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On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities

Identification of the majority of organisms present in human-associated microbial communities is feasible with the advent of high throughput sequencing technology. As substantial variability in microbiota communities is seen across subjects, the use of longitudinal study designs is important to bett...

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Autores principales: Wagner, Brandie D., Grunwald, Gary K., Zerbe, Gary O., Mikulich-Gilbertson, Susan K., Robertson, Charles E., Zemanick, Edith T., Harris, J. Kirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972327/
https://www.ncbi.nlm.nih.gov/pubmed/29872428
http://dx.doi.org/10.3389/fmicb.2018.01037
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author Wagner, Brandie D.
Grunwald, Gary K.
Zerbe, Gary O.
Mikulich-Gilbertson, Susan K.
Robertson, Charles E.
Zemanick, Edith T.
Harris, J. Kirk
author_facet Wagner, Brandie D.
Grunwald, Gary K.
Zerbe, Gary O.
Mikulich-Gilbertson, Susan K.
Robertson, Charles E.
Zemanick, Edith T.
Harris, J. Kirk
author_sort Wagner, Brandie D.
collection PubMed
description Identification of the majority of organisms present in human-associated microbial communities is feasible with the advent of high throughput sequencing technology. As substantial variability in microbiota communities is seen across subjects, the use of longitudinal study designs is important to better understand variation of the microbiome within individual subjects. Complex study designs with longitudinal sample collection require analytic approaches to account for this additional source of variability. A common approach to assessing community changes is to evaluate the change in alpha diversity (the variety and abundance of organisms in a community) over time. However, there are several commonly used alpha diversity measures and the use of different measures can result in different estimates of magnitude of change and different inferences. It has recently been proposed that diversity profile curves are useful for clarifying these differences, and may provide a more complete picture of the community structure. However, it is unclear how to utilize these curves when interest is in evaluating changes in community structure over time. We propose the use of a bi-exponential function in a longitudinal model that accounts for repeated measures on each subject to compare diversity profiles over time. Furthermore, it is possible that no change in alpha diversity (single community/sample) may be observed despite the presence of a highly divergent community composition. Thus, it is also important to use a beta diversity measure (similarity between multiple communities/samples) that captures changes in community composition. Ecological methods developed to evaluate temporal turnover have currently only been applied to investigate changes of a single community over time. We illustrate the extension of this approach to multiple communities of interest (i.e., subjects) by modeling the beta diversity measure over time. With this approach, a rate of change in community composition is estimated. There is a need for the extension and development of analytic methods for longitudinal microbiota studies. In this paper, we discuss different approaches to model alpha and beta diversity indices in longitudinal microbiota studies and provide both a review of current approaches and a proposal for new methods.
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spelling pubmed-59723272018-06-05 On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities Wagner, Brandie D. Grunwald, Gary K. Zerbe, Gary O. Mikulich-Gilbertson, Susan K. Robertson, Charles E. Zemanick, Edith T. Harris, J. Kirk Front Microbiol Microbiology Identification of the majority of organisms present in human-associated microbial communities is feasible with the advent of high throughput sequencing technology. As substantial variability in microbiota communities is seen across subjects, the use of longitudinal study designs is important to better understand variation of the microbiome within individual subjects. Complex study designs with longitudinal sample collection require analytic approaches to account for this additional source of variability. A common approach to assessing community changes is to evaluate the change in alpha diversity (the variety and abundance of organisms in a community) over time. However, there are several commonly used alpha diversity measures and the use of different measures can result in different estimates of magnitude of change and different inferences. It has recently been proposed that diversity profile curves are useful for clarifying these differences, and may provide a more complete picture of the community structure. However, it is unclear how to utilize these curves when interest is in evaluating changes in community structure over time. We propose the use of a bi-exponential function in a longitudinal model that accounts for repeated measures on each subject to compare diversity profiles over time. Furthermore, it is possible that no change in alpha diversity (single community/sample) may be observed despite the presence of a highly divergent community composition. Thus, it is also important to use a beta diversity measure (similarity between multiple communities/samples) that captures changes in community composition. Ecological methods developed to evaluate temporal turnover have currently only been applied to investigate changes of a single community over time. We illustrate the extension of this approach to multiple communities of interest (i.e., subjects) by modeling the beta diversity measure over time. With this approach, a rate of change in community composition is estimated. There is a need for the extension and development of analytic methods for longitudinal microbiota studies. In this paper, we discuss different approaches to model alpha and beta diversity indices in longitudinal microbiota studies and provide both a review of current approaches and a proposal for new methods. Frontiers Media S.A. 2018-05-22 /pmc/articles/PMC5972327/ /pubmed/29872428 http://dx.doi.org/10.3389/fmicb.2018.01037 Text en Copyright © 2018 Wagner, Grunwald, Zerbe, Mikulich-Gilbertson, Robertson, Zemanick and Harris. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wagner, Brandie D.
Grunwald, Gary K.
Zerbe, Gary O.
Mikulich-Gilbertson, Susan K.
Robertson, Charles E.
Zemanick, Edith T.
Harris, J. Kirk
On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title_full On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title_fullStr On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title_full_unstemmed On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title_short On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities
title_sort on the use of diversity measures in longitudinal sequencing studies of microbial communities
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972327/
https://www.ncbi.nlm.nih.gov/pubmed/29872428
http://dx.doi.org/10.3389/fmicb.2018.01037
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