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1.
Anal Biochem ; 434(1): 39-43, 2013 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-23123426

RESUMO

We adapted the protocols of reducing sugar measurements with dinitrosalicylic acid and bicinchoninic acid for thermocyclers and their use in enzymatic assays for hydrolases such as amylase and ß-1,3-glucanase. The use of thermocyclers for these enzymatic assays resulted in a 10 times reduction in the amount of reagent and volume of the sample needed when compared with conventional microplate protocols. We standardized absorbance readings from the polymerase chain reaction plates, which allowed us to make direct readings of the techniques above, and a ß-glycosidase assay was also established under the same conditions. Standardization of the enzymatic reaction in thermocyclers resulted in less time-consuming temperature calibrations and without loss of volume through leakage or evaporation from the microplate. Kinetic parameters were successfully obtained, and the use of the thermocycler allowed the measurement of enzymatic activities in biological samples from the field with a limited amount of protein.


Assuntos
Amilases/metabolismo , Ensaios Enzimáticos/métodos , Glucana 1,3-beta-Glucosidase/metabolismo , Miniaturização/instrumentação , Ensaios Enzimáticos/instrumentação , Humanos , Cinética , Quinolinas/química , Salicilatos/química , Saliva/enzimologia , Amido/metabolismo
2.
J Insect Physiol ; 58(12): 1620-5, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23085484

RESUMO

Physalin B is a natural secosteroidal, extracted from the Solanaceae plant, Physalis angulata, and it presents immune-modulator effects on the bloodsucking bug, Rhodnius prolixus. In this work, R. prolixus was treated with physalin B at a concentration of 1 mg/ml of blood meal (oral application), or 20 ng/insect (applied topically) or 57 ng/cm(2) of filter paper (contact treatment), and infected with Trypanosoma cruzi Dm28c clone (2×10(6) epimastigotes/insect). The three types of applications significantly decreased the number of T. cruzi Dm28c in the gut comparing with the non-treated infected insects (controls). All groups of infected insects treated with physalin B had higher numbers of bacterial microbiota in the gut than the non-treated controls infected with T. cruzi. We observed that the infected physalin B insects with topical and contact treatments had a lower antibacterial activity in the gut when compared with control infected insects. Furthermore, infected insects with the physalin B oral treatment produced higher levels of nitrite and nitrate in the gut than control infected insects. These results demonstrate that physalin B decreases the T. cruzi transmission by inhibiting the parasite development in the insect vector R. prolixus. Herein the importance of physalin B modulation on the immune system and microbiota population in terms of parasite development and transmission are discussed.


Assuntos
Interações Hospedeiro-Parasita/efeitos dos fármacos , Rhodnius/efeitos dos fármacos , Secoesteroides/farmacologia , Trypanosoma cruzi/efeitos dos fármacos , Animais , Metagenoma/efeitos dos fármacos , Muda/efeitos dos fármacos , Nitratos/metabolismo , Nitritos/metabolismo , Espécies Reativas de Nitrogênio/metabolismo , Rhodnius/imunologia , Rhodnius/metabolismo , Rhodnius/microbiologia , Rhodnius/parasitologia
3.
J Insect Physiol ; 58(10): 1314-24, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22841889

RESUMO

Lutzomyia longipalpis is the principal species of phlebotomine incriminated as vector of Leishmania infantum, the etiological agent of visceral leishmaniasis in the Americas. Despite its importance as vector, almost nothing related to the larval biology, especially about its digestive system has been published. The objective of the present study was to obtain an overview of carbohydrate digestion by the larvae. Taking in account that phlebotomine larvae live in the soil rich in decaying materials and microorganisms we searched principally for enzymes capable to hydrolyze carbohydrates present in this kind of substrate. The principal carbohydrases encountered in the midgut were partially characterized. One of them is a α-amylase present in the anterior midgut. It is probably involved with the digestion of glycogen, the reserve carbohydrate of fungi. Two other especially active enzymes were present in the posterior midgut, a membrane bound α-glucosidase and a membrane bound trehalase. The first, complete the digestion of glycogen and the other probably acts in the digestion of trehalose, a carbohydrate usually encountered in microorganisms undergoing hydric stress. In a screening done with the use of p-nitrophenyl-derived substrates other less active enzymes were also observed in the midgut. A general view of carbohydrate digestion in L. longipalpis was presented. Our results indicate that soil microorganisms appear to be the main source of nutrients for the larvae.


Assuntos
Metabolismo dos Carboidratos , Glicosídeo Hidrolases/metabolismo , Psychodidae/metabolismo , Animais , Trato Gastrointestinal/enzimologia , Glicólise , Larva/metabolismo , Psychodidae/enzimologia , Trealase/metabolismo , alfa-Amilases/metabolismo , alfa-Glucosidases/metabolismo
4.
PLoS One ; 7(5): e36591, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22574189

RESUMO

Trypanosoma cruzi in order to complete its development in the digestive tract of Rhodnius prolixus needs to overcome the immune reactions and microbiota trypanolytic activity of the gut. We demonstrate that in R. prolixus following infection with epimastigotes of Trypanosoma cruzi clone Dm28c and, in comparison with uninfected control insects, the midgut contained (i) fewer bacteria, (ii) higher parasite numbers, and (iii) reduced nitrite and nitrate production and increased phenoloxidase and antibacterial activities. In addition, in insects pre-treated with antibiotic and then infected with Dm28c, there were also reduced bacteria numbers and a higher parasite load compared with insects solely infected with parasites. Furthermore, and in contrast to insects infected with Dm28c, infection with T. cruzi Y strain resulted in a slight decreased numbers of gut bacteria but not sufficient to mediate a successful parasite infection. We conclude that infection of R. prolixus with the T. cruzi Dm28c clone modifies the host gut immune responses to decrease the microbiota population and these changes are crucial for the parasite development in the insect gut.


Assuntos
Intestinos/imunologia , Intestinos/parasitologia , Metagenoma/imunologia , Rhodnius/microbiologia , Rhodnius/parasitologia , Trypanosoma cruzi/crescimento & desenvolvimento , Animais , Antibacterianos/farmacologia , Doença de Chagas/imunologia , Doença de Chagas/metabolismo , Doença de Chagas/microbiologia , Imunidade Humoral/efeitos dos fármacos , Imunidade Humoral/imunologia , Mucosa Intestinal/metabolismo , Intestinos/efeitos dos fármacos , Metagenoma/efeitos dos fármacos , Monofenol Mono-Oxigenase/metabolismo , Nitratos/metabolismo , Nitritos/metabolismo , Rhodnius/efeitos dos fármacos , Rhodnius/metabolismo , Especificidade da Espécie , Análise de Sobrevida , Trypanosoma cruzi/patogenicidade
5.
Exp Parasitol ; 122(2): 84-90, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19303010

RESUMO

In this paper, the lytic activity of two variants of Serratia marcescens against promastigotes of Leishmania braziliensis was studied. In vitro assays showed that S. marcescens variant SM365 lyses L. braziliensis promastigotes, while the variant DB11 did not. Scanning electron microscopy (SEM) revealed that S. marcescens SM365 adheres to all cellular body and flagellum of the parasite. Several filamentous structures were formed and identified as biofilms. After 120min incubation, they connect the protozoan to the developing bacterial clusters. SEM also demonstrated that bacteria, adhered onto L. braziliensis promastigote surface, formed small filamentous structures which apparently penetrates into the parasite membrane. d-mannose protects L. braziliensis against the S. marcescens SM365 lytic effect in a dose dependent manner. SM365 variant pre cultivated at 37 degrees C did not synthesize prodigiosin although the adherence and lysis of L. braziliensis were similar to the effect observed with bacteria cultivated at 28 degrees C, which produce high concentrations of prodigiosin. Thus, we suggest that prodigiosin is not involved in the lysis of promastigotes and that adherence promoted by bacterial mannose-sensitive (MS) fimbriae is a determinant factor in the lysis of L. braziliensis by S. marcescens SM365.


Assuntos
Fímbrias Bacterianas/metabolismo , Leishmania braziliensis/metabolismo , Prodigiosina/metabolismo , Serratia marcescens/fisiologia , Animais , Aderência Bacteriana , Carboidratos/farmacologia , Fímbrias Bacterianas/efeitos dos fármacos , Cinética , Leishmania braziliensis/efeitos dos fármacos , Leishmania braziliensis/ultraestrutura , Manose/farmacologia , Microscopia Eletrônica de Varredura , Prodigiosina/isolamento & purificação , Serratia marcescens/química , Serratia marcescens/ultraestrutura
6.
Exp Parasitol ; 118(4): 561-8, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18206142

RESUMO

Studies on the lysis of L. chagasi caused by the bacteria Serratia marcescens were carried out. In vitro experiments demonstrated that S. marcescens variant SM 365, a prodigiosin pigment producer, lysed this species of Leishmania but variant DB11, a nonpigmented bacteria, was unable to lyse the parasite. High concentrations of d-mannose were found to protect L. chagasi markedly diminishing the lysis by S. marcescens SM 365. Promastigotes of L. chagasi bound the lectin Concanavalin A conjugated with FITC, the fluorescence was intensely found at the base of the flagellum (flagellar pocket). Scanning electron microscopy revealed that the bacteria adherence occurred mainly in the flagellar pocket. S. marcescens SM 365 formed filamentous structures, identified as biofilms, which connect the protozoan to the developing bacterial clusters, in low concentrations of bacteria after 30 min incubation time. We suggest that bacterial mannose-sensitive (MS) fimbriae are relevant to S. marcescens SM 365 in the lysis of L. chagasi.


Assuntos
Leishmania infantum/microbiologia , Serratia marcescens/fisiologia , Animais , Aderência Bacteriana/fisiologia , Biofilmes , Concanavalina A/química , Relação Dose-Resposta a Droga , Fímbrias Bacterianas/fisiologia , Flagelos/microbiologia , Flagelos/ultraestrutura , Fluoresceína-5-Isotiocianato/análogos & derivados , Fluoresceína-5-Isotiocianato/química , Interações Hospedeiro-Patógeno , Cinética , Leishmania infantum/metabolismo , Leishmania infantum/ultraestrutura , Manose/metabolismo , Manose/farmacologia , Microscopia Eletrônica de Varredura , Microscopia de Fluorescência , Microscopia de Interferência , Serratia marcescens/ultraestrutura
7.
Exp Parasitol ; 115(2): 200-4, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16989812

RESUMO

Studies were carried out on the effects of different carbohydrates on the lysis of Trypanosoma cruzi, Trypanosoma rangeli and erythocytes caused by the bacteria Serratia marcescens variants SM 365 and RPH. High concentrations of d-mannose were found to protect T. cruzi and T. rangeli markedly diminishing the lysis caused by S. marcescens. However, this carbohydrate is unable to interfere with the hemolysis induced by SM 365 and RPH variants. These results showed that the trypanolytic effect induced by S. marcescens SM 365 and RPH variants is dependent on d-mannose and distinct from the hemolytic activity, strongly suggesting that bacterial fimbriae are relevant to S. marcescens in lysis of parasites.


Assuntos
Hemólise/efeitos dos fármacos , Manose/fisiologia , Serratia marcescens/fisiologia , Trypanosoma cruzi/metabolismo , Animais , Eritrócitos/efeitos dos fármacos , Eritrócitos/microbiologia , Fímbrias Bacterianas/fisiologia , Humanos , Cinética , Manose/farmacologia , Serratia marcescens/efeitos dos fármacos , Serratia marcescens/patogenicidade , Trypanosoma cruzi/efeitos dos fármacos , Trypanosoma cruzi/microbiologia
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