IJMS_2026v16n1

International Journal of Marine Science, 2026, Vol.16, No.1, 55-65 http://www.aquapublisher.com/index.php/ijms 63 Effective integrated management requires surveillance systems designed for early detection rather than only proof of disease freedom. Expert-guided design for OsHV-1 highlights that observational (farmer-based) surveillance, when carefully structured and combined with targeted active sampling and strong industry-government partnerships, can greatly enhance system sensitivity and confidence in disease freedom, whereas active testing alone is unlikely to detect outbreaks in time. Farmer reporting is central to such systems; behavioural studies in France show that financial compensation, awareness of reporting objectives, and participatory education strongly influence whether and how quickly farmers notify unexplained mortalities, directly affecting early-warning performance. New molecular and environmental tools expand early-warning capacity. Suites of droplet digital PCR assays enable highresolution, simultaneous quantification of multiple oyster-relevant pathogens in farm-proximal waters, revealing spatiotemporal hotspots where mortality risk increases and allowing farmers to adjust practices as pathogen loads rise. In parallel, temperature-based outlooks and spatial risk maps that integrate sea-temperature thresholds, turbidity and terrestrial inputs can guide targeted surveillance and proactive management of marine diseases, illustrating how environmental monitoring can be coupled with aquaculture health systems as oceans warm. References Alfaro A., Nguyen T.V., and Merien F., 2019, The complex interactions of Ostreid herpesvirus 1, Vibrio bacteria, environment and host factors in mass mortality outbreaks of Crassostrea gigas, Reviews in Aquaculture, 11(4): 1148-1168. https://doi.org/10.1111/raq.12284 Batchelor S., Harrison J.S., Greiman S., Treible L.M., and Carroll J.M., 2023, Assessment of infection prevalence and intensity of disease-causing parasitic protozoans Perkinsus marinus and Haplosporidium nelsoni in Georgia oysters, Microorganisms, 11(7): 1808. https://doi.org/10.3390/microorganisms11071808 Botta R., Asche F., Borsum J., and Camp E., 2020, A review of global oyster aquaculture production and consumption, Marine Policy, 117: 103952. https://doi.org/10.1016/j.marpol.2020.103952 Bradley T., Mohr P.G., Humphrey J.D., Moody N., Cummins D., Slater J., and Crane M., 2025, Bonamia exitiosa: the cause of bonamiasis in native oysters Ostrea angasi in Australia in 2015, Diseases of Aquatic Organisms, 162: 99-113. https://doi.org/10.3354/dao03853 Cain G., Liu O., Whittington R., and Hick P., 2021, Reduction in virulence over time in Ostreid herpesvirus 1 (OsHV-1) microvariants between 2011 and 2015 in Australia, Viruses, 13(5): 946. https://doi.org/10.3390/v13050946 Chen Y., and Wang W.X., 2025, Immune resilience and subcellular adaptation of oyster hemocytes under hypoxic stress, Environmental Science and Technology, 59(31): 16332-16343. https://doi.org/10.1021/acs.est.5c05254 De Kantzow M.C., Hick P., Dhand N., and Whittington R., 2017, Risk factors for mortality during the first occurrence of Pacific Oyster Mortality Syndrome due to Ostreid herpesvirus-1 in Tasmania, 2016, Aquaculture, 468: 328-336. https://doi.org/10.1016/j.aquaculture.2016.10.025 De La Forest Divonne S., Pouzadoux J., Romatif O., Montagnani C., Mitta G., Destoumieux-Garzón D., Gourbal B., Charrière G., and Vignal E., 2025, Diversity and functional specialization of oyster immune cells uncovered by integrative single-cell level investigations, eLife, 13: RP102622. https://doi.org/10.7554/elife.102622 De Lorgeril J., Escoubas J., Loubière V., Pernet F., Le Gall P., Vergnes A., Aujoulat F., Jeannot J., Jumas-Bilak E., Got P., Guéguen Y., Destoumieux-Garzón D., and Bachère E., 2018, Inefficient immune response is associated with microbial permissiveness in juvenile oysters affected by mass mortalities in the field, Fish and Shellfish Immunology, 77: 156-163. https://doi.org/10.1016/j.fsi.2018.03.027 De Lorgeril J., Petton B., Lucasson A., Perez V., Stenger P., Dégremont L., Montagnani C., Escoubas J., Haffner P., Allienne J., Leroy M., Lagarde F., VidalDupiol J., Guéguen Y., and Mitta G., 2020, Differential basal expression of immune genes confers Crassostrea gigas resistance to Pacific oyster mortality syndrome, BMC Genomics, 21(1): 63. https://doi.org/10.1186/s12864-020-6471-x Delisle L., Laroche O., Hilton Z., Burguin J., Rolton A., Berry J., Pochon X., Boudry P., and Vignier J., 2022, Understanding the dynamics of POMS infection and the role of microbiota composition in the survival of Pacific oysters Crassostrea gigas, Microbiology Spectrum, 10(6): e01959-22. https://doi.org/10.1128/spectrum.01959-22 Delisle L., Rolton A., and Vignier J., 2023, Inactivated Ostreid herpesvirus-1 induces an innate immune response in the Pacific oyster Crassostrea gigas hemocytes, Frontiers in Immunology, 14: 1161145. https://doi.org/10.3389/fimmu.2023.1161145 Destoumieux-Garzón D., Canesi L., Oyanedel D., Travers M., Charrière G., Pruzzo C., and Vezzulli L., 2020, Vibrio-bivalve interactions in health and disease, Environmental Microbiology, 22(10): 4323-4341. https://doi.org/10.1111/1462-2920.15055

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