New #RSOS paper: Machine learning reveals distinct gene expression signatures across tissue states in stony #coral tissue loss disease: royalsocietypublishing.org/doi/10.1098/... @kelseybeavers.bsky.social @mad-em.bsky.social @emily-vanburen.bsky.social

Our findings suggest even visibly healthy tissue is responding to SCTLD by increasing symbiont (or pathogen) uptake via Rab5a.

If SCTLD involves a symbiont-borne pathogen, this would worsen infection rather than fight it!

Understanding this may be key to detecting and stopping SCTLD earlier.

Many intracellular pathogens, including some bacteria and parasites, can hijack Rab5a to evade immune defenses and survive inside host cells.

So in HD tissue, Rab5a may reflect:
— symbiont uptake and retention
— early pathogen manipulation
— early host–symbiont dysregulation

In cnidarians, Rab proteins play a key role in symbiosis by mediating symbiosome stabilization within host cells.

In Aiptasia, Rab5a localizes to symbiosomes only when they contain viable, newly acquired symbionts (Fig from Chen et al. 2004: doi.org/10.1016/j.bb...)

But there's a twist...

What was REALLY fascinating was what we found in HD tissue: it’s not just “in-between” HH and LD—it’s a biologically distinct state.

One gene stood out: Rab5a, which plays a key role in symbiont uptake and intracellular trafficking in cnidarians.

In lesion tissue (LD), we found signatures of NF-κB immune activation, autophagy, oxidative stress and cytoskeletal/ECM breakdown in the coral host, alongside chloroplast dysfunction in the symbionts.

Together, these signal a complete collapse of holobiont homeostasis.

In healthy tissue, we found strong signatures of TGFβ signaling in the top-ranked genes (Tmem145, INHBB). This pathway is known to suppress inflammation and support symbiosis in cnidarians. We also observed high expression of Dmbt1, a gene associated with mucosal homeostasis and microbial balance.

This study was SO cool because for the first time we were able to describe how SCTLD progresses at the gene expression level as a coral goes from healthy to diseased.

Some of what we found made perfect sense, but some other findings totally surprised us! ‼️

Instead of just asking which genes are differentially expressed, we asked:
👉 Which genes best distinguish coral health states?

This ML approach ranks genes by their predictive power, and we applied it to both the coral (M. cavernosa) and its main algal symbiont (C. goreaui)

We used an algorithm that combines supervised ML with differential expression stats to identify gene expression signatures characteristic of three tissue states in SCTLD:
— HH = healthy tissue on a healthy colony
— HD = “healthy” tissue on a diseased colony
— LD = active lesion tissue

🎉 Exciting news! The last manuscript from my dissertation was just published in Royal Society Open Science!
And in a fun twist of fate, the cover of this issue happens to feature a Caribbean coral colony 🪸 (not from our study, but still serendipitous nonetheless!)

TACC is offering a week-long "Machine Learning in Life Sciences" workshop, happening May 19–24 in Austin! If you're working in a bio-related field and want hands-on training—from ML fundamentals to cutting-edge deep learning applications—this is the place to be 🚀

We hope to see you there!

I'll start 🙂 I do #coral #transcriptomics, and a huge time constraint has been conducting literature searches for each and every gene on my (many) gene lists! While I recognize the value of lit reviews, this process feels very inefficient in terms of time-to-discovery

Calling all 'omics researchers:

What are the most challenging or time-consuming aspects of your research? Whether it’s locating the data you need, assembly challenges, or something else, I’d love to hear about the roadblocks you’ve encountered. #Omics #Bioinformatics #Research

If you're in Atlanta for SC24, please join us in our booth for beverages and hors d'oeuvres as we announce the launch of the U.S. National Science Foundation Leadership-Class Computing Facility (NSF LCCF). We look forward to seeing you there!

Tuesday, November 19
3pm-5pm ET
TACC Booth #1203