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Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens

BACKGROUND: Campylobacter jejuni is a pervasive pathogen of major public health concern with a complex ecology requiring accurate and informative approaches to define pathogen diversity during outbreak investigations. Source attribution analysis may be confounded if the genetic diversity of a C. jej...

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Autores principales: Djeghout, Bilal, Bloomfield, Samuel J., Rudder, Steven, Elumogo, Ngozi, Mather, Alison E., Wain, John, Janecko, Nicol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727990/
https://www.ncbi.nlm.nih.gov/pubmed/36476389
http://dx.doi.org/10.1186/s13099-022-00520-1
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author Djeghout, Bilal
Bloomfield, Samuel J.
Rudder, Steven
Elumogo, Ngozi
Mather, Alison E.
Wain, John
Janecko, Nicol
author_facet Djeghout, Bilal
Bloomfield, Samuel J.
Rudder, Steven
Elumogo, Ngozi
Mather, Alison E.
Wain, John
Janecko, Nicol
author_sort Djeghout, Bilal
collection PubMed
description BACKGROUND: Campylobacter jejuni is a pervasive pathogen of major public health concern with a complex ecology requiring accurate and informative approaches to define pathogen diversity during outbreak investigations. Source attribution analysis may be confounded if the genetic diversity of a C. jejuni population is not adequately captured in a single specimen. The aim of this study was to determine the genomic diversity of C. jejuni within individual stool specimens from four campylobacteriosis patients. Direct plating and pre-culture filtration of one stool specimen per patient was used to culture multiple isolates per stool specimen. Whole genome sequencing and pangenome level analysis were used to investigate genomic diversity of C. jejuni within a patient. RESULTS: A total 92 C. jejuni isolates were recovered from four patients presenting with gastroenteritis. The number of isolates ranged from 13 to 30 per patient stool. Three patients yielded a single C. jejuni multilocus sequence type: ST-21 (n = 26, patient 4), ST-61 (n = 30, patient 1) and ST-2066 (n = 23, patient 2). Patient 3 was infected with two different sequence types [ST-51 (n = 12) and ST-354 (n = 1)]. Isolates belonging to the same sequence type from the same patient specimen shared 12–43 core non-recombinant SNPs and 0–20 frameshifts with each other, and the pangenomes of each sequence type consisted of 1406–1491 core genes and 231–264 accessory genes. However, neither the mutation nor the accessory genes were connected to a specific functional gene category. CONCLUSIONS: Our findings show that the C. jejuni population recovered from an individual patient’s stool are genetically diverse even within the same ST and may have shared common ancestors before specimens were obtained. The population is unlikely to have evolved from a single isolate at the time point of initial patient infection, leading us to conclude that patients were likely infected with a heterogeneous C. jejuni population. The diversity of the C. jejuni population found within individual stool specimens can inform future methodological approaches to attribution and outbreak investigations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00520-1.
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spelling pubmed-97279902022-12-08 Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens Djeghout, Bilal Bloomfield, Samuel J. Rudder, Steven Elumogo, Ngozi Mather, Alison E. Wain, John Janecko, Nicol Gut Pathog Research BACKGROUND: Campylobacter jejuni is a pervasive pathogen of major public health concern with a complex ecology requiring accurate and informative approaches to define pathogen diversity during outbreak investigations. Source attribution analysis may be confounded if the genetic diversity of a C. jejuni population is not adequately captured in a single specimen. The aim of this study was to determine the genomic diversity of C. jejuni within individual stool specimens from four campylobacteriosis patients. Direct plating and pre-culture filtration of one stool specimen per patient was used to culture multiple isolates per stool specimen. Whole genome sequencing and pangenome level analysis were used to investigate genomic diversity of C. jejuni within a patient. RESULTS: A total 92 C. jejuni isolates were recovered from four patients presenting with gastroenteritis. The number of isolates ranged from 13 to 30 per patient stool. Three patients yielded a single C. jejuni multilocus sequence type: ST-21 (n = 26, patient 4), ST-61 (n = 30, patient 1) and ST-2066 (n = 23, patient 2). Patient 3 was infected with two different sequence types [ST-51 (n = 12) and ST-354 (n = 1)]. Isolates belonging to the same sequence type from the same patient specimen shared 12–43 core non-recombinant SNPs and 0–20 frameshifts with each other, and the pangenomes of each sequence type consisted of 1406–1491 core genes and 231–264 accessory genes. However, neither the mutation nor the accessory genes were connected to a specific functional gene category. CONCLUSIONS: Our findings show that the C. jejuni population recovered from an individual patient’s stool are genetically diverse even within the same ST and may have shared common ancestors before specimens were obtained. The population is unlikely to have evolved from a single isolate at the time point of initial patient infection, leading us to conclude that patients were likely infected with a heterogeneous C. jejuni population. The diversity of the C. jejuni population found within individual stool specimens can inform future methodological approaches to attribution and outbreak investigations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00520-1. BioMed Central 2022-12-07 /pmc/articles/PMC9727990/ /pubmed/36476389 http://dx.doi.org/10.1186/s13099-022-00520-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Djeghout, Bilal
Bloomfield, Samuel J.
Rudder, Steven
Elumogo, Ngozi
Mather, Alison E.
Wain, John
Janecko, Nicol
Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title_full Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title_fullStr Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title_full_unstemmed Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title_short Comparative genomics of Campylobacter jejuni from clinical campylobacteriosis stool specimens
title_sort comparative genomics of campylobacter jejuni from clinical campylobacteriosis stool specimens
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727990/
https://www.ncbi.nlm.nih.gov/pubmed/36476389
http://dx.doi.org/10.1186/s13099-022-00520-1
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