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Microbial characterization based on multifractal analysis of metagenomes
INTRODUCTION: The species diversity of microbiomes is a cutting-edge concept in metagenomic research. In this study, we propose a multifractal analysis for metagenomic research. METHOD AND RESULTS: Firstly, we visualized the chaotic game representation (CGR) of simulated metagenomes and real metagen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910082/ https://www.ncbi.nlm.nih.gov/pubmed/36779183 http://dx.doi.org/10.3389/fcimb.2023.1117421 |
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author | Xie, Xian-hua Huang, Yu-jie Han, Guo-sheng Yu, Zu-guo Ma, Yuan-lin |
author_facet | Xie, Xian-hua Huang, Yu-jie Han, Guo-sheng Yu, Zu-guo Ma, Yuan-lin |
author_sort | Xie, Xian-hua |
collection | PubMed |
description | INTRODUCTION: The species diversity of microbiomes is a cutting-edge concept in metagenomic research. In this study, we propose a multifractal analysis for metagenomic research. METHOD AND RESULTS: Firstly, we visualized the chaotic game representation (CGR) of simulated metagenomes and real metagenomes. We find that metagenomes are visualized with self-similarity. Then we defined and calculated the multifractal dimension for the visualized plot of simulated and real metagenomes, respectively. By analyzing the Pearson correlation coefficients between the multifractal dimension and the traditional species diversity index, we obtain that the correlation coefficients between the multifractal dimension and the species richness index and Shannon diversity index reached the maximum value when q = 0, 1, and the correlation coefficient between the multifractal dimension and the Simpson diversity index reached the maximum value when q = 5. Finally, we apply our method to real metagenomes of the gut microbiota of 100 infants who are newborn and 4 and 12 months old. The results show that the multifractal dimensions of an infant's gut microbiomes can distinguish age differences. CONCLUSION AND DISCUSSION: There is self-similarity among the CGRs of WGS of metagenomes, and the multifractal spectrum is an important characteristic for metagenomes. The traditional diversity indicators can be unified under the framework of multifractal analysis. These results coincided with similar results in macrobial ecology. The multifractal spectrum of infants’ gut microbiomes are related to the development of the infants. |
format | Online Article Text |
id | pubmed-9910082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99100822023-02-10 Microbial characterization based on multifractal analysis of metagenomes Xie, Xian-hua Huang, Yu-jie Han, Guo-sheng Yu, Zu-guo Ma, Yuan-lin Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: The species diversity of microbiomes is a cutting-edge concept in metagenomic research. In this study, we propose a multifractal analysis for metagenomic research. METHOD AND RESULTS: Firstly, we visualized the chaotic game representation (CGR) of simulated metagenomes and real metagenomes. We find that metagenomes are visualized with self-similarity. Then we defined and calculated the multifractal dimension for the visualized plot of simulated and real metagenomes, respectively. By analyzing the Pearson correlation coefficients between the multifractal dimension and the traditional species diversity index, we obtain that the correlation coefficients between the multifractal dimension and the species richness index and Shannon diversity index reached the maximum value when q = 0, 1, and the correlation coefficient between the multifractal dimension and the Simpson diversity index reached the maximum value when q = 5. Finally, we apply our method to real metagenomes of the gut microbiota of 100 infants who are newborn and 4 and 12 months old. The results show that the multifractal dimensions of an infant's gut microbiomes can distinguish age differences. CONCLUSION AND DISCUSSION: There is self-similarity among the CGRs of WGS of metagenomes, and the multifractal spectrum is an important characteristic for metagenomes. The traditional diversity indicators can be unified under the framework of multifractal analysis. These results coincided with similar results in macrobial ecology. The multifractal spectrum of infants’ gut microbiomes are related to the development of the infants. Frontiers Media S.A. 2023-01-26 /pmc/articles/PMC9910082/ /pubmed/36779183 http://dx.doi.org/10.3389/fcimb.2023.1117421 Text en Copyright © 2023 Xie, Huang, Han, Yu and Ma https://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(s) 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 | Cellular and Infection Microbiology Xie, Xian-hua Huang, Yu-jie Han, Guo-sheng Yu, Zu-guo Ma, Yuan-lin Microbial characterization based on multifractal analysis of metagenomes |
title | Microbial characterization based on multifractal analysis of metagenomes |
title_full | Microbial characterization based on multifractal analysis of metagenomes |
title_fullStr | Microbial characterization based on multifractal analysis of metagenomes |
title_full_unstemmed | Microbial characterization based on multifractal analysis of metagenomes |
title_short | Microbial characterization based on multifractal analysis of metagenomes |
title_sort | microbial characterization based on multifractal analysis of metagenomes |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910082/ https://www.ncbi.nlm.nih.gov/pubmed/36779183 http://dx.doi.org/10.3389/fcimb.2023.1117421 |
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