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S.L. Kaattari

Publications and source records attributed to S.L. Kaattari.

3 recordsLinked to original sources
USGS2002

Status and opportunities for genomics research with rainbow trout

The rainbow trout (Oncorhynchus mykiss) is one of the most widely studied of model fish species. Extensive basic biological information has been collected for this species, which because of their large size relative to other model fish species are particularly suitable for studies requiring ample quantities of specific cells and tissue types. Rainbow trout have been widely utilized for research in carcinogenesis, toxicology, comparative immunology, disease ecology, physiology and nutrition. They are distinctive in having evolved from a relatively recent tetraploid event, resulting in a high incidence of duplicated genes. Natural populations are available and have been well characterized for chromosomal, protein, molecular and quantitative genetic variation. Their ease of culture, and experimental and aquacultural significance has led to the development of clonal lines and the widespread application of transgenic technology to this species. Numerous microsatellites have been isolated and two relatively detailed genetic maps have been developed. Extensive sequencing of expressed sequence tags has begun and four BAC libraries have been developed. The development and analysis of additional genomic sequence data will provide distinctive opportunities to address problems in areas such as evolution of the immune system and duplicate genes. ?? 2002 Elsevier Science Inc. All rights reserved.

Conference Paper↗
USGS2001

Detection of Perkinsus marinus extracellular proteins tissues of the eastern oyster Crassostrea virginica: Potential use diagnostic assays

Perkinsus marinus , the cause of serious losses of the eastern oyster Crassostrea virginica , secretes extracellular proteins (ECP) in culture (in vitro) including serine proteases. The production of similar ECP in the eastern oyster (in vivo) and their role in pathogenicity, however, remain to be elucidated. The induction and dissemination of these proteins within infected eastern oysters could be critical to understanding the pathologic mechanisms employed as well as to providing the means for rapid and specific diagnosis. To quantify and examine the production of these proteins in the host, polyclonal antibodies were produced against ECP produced during the in vitro culture of P. marinus. By the use of a Western blot technique, these antibodies were shown to recognize a 62-kDa protein antigen expressed in lightly infected oysters, whereas three antigens (62, 38, and 28 kDa) were recognized in heavily infected oysters. Additionally, there was an antigen that is expressed in vitro (40 kDa) that was not detected in vivo and two that were detected in vivo (120 and 32 kDa) but not in vitro. An enzyme-linked immunosorbent assay (ELISA) employing these antibodies indicated that the concentration of secreted antigens is significantly related ( P < 0.05) to the number of cells of P. marinus in infected eastern oyster tissues, as determined by the standard Ray's fluid thioglycollate medium (RFTM) assay. Significant differences ( P < 0.025) between the ELISA and RFTM assays were only observed when oysters possessed less than one hypnospore per gram of tissue. Thus this ELISA proved to be an excellent diagnostic tool, generating values that correlated with the number of protozoal cells present within infected tissues.

Virginia↗