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Wikberg, E.

Publications and source records attributed to Wikberg, E..

2 recordsLinked to original sources

Social interactions across groups of colobus monkeys (Colobus vellerosus) explain similarities in their gut microbiomes

The gut microbiome is structured by social groups in a variety of host taxa. Whether this pattern is driven by relatedness, similar diets, or shared social environments is under debate because few studies have had access to the data necessary to disentangle these factors in wild populations. We investigated whether diet, relatedness, or the 1-meter proximity network best explains differences in the gut microbiome among 45 female colobus monkeys in 8 social groups residing at Boabeng-Fiema, Ghana. We combined demographic and behavioural data collected May-August 2007 and October 2008-April 2009 with 16S rRNA sequencing of faecal samples collected during the latter part of each observation period. Social group identity explained a large percentage of the variation in gut microbiome beta-diversity. When comparing the predictive power of dietary dissimilarity, relatedness, and connectedness in the 1-meter proximity network, the models with social connectedness received the strongest support, even in our analyses that excluded within-group dyads. This novel finding indicates that microbes may be transmitted during intergroup encounters, which could occur either indirectly via shared environments or directly via social contact. Lastly, some of the gut microbial taxa that appear to be transmitted via 1-meter proximity are associated with digestion of plant material, but further research is needed to investigate whether this type of gut microbe transmission yields health benefits, which could provide an incentive for the formation and maintenance of social bonds within and between social groups.

microbiology

Divergence in gut microbial communities mirrors a social group fission event in a black-and-white colobus monkey (Colobus vellerosus)

Host behavior and social factors have increasingly been implicated in structuring the composition of gut microbial communities. In social animals, distinct microbial communities characterize different social groups across a variety of taxa, although little longitudinal research has been conducted that demonstrates how this divergence occurs. Our study addresses this question by characterizing the gut microbial composition of an African Old World monkey, the black-and-white colobus (Colobus vellerosus), prior to and after a social group fission event. Gut microbial taxonomic composition of these monkeys was profiled using the V-4 hypervariable region of the bacterial 16s rRNA gene, and pairwise-relatedness values were calculated for all individuals using 17 STR loci and partial pedigree information. The two social groups in this study were found to harbor distinct microbial signatures after the fission event from which they emerged, while these communities were not divergent in the same individuals prior to this event. Three genera were found to differ in abundance between the two new social groups: Parabacteroides, Coprococcus, and Porphyromonadaceae. Additionally, although this fission happened partially along lines of relatedness, relatedness did not structure the differences that we found. Taken together, this study suggests that distinct gut microbial profiles can emerge in social groups in less than one year and recommends further work into more finely mapping the timescales, causes, and potentially adaptive effects of this recurring trend toward distinct group microbial signatures. Research highlightsO_LIDistinct gut microbial profiles emerge in two social groups of C. vellerosus less than nine months after a fission event. C_LIO_LIThree genera differ in abundance between the two new social groups. C_LIO_LIRelatedness does not structure differences in microbial composition between the groups. C_LI

ecology