Summary of Study ST001187
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000799. The data can be accessed directly via it's Project DOI: 10.21228/M8D98R This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.
Study ID | ST001187 |
Study Title | Effects of selenate and cadmium exposure on the honey bee metabolome (part-I) |
Study Summary | We moved one frame of brood each from five healthy honey bee colonies with marked Italian queens and housed them in a hive body at 35°C and 50% humidity under constant darkness. We then allowed the bees to emerge, mixed the newly emerged workers (NEWs) to randomize their colony of origin and placed NEWs into 13 cm x 10.5 cm x 6.5 cm wire cages equipped with feeders containing 35mL of deionized water and 35mL 50% sucrose. We also provided a pollen patty to each cage of bees consisting of 269g corn syrup, 113g sucrose and 113g of Bee Pro (Mann Lake, Hackensack, MN). To inoculate the newly emerged workers with their “core” microbiome, we collected 50 mL of foragers from the source hives of the NEWs, immobilized the bees at 4°C, aseptically dissected out the abdomens and macerated the whole abdomens in 50% sucrose. We added 1 mL of the resulting slurry to 34 mL of 50% sucrose solution and fed it to the NEWs. We allowed the bees to feed ad libitium on the mixture for two days before replacing the feeders with 50% sucrose. We allowed the bees to feed for three more days to fully establish a microbiome. Once the bees had an established microbiome, we prepared treatment feeding solutions of 50% sucrose (as a no metal/metalloid control), 50% sucrose spiked with 0.6 mg/L sodium selenate or 50% sucrose with 0.24 mg/L cadmium chloride (Alfa Aesar, Ward Hill, MA) and pollen patties spiked with either 6.0 mg/L selenium or 0.46 mg/L cadmium as in Hladun et al 2015. We again allowed the bees to feed ad libitium. We sampled three bees from 13 cages after four days of continuous exposure to the above-mentioned treatments and immediately placed the samples on dry ice, followed by long-term storage at -80 °C. |
Institute | University of California, Riverside |
Last Name | Rothman |
First Name | Jason |
Address | 900 University Ave. |
jroth002@ucr.edu | |
Phone | 9518275817 |
Submit Date | 2019-05-31 |
Raw Data Available | Yes |
Raw Data File Type(s) | raw(Waters) |
Analysis Type Detail | LC-MS |
Release Date | 2019-07-17 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000799 |
Project DOI: | doi: 10.21228/M8D98R |
Project Title: | Untargeted metabolomics of honey bees exposed to selenate or cadmium |
Project Summary: | Effects of selenate and cadmium exposure on honey bees. |
Institute: | University of California, Riverside |
Last Name: | Rothman |
First Name: | Jason |
Address: | 900 University Ave., Riverside, CA, 91766, USA |
Email: | jroth002@ucr.edu |
Phone: | 9518275817 |
Subject:
Subject ID: | SU001254 |
Subject Type: | Insect |
Subject Species: | Apis mellifera |
Taxonomy ID: | 7460 |
Factors:
Subject type: Insect; Subject species: Apis mellifera (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment |
---|---|---|
SA082474 | HBCD-4 | Cadmium |
SA082475 | HBCD-2 | Cadmium |
SA082476 | HBCD-1 | Cadmium |
SA082477 | HBCD-3 | Cadmium |
SA082478 | HBCT-1 | Control |
SA082479 | HBCT-2 | Control |
SA082480 | HBCT-4 | Control |
SA082481 | HBCT-3 | Control |
SA082482 | QC-5 | Pool |
SA082483 | QC-4 | Pool |
SA082484 | QC-1 | Pool |
SA082485 | QC-2 | Pool |
SA082486 | QC-3 | Pool |
SA082487 | HBSE-3 | Selenate |
SA082488 | HBSE-1 | Selenate |
SA082489 | HBSE-2 | Selenate |
SA082490 | HBSE-4 | Selenate |
SA082491 | HBSE-5 | Selenate |
Showing results 1 to 18 of 18 |
Collection:
Collection ID: | CO001248 |
Collection Summary: | We sampled three bees from 13 cages after four days of continuous exposure to the treatments and immediately placed the samples on dry ice, followed by long-term storage at -80 °C. |
Sample Type: | Insect tissue |
Storage Conditions: | Described in summary |
Treatment:
Treatment ID: | TR001269 |
Treatment Summary: | Once the bees had an established microbiome, we prepared treatment feeding solutions of 50% sucrose (as a no metal/metalloid control), 50% sucrose spiked with 0.6 mg/L sodium selenate or 50% sucrose with 0.24 mg/L cadmium chloride (Alfa Aesar, Ward Hill, MA) and pollen patties spiked with either 6.0 mg/L selenium or 0.46 mg/L cadmium and allowed the bees to feed ad libitium. |
Sample Preparation:
Sampleprep ID: | SP001262 |
Sampleprep Summary: | Samples were freeze-dried, homogenized, and extracted with 30:30:20:20 acetonitrile:methanol:water:isopropanol. Samples were then sonicated, vortexed, and centrifuged before analysis. |
Combined analysis:
Analysis ID | AN001979 |
---|---|
Analysis type | MS |
Chromatography type | Normal phase |
Chromatography system | Waters Acquity I-Class |
Column | Waters Acquity CSH C18 (100 x 2.1mm,1.7um) |
MS Type | ESI |
MS instrument type | QTOF |
MS instrument name | Waters Synapt-G2-Si |
Ion Mode | POSITIVE |
Units | peak area |
Chromatography:
Chromatography ID: | CH001428 |
Instrument Name: | Waters Acquity I-Class |
Column Name: | Waters Acquity CSH C18 (100 x 2.1mm,1.7um) |
Column Temperature: | 40 |
Flow Gradient: | 0 min, 1% B; 1 min, 1% B; 8 min, 40% B; 24 min, 100% B; 26.5 min, 100% B; 27 min, 1% B |
Flow Rate: | 250 ul/min |
Solvent A: | 100% water; 0.1% formic acid |
Solvent B: | 100% acetonitrile; 0.1% formic acid |
Chromatography Type: | Normal phase |
MS:
MS ID: | MS001833 |
Analysis ID: | AN001979 |
Instrument Name: | Waters Synapt-G2-Si |
Instrument Type: | QTOF |
MS Type: | ESI |
MS Comments: | We processed the metabolite data (peak picking, alignment, deconvolution, integration, normalization, and spectral matching) with Progenesis Qi software (Nonlinear Dynamics, Durham, NC). |
Ion Mode: | POSITIVE |