Cargando…

Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission

Bacterial whole genome sequencing offers the prospect of rapid and high precision investigation of infectious disease outbreaks. Close genetic relationships between microorganisms isolated from different infected cases suggest transmission is a strong possibility, whereas transmission between cases...

Descripción completa

Detalles Bibliográficos
Autores principales: Eyre, David W., Cule, Madeleine L., Griffiths, David, Crook, Derrick W., Peto, Tim E. A., Walker, A. Sarah, Wilson, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642043/
https://www.ncbi.nlm.nih.gov/pubmed/23658511
http://dx.doi.org/10.1371/journal.pcbi.1003059
_version_ 1782268087882481664
author Eyre, David W.
Cule, Madeleine L.
Griffiths, David
Crook, Derrick W.
Peto, Tim E. A.
Walker, A. Sarah
Wilson, Daniel J.
author_facet Eyre, David W.
Cule, Madeleine L.
Griffiths, David
Crook, Derrick W.
Peto, Tim E. A.
Walker, A. Sarah
Wilson, Daniel J.
author_sort Eyre, David W.
collection PubMed
description Bacterial whole genome sequencing offers the prospect of rapid and high precision investigation of infectious disease outbreaks. Close genetic relationships between microorganisms isolated from different infected cases suggest transmission is a strong possibility, whereas transmission between cases with genetically distinct bacterial isolates can be excluded. However, undetected mixed infections—infection with ≥2 unrelated strains of the same species where only one is sequenced—potentially impairs exclusion of transmission with certainty, and may therefore limit the utility of this technique. We investigated the problem by developing a computationally efficient method for detecting mixed infection without the need for resource-intensive independent sequencing of multiple bacterial colonies. Given the relatively low density of single nucleotide polymorphisms within bacterial sequence data, direct reconstruction of mixed infection haplotypes from current short-read sequence data is not consistently possible. We therefore use a two-step maximum likelihood-based approach, assuming each sample contains up to two infecting strains. We jointly estimate the proportion of the infection arising from the dominant and minor strains, and the sequence divergence between these strains. In cases where mixed infection is confirmed, the dominant and minor haplotypes are then matched to a database of previously sequenced local isolates. We demonstrate the performance of our algorithm with in silico and in vitro mixed infection experiments, and apply it to transmission of an important healthcare-associated pathogen, Clostridium difficile. Using hospital ward movement data in a previously described stochastic transmission model, 15 pairs of cases enriched for likely transmission events associated with mixed infection were selected. Our method identified four previously undetected mixed infections, and a previously undetected transmission event, but no direct transmission between the pairs of cases under investigation. These results demonstrate that mixed infections can be detected without additional sequencing effort, and this will be important in assessing the extent of cryptic transmission in our hospitals.
format Online
Article
Text
id pubmed-3642043
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36420432013-05-08 Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission Eyre, David W. Cule, Madeleine L. Griffiths, David Crook, Derrick W. Peto, Tim E. A. Walker, A. Sarah Wilson, Daniel J. PLoS Comput Biol Research Article Bacterial whole genome sequencing offers the prospect of rapid and high precision investigation of infectious disease outbreaks. Close genetic relationships between microorganisms isolated from different infected cases suggest transmission is a strong possibility, whereas transmission between cases with genetically distinct bacterial isolates can be excluded. However, undetected mixed infections—infection with ≥2 unrelated strains of the same species where only one is sequenced—potentially impairs exclusion of transmission with certainty, and may therefore limit the utility of this technique. We investigated the problem by developing a computationally efficient method for detecting mixed infection without the need for resource-intensive independent sequencing of multiple bacterial colonies. Given the relatively low density of single nucleotide polymorphisms within bacterial sequence data, direct reconstruction of mixed infection haplotypes from current short-read sequence data is not consistently possible. We therefore use a two-step maximum likelihood-based approach, assuming each sample contains up to two infecting strains. We jointly estimate the proportion of the infection arising from the dominant and minor strains, and the sequence divergence between these strains. In cases where mixed infection is confirmed, the dominant and minor haplotypes are then matched to a database of previously sequenced local isolates. We demonstrate the performance of our algorithm with in silico and in vitro mixed infection experiments, and apply it to transmission of an important healthcare-associated pathogen, Clostridium difficile. Using hospital ward movement data in a previously described stochastic transmission model, 15 pairs of cases enriched for likely transmission events associated with mixed infection were selected. Our method identified four previously undetected mixed infections, and a previously undetected transmission event, but no direct transmission between the pairs of cases under investigation. These results demonstrate that mixed infections can be detected without additional sequencing effort, and this will be important in assessing the extent of cryptic transmission in our hospitals. Public Library of Science 2013-05-02 /pmc/articles/PMC3642043/ /pubmed/23658511 http://dx.doi.org/10.1371/journal.pcbi.1003059 Text en © 2013 Eyre et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Eyre, David W.
Cule, Madeleine L.
Griffiths, David
Crook, Derrick W.
Peto, Tim E. A.
Walker, A. Sarah
Wilson, Daniel J.
Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title_full Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title_fullStr Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title_full_unstemmed Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title_short Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission
title_sort detection of mixed infection from bacterial whole genome sequence data allows assessment of its role in clostridium difficile transmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642043/
https://www.ncbi.nlm.nih.gov/pubmed/23658511
http://dx.doi.org/10.1371/journal.pcbi.1003059
work_keys_str_mv AT eyredavidw detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT culemadeleinel detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT griffithsdavid detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT crookderrickw detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT petotimea detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT walkerasarah detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission
AT wilsondanielj detectionofmixedinfectionfrombacterialwholegenomesequencedataallowsassessmentofitsroleinclostridiumdifficiletransmission