RESUMO
Dioctophyme renale is a nematode with zoonotic potential that affects the kidneys of carnivorous, wild, and domestic mammals. In this study, we sought to evaluate the indirect ELISA method against routine methods used to diagnose dioctophimosis. Hence, 38 dogs parasitized by D. renale, as confirmed by surgery, were selected. The dogs were evaluated by abdominal ultrasound and urinalysis, and their sera were tested by indirect ELISA using D. renale adult secretion and excretion antigen (DES). Five dogs were followed up with serum collections on day 0 (day of surgery) and 30, 60, and 90 days after surgery to evaluate antibody kinetics. Abdominal ultrasound and indirect ELISA successfully diagnosed 37 dogs parasitized by D. renale, while urinalysis diagnosed 29 animals. The positive animals were parasitized with 1-7 parasites; 17 dogs were infected by male and female parasites, 15 only by female parasites, and six were parasitized only by male parasites. When assessing specificity and sensitivity, all techniques showed 100% specificity and 81.6%, 97.4%, and 97.4% sensitivity for urinalysis, ultrasound, and ELISA, respectively (p < 0.001). The five positive dogs that were followed up after surgery showed a progressive decrease in mean absorbances in indirect ELISA (0.644, 0.516, 0.511, and 0.440, respectively). This study demonstrated that the indirect ELISA using the DE antigen could diagnose dioctophimosis regardless of the number, sex, and location of the parasites, with the potential to be used in epidemiological research and implementing immunological and molecular studies, opening new lines of research on D. renale.
Dioctophyme renale é um nematódeo que possui potencial zoonótico e acomete o rim de mamíferos carnívoros, silvestres e domésticos. Neste estudo busca-se avaliar a técnica de ELISA indireto frente metodologias de rotina utilizadas no diagnóstico da dioctofimose. Para isto, 38 cães participaram do estudo, sendo todos parasitados por D. renale, confirmados por cirurgia. Esses cães foram avaliados por ultrassom abdominal, urinálise e seus soros testado por ELISA indireto utilizando antígeno de excreção e secreção (DES) de adultos de D. renale. Destes, cinco cães foram acompanhados com coletas de soro, no dia zero (dia da cirurgia) e após 30, 60 e 90 dias da cirurgia para avaliar a cinética dos anticorpos. O ultrassom abdominal e ELISA indireto apresentaram sucesso no diagnóstico de 37 cães parasitados por D. renale, enquanto que a urinálise diagnosticou 29 animais. Os animais positivos possuíam de um a sete parasitos, 17 cães apresentaram infecções por macho e fêmeas, 15 somente por fêmeas e seis foram parasitados apenas por machos. Na avaliação da especificidade e sensibilidade, todas as técnicas apresentaram 100% de especificidade e 81,6%, 97,4%, 97,4% de sensibilidade para urinálise, ultrassom e ELISA, respectivamente (p < 0,001). Os cinco cães positivos que foram acompanhados após a cirurgia apresentaram diminuição progressiva nas médias de absorbâncias no ELISA indireto (0,644, 0,516, 0,511 e 0,440, respectivamente). O estudo demonstrou que o ELISA indireto utilizando o antígeno DES poderia diagnosticar dioctofimose, independentemente do número, sexo e localização dos parasitos, com potencial para ser utilizada em estudos epidemiológicos e na implementação de estudos imunológicos e moleculares, abrindo novas linhas de pesquisa sobre Dioctophyme renale.
RESUMO
This study sought to make a literature review of the medicinal plants Origanum majorana, Origanum vulgare L., Thymus vulgaris L., Cuminum cynimum L., and Rosmarinus officinalis L. with antiparasitic potential. Articles and theses were selected from the LILACS, PubMed, and Google Scholar databases, which comprised the period from 2000 to 2021 (22 years). In all, 49 studies were selected, and the majority were with the plant Origanum vulgare L. (oregano), followed by Thymus vulgaris L. (thyme). Twenty-five genera of parasites were detected, which were described being tested with phytotherapic. The nematode Haemonchus spp. was the most evaluated in these studies, followed by the parasite genera Leishmania, Trichostrongylus, and Toxocara. All plants showed antiparasitic effects, with more or less action, therefore with the potential to continue research in the search for biomolecules to control these parasites.
O presente trabalho faz uma revisão bibliográfica das plantas medicinais Origanum majorana, Origanum vulgare L., Thymus vulgaris L., Cuminum cynimum L. e Rosmarinus officinalis L. com potencial antiparasitário. Foram selecionados artigos e teses nos bancos de dados LILACS, PubMed e Google Acadêmico que compreendiam o período de publicação de 2000 a 2021 (22 anos). Ao todo, foram selecionados 49 estudos, sendo que na maioria constava a planta Origanum vulgare L. (orégano), seguido de Thymus vulgaris L. (tomilho). Foram detectados 25 gêneros de parasitos, os quais foram descritos sendo testados frente a algum fitoterápico. O nematoda Haemonchus spp. foi o mais avaliado nestes estudos, seguido dos gêneros dos parasitos Leishmania, Trichostrongylus e Toxocara. Todas as plantas apresentaram efeitos antiparasitários, com maior ou menos ação, portanto com potencial para dar continuidade aos estudos em buscas de biomoléculas para controle destes parasitos.
RESUMO
The objective of this work was to evaluate the early and late immunological modulation of an experimental infection of T. canis larvae in mice. Mice were infected with 100 infective larvae and euthanized at different period: 24, 48 hours post infection (HPI), 15- and 30 days post infection (DPI). The humoral response was evaluated by indirect ELISA. Quantitative RT-PCR (qPCR) was used to quantify the mRNA transcription of cytokines IL4, IL10, IL12 and Ym1 in the early and late infection periods. Infection with T. canis was able to generate specific total IgG at 15- and 30- DPI. Analyzing the IgG isotype revealed a significant differentiation for IgG1 compared with IgG2a, IgG2b and IgG3, characterizing a Th-2 response. Evaluating the gene transcription at the early phase of infection, higher transcription levels of IL10, IL4 and Ym1 and a downregulation of IL12 were observed. By the late phase, increased transcription levels of IL4, Ym1 and IL12 were observed, and downregulation of IL-10 transcription was observed. The data obtained suggest that during experimental infection with T. canis, the participation of the IL4, IL10, IL12 cytokines and Ym1 can play an important role in T. canis immunomodulation.(AU)
O objetivo deste trabalho foi avaliar a modulação imunológica precoce e tardia da infecção experimental de larvas de T. canis em camundongos. Estes foram infectados com 100 larvas infectantes e eutanasiados em diferentes períodos: 24 e 48 horas pós infecção (HPI), 15 e 30 dias após a infecção (DPI). A resposta humoral foi avaliada por ELISA indireto. RT-PCR quantitativo (qPCR) foi usado para quantificar a transcrição de mRNA das citocinas IL4, IL10, IL12 e Ym1 nos períodos de infecção precoce e tardia. A infecção por T. canis foi capaz de gerar IgG total específico aos 15 e 30 DPI. A análise do isótipo IgG revelou uma diferenciação significativa para IgG1 em comparação com IgG2a, IgG2b e IgG3, caracterizando uma resposta Th-2. Avaliando-se a transcrição gênica na fase inicial da infecção, foram observados níveis mais elevados de transcrição de IL10, IL4 e Ym1 e a regulação negativa de IL12. Na fase tardia, foram observados níveis aumentados de transcrição de IL4, Ym1 e IL12, e foi observada regulação negativa da transcrição de IL-10. Os dados obtidos sugerem, que durante a infecção experimental com T. canis, a participação das citocinas IL4, IL10, IL12 e Ym1 podem desempenhar um papel importante na imunomodulação de T. canis.(AU)
Assuntos
Animais , Camundongos , Toxocaríase/diagnóstico , Toxocara canis/imunologia , Imunomodulação , Camundongos/parasitologia , Larva Migrans/imunologiaRESUMO
Human toxocariasis consists of chronic tissue parasitosis that is difficult to treat and control. This study aimed to evaluate the action of the probiotic Lactobacillus acidophilus ATCC 4356 on larvae of Toxocara canis and the effect of IFN-γ cytokine on parasite-host in vivo (1.109 CFU) and in vitro (1.106, 1.107, 1.108, 1.109 CFU) interactions. Four groups of six BALB/c mice were formed: G1 - L. acidophilus supplementation and T. canis infection; G2 - T. canis infection; G3 - L. acidophilus supplementation; and G4 - PBS administration. Mice were intragastrically suplemented with probiotics for 15 days before inoculation and 48 h after inoculation with 100 T. canis eggs. The inoculation of T. canis was also perfomed intragastrically. The recovery of larvae took place through digestion of liver and lung tissues; the evaluation of IFN-γ gene transcription in leukocytes was performed by qPCR. The in vitro test consisted of incubating the probiotic with T. canis larvae. The supplementation of probiotics produced a reduction of 57.7% (p = 0.025) in the intensity of infection of T. canis larvae in mice, whereas in the in vitro test, there was no larvicidal effect. In addition, a decrease in the IFN-γ gene transcription was observed in both, T. canis-infected and uninfected mice, regardless of whether or not they received supplementation. The probiotic L. acidophilus ATCC 4356 reduced T. canis infection intensity in mice, however, the probiotic did not have a direct effect on larvae, demonstrating the need of interaction with the host for the beneficial effect of the probiotic to occur. Yet, the proinflammatory cytokine IFN-γ did not apparently contributed to the observed beneficial effect of probiotics.
Assuntos
Lactobacillus acidophilus/efeitos dos fármacos , Probióticos/administração & dosagem , Toxocara canis/efeitos dos fármacos , Toxocaríase/tratamento farmacológico , Toxocaríase/prevenção & controle , Animais , Lactobacillus , Larva/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos BALB C , Probióticos/farmacologia , Toxocara canis/microbiologia , Toxocara canis/fisiologia , Toxocaríase/parasitologiaRESUMO
The nematode Toxocara canis is of public health importance and is the main causative agent of toxocariasis in humans. This disease is difficult to diagnose due to several factors, including the possibility of cross-reactions with other nematodes in the ELISA. To overcome this problem, molecular tests have been recommended as an alternative to identify the parasite. The quantitative real-time polymerase chain reaction (qPCR) technique was used in this study to identify and quantify the parasite load of T. canis in the mouse brain. To this end, 24 mice were divided into six groups, five of which were challenged with different infective doses of T. canis larvae (L3) (1000, 500, 250, 100 and 50 larvae), while the sixth group, uninfected, acted as negative control. Forty-five days after infection, the animals were euthanized to collect the brain, from which two portions of 20 mg of tissue were taken for DNA extraction, while the rest of the brain tissue was digested to quantify the number of larvae by microscopy. The number of DNA copies was calculated from the standard DNA quantification curve, showing values of E = 93.4%, R2 = 0.9655 and Y = -3.415. A strong positive correlation (R = 0, 81; p < .001) was found between the number of copies and the recovery of larvae from brain. However, the parasite's DNA was also identified even in animals from whose brain no larvae were recovered after tissue digestion. The results of this study therefore confirm that the qPCR technique can be a valuable tool for the detection and quantification of T. canis DNA in murine hosts, even in animals whose with tissues contain very few parasites.
Assuntos
Encéfalo/parasitologia , DNA de Helmintos/análise , Olho/parasitologia , Carga Parasitária/métodos , Parasitologia/métodos , Reação em Cadeia da Polimerase em Tempo Real/métodos , Toxocara canis/isolamento & purificação , Animais , Feminino , Larva/crescimento & desenvolvimento , Camundongos , Carga Parasitária/instrumentação , Parasitologia/instrumentação , Toxocara canis/crescimento & desenvolvimentoRESUMO
Este estudo avaliou a ação in vitro e in vivo de extratos de Eugenia uniflora em nematódeos gastrintestinais de ovinos. No teste de inibição da eclodibilidade dos ovos, extratos aquosos e hidroalcoólicos foram testados nas concentrações de 40 a 1,25 mg/mL. O efeito citotóxico foi mensurado através do ensaio de MTT em células VERO nas concentrações de 4000 a 1,95 µg/mL. A composição química foi analisada através da marcha fitoquímica qualitativa. No teste in vivo, foram administrados 100 mg/kg, por via oral, do extrato hidroalcoólico por três dias em ovinos naturalmente infectados e realizada coleta de fezes para estimar a redução de ovos por grama de fezes (OPG). Diferentes extratos de E. uniflora inibiram a eclodibilidade dos ovos, com percentual de inibição variando de 14,56 a 99,75%, sendo os hidroalcoólicos mais promissores que os aquosos. Na marcha fitoquímica, compostos com ação anti-helmíntica comprovada foram observados, como flavonoides, saponinas, taninos e triterpenos. Nas condições testadas, os extratos apresentaram citotoxicidade nula a moderada. In vivo, a redução do OPG foi observada apenas no grupo controle (anti-helmíntico). Os extratos de E. uniflora mostraram-se promissores com ação in vitro, necessitando estudos que avaliem outras concentrações e formas de administração in vivo.(AU)
This study evaluated the in vitro and in vivo action of Eugenia uniflora extracts on sheep gastrointestinal nematode. In the egg hatchability inhibition assay, aqueous and hydroalcoholic extracts were tested in the concentrations ranging from 40 to 1.25 mg/mL. The cytotoxic effect was measured using the MTT assay on VERO cells at concentrations ranging from 4000 to 1.95 μg/mL. The chemical composition was analyzed through the qualitative phytochemical screening. In the in vivo test, 100 mg/kg of the hydroalcoholic extract was administered orally for three days in sheep naturally infected and fecal collection was performed to estimate the egg count per gram of faeces (EPG). Different extracts of E. uniflora inhibited hatchability of eggs with a percentage of inhibition ranging from 14.56 to 99.75%, being the hydroalcoholic most effective than the aqueous. In phytochemical analysis, compounds with anthelmintic action were observed, such as flavonoids, saponins, tannins and triterpenes. Extracts showed moderate to null cytotoxicity under the conditions tested. Reduction of EPG was observed only in control group (anthelmintic). The extracts of E. uniflora proved promising with in vitro action, requiring studies that assess other concentrations and forms of in vivo administration.(AU)
Assuntos
Animais , Eugenia/química , Extratos Vegetais/uso terapêutico , Nematoides , Ovinos/parasitologia , Haemonchus , Plantas MedicinaisRESUMO
Toxocara spp. are responsible for causing toxocariasis, a zoonotic disease of global importance, which is difficult to treat as the available drugs have moderate efficacy in the clinical resolution of the disease. A promising alternative to the existing drugs is Propolis, which is known for having biological and pharmacological properties such as antiparasitic, antioxidant, and antitumor activities. In this study, we report the in vitro anthelmintic activity of essential oil from Brazilian Red Propolis (EOP) against larvae of Toxocara cati. Approximately 100 larvae per well were cultivated in microplates containing RPMI-1640 medium and incubated in the presence of EOP (18.75, 37.5, 75, 150, 300 and 600⯵g/mL) to determine the Minimum Inhibitory Concentration (MIC) and IC50 (concentration required to inhibit 50% of the population) values. Then, T. cati larvae treated with the MIC of EOP were inoculated in mice to evaluate their progression in vivo. A concentration of 600⯵g/mL of EOP showed 100% larvicidal activity after exposure for 48â¯h, while 300⯵g/mL represented the IC50 and CC50. The anthelmintic activity of EOP was confirmed by the inability of the treated T. cati larvae to infect the mice. Our findings demonstrate the potential of EOP as an anthelmintic.
Assuntos
Anti-Helmínticos/farmacologia , Óleos Voláteis/farmacologia , Própole/química , Toxocara/efeitos dos fármacos , Animais , Anti-Helmínticos/isolamento & purificação , Anti-Helmínticos/toxicidade , Células CHO , Corantes , Cricetinae , Cricetulus , Feminino , Concentração Inibidora 50 , Cinética , Larva/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos BALB C , Testes de Sensibilidade Microbiana , Movimento/efeitos dos fármacos , Óleos Voláteis/isolamento & purificação , Óleos Voláteis/toxicidade , Toxocara/fisiologia , Azul TripanoRESUMO
Toxocariasis is a zoonotic disease that affects humans and animals alike. Although recombinant proteins are widely used for its diagnosis in humans, their performance in companion and production animals remains unknown. This study aimed to investigate the serodiagnostic potential of the recombinant proteins rTES-30 and rTES-120 from Toxocara canis in an indirect ELISA for cattle, horses, and sheep. Serum samples collected from the animals were tested with indirect ELISA and Western Blotting using T. canis TES-30 and TES-120 recombinant proteins produced in Escherichia coli, as well as native-TES. In the ELISA, rTES-30 showed high serodiagnostic potential in sheep and horses (92.6% and 85.2%, respectively), while the sensitivity of rTES-120 was higher in cattle and horses (97.2% and 92.6%, respectively). Furthermore, a highly positive association was observed between native and recombinant proteins in seropositive samples, while a moderately positive association was observed in seronegative samples, probably due to the lower specificity of native TES. In conclusion, our study indicates that the use of recombinant proteins in an indirect ELISA is an effective tool for the serodiagnosis of toxocariasis in animals, with the choice of protein being species-dependent.
Assuntos
Proteínas de Helminto/imunologia , Proteínas Recombinantes/imunologia , Testes Sorológicos/métodos , Toxocara canis/imunologia , Toxocaríase/diagnóstico , Animais , Bovinos , Feminino , Cavalos , Masculino , Ovinos , Toxocaríase/imunologia , Toxocaríase/parasitologiaRESUMO
Este estudo avaliou a ação in vitro e in vivo de extratos de Eugenia uniflora em nematódeos gastrintestinais de ovinos. No teste de inibição da eclodibilidade dos ovos, extratos aquosos e hidroalcoólicos foram testados nas concentrações de 40 a 1,25 mg/mL. O efeito citotóxico foi mensurado através do ensaio de MTT em células VERO nas concentrações de 4000 a 1,95 µg/mL. A composição química foi analisada através da marcha fitoquímica qualitativa. No teste in vivo, foram administrados 100 mg/kg, por via oral, do extrato hidroalcoólico por três dias em ovinos naturalmente infectados e realizada coleta de fezes para estimar a redução de ovos por grama de fezes (OPG). Diferentes extratos de E. uniflora inibiram a eclodibilidade dos ovos, com percentual de inibição variando de 14,56 a 99,75%, sendo os hidroalcoólicos mais promissores que os aquosos. Na marcha fitoquímica, compostos com ação anti-helmíntica comprovada foram observados, como flavonoides, saponinas, taninos e triterpenos. Nas condições testadas, os extratos apresentaram citotoxicidade nula a moderada. In vivo, a redução do OPG foi observada apenas no grupo controle (anti-helmíntico). Os extratos de E. uniflora mostraram-se promissores com ação in vitro, necessitando estudos que avaliem outras concentrações e formas de administração in vivo.
This study evaluated the in vitro and in vivo action of Eugenia uniflora extracts on sheep gastrointestinal nematode. In the egg hatchability inhibition assay, aqueous and hydroalcoholic extracts were tested in the concentrations ranging from 40 to 1.25 mg/mL. The cytotoxic effect was measured using the MTT assay on VERO cells at concentrations ranging from 4000 to 1.95 μg/mL. The chemical composition was analyzed through the qualitative phytochemical screening. In the in vivo test, 100 mg/kg of the hydroalcoholic extract was administered orally for three days in sheep naturally infected and fecal collection was performed to estimate the egg count per gram of faeces (EPG). Different extracts of E. uniflora inhibited hatchability of eggs with a percentage of inhibition ranging from 14.56 to 99.75%, being the hydroalcoholic most effective than the aqueous. In phytochemical analysis, compounds with anthelmintic action were observed, such as flavonoids, saponins, tannins and triterpenes. Extracts showed moderate to null cytotoxicity under the conditions tested. Reduction of EPG was observed only in control group (anthelmintic). The extracts of E. uniflora proved promising with in vitro action, requiring studies that assess other concentrations and forms of in vivo administration.
Assuntos
Animais , Eugenia/química , Extratos Vegetais/uso terapêutico , Haemonchus , Nematoides , Ovinos/parasitologia , Plantas MedicinaisRESUMO
Due to the growing population of pets, especially homeless dogs and cats, zoonoses still represent a significant public health problem. Toxoplasma gondii and Toxocara spp. are epidemiologically important zoonotic agents as they are etiological factors of human toxoplasmosis and toxocariasis, respectively. These parasites remain neglected even though they are substantially prevalent in rural areas. The aim of this study was to investigate T. gondii and T. canis seroprevalence and risk factors of seropositivity in a rural population in Pelotas municipality, Brazil. The study participants (n=344) were patients of a Basic Healthcare Unit (BHU) located in Cerrito Alegre. Blood samples were collected and tested for T. gondii antibodies by indirect immunofluorescence and T. canis antibodies by an indirect ELISA that targets an excreted-secreted antigen (TES). T. gondii seropositivity was 53.2%, with higher titers (1:256 - 1:1,024) in individuals who habitually eat pork, beef, or chicken, while T. canis seropositivity was 71.8% and concomitant T. gondii and T. canis seropositivity was 38.3%. Among the seropositivity risk factors assessed, only habitual undercooked meat consumption was significant (p = 0.046; OR = 3.7) for T. gondii and none of them were associated with T. canis seropositivity. Both parasites have a high prevalence in rural areas, which reinforces the need to invest in rural community education and health.