Summary of Study ST001885
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 PR001188. The data can be accessed directly via it's Project DOI: 10.21228/M84X4Z 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 | ST001885 |
Study Title | MS Differentiating toxic and nontoxic congeneric harmful algae using the non-polar metabolome |
Study Summary | Recognition and rejection of chemically defended prey is critical to maximizing fitness for predators. Paralytic shellfish toxins (PSTs) which strongly inhibit voltage-gated sodium channels in diverse animal taxa are produced by several species of the bloom-forming algal genus Alexandrium where they appear to function as chemical defenses against grazing copepods. Despite PSTs being produced and localized within phytoplankton cells, some copepods distinguish toxic from non-toxic prey, selectively ingesting less toxic cells, in ways that suggest cell surface recognition perhaps associated with non-polar metabolites. In this study LC/MS and NMR-based metabolomics revealed that the non-polar metabolomes of two toxic species (Alexandrium catenella and Alexandrium pacificum) vary considerably from their non-toxic congener Alexandrium tamarense despite all three being very closely related. Toxic and non-toxic Alexandrium spp. were distinguished from each other by metabolites belonging to seven lipid classes. Of these, 17 specific metabolites were significantly more abundant in both toxic A. catenella and A. pacificum compared to non-toxic A. tamarense suggesting that just a small portion of the observed metabolic variability is associated with toxicity. Future experiments aimed at deciphering chemoreception mechanisms of copepod perception of Alexandrium toxicity should consider these metabolites, and the broader lipid classes phosphatidylcholines and sterols, as potential candidate cues. |
Institute | Georgia Institute of Technology |
Last Name | Brown |
First Name | Emily |
Address | 950 Atlantic Dr Atlanta GA 30332, USA |
julia.kubanek@biosci.gatech.edu | |
Phone | 404-894-8424 |
Submit Date | 2021-07-22 |
Raw Data Available | Yes |
Raw Data File Type(s) | mzML |
Analysis Type Detail | LC-MS |
Release Date | 2021-08-09 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR001188 |
Project DOI: | doi: 10.21228/M84X4Z |
Project Title: | Differentiating toxic and nontoxic congeneric harmful algae using the non-polar metabolome |
Project Summary: | Recognition and rejection of chemically defended prey is critical to maximizing fitness for predators. Paralytic shellfish toxins (PSTs) which strongly inhibit voltage-gated sodium channels in diverse animal taxa are produced by several species of the bloom-forming algal genus Alexandrium where they appear to function as chemical defenses against grazing copepods. Despite PSTs being produced and localized within phytoplankton cells, some copepods distinguish toxic from non-toxic prey, selectively ingesting less toxic cells, in ways that suggest cell surface recognition perhaps associated with non-polar metabolites. In this study LC/MS and NMR-based metabolomics revealed that the non-polar metabolomes of two toxic species (Alexandrium catenella and Alexandrium pacificum) vary considerably from their non-toxic congener Alexandrium tamarense despite all three being very closely related. Toxic and non-toxic Alexandrium spp. were distinguished from each other by metabolites belonging to seven lipid classes. Of these, 17 specific metabolites were significantly more abundant in both toxic A. catenella and A. pacificum compared to non-toxic A. tamarense suggesting that just a small portion of the observed metabolic variability is associated with toxicity. Future experiments aimed at deciphering chemoreception mechanisms of copepod perception of Alexandrium toxicity should consider these metabolites, and the broader lipid classes phosphatidylcholines and sterols, as potential candidate cues. |
Institute: | Georgia Institute of Technology |
Last Name: | Brown |
First Name: | Emily |
Address: | 950 Atlantic Dr Atlanta GA 30332, USA |
Email: | julia.kubanek@biosci.gatech.edu |
Phone: | 404-894-8424 |
Subject:
Subject ID: | SU001963 |
Subject Type: | Other organism |
Subject Species: | Alexandrium catenella;Alexandrium tamarense;Alexandrium pacificum |
Taxonomy ID: | 2925;2926;1565494 |
Species Group: | Alexandrium catenella; Alexandrium tamarense; Alexandrium pacificum |
Factors:
Subject type: Other organism; Subject species: Alexandrium catenella;Alexandrium tamarense;Alexandrium pacificum (Factor headings shown in green)
mb_sample_id | local_sample_id | factor |
---|---|---|
SA175199 | QC06 | QC |
SA175200 | QC07 | QC |
SA175201 | QC08 | QC |
SA175202 | QC10 | QC |
SA175203 | QC05 | QC |
SA175204 | QC03 | QC |
SA175205 | Blank01 | QC |
SA175206 | Blank02 | QC |
SA175207 | QC01 | QC |
SA175208 | QC02 | QC |
SA175209 | QC04 | QC |
SA175210 | QC09 | QC |
SA175211 | 74_3ERB74_AC_14 | Treatment;Alexandrium_catenella |
SA175212 | 74_3ERB74_AC_7 | Treatment;Alexandrium_catenella |
SA175213 | 74_3ERB74_AC_5 | Treatment;Alexandrium_catenella |
SA175214 | 74_3ERB74_AC_4 | Treatment;Alexandrium_catenella |
SA175215 | 74_3ERB74_AC_2 | Treatment;Alexandrium_catenella |
SA175216 | 74_3ERB74_AC_3 | Treatment;Alexandrium_catenella |
SA175217 | 74_3ERB74_AC_8 | Treatment;Alexandrium_catenella |
SA175218 | 74_3ERB74_AC_6 | Treatment;Alexandrium_catenella |
SA175219 | 74_3ERB74_AC_13 | Treatment;Alexandrium_catenella |
SA175220 | 74_3ERB74_AC_9 | Treatment;Alexandrium_catenella |
SA175221 | 74_3ERB74_AC_12 | Treatment;Alexandrium_catenella |
SA175222 | 74_3ERB74_AC_15 | Treatment;Alexandrium_catenella |
SA175223 | 74_3ERB74_AC_1 | Treatment;Alexandrium_catenella |
SA175224 | 74_3ERB74_AC_10 | Treatment;Alexandrium_catenella |
SA175225 | 74_3ERB74_AC_11 | Treatment;Alexandrium_catenella |
SA175226 | 75_3ERB75_AP_9 | Treatment;Alexandrium_pacificum |
SA175227 | 75_3ERB75_AP_7 | Treatment;Alexandrium_pacificum |
SA175228 | 75_3ERB75_AP_10 | Treatment;Alexandrium_pacificum |
SA175229 | 75_3ERB75_AP_14 | Treatment;Alexandrium_pacificum |
SA175230 | 75_3ERB75_AP_15 | Treatment;Alexandrium_pacificum |
SA175231 | 75_3ERB75_AP_13 | Treatment;Alexandrium_pacificum |
SA175232 | 75_3ERB75_AP_11 | Treatment;Alexandrium_pacificum |
SA175233 | 75_3ERB75_AP_6 | Treatment;Alexandrium_pacificum |
SA175234 | 75_3ERB75_AP_1 | Treatment;Alexandrium_pacificum |
SA175235 | 75_3ERB75_AP_5 | Treatment;Alexandrium_pacificum |
SA175236 | 75_3ERB75_AP_2 | Treatment;Alexandrium_pacificum |
SA175237 | 75_3ERB75_AP_3 | Treatment;Alexandrium_pacificum |
SA175238 | 75_3ERB75_AP_4 | Treatment;Alexandrium_pacificum |
SA175239 | 74_3ERB74_AT_10 | Treatment;Alexandrium_tamarense |
SA175240 | 74_3ERB74_AT_8 | Treatment;Alexandrium_tamarense |
SA175241 | 74_3ERB74_AT_9 | Treatment;Alexandrium_tamarense |
SA175242 | 74_3ERB74_AT_13 | Treatment;Alexandrium_tamarense |
SA175243 | 74_3ERB74_AT_7 | Treatment;Alexandrium_tamarense |
SA175244 | 74_3ERB74_AT_12 | Treatment;Alexandrium_tamarense |
SA175245 | 74_3ERB74_AT_11 | Treatment;Alexandrium_tamarense |
SA175246 | 74_3ERB74_AT_4 | Treatment;Alexandrium_tamarense |
SA175247 | 74_3ERB74_AT_1 | Treatment;Alexandrium_tamarense |
SA175248 | 74_3ERB74_AT_14 | Treatment;Alexandrium_tamarense |
SA175249 | 74_3ERB74_AT_15 | Treatment;Alexandrium_tamarense |
SA175250 | 74_3ERB74_AT_2 | Treatment;Alexandrium_tamarense |
SA175251 | 74_3ERB74_AT_3 | Treatment;Alexandrium_tamarense |
SA175252 | 74_3ERB74_AT_6 | Treatment;Alexandrium_tamarense |
SA175253 | 74_3ERB74_AT_5 | Treatment;Alexandrium_tamarense |
SA175254 | 75_3ERB75_AT_15 | Treatment;Alexandrium_tamarense2 |
SA175255 | 75_3ERB75_AT_11 | Treatment;Alexandrium_tamarense2 |
SA175256 | 75_3ERB75_AT_4 | Treatment;Alexandrium_tamarense2 |
SA175257 | 75_3ERB75_AT_5 | Treatment;Alexandrium_tamarense2 |
SA175258 | 75_3ERB75_AT_3 | Treatment;Alexandrium_tamarense2 |
SA175259 | 75_3ERB75_AT_2 | Treatment;Alexandrium_tamarense2 |
SA175260 | 75_3ERB75_AT_1 | Treatment;Alexandrium_tamarense2 |
SA175261 | 75_3ERB75_AT_6 | Treatment;Alexandrium_tamarense2 |
SA175262 | 75_3ERB75_AT_7 | Treatment;Alexandrium_tamarense2 |
SA175263 | 75_3ERB75_AT_12 | Treatment;Alexandrium_tamarense2 |
SA175264 | 75_3ERB75_AT_13 | Treatment;Alexandrium_tamarense2 |
SA175265 | 75_3ERB75_AT_10 | Treatment;Alexandrium_tamarense2 |
SA175266 | 75_3ERB75_AT_9 | Treatment;Alexandrium_tamarense2 |
SA175267 | 75_3ERB75_AT_8 | Treatment;Alexandrium_tamarense2 |
SA175268 | 75_3ERB75_AT_14 | Treatment;Alexandrium_tamarense2 |
Showing results 1 to 70 of 70 |
Collection:
Collection ID: | CO001956 |
Collection Summary: | Alexandrium cells were collected by vacuum filtration onto GF/F filters and quenched with liquid nitrogen. Frozen cells with filters were stored in foil(previously muffled for 3 h at 450 °C) at -80 °C until extraction. |
Sample Type: | Algae |
Treatment:
Treatment ID: | TR001975 |
Treatment Summary: | Metabolomes of toxic versus non-toxic species were compared using the following experimental pairings: A. tamarense (n=15) with A. catenella (n=15) (Experiment 1) and A. tamarense (n=15) with A. pacificum (n=15) (Experiment 2). The same non-toxic strain of A. tamarense was used in both experiments but the two experiments were conducted separately, in different months, to make the experiment manageable based on availability of batches grown from stock cultures. For both experiments, Alexandrium spp. cultures at a cell density of 12,000 to 13,000 cells mL-1 were split into fifteen 300 mL subcultures of each species which grew for two days. At the end of each experiment, during harvesting, a 1.0 mL aliquot from each culture was preserved with Lugol’s solution to measure cell concentrations |
Sample Preparation:
Sampleprep ID: | SP001969 |
Sampleprep Summary: | IPA: ACN (2:1) extract 4.54e6 cells per 1mL |
Combined analysis:
Analysis ID | AN003049 | AN003050 |
---|---|---|
Analysis type | MS | MS |
Chromatography type | Reversed phase | Reversed phase |
Chromatography system | Thermo Vanquish | Thermo Vanquish |
Column | Thermo Accucore C30 (150 x 2.1mm,2.6um) | Thermo Accucore C30 (150 x 2.1mm,2.6um) |
MS Type | ESI | ESI |
MS instrument type | orbitrap and ion trap | orbitrap and ion trap |
MS instrument name | Thermo Orbitrap ID-X Tribrid | Thermo Orbitrap ID-X Tribrid |
Ion Mode | POSITIVE | NEGATIVE |
Units | peak area | peak area |
Chromatography:
Chromatography ID: | CH002259 |
Instrument Name: | Thermo Vanquish |
Column Name: | Thermo Accucore C30 (150 x 2.1mm,2.6um) |
Chromatography Type: | Reversed phase |
MS:
MS ID: | MS002836 |
Analysis ID: | AN003049 |
Instrument Name: | Thermo Orbitrap ID-X Tribrid |
Instrument Type: | orbitrap and ion trap |
MS Type: | ESI |
MS Comments: | compound discoverer |
Ion Mode: | POSITIVE |
MS ID: | MS002837 |
Analysis ID: | AN003050 |
Instrument Name: | Thermo Orbitrap ID-X Tribrid |
Instrument Type: | orbitrap and ion trap |
MS Type: | ESI |
MS Comments: | compound discoverer |
Ion Mode: | NEGATIVE |