ABSTRACT
Rhodnius prolixus é um dos principais insetos vetores de Trypanosomacruzi e de Trypanosoma rangeli na América Latina. A produção de peptídeosantimicrobianos (AMPs) no trato digestivo ou corpo gorduroso do inseto é vitalpara evitar a proliferação de microrganismos patogênicos além de manter ahomeostasia da microbiota nativa. O presente trabalho focou na modulação daimunidade humoral do intestino médio de R. prolixus desafiados oralmente coma bactéria Gram-positiva Staphylococcus aureus e Gram-negativa Escherichiacoli, além de seus tripanosomatídeos naturais T. rangeli e T. cruzi, considerandoa influência do desenvolvimento dos parasitas sobre a microbiota intestinal. Emcondições normais, a região anterior do intestino médio houve maior abundânciade transcritos de genes de lisozimas (lis) e defensinas (def), enquanto naposterior, do gene da prolixicina (prol). Insetos alimentados com bactérias Gramnegativasapresentaram maior quantidade de transcritos de defC e prol,enquanto a ingestão de bactérias Gram-positivas induziu a expressão de defA edefB no intestino médio. A infecção por T. rangeli cepa Macias diminuiu aatividade fenoloxidásica, os níveis de expressão de lisozimas e prolixicina, aomesmo tempo em que induziu aumento de atividade antibacteriana e dos níveisde defensina C no tubo digestivo do inseto, também modificando a composiçãode bactérias nativas...
Rhodnius prolixus is a major vector of Trypanosoma rangeli andTrypanosoma cruzi, in Latin America. The production of antimicrobial peptides(AMPs) in the midgut of the insect is vital to control possible infection, and tomaintain the microbiota already present in the digestive tract. This work focuseson the modulation of the humoral immune responses of the midgut of R. prolixusorally challenged with Gram positive and Gram negative bacteria as well with T.rangeli Macias strain, T. cruzi Dm 28c and Y strain, considering the influence ofthe parasites on the intestinal microbiota. Our results showed that the anteriormidgut contents of control insects contain a higher inducible antibacterial activityand AMPs transcript abundance than those of the posterior midgut. Insects orallyfed with Gram-negative bacteria presented higher amount of defC and proltranscripts, while the ingestion of Gram-positive induced defA and defBexpression in the midgut. T. rangeli Macias strain successfully colonized R.prolixus midgut through a decreasing in PO activities, prolixicin and lysozymelevels, while at the same time induced an increase in antibacterial activity andupregulated defC levels in the insect anterior midgut. T. rangeli infection alsodiminishes the amount of cultivable gut bacteria as well modified the compositionof indigenous microorganisms. Furthermore, different T. cruzi strains presentdistinct profiles of immune system and microbiota modulation in R. prolixusmidgut, where T. cruzi Dm 28c was able to induce an increase in defensin Cgenes and a depression in prolixicin genes, while drastically reduce the cultivablebacteria population. In the other hand T. cruzi Y was not competent to induceAMPs expression in the gut or considerably reduce the microbiota in the anteriormidgut...
Subject(s)
Animals , Antimicrobial Cationic Peptides , Rhodnius/immunology , Trypanosoma rangeli , Trypanosoma cruzi/immunology , Phagocytosis , Plant Root NodulationABSTRACT
Semiconductor nanoparticles, such as quantum dots (QDs), were used to carry out experiments in vivo and ex vivo with Trypanosoma cruzi. However, questions have been raised regarding the nanotoxicity of QDs in living cells, microorganisms, tissues and whole animals. The objective of this paper was to conduct a QD nanotoxicity study on living T. cruzi protozoa using analytical methods. This was accomplished using in vitro experiments to test the interference of the QDs on parasite development, morphology and viability. Our results show that after 72 h, a 200 μM cadmium telluride (CdTe) QD solution induced important morphological alterations in T. cruzi, such as DNA damage, plasma membrane blebbing and mitochondrial swelling. Flow cytometry assays showed no damage to the plasma membrane when incubated with 200 μM CdTe QDs for up to 72 h (propidium iodide cells), giving no evidence of classical necrosis. Parasites incubated with 2 μM CdTe QDs still proliferated after seven days. In summary, a low concentration of CdTe QDs (2 μM) is optimal for bioimaging, whereas a high concentration (200 μM CdTe) could be toxic to cells. Taken together, our data indicate that 2 μM QD can be used for the successful long-term study of the parasite-vector interaction in real time.