Vibriosis control in Vannamei Shrimp: Intestinal and mangrove-derived bacteriophages

Open Access

Issue		BIO Web Conf. Volume 143, 2024 The 5^th International Conference on Bioenergy and Environmentally Sustainable Agriculture Technology (ICoN-BEAT 2024)


Article Number		02007
Number of page(s)		13
Section		Fishery and Animal Science
DOI		https://doi.org/10.1051/bioconf/202414302007
Published online		25 November 2024

N. A. D. Kah Sem, S. Abd Gani, C. M. Chong, I. Natrah, S. Shamsi, Management and Mitigation of Vibriosis in Aquaculture: Nanoparticles as Promising Alternatives. Int J Mol Sci. 24(16) (2023). [Google Scholar]
G. M. M. Sanches-Fernandes, I. Sá-Correia, R. Costa, 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 (2022). [CrossRef] [PubMed] [Google Scholar]
D. I. Haris, J. Yaminudin, S. H. Othman, K. C. Lim, I. Ismail, P. D. Wulan Sari, M. Karim, The use of commercial feed and microdiets incorporated with probiotics in Penaeid shrimp culture: a short review. Latin american journal of aquatic research. 52(3), 350–367 (2024). [CrossRef] [Google Scholar]
C. de Souza Valente, A. H. L. Wan, Vibrio and major commercially important vibriosis diseases in decapod crustaceans. Journal of Invertebrate Pathology. 181, 107527 (2021). [CrossRef] [PubMed] [Google Scholar]
B. T. Iber, N. A. Kasan, Recent advances in Shrimp aquaculture wastewater management. Heliyon. 7(11), e08283 (2021). [CrossRef] [PubMed] [Google Scholar]
C. Aranaga, L. D. Pantoja, E. A. Martínez, A. Falco, Phage therapy in the era of multidrug resistance in bacteria: a systematic review. International journal of molecular sciences. 23(9), 4577 (2022). [CrossRef] [PubMed] [Google Scholar]
A. Broncano-Lavado, G. Santamaría-Corral, J. Esteban, M. García-Quintanilla, Advances in bacteriophage therapy against relevant multidrug-resistant pathogens. Antibiotics. 10(6), 672 (2021). [CrossRef] [PubMed] [Google Scholar]
M. Reuter, D. H. Kruger, Approaches to optimize therapeutic bacteriophage and bacteriophage-derived products to combat bacterial infections. Virus Genes. 56(2), 136149 (2020). [CrossRef] [PubMed] [Google Scholar]
N. Düzgüneş, M. Sessevmez, M. Yildirim, Bacteriophage therapy of bacterial infections: the rediscovered frontier. Pharmaceuticals. 14(1), 34 (2021). [PubMed] [Google Scholar]
N. J. Anyaegbunam, C. C. Anekpo, Z. K. G. Anyaegbunam, Y. Doowuese, C. B. Chinaka, O. J. Odo, H. C. Sharndama, O. P. Okeke, I. E. Mba, The resurgence of phagebased therapy in the era of increasing antibiotic resistance: From research progress to challenges and prospects. Microbiological Research. 264, 127155 (2022). [CrossRef] [PubMed] [Google Scholar]
M. Taati Moghadam, N. Amirmozafari, A. Shariati, M. Hallajzadeh, S. Mirkalantari, A. Khoshbayan, F. Masjedian Jazi, How Phages Overcome the Challenges of Drug Resistant Bacteria in Clinical Infections. Infect Drug Resist. 13, 45–61 (2020). [CrossRef] [Google Scholar]
T. Zhang, M. Zhang, Y. Chen, M. Yu, R. Zeng, M. Jin, Isolation, characterization, and comparative genomic analysis of vB_BviS-A10Y, a novel bacteriophage from mangrove sediments. Archives of Virology. 168(2), 54 (2023). [CrossRef] [PubMed] [Google Scholar]
A. Sekar, R. S. Chinnappan, K. Kandasamy, Therapeutic effect of mangrove-derived bacteriophages on biofilm forming bacteria isolated from mice bearing lung-cancer. World J Pharm Res. 5(4), 875–891 (2015). [Google Scholar]
J. Fu, Y. Li, L. Zhao, C. Wu, Z. He, Characterization of vB_ValM_PVA8, a broad-hostrange bacteriophage infecting Vibrio alginolyticus and Vibrio parahaemolyticus. Frontiers in Microbiology. 14, 1105924 (2023). [CrossRef] [PubMed] [Google Scholar]
J. Fu, Y. Li, L. Zhao, C. Wu, Z. He, Characterization and genomic analysis of a bacteriophage with potential in lysing Vibrio alginolyticus. Viruses. 15(1), 135 (2022). [CrossRef] [PubMed] [Google Scholar]
B. K. Shrestha, M. Tumbahangphe, J. Shakya, S. Chauhan, B. Dhungana, R. Shrestha, J. Limbu, K. Khadka, A. Rai, Laboratory Protocols for Isolation and Identification of Toxigenic Strains of Vibrio cholerae: A Review. International Journal for Research in Applied Sciences and Biotechnology. 7(6), 181–189 (2020). [CrossRef] [Google Scholar]
J.-M. Lee, R. N. Azizah, K.-S. Kim, Comparative evaluation of three agar media-based methods for presumptive identification of seafood-originated Vibrio parahaemolyticus strains. Food Control. 116, 107308 (2020). [CrossRef] [Google Scholar]
J. Fu, Y. Li, L. Zhao, C. Wu, Z. He, Characterization of vB_ValM_PVA8, a broad-hostrange bacteriophage infecting Vibrio alginolyticus and Vibrio parahaemolyticus. Front Microbiol. 14, 1105924 (2023). [CrossRef] [PubMed] [Google Scholar]
D. M. a. Fadlilah, A. W. Setiawan, Y. A. Handoko, [Isolation, characterisation and pH stability test of bacteriophage Xanthomonas oryzae from paddy fields]. Jurnal Ilmiah Pertanian. 19(2), 118–125 (2022). [Google Scholar]
F. A. Choliq, M. Martosudiro, I. Istiqomah, M. F. Nijami, [Isolation and test of the ability of bacteriophages as control agents of bacterial wilt disease (Ralstonia solanacearum) on tomato plants]. VIABEL: Jurnal Ilmiah Ilmu-Ilmu Pertanian. 14(1), 8–20 (2020). [CrossRef] [Google Scholar]
U. Ni’mah, D. Pringgenies, G. W. Santosa, [Effect of Stichopus hermanii Semper, 1868 (Stichopodidae, Holothuroidea) extract on the total haemocyte count of Litopenaeus vannamei Boone, 1931 (Penaeidae, Crustacea)]. Journal of Marine Research. 10(3), 387–394 (2021). [CrossRef] [Google Scholar]
U. Devitha Tri, P. Slamet Budi, H. Sri, S. Ayi, [Overview of hematological parameters in tilapia (Oreochromis niloticus) given Streptococcus iniae DNA vaccine with different doses]. Journal of Aquaculture Management and Technology. 2(4), 7–20 (2013). [Google Scholar]
O. D. Nigro G. F. Steward, Differential specificity of selective culture media for enumeration of pathogenic vibrios: Advantages and limitations of multi-plating methods. Journal of Microbiological Methods. 111, 24–30 (2015). [CrossRef] [PubMed] [Google Scholar]
Y. Nakashima, M. Oho, K. Kusaba, Z. Nagasawa, O. Komatsu, I. Manome, K. Araki, H. Oishi, M. Nakashima, A chromogenic substrate culture plate for early identification of Vibrio vulnificus and isolation of other marine Vibrios. Ann Clin Lab Sci. 37(4), 330–4 (2007). [PubMed] [Google Scholar]
E. Ogayar, I. Larrañaga, A. Lomba, V. R. Kaberdin, I. Arana, M. Orruño, Efficiency and specificity of CARD‐FISH probes in detection of marine vibrios. Environmental Microbiology Reports. 13(6), 928–933 (2021). [CrossRef] [PubMed] [Google Scholar]
C. C. Glackin, S. Dupke, T. S. Chandra, D. Riedinger, M. Labrenz, Combined TCBS and CHROMagar Analyses Allow for Basic Identification of Vibrio vulnificus within a 48 h Incubation Period in the Coastal Baltic Sea. Microorganisms. 12(3), 614 (2024). [CrossRef] [PubMed] [Google Scholar]
L. H. B. Ngoc, N. T. L. Anh, V. N. T. Anh, N. T. P. Uyen, L. V. Dung, T. T. B. Van, Infectious characteristics of some Vibrio spp. phages isolated in shrimp farming of the Mekong delta. Journal of Applied Biology & Biotechnology. 12, 48–54 (2024). [Google Scholar]
Q. Hao, Y. Bai, H. Zhou, X. Bao, H. Wang, L. Zhang, M. Lyu, S. Wang, Isolation and characterization of bacteriophage VA5 against Vibrio alginolyticus. Microorganisms. 11(12), 2822 (2023). [CrossRef] [PubMed] [Google Scholar]
A. D. Tadeu, J. Duarte, D. Trindade, P. Costa, C. Venâncio, I. Lopes, V. Oliveira, N. C. Gomes, A. Almeida, C. Pereira, Bacteriophages to control Vibrio alginolyticus in live feeds prior to their administration in larviculture. Journal of Applied Microbiology. 135(5), lxae115 (2024). [CrossRef] [PubMed] [Google Scholar]
S. Liu, S.-Y. Quek, K. Huang, Advanced strategies to overcome the challenges of bacteriophage-based antimicrobial treatments in food and agricultural systems. Critical Reviews in Food Science and Nutrition. 1–25 (2023). [Google Scholar]
T. Dharmaraj, M. J. Kratochvil, J. D. Pourtois, Q. Chen, M. Hajfathalian, A. Hargil, Y.-H. Lin, Z. Evans, A. Oromí-Bosch, J. D. Berry, Rapid assessment of changes in phage bioactivity using dynamic light scattering. PNAS nexus. 2(12), 406 (2023). [CrossRef] [Google Scholar]
L. D. Moda-Silva, V. D. Oliveira, T. A. da Cruz, A. C. da Rocha, E. Watanabe, The Antibacterial Activity of Novel Bacteriophages and the Emergence of Bacterial Resistance to Phage Infections: An In Vitro Study. Applied Biosciences, 3(2), 186–196 (2024). DOI: 10.3390/applbiosci3020012. [CrossRef] [Google Scholar]
W. Liu, Y. Wu, H. Wang, H. Wang, and M. Zhou, Isolation Biological Characteristics of a Novel Phage and Its Application to Control Vibrio Parahaemolyticus in Shellfish Meat. Foodborne Pathogens and Disease. (2024). [Google Scholar]
J. P. González-Gómez, S. A. Soto-Rodriguez, B. Gomez-Gil, J. M. Serrano-Hernández, R. Lozano-Olvera, O. López-Cuevas, N. Castro-del Campo, C. Chaidez, Effect of phage therapy on survival, histopathology, and water microbiota of Penaeus vannamei challenged with Vibrio parahaemolyticus causing acute hepatopancreatic necrosis disease (AHPND). Aquaculture. 576, 739851 (2023). [CrossRef] [Google Scholar]
K. Alagappan, V. Karuppiah, B. Deivasigamani, Protective effect of phages on experimental V. parahaemolyticus infection and immune response in shrimp (Fabricius, 1798). Aquaculture. 453, 86–92 (2016). [CrossRef] [Google Scholar]
S. Jeyachandran, K. Park, I. S. Kwak, V. Baskaralingam, Morphological and functional characterization of circulating hemocytes using microscopy techniques. Microscopy research and technique. 83(7), 736–743 (2020). [CrossRef] [PubMed] [Google Scholar]
Y. Luo, W.-X. Wang, Immune responses of oyster hemocyte subpopulations to in vitro and in vivo zinc exposure. Aquatic Toxicology. 242, 106022 (2022). [CrossRef] [Google Scholar]
M. M. M. Hossain, L. N. Tanni, M. A. Rahman, N. Farjana, R. S. Moon, N. Z. Tonni, M. R. Mekat, S. Mojumdar, N. R. Prince, S. A. Rojoni, Bacteriophage and nonpathogenic vibrio to control diseases in black tiger shrimp (Penaeus monodon) aquaculture. (2023). [Google Scholar]
M. Benala, M. Vaiyapuri, V. Sivam, K. Raveendran, M. P. Mothadaka, M. R. Badireddy, Genome characterization and infectivity potential of vibriophage-ϕLV6 with lytic activity against luminescent vibrios of Penaeus vannamei shrimp aquaculture. Viruses. 15(4), 868 (2023). [CrossRef] [PubMed] [Google Scholar]
D. Wahjuningrum, P. Ramhirez, L. Nuzullia, M. Yuhana, S. Sukenda, H. Nasrullah, Isolation of Lytic Bacteriophages infected Indonesian-strain Vibrio parahaemolyticus and its Protective Effects on Brine Shrimp (Artemia sp.). Jurnal Ilmiah Perikanan dan Kelautan. (2023). [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.