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Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals

Klebsiella pneumoniae is an important nosocomial infectious agent with a high antimicrobial resistance (AMR) burden. The application of long read sequencing technologies is providing insights into bacterial chromosomal and putative extra-chromosomal genetic elements (PEGEs) associated with AMR, but...

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Autores principales: Spadar, Anton, Perdigão, João, Phelan, Jody, Charleston, James, Modesto, Ana, Elias, Rita, de Sessions, Paola Florez, Hibberd, Martin L., Campino, Susana, Duarte, Aida, Clark, Taane G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985491/
https://www.ncbi.nlm.nih.gov/pubmed/33753763
http://dx.doi.org/10.1038/s41598-021-85724-2
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author Spadar, Anton
Perdigão, João
Phelan, Jody
Charleston, James
Modesto, Ana
Elias, Rita
de Sessions, Paola Florez
Hibberd, Martin L.
Campino, Susana
Duarte, Aida
Clark, Taane G.
author_facet Spadar, Anton
Perdigão, João
Phelan, Jody
Charleston, James
Modesto, Ana
Elias, Rita
de Sessions, Paola Florez
Hibberd, Martin L.
Campino, Susana
Duarte, Aida
Clark, Taane G.
author_sort Spadar, Anton
collection PubMed
description Klebsiella pneumoniae is an important nosocomial infectious agent with a high antimicrobial resistance (AMR) burden. The application of long read sequencing technologies is providing insights into bacterial chromosomal and putative extra-chromosomal genetic elements (PEGEs) associated with AMR, but also epigenetic DNA methylation, which is thought to play a role in cleavage of foreign DNA and expression regulation. Here, we apply the PacBio sequencing platform to eight Portuguese hospital isolates, including one carbapenemase producing isolate, to identify methylation motifs. The resulting assembled chromosomes were between 5.2 and 5.5Mbp in length, and twenty-six PEGEs were found. Four of our eight samples carry bla(CTX-M-15), a dominant Extended Spectrum Beta Lactamase in Europe. We identified methylation motifs that control Restriction–Modification systems, including GATC of the DNA adenine methylase (Dam), which methylates N6-methyladenine (m6A) across all our K. pneumoniae assemblies. There was a consistent lack of methylation by Dam of the GATC motif downstream of two genes: fosA, a locus associated with low level fosfomycin resistance, and tnpB transposase on IncFIB(K) plasmids. Overall, we have constructed eight high quality reference genomes of K. pneumoniae, with insights into horizontal gene transfer and methylation m6A motifs.
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spelling pubmed-79854912021-03-25 Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals Spadar, Anton Perdigão, João Phelan, Jody Charleston, James Modesto, Ana Elias, Rita de Sessions, Paola Florez Hibberd, Martin L. Campino, Susana Duarte, Aida Clark, Taane G. Sci Rep Article Klebsiella pneumoniae is an important nosocomial infectious agent with a high antimicrobial resistance (AMR) burden. The application of long read sequencing technologies is providing insights into bacterial chromosomal and putative extra-chromosomal genetic elements (PEGEs) associated with AMR, but also epigenetic DNA methylation, which is thought to play a role in cleavage of foreign DNA and expression regulation. Here, we apply the PacBio sequencing platform to eight Portuguese hospital isolates, including one carbapenemase producing isolate, to identify methylation motifs. The resulting assembled chromosomes were between 5.2 and 5.5Mbp in length, and twenty-six PEGEs were found. Four of our eight samples carry bla(CTX-M-15), a dominant Extended Spectrum Beta Lactamase in Europe. We identified methylation motifs that control Restriction–Modification systems, including GATC of the DNA adenine methylase (Dam), which methylates N6-methyladenine (m6A) across all our K. pneumoniae assemblies. There was a consistent lack of methylation by Dam of the GATC motif downstream of two genes: fosA, a locus associated with low level fosfomycin resistance, and tnpB transposase on IncFIB(K) plasmids. Overall, we have constructed eight high quality reference genomes of K. pneumoniae, with insights into horizontal gene transfer and methylation m6A motifs. Nature Publishing Group UK 2021-03-22 /pmc/articles/PMC7985491/ /pubmed/33753763 http://dx.doi.org/10.1038/s41598-021-85724-2 Text en © The Author(s) 2021 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 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/.
spellingShingle Article
Spadar, Anton
Perdigão, João
Phelan, Jody
Charleston, James
Modesto, Ana
Elias, Rita
de Sessions, Paola Florez
Hibberd, Martin L.
Campino, Susana
Duarte, Aida
Clark, Taane G.
Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title_full Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title_fullStr Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title_full_unstemmed Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title_short Methylation analysis of Klebsiella pneumoniae from Portuguese hospitals
title_sort methylation analysis of klebsiella pneumoniae from portuguese hospitals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985491/
https://www.ncbi.nlm.nih.gov/pubmed/33753763
http://dx.doi.org/10.1038/s41598-021-85724-2
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