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Authordc.contributor.authorRojas, Rodrigo 
Authordc.contributor.authorMiranda, Claudio D. es_CL
Authordc.contributor.authorAmaro Sepúlveda, Ana María es_CL
Admission datedc.date.accessioned2010-04-27T14:34:13Z
Available datedc.date.available2010-04-27T14:34:13Z
Publication datedc.date.issued2008
Cita de ítemdc.identifier.citationMicrob Ecolen_US
Identifierdc.identifier.otherDOI 10.1007/s00248-008-9401-z
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/128499
Abstractdc.description.abstractMass mortalities of larval cultures of Chilean scallop Argopecten purpuratus have repeatedly occurred in northern Chile, characterized by larval agglutination and accumulation in the bottom of rearing tanks. The exopolysaccharide slime (EPS) producing CAM2 strain was isolated as the primary organism from moribund larvae in a pathogenic outbreak occurring in a commercial hatchery producing larvae of the Chilean scallop Argopecten purpuratus located in Bahía Inglesa, Chile. The CAM2 strain was characterized biochemically and was identified by polymerase chain reaction amplification of 16S rRNA as Halomonas sp. (Accession number DQ885389.1). Healthy 7-day-old scallop larvae cultures were experimentally infected for a 48-h period with an overnight culture of the CAM2 strain at a final concentration of ca. 105 cells per milliliter, and the mortality and vital condition of larvae were determined by optical and scanning electron microscopy (SEM) to describe the chronology of the disease. Pathogenic action of the CAM2 strain was clearly evidenced by SEM analysis, showing a high ability to adhere and detach larvae velum cells by using its “slimy” EPS, producing agglutination, loss of motility, and a posterior sinking of scallop larvae. After 48 h, a dense bacterial slime on the shell surface was observed, producing high percentages of larval agglutination (63.28±7.87%) and mortality (45.03±4.32%) that were significantly (P<0.05) higher than those of the unchallenged control cultures, which exhibited only 3.20±1.40% dead larvae and no larval agglutination. Furthermore, the CAM2 strain exhibited a high ability to adhere to fiberglass pieces of tanks used for scallop larvae rearing (1.64×105 cells adhered per square millimeters at 24 h postinoculation), making it very difficult to eradicate it from the culture systems. This is the first report of a pathogenic activity on scallop larvae of Halomonas species, and it prompts the necessity of an appraisal on biofilm-producing bacteria in Chilean scallop hatcheries.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherSpringeren_US
Títulodc.titlePathogenicity of a Highly Exopolysaccharide-producing Halomonas Strain Causing Epizootics in Larval Cultures of the Chilean Scallop Argopecten purpuratus (Lamarck, 1819)en_US
Document typedc.typeArtículo de revista


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