Active microbiome data of Penaeus stylirostris hemolymph and its rearing water under contrasting conditions
Metabarcoding data from water and shrimp's hemolymph in order to assess the microbial structure, variability with rearing conditions and identify possible biomarkers of healthy shrimps.
Data accessChemin d'accès | /home/ref-bioinfo/ifremer/leadnc/comistyl |
Date(s)Date(s) |
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Author(s)Auteur(s) | Callac Nolwenn
(IFREMER)
Boulo Viviane (IFREMER) Ansquer Dominique (IFREMER) Belliard Corine (IFREMER) Plougoulen Gwen (IFREMER) Wabete Nelly (IFREMER) Pham Dominique (IFREMER) Saulnier Denis (IFREMER) Le Luyer Jeremy (IFREMER) Loyat Alain (IFREMER) Lafille Marc André (DRM) Basset Caline (IFREMER) Lam Jean-Sebastien (IFREMER) Mailliez Jean-René (IFREMER) Lau Christophe (DRM) Elissondo Carine (CAPF) Delecheneau Jean-Michel (CAPF) Brun Pierre (IFREMER) Matehau Ariora (IFREMER) Taupua (CAPF) Ballan Valentine (IFREMER) Le Rhollec Julien (IFREMER) |
Contact(s)Contact(s) | IFREMER
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SourceSource |
Projet COMISTYL |
LineageGénéalogie |
Sequencing data for this project were acquired from extraction of total RNA from the hemolymph of Penaeus stylirostris shrimp and from the water of their environment. The shrimp were reared under contrasting conditions: two rearing waters (earthen pond and clear water tanks), at two sampling times (beginning of the experiment, 9 months old shrimp reared in earthen ponds then partially transferred to clear water tanks and reared in both waters in parallel for one month, end of the experiment), during two seasons (warm and cold) and on two sites (New Caledonia and French Polynesia). RNA extractions in hemolymph samples were performed with the Direct-Zol Mini-Prep kit (Zymo Research) according to the manufacturer's protocol. RNA extractions in water samples were performed according to the manufacturer's protocol with the RNeasy PowerWater kit (Qiagen). The extracted RNAs were reverse transcribed into cDNA by M-MLV reverse transcriptase (PROMEGA) in a thermocycler (Verity TM, Biosystems). Finally, all cDNAs were sequenced by MrDNA (Shallowater, TX, Uited Sates) with primers 515F/806Rs on Illumina HiSeq, 2 x 300 bases and an average sequencing depth of 20,000 reads. |
ConstraintsContraintes |
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Spatial informationsInformations géographiques |
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