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Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host
Campylobacteriosis typically manifests as a short-lived, self-limiting gastrointestinal infection in humans, however prolonged infection can be seen in cases with underlying immunodeficiency. Public Health England received 25 isolates of Campylobacter jejuni from an individual with combined variable...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308304/ https://www.ncbi.nlm.nih.gov/pubmed/32572150 http://dx.doi.org/10.1038/s41598-020-66771-7 |
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author | Barker, Clare R. Painset, Anaïs Swift, Craig Jenkins, Claire Godbole, Gauri Maiden, Martin C. J. Dallman, Timothy J. |
author_facet | Barker, Clare R. Painset, Anaïs Swift, Craig Jenkins, Claire Godbole, Gauri Maiden, Martin C. J. Dallman, Timothy J. |
author_sort | Barker, Clare R. |
collection | PubMed |
description | Campylobacteriosis typically manifests as a short-lived, self-limiting gastrointestinal infection in humans, however prolonged infection can be seen in cases with underlying immunodeficiency. Public Health England received 25 isolates of Campylobacter jejuni from an individual with combined variable immunodeficiency over a period of 15 years. All isolates were typed and archived at the time of receipt. Whole genome sequencing (WGS) and antimicrobial susceptibility testing were performed to examine the relatedness of the isolates and to investigate the changes in the genome that had taken place over the course of the infection. Genomic typing methods were compared to conventional phenotypic methods, and revealed that the infection was caused by a single, persistent strain of C. jejuni belonging to clonal complex ST-45, with evidence of adaptation and selection in the genome over the course of the infection. Genomic analysis of sequence variants associated with antimicrobial resistance identified the genetic background behind rRNA gene mutations causing variable levels of resistance to erythromycin. This application of WGS to examine a persistent case of campylobacteriosis provides insight into the mutations and selective pressures occurring over the course of an infection, some of which have important clinical relevance. |
format | Online Article Text |
id | pubmed-7308304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73083042020-06-23 Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host Barker, Clare R. Painset, Anaïs Swift, Craig Jenkins, Claire Godbole, Gauri Maiden, Martin C. J. Dallman, Timothy J. Sci Rep Article Campylobacteriosis typically manifests as a short-lived, self-limiting gastrointestinal infection in humans, however prolonged infection can be seen in cases with underlying immunodeficiency. Public Health England received 25 isolates of Campylobacter jejuni from an individual with combined variable immunodeficiency over a period of 15 years. All isolates were typed and archived at the time of receipt. Whole genome sequencing (WGS) and antimicrobial susceptibility testing were performed to examine the relatedness of the isolates and to investigate the changes in the genome that had taken place over the course of the infection. Genomic typing methods were compared to conventional phenotypic methods, and revealed that the infection was caused by a single, persistent strain of C. jejuni belonging to clonal complex ST-45, with evidence of adaptation and selection in the genome over the course of the infection. Genomic analysis of sequence variants associated with antimicrobial resistance identified the genetic background behind rRNA gene mutations causing variable levels of resistance to erythromycin. This application of WGS to examine a persistent case of campylobacteriosis provides insight into the mutations and selective pressures occurring over the course of an infection, some of which have important clinical relevance. Nature Publishing Group UK 2020-06-22 /pmc/articles/PMC7308304/ /pubmed/32572150 http://dx.doi.org/10.1038/s41598-020-66771-7 Text en © The Author(s) 2020 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 Barker, Clare R. Painset, Anaïs Swift, Craig Jenkins, Claire Godbole, Gauri Maiden, Martin C. J. Dallman, Timothy J. Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title | Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title_full | Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title_fullStr | Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title_full_unstemmed | Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title_short | Microevolution of Campylobacter jejuni during long-term infection in an immunocompromised host |
title_sort | microevolution of campylobacter jejuni during long-term infection in an immunocompromised host |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308304/ https://www.ncbi.nlm.nih.gov/pubmed/32572150 http://dx.doi.org/10.1038/s41598-020-66771-7 |
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