<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Coral Holobiont | del Campo Lab - Microbial Ecology and Evolution</title><link>https://delcampolab.com/tag/coral-holobiont/</link><atom:link href="https://delcampolab.com/tag/coral-holobiont/index.xml" rel="self" type="application/rss+xml"/><description>Coral Holobiont</description><generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Sun, 30 Jun 2024 00:00:00 +0000</lastBuildDate><image><url>https://delcampolab.com/media/logo_hu3705697567409936087.png</url><title>Coral Holobiont</title><link>https://delcampolab.com/tag/coral-holobiont/</link></image><item><title>Koch at the reef — Understanding coral disease</title><link>https://delcampolab.com/project/disease/</link><pubDate>Sun, 30 Jun 2024 00:00:00 +0000</pubDate><guid>https://delcampolab.com/project/disease/</guid><description>&lt;p>Corals are host to a mixture of microbes — prokaryotes, protists, and viruses — that play critical functional roles within their host. During unfavourable environmental conditions, coral immunity becomes compromised, fostering the proliferation of alien pathogens or previously resident microbes that turn pathogenic. Coral disease can persist over months or years, pushing the coral into a chronically stressed state. In severe cases, epizootics such as Stony Coral Tissue Loss Disease (SCTLD) can spread through entire reefscapes, turning vibrant communities from reefs to rubble.&lt;/p>
&lt;p>Here we explore several coral diseases — black band disease, red band disease, Caribbean ciliate infection, SCTLD, and dark spots disease — teasing apart pathobiome structure, dynamics, and expression during pathogenesis across multiple scleractinian hosts: &lt;em>Pseudodiploria strigosa&lt;/em>, &lt;em>Orbicella faveolata&lt;/em>, &lt;em>Diploria labyrinthiformis&lt;/em>, &lt;em>Dendrogyra cylindrus&lt;/em>, and &lt;em>Stephanocoenia intercepta&lt;/em>. Sampling was conducted in Curaçao off the leeward coast at multiple sites during October 2022 and March 2023. Triplicate coral samples were taken from healthy tissues, apparently healthy tissue from diseased hosts, the disease transition zone, and dead skeleton. Coral 16S/18S rRNA genes were sequenced from ~250 samples, allowing exploration of both prokaryotic and microeukaryotic community dynamics across diseases. Additionally, RNA sequencing was conducted using poly-A selection/enrichment to observe the host transcriptional response through disease progression.&lt;/p>
&lt;p>We aim to characterise the prokaryotic and eukaryotic taxa recovered from several diseases to disentangle microbial variability between visually healthy and diseased individuals, and to identify the host response and likely immunological functions at the cellular level through disease progression.&lt;/p></description></item><item><title>The rhythm of the reef — Diel cycles of the coral holobiont</title><link>https://delcampolab.com/project/rhythm/</link><pubDate>Sun, 30 Jun 2024 00:00:00 +0000</pubDate><guid>https://delcampolab.com/project/rhythm/</guid><description>&lt;p>Coral physiology is intimately dependent on diel cycles, as fluctuations in light intensity and spectrum, nutrient availability, and temperature directly change the respiration and energy assimilation capabilities of the coral colony. As complex sessile organisms, corals harbour incredibly diverse microbial assemblages of prokaryotes and microeukaryotes that provide functional roles in the coral ecosphere. Corals and Symbiodiniaceae have co-evolved, resulting in a symbiotic life strategy that benefits the coral host through the intracellular production of organic compounds such as carbon and oxygen. During sunlit hours, photosynthetic efficiency has been observed to increase oxygen levels ~250% of air saturation, stimulating hyperoxic environments. Corals and their aerobic microbial associates consume available oxygen through the night, where levels can become hypoxic. Given this extreme variation in abiotic parameters, it is likely that microbial communities reflect measurable changes through diel cycles, while cellular mechanisms help corals adapt to these extreme abiotic shifts.&lt;/p>
&lt;p>This project explored three scleractinian corals — &lt;em>Pseudodiploria strigosa&lt;/em>, &lt;em>Orbicella faveolata&lt;/em>, and &lt;em>Diploria labyrinthiformis&lt;/em> — through three diel cycles to characterise their microbial associates (including surrounding seawater) and the host transcriptional response. Coral samples were collected in triplicate and 1L reference seawater samples were acquired off the leeward side of Curaçao at 6-hour intervals over three days, resulting in a total of 3 replicated diel cycles. DNA was isolated, amplified using the V4 region of the 16S and 18S rRNA genes, and sequenced using Illumina MiSeq 2×250bp; RNA was sequenced using poly-A selection/enrichment.&lt;/p>
&lt;p>We hypothesise that microbial taxa follow trends in abundance with respect to anoxic and hyperoxic conditions, and that circadian genes such as &lt;em>cry1&lt;/em>, &lt;em>cry2&lt;/em>, &lt;em>clock&lt;/em>, and &lt;em>cycle&lt;/em> show diel oscillations in expression. This work was published in &lt;a href="https://doi.org/10.1016/j.chom.2026.01.004" target="_blank" rel="noopener">&lt;em>Cell Host &amp;amp; Microbe&lt;/em> (Weiler et al. 2026)&lt;/a>.&lt;/p></description></item></channel></rss>