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Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia

Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas13a, previously known as CRISPR-C2c2, is the most recently identified RNA-guided RNA-targeting CRISPR-Cas system that has the unique characteristics of both targeted and collateral single-stranded RNA (ssRNA) cleavage activities....

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Autores principales: Watanabe, Shinya, Cui, Bintao, Kiga, Kotaro, Aiba, Yoshifumi, Tan, Xin-Ee, Sato’o, Yusuke, Kawauchi, Moriyuki, Boonsiri, Tanit, Thitiananpakorn, Kanate, Taki, Yusuke, Li, Fen-Yu, Azam, Aa Haeruman, Nakada, Yumi, Sasahara, Teppei, Cui, Longzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914741/
https://www.ncbi.nlm.nih.gov/pubmed/31921024
http://dx.doi.org/10.3389/fmicb.2019.02838
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author Watanabe, Shinya
Cui, Bintao
Kiga, Kotaro
Aiba, Yoshifumi
Tan, Xin-Ee
Sato’o, Yusuke
Kawauchi, Moriyuki
Boonsiri, Tanit
Thitiananpakorn, Kanate
Taki, Yusuke
Li, Fen-Yu
Azam, Aa Haeruman
Nakada, Yumi
Sasahara, Teppei
Cui, Longzhu
author_facet Watanabe, Shinya
Cui, Bintao
Kiga, Kotaro
Aiba, Yoshifumi
Tan, Xin-Ee
Sato’o, Yusuke
Kawauchi, Moriyuki
Boonsiri, Tanit
Thitiananpakorn, Kanate
Taki, Yusuke
Li, Fen-Yu
Azam, Aa Haeruman
Nakada, Yumi
Sasahara, Teppei
Cui, Longzhu
author_sort Watanabe, Shinya
collection PubMed
description Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas13a, previously known as CRISPR-C2c2, is the most recently identified RNA-guided RNA-targeting CRISPR-Cas system that has the unique characteristics of both targeted and collateral single-stranded RNA (ssRNA) cleavage activities. This system was first identified in Leptotrichia shahii. Here, the complete whole genome sequences of 11 Leptotrichia strains were determined and compared with 18 publicly available Leptotrichia genomes in regard to the composition, occurrence and diversity of the CRISPR-Cas13a, and other CRISPR-Cas systems. Various types of CRISPR-Cas systems were found to be unevenly distributed among the Leptotrichia genomes, including types I-B (10/29, 34.4%), II-C (1/29, 2.6%), III-A (6/29, 15.4%), III-D (6/29, 15.4%), III-like (3/29, 7.7%), and VI-A (11/29, 37.9%), while 8 strains (20.5%) had no CRISPR-Cas system at all. The Cas13a effectors were found to be highly divergent with amino acid sequence similarities ranging from 61% to 90% to that of L. shahii, but their collateral ssRNA cleavage activities leading to impediment of bacterial growth were conserved. CRISPR-Cas spacers represent a sequential achievement of former intruder encounters, and the retained spacers reflect the evolutionary phylogeny or relatedness of strains. Analysis of spacer contents and numbers among Leptotrichia species showed considerable diversity with only 4.4% of spacers (40/889) were shared by two strains. The organization and distribution of CRISPR-Cas systems (type I-VI) encoded by all registered Leptotrichia species revealed that effector or spacer sequences of the CRISPR-Cas systems were very divergent, and the prevalence of types I, III, and VI was almost equal. There was only one strain carrying type II, while none carried type IV or V. These results provide new insights into the characteristics and divergences of CRISPR-Cas systems among Leptotrichia species.
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spelling pubmed-69147412020-01-09 Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia Watanabe, Shinya Cui, Bintao Kiga, Kotaro Aiba, Yoshifumi Tan, Xin-Ee Sato’o, Yusuke Kawauchi, Moriyuki Boonsiri, Tanit Thitiananpakorn, Kanate Taki, Yusuke Li, Fen-Yu Azam, Aa Haeruman Nakada, Yumi Sasahara, Teppei Cui, Longzhu Front Microbiol Microbiology Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas13a, previously known as CRISPR-C2c2, is the most recently identified RNA-guided RNA-targeting CRISPR-Cas system that has the unique characteristics of both targeted and collateral single-stranded RNA (ssRNA) cleavage activities. This system was first identified in Leptotrichia shahii. Here, the complete whole genome sequences of 11 Leptotrichia strains were determined and compared with 18 publicly available Leptotrichia genomes in regard to the composition, occurrence and diversity of the CRISPR-Cas13a, and other CRISPR-Cas systems. Various types of CRISPR-Cas systems were found to be unevenly distributed among the Leptotrichia genomes, including types I-B (10/29, 34.4%), II-C (1/29, 2.6%), III-A (6/29, 15.4%), III-D (6/29, 15.4%), III-like (3/29, 7.7%), and VI-A (11/29, 37.9%), while 8 strains (20.5%) had no CRISPR-Cas system at all. The Cas13a effectors were found to be highly divergent with amino acid sequence similarities ranging from 61% to 90% to that of L. shahii, but their collateral ssRNA cleavage activities leading to impediment of bacterial growth were conserved. CRISPR-Cas spacers represent a sequential achievement of former intruder encounters, and the retained spacers reflect the evolutionary phylogeny or relatedness of strains. Analysis of spacer contents and numbers among Leptotrichia species showed considerable diversity with only 4.4% of spacers (40/889) were shared by two strains. The organization and distribution of CRISPR-Cas systems (type I-VI) encoded by all registered Leptotrichia species revealed that effector or spacer sequences of the CRISPR-Cas systems were very divergent, and the prevalence of types I, III, and VI was almost equal. There was only one strain carrying type II, while none carried type IV or V. These results provide new insights into the characteristics and divergences of CRISPR-Cas systems among Leptotrichia species. Frontiers Media S.A. 2019-12-10 /pmc/articles/PMC6914741/ /pubmed/31921024 http://dx.doi.org/10.3389/fmicb.2019.02838 Text en Copyright © 2019 Watanabe, Cui, Kiga, Aiba, Tan, Sato’o, Kawauchi, Boonsiri, Thitiananpakorn, Taki, Li, Azam, Nakada, Sasahara and Cui. 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
Watanabe, Shinya
Cui, Bintao
Kiga, Kotaro
Aiba, Yoshifumi
Tan, Xin-Ee
Sato’o, Yusuke
Kawauchi, Moriyuki
Boonsiri, Tanit
Thitiananpakorn, Kanate
Taki, Yusuke
Li, Fen-Yu
Azam, Aa Haeruman
Nakada, Yumi
Sasahara, Teppei
Cui, Longzhu
Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title_full Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title_fullStr Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title_full_unstemmed Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title_short Composition and Diversity of CRISPR-Cas13a Systems in the Genus Leptotrichia
title_sort composition and diversity of crispr-cas13a systems in the genus leptotrichia
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914741/
https://www.ncbi.nlm.nih.gov/pubmed/31921024
http://dx.doi.org/10.3389/fmicb.2019.02838
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