Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases

Group B <i>Streptococcus</i> (GBS) is an important pathogen of neonatal infections, and the clonal complex (CC)-17/serotype III GBS strain has emerged as the dominant strain. The clinical manifestations of CC17/III GBS sepsis may vary greatly but have not been well-investigated. A total...

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Autores principales: Jen-Fu Hsu, Jang-Jih Lu, Chih Lin, Shih-Ming Chu, Lee-Chung Lin, Mei-Yin Lai, Hsuan-Rong Huang, Ming-Chou Chiang, Ming-Horng Tsai
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/7f0b4f77ba79480596f21f4377a55b19
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spelling oai:doaj.org-article:7f0b4f77ba79480596f21f4377a55b192021-11-11T17:06:12ZClustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases10.3390/ijms2221116261422-00671661-6596https://doaj.org/article/7f0b4f77ba79480596f21f4377a55b192021-10-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11626https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Group B <i>Streptococcus</i> (GBS) is an important pathogen of neonatal infections, and the clonal complex (CC)-17/serotype III GBS strain has emerged as the dominant strain. The clinical manifestations of CC17/III GBS sepsis may vary greatly but have not been well-investigated. A total of 103 CC17/III GBS isolates that caused neonatal invasive diseases were studied using a new approach based on clustered regularly interspaced short palindromic repeats (CRISPR) loci and restriction fragment length polymorphism (RFLP) analyses. All spacers of CRISPR loci were sequenced and analyzed with the clinical presentations. After CRISPR-RFLP analyses, a total of 11 different patterns were observed among the 103 CRISPR-positive GBS isolates. GBS isolates with the same RFLP patterns were found to have highly comparable spacer contents. Comparative sequence analysis of the CRISPR1 spacer content revealed that it is highly diverse and consistent with the dynamics of this system. A total of 29 of 43 (67.4%) spacers displayed homology to reported phage and plasmid DNA sequences. In addition, all CC17/III GBS isolates could be categorized into three subgroups based on the CRISPR-RFLP patterns and eBURST analysis. The CC17/III GBS isolates with a specific CRISPR-RFLP pattern were more significantly associated with occurrences of severe sepsis (57.1% vs. 29.3%, <i>p</i> = 0.012) and meningitis (50.0% vs. 20.8%, <i>p</i> = 0.009) than GBS isolates with RFLP lengths between 1000 and 1300 bp. Whole-genome sequencing was also performed to verify the differences between CC17/III GBS isolates with different CRISPR-RFLP patterns. We concluded that the CRISPR-RFLP analysis is potentially applicable to categorizing CC17/III GBS isolates, and a specific CRISPR-RFLP pattern could be used as a new biomarker to predict meningitis and illness severity after further verification.Jen-Fu HsuJang-Jih LuChih LinShih-Ming ChuLee-Chung LinMei-Yin LaiHsuan-Rong HuangMing-Chou ChiangMing-Horng TsaiMDPI AGarticlegroup B <i>Streptococcus</i>CRISPRmultilocus sequence typingantimicrobial resistancephageBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11626, p 11626 (2021)
institution DOAJ
collection DOAJ
language EN
topic group B <i>Streptococcus</i>
CRISPR
multilocus sequence typing
antimicrobial resistance
phage
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle group B <i>Streptococcus</i>
CRISPR
multilocus sequence typing
antimicrobial resistance
phage
Biology (General)
QH301-705.5
Chemistry
QD1-999
Jen-Fu Hsu
Jang-Jih Lu
Chih Lin
Shih-Ming Chu
Lee-Chung Lin
Mei-Yin Lai
Hsuan-Rong Huang
Ming-Chou Chiang
Ming-Horng Tsai
Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
description Group B <i>Streptococcus</i> (GBS) is an important pathogen of neonatal infections, and the clonal complex (CC)-17/serotype III GBS strain has emerged as the dominant strain. The clinical manifestations of CC17/III GBS sepsis may vary greatly but have not been well-investigated. A total of 103 CC17/III GBS isolates that caused neonatal invasive diseases were studied using a new approach based on clustered regularly interspaced short palindromic repeats (CRISPR) loci and restriction fragment length polymorphism (RFLP) analyses. All spacers of CRISPR loci were sequenced and analyzed with the clinical presentations. After CRISPR-RFLP analyses, a total of 11 different patterns were observed among the 103 CRISPR-positive GBS isolates. GBS isolates with the same RFLP patterns were found to have highly comparable spacer contents. Comparative sequence analysis of the CRISPR1 spacer content revealed that it is highly diverse and consistent with the dynamics of this system. A total of 29 of 43 (67.4%) spacers displayed homology to reported phage and plasmid DNA sequences. In addition, all CC17/III GBS isolates could be categorized into three subgroups based on the CRISPR-RFLP patterns and eBURST analysis. The CC17/III GBS isolates with a specific CRISPR-RFLP pattern were more significantly associated with occurrences of severe sepsis (57.1% vs. 29.3%, <i>p</i> = 0.012) and meningitis (50.0% vs. 20.8%, <i>p</i> = 0.009) than GBS isolates with RFLP lengths between 1000 and 1300 bp. Whole-genome sequencing was also performed to verify the differences between CC17/III GBS isolates with different CRISPR-RFLP patterns. We concluded that the CRISPR-RFLP analysis is potentially applicable to categorizing CC17/III GBS isolates, and a specific CRISPR-RFLP pattern could be used as a new biomarker to predict meningitis and illness severity after further verification.
format article
author Jen-Fu Hsu
Jang-Jih Lu
Chih Lin
Shih-Ming Chu
Lee-Chung Lin
Mei-Yin Lai
Hsuan-Rong Huang
Ming-Chou Chiang
Ming-Horng Tsai
author_facet Jen-Fu Hsu
Jang-Jih Lu
Chih Lin
Shih-Ming Chu
Lee-Chung Lin
Mei-Yin Lai
Hsuan-Rong Huang
Ming-Chou Chiang
Ming-Horng Tsai
author_sort Jen-Fu Hsu
title Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
title_short Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
title_full Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
title_fullStr Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
title_full_unstemmed Clustered Regularly Interspaced Short Palindromic Repeat Analysis of Clonal Complex 17 Serotype III Group B <i>Streptococcus</i> Strains Causing Neonatal Invasive Diseases
title_sort clustered regularly interspaced short palindromic repeat analysis of clonal complex 17 serotype iii group b <i>streptococcus</i> strains causing neonatal invasive diseases
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/7f0b4f77ba79480596f21f4377a55b19
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