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Biology subjects

Dominguez, J. H.

Publications and source records attributed to Dominguez, J. H..

2 recordsLinked to original sources

Does host diversity beget microbiome diversity? Effects of zooplankton diversity and composition on environmental and host-associated microbes

Microbiomes alter host health and are shaped by transmission within and among host taxa. Microbes can alter host communities, yet whether the diversity of hosts reciprocally shapes microbial communities remains poorly resolved. Diverse host communities may promote microbiome diversity through elevated cross-species microbial spillover or reduce it by diluting conspecific transmission. Here, we manipulated the composition and diversity of pond zooplankton communities to test how host diversity and density alter host-associated and environmental microbiomes. Host diversity had opposing effects on microbiome alpha diversity for different zooplankton host species, increasing microbiome diversity in calanoid copepods while reducing it in Daphnia, with no effect on environmental microbes. Host diversity amplified cross-species microbial spillover for subordinate competitors (calanoid copepods) and diluted conspecific transmission for the dominant competitor (Daphnia). These contrasting responses reflected shifts in indicator microbes associated with each host taxon. Increasing host turnover generated higher microbiome turnover, demonstrating that microbiome assembly depends on host community composition. Our results indicate that contact with both conspecifics and heterospecifics alters animal microbiomes, and that host diversity can either promote the spillover or dilute the transmission of microbes in different zooplankton with potential effects on host health and ecosystems.

ecology↗

Consistent, scale-dependent differences in the biogeography of host-associated and free-living microbiomes across systems

Microbial communities are critical to the functioning of ecosystems and shape the ecology and evolution of host organisms. However, we have a limited understanding of how host-associated and free-living microbes differ in their structure and biogeography. Here, we test whether host-associated (fish gut) and free-living (lake bacterioplankton) microbes exhibit different metacommunity structure, spatial turnover, and consistency with neutral expectations using two independent lake systems. We characterized microbial communities in lake water (Vancouver Island and Sierra Nevada) and guts in two fish species (stickleback and brook trout) using 16S amplicon sequencing. We compared alpha and beta diversity within lakes, quantified spatial turnover (distance-decay), and tested for departure from neutral abundance-occurrence expectations between bacterioplankton and fish gut microbiomes. Fish microbiomes had lower alpha diversity compared to bacterioplankton, but higher beta diversity within lakes. Bacterioplankton were more similar across lakes yet showed stronger patterns of spatial turnover with distance than fish gut microbiomes. A neutral model explained a substantial proportion of abundance-occurrence relationships in bacterioplankton communities but performed poorly for fish-associated microbes. Our study indicates that host-associated and free-living microbes have disparate patterns of metacommunity structure and spatial turnover consistent with differences in the strength of neutral ecological processes. Fish microbiomes were less diverse at the local scale but more variable across space and time than bacterioplankton communities, suggestive of potentially strong local selection and/or reduced microbial exchange among hosts compared to environmental communities. Importantly, we observed highly consistent patterns across both lake systems despite differences in host species, sampling design, and region, demonstrating that differences in the distribution of host and environmental microbes are potentially widespread. This study demonstrates how host association fundamentally alters the diversity and spatial distribution of microbes, emphasizing the need to incorporate hosts into broader frameworks of microbial biogeography.

ecology↗