10760297

umls-concept:C0010453, umls-concept:C0012470, umls-concept:C0012854, umls-concept:C0012933, umls-concept:C0014406, umls-concept:C0162326, umls-concept:C0337051, umls-concept:C0370003, umls-concept:C0425245, umls-concept:C0439849, umls-concept:C0439855, umls-concept:C0445223, umls-concept:C0522430, umls-concept:C1509144, umls-concept:C1519249, umls-concept:C1552132, umls-concept:C1552599, umls-concept:C1704787, umls-concept:C1711351, umls-concept:C1880355, umls-concept:C2347026

2000-5-17

The newly described heterotrophic estuarine dinoflagellate Pfiesteria piscicida has been linked with fish kills in field and laboratory settings, and with a novel clinical syndrome of impaired cognition and memory disturbance among humans after presumptive toxin exposure. As a result, there is a pressing need to better characterize the organism and these associations. Advances in Pfiesteria research have been hampered, however, by the absence of genomic sequence data. We employed a sequencing strategy directed by heteroduplex mobility assay to detect Pfiesteria piscicida 18S rDNA "signature" sequences in complex pools of DNA and used those data as the basis for determination of the complete P. piscicida 18S rDNA sequence. Specific PCR assays for P. piscicida and other estuarine heterotrophic dinoflagellates were developed, permitting their detection in algal cultures and in estuarine water samples collected during fish kill and fish lesion events. These tools should enhance efforts to characterize these organisms and their ecological relationships. Heteroduplex mobility assay-directed sequence discovery is broadly applicable, and may be adapted for the detection of genomic sequence data of other novel or nonculturable organisms in complex assemblages.

eng

IM

MEDLINE

0027-8424

Print

97

Y

2010-11-18

2000

Institute of Human Virology and University of Maryland School of Medicine, Baltimore, MD 21201, USA. oldach@umbi.umd.edu