MALDI-FISH for co-localization of brominated metabolites and Pseudovibrio spp. in Aplysina tissue

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This paper investigates whether bromotyrosine-containing natural products in the marine sponge Aplysina aerophoba originate from the sponge itself, its microbiota, or both, focusing on the brominated metabolite fistularin-3. Using MALDI-MSI paired with fluorescent in situ hybridization (FISH) on the same sponge cryosections, the authors measured fistularin-3 distribution and co-localized it with Pseudovibrio brasiliensis after inoculating sponges with the bacterium. They report fistularin-3 presence in inoculated samples and assess spatial co-localization, motivated by a prior unreplicated claim that P. brasiliensis can produce fistularin-3 in pure culture. A key caveat noted is that the study cannot definitively establish production source, though the authors conclude their data is consistent with a scenario where both sponge and microbe may be involved. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Bromotyrosine-containing natural products have long been isolated from marine sponges of the order Verongiida . Recent studies have questioned the source of these natural products whether production occurs through the sponge, its diverse microbiota, or perhaps a combination of both. While studying the uptake of engineered bacterial strains by sponges, we have observed production of fistularin-3 in sponge. To explore these results further, we employed multimodal imaging techniques to co-localize microbial metabolites with fluorescent in situ hybridization (FISH) probes. Here, we built on previously developed MALDI-FISH methods to add to the conversation on brominated metabolite production in marine sponges. Using MALDI-MSI, we measured fistularin-3, a poly-brominated natural product previously isolated from Aplysina aerophoba , present in our A. aerophoba samples that were inoculated with Pseudovibrio brasiliensis . A recent study reported that P. brasiliensis produced fistularin-3 in pure culture, but this data has not yet been reproduced. We employed MALDI-MSI and FISH on the same sponge cryosections to colocalize the spatial distribution of fistularin-3 with P. brasiliensis in sponge tissue. Despite the caveats of this study, our data suggests that perhaps both sponge and microbe may be required for production of fistularin-3.
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Abstract Bromotyrosine-containing natural products have long been isolated from marine sponges of the order Verongiida. Recent studies have questioned the source of these natural products whether production occurs through the sponge, its diverse microbiota, or perhaps a combination of both. While studying the uptake of engineered bacterial strains by sponges, we have observed production of fistularin-3 in sponge. To explore these results further, we employed multimodal imaging techniques to co-localize microbial metabolites with fluorescent in situ hybridization (FISH) probes. Here, we built on previously developed MALDI-FISH methods to add to the conversation on brominated metabolite production in marine sponges. Using MALDI-MSI, we measured fistularin-3, a poly-brominated natural product previously isolated from Aplysina aerophoba, present in our A. aerophoba samples that were inoculated with Pseudovibrio brasiliensis. A recent study reported that P. brasiliensis produced fistularin-3 in pure culture, but this data has not yet been reproduced. We employed MALDI-MSI and FISH on the same sponge cryosections to colocalize the spatial distribution of fistularin-3 with P. brasiliensis in sponge tissue. Despite the caveats of this study, our data suggests that perhaps both sponge and microbe may be required for production of fistularin-3. Competing Interest Statement The authors have declared no competing interest.

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