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IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis
Salmonella genomic island 1 (SGI1) is an integrative mobilizable element integrated into the chromosome of bacteria, which plays an important role in the dissemination of antimicrobial resistance genes. Lots of SGI1 variants are found mainly in Salmonella enterica and Proteus mirabilis. In this stud...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769106/ https://www.ncbi.nlm.nih.gov/pubmed/31608048 http://dx.doi.org/10.3389/fmicb.2019.02245 |
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author | Wang, Xue-Chun Lei, Chang-Wei Kang, Zhuang-Zhuang Zhang, Yu Wang, Hong-Ning |
author_facet | Wang, Xue-Chun Lei, Chang-Wei Kang, Zhuang-Zhuang Zhang, Yu Wang, Hong-Ning |
author_sort | Wang, Xue-Chun |
collection | PubMed |
description | Salmonella genomic island 1 (SGI1) is an integrative mobilizable element integrated into the chromosome of bacteria, which plays an important role in the dissemination of antimicrobial resistance genes. Lots of SGI1 variants are found mainly in Salmonella enterica and Proteus mirabilis. In this study, a total of 157 S. enterica and 132 P. mirabilis strains were collected from food-producing animals in Sichuan Province of China between December 2016 and November 2017. Detection of the SGI1 integrase gene showed that three S. enterica and five P. mirabilis strains were positive for SGI1, which displayed different multidrug resistance profiles. Five different SGI1 variants, including two novel variants (SGI1-PmBC1123 and SGI1-PmSC1111), were characterized by whole genome sequencing and PCR linkage. In two novel SGI1 variants, IS26-mediated rearrangements resulted in large sequence inversions of the MDR regions extending outside the SGI1 backbone. The sul3-type III class 1 integron (5′CS-sat-psp-aadA2-cmlA1-aadA1-qacH-IS440-sul3) and gene cassettes aac(6′)-Ib-cr-bla(OXA–)(1)-catB3-arr-3 are found in SGI1-PmSC1111. Mobilization experiments indicated that three known variants were conjugally mobilized in trans to Escherichia coli with the help of a conjugative IncC plasmid. However, the two novel variants seemed to lose the mobilization, which might result from the sequence inversion of partial SGI1 backbone. The identification of the two novel SGI1 variants in this study suggested that IS26-mediated rearrangements promote the diversity of SGI1. |
format | Online Article Text |
id | pubmed-6769106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67691062019-10-11 IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis Wang, Xue-Chun Lei, Chang-Wei Kang, Zhuang-Zhuang Zhang, Yu Wang, Hong-Ning Front Microbiol Microbiology Salmonella genomic island 1 (SGI1) is an integrative mobilizable element integrated into the chromosome of bacteria, which plays an important role in the dissemination of antimicrobial resistance genes. Lots of SGI1 variants are found mainly in Salmonella enterica and Proteus mirabilis. In this study, a total of 157 S. enterica and 132 P. mirabilis strains were collected from food-producing animals in Sichuan Province of China between December 2016 and November 2017. Detection of the SGI1 integrase gene showed that three S. enterica and five P. mirabilis strains were positive for SGI1, which displayed different multidrug resistance profiles. Five different SGI1 variants, including two novel variants (SGI1-PmBC1123 and SGI1-PmSC1111), were characterized by whole genome sequencing and PCR linkage. In two novel SGI1 variants, IS26-mediated rearrangements resulted in large sequence inversions of the MDR regions extending outside the SGI1 backbone. The sul3-type III class 1 integron (5′CS-sat-psp-aadA2-cmlA1-aadA1-qacH-IS440-sul3) and gene cassettes aac(6′)-Ib-cr-bla(OXA–)(1)-catB3-arr-3 are found in SGI1-PmSC1111. Mobilization experiments indicated that three known variants were conjugally mobilized in trans to Escherichia coli with the help of a conjugative IncC plasmid. However, the two novel variants seemed to lose the mobilization, which might result from the sequence inversion of partial SGI1 backbone. The identification of the two novel SGI1 variants in this study suggested that IS26-mediated rearrangements promote the diversity of SGI1. Frontiers Media S.A. 2019-09-24 /pmc/articles/PMC6769106/ /pubmed/31608048 http://dx.doi.org/10.3389/fmicb.2019.02245 Text en Copyright © 2019 Wang, Lei, Kang, Zhang and Wang. 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 Wang, Xue-Chun Lei, Chang-Wei Kang, Zhuang-Zhuang Zhang, Yu Wang, Hong-Ning IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title_full | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title_fullStr | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title_full_unstemmed | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title_short | IS26-Mediated Genetic Rearrangements in Salmonella Genomic Island 1 of Proteus mirabilis |
title_sort | is26-mediated genetic rearrangements in salmonella genomic island 1 of proteus mirabilis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769106/ https://www.ncbi.nlm.nih.gov/pubmed/31608048 http://dx.doi.org/10.3389/fmicb.2019.02245 |
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