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Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype
Shiga toxin (Stx) is the key virulent factor in Shiga toxin-producing Escherichia coli (STEC). To date, three Stx1 subtypes and seven Stx2 subtypes have been described in E. coli, which differed in receptor preference and toxin potency. Here, we identified a novel Stx2 subtype designated Stx2h in E....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928088/ https://www.ncbi.nlm.nih.gov/pubmed/29712985 http://dx.doi.org/10.1038/s41598-018-25233-x |
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author | Bai, Xiangning Fu, Shanshan Zhang, Ji Fan, Ruyue Xu, Yanmei Sun, Hui He, Xiaohua Xu, Jianguo Xiong, Yanwen |
author_facet | Bai, Xiangning Fu, Shanshan Zhang, Ji Fan, Ruyue Xu, Yanmei Sun, Hui He, Xiaohua Xu, Jianguo Xiong, Yanwen |
author_sort | Bai, Xiangning |
collection | PubMed |
description | Shiga toxin (Stx) is the key virulent factor in Shiga toxin-producing Escherichia coli (STEC). To date, three Stx1 subtypes and seven Stx2 subtypes have been described in E. coli, which differed in receptor preference and toxin potency. Here, we identified a novel Stx2 subtype designated Stx2h in E. coli strains isolated from wild marmots in the Qinghai-Tibetan plateau, China. Stx2h shares 91.9% nucleic acid sequence identity and 92.9% amino acid identity to the nearest Stx2 subtype. The expression of Stx2h in type strain STEC299 was inducible by mitomycin C, and culture supernatant from STEC299 was cytotoxic to Vero cells. The Stx2h converting prophage was unique in terms of insertion site and genetic composition. Whole genome-based phylo- and patho-genomic analysis revealed STEC299 was closer to other pathotypes of E. coli than STEC, and possesses virulence factors from other pathotypes. Our finding enlarges the pool of Stx2 subtypes and highlights the extraordinary genomic plasticity of E. coli strains. As the emergence of new Shiga toxin genotypes and new Stx-producing pathotypes pose a great threat to the public health, Stx2h should be further included in E. coli molecular typing, and in epidemiological surveillance of E. coli infections. |
format | Online Article Text |
id | pubmed-5928088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59280882018-05-07 Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype Bai, Xiangning Fu, Shanshan Zhang, Ji Fan, Ruyue Xu, Yanmei Sun, Hui He, Xiaohua Xu, Jianguo Xiong, Yanwen Sci Rep Article Shiga toxin (Stx) is the key virulent factor in Shiga toxin-producing Escherichia coli (STEC). To date, three Stx1 subtypes and seven Stx2 subtypes have been described in E. coli, which differed in receptor preference and toxin potency. Here, we identified a novel Stx2 subtype designated Stx2h in E. coli strains isolated from wild marmots in the Qinghai-Tibetan plateau, China. Stx2h shares 91.9% nucleic acid sequence identity and 92.9% amino acid identity to the nearest Stx2 subtype. The expression of Stx2h in type strain STEC299 was inducible by mitomycin C, and culture supernatant from STEC299 was cytotoxic to Vero cells. The Stx2h converting prophage was unique in terms of insertion site and genetic composition. Whole genome-based phylo- and patho-genomic analysis revealed STEC299 was closer to other pathotypes of E. coli than STEC, and possesses virulence factors from other pathotypes. Our finding enlarges the pool of Stx2 subtypes and highlights the extraordinary genomic plasticity of E. coli strains. As the emergence of new Shiga toxin genotypes and new Stx-producing pathotypes pose a great threat to the public health, Stx2h should be further included in E. coli molecular typing, and in epidemiological surveillance of E. coli infections. Nature Publishing Group UK 2018-04-30 /pmc/articles/PMC5928088/ /pubmed/29712985 http://dx.doi.org/10.1038/s41598-018-25233-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bai, Xiangning Fu, Shanshan Zhang, Ji Fan, Ruyue Xu, Yanmei Sun, Hui He, Xiaohua Xu, Jianguo Xiong, Yanwen Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title | Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title_full | Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title_fullStr | Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title_full_unstemmed | Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title_short | Identification and pathogenomic analysis of an Escherichia coli strain producing a novel Shiga toxin 2 subtype |
title_sort | identification and pathogenomic analysis of an escherichia coli strain producing a novel shiga toxin 2 subtype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928088/ https://www.ncbi.nlm.nih.gov/pubmed/29712985 http://dx.doi.org/10.1038/s41598-018-25233-x |
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