18 research outputs found
Corrimentos vaginais em gestantes: comparacao da abordagem sindromica com exames da pratica clinica da enfermagem
Abstracts of presentations on plant protection issues at the xth international congress of virology: August 11-16,1996 Binyanei haOoma, Jerusalem, Israel Part 2 Plenary Lectures
In vitro effects of metal pollution on Mediterranean sponges: Species-specific inhibition of 2 ‘,5 ‘-oligoadenylate synthetase.
7 páginas, 5 figuras, 1 tabla.Heavy metals are among the main pollutants of the Mediterranean coastal waters where they can harm
sublittoral biota. Filter-feeder, long-living invertebrates that remain fixed to the rocky bottom, such as
sponges, are good targets tometal contamination studies since theymay be exposed to potential lowlevels
of contamination for years. Several molecular and biochemical mechanisms are developed by sponges
to counteract the effects of noxious metals. As a result, some of the normal cell functions can be altered.
Herewe showthat the main heavy metals that can be found in marine sublittoralwaters (i.e. copper, iron,
zinc and manganese) may alter the immune system of sponges by inhibiting the activity of the sponge
2 ,5 -oligoadenylate synthetase (2-5A synthetase), which is an enzyme involved in the immune system
of vertebrates. We selected the widespread Mediterranean sponges Geodia cydonium, Crella elegans and
Chondrosia reniformis for the study. They exerted a high 2-5A synthetase activity and gave a unique profile
of 2 ,5 -oligoadenylate product production. Several metals alter the 2-5A synthetase activity differently,
in a species-specific manner. 2-5A synthetases from G. cydonium and C. elegans were inhibited by all the
metal ions assayed. However, in C. reniformis, 2-5A synthetase was either activated or inhibited by the
same ions depending on their final concentrations. Like in humans, metal contamination may have an
effect on the OAS activity and thus it might alter the sponge immune system. However, since the effects
are species-specific, 2-5A synthetase cannot be used as general biomarker of metal pollutions.This work was supported by the European Union with
the Marie Curie Research Training Network, BIOCAPITAL FP6
and by the Spanish Government with the projects INTERGEN,
CICYT: CTM2004-05265-C02/MAR and MARMOL, CICYT:
CTM2007-66635-CO2.Peer reviewe
2′-phosphodiesterase and 2′,5′-oligoadenylate synthetase activities in the lowest metazoans, sponge [porifera]
4 páginas, 1 tabla, 1 figura.Sponges [porifera], the most ancient metazoans, contain modules related to the vertebrate immune system,
including the 2
0
,5
0
-oligoadenylate synthetase (OAS). The components of the antiviral 2
0
,5
0
-oligoadenylate
(2–5A) system (OAS, 2
0
-Phosphodiesterase (2
0
-PDE) and RNAse L) of vertebrates have not all been identified
in sponges. Here, we demonstrate for the first time that in addition to the OAS activity, sponges possess
a 2
0
-PDE activity, which highlights the probable existence of a premature 2–5A system. Indeed, Suberites
domuncula and Crella elegans exhibited this 2–5A degrading activity. Upon this finding, two out of three
elements forming the 2–5A system have been found in sponges, only a endoribonuclease, RNAse L or similar,
has to be found. We suspect the existence of a complex immune system in sponges, besides the self/non-self
recognition system and the use of phagocytosis and secondary metabolites against pathogens.This work was supported by the European Union with the Marie
Curie Research Training Network, BIOCAPITAL FP6 and by the
Spanish Government with the project MARMOL, CI-CYT: CTM2007-
66635-CO2.Peer reviewe
Evolution of the 2′-5′-Oligoadenylate Synthetase Family in Eukaryotes and Bacteria
13 páginas, 5 figuras, 3 tablas.The 2
0
-5
0
-oligoadenylate synthetase (OAS)
belongs to a nucleotidyl transferase family that includes
poly(A) polymerases and CCA-adding enzymes. In mammals and birds, the OAS functions in the interferon system
but it is also present in an active form in sponges, which are
devoid of the interferon system. In view of these observations, we have pursued the idea that OAS genes could be
present in other metazoans and in unicellular organisms as
well. We have identified a number of OAS1 genes in
annelids, mollusks, a cnidarian, chordates, and unicellular
eukaryotes and also found a family of proteins in bacteria
that contains the five OAS-specific motifs. This indicates a
specific relationship to OAS. The wide distribution of the
OAS genes has made it possible to suggest how the OAS1
gene could have evolved from a common ancestor to choanoflagellates and metazoans. Furthermore, we suggest that
the OASL may have evolved from an ancestor of cartilaginous fishes, and that the OAS2 and the OAS3 genes
evolved from a mammalian ancestor. OAS proteins function in the interferon system in mammals. This system is
only found in jawed vertebrates. We therefore suggest that
the original function of OAS may differ from its function in
the interferon system, and that this original function of OAS
is preserved even in OAS genes that code for proteins,
which do not have 2
0
-5
0
-oligoadenylate synthetase activity.The work was initially supported by a
grant from the Danish Natural Science Council and the Carlsberg
Foundation. The work was supported by the Estonian Science
Foundation (Grant no. 7421).Peer reviewe