Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.

The large amounts of engineered titanium dioxide nanoparticles (TiO2NPs) that have been manufactured have inevitably been released into the ecosystem. Reports have suggested that TiO2 is a relatively inert material that has low toxicity to animals. However, as various types of NPs increasingly accum...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Chiao-Yi Huang, Wei-Sheng Yu, Geng-Chia Liu, Shih-Che Hung, Jen-Hsiang Chang, Jen-Che Chang, Chia-Liang Cheng, Der-Shan Sun, Ming-Der Lin, Wen-Ying Lin, Yin-Jeh Tzeng, Hsin-Hou Chang
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/1f75e334fc4a4408bf030a04e569db51
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:1f75e334fc4a4408bf030a04e569db51
record_format dspace
spelling oai:doaj.org-article:1f75e334fc4a4408bf030a04e569db512021-12-02T20:05:00ZOpportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.1932-620310.1371/journal.pone.0247859https://doaj.org/article/1f75e334fc4a4408bf030a04e569db512021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0247859https://doaj.org/toc/1932-6203The large amounts of engineered titanium dioxide nanoparticles (TiO2NPs) that have been manufactured have inevitably been released into the ecosystem. Reports have suggested that TiO2 is a relatively inert material that has low toxicity to animals. However, as various types of NPs increasingly accumulate in the ocean, their effects on aquatic life-forms remain unclear. In this study, a zebrafish model was used to investigate TiO2NP-induced injury and mortality. We found that the treatment dosages of TiO2NP are positively associated with increased motility of zebrafish and the bacterial counts in the water. Notably, gill but not dorsal fin and caudal fin of the zebrafish displayed considerably increased bacterial load. Metagenomic analysis further revealed that gut microflora, such as phyla Proteobacteria, Bacteroidetes, and Actinobacteria, involving more than 95% of total bacteria counts in the NP-injured zebrafish gill samples. These results collectively suggest that opportunistic bacterial infections are associated with TiO2NP-induced mortality in zebrafish. Infections secondary to TiO2NP-induced injury could be a neglected factor determining the detrimental effects of TiO2NPs on wild fish.Chiao-Yi HuangWei-Sheng YuGeng-Chia LiuShih-Che HungJen-Hsiang ChangJen-Che ChangChia-Liang ChengDer-Shan SunMing-Der LinWen-Ying LinYin-Jeh TzengHsin-Hou ChangPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 7, p e0247859 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Chiao-Yi Huang
Wei-Sheng Yu
Geng-Chia Liu
Shih-Che Hung
Jen-Hsiang Chang
Jen-Che Chang
Chia-Liang Cheng
Der-Shan Sun
Ming-Der Lin
Wen-Ying Lin
Yin-Jeh Tzeng
Hsin-Hou Chang
Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
description The large amounts of engineered titanium dioxide nanoparticles (TiO2NPs) that have been manufactured have inevitably been released into the ecosystem. Reports have suggested that TiO2 is a relatively inert material that has low toxicity to animals. However, as various types of NPs increasingly accumulate in the ocean, their effects on aquatic life-forms remain unclear. In this study, a zebrafish model was used to investigate TiO2NP-induced injury and mortality. We found that the treatment dosages of TiO2NP are positively associated with increased motility of zebrafish and the bacterial counts in the water. Notably, gill but not dorsal fin and caudal fin of the zebrafish displayed considerably increased bacterial load. Metagenomic analysis further revealed that gut microflora, such as phyla Proteobacteria, Bacteroidetes, and Actinobacteria, involving more than 95% of total bacteria counts in the NP-injured zebrafish gill samples. These results collectively suggest that opportunistic bacterial infections are associated with TiO2NP-induced mortality in zebrafish. Infections secondary to TiO2NP-induced injury could be a neglected factor determining the detrimental effects of TiO2NPs on wild fish.
format article
author Chiao-Yi Huang
Wei-Sheng Yu
Geng-Chia Liu
Shih-Che Hung
Jen-Hsiang Chang
Jen-Che Chang
Chia-Liang Cheng
Der-Shan Sun
Ming-Der Lin
Wen-Ying Lin
Yin-Jeh Tzeng
Hsin-Hou Chang
author_facet Chiao-Yi Huang
Wei-Sheng Yu
Geng-Chia Liu
Shih-Che Hung
Jen-Hsiang Chang
Jen-Che Chang
Chia-Liang Cheng
Der-Shan Sun
Ming-Der Lin
Wen-Ying Lin
Yin-Jeh Tzeng
Hsin-Hou Chang
author_sort Chiao-Yi Huang
title Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
title_short Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
title_full Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
title_fullStr Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
title_full_unstemmed Opportunistic gill infection is associated with TiO2 nanoparticle-induced mortality in zebrafish.
title_sort opportunistic gill infection is associated with tio2 nanoparticle-induced mortality in zebrafish.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/1f75e334fc4a4408bf030a04e569db51
work_keys_str_mv AT chiaoyihuang opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT weishengyu opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT gengchialiu opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT shihchehung opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT jenhsiangchang opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT jenchechang opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT chialiangcheng opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT dershansun opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT mingderlin opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT wenyinglin opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT yinjehtzeng opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
AT hsinhouchang opportunisticgillinfectionisassociatedwithtio2nanoparticleinducedmortalityinzebrafish
_version_ 1718375527976271872