» Articles » PMID: 26176852

Up in Arms: Immune and Nervous System Response to Sea Star Wasting Disease

Abstract

Echinoderms, positioned taxonomically at the base of deuterostomes, provide an important system for the study of the evolution of the immune system. However, there is little known about the cellular components and genes associated with echinoderm immunity. The 2013-2014 sea star wasting disease outbreak is an emergent, rapidly spreading disease, which has led to large population declines of asteroids in the North American Pacific. While evidence suggests that the signs of this disease, twisting arms and lesions, may be attributed to a viral infection, the host response to infection is still poorly understood. In order to examine transcriptional responses of the sea star Pycnopodia helianthoides to sea star wasting disease, we injected a viral sized fraction (0.2 μm) homogenate prepared from symptomatic P. helianthoides into apparently healthy stars. Nine days following injection, when all stars were displaying signs of the disease, specimens were sacrificed and coelomocytes were extracted for RNA-seq analyses. A number of immune genes, including those involved in Toll signaling pathways, complement cascade, melanization response, and arachidonic acid metabolism, were differentially expressed. Furthermore, genes involved in nervous system processes and tissue remodeling were also differentially expressed, pointing to transcriptional changes underlying the signs of sea star wasting disease. The genomic resources presented here not only increase understanding of host response to sea star wasting disease, but also provide greater insight into the mechanisms underlying immune function in echinoderms.

Citing Articles

A reference genome for ecological restoration of the sunflower sea star, Pycnopodia helianthoides.

Schiebelhut L, DeBiasse M, Gabriel L, Hoff K, Dawson M J Hered. 2023; 115(1):86-93.

PMID: 37738158 PMC: 10838127. DOI: 10.1093/jhered/esad054.


Sea stars resist wasting through active immune and collagen systems.

Pespeni M, Lloyd M Proc Biol Sci. 2023; 290(2002):20230347.

PMID: 37403510 PMC: 10320347. DOI: 10.1098/rspb.2023.0347.


Two decades of change in sea star abundance at a subtidal site in Puget Sound, Washington.

Casendino H, McElroy K, Sorel M, Quinn T, Wood C PLoS One. 2023; 18(6):e0286384.

PMID: 37294819 PMC: 10256211. DOI: 10.1371/journal.pone.0286384.


A Review of Asteroid Biology in the Context of Sea Star Wasting: Possible Causes and Consequences.

Oulhen N, Byrne M, Duffin P, Gomez-Chiarri M, Hewson I, Hodin J Biol Bull. 2022; 243(1):50-75.

PMID: 36108034 PMC: 10642522. DOI: 10.1086/719928.


A chromosome-level reference genome for the giant pink sea star, Pisaster brevispinus, a species severely impacted by wasting.

DeBiasse M, Schiebelhut L, Escalona M, Beraut E, Fairbairn C, Marimuthu M J Hered. 2022; 113(6):689-698.

PMID: 36044245 PMC: 9709977. DOI: 10.1093/jhered/esac044.


References
1.
Cameron R, Samanta M, Yuan A, He D, Davidson E . SpBase: the sea urchin genome database and web site. Nucleic Acids Res. 2008; 37(Database issue):D750-4. PMC: 2686435. DOI: 10.1093/nar/gkn887. View

2.
Franzenburg S, Fraune S, Kunzel S, Baines J, Domazet-Loso T, Bosch T . MyD88-deficient Hydra reveal an ancient function of TLR signaling in sensing bacterial colonizers. Proc Natl Acad Sci U S A. 2012; 109(47):19374-9. PMC: 3511086. DOI: 10.1073/pnas.1213110109. View

3.
Hewson I, Button J, Gudenkauf B, Miner B, Newton A, Gaydos J . Densovirus associated with sea-star wasting disease and mass mortality. Proc Natl Acad Sci U S A. 2014; 111(48):17278-83. PMC: 4260605. DOI: 10.1073/pnas.1416625111. View

4.
Dheilly N, Raftos D, Haynes P, Smith L, Nair S . Shotgun proteomics of coelomic fluid from the purple sea urchin, Strongylocentrotus purpuratus. Dev Comp Immunol. 2013; 40(1):35-50. DOI: 10.1016/j.dci.2013.01.007. View

5.
Akira S, Uematsu S, Takeuchi O . Pathogen recognition and innate immunity. Cell. 2006; 124(4):783-801. DOI: 10.1016/j.cell.2006.02.015. View