Bacterial infections and antibiotic resistance in stranded dugongs (Dugong dugon) from the Andaman Sea, Thailand https://doi.org/10.12982/VIS.2026.052
Main Article Content
Abstract
Bacterial infections are recognized as important contributors to mortality in dugongs (Dugong dugon), endangered marine mammals inhabiting Thai coastal waters, yet information on their pathogenic bacteria, pathological findings, and antibiotic resistance remains limited. This study investigated the occurrence of bacterial infections and antibiotic resistance profiles in samples collected during necropsy examinations of freshly stranded dugong carcasses recovered from the Andaman Sea, Thailand, between 2024 and 2025. Necropsy, histopathology, bacterial culture, antimicrobial susceptibility testing, and PCR detection of antibiotic resistance genes (ARGs) were performed. Ten bacterial isolates representing eight species were identified, predominantly Vibrio spp. and Photobacterium damselae, associated with lesions consistent with septicemia. Members of the family Vibrionaceae were predominant (60%), while other isolates included Achromobacter xylosoxidans, Shewanella putrefaciens, Sphingomonas paucimobilis, and Enterococcus faecalis. Lesions were characterized by inflammation, congestion, and hemorrhage, consistent with systemic bacterial infection. Antibiotic susceptibility testing in Gram-negative bacteria revealed variable resistance to amikacin (AK), cefazolin (KZ), ceftazidime (CAZ), oxytetracycline (OT), and enrofloxacin (ENR), whereas all isolates were susceptible to amoxicillin–clavulanic acid (AMC), imipenem (IPM), and sulfamethoxazole/ trimethoprim (SXT). In contrast, E. faecalis exhibited resistance to OT and ENR. PCR screening demonstrated that 90% of isolates carried one or more ARGs, most frequently blaCTX-M (60%), blaOXA-1 (40%), and tetM (40%), with aac(3)-IIa, ant(2′′)-Ia, sul1, sul2, gyrA, blaTEM, and blaSHV also detected. Notably, some resistance genes were identified in phenotypically susceptible isolates, suggesting a latent resistance reservoir. These findings establish baseline data on bacterial pathogens and antibiotic resistance in Thai dugongs, emphasizing the need for antibiotic resistance monitoring in marine ecosystems and supporting improved therapeutic management of stranded marine mammals.
Article Details

This work is licensed under a Creative Commons Attribution 4.0 International License.
Publishing an article with open access in Veterinary Integrative Sciences leaves the copyright with the author. The article is published under the Creative Commons Attribution License 4.0 (CC-BY 4.0), which allows users to read, copy, distribute and make derivative works from the material, as long as the author of the original work is cited.
References
Abat, C., Huart, M., Garcia, V., Dubourg, G., Raoult, D., 2016. Enterococcus faecalis urinary-tract infections: Do they have a zoonotic origin?. J. Infect. 73(4), 305-313.
Abdi-Hachesoo, B., Khoshbakht, R., Sharifiyazdi, H., Tabatabaei, M., Hosseinzadeh, S., Asasi, K., 2014. Tetracycline resistance genes in Campylobacter jejuni and C. coli isolated from poultry carcasses. Jundishapur. J. Microbiol. 7(9), e12129.
Akasaka, T., Tanaka, M., Yamaguchi, A., Sato, K., 2001. Type II topoisomerase mutations in fluoroquinolone-resistant clinical strains of Pseudomonas aeruginosa isolated in 1998 and 1999: role of target enzyme in mechanism of fluoroquinolone resistance. Antimicrob. Agents. Chemother. 45(8), 2263-2268.
Amarasiri, M., Sano, D., Suzuki, S., 2020. Understanding human health risks caused by antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARG) in water environments: Current knowledge and questions to be answered. Crit. Rev. Environ. Sci. Technol. 50(19), 2016-2059.
Baek, S.M., Lee, S.W., Kim, T.U., Kim, J.H., Lee, Y.J., Yim, J.H., Kim, W.J., Choi, S.K., Han, J.E., Jeong, K.S., Park, J.K., 2023. Case report: Fatal neonatal sepsis associated with Escherichia fergusonii infection in a common bottlenose dolphin (Tursiops truncatus). Front. Vet. Sci. 10, 1242599.
Battistini, R., Masotti, C., Giorda, F., Grattarola, C., Peletto, S., Testori, C., Zoppi, S., Berio, E., Crescio, M. I., Pussini, N., Serracca, L., Casalone, C., 2024. Photobacterium damselae subsp. damselae in stranded cetaceans: A 6-year monitoring of the Ligurian Sea in Italy. Animals (Basel). 14(19), 2825.
Bourque, M., Quintiliani, R., Tilton, R.C., 1976. Synergism of cefazolin-gentamicin against enterococci. Antimicrob. Agents. Chemother. 10(1), 157-163.
Candelli, M., Sacco Fernandez, M., Triunfo, C., Piccioni, A., Ojetti, V., Franceschi, F., Pignataro, G., 2025. Vibrio vulnificus-A review with a special focus on sepsis. Microorganisms. 13(1), 128.
Cha, T.S., Park, S.Y., Lee, K., Park, E.J., Na, J.B., Kim, Y.B., Lee, K., Lim, S., Uh, N., Jung, J.Y., Kim, B.Y., Kim, B., Han, J.E., Kim, J.H., 2025. Characterization of Photobacterium damselae subsp. damselae isolated from a spotted seal (Phoca largha) (Pinnipedia: Phocidae) stranded in Korea. Front. Vet. Sci. 12, 1574705.
CLSI, 2002. Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals; approved standard CLSI/NCCLS document M31-A2, 2nd edition. Clinical and Laboratory Standards Institute, Wayne, PA.
CLSI, 2015a. Methods for antimicrobial dilution and disk susceptibility testing of infrequently isolated or fastidious bacteria, 3rd edition. CLSI guideline M45. Clinical and Laboratory Standards Institute, Wayne, PA.
CLSI, 2015b. Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals, 3rd edition. CLSI guideline VET01S. Clinical and Laboratory Standards Institute, Wayne, PA.
CLSI, 2021. Performance standards for antimicrobial susceptibility testing, 31st edition. CLSI guideline M100. Clinical and Laboratory Standards Institute, Wayne, PA.
CLSI, 2020. Methods for antimicrobial broth dilution and disk diffusion susceptibility testing of bacteria isolated from aquatic animals, 2nd edition. CLSI guideline VET03. Clinical and Laboratory Standards Institute, Wayne, PA.
Daochai, C., Sornying, P., Keawchana, N., Manmoo, S., Khumraksa, P., Kaewmong, P., Ninwat, S., Upanoi, T., Sukkarun, P., Suyapoh, W., 2024. Investigation into the causes of mortality in cetaceans and sirenian populations in the Andaman Sea, Thailand: A retrospective analysis spanning 2018-2023. Vet. World. 17(12), 2889-2898.
de Sousa, G.P., Soares, R.M., Borges, J.C.G., Brito, A.P.D., Oliveira, D.C.R., Faita, T., Attademo, F.L.N., Luna, F.O., de Oliveira, R.E.M., Freitas, C.I.A., Vergara-Parente, J.E., Keid, L.B., 2021. Brucella infection investigation in cetaceans and manatees in Northeast Brazil. J. Aquat. Anim. Health. 33(3), 125-132.
Department of Marine and Coastal Resources, 2013. Dugong necropsy manual in Thailand. DMCR Publications, Bangkok. (In Thai)
Di Renzo, L., Di Francesco, G., Profico, C., Di Francesco, C. E., Ferri, N., Averaimo, D., Di Guardo, G., 2017. Vibrio parahaemolyticus- and V. alginolyticus-associated meningo-encephalitis in a bottlenose dolphin (Tursiops truncatus) from the Adriatic coast of Italy. Res. Vet. Sci. 115, 363-365.
Dunn, J.L., Buck, J.D., Robeck, T.R., 2001. Bacterial diseases of cetaceans and pinnipeds. In: Dunn, J.L., Buck, J.D., Robeck, T.R. (Eds.), CRC handbook of marine mammal medicine, CRC Press, pp. 359-386.
Eiamcharoen, P., Khumraksa, P., Ninwat, S., Suttiboon, T., Keawchana, N., Sornying, P., Suyapoh, W., 2025. Novel insight into dugong mortality: first report of systemic Achromobacter xylosoxidans infection, disseminated intravascular coagulation, and associated pathogenesis. Animals (Basel). 15(16), 2441.
El-Gohary, F.A., Abdel-Hafez, L.J.M., Zakaria, A.I., Shata, R.R., Tahoun, A., El-Mleeh, A., Abo Elfadl, E.A., Elmahallawy, E.K., 2020. Enhanced antibacterial activity of silver nanoparticles combined with hydrogen peroxide against multidrug-resistant pathogens isolated from dairy farms and beef slaughterhouses in Egypt. Infect. Drug. Resist. 13, 3485-3499.
Enne, V.I., Delsol, A.A., Roe, J.M., Bennett, P.M., 2006. Evidence of antibiotic resistance gene silencing in Escherichia coli. Antimicrob. Agents. Chemother. 50(9), 3003-3010.
Eros, C., Marsh, H., Bonde, R.K., O’Shea, T.A., Beck, C.A., Recchia, C., Dobbs, K., Turner, M., Lemm, S., Pears, R., Bowater, R., 2007. Procedures for the salvage and necropsy of the Dugong (Dugong dugon). Research Publication No. 85., Queensland.
Ewing, R.Y., Rotstein, D.S., McLellan, W.A., Costidis, A.M., Lovewell, G., Schaefer, A.M., Romero, C.H., Bossart, G.D., 2020. Macroscopic and histopathologic findings from a mass stranding of rough-toothed dolphins (Steno bredanensis) in 2005 on Marathon Key, Florida, USA. Front. Vet. Sci. 7, 572.
Fernandez, A., Jepson, P.D., Diaz-Delgado, J., de Quiros, Y.B., Sierra, E., Mompeo, B., Vela, A.I., Di Guardo, G., Suarez-Santana, C., de Los Monteros, A.E., Herraez, P., Andrada, M., Caballero, M.J., Rivero, M., Consoli, F., Castro-Alonso, A., Quesada-Canales, O., Arbelo, M., 2022. Budd-Chiari-like pathology in dolphins. Sci. Rep. 12(1), 12635.
Freitas, A.R., Werner, G., 2023. Nosocomial pathogens and antimicrobial resistance: Modern challenges and future opportunities. Microorganisms. 11(7), 1685.
Fujioka, R.S., Greco, S.B., Cates, M.B., Schroeder, J.P., 1987. Isolation of Vibrio vulnificus from internal organs of a suddenly expired atlantic bottlenose dolphin. Veterinary Information Network.
Georgi, C., Buerger, J., Hillen, W., Berens, C., 2012. Promoter strength driving TetR determines the regulatory properties of Tet-controlled expression systems. PloS. one. 7(7), e41620.
Grape, M., Sundström, L., Kronvall, G., 2003. Sulphonamide resistance gene sul3 found in Escherichia coli isolates from human sources. J. Antimicrob. Chemother. 52(6), 1022-1024.
Grenni, P., 2022. Antimicrobial resistance in rivers: a review of the genes detected and new challenges. Environ. Toxicol. Chem. 41(3), 687-714.
Harris, H., Stambaugh, H., Jacobs, E., Bhalodi, A., Chandrasekaran, S., Cole, N.C., Lu, J., Tekle, T., Humphries, R., Simner, P.J., 2025. Defining antimicrobial susceptibility testing methods and breakpoints among Achromobacter species. J. Clin. Microbiol. 63(6), e0026425.
Hasan, K.A., Ali, S.A., Rehman, M., Bin-Asif, H., Zahid, S., 2018. The unravelled Enterococcus faecalis zoonotic superbugs: Emerging multiple resistant and virulent lineages isolated from poultry environment. Zoonoses. Public. Health. 65(8), 921-935.
Hedayatianfard, K., Akhlaghi, M., Sharifiyazdi, H., 2014. Detection of tetracycline resistance genes in bacteria isolated from fish farms using polymerase chain reaction. Vet. Res. Forum. 5(4), 269-275.
Hossain, S., De Silva, B.C.J., Wimalasena, S.H.M.P., Pathirana, H.N.K.S., Heo, G.J., 2017. High prevalence of quinolone resistance genes in Citrobacter freundii isolated from pet turtles. Asian. J. Anim. Vet. Adv. 12(4), 212-217.
Huang, Z., Yu, K., Fu, S., Xiao, Y., Wei, Q., Wang, D., 2022. Genomic analysis reveals high intra-species diversity of Shewanella algae. Microb. Genom. 8(2), 000786.
Jones, M.K., Oliver, J.D., 2009. Vibrio vulnificus: disease and pathogenesis. Infect. Immun. 77(5), 1723-1733.
La Rosa, M.C., Maugeri, A., Favara, G., La Mastra, C., Magnano San Lio, R., Barchitta, M., Agodi, A., 2025. The impact of wastewater on antimicrobial resistance: A scoping review of transmission pathways and contributing factors. Antibiotics (Basel). 14(2), 131.
Lajqi Berisha, N., Poceva Panovska, A., Hajrulai-Musliu, Z., 2024. Antibiotic resistance and aquatic systems: Importance in public health. Water. 16(17), 2362.
Landsberg, J.H., Tabuchi, M., Rotstein, D.S., Subramaniam, K., Rodrigues, T.C.S., Waltzek, T.B., Stacy, N.I., Wilson, P.W., Kiryu, Y., Uzal, F.A., de Wit, M., 2022. Novel lethal clostridial infection in Florida manatees (Trichechus manatus latirostris): Cause of the 2013 unusual mortality event in the Indian River Lagoon. Front. Mar. Sci. 9, 841857.
Li, M., Zhao, L., Ma, J., Zhao, N., Luo, J., Wang, C., Chen, L., Ma, G., Wang, Y., He, H., 2018. Vibrio vulnificus in aquariums is a novel threat to marine mammals and public health. Transbound. Emerg. Dis. 65(6), 1863-1871.
Liguori, K., Keenum, I., Davis, B.C., Calarco, J., Milligan, E., Harwood, V.J., Pruden, A., 2022. Antimicrobial resistance monitoring of water environments: A framework for standardized methods and quality control. Environ. Sci. Technol. 56(13), 9149-9160.
Lo, C., Li, W.T., Yang, W.C., 2016. Oropharyngeal foreign body and antibiotic-resistant Vibrio parahaemolyticus infection in a stranded juvenile fraser's dolphin (Lagenodelphis hosei). Available online: https://www.vin.com/apputil/content/default adv1.aspx?pId=14818&id=7312345.
Mahieddine, F.C., Mathieu-Denoncourt, A., Duperthuy, M., 2025. Temperature influences antimicrobial resistance and virulence of Vibrio parahaemolyticus clinical isolates from Quebec, Canada. Pathogens. 14(6), 521.
Marsh, H., 1980. Age determination of the dugong (Dugong dugon (Miiller)) in Northern Australia and its biological implications. Rep. Int. Whal. Commn. 3, 181-201.
Milijasevic, M., Veskovic-Moracanin, S., Babic Milijasevic, J., Petrovic, J., Nastasijevic, I., 2024. Antimicrobial resistance in aquaculture: Risk mitigation within the One Health Context. Foods. 13(15), 2448.
Ng, W.W., Shum, H.P., To, K.K., Sridhar, S., 2022. Emerging infections due to Shewanella spp.: A case series of 128 cases over 10 years. Front. Med. 9, 850938.
Nielsen, K.A., Owen, H.C., Mills, P.C., Flint, M., Gibson, J.S., 2013. Bacteria isolated from dugongs (Dugong dugon) submitted for postmortem examination in Queensland, Australia, 2000-2011. J. Zoo. Wildl. Med. 44(1), 35-41.
Norman, S.A., Lambourn, D.M., Huggins, J.L., Gaydos, J.K., Dubpernell, S., Berta, S., Olson, J.K., Souze, V., Evans, A., Carlson, B., Johnson, M., Mayer, R., King, C., Scott, A., 2021 Antibiotic resistance of bacteria in two marine mammal species, harbor seals and harbor porpoises, living in an urban marine ecosystem, the Salish Sea, Washington State, USA. Oceans. 2(1), 86-104.
Obusan, M.C.M., Aragones, L.V., Rivera, W.L., Siringan, M.A.T., 2018. Antibiotic susceptibility patterns of bacteria isolated from cetaceans stranded in the Philippines. Aquat. Mamm. 44(5), 558-569.
Obusan, M.C.M., Caras, J.A.A., Lumang, L.S.L., Calderon, E.J.S., Villanueva, R.M.D., Salibay, C.C., Siringan, M.A.T., Rivera, W.L., Masangkay, J.S., Aragones, L.V., 2021. Bacteriological and histopathological findings in cetaceans that stranded in the Philippines from 2017 to 2018. PLoS. One. 16(11), e0243691.
Owen, H., Gillespie, A., Wilkie, I., 2012. Postmortem findings from Dugong (Dugong dugon) submissions to the University of Queensland: 1997-2010. J. Wildl. Dis. 48(4), 962-970.
Owen, H.C., Flint, M., Limpus, C.J., Palmieri, C., Mills, P.C., 2013. Evidence of sirenian cold stress syndrome in dugongs Dugong dugon from southeast Queensland, Australia. Dis. Aquat. Organ. 103(1), 1-7.
Panyawai, J., Prathep, A., 2022. A systematic review of the status, knowledge, and research gaps of dugong in Southeast Asia. Aquat. Mamm. 48(3), 203-222.
Poommouang, A., Piboon, P., Buddhachat, K., Brown, J.L., Kriangwanich, W., Chomdej, S., Kampuansai, J., Mekchay, S., Kaewmong, P., Kittiwattanawong, K., Nganvongpanit, K., 2022. Microsatellite polymorphism and the population structure of dugongs (Dugong dugon) in Thailand. Animals (Basel). 12(3), 235.
Prasad, P., Reshi, S., Nataraj, G., 2019. Topic: Shewanella species: case series on a rare emerging pathogen. Indian. J. Microbiol. Res. 6(4), 303-307.
Pugliares, K.R., Bogomolni, A., Touhey, K.M., Herzig, S.M., Harry, C.T., Moore, M.J., 2007. Marine mammal necropsy: an introductory guide for stranding responders and field biologists. Woods Hole Oceanographic Institution, Woods Hole, MA.
Raharjo, H.M., Budiyansah, H., Mursalim, M.F., Chokmangmeepisarn, P., Sakulworakan, R., Madyod, S., Sewaka, M., Sonthi, M., Debnath, P.P., Elayaraja, S., Rung-Ruangkijkrai, T., Dong, H.T., Rodkhum, C., 2022. Distribution of vibrionaceae in farmed Asian sea bass, Lates calcarifer in Thailand and their high prevalence of antimicrobial resistance. J. Fish. Dis. 45(9), 1355-1371.
Rajni, E., Kataria, S., Sarna, M.K., Garg, V.K., 2023. A case of bacteremia by Achromobacter xylosoxidans in an immunocompromised host and review of literature. Arch. Med. Health. Sci. 11(1), 141-144.
Sanches-Fernandes, G.M.M., Sá-Correia, I., Costa, R., 2022. Vibriosis outbreaks in aquaculture: addressing environmental and public health concerns and preventive therapies using gilthead seabream farming as a model system. Front. Microbiol. 13, 904815.
Sato, T., Shibuya, H., Ohba, S., Nojiri, T., Shirai, W., 2003. Mycobacteriosis in two captive Florida manatees (Trichechus manatus latirostris). J. Zoo. Wildl. Med. 34(2), 184-188.
Schroeder, J.P., Wallace, J.G., Cates, M.B., Greco, S.B., Moore, P.W., 1985. An infection by Vibrio alginolyticus in an Atlantic bottlenose dolphin housed in an open ocean pen. J. Wildl. Dis. 21(4), 437-438.
Sezgin, S.S., Yılmaz, M., Arslan, T., Kubilay, A., 2023. Current antibiotic sensitivity of Lactococcus garvieae in rainbow trout (Oncorhynchus mykiss) farms from Southwestern Turkey. J. Agr. Sci. 29(2), 630-642.
Sharma, J., Sharma, M., Ray, P., 2010. Detection of TEM & SHV genes in Escherichia coli & Klebsiella pneumoniae isolates in a tertiary care hospital from India. Indian. J. Med. Res. 132, 332-336.
Sheikh, H.I., Alhamadin, N.I.I., Liew, H.J., Fadhlina, A., Wahid, M.E.A., Musa, N., Jalal, K.C.A., 2024. Virulence factors of the zoonotic pathogen Vibrio alginolyticus: a review and bibliometric analysis. Appl. Biochem. Microbiol. 60(3), 514-531.
Silva, M.C., Attademo, F.F., Freire, A.C., Sousa, G.P., Luna, F.O., Lima, D.C., Mota, R.A., Mendes, E.S., Silva, J.C., 2017. Identification of bacteria in blood cultures from clinically ill captive Antillean manatees (Trichechus manatus manatus). J. Zoo. Wildl. Med. 48(1), 13-17.
Soleimani, N., Aganj, M., Ali, L., Shokoohizadeh, L., Sakinc, T., 2014. Frequency distribution of genes encoding aminoglycoside modifying enzymes in uropathogenic E. coli isolated from Iranian hospital. BMC. Res. Notes. 7, 842.
Sornying, P., Kaewnoi, D., Keawchana, N., Khumraksa, P., Ruangpoon, S., Ninwat, S., Sukkarun, P., Arnuphapprasert, A., Suyapoh, W., 2025. The hidden burden: morphological, histological, and pathological features of Paradujardinia halicoris in dugongs (Dugong dugon) from the Andaman coast of Thailand: Characterizing the nematode-induced gastrointestinal lesions in a threatened sirenian species. Vet. Integr. Sci. 24(2), 1-16.
Sornying, P., Keawchana, N., Yakoh, A., Nookamsuan, K., Maitrimitr, W., Sarawaree, K., Jantrakajorn, S., Suyapoh, W., 2025. Piscine intestinal coccidial infections in Pearl Gentian groupers (Epinephelus lanceolatus ♂ × E. fuscoguttatus ♀): Pathogenesis, and host intestinal response. Fish. Pathol. 60(3), 1-12.
Steward, C.D., Rasheed, J.K., Hubert, S.K., Biddle, J.W., Raney, P.M., Anderson, G.J., Williams, P.P., Brittain, K.L., Oliver, A., McGowan, J.E. Jr., Tenover, F.C., 2001. Characterization of clinical isolates of Klebsiella pneumoniae from 19 laboratories using the National Committee for Clinical Laboratory Standards extended-spectrum β-lactamase detection methods. J. Clin. Microbiol. 39(8), 2864-2872.
Suzzi, A.L., Stat, M., Gaston, T.F., Siboni, N., Williams, N.L.R., Seymour, J.R., Huggett, M.J., 2022. Elevated estuary water temperature drives fish gut dysbiosis and increased loads of pathogenic vibrionaceae. Environ. Res. 219, 115144.
Tang, K.W.K., Millar, B.C., Moore, J.E., 2023. Antimicrobial resistance (AMR). Br. J. Biomed. Sci. 80, 11387.
Trinh, S.A., Gavin, H.E., Satchell, K.J.F., 2017. Efficacy of ceftriaxone, cefepime, doxycycline, ciprofloxacin, and combination therapy for Vibrio vulnificus foodborne septicemia. Antimicrob. Agents. Chemother. 61(12), e01106-01117.
Vega-Sánchez, V., Latif-Eugenín, F., Soriano-Vargas, E., Beaz-Hidalgo, R., Figueras, M.J., Aguilera-Arreola, M.G., Castro-Escarpulli, G., 2014. Re-identification of Aeromonas isolates from rainbow trout and incidence of class 1 integron and β-lactamase genes. Vet. Microbiol. 172(3-4), 528-533.
Vergara-Parente, J.E., Sidrim, J.J.C., Pessoa, A., Parente, C.L., Marcondes, M.C.C., Teixeira, M., Rocha, M.F.G., 2003. Salmonellosis in an Antillean manatee (Trichechus manatus manatus) calf: a fatal case. Aquat. Mamm. 29(1), 131-136.
Wallace, C.C., Yund, P.O., Ford, T.E., Matassa, K.A., Bass, A.L., 2013. Increase in antimicrobial resistance in bacteria isolated from stranded marine mammals of the Northwest Atlantic. EcoHealth. 10(2), 201-210.
Walsh, M.T., Bossart, G.D., Young, W.G. Jr., Rose, P.M., 1987. Omphalitis and peritonitis in a young West Indian manatee (Trichechus manatus). J. Wildl. Dis. 23(4), 702-704.
Waltzek, T.B., Cortés-Hinojosa, G., Wellehan, J.F. Jr., Gray, G.C., 2012. Marine mammal zoonoses: a review of disease manifestations. Zoonoses. Public. Health. 59(8), 521-535.
Wang, B., Liu, K., Sakornwimon, W., Huang, W., Li, T., Lai, X., Li, C., Zhao, L., Cong, B., Liu, S., 2025. Spatial planning for dugong conservation: assessing habitat suitability and conservation gaps in Indo-Pacific Convergence Zone. Mar. Policy. 180, 106777.
Warsa, U.C., Nonoyama, M., Ida, T., Okamoto, R., Okubo, T., Shimauchi, C., Kuga, A., Inoue, M., 1996. Detection of tet(K) and tet(M) in Staphylococcus aureus of Asian countries by the polymerase chain reaction. J. Antibiot. 49(11), 1127-1132.
Wirsing, A.J., Kiszka, J.J., Allen, A.Â‐C., Heithaus, M.R., 2022. Ecological roles and importance of sea cows (Order: Sirenia): a review and prospectus. Mar. Ecol. Prog. Ser. 689, 191-215.
Wu, Q., Wang, Y., Zhang, X., Gu, X., He, H., Jin, X., 2023. Pyogranulomatous dermatitis with Enterococcus faecalis in a spotted seal (Phoca larga). Vet. Med. Sci. 9(2), 985-991.
Yano, Y., Hamano, K., Satomi, M., Tsutsui, I., Aue‐umneoy, D., 2011. Diversity and characterization of oxytetracycline‐resistant bacteria associated with non‐native species, white‐leg shrimp (Litopenaeus vannamei), and native species, black tiger shrimp (Penaeus monodon), intensively cultured in Thailand. J. Appl. Microbiol. 110(3), 713-722.
Yano, Y., Hamano, K., Satomi, M., Tsutsui, I., Ban, M., Aue‐Umneoy, D., 2014. Prevalence and antimicrobial susceptibility of Vibrio species related to food safety isolated from shrimp cultured at inland ponds in Thailand. Food. Control. 38, 30-36.