Biology subjects

Manns, H.

Publications and source records attributed to Manns, H..

3 recordsLinked to original sources

bioRxiv2026

The genome of the reef-building coral Porites harrisoni from the southern Persian/Arabian Gulf

We present a genome assembly from the coral species Porites harrisoni from the southern Persian/Arabian Gulf, the hottest ocean basin where corals live. The assembly is 626.7 Mb in size, spanning 1,883 contigs with a contig N50 of 807.4 kb, including a single-contig mitochondrial genome. The assembly has a BUSCO completeness of 86.3% (single = 72.5%, duplicated = 13.7%, fragmented = 1.2%, missing = 12.5%) using the eukaryota_odb10 reference set (n = 255). A total of 59.23% of the nuclear genome consists of repeats, comprising 15.89% retroelements, 10.00% DNA transposons, and 31.71% unclassified repeats. Gene annotation of this nuclear genome assembly identified 27,823 protein-coding genes. The mitogenome has an assembly size of 18,639 bp with 13 protein-coding genes as well as 2 tRNAs and 2 rRNAs. The genome of P. harrisoni provides a valuable genomic resource of a coral from an extreme environment, which will enable comparative analyses, enhancing our understanding of the genomic architecture underlying thermal resilience. Such comparisons will contribute to elucidating the evolutionary basis of heat tolerance and adaptive capacity of corals in the context of rapid climate change.

genomics↗

bioRxiv2025

Evolutionary Genomics Guides Scalable Coral Probiotics for Climate Resilience

A universal bottleneck limiting probiotic efficacy in medicine, aquaculture, agriculture, and wildlife conservation is uncertain long-term colonization, necessitating repeated administration. We present an evolution-guided framework for probiotic identification based on genomic hallmarks of emerging host dependency, including widespread pseudogenization and insertion sequence proliferation driving genomic restructuring. Applied to coral reefs, we screened over 1,200 coral-associated bacterial isolates and identified Ruegeria MC10 as exhibiting these signatures. Its presence was associated with increased thermal tolerance of a model cnidarian. Following nursery application, MC10 persisted in reef corals for an 8-month monitoring period through a natural bleaching event, improving color retention and retaining algal photosynthesis performance. This work establishes a predictive, scalable pipeline for selecting persistent probiotics, directly addressing a central constraint on microbiome-based interventions across host systems.

microbiology↗

bioRxiv2023

Short-term heat stress assays provide a standardized screening tool to assess impacts of microbiome manipulation on Aiptasia thermal stress tolerance

The ongoing loss of corals and their reef ecosystems hastens the need to develop approaches that mitigate the impacts of climate change. Given the strong reliance of corals on their associated prokaryotic and microalgal symbionts, microbiome-targeted interventions in the form of probiotics or microbiome transplants are emerging as potential solutions. Although inoculation with beneficial microorganisms was shown to improve coral bleaching recovery, the mechanistic underpinnings and extent to which microbiomes can be manipulated are largely unknown. Research progress in this regard is often hindered by coral holobiont complexity and a lack of standardized diagnostics to assess physiological and phenotypic changes following microbial manipulation. Here we address these shortcomings by establishing short-term acute thermal stress assays using the CBASS (Coral Bleaching Automated Stress System) as a standardized and reproducible experimental platform to assess the impact of microbiome manipulation on stress tolerance phenotypes of the coral model Aiptasia. We show that thermal tolerance phenotypes following acute heat stress assays are highly reproducible, host species-specific, and can exert legacy effects with consequences for long-term thermal resilience. We further demonstrate the ability to resolve phenotypic differences in thermal tolerance following microbiome manipulation through pathogen incubation. By employing acute heat stress assays in conjunction with a tractable model organism, we present a standardized experimental platform that allows functional screening for microbes that affect thermal stress tolerance. Such effort may accelerate the discovery of microbes and microbial mechanisms mediating thermal tolerance and our ability to harness them to increase stress resilience.

microbiology↗