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Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms
This study reports the comparative analyses of four Flavobacterium columnare isolates that have different virulence and antimicrobial resistance patterns. The main research goal was to reveal new insights into possible virulence genes by comparing the genomes of bacterial isolates that could induce...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881675/ https://www.ncbi.nlm.nih.gov/pubmed/33579339 http://dx.doi.org/10.1186/s13567-021-00899-w |
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author | Declercq, Annelies Maria Tilleman, Laurentijn Gansemans, Yannick De Witte, Chloë Haesebrouck, Freddy Van Nieuwerburgh, Filip Smet, Annemieke Decostere, Annemie |
author_facet | Declercq, Annelies Maria Tilleman, Laurentijn Gansemans, Yannick De Witte, Chloë Haesebrouck, Freddy Van Nieuwerburgh, Filip Smet, Annemieke Decostere, Annemie |
author_sort | Declercq, Annelies Maria |
collection | PubMed |
description | This study reports the comparative analyses of four Flavobacterium columnare isolates that have different virulence and antimicrobial resistance patterns. The main research goal was to reveal new insights into possible virulence genes by comparing the genomes of bacterial isolates that could induce tissue damage and mortality versus the genome of a non-virulent isolate. The results indicated that only the genomes of the virulent isolates possessed unique genes encoding amongst others a methyl-accepting chemotaxis protein possibly involved in the initial colonization of tissue, and several VgrG proteins engaged in interbacterial competition. Furthermore, comparisons of genes unique for the genomes of the highly virulent (HV) carp and trout isolates versus the, respectively, low and non-virulent carp and trout isolates were performed. An important part of the identified unique virulence genes of the HV-trout isolate was located in one particular gene region identified as a genomic island. This region contained araC and nodT genes, both linked to pathogenic and multidrug-resistance, and a luxR-gene, functional in bacterial cell-to-cell communication. Furthermore, the genome of the HV-trout isolate possessed unique sugar-transferases possibly important in bacterial adhesion. The second research goal was to obtain insights into the genetic basis of acquired antimicrobial resistance. Several point-mutations were discovered in gyrase-genes of an isolate showing phenotypic resistance towards first and second-generation quinolones, which were absent in isolates susceptible to quinolones. Tetracycline-resistance gene tetA was found in an isolate displaying acquired phenotypic resistance towards oxytetracycline. Although not localized on a prophage, several flanking genes were indicative of the gene’s mobile character. |
format | Online Article Text |
id | pubmed-7881675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78816752021-02-17 Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms Declercq, Annelies Maria Tilleman, Laurentijn Gansemans, Yannick De Witte, Chloë Haesebrouck, Freddy Van Nieuwerburgh, Filip Smet, Annemieke Decostere, Annemie Vet Res Research Article This study reports the comparative analyses of four Flavobacterium columnare isolates that have different virulence and antimicrobial resistance patterns. The main research goal was to reveal new insights into possible virulence genes by comparing the genomes of bacterial isolates that could induce tissue damage and mortality versus the genome of a non-virulent isolate. The results indicated that only the genomes of the virulent isolates possessed unique genes encoding amongst others a methyl-accepting chemotaxis protein possibly involved in the initial colonization of tissue, and several VgrG proteins engaged in interbacterial competition. Furthermore, comparisons of genes unique for the genomes of the highly virulent (HV) carp and trout isolates versus the, respectively, low and non-virulent carp and trout isolates were performed. An important part of the identified unique virulence genes of the HV-trout isolate was located in one particular gene region identified as a genomic island. This region contained araC and nodT genes, both linked to pathogenic and multidrug-resistance, and a luxR-gene, functional in bacterial cell-to-cell communication. Furthermore, the genome of the HV-trout isolate possessed unique sugar-transferases possibly important in bacterial adhesion. The second research goal was to obtain insights into the genetic basis of acquired antimicrobial resistance. Several point-mutations were discovered in gyrase-genes of an isolate showing phenotypic resistance towards first and second-generation quinolones, which were absent in isolates susceptible to quinolones. Tetracycline-resistance gene tetA was found in an isolate displaying acquired phenotypic resistance towards oxytetracycline. Although not localized on a prophage, several flanking genes were indicative of the gene’s mobile character. BioMed Central 2021-02-12 2021 /pmc/articles/PMC7881675/ /pubmed/33579339 http://dx.doi.org/10.1186/s13567-021-00899-w Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Declercq, Annelies Maria Tilleman, Laurentijn Gansemans, Yannick De Witte, Chloë Haesebrouck, Freddy Van Nieuwerburgh, Filip Smet, Annemieke Decostere, Annemie Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title | Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title_full | Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title_fullStr | Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title_full_unstemmed | Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title_short | Comparative genomics of Flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
title_sort | comparative genomics of flavobacterium columnare unveils novel insights in virulence and antimicrobial resistance mechanisms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881675/ https://www.ncbi.nlm.nih.gov/pubmed/33579339 http://dx.doi.org/10.1186/s13567-021-00899-w |
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