Academic literature on the topic 'Vibrio marinus'
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Journal articles on the topic "Vibrio marinus"
Urakawa, Hidetoshi, Kumiko Kita-Tsukamoto, and Kouichi Ohwada. "Restriction fragment length polymorphism analysis of psychrophilic and psychrotrophic Vibrio and Photobacterium from the north-western Pacific Ocean and Otsuchi Bay, Japan." Canadian Journal of Microbiology 45, no. 1 (January 1, 1999): 67–76. http://dx.doi.org/10.1139/w98-128.
Full textTall, B. D., J. F. La Peyre, J. W. Bier, M. D. Miliotis, D. E. Hanes, M. H. Kothary, D. B. Shah, and M. Faisal. "Perkinsus marinus Extracellular Protease Modulates Survival of Vibrio vulnificus in Eastern Oyster (Crassostrea virginica) Hemocytes." Applied and Environmental Microbiology 65, no. 9 (September 1, 1999): 4261–63. http://dx.doi.org/10.1128/aem.65.9.4261-4263.1999.
Full textBAUMEISTER, LESLIE, MONA E. HOCHMAN, JOHN R. SCHWARZ, and ROBIN BRINKMEYER. "Occurrence of Vibrio vulnificus and Toxigenic Vibrio parahaemolyticus on Sea Catfishes from Galveston Bay, Texas." Journal of Food Protection 77, no. 10 (October 1, 2014): 1784–86. http://dx.doi.org/10.4315/0362-028x.jfp-14-175.
Full textLangridge, Patricia, R. D. Haight, and R. Y. Morita. "Use of heat for obtaining malic dehydrogenase from cells of Vibrio marinus." Zeitschrift für allgemeine Mikrobiologie 8, no. 3 (January 24, 2007): 221–23. http://dx.doi.org/10.1002/jobm.19680080308.
Full textMasuda, K. V., and L. J. Albright. "Hydrostatic pressure effects upon cellular leakage and active transport by Vibrio marinus." Zeitschrift für allgemeine Mikrobiologie 18, no. 10 (January 24, 2007): 731–40. http://dx.doi.org/10.1002/jobm.19780181005.
Full textTokárová, Viola, Ayyappasamy Sudalaiyadum Perumal, Monalisha Nayak, Henry Shum, Ondřej Kašpar, Kavya Rajendran, Mahmood Mohammadi, et al. "Patterns of bacterial motility in microfluidics-confining environments." Proceedings of the National Academy of Sciences 118, no. 17 (April 19, 2021): e2013925118. http://dx.doi.org/10.1073/pnas.2013925118.
Full textBirkbeck, T. H., B. Billcliffe, A. Laidler, and D. I. Cox. "The relationship between Aeromonas sp. NCIMB 2263, a causative agent of skin lesions in Atlantic salmon, Vibrio marinus (Moritella marina) and Vibrio viscosus." Journal of Fish Diseases 23, no. 4 (July 2000): 281–83. http://dx.doi.org/10.1046/j.1365-2761.2000.00228.x.
Full textSOKOLOVA, INNA M., JAMES D. OLIVER, and LARRY J. LEAMY. "AN AFLP APPROACH TO IDENTIFY GENETIC MARKERS ASSOCIATED WITH RESISTANCE TO VIBRIO VULNIFICUS AND PERKINSUS MARINUS IN EASTERN OYSTERS." Journal of Shellfish Research 25, no. 1 (April 2006): 95–100. http://dx.doi.org/10.2983/0730-8000(2006)25[95:aaatig]2.0.co;2.
Full textBen Dhia Thabet, O., M. L. Fardeau, C. Suarez-Nuñez, M. Hamdi, P. Thomas, B. Ollivier, and D. Alazard. "Desulfovibrio marinus sp. nov., a moderately halophilic sulfate-reducing bacterium isolated from marine sediments in Tunisia." International Journal of Systematic and Evolutionary Microbiology 57, no. 9 (September 1, 2007): 2167–70. http://dx.doi.org/10.1099/ijs.0.64790-0.
Full textHernández Mendoza, Dulce Maripaz, Pablo San Martín del Ángel, Catya Jiménez Torres, and Rosa Idalia Hernández Herrera. "Monitoreo de vibrio spp. en ostiones Crassostrea virginica de las lagunas de Tamiahua y Tampamachoco, Veracruz, México." Revista Biológico Agropecuaria Tuxpan 9, no. 1 (July 1, 2021): 122–41. http://dx.doi.org/10.47808/revistabioagro.v9i1.346.
Full textDissertations / Theses on the topic "Vibrio marinus"
Robino, Etienne. "Etude des amibes marines et de leurs interactions avec les vibrios pathogènes d’huître." Thesis, Montpellier, 2019. http://www.theses.fr/2019MONTG041.
Full textFree living amoebae inhabit aquatic environments and use phagocytosis of bacteria for their nutrition. According to the hypothesis of coincidental evolution of virulence, the cellular and molecular mechanisms of phagocytosis being preserved from amoebae to the immune cells of animals, the predation exerted by amoebae could favor the emergence of pathogenic bacteria resistant to phagocytosis. Since 2008, Crassostrea gigas oysters have suffered from over-mortality in France. This poly-microbial disease involves the Herpes OsHV-1 μvar virus which causes an immunosuppression of oysters that are then colonized by various opportunistic pathogenic bacteria including vibrios inducing the death of the animal. V. tasmaniensis LGP32 is a facultative intracellular pathogen of oyster hemocytes that resists phagocytosis and destroys hemocytes using different virulence factors. We have therefore undertaken to study the interactions between marine amoebae of the oyster environment and the vibrios in order to verify if some mechanisms of virulence could also play a role in this type of interactions. By performing field sampling, we demonstrated that the interaction between vibrios and amoebae is ecologically realistic and observed a low diversity of heterotrophic protists near the oyster tables of the Thau Lagoon compared to other less anthropogenic environments. Functional studies between LGP32 and the amoeba Vannella sp. AP1411 showed that LGP32 is able to resist amoeba predation involving certain virulence factors such as Vsm metalloprotease and CopA P-ATPase copper efflux pump which are also involved in the interaction of LGP32 with oysters. In contrast, other virulence factors implicated in the oyster are not involved in amoeba-predation resistance indicating that some factors are involved in interactions with various hosts while others would be involved in more specific interactions
Poirier, Aurore. "Etude comparative des interactions Vibrio - phagocytes dans l'environnement marin." Thesis, Montpellier, 2015. http://www.theses.fr/2015MONTS062/document.
Full textVibrio strains belonging to the Splendidus clade have been repeatedly found in juvenile diseased oysters affected by summer mortalities. V. tasmaniensis LGP32 is an intracellular pathogen of oyster hemocytes which has been reported to alter the oxidative burst and inhibit phagosome maturation.We here focus on the interactions between phagocytes and V. tasmaniensis LGP32, at molecular, cellular and environmental scales. In the first part of this work, we uncover anunknown antimicrobial mechanism of C. gigas hemocytes: the formation of DNA extracellular traps (ETs). These ETs are associated with antimicrobial histones and are able to entrap bacteria. As in vertebrates, ETs formation depends on reactive oxygen species production. In addition, the presence of ETs was confirmed in vivo and has been associated with antimicrobial histones accumulation in tissues, in response to injury or infection. In the second part of this work, we studied the interactions between V. tasmaniensis LGP32 and heterotrophic protists found in the oyster’s environment, such as amoebae and ciliates, which feed on microorganisms by phagocytosis. An important result of this workwas that V. tasmaniensis LGP32 resists to phagocytosis by environmental heterotrophic protists, as well as to oyster hemocytes. To our knowledge, this is the first mechanical description of an interaction between marine amoebae and marine pathogenic bacteria. As the amoebae were isolated from the direct environment of oysters, we can presume that the selective pressure exerted by environmental phagocytes could select for virulence and/or phagocytosis resistance traits in marine bacteria as in the case of V. tasmaniensis LGP32
Dueñas, Peña Talia Greta Amalia. "Recuento de Vibrio parahaemolyticus Kanagawa positivo en especies marinas de consumo en Lima Metropolitana y Callao." Bachelor's thesis, Universidad Nacional Mayor de San Marcos, 2008. https://hdl.handle.net/20.500.12672/1628.
Full text-- The aim of this research was performing a count of Vibrio parahaemolyticus Kanagawa positive out of 50 samples including raw fish, mollusks and crustaceans collected from fishermen’s wharf, fisheries, and supermarkets of edible character in Metropolitan Lima and Callao between november 1999 and april 2000. The microbiological analysis was performed according to Bacteriological Analytical Manual (BAM, 7 ed.). Vibrio parahaemolyticus Kanagawa positive was found in 4 samples from 5 strains with biochemical features that met those of Vibrio parahaemolyticus out of a total of 568 analized strains. The Most Probable Number (NMP) values found are as follows: Fish and crustaceans 3/g each, while molluscs had a minimum value of 3/g and a maximum of 7,4/g. Vibrio parahaemolyticus Kanagawa positive samples (n=4) represented 8% out of the total marine samples (n=50), being the percentages found in fish 2% (n=1), mollusks 4% (n=2) and crustaceans 2% (n=1) out of the total number of samples as well. -- Key Words: Vibrio parahaemolyticus, fish, mollusks, crustaceans, Kanagawa positive, MPN, Metropolitan Lima and Callao.
Tesis
Bienlien, Lydia M. "Influence of Perkinsus Marinus Infection and Oyster Health on Levels of Human-Pathogenic Vibrios in Oysters." W&M ScholarWorks, 2016. https://scholarworks.wm.edu/etd/1477068161.
Full textCARVALHO, Joana Angélica Lyra Vogeley de. "Efeito do uso de bactérias probióticas na sobrevivência de larvas de Litopenaeus vannamei expostas à infecção experimental por Vibrio spp." Universidade Federal Rural de Pernambuco, 2011. http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/6339.
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This study aimed to evaluate the survival of Litopenaeus vannamei shrimp larvae treated with probiotic bacteria and subsequently infected by Vibrio harveyi and Vibrio alginolyticus. Shrimp were kept in two 80L tanks under similar culture conditions, but only one tank was previously treated with commercial probiotic (Bacillus spp.) added daily in the water at a concentration of 105 CFU/ml. This protocol was maintained until the animals reach the stage of development needed for the infection experiments by Vibrio spp. Three independent infection experiments were performed: Zoea1 to Zoea3, Mysis1 to Mysis3 and Postlarvae (PL)10 to PL14 with the following treatments with four replicates each: only V. harveyi; commercial probiotic + V. harveyi; only V. alginolyticus; commercial probiotic + V. alginolyticus; and without Vibrio spp. and probiotic (Control). In the experiment with PL, only the treatments with V. harveyi; commercial probiotic + V. harveyi and control were used. Vibrio species were inoculated only at the beginning of each experiment at a concentration of 107 CFU/ml. At the end of experiments, a sample of water and shrimp from each experimental unit was submitted to quantification of Vibrio spp. Additionally, was realized an antagonism test of Bacillus spp. against Vibrio spp. In the experiments with zoea and mysis, larvae cultured in treatment V. harveyi had a significantly lower survival when compared with treatments V. alginolyticus and control. There was a significant increase in survival of zoea and mysis larvae treated with probiotic + V. harveyi with 81.07 and 90.13%, differentiating the larvae infected only with V. harveyi with 12.80 and 69.13%, respectively. There were no significant differences in survival of postlarvae among treatments. Total Vibrio spp. counts decreased in the water and shrimp of treatments with the use of probiotic. The probiotic (Bacillus spp.) showed inhibitory activity against Vibrio spp. in vitro. The results indicated an increase in the survival of early larval stages (zoea and mysis) infected by V. harveyi after treatment with Bacillus spp. The administration of probiotic bacteria is a promising alternative for the prevention of Vibrio spp. in larviculture of L. vannamei.
O presente estudo teve como objetivo avaliar a sobrevivência de larvas de Litopenaeus vannamei tratadas com bactérias probióticas e posteriormente infectadas por Vibrio harveyi e Vibrio alginolyticus. Os camarões foram mantidos em dois tanques de 80L nas mesmas condições, mas apenas um deles foi previamente tratado com probiótico comercial (Bacillus spp.) adicionado diariamente na água na concentração de 105 UFC/ml. Este protocolo foi mantido até os animais alcançarem o estágio de desenvolvimento larval necessário para os experimentos de infecção por Vibrio spp. Foram realizados três experimentos independentes de infecção: Zoea1 a Zoea3, Mísis1 a Mísis3 e Pós-larvas (PL)10 a PL14 com os seguintes tratamentos com quatro repetições cada: somente V.harveyi; probiótico comercial + V. harveyi; somente V. alginolyticus; probiótico comercial + V. alginolyticus; sem Vibrio spp. e probiótico (controle). No experimento com PL, somente os tratamentos com V. harveyi; probiótico comercial + V. harveyi e controle foram utilizados. As espécies de Vibrio foram inoculadas apenas no início de cada experimento na concentração de 107 UFC/ml. Ao final dos experimentos, uma amostra de água e camarão de cada parcela experimental foi submetida à quantificação de Vibrio spp. Adicionalmente foi realizado um teste de antagonismo in vitro de Bacillus spp. contra Vibrio spp. Nos experimentos com zoea e mísis, as larvas cultivadas no tratamento V. harveyi apresentaram uma sobrevivência significativamente inferior quando comparadas com as dos tratamentos V. alginolyticus e controle. Houve um aumento significativo na sobrevivência de larvas zoea e mísis tratadas com probiótico + V. harveyi com 81,07 e 90,13%, em comparação com as larvas infectadas apenas com V. harveyi com 12,80 e 69,13%, respectivamente. Não foram observadas diferenças significativas na sobrevivência das pós-larvas entre tratamentos. A quantidade total de Vibrio spp. na água e camarões diminuiu nos tratamentos com o uso de probiótico. O probiótico (Bacillus spp.) apresentou atividade inibitória contra Vibrio spp. in vitro. Os resultados indicaram um aumento na sobrevivência dos estágios larvais iniciais (zoea e mísis) infectadas por V. harveyi após tratamento com Bacillus spp. A administração de bactérias probióticas é uma alternativa promissora para a prevenção de Vibrio spp. na larvicultura de L. vannamei.
Trubitsyn, Denis. "Magnetosome formation in marine vibrio MV-1." Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/7589.
Full textFlores, Dominick Violeta de Jesús. "Aislamiento y caracterización de un bacteriófago con actividad lítica para Vibrio fluvialis." Master's thesis, Universidad Nacional Mayor de San Marcos, 2017. https://hdl.handle.net/20.500.12672/7007.
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Girard, Léa. "Quorum Sensing in Vibrio spp. : AHL diversity, temporal dynamic and niche partitioning." Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066650/document.
Full textQuorum sensing is an important mechanism among Vibrio species and is involved in many vital functions such as niche colonization, survival strategies or virulence. However, AHL diversity still largely underestimated for the majority of Vibrio species and the current knowledge on AHL-mediated QS is limited to a few pathogenic or bioluminescent species. Nonetheless, these species are weakly abundant in seawater while dominant species in the environment are poorly studied. Our results revealed a unexpected diversity of AHL molecules but also a quite surprising intra-species diversity of AHL production phenotypes. For the first time, we showed that different isolates of a single genotype switched between different AHL production phenotypes among time and we revealed the potential involvement of abiotic and biotic parameters in these variations. However, it appears that when studied at a microscale, Vibrio populations are showing a functional structuration in ecological units consisting of phylogenetically close strains sharing habitat and social traits. In this context, it was necessary to determine if these different AHL production phenotypes were associated to different micro-habitats in the water column. We did not demonstrate that a common language was spoken within ecological populations. This thesis work provide new insights on AHL-mediated QS among a broader range of species and among Vibrio populations and depicts the potential impact of multiple aspects of marine environments on AHL production
Lavezzo, Lígia Carolina. "Caracterização das especies de vibrios isoladas em amostras de água do mar, plâncton e bivalves da zona litorânea do Estado de São Paulo." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-18112015-192329/.
Full textThe aim of this study was to characterize at the molecular level Vibrio species isolated from seawater, plankton, bivalves samples from Canal de São Sebastião (n=78), Baixada Santista (n=37) and Ubatuba (n=17), to analyze antimicrobial susceptibility and the major virulence-associated genes. The results showed ciprofloxacin, meropenem, nalidixic acid sensitivity, ampicillin, and cephalothin resistance, and a significant percentage of multidrug resistance (Ubatuba: 64.7%; Baixada Santista: 48.6%; Canal de São Sebastião: 43%). Four seawater isolates were found positive for the stn/sto virulence gene. MLSA allowed the identification of V.alginolyticus, V.fluvialis, V.campbellii, V.harveyi in Ubatuba; V.fluvialis, V.alginolyticus, V.campbellii, V.rotiferianus, V.harveyi, V.diabolicus, V.atypicus, V.coralliilyticus, V.maritimus, V.parahaemolyticus and V.tubiashii in Canal de São Sebastião, and V.alginolyticus, V.parahaemolyticus, V.rotiferianus, V.campbellii, V.harveyi, V.communis, V.maritimus, V.fluvialis, V.fortis, V.natriegens, and V.navarrensis in Baixada Santista.
Neto, Antonio Alves dos Santos. "Biologia computacional aplicada à análise de dados de microarranjos do genoma da bactéria marinha vibrio parahaemolyticus em presença de n-acetilglicosamina." Laboratório Nacional de Computação Científica, 2010. http://www.lncc.br/tdmc/tde_busca/arquivo.php?codArquivo=210.
Full textLarge scale gene expression analysis has fundamental importance for understanding cellular function and gene regulation mechanics. It enables the measurement of expression levels of thousands of genes simultaneously, and makes possible a wider understanding of the biological system. Among the main experimental techniques available for this purpose, microarray technology has been widely used. The objective of this work was to determine the genes of Vibrio parahaemolyticus which have their expression induced or repressed in presence of amino-sugars N-acetylglucosamine (NAG). V. parahaemolyticus is a marine bacterium, commonly found in water and in association with marine organisms. NAG is one of the most abundant amino sugars in the marine environment. For this, V. parahaemolyticus RIMD2210633, was cultivated in two media as sources of energy. The first medium consists of maltose and NAG (control) and the second only by NAG (treatment). Bacterial culture was done under aerobic conditions and low agitation at 28C. Two samples were drawn from the medium 24 hours after the experiment beginning in order to perform the extraction of mRNA and preparation of cDNA. Three replicas of the experiments were made. Mixtures of cDNA prepared from RNA extracted from each replicate were used in hybridizations in microarray slides containing a total of 4832 ORFS from the V. parahaemolyticus RIMD2210633 genome. Comparative analysis of gene expression of V. parahaemolyticus in two culture conditions resulted in detection of 59 genes with expression induced, 38 repressed genes, and 4245 without modified expression (increased or decreased) in presence of NAG. In total, 523 genes were excluded from this comparison because the hybridization was unsatisfactory. There was a gene ordination following the functional classification of the database TIGR-CMR and KEGG. The genes with induced expression mainly belong to classes of regulatory functions, energy metabolism, and transport proteins. PilA and Chemotaxis proteins were found, suggesting a role of NAG in the transformation. Repressed expression genes are mainly included in the functions of energy metabolism, cell address, and hypothetical proteins. This study demonstrated that NAG interfere in regulation of different cell processes, including the ability to capture DNA from the medium by V. parahaemolyticus.
Books on the topic "Vibrio marinus"
Göteborgs universitet. Dept. of General and Marine Microbiology., ed. On starvation and chemotactic responses by a marine Vibrio sp. S14. Göteborg, Sweden: Dept. of General and Marine Microbiology, University of Göteborg, 1990.
Find full textCuttle, Lisa. Dermatologic Manifestations of Infectious Disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0044.
Full textPérez Reytor,, Diliana Celeste. Identificación de nuevos marcadores de virulencia en cepas no toxigénicas de vibrio parahaemolyticus. Universidad Autónoma de Chile, 2019. http://dx.doi.org/10.32457/20.500.12728/87462019dcbm7.
Full textBook chapters on the topic "Vibrio marinus"
McFall-Ngai, M., C. Brennan, V. Weis, and L. Lamarcq. "Mannose Adhesin—Glycan Interactions in the Euprymna Scolopes—Vibrio Fischeri Symbiosis." In New Developments in Marine Biotechnology, 273–76. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-5983-9_58.
Full textLizárraga-Partida, Marcial Leonardo, Irma Wong-Chang, Guadalupe Barrera-Escorcia, Alfonso, and V. Botello. "Detection of Culturable and Non-Culturable Vibrio Cholerae 01 in Mexico." In New Developments in Marine Biotechnology, 307–10. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-5983-9_65.
Full textAndersen, Kristian Gjerrestad, Gbanaibolou Jombo, Sikiru Oluwarotimi Ismail, Yong Kang Chen, Hom Nath Dhakal, and Yu Zhang. "Damage Characterisation in Composite Laminates Using Vibro-Acoustic Technique." In Springer Proceedings in Energy, 275–82. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63916-7_34.
Full textJiang, Sunny C. "Vibrio cholerae in recreational beach waters and tributaries of Southern California." In The Ecology and Etiology of Newly Emerging Marine Diseases, 157–64. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-017-3284-0_14.
Full textNirajkumar, Sojitra, Satya P. Singh, and John J. Georrge. "In Silico Identification of Drug Targets and Drug-Like Molecules against Vibrio splendidus LGP32." In Marine Niche: Applications in Pharmaceutical Sciences, 401–14. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5017-1_22.
Full textVisick, Karen L., and Edward G. Ruby. "Temporal Control of Lux Gene Expression in the Symbiosis between Vibrio Fischeri and Its Squid Host." In New Developments in Marine Biotechnology, 277–79. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-5983-9_59.
Full textSinger, John T., Jacqueline H. Edgar, and Bruce L. Nicholson. "Expression of Capsid Proteins from Infectious Pancreatic Necrosis Virus (IPNV) in the Marine Bacterium Vibrio Anguillarum." In New Developments in Marine Biotechnology, 303–6. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-5983-9_64.
Full textLipp, Erin K., Cesar Rodriguez-Palacios, and Joan B. Rose. "Occurrence and distribution of the human pathogen Vibrio vulnificus in a subtropical Gulf of Mexico estuary." In The Ecology and Etiology of Newly Emerging Marine Diseases, 165–73. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-017-3284-0_15.
Full textHuang, Lixing, Qiancheng Gao, Youyu Zhang, Wei Xu, and Qingpi Yan. "Community Change and Pathogenicity of Vibrio." In Vibrios [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96515.
Full textChellapandian, Hethesh, Jeyachandran Sivakamavalli, A. Vijay Anand, and Balamuralikrishnan Balasubramanian. "Challenges in Controlling Vibriosis in Shrimp Farms." In Infectious Diseases and Sepsis [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97018.
Full textConference papers on the topic "Vibrio marinus"
Blanchet, D. "Vibro Acoustic Modeling of Marine Structures and Underwater Sound Radiation of Vibrating Structures." In 5th International Conference on Technology and Operation of Offshore Support Vessels. Singapore: Research Publishing Services, 2013. http://dx.doi.org/10.3850/978-981-07-7338-0_osv2013-15.
Full text"Phenotypic characterization of marine phage cocktail from Batangas Philippines against Multi-Drug Resistant Pseudomonas aeruginosa, Methicillin Resistant Staphylococcus aureus, and Vibrio cholera." In Multi-Disciplinary Manila (Philippines) Conferences Jan. 23-24, 2017, Manila (Philippines). Universal Researchers (UAE), 2017. http://dx.doi.org/10.17758/uruae.ae0117608.
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