Journal
ECOLOGY AND EVOLUTION
Volume 12, Issue 12, Pages -Publisher
WILEY
DOI: 10.1002/ece3.9674
Keywords
16 S rRNA gene sequencing; fish; gut microbiome; parallel evolution; trophic ecology
Categories
Funding
- Deutsche Forschungsgemeinschaft [458274593]
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Parallel evolution of host organisms is often accompanied by parallel changes of their associated microbial communities. However, quantitative approaches to studying microbiota parallelism have been rarely used. This study advocates for the use of multivariate vector analysis to quantify microbiota changes and provides an analytical framework for comparing host lineages. The results show that parallelism estimates are consistent with other statistical methods and might be stronger for microbiota function compared to taxonomic composition.
Parallel evolution of phenotypic traits is regarded as strong evidence for natural selection and has been studied extensively in a variety of taxa. However, we have limited knowledge of whether parallel evolution of host organisms is accompanied by parallel changes of their associated microbial communities (i.e., microbiotas), which are crucial for their hosts' ecology and evolution. Determining the extent of microbiota parallelism in nature can improve our ability to identify the factors that are associated with (putatively adaptive) shifts in microbial communities. While it has been emphasized that (non)parallel evolution is better considered as a quantitative continuum rather than a binary phenomenon, quantitative approaches have rarely been used to study microbiota parallelism. We advocate using multivariate vector analysis (i.e., phenotypic change vector analysis) to quantify direction and magnitude of microbiota changes and discuss the applicability of this approach for studying parallelism, and we compiled an R package for multivariate vector analysis of microbial communities ('multivarvector'). We exemplify its use by reanalyzing gut microbiota data from multiple fish species that exhibit parallel shifts in trophic ecology. We found that multivariate vector analysis results were largely consistent with other statistical methods, parallelism estimates were not affected by the taxonomic level at which the microbiota is studied, and parallelism might be stronger for gut microbiota function compared to taxonomic composition. This approach provides an analytical framework for quantitative comparisons across host lineages, thereby providing the potential to advance our capacity to predict microbiota changes. Hence, we emphasize that the development and application of quantitative measures, such as multivariate vector analysis, should be further explored in microbiota research in order to better understand the role of microbiota dynamics during their hosts' adaptive evolution, particularly in settings of parallel evolution.
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