TY - JOUR
T1 - Discovery of genes expressed in response to Perkinsus marinus challenge in Eastern (Crassostrea virginica) and Pacific (C. gigas) oysters
AU - Tanguy, Arnaud
AU - Guo, Ximing
AU - Ford, Susan E.
N1 - Funding Information:
The authors like to thank G. DeBrosse and G. King for providing some of experimental oysters. Drs. G.R. Vasta and J.A.F. Robledo kindly assisted in searching for P. marinus sequences. This work is supported by a postdoctoral fellowship from Institute of Marine and Coastal Sciences, Rutgers University, and grants from the National Sea Grant (OD-9915 and ODRP-29) and New Jersey Commission on Science and Technology (00-2042-007-20). This is publication IMCS-04-08 and NJMSC-04-565.
PY - 2004/8/18
Y1 - 2004/8/18
N2 - The protozoan pathogen Perkinsus marinus is the causative agent of Dermo, a lethal disease of the eastern oyster Crassostrea virginica, but not the Pacific oyster Crassostrea gigas. To understand the response of these two oysters to parasite exposure, a suppression subtractive hybridization (SSH) method was employed to characterize genes up-regulated during parasite challenge in both hemocytes and gills. The number of differentially expressed gene sequences obtained was 107 for C. virginica and 69 for C. gigas, including 46 and 37 sequences, respectively, that matched known genes in GenBank. Most of the sequences have not been characterized in other molluscs. Nineteen genes involved in immune system and cell communication, protein regulation and transcription, cell cycle, respiratory chain and cytoskeleton were selected for expression analysis by semi-quantitative PCR. Although varying in magnitude and timing post exposure, all genes screened showed over-expression in challenged oysters in both species, validating the SSH method. Results of this study highlighted some differences in gene expression between the two oysters in response to P. marinus infection, providing candidate genes and pathways for further analysis.
AB - The protozoan pathogen Perkinsus marinus is the causative agent of Dermo, a lethal disease of the eastern oyster Crassostrea virginica, but not the Pacific oyster Crassostrea gigas. To understand the response of these two oysters to parasite exposure, a suppression subtractive hybridization (SSH) method was employed to characterize genes up-regulated during parasite challenge in both hemocytes and gills. The number of differentially expressed gene sequences obtained was 107 for C. virginica and 69 for C. gigas, including 46 and 37 sequences, respectively, that matched known genes in GenBank. Most of the sequences have not been characterized in other molluscs. Nineteen genes involved in immune system and cell communication, protein regulation and transcription, cell cycle, respiratory chain and cytoskeleton were selected for expression analysis by semi-quantitative PCR. Although varying in magnitude and timing post exposure, all genes screened showed over-expression in challenged oysters in both species, validating the SSH method. Results of this study highlighted some differences in gene expression between the two oysters in response to P. marinus infection, providing candidate genes and pathways for further analysis.
KW - EST
KW - FSW-PS
KW - Gene expression
KW - Immune system
KW - MAPK
KW - Mollusca
KW - Parasite
KW - RFTM
KW - RT-PCR
KW - Ray's Fluid Thioglycollate Medium
KW - Substractive libraries
KW - expressed sequence tag
KW - filtered sea water with penicillin and streptomycin
KW - reverse transcription poly chain reaction
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U2 - 10.1016/j.gene.2004.05.019
DO - 10.1016/j.gene.2004.05.019
M3 - Article
C2 - 15302413
AN - SCOPUS:4143143353
SN - 0378-1119
VL - 338
SP - 121
EP - 131
JO - Gene
JF - Gene
IS - 1
ER -