Genomic Microsatellites Underscore the Distinctiveness of Closely Related Pseudoperonospora cubensis and Pseudoperonospora humuli and Provide New Insights Into Their Evolutionary Past
title_sort “jumping jack”: genomic microsatellites underscore the distinctiveness of closely related pseudoperonospora cubensis and pseudoperonospora humuli and provide new insights into their evolutionary past
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317435/
https://www.ncbi.nlm.nih.gov/pubmed/34335513
http://dx.doi.org/10.3389/fmicb.2021.686759
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