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Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond

The freshwater cyanobacterium Microcystis aeruginosa frequently forms toxic massive blooms and exists in an arms race with its infectious phages in aquatic natural environments, and as a result, has evolved extremely diverse and elaborate antiviral defense systems, including the clustered regularly...

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Autores principales: Kimura, Shigeko, Uehara, Mika, Morimoto, Daichi, Yamanaka, Momoko, Sako, Yoshihiko, Yoshida, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852275/
https://www.ncbi.nlm.nih.gov/pubmed/29568293
http://dx.doi.org/10.3389/fmicb.2018.00425
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author Kimura, Shigeko
Uehara, Mika
Morimoto, Daichi
Yamanaka, Momoko
Sako, Yoshihiko
Yoshida, Takashi
author_facet Kimura, Shigeko
Uehara, Mika
Morimoto, Daichi
Yamanaka, Momoko
Sako, Yoshihiko
Yoshida, Takashi
author_sort Kimura, Shigeko
collection PubMed
description The freshwater cyanobacterium Microcystis aeruginosa frequently forms toxic massive blooms and exists in an arms race with its infectious phages in aquatic natural environments, and as a result, has evolved extremely diverse and elaborate antiviral defense systems, including the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated genes (Cas) system. Here, to assess Microcystis population dynamics associated with exogenous mobile genetic elements such as phages and plasmids, we examined the temporal variation in CRISPR genotypes (CTs) by analyzing spacer sequences detected in a natural pond between June and October 2013 when a cyanobacterial bloom occurred. A total of 463,954 high-quality leader-end CRISPR sequences were obtained and the sequences containing spacers were classified into 31 previously reported CTs and 68 new CTs based on the shared order of the leader-end spacers. CT19 was the most dominant genotype (32%) among the 16 most common CTs, followed by CT52 (14%) and CT58 (9%). Spacer repertoires of CT19 showed mainly two different types; CT19(origin), which was identical to the CT19 spacer repertoire of previously isolated strains, and CT19(new+), which contained a new spacer at the leader-end of the CRISPR region of CT19(origin), which were present in almost equal abundance, accounting for up to 99.94% of CT19 sequences. Surprisingly, we observed the spacer repertoires of the second to tenth spacers of CT19(origin) at the most leader-end of proto-genotype sequences of CT19(origin). These were observed during the sampling in this study and our previous study at the same ecosystem in 2010 and 2011, suggesting these CTs persisted from 2011 to 2013 in spite of phage pressure. The leader-end variants were observed in other CT genotypes. These findings indicated an incomplete selective sweep of Microcystis populations. We explained the phenomenon as follow; the abundance of Microcystis varied seasonally and drastically, resulting that Microcystis populations experience a bottleneck once a year, and thereby founder effects following a bottleneck mean that older CTs have an equal chance of increasing in prevalence as the CTs generated following acquisition of newer spacers.
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spelling pubmed-58522752018-03-22 Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond Kimura, Shigeko Uehara, Mika Morimoto, Daichi Yamanaka, Momoko Sako, Yoshihiko Yoshida, Takashi Front Microbiol Microbiology The freshwater cyanobacterium Microcystis aeruginosa frequently forms toxic massive blooms and exists in an arms race with its infectious phages in aquatic natural environments, and as a result, has evolved extremely diverse and elaborate antiviral defense systems, including the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated genes (Cas) system. Here, to assess Microcystis population dynamics associated with exogenous mobile genetic elements such as phages and plasmids, we examined the temporal variation in CRISPR genotypes (CTs) by analyzing spacer sequences detected in a natural pond between June and October 2013 when a cyanobacterial bloom occurred. A total of 463,954 high-quality leader-end CRISPR sequences were obtained and the sequences containing spacers were classified into 31 previously reported CTs and 68 new CTs based on the shared order of the leader-end spacers. CT19 was the most dominant genotype (32%) among the 16 most common CTs, followed by CT52 (14%) and CT58 (9%). Spacer repertoires of CT19 showed mainly two different types; CT19(origin), which was identical to the CT19 spacer repertoire of previously isolated strains, and CT19(new+), which contained a new spacer at the leader-end of the CRISPR region of CT19(origin), which were present in almost equal abundance, accounting for up to 99.94% of CT19 sequences. Surprisingly, we observed the spacer repertoires of the second to tenth spacers of CT19(origin) at the most leader-end of proto-genotype sequences of CT19(origin). These were observed during the sampling in this study and our previous study at the same ecosystem in 2010 and 2011, suggesting these CTs persisted from 2011 to 2013 in spite of phage pressure. The leader-end variants were observed in other CT genotypes. These findings indicated an incomplete selective sweep of Microcystis populations. We explained the phenomenon as follow; the abundance of Microcystis varied seasonally and drastically, resulting that Microcystis populations experience a bottleneck once a year, and thereby founder effects following a bottleneck mean that older CTs have an equal chance of increasing in prevalence as the CTs generated following acquisition of newer spacers. Frontiers Media S.A. 2018-03-08 /pmc/articles/PMC5852275/ /pubmed/29568293 http://dx.doi.org/10.3389/fmicb.2018.00425 Text en Copyright © 2018 Kimura, Uehara, Morimoto, Yamanaka, Sako and Yoshida. 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 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
Kimura, Shigeko
Uehara, Mika
Morimoto, Daichi
Yamanaka, Momoko
Sako, Yoshihiko
Yoshida, Takashi
Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title_full Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title_fullStr Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title_full_unstemmed Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title_short Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond
title_sort incomplete selective sweeps of microcystis population detected by the leader-end crispr fragment analysis in a natural pond
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852275/
https://www.ncbi.nlm.nih.gov/pubmed/29568293
http://dx.doi.org/10.3389/fmicb.2018.00425
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