Centrocins: Isolation and characterization of novel dimeric antimicrobial peptides from the green sea urchin, Strongylocentrotus droebachiensis

2010 ◽  
Vol 34 (9) ◽  
pp. 959-968 ◽  
Author(s):  
Chun Li ◽  
Tor Haug ◽  
Morten K. Moe ◽  
Olaf B. Styrvold ◽  
Klara Stensvåg
1979 ◽  
Vol 83 (1) ◽  
pp. 109-115 ◽  
Author(s):  
K T Edds

Isolated petaloid coelomocytes from the sea urchin Strongylocentrotus droebachiensis transform to a filopodial morphology in hypotonic media. Electron micrographs of negatively stained Triton-insoluble cytoskeletons show that the petaloid form consists of a loose net of microfilaments while the filopodial form consists of paracrystalline bundles of microfilaments. Actin is the major protein of both forms of the cytoskeleton. Additional polypeptides have molecular weights of approximately 220,000, 64,000, 57,000, and 27,000 daltons. Relative to actin the filopodial cytoskeletons have an average of 2.5 times as much 57k polypeptide as the petaloid cytoskeletons. Treatment with 0.25 M NaCl dissociates the filament bundles into individual actin filaments free of the actin-associated polypeptides. Thus, one or more of these actin-associated polypeptides may be responsible for crosslinking the actin filaments into bundles and maintaining the three-dimensional nature of the cytoskeletons.


2015 ◽  
Vol 17 ◽  
pp. 227-234 ◽  
Author(s):  
Olga N. Pozharitskaya ◽  
Alexander N. Shikov ◽  
Into Laakso ◽  
Tuulikki Seppänen-Laakso ◽  
Igor E. Makarenko ◽  
...  

2008 ◽  
Vol 32 (12) ◽  
pp. 1430-1440 ◽  
Author(s):  
Chun Li ◽  
Tor Haug ◽  
Olaf B. Styrvold ◽  
Trond Ø. Jørgensen ◽  
Klara Stensvåg

1992 ◽  
Vol 267 (4) ◽  
pp. 2228-2233 ◽  
Author(s):  
B P Cammue ◽  
M F De Bolle ◽  
F R Terras ◽  
P Proost ◽  
J Van Damme ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
pp. 699 ◽  
Author(s):  
Marc B Anglès d’Auriac ◽  
Anders Hobæk ◽  
Hartvig Christie ◽  
Hege Gundersen ◽  
Camilla Fagerli ◽  
...  

2021 ◽  
Author(s):  
Jonathan Hira ◽  
Klara Stensvåg

Abstract “Sea urchin lesion syndrome” is known as sea urchins disease with the progressive development of necrotic epidermal tissue and loss of external organs, including appendages on the outer body surface. Recently, a novel strain, Vibrio echinoideorum has been isolated from the lesions of green sea urchin (Strongylocentrotus droebachiensis), an economically important mariculture species in Norway. V. echinoideorum has not been reported elsewhere in association of with green sea urchin lesion syndrome. Therefore, in this study, an immersion based bacterial challenge experiment was performed to expose sea urchins (wounded and non-wounded) to V. echinoideorum, thereby mimicking a nearly natural host-pathogen interaction under controlled conditions. This infection experiment demonstrated that only the injured sea urchins developed the lesion to a significant degree when exposed to V. echinoideorum. Pure cultures of the employed bacterial strain was recovered from the infected animals and its identity was confirmed by the MALDI-TOF MS spectra profiling. Additionally, the hemolytic phenotype of V. echinoideorum substantiated its virulence potential towards the host, and this was also supported by the cytolytic effect on red spherule cells of sea urchins. Furthermore, the genome sequence of V. echinoideorum was assumed to encode potential virulence genes and were subjected for in silico comparison with the established virulence factors of Vibrio vulnificus and Vibrio tasmaniensis. This comparative virulence profile provided novel insights about virulence genes and their putative functions related to chemotaxis, adherence, invasion, evasion of the host immune system, and damage of host tissue and cells. Thus, it supports the pathogenicity of V. echinoideorum. In conclusion, the interaction of V. echinoideorum with injured sea urchins appears to be essential for the development of lesion syndrome and therefore, revealing its potentiality as an opportunistic pathogen.


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