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Fingerprinting cities: differentiating subway microbiome functionality

BACKGROUND: Accumulating evidence suggests that the human microbiome impacts individual and public health. City subway systems are human-dense environments, where passengers often exchange microbes. The MetaSUB project participants collected samples from subway surfaces in different cities and perfo...

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Autores principales: Zhu, Chengsheng, Miller, Maximilian, Lusskin, Nick, Mahlich, Yannick, Wang, Yanran, Zeng, Zishuo, Bromberg, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822482/
https://www.ncbi.nlm.nih.gov/pubmed/31666099
http://dx.doi.org/10.1186/s13062-019-0252-y
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author Zhu, Chengsheng
Miller, Maximilian
Lusskin, Nick
Mahlich, Yannick
Wang, Yanran
Zeng, Zishuo
Bromberg, Yana
author_facet Zhu, Chengsheng
Miller, Maximilian
Lusskin, Nick
Mahlich, Yannick
Wang, Yanran
Zeng, Zishuo
Bromberg, Yana
author_sort Zhu, Chengsheng
collection PubMed
description BACKGROUND: Accumulating evidence suggests that the human microbiome impacts individual and public health. City subway systems are human-dense environments, where passengers often exchange microbes. The MetaSUB project participants collected samples from subway surfaces in different cities and performed metagenomic sequencing. Previous studies focused on taxonomic composition of these microbiomes and no explicit functional analysis had been done till now. RESULTS: As a part of the 2018 CAMDA challenge, we functionally profiled the available ~ 400 subway metagenomes and built predictor for city origin. In cross-validation, our model reached 81% accuracy when only the top-ranked city assignment was considered and 95% accuracy if the second city was taken into account as well. Notably, this performance was only achievable if the similarity of distribution of cities in the training and testing sets was similar. To assure that our methods are applicable without such biased assumptions we balanced our training data to account for all represented cities equally well. After balancing, the performance of our method was slightly lower (76/94%, respectively, for one or two top ranked cities), but still consistently high. Here we attained an added benefit of independence of training set city representation. In testing, our unbalanced model thus reached (an over-estimated) performance of 90/97%, while our balanced model was at a more reliable 63/90% accuracy. While, by definition of our model, we were not able to predict the microbiome origins previously unseen, our balanced model correctly judged them to be NOT-from-training-cities over 80% of the time. Our function-based outlook on microbiomes also allowed us to note similarities between both regionally close and far-away cities. Curiously, we identified the depletion in mycobacterial functions as a signature of cities in New Zealand, while photosynthesis related functions fingerprinted New York, Porto and Tokyo. CONCLUSIONS: We demonstrated the power of our high-speed function annotation method, mi-faser, by analysing ~ 400 shotgun metagenomes in 2 days, with the results recapitulating functional signals of different city subway microbiomes. We also showed the importance of balanced data in avoiding over-estimated performance. Our results revealed similarities between both geographically close (Ofa and Ilorin) and distant (Boston and Porto, Lisbon and New York) city subway microbiomes. The photosynthesis related functional signatures of NYC were previously unseen in taxonomy studies, highlighting the strength of functional analysis.
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spelling pubmed-68224822019-11-06 Fingerprinting cities: differentiating subway microbiome functionality Zhu, Chengsheng Miller, Maximilian Lusskin, Nick Mahlich, Yannick Wang, Yanran Zeng, Zishuo Bromberg, Yana Biol Direct Research BACKGROUND: Accumulating evidence suggests that the human microbiome impacts individual and public health. City subway systems are human-dense environments, where passengers often exchange microbes. The MetaSUB project participants collected samples from subway surfaces in different cities and performed metagenomic sequencing. Previous studies focused on taxonomic composition of these microbiomes and no explicit functional analysis had been done till now. RESULTS: As a part of the 2018 CAMDA challenge, we functionally profiled the available ~ 400 subway metagenomes and built predictor for city origin. In cross-validation, our model reached 81% accuracy when only the top-ranked city assignment was considered and 95% accuracy if the second city was taken into account as well. Notably, this performance was only achievable if the similarity of distribution of cities in the training and testing sets was similar. To assure that our methods are applicable without such biased assumptions we balanced our training data to account for all represented cities equally well. After balancing, the performance of our method was slightly lower (76/94%, respectively, for one or two top ranked cities), but still consistently high. Here we attained an added benefit of independence of training set city representation. In testing, our unbalanced model thus reached (an over-estimated) performance of 90/97%, while our balanced model was at a more reliable 63/90% accuracy. While, by definition of our model, we were not able to predict the microbiome origins previously unseen, our balanced model correctly judged them to be NOT-from-training-cities over 80% of the time. Our function-based outlook on microbiomes also allowed us to note similarities between both regionally close and far-away cities. Curiously, we identified the depletion in mycobacterial functions as a signature of cities in New Zealand, while photosynthesis related functions fingerprinted New York, Porto and Tokyo. CONCLUSIONS: We demonstrated the power of our high-speed function annotation method, mi-faser, by analysing ~ 400 shotgun metagenomes in 2 days, with the results recapitulating functional signals of different city subway microbiomes. We also showed the importance of balanced data in avoiding over-estimated performance. Our results revealed similarities between both geographically close (Ofa and Ilorin) and distant (Boston and Porto, Lisbon and New York) city subway microbiomes. The photosynthesis related functional signatures of NYC were previously unseen in taxonomy studies, highlighting the strength of functional analysis. BioMed Central 2019-10-30 /pmc/articles/PMC6822482/ /pubmed/31666099 http://dx.doi.org/10.1186/s13062-019-0252-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhu, Chengsheng
Miller, Maximilian
Lusskin, Nick
Mahlich, Yannick
Wang, Yanran
Zeng, Zishuo
Bromberg, Yana
Fingerprinting cities: differentiating subway microbiome functionality
title Fingerprinting cities: differentiating subway microbiome functionality
title_full Fingerprinting cities: differentiating subway microbiome functionality
title_fullStr Fingerprinting cities: differentiating subway microbiome functionality
title_full_unstemmed Fingerprinting cities: differentiating subway microbiome functionality
title_short Fingerprinting cities: differentiating subway microbiome functionality
title_sort fingerprinting cities: differentiating subway microbiome functionality
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822482/
https://www.ncbi.nlm.nih.gov/pubmed/31666099
http://dx.doi.org/10.1186/s13062-019-0252-y
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