ANTIBACTERIAL ACTIVITY IN THE BLOOD-CELLS OF THE SOLITARY ASCIDIAN, CIONA-INTESTINALIS, IN-VITRO

Citation
C. Findlay et Vj. Smith, ANTIBACTERIAL ACTIVITY IN THE BLOOD-CELLS OF THE SOLITARY ASCIDIAN, CIONA-INTESTINALIS, IN-VITRO, The Journal of experimental zoology, 273(5), 1995, pp. 434-444
Citations number
32
Categorie Soggetti
Zoology
ISSN journal
0022104X
Volume
273
Issue
5
Year of publication
1995
Pages
434 - 444
Database
ISI
SICI code
0022-104X(1995)273:5<434:AAITBO>2.0.ZU;2-5
Abstract
The antibacterial properties of the blood cells of the solitary ascidi an, Ciona intestinalis, were investigated in vitro. The results show t hat blood cell lysate supernatants have potent antibacterial activity against a wide range of bacteria. Activity was strongest against Gram positive bacteria, where typically there was a 95-99% reduction in bac terial viability within 1 h. By contrast, Gram negative bacteria were less susceptible to-the antibacterial effects, with the viability of t hese bacteria generally reduced by approximately 20-40% after 3 h. Act ivity against both types of bacteria was further found to be heat-stab le (even after heating to 100 degrees C for 10 min or freezing to -20 degrees C for up to 1 month), Ca2+- but not Mg2+-dependent, and active at very low titres. Comparison of the antibacterial vigour of lysate supernatants made from separated blood cell populations revealed that activity resides mainly in the morula cells with some, albeit weaker, activity also detectable in the hyaline amoebocytes. No activity was p resent in the plasma. Preliminary investigations into the mode of acti on of the active factors indicate that the response is not due to lyso zyme, is not directly lytic in character, and is not attributable to a gglutination. Instead, as preliminary characterization by gel filtrati on on Sephadex G-75 revealed 4 main protein peaks, with antibacterial activity confined to peak 3 (molecular weight range of 8-15 kDa), the phenomenon seems to be due to the action of one or more low molecular weight proteins. The location, action, and release of these factors ap pear to differ from those of the cecropins and defensins described in other animal groups. (C) 1995 Wiley-Liss, Inc.