Copepods are one of the most abundant invertebrate groups in the seas and oceans and are a significant food source for marine animals. Copepods are also particularly sensitive to elevated temperatures. However, it is relatively unknown how the internal microbiome influences copepod susceptibility to warming. We addressed this fundamental knowledge gap by assessing key life history traits (survival, development, and reproduction) and changes in the internal microbiome in the tropical calanoid copepod Acartia sp. in response to warming (26°C, 30°C, and 34°C). Copepod microbiomes were analyzed using high throughput DNA sequencing of V1–V9 of 16S rRNA hypervariable regions. Copepod performance was better at 30°C than at 26°C, as indicated by faster development, a higher growth rate, and fecundity. However, these parameters strongly decreased at 34°C. We recorded 1,262,987 amplicon sequence reads, corresponding to 392 total operational taxonomic units (OTUs) at 97% similarity. Warming did not affect OTU numbers and the biodiversity indices, but it substantially changed the relative abundance of three major phyla: Proteobacteria, Actinobacteria, and Bacteroidota. The thermophilic and opportunistic Proteobacteria and Bacteroidota increased under extreme temperatures (34°C) while Actinobacteria abundance was strongly reduced. Changes in the relative abundance of these bacteria might be related to reduced copepod growth, survival, and reproduction under extreme temperatures. Profiling the functional role of all internal bacterial groups in response to the temperature change will fundamentally advance our mechanistic understanding of the performance of tropical copepods and, more generally, marine invertebrates to a warming climate.
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