Ocean acidification weakens the immune response of blood clam through hampering the NF-kappa beta and toll-like receptor pathways

DOI

The impact of pCO2 driven ocean acidification on marine bivalve immunity remains poorly understood. To date, this impact has only been investigated in a few bivalve species and the underlying molecular mechanism remains unknown. In the present study, the effects of the realistic future ocean pCO2 levels (pH at 8.1, 7.8, and 7.4) on the total number of haemocyte cells (THC), phagocytosis status, blood cell types composition, and expression levels of twelve genes from the NF-kappa beta signaling and toll-like receptor pathways of a typical bottom burrowing bivalve, blood clam (Tegillarca granosa), were investigated. The results obtained showed that while both THC number and phagocytosis frequency were significantly reduced, the percentage of red and basophil granulocytes were significantly decreased and increased, respectively, upon exposure to elevated pCO2. In addition, exposure to pCO2 acidified seawater generally led to a significant down-regulation in the inducer and key response genes of NF-kappa beta signaling and toll-like receptor pathways. The results of the present study revealed that ocean acidification may hamper immune responses of the bivalve T. granosa which subsequently render individuals more susceptible to pathogens attacks such as those from virus and bacteria.

In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Gattuso et al, 2015) was used to compute a complete and consistent set of carbonate system variables, as described by Nisumaa et al. (2010). In this dataset the original values were archived in addition with the recalculated parameters (see related PI). The date of carbonate chemistry calculation is 2016-06-21.

Supplement to: Liu, Saixi; Shi, Wei; Guo, Cheng; Zhao, Xinguo; Han, Yu; Peng, Chao; Chai, Xueliang; Liu, Guangxu (2016): Ocean acidification weakens the immune response of blood clam through hampering the NF-kappa beta and toll-like receptor pathways. Fish & Shellfish Immunology, 54, 322-327

Identifier
DOI https://doi.org/10.1594/PANGAEA.861971
Related Identifier IsSupplementTo https://doi.org/10.1016/j.fsi.2016.04.030
Related Identifier IsDocumentedBy https://cran.r-project.org/package=seacarb
Metadata Access https://ws.pangaea.de/oai/provider?verb=GetRecord&metadataPrefix=datacite4&identifier=oai:pangaea.de:doi:10.1594/PANGAEA.861971
Provenance
Creator Liu, Saixi; Shi, Wei ORCID logo; Guo, Cheng; Zhao, Xinguo ORCID logo; Han, Yu; Peng, Chao; Chai, Xueliang; Liu, Guangxu ORCID logo
Publisher PANGAEA
Contributor Yang, Yan
Publication Year 2016
Rights Creative Commons Attribution 3.0 Unported; https://creativecommons.org/licenses/by/3.0/
OpenAccess true
Representation
Resource Type Supplementary Dataset; Dataset
Format text/tab-separated-values
Size 1503 data points
Discipline Immunology; Life Sciences; Medicine; Microbiology, Virology and Immunology