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1.
Sci Total Environ ; 896: 164981, 2023 Oct 20.
Article in English | MEDLINE | ID: mdl-37364846

ABSTRACT

Since the 2019 oil spill on the northeastern coast of Brazil, oil materials have washed up on the beaches. A characteristic of the recent oil spill that began in late August was that some of the oiled material, such as tarballs, contained the goose barnacle species Lepas anatifera (Cirripedia, Lepadomorpha), which is well-known for its cosmopolitan distribution and wide occurrence in the oceans. The findings of this study provide information on the occurrence and contamination of petroleum hydrocarbons in animals adhered to the surfaces of tarballs sampled from beaches in the Brazilian states of Ceará and Rio Grande do Norte, between September and November 2022. The size of the barnacles varied from 0.122 to 2.20 cm, suggesting that the tarballs had been floating in the ocean for at least a month. All groups of L. anatifera collected from the tarballs had polycyclic aromatic hydrocarbons (PAHs) present (∑21PAHs from 476.33 to 3816.53 ng g-1). In comparison to high-molecular-weight PAHs, which are primarily from pyrolytic sources, low-molecular-weight PAHs, such as naphthalene and phenanthrene, which are mostly related to petrogenic sources, were shown to be more abundant. In addition, dibenzothiophene, which is exclusive of petrogenic origin, was found in all samples (30.74-537.76 ng g-1). The aliphatic hydrocarbons (AHs): n-alkanes, pristane, and phytane were also found and displayed petroleum characteristics. These results highlight the danger of increasing the absorption of petrogenic PAHs and AHs by organisms that use tarballs as substrates. L. anatifera is a crucial component of the food chain because many animals such as crabs, starfish, and gastropods consume it.


Subject(s)
Petroleum Pollution , Petroleum , Polycyclic Aromatic Hydrocarbons , Thoracica , Water Pollutants, Chemical , Animals , Petroleum/analysis , Brazil , Environmental Monitoring/methods , Hydrocarbons/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Petroleum Pollution/adverse effects , Petroleum Pollution/analysis , Eating , Water Pollutants, Chemical/analysis , Geologic Sediments/chemistry
2.
Article in English | MEDLINE | ID: mdl-27313992

ABSTRACT

Toxoplasmosis is a zoonosis distributed all over the world, which the etiologic agent is an intracellular protozoan parasite, Toxoplasma gondii. This disease may cause abortions and severe diseases in many warm-blood hosts, including humans, particularly the immunocompromised patients. The parasite specialized secretory organelles, as micronemes, rhoptries and dense granules, are critical for the successful parasitism. The dense granule protein 2 (GRA2) is a parasite immunogenic protein secreted during infections and previous studies have been shown that this parasite component is crucial for the formation of intravacuolar membranous nanotubular network (MNN), as well as for secretion into the vacuole and spatial organization of the parasites within the vacuole. In the present study, we produced a monoclonal antibody to GRA2 (C3C5 mAb, isotype IgG2b), mapped the immunodominant epitope of the protein by phage display and built GRA2 synthetic epitopes to evaluate their ability to protect mice in a model of experimental infection. Our results showed that synthetic peptides for B- and T-cell epitopes are able to improve survival of immunized animals. In contrast with non-immunized animals, the immunized mice with both B- and T-cell epitopes had a better balance of cytokines and demonstrated higher levels of IL-10, IL-4 and IL-17 production, though similar levels of TNF-α and IL-6 were observed. The immunization with both B- and T-cell epitopes resulted in survival rate higher than 85% of the challenged mice. Overall, these results demonstrate that immunization with synthetic epitopes for both B- and T-cells from GRA2 protein can be more effective to protect against infection by T. gondii.


Subject(s)
Antigens, Protozoan/immunology , Epitopes, B-Lymphocyte/immunology , Epitopes, T-Lymphocyte/immunology , Peptides/immunology , Protozoan Proteins/immunology , Protozoan Vaccines/immunology , Toxoplasma/immunology , Toxoplasmosis/prevention & control , Adjuvants, Immunologic , Amino Acid Sequence , Animals , Antibodies, Monoclonal/chemistry , Antibodies, Monoclonal/immunology , Antibodies, Protozoan/blood , Antigens, Protozoan/genetics , Cytokines/metabolism , Disease Models, Animal , Female , Fluorescent Antibody Technique, Indirect , Immunity, Humoral , Interleukins/immunology , Interleukins/metabolism , Mice , Mice, Inbred C57BL , Models, Structural , Peptides/chemical synthesis , Peptides/genetics , Protein Conformation , Protozoan Vaccines/chemical synthesis , Protozoan Vaccines/genetics , Survival Rate , Toxoplasma/chemistry , Toxoplasmosis/immunology , Toxoplasmosis/parasitology , Treatment Outcome
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