CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.

Streptococcus pyogenes, one of the major human pathogens, is a unique species since it has acquired diverse strain-specific virulence properties mainly through the acquisition of streptococcal prophages. In addition, S. pyogenes possesses clustered regularly interspaced short palindromic repeats (CR...

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Autores principales: Takashi Nozawa, Nayuta Furukawa, Chihiro Aikawa, Takayasu Watanabe, Bijaya Haobam, Ken Kurokawa, Fumito Maruyama, Ichiro Nakagawa
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:c7bab222ff0742e5a802f5f0abe26c4b2021-11-18T06:54:21ZCRISPR inhibition of prophage acquisition in Streptococcus pyogenes.1932-620310.1371/journal.pone.0019543https://doaj.org/article/c7bab222ff0742e5a802f5f0abe26c4b2011-05-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21573110/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Streptococcus pyogenes, one of the major human pathogens, is a unique species since it has acquired diverse strain-specific virulence properties mainly through the acquisition of streptococcal prophages. In addition, S. pyogenes possesses clustered regularly interspaced short palindromic repeats (CRISPR)/Cas systems that can restrict horizontal gene transfer (HGT) including phage insertion. Therefore, it was of interest to examine the relationship between CRISPR and acquisition of prophages in S. pyogenes. Although two distinct CRISPR loci were found in S. pyogenes, some strains lacked CRISPR and these strains possess significantly more prophages than CRISPR harboring strains. We also found that the number of spacers of S. pyogenes CRISPR was less than for other streptococci. The demonstrated spacer contents, however, suggested that the CRISPR appear to limit phage insertions. In addition, we found a significant inverse correlation between the number of spacers and prophages in S. pyogenes. It was therefore suggested that S. pyogenes CRISPR have permitted phage insertion by lacking its own spacers. Interestingly, in two closely related S. pyogenes strains (SSI-1 and MGAS315), CRISPR activity appeared to be impaired following the insertion of phage genomes into the repeat sequences. Detailed analysis of this prophage insertion site suggested that MGAS315 is the ancestral strain of SSI-1. As a result of analysis of 35 additional streptococcal genomes, it was suggested that the influences of the CRISPR on the phage insertion vary among species even within the same genus. Our results suggested that limitations in CRISPR content could explain the characteristic acquisition of prophages and might contribute to strain-specific pathogenesis in S. pyogenes.Takashi NozawaNayuta FurukawaChihiro AikawaTakayasu WatanabeBijaya HaobamKen KurokawaFumito MaruyamaIchiro NakagawaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 5, p e19543 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Takashi Nozawa
Nayuta Furukawa
Chihiro Aikawa
Takayasu Watanabe
Bijaya Haobam
Ken Kurokawa
Fumito Maruyama
Ichiro Nakagawa
CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
description Streptococcus pyogenes, one of the major human pathogens, is a unique species since it has acquired diverse strain-specific virulence properties mainly through the acquisition of streptococcal prophages. In addition, S. pyogenes possesses clustered regularly interspaced short palindromic repeats (CRISPR)/Cas systems that can restrict horizontal gene transfer (HGT) including phage insertion. Therefore, it was of interest to examine the relationship between CRISPR and acquisition of prophages in S. pyogenes. Although two distinct CRISPR loci were found in S. pyogenes, some strains lacked CRISPR and these strains possess significantly more prophages than CRISPR harboring strains. We also found that the number of spacers of S. pyogenes CRISPR was less than for other streptococci. The demonstrated spacer contents, however, suggested that the CRISPR appear to limit phage insertions. In addition, we found a significant inverse correlation between the number of spacers and prophages in S. pyogenes. It was therefore suggested that S. pyogenes CRISPR have permitted phage insertion by lacking its own spacers. Interestingly, in two closely related S. pyogenes strains (SSI-1 and MGAS315), CRISPR activity appeared to be impaired following the insertion of phage genomes into the repeat sequences. Detailed analysis of this prophage insertion site suggested that MGAS315 is the ancestral strain of SSI-1. As a result of analysis of 35 additional streptococcal genomes, it was suggested that the influences of the CRISPR on the phage insertion vary among species even within the same genus. Our results suggested that limitations in CRISPR content could explain the characteristic acquisition of prophages and might contribute to strain-specific pathogenesis in S. pyogenes.
format article
author Takashi Nozawa
Nayuta Furukawa
Chihiro Aikawa
Takayasu Watanabe
Bijaya Haobam
Ken Kurokawa
Fumito Maruyama
Ichiro Nakagawa
author_facet Takashi Nozawa
Nayuta Furukawa
Chihiro Aikawa
Takayasu Watanabe
Bijaya Haobam
Ken Kurokawa
Fumito Maruyama
Ichiro Nakagawa
author_sort Takashi Nozawa
title CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
title_short CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
title_full CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
title_fullStr CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
title_full_unstemmed CRISPR inhibition of prophage acquisition in Streptococcus pyogenes.
title_sort crispr inhibition of prophage acquisition in streptococcus pyogenes.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/c7bab222ff0742e5a802f5f0abe26c4b
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