Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.01.09.698610

Roseobacter enrichment early in life facilitates future colonization of Roseobacter bacteria and improves long-term survival against Vibrio aestuarianus in the Pacific oyster

Abstract

Exposure to beneficial bacteria during early immune development may promote long-term survival against pathogens, known as "microbial education." As marine diseases intensify with ocean warming, methods to improve marine organisms robustness against disease will be valuable for mitigation. Here, we experimentally tested whether exposure to high temperature seawater, seawater enrichment with Roseobacter bacteria, or a combination of both during the first 24 hours of life enhances long-term survival of the Pacific oyster (Crassostrea gigas) against the widespread marine pathogen, Vibrio aestuarianus subsp. francensis, at high temperatures (24 {degrees}C). Exposure to high temperatures early in life did not improve future survival during disease challenges and caused high larval mortality. Conversely, Roseobacter enrichment during high temperature exposure resulted in a "microbial rescue effect," improving larval survival. We found that Roseobacter enrichment during the first 24 hours of life improved future survival against V. aestuarianus at high temperatures by up to [~]28% at 13 days post-fertilization (dpf) and [~]30% at 90 dpf. Ultimately, the supplemented Roseobacter species did not remain associated with the host microbiome but instead was replaced by a high abundance of other Roseobacter bacteria at 90 dpf. These findings suggest that early Roseobacter enrichment facilitates future colonization by other Roseobacter species, which may in turn protect against pathogenic V. aestuarianus, supporting the concept of microbial education in marine invertebrates and its potential use to combat marine diseases. ImportanceThis research identifies key aspects of early developmental processes in a marine invertebrate, Crassostrea gigas, and explores how these processes can be utilized to alter host-microbe interactions later in life.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wright-LaGreca, M. D., Loudon, A., Bates, A., Moody, D., Dennis-Orr, J., Gilchrist, K., Falk, F., Green, T. J.. 2026-01-09. Roseobacter enrichment early in life facilitates future colonization of Roseobacter bacteria and improves long-term survival against Vibrio aestuarianus in the Pacific oyster. https://doi.org/10.64898/2026.01.09.698610

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A population-scale landscape of the subgingival microbiome reveals divergent routes to periodontal dysbiosis

Periodontitis is an archetypical mucosal inflammatory disease in which microbiome dysbiosis at the tooth-epithelial interface interacts with host genetic and behavioral risk factors to drive immune-mediated tissue destruction. Although subgingival microbiome compositional shifts are thought to parallel disease severity, microbiome variation at the population-level and its relationship to periodontal clinical phenotypes and disease-modifying factors remain poorly defined. Here, we use unsupervised manifold learning to map the compositional landscape of the subgingival microbiome in 1,355 adults spanning periodontal health to severe periodontitis. We identified eight latent microbiome states organized along a branching continuum from eubiosis to dysbiosis. An intermediate microbial configuration marked ecological destabilization and bifurcation into two distinct periodontitis-associated dysbiotic trajectories, distinguished by links to gingival inflammation and smoking. Although the microbiome trajectories broadly tracked periodontal destruction, a minority of individuals showed discordant microbiome-clinical phenotypes, with some individuals with periodontitis retaining otherwise eubiotic microbiomes enriched for low-abundance pathobionts, while some cases of health or mild disease had highly dysbiotic communities, suggesting distinct host susceptibility. Together, these findings define a population-scale ecological landscape of the subgingival microbiome, reveal divergent trajectories to periodontal dysbiosis, and highlight heterogeneity in the relationship between microbial community structure and clinical disease expression.

microbiology↗

Beta-lactam enhancement against methicillin-resistant Staphylococcus aureus by cell wall blockade is autolysis-dependent: a butyrolactone derivative as case in point

Methicillin-resistant Staphylococcus aureus (MRSA) is non-susceptible to beta-lactams. Blockade of cell wall biosynthesis is a potential target for beta-lactam enhancement but requires further investigation. A butyrolactone derivative enhanced beta-lactams against MRSA strains by reducing the availability of D-Ala-D-Ala. Unlike D-cycloserine, it did not inhibit D-Ala-D-Ala ligase (Ddl). Nor did it show an additive or synergistic effect when combined with cycloserine, indicating a unique mechanism for blocking cell wall precursor production that does not involve the traditional Lipid II pathway. Notably, beta-lactam potentiation by our chemical or D-cycloserine was highly dependent on the intrinsic autolytic ability of the tested MRSA strains. Strains that resisted lysis upon Triton X-100 exposure showed a minimal increase in beta-lactam susceptibility, whereas highly autolytic strains showed significant changes in their beta-lactam MICs. We have thus identified autolytic ability as the Achilles Heel in the strategy of targeting cell wall biosynthesis for beta-lactam potentiation.

microbiology↗

Rapid and largely reversible shifts in the canine fecal metabolome during dietary change

Diet can rapidly change the fecal metabolome, but less is known about recovery after the original diet is restored. We used untargeted UPLC-MS metabolomics to analyze 72 fecal samples from nine Pumi dogs during an owner-managed switch from dry food to raw food and back to dry food. Diet phase accounted for a large proportion of variation in both ionization modes. More than 13,000 LC-MS features changed at the first sampling point after the switch to raw food, with a similarly large response after return to dry food. Among features significant in both comparisons, more than 99% changed in opposite directions. At the final sampling point, no positive-mode (ESI+) features and only 13 negative-mode (ESI-) features differed from the second dry-food baseline under the same threshold. BARF-associated patterns persisted in analyses excluding individual dogs and in pedigree-adjusted candidate models, although individual feature effects depended on normalization. Putative metabolites from several biochemical classes differed in their response and recovery. The fecal metabolome therefore changed rapidly and returned largely toward baseline, with differences among dogs.

microbiology↗