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Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae

Absorption and accumulation of bioavailable cyanobacterial metabolites (including cyanotoxins) are likely in fish after senescence and the rupturing of cells during bloom episodes. We determined the toxicity of cyanopeptides identified from two strains of Microcystis (M. panniformis MIRS-04 and M. a...

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Autores principales: Fernandes, Kelly, Gomes, Andreia, Calado, Leonardo, Yasui, George, Assis, Diego, Henry, Theodore, Fonseca, Ana, Pinto, Ernani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520764/
https://www.ncbi.nlm.nih.gov/pubmed/31013880
http://dx.doi.org/10.3390/toxins11040220
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author Fernandes, Kelly
Gomes, Andreia
Calado, Leonardo
Yasui, George
Assis, Diego
Henry, Theodore
Fonseca, Ana
Pinto, Ernani
author_facet Fernandes, Kelly
Gomes, Andreia
Calado, Leonardo
Yasui, George
Assis, Diego
Henry, Theodore
Fonseca, Ana
Pinto, Ernani
author_sort Fernandes, Kelly
collection PubMed
description Absorption and accumulation of bioavailable cyanobacterial metabolites (including cyanotoxins) are likely in fish after senescence and the rupturing of cells during bloom episodes. We determined the toxicity of cyanopeptides identified from two strains of Microcystis (M. panniformis MIRS-04 and M. aeruginosa NPDC-01) in a freshwater tropical fish, Astyanax altiparanae (yellowtail tetra, lambari). Aqueous extracts of both Microcystis strains were prepared in order to simulate realistic fish exposure to these substances in a freshwater environment. Both strains were selected because previous assays evidenced the presence of microcystins (MCs) in MIRS-04 and lack of cyanotoxins in NPDC-01. Identification of cyanobacterial secondary metabolites was performed by LC-HR-QTOF-MS and quantification of the MC-LR was carried out by LC-QqQ-MS/MS. MIRS-04 produces the MCs MC-LR, MC-LY and MC-HilR as well as micropeptins B, 973, 959 and k139. NPCD-01 biosynthetizes microginins FR1, FR2/FR4 and SD-755, but does not produce MCs. Larval fish survival and changes in morphology were assessed for 96 h exposure to aqueous extracts of both strains at environmentally relevant concentrations from 0.1 to 0.5 mg (dry weight)/mL, corresponding to 0.15 to 0.74 μg/mL of MC-LR (considering dried amounts of MIRS-04 for comparison). Fish mortality increased with concentration and time of exposure for both strains of Microcystis. The frequencies of morphological abnormalities increased with concentration in both strains, and included abdominal and pericardial oedema, and spinal curvature. Results demonstrate that toxicity was not solely caused by MCs, other classes of cyanobacterial secondary metabolites contributed to the observed toxicity.
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spelling pubmed-65207642019-05-31 Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae Fernandes, Kelly Gomes, Andreia Calado, Leonardo Yasui, George Assis, Diego Henry, Theodore Fonseca, Ana Pinto, Ernani Toxins (Basel) Article Absorption and accumulation of bioavailable cyanobacterial metabolites (including cyanotoxins) are likely in fish after senescence and the rupturing of cells during bloom episodes. We determined the toxicity of cyanopeptides identified from two strains of Microcystis (M. panniformis MIRS-04 and M. aeruginosa NPDC-01) in a freshwater tropical fish, Astyanax altiparanae (yellowtail tetra, lambari). Aqueous extracts of both Microcystis strains were prepared in order to simulate realistic fish exposure to these substances in a freshwater environment. Both strains were selected because previous assays evidenced the presence of microcystins (MCs) in MIRS-04 and lack of cyanotoxins in NPDC-01. Identification of cyanobacterial secondary metabolites was performed by LC-HR-QTOF-MS and quantification of the MC-LR was carried out by LC-QqQ-MS/MS. MIRS-04 produces the MCs MC-LR, MC-LY and MC-HilR as well as micropeptins B, 973, 959 and k139. NPCD-01 biosynthetizes microginins FR1, FR2/FR4 and SD-755, but does not produce MCs. Larval fish survival and changes in morphology were assessed for 96 h exposure to aqueous extracts of both strains at environmentally relevant concentrations from 0.1 to 0.5 mg (dry weight)/mL, corresponding to 0.15 to 0.74 μg/mL of MC-LR (considering dried amounts of MIRS-04 for comparison). Fish mortality increased with concentration and time of exposure for both strains of Microcystis. The frequencies of morphological abnormalities increased with concentration in both strains, and included abdominal and pericardial oedema, and spinal curvature. Results demonstrate that toxicity was not solely caused by MCs, other classes of cyanobacterial secondary metabolites contributed to the observed toxicity. MDPI 2019-04-13 /pmc/articles/PMC6520764/ /pubmed/31013880 http://dx.doi.org/10.3390/toxins11040220 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fernandes, Kelly
Gomes, Andreia
Calado, Leonardo
Yasui, George
Assis, Diego
Henry, Theodore
Fonseca, Ana
Pinto, Ernani
Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title_full Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title_fullStr Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title_full_unstemmed Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title_short Toxicity of Cyanopeptides from Two Microcystis Strains on Larval Development of Astyanax altiparanae
title_sort toxicity of cyanopeptides from two microcystis strains on larval development of astyanax altiparanae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520764/
https://www.ncbi.nlm.nih.gov/pubmed/31013880
http://dx.doi.org/10.3390/toxins11040220
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