in

An exploratory investigation into the microbial and cyanobacterial presence on skin epibiotia and orofacial lesions in estuarine common bottlenose dolphins (Tursiops truncatus) through metabarcoding


Abstract

Estuarine common bottlenose dolphins (Tursiops truncatus) inhabiting the Indian River Lagoon (IRL) have been documented with light brown skin lesions, loosely categorized as “algal sheens”. In recent years, dolphins from the IRL have also exhibited unusual necro-ulcerative orofacial lesions. To date, no metabarcoding investigation has been conducted to determine whether “algal sheens” observed on the dolphins are pathogenic, opportunistic or are indicators of poor health or water quality. The aim of this study was to investigate the etiology of “algal sheens” and orofacial lesions, to assess the pathogenic potential. In this study, 13 skin and “algal sheen” swabs from 11 dolphins were sequenced using metabarcoding techniques. Genus-level identification was achieved and compared. Results from both “algal sheen” and orofacial lesion samples demonstrated higher bacterial diversity than reported in normal bottlenose dolphin skin microbiomes. Previously unreported bacterial genera were identified, genera containing pathogenic species found in both sample types. Species responsible for “algal sheens” were not definitively identified. Numerous cyanobacterial genera typically found in eutrophic conditions were identified.

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Data availability

This data has been submitted to Genbank Biosample (accession numbers SAMN47938985-SAMN47938997) that will become publicly available after publication.

References

  1. Costa, A. P., Mcfee, W., Wilcox, L. A., Archer, F. I. & Rosel, P. E. The common bottlenose dolphin (Tursiops truncatus) ecotypes of the western North Atlantic revisited: an integrative taxonomic investigation supports the presence of distinct species. Zool. J. Linn. Soc. 196, 1608–1636 (2022).

    Google Scholar 

  2. Hart, L. B. et al. Skin lesions on common bottlenose dolphins (Tursiops truncatus) from three sites in the Northwest Atlantic, USA. PLoS ONE 7, e33081 (2012).

    Google Scholar 

  3. Toms, C. N., Stone, T. & Och-Adams, T. Visual-only assessments of skin lesions on free-ranging common bottlenose dolphins (Tursiops truncatus): Reliability and utility of quantitative tools. Mar. Mamm. Sci. 36, 744–773 (2020).

    Google Scholar 

  4. Taylor, J. S., Hart, L. B. & Adams, J. Skin lesion prevalence of estuarine common bottlenose dolphins (Tursiops truncatus) in North Carolina, with comparisons to other east coast study sites. Mar. Mamm. Sci. 37, 127–141 (2021).

    Google Scholar 

  5. Zabka, T. S. & Romano, T. A. Distribution of MHC II (+) cells in skin of the Atlantic bottlenose dolphin (Tursiops truncatus): an initial investigation of dolphin dendritic cells. Anat. Rec. Part A Discov. Mol. Cell. Evol. Biol. 273, 636–647 (2003).

  6. Hicks, B. D., Aubin, D. J. S., Geraci, J. R. & Brown, W. R. Epidermal growth in the bottlenose dolphin. Tursiops truncatus. J. Invest. Derm. 85, 60–63 (1985).

    Google Scholar 

  7. Van Bressem, M. F. et al. Epidemiological characteristics of skin disorders in cetaceans from South American waters. Lat. Am. J. Aquat. Mamm. 10, 20–32 (2015).

    Google Scholar 

  8. Duignan, P. J., Stephens, N. S. & Robb, K. Fresh water skin disease in dolphins: a case definition based on pathology and environmental factors in Australia. Sci. Rep. 10, 21979 (2020).

    Google Scholar 

  9. Brown, A. O. et al. A new species of cryptic cyanobacteria isolated from the epidermis of a bottlenose dolphin and as a bioaerosol. Phycologia 60, 603–618 (2021).

    Google Scholar 

  10. Russo, C. D. et al. Bacterial species identified on the skin of bottlenose dolphins off southern California via next generation sequencing techniques. Microb. Ecol. 75, 303–309 (2018).

    Google Scholar 

  11. Urian, K. W. & Wells, R. S. Bottlenose Dolphin the Moray Firth, Scotland: A population at the north-Photo-Identification Workshop. NOAA Technical Memo NMFS-SEFSC-393. (1996).

  12. Durden, W. N., et al. Robust design capture-recapture analysis of abundance and demographic parameters of Indian River Lagoon common bottlenose dolphins (Tursiops truncatus truncatus). Plos One 16, e0250657; https://doi.org/10.1371/journal.pone.0250657 (2021).

  13. Chiarello, M., Villeger, S., Bouvier, C., Auguet, J. & Bouvier, T. Captive bottlenose dolphins and killer whales harbor a species-specific skin microbiota that varies among individuals. Sci. Rep. 7, 15269; https://doi.org/10.1038/s41598-017-15220-z (2017).

  14. Smith, N. P. Tidal and nontidal flushing of Florida’s Indian River Lagoon. Estuaries 16, 739–746 (1993).

    Google Scholar 

  15. Lewis, D. M., Thompson, K. A., MacDonald, T. C. & Cook, G. S. Understanding shifts in estuarine fish communities following disturbances using an ensemble modeling framework. Ecol. Ind. 126, 107623 (2021).

    Google Scholar 

  16. Morris, L. J. et al. Seagrass in a changing estuary, the Indian River Lagoon, Florida. United States. Front. Mar. Sci. 8, 789818 (2022).

    Google Scholar 

  17. Durden, W. N. et al. Morbidity and mortality patterns of Indian River Lagoon common bottlenose dolphins (Tursiops truncatus truncatus) 2002–2020. J. Wildl. Dis. 59, 616–628 (2023).

    Google Scholar 

  18. Schaefer, A. M. et al. Risk factors for colonization of E. coli in atlantic bottlenose dolphins (Tursiops truncatus) in the Indian River Lagoon. Florida. J. Environ. Pub. Health https://doi.org/10.1155/2011/597073 (2011).

    Google Scholar 

  19. Durden, W. N., Stolen, M. K., Adams, D. H. & Stolen, E. D. Mercury and selenium concentrations in stranded bottlenose dolphins from the Indian River Lagoon system. Florida. Bull. Mar. Sci. 81, 37–54 (2007).

    Google Scholar 

  20. Bossart, G. D. et al. Pathologic findings in stranded Atlantic bottlenose dolphins (Tursiops truncatus) from the Indian River Lagoon. Florida. Fl. Sci. 66, 226–238 (2003).

    Google Scholar 

  21. Mazzoil, M. et al. Home ranges of bottlenose dolphins (Tursiops truncatus) in the Indian River Lagoon, Florida: environmental correlates and implications for management strategies. EcoHealth 5, 278–288 (2008).

    Google Scholar 

  22. Durden, W. N. et al. Small-scale movement patterns, activity budgets, and association patterns of radio-tagged Indian River Lagoon bottlenose dolphins (Tursiops truncatus). Aquat. Mamm. 45, 66–87 (2017).

    Google Scholar 

  23. Durden, W. N., Fabry, A. & Jablonski, T. Assessing nutritional condition in common bottlenose dolphins (Tursiops truncatus truncatus) inhabiting the northern Indian River Lagoon. Final Technical Report. Pp 522–538. Submitted to: Florida Institute of Technology, Restore Lagoon In: Flow Research: https://research.fit.edu/media/site-specific/wwwfitedu/indian-river-lagoon/documents/restore-lagoon-inflow-research/RLI-Phase-3-Final-Summary-Report.pdf (2023).

  24. Geraci, J. R. & Lounsbury, V. J. Marine mammals ashore: A field guide for strandings, 2nd Ed. National Aquarium in Baltimore, Baltimore, Maryland, 371 pp (2005)

  25. Wells, R. S., Scott, M. D. & Irvine, A. B. The social structure of free-ranging bottlenose dolphins in Current mammalogy (ed. Genoways, H. H.) 247–305 (Plenum Press, 1987).

  26. Akin, P. A, Peltier, K. M. & Miller, R. B. Techniques for the Preparation and Examination of Reproductive Samples Collected from Dolphins in the Eastern Tropical Pacific. NOAA Technical Memorandum NMFS-SWFSC-192. U.S. Department of Commerce, Washington, DC, 26 pp. (1993)

  27. Fair, P. A. et al. Protocols for Conducting Dolphin Capture–Release Health Assessment Studies. NOAA Technical Memorandum. https://repository.library.noaa.gov/view/noaa/17775 (2006)

  28. Read, A. J. & Murray, K. T. Gross Evidence of Human Induced Mortality in Small Cetaceans. U.S. Department of Commerce, NOAA Technical Memorandum NMFS-OPR-15, (2020).

  29. Moore, K. T. & Barco, S. G. Handbook for Recognizing, Evaluating, and Documenting Human Interaction in Stranded Cetaceans and Pinnipeds. U.S. Department of Commerce (2013).

  30. Harzen, S. & Brunnick, B. J. Skin disorders in bottlenose dolphins (Tursiops truncatus), resident in the Sado estuary. Portugal. Aquat. Mamm. 21, 59–68 (1997).

    Google Scholar 

  31. Bertulli, C. G., Cecchetti, A., Van Bressem, M. F. & Waerebeek, K. V. Skin disorders in common minke whales and white-beaked dolphins off Iceland, a photographic assessment. J. Mar. Anim. Ecol. 5, 29–40 (2012).

    Google Scholar 

  32. Sanino, G. P, Van Bressem, M., Van Waerebeek, K. & Pozo, N. Skin disorders of coastal dolphins at Añihué Reserve, Chilean Patagonia: A matter of concern. Bol. Del Museo Nacion. Hist. Nat., Chile 63, 127–157 (2014).

  33. Vilela, R. et al. Cutaneous granulomas in dolphins caused by novel uncultivated Paracoccidiodes brasiliensis. Emerg. Infec. Dis. 22, 2063–2069 (2016).

    Google Scholar 

  34. Herr, H., Burkhardt-Holm, P., Heyer, K., Siebert, U. & Selling, J. Injuries, malformations, and epidermal conditions in cetaceans of the Strait of Gibraltar. Aquat. Mamm. 46, 215–235 (2020).

    Google Scholar 

  35. Bearzi, M., Rapoport, S., Chau, J., & Saylan, C. Skin lesions and physical deformities of coastal and offshore common bottlenose dolphins (Tursiops truncatus) in Santa Monica Bay and adjacent areas, California. AMBIO: A J. of the Human Environ., 38, 66–71 (2009).

  36. Knowlton, A. R. et al. Effects of fishing rope strength on the severity of large whale entanglements. Cons. Biol. 30, 318–328 (2015).

    Google Scholar 

  37. Illumina. Best Practices for High Sensitivity Applications: Minimizing Sample Carryover. Available: https://my.illumina.com/MyIllumina/Bulletin/ DVzvSUldoEqh4oUyPaxoXA/best-practices-for-high-sensitivity-applicationsm. (2013)

  38. Martin, M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet J. 17, 10–12 (2011).

    Google Scholar 

  39. Callahan, B. et al. DADA2: High-resolution sample inference from Illumina amplicon data. Nat. Methods 13, 581–583 (2016).

    Google Scholar 

  40. Quast, C. et al. The SILVA ribosomal RNA gene database project: Improved data processing and web-based tools. Nucl. Acids Res. https://doi.org/10.1093/nar/gks1219 (2013).

    Google Scholar 

  41. Lefler, F. W., Berthold, D. E. & Laughinghouse, H. D. IV. Cyanoseq: A database of cyanobacterial 16S rRNA gene sequences with curated taxonomy. J. Phycol. 59, 470–480 (2023).

    Google Scholar 

  42. Stolen, M. K. & Barlow, J. A model life table for bottlenose dolphins (Tursiops truncatus) from the Indian River Lagoon System, Florida. USA. Mar. Mamm. Sci. 19, 630–649 (2003).

    Google Scholar 

  43. Robles-Malagamba, M. J. et al. Characterization of the bacterial microbiome among free-ranging bottlenose dolphins (Tursiops truncatus). Heliyon https://doi.org/10.1016/j.heliyon.2020 (2020).

    Google Scholar 

  44. Kiu, R. & Hall, L. J. An update on the human and animal enteric pathogen Clostridium perfringens. Emerg. Microbes Infect. https://doi.org/10.1038/s41426-018-0144-8 (2018).

    Google Scholar 

  45. Acuña-Amador, L. & Barloy-Hubler, F. Porphyromonas spp. have an extensive host range in ill and healthy individuals and an unexpected environmental distribution: A systematic review and meta-analysis. Anaerobe 66, 102280; https://doi.org/10.1016/j.anaerobe.2020.102280 (2020).

  46. Johnson, W. R. et al. Novel diversity of bacterial communities associated with bottlenose dolphin upper respiratory tracts. Environ. Microbiol. Rep. 1, 555–562 (2009).

    Google Scholar 

  47. Li, C. et al. Insights on gut and skin wound microbiome in stranded Indo-Pacific finless porpoise (Neophocaena phocaenoides). Microorganisms 10, 1295 (2022).

    Google Scholar 

  48. Mada, P. K. & Khan, M. H. Hathewaya limosa empyema: A case report. Cureus https://doi.org/10.7759/cureus.55156 (2024).

    Google Scholar 

  49. Mabrok, M. et al. Tenacibaculosis caused by Tenacibaculum maritimum: Updated knowledge of this marine bacterial fish pathogen. Front. Cell Infect. Microbiol. 12, 1068000 (2023).

    Google Scholar 

  50. Nematollahi, A., Decostere, A., Pasmans, F. & Haesebrouck, F. Flavobacterium psychrophilum infections in salmonid fish. J. Fish Dis. 26, 563–574 (2003).

    Google Scholar 

  51. Hosoya, S., Arunpairojana, V., Suwannachart, C., Kanjana-Opas, A. & Yokota, A. Aureispira marina gen. nov., sp. nov., a gliding, arachidonic acid-containing bacterium isolated from the southern coastline of Thailand. Int. J. Syst. Evol. Microbiol. 56, 2931–2935 (2006).

  52. Coenye, T. & Vandamme, P. Diversity and significance of Burkholderia species occupying diverse ecological niches. Environ. Microbiol. 5, 719–729 (2003).

    Google Scholar 

  53. Van Zandt, K. E., Greer, M. T. & Gelhaus, H. C. Glanders: An overview of infection in humans. Orphanet J. Rare Dis. https://doi.org/10.1186/1750-1172-8-131 (2013).

    Google Scholar 

  54. Puri, A., Padda, K. P. & Chanway, C. P. Can naturally-occurring endophytic nitrogen-fixing bacteria of hybrid white spruce sustain boreal forest tree growth on extremely nutrient-poor soils?. Soil Biol. Biochem. 140, 107642 (2020).

    Google Scholar 

  55. Dominguez-Sanchez, C.A., Ferguson, S.H., Edkins, T., Young, B.G. & Kringorn, J. Pilot study: decoding the skin microbiome of bowhead (Balaena mysticetus) and killer whales (Orcinus orca) in Nunavut, Canada. Arc. Sci. 10, 169–188. https://doi.org/10.1139/as-2023-0028 (2024)

  56. Bowman, J. P. The Genus Psychrobacter in The Prokaryotes (eds. Dworkin, M., Falkow, S., Rosenberg, E., Schleifer, K. H. & Stackebrandt, E.) 920–930 (Springer, 2006).

  57. Guilloux, C. A., Lamoureux, C., Beauruelle, C. & Héry-Arnaud, G. Porphyromonas: A neglected potential key genus in human microbiomes. Anaerobe 68, 102230; https://doi.org/10.1016/j.anaerobe.2020.102230 (2021).

  58. Radolf, J. D. Treponema in Medical Microbiology, 4th edition (ed. Baron, S.) (University of Texas, Galveston; 1996).

  59. Majander, K. et al. Redefining the treponemal history through pre-Columbian genomes from Brazil. Nature 627, 182–188 (2024).

    Google Scholar 

  60. Ngono, J. N. et al. Ulcerative skin lesions among children in Cameroon: It is not always Yaws. PLoS Negl. Trop. Dis. https://doi.org/10.1371/journal.pntd.0009180 (2021).

    Google Scholar 

  61. Avendaño-Herrera, R., Toranzo, A. E. & Magariños, B. Tenacibaculosis infection in marine fish caused by Tenacibaculum maritimum: A review. Dis. Aquat. Org. 71, 255–266 (2006).

    Google Scholar 

  62. Cato, E. P., Cummins, C. S. & Smith, L. D. Clostridium limosum André in Prévot 1948, 165 amended description and pathogenic characteristics. Int. J. Syst. Evol. Microbiol. 20, 305–316 (1970).

    Google Scholar 

  63. Hatheway, C. L. Toxigenic Clostridia. Clin. Microbiol. Rev. 3, 86–87 (1990).

    Google Scholar 

  64. Holmes, R. W., Nagasawa, S. & Takano, H. The morphology and geographic distribution of epidermal diatoms of the Dall’s porpoise (Phocoenoides dalli True) in the northern Pacific Ocean. Bull. Nat. Sci. Mus. Tokyo, Ser. B 19, 1–18. (1993).

  65. Nagasawa, S., Holmes, R. W. & Nemoto, T. Occurrence of cetacean diatoms in the sediments of Otsuchi Bay, Iwate. Japan. Proc. Jap. Acad. Ser. B 65, 80–83 (1989).

    Google Scholar 

  66. Ashworth, M. P. et al. Cultivating epizoic diatoms provides insights into the evolution and ecology of both epibionts and hosts. Sci. Rep. 12, 15116 (2022).

    Google Scholar 

  67. Majewska, R. et al. Chelonicola and Poulinea, two new gomphonemoid diatom genera (Bacillariophyta) living on marine turtles from Costa Rica. Phytotaxa 233, 236–250 (2015).

    Google Scholar 

  68. Frankovich, T. A., Ashworth, M. P., Sullivan, M. J., Theriot, E., C. & Stacy, N. I. Epizoic and apochlorotic Tursiocola species (Bacillariophyta) from the skin of Florida manatees (Trichechus manatus latirostris). Protist 169, 539–568 (2018).

  69. Diéguez, A. L., Pichon, P., Balboa, S., Magnesen, T. & Romalde, J. L. Complete characterization of new isolates of Neptunomonas phycophila leads to emend its description and opens possibilities of biotechnological applications. Microbiol. Open https://doi.org/10.1002/mbo3.519 (2017).

    Google Scholar 

  70. Yang, T. et al. Following the oil fallout: Bacterial community succession in Gulf of Mexico seafloor sediment after the 2010 Deepwater Horizon blowout. Front. Microbiol. https://doi.org/10.3389/fmicb.2016.013842016 (2016).

    Google Scholar 

  71. Tsuboi, S., Kohzu, A., Imai, A., Iwasaki, K. & Yamamura, S. Vertical variation of bulk and metabolically active prokaryotic community in sediment of a hypereutrophic freshwater lake. Environ. Sci. Poll. Res. 26, 9379–9389 (2019).

    Google Scholar 

  72. Wei, C., Zeng, Y., Tang, K. & Jiao, N. Comparison of bacterioplankton communities in three mariculture ponds farming different commercial animals in subtropical Chinese coast. Hydrobiologia 632, 107–126 (2009).

    Google Scholar 

  73. Houghton, K. A. Responses in Bacterioplankton Production and Community Structure After Exposure to Oil and Dispersant in the Northeastern Gulf of Mexico. University of West Florida Dissertation, 60 pp. (2015)

  74. Crump, B. C., Peranteau, C., Beckingham, B. & Cornwell, J. C. Respiratory succession and community succession of bacterioplankton in seasonally anoxic estuarine waters. Appl. Environ. Microbiol. 73, 6802–6810 (2007).

    Google Scholar 

  75. He, J. et al. Primer selection impacts the evaluation of microecological patterns in environmental microbiomes. iMeta 2, e135. https://doi.org/10.1002/imt2.135 (2023).

    Google Scholar 

  76. Krzyszczyk, E., Patterson, E. M., Stanton, M. A. & Mann, J. The transition to independence: Sex differences in social and behavioral development of wild bottlenose dolphins. Anim. Behav. 129, 43–59 (2017).

    Google Scholar 

  77. Stolen, M. K., Durden, W. N. & Odell, D. K. Historical synthesis of bottlenose dolphin (Tursiops truncatus) stranding data in the Indian River Lagoon system, Florida, from 1977–2005. Fl. Scient. 70, 45–54 (2007).

    Google Scholar 

  78. Marks, W. et al. A case study of monofilament line entanglement in a common bottlenose dolphin (Tursiops truncatus): Entanglement, disentanglement, and subsequent death. BCM Vet. Res. 16, 223 (2020).

    Google Scholar 

  79. Elorriaga-Verplancken, F. R., Tobar-Hurtado, S., Medina-López, M. A., de la Cruz, D. B. & Urbán, J. R. Potential morphological contributions to a live stranding: Abnormal snout and Conchoderma auritum infestation in a bottlenose dolphin (Tursiops truncatus). Aquat. Mam. 41, 198 (2015).

    Google Scholar 

  80. Sharp, S. M. et al. Gross and histopathologic diagnoses from North Atlantic right whale Eubalaena glacialis mortalities between 2003 and 2018. Dis. Aquat. Org. 135, 1–31 (2019).

    Google Scholar 

  81. Indian River Lagoon National Estuary Program (IRLNEP). Indian River Lagoon: An Introduction to a Natural Treasure. Available at: https://www.epa.gov/sites/default/files/2018-01/documents/58692_an_river_lagoon_an_introduction_to_a_natural_treasure_2007.pdf (2007).

  82. Indian River Lagoon National Estuary Program (IRLNEP). Looking ahead to 2030: A 10-year comprehensive conservation and management plan for the Indian River Lagoon, Florida. Available at: https://onelagoon.org/wp-content/uploads/8_IRLNEP_CCMP-_FINAL2020_01062020.pdf (2020).

  83. Environmental Protection Agency, National Estuary Program, Indian River Lagoon. Available at: www.epa.gov/owow/estuaries/programs/irl.htm (2024).

  84. Barbarite, G.M. The Occurrence of Vibrio vulnificus, V. parahaemolyticus and V. cholerae in the Indian River Lagoon, Florida, with Implications for Human Health. Florida Atlantic University Dissertation, 155 pp. (2016).

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Acknowledgements

We sincerely thank Teresa Jablonski, Agatha Fabry, SeaWorld Orlando rescue team and vet services staff, and HSWRI volunteers for their support of this study. This work was funded in part by the John H. Prescott Marine Mammal Rescue Assistance Grant, SeaWorld Busch Gardens Conservation Fund, Discover Florida Ocean’s License Plate, Brevard County Tourism and Development Council, and Protect Wild Dolphin’s License plate. We also sincerely thank the Coastal Biology Flagship Program and the Institute of Environmental Research and Education at the University of North Florida.

Funding

This work was funded in part by the John H. Prescott Marine Mammal Rescue Assistance Grant, SeaWorld Busch Gardens Conservation Fund, Discover Florida Ocean’s License Plate, Brevard County Tourism and Development Council, and Protect Wild Dolphin’s License plate. We also sincerely thank the Coastal Biology Flagship Program and the Institute of Environmental Research and Education at the University of North Florida.

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AB wrote the main manuscript text and DAC extracted and amplified all samples and provided funding. WND collected all life history information for all sampled dolphins. AB and WND prepared Table 1, WND prepared Fig. 1, AB and WND prepared Figs. 2, AB prepared Figs 3, 4, and 5 and 3. CM prepared Figs 6, 7, 8 and 9. All authors reviewed the manuscript.

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Amber O. Brown.

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Brown, A.O., Durden, W.N., McGovern, C. et al. An exploratory investigation into the microbial and cyanobacterial presence on skin epibiotia and orofacial lesions in estuarine common bottlenose dolphins (Tursiops truncatus) through metabarcoding.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-37434-w

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Keywords

  • Dolphin mortality
  • Metabarcoding
  • Pathogenic

  • Tursiops truncatus


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