De novo transcriptome assembly and differential gene expression analysis of the calanoid copepod Acartia tonsa exposed to nickel for nanoparticles

被引:26
|
作者
Zhou, Chao [1 ]
Carotenuto, Ylenia [2 ]
Vitiello, Valentina [3 ]
Wu, Changwen [1 ]
Zhang, Jianshe [1 ]
Buttino, Isabella [2 ,3 ]
机构
[1] Zhejiang Ocean Univ, Coll Marine Sci & Technol, Natl Engn Res Ctr Marine Facil Aquaculture, 1 Haida South Rd, Zhoushan 316022, Zhejiang, Peoples R China
[2] Dept Integrat Marine Ecol, Stn Zool Anton Dohrn, Naples, Italy
[3] ISPRA, Via Cedro 38, I-57122 Livorno, Italy
关键词
Toxicogenomic; Ecotoxicology; Downregulated genes; Xenobiotic; Egg hatching success; TIGRIOPUS-JAPONICUS; RIBOSOME BIOGENESIS; COLD-STORAGE; ENGINEERED NANOPARTICLES; EGG-PRODUCTION; TOXICITY; POPULATION; IDENTIFICATION; REPRODUCTION; ECOTOXICITY;
D O I
10.1016/j.chemosphere.2018.06.096
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The calanoid copepod Acartia tonsa is a reference species in standardized ecotoxicology bioassay. Despite this interest, there is a lack of knowledge on molecular responses of A. tonsa to contaminants. We generated a de novo assembled transcriptome of A. tonsa exposed 4 days to 8.5 and 17 mg/L nickel nanoparticles (NiNP5), which have been shown to reduce egg hatching success and larval survival but had no effects on the adults. Aims of our study were to 1) improve the knowledge on the molecular responses of A. tonsa copepod and 2) increase the genomic resources of this copepod for further identification of potential biomarkers of NP exposure. The de novo assembled transcriptome of A. tonsa consisted of 53,619 unigenes, which were further annotated to nr, GO, KOG and KEGG databases. In particular, most unigenes were assigned to Metabolic and Cellular processes (34-45%) GO terms, and to Human disease (28%) and Organismal systems (23%) KEGG categories. Comparison among treatments showed that 373 unigenes were differentially expressed in A. tonsa exposed to NiNPs at 8.5 and 17 mg/L, with respect to control. Most of these genes were downregulated and took part in ribosome biogenesis, translation and protein turnover, thus suggesting that NiNP5 could affect the copepod ribosome synthesis machinery and functioning. Overall, our study highlights the potential of toxicogenomic approach in gaining more mechanistic and functional information about the mode of action of emerging compounds on marine organisms, for biomarker discovering in crustaceans. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 172
页数:10
相关论文
共 50 条
  • [1] Toxicity of nickel in the marine calanoid copepod Acartia tonsa: Nickel chloride versus nanoparticles
    Zhou, C.
    Vitiello, V.
    Casals, E.
    Puntes, V. F.
    Iamunno, F.
    Pellegrini, D.
    Changwen, W.
    Benvenuto, G.
    Buttino, I.
    AQUATIC TOXICOLOGY, 2016, 170 : 1 - 12
  • [2] Insights into the molecular response of Dioithona rigida to selenium nanoparticles: de novo transcriptome assembly and differential gene expression analysis
    Meethalepurayil, Vineeth Kumar Chirayil
    Velu, Karthick
    Dhinakarasamy, Inbakandan
    Shrestha, Lok Kumar
    Ariga, Katsuhiko
    Rene, Eldon Raj
    Vijayakumar, Ganesh Kumar
    Mani, Ravi
    Radhakrishnapillai, Aravind
    Tharmathass, Stalin Dhas
    Prasad, Sowmiya
    SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS, 2024, 25 (01)
  • [3] De novo transcriptome assembly of the calanoid copepod Neocalanus flemingeri: A new resource for emergence from diapause
    Roncalli, Vittoria
    Cieslak, Matthew C.
    Sommer, Stephanie A.
    Hoperoft, Russell R.
    Lenz, Petra H.
    MARINE GENOMICS, 2018, 37 : 114 - 119
  • [4] Comprehensive evaluation of de novo transcriptome assembly programs and their effects on differential gene expression analysis
    Wang, Sufang
    Gribskov, Michael
    BIOINFORMATICS, 2017, 33 (03) : 327 - 333
  • [5] De novo transcriptome assembly and analysis of differential gene expression in response to drought in European beech
    Mueller, Markus
    Seifert, Sarah
    Luebbe, Torben
    Leuschner, Christoph
    Finkeldey, Reiner
    PLOS ONE, 2017, 12 (09):
  • [6] De novo assembly of a tadpole shrimp (Triops newberryi) transcriptome and preliminary differential gene expression analysis
    Horn, Rebekah L.
    Ramaraj, Thiruvarangan
    Devitt, Nicholas P.
    Schilkey, Faye D.
    Cowley, David E.
    MOLECULAR ECOLOGY RESOURCES, 2017, 17 (02) : 161 - 171
  • [7] Transcriptome Sequencing, De Novo Assembly and Differential Gene Expression Analysis of the Early Development of Acipenser baeri
    Song, Wei
    Jiang, Keji
    Zhang, Fengying
    Lin, Yu
    Ma, Lingbo
    PLOS ONE, 2015, 10 (09):
  • [8] De novo transcriptome assembly and analysis of differential gene expression following lipopolysaccharide challenge in Pelteobagrus fulvidraco
    Liu, Qiu-Ning
    Xin, Zhao-Zhe
    Liu, Yu
    Zhang, Dai-Zhen
    Jiang, Sen-Hao
    Chai, Xin-Yue
    Wang, Zheng-Fei
    Zhang, Hua-Bin
    Bian, Xun-Guang
    Zhou, Chun-Lin
    Tang, Bo-Ping
    FISH & SHELLFISH IMMUNOLOGY, 2018, 73 : 84 - 91
  • [9] Differential gene expression profile of the calanoid copepod, Pseudodiaptomus annandalei, in response to nickel exposure
    Jiang, Jie-Lan
    Wang, Gui-Zhong
    Mao, Ming-Guang
    Wang, Ke-Jian
    Li, Shao-Jing
    Zeng, Chao-Shu
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2013, 157 (02): : 203 - 211
  • [10] De novo transcriptome assembly and analysis of differential gene expression following peptidoglycan (PGN) challenge in Antheraea pernyi
    Liu, Yu
    Xin, Zhao-Zhe
    Zhang, Dai-Zhen
    Zhu, Xiao-Yu
    Wang, Ying
    Chen, Li
    Tang, Bo-Ping
    Zhou, Chun-Lin
    Chai, Xin-Yue
    Tian, Ji-Wu
    Liu, Qiu-Ning
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 112 : 1199 - 1207