Machine learning to predict the source of campylobacteriosis using whole genome data.

Campylobacteriosis is among the world's most common foodborne illnesses, caused predominantly by the bacterium Campylobacter jejuni. Effective interventions require determination of the infection source which is challenging as transmission occurs via multiple sources such as contaminated meat,...

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Autores principales: Nicolas Arning, Samuel K Sheppard, Sion Bayliss, David A Clifton, Daniel J Wilson
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/cc79937e580e4d55b76229528d8bdca3
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spelling oai:doaj.org-article:cc79937e580e4d55b76229528d8bdca32021-12-02T20:03:31ZMachine learning to predict the source of campylobacteriosis using whole genome data.1553-73901553-740410.1371/journal.pgen.1009436https://doaj.org/article/cc79937e580e4d55b76229528d8bdca32021-10-01T00:00:00Zhttps://doi.org/10.1371/journal.pgen.1009436https://doaj.org/toc/1553-7390https://doaj.org/toc/1553-7404Campylobacteriosis is among the world's most common foodborne illnesses, caused predominantly by the bacterium Campylobacter jejuni. Effective interventions require determination of the infection source which is challenging as transmission occurs via multiple sources such as contaminated meat, poultry, and drinking water. Strain variation has allowed source tracking based upon allelic variation in multi-locus sequence typing (MLST) genes allowing isolates from infected individuals to be attributed to specific animal or environmental reservoirs. However, the accuracy of probabilistic attribution models has been limited by the ability to differentiate isolates based upon just 7 MLST genes. Here, we broaden the input data spectrum to include core genome MLST (cgMLST) and whole genome sequences (WGS), and implement multiple machine learning algorithms, allowing more accurate source attribution. We increase attribution accuracy from 64% using the standard iSource population genetic approach to 71% for MLST, 85% for cgMLST and 78% for kmerized WGS data using the classifier we named aiSource. To gain insight beyond the source model prediction, we use Bayesian inference to analyse the relative affinity of C. jejuni strains to infect humans and identified potential differences, in source-human transmission ability among clonally related isolates in the most common disease causing lineage (ST-21 clonal complex). Providing generalizable computationally efficient methods, based upon machine learning and population genetics, we provide a scalable approach to global disease surveillance that can continuously incorporate novel samples for source attribution and identify fine-scale variation in transmission potential.Nicolas ArningSamuel K SheppardSion BaylissDavid A CliftonDaniel J WilsonPublic Library of Science (PLoS)articleGeneticsQH426-470ENPLoS Genetics, Vol 17, Iss 10, p e1009436 (2021)
institution DOAJ
collection DOAJ
language EN
topic Genetics
QH426-470
spellingShingle Genetics
QH426-470
Nicolas Arning
Samuel K Sheppard
Sion Bayliss
David A Clifton
Daniel J Wilson
Machine learning to predict the source of campylobacteriosis using whole genome data.
description Campylobacteriosis is among the world's most common foodborne illnesses, caused predominantly by the bacterium Campylobacter jejuni. Effective interventions require determination of the infection source which is challenging as transmission occurs via multiple sources such as contaminated meat, poultry, and drinking water. Strain variation has allowed source tracking based upon allelic variation in multi-locus sequence typing (MLST) genes allowing isolates from infected individuals to be attributed to specific animal or environmental reservoirs. However, the accuracy of probabilistic attribution models has been limited by the ability to differentiate isolates based upon just 7 MLST genes. Here, we broaden the input data spectrum to include core genome MLST (cgMLST) and whole genome sequences (WGS), and implement multiple machine learning algorithms, allowing more accurate source attribution. We increase attribution accuracy from 64% using the standard iSource population genetic approach to 71% for MLST, 85% for cgMLST and 78% for kmerized WGS data using the classifier we named aiSource. To gain insight beyond the source model prediction, we use Bayesian inference to analyse the relative affinity of C. jejuni strains to infect humans and identified potential differences, in source-human transmission ability among clonally related isolates in the most common disease causing lineage (ST-21 clonal complex). Providing generalizable computationally efficient methods, based upon machine learning and population genetics, we provide a scalable approach to global disease surveillance that can continuously incorporate novel samples for source attribution and identify fine-scale variation in transmission potential.
format article
author Nicolas Arning
Samuel K Sheppard
Sion Bayliss
David A Clifton
Daniel J Wilson
author_facet Nicolas Arning
Samuel K Sheppard
Sion Bayliss
David A Clifton
Daniel J Wilson
author_sort Nicolas Arning
title Machine learning to predict the source of campylobacteriosis using whole genome data.
title_short Machine learning to predict the source of campylobacteriosis using whole genome data.
title_full Machine learning to predict the source of campylobacteriosis using whole genome data.
title_fullStr Machine learning to predict the source of campylobacteriosis using whole genome data.
title_full_unstemmed Machine learning to predict the source of campylobacteriosis using whole genome data.
title_sort machine learning to predict the source of campylobacteriosis using whole genome data.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/cc79937e580e4d55b76229528d8bdca3
work_keys_str_mv AT nicolasarning machinelearningtopredictthesourceofcampylobacteriosisusingwholegenomedata
AT samuelksheppard machinelearningtopredictthesourceofcampylobacteriosisusingwholegenomedata
AT sionbayliss machinelearningtopredictthesourceofcampylobacteriosisusingwholegenomedata
AT davidaclifton machinelearningtopredictthesourceofcampylobacteriosisusingwholegenomedata
AT danieljwilson machinelearningtopredictthesourceofcampylobacteriosisusingwholegenomedata
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