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Perkinsus chesapeaki ATCC PRA-65

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Principle Investigator(s) Senjie Lin
External sample IDPerchexp
NCGR Sample IDMMETSP0924C
Sample accession numberCAM_SMPL_002745
Assembly accession numberCAM_ASM_000563
Combined Assembly NamePerkinsus-chesapeaki-ATCC_PRA_65
GenusPerkinsus
Specieschesapeaki
StrainATCC PRA-65
ClonalYes
AxenicNo
Prelim. NCBI Taxon ID321610
18S rRNA
Importance of organism and transcriptomesPerkinsus chesapeaki is a pathogenic protist that infects at least 6 species of clams in both Chesapeake Bay and Delaware Bay, at prevalences that commonly reach 100% among clam samples (Reece et al. 2008, Dis. Aquat. Org. 82:237-248). Members of the genus Perkinsus are closely related to, but distinct from, dinoflagellates. It has two spliced leaders.
Additional citations and referencesBurreson et al. 2005, J. Eukaryot. Microbiol. 52:258-270.
Environmental Data
Primary citation for organism's characterization, if availableZhang, H., Campbell, D. A, Strum, N. R., Dungan, C. F. and Lin, S. 2011. Spliced leader RNA, mitochondrial gene frameshifts, and multi-protein phylogeny expand support for Perkinsus as a unique alveolate. PLoS ONE 6(5): e19933. Doi:10.1371/journal.pone.0019933.
Latitude38.9944
Longitude76.2141
Depth (m)4
Salinity (psu)13.5
Temperature (ºC)27.8
Collection date27-AUG-02
Sample collection siteChesapeake Bay
Other collection site infoChester River, Buoy Rock, Maryland
Sample material (e.g. "seawater," "sediment," etc.)Mya arenaria host clam
Habitat descriptionThe host clam was infaunal within a benthic sand and mud substrate from which it was excavated.
Habitatorganism-associated habitat
CountryUNITED STATES
Experimental Data
Date of experiment13-MAY-11
Growth medium850 mOsm/kg DME:Ham's F-12 (Burreson et al. 2005, J. Eukaryot. Microbiol. 52:258-270)
Modifications to growth medium3% (v/v) FBS, 100 ?g/ml streptomycin, 100 U/ml penicillin
Temperature (ºC)27
Salinty (psu)29
pH7
Pressure (atm)1
Investigation typeEukaryotes
Other experimental metadata availablesubmitted is Perkinsus spliced leader based cDNA prepared when culture was in exponential phase.