6 research outputs found

    Evaluation of Cuspidaria pulchra and its Isolated Compounds Against Schistosoma mansoni Adult Worms

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    The present study has investigated the chemical composition of the bioactive EtOAc fraction of Cuspidaria pulchra aerial parts, as well as its schistosomicidal activities against Schistosoma mansoni adult worms in vitro. To this end, the crude ethanol extract obtained from the aerial parts of C. pulchra (Bignoniaceae) was partitioned with n-hexane, EtOAc, and n-BuOH. The EtOAc fraction was purified by preparative HPLC, which afforded 3,4-dihydroxybenzaldehyde (1), p-coumaric acid (2), p-hydroxybenzoic acid (3), ursolic acid (4), and oleanolic acid (5). The bioassay results indicated that the crude ethanol extract and the EtOAc fraction at 100 µg/mL killed the adult schistosomes in vitro. Compounds 1 and 3 at 100 µm were only able to separate coupled S. mansoni adult worms

    Case report: Urbanized non-human primates as sentinels for human zoonotic diseases: a case of acute fatal toxoplasmosis in a free-ranging marmoset in coinfection with yellow fever virus

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    Free-ranging non-human primates (NHP) can live in anthropized areas or urban environments in close contact with human populations. This condition can enable the emergence and transmission of high-impact zoonotic pathogens. For the first time, we detected a coinfection of the yellow fever (YF) virus with Toxoplasma gondii in a free-ranging NHP in a highly urbanized area of a metropolis in Brazil. Specifically, we observed this coinfection in a black-tufted marmoset found dead and taken for a necropsy by the local health surveillance service. After conducting an epidemiological investigation, characterizing the pathological features, and performing molecular assays, we confirmed that the marmoset developed an acute fatal infection caused by T. gondii in coinfection with a new YF virus South American-1 sub-lineage. As a result, we have raised concerns about the public health implications of these findings and discussed the importance of diagnosis and surveillance of zoonotic agents in urbanized NHPs. As competent hosts of zoonotic diseases such as YF and environmental sentinels for toxoplasmosis, NHPs play a crucial role in the One Health framework to predict and prevent the emergence of dangerous human pathogens

    Synthesis of the Silaisocyanoacetylene Molecule

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    The hitherto elusive silaisocyanoacetylene molecule (HCCNSi)a member of the silaisocyanide familyhas been synthesized for the first time through the reaction of the silicon nitride radical (SiN) with acetylene (C<sub>2</sub>H<sub>2</sub>) in the gas phase under single collision conditions. Compared to the isoelectronic reaction of the cyano radical (CN) with acetylene, the replacement of the carbon atom in the cyano group by an isovalent silicon atom has a pronounced effect on the reactivity. Whereas the silicon nitride radical was found to pass an entrance barrier and adds with the nitrogen atom to the acetylene molecule, the cyano radical adds barrierlessly with the carbon atom forming the HCCH­(NSi) and HCCH­(CN) intermediates, respectively. These structures undergo hydrogen loss to form the linear silaisocyanoacetylene (HCCNSi) and cyanoacetylene molecules (HCCCN), respectively. Therefore, the isovalency of the silicon atom was found to bear little resemblance with the carbon atom having a dramatic effect not only on the reactivity, but also on the reaction mechanism, thermochemistry, and chemical bonding of the isoelectronic silaisocyanoacetylene and cyanoacetylene products, effectively reversing the thermodynamical stability of the nitrile versus isonitrile and silanitrile versus isosilanitrile isomer pairs

    Hepato-pathological hallmarks for the surveillance of Yellow Fever in South American non-human primates

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    University of Brasília. Graduate Program in Animal Science. Brasilia, DF, Brazil / Brazilian Ministry of Health. Brasilia, DF, BrazilBrazilian Ministry of Health. Brasilia, DF, BrazilBrazilian Ministry of Health. Brasilia, DF, BrazilBrazilian Ministry of Health. Brasilia, DF, BrazilThe University of Sydney. Sydney, New South Wales, AustraliaFundação Oswaldo Cruz. Rio de Janeiro, RJ, BrazilUniversidade do Estado do Pará. Belém, PA, BrazilMinistério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, BrasilUniversidade do Estado do Pará. Belém, PA, BrazilUniversity of Brasília. Graduate Program in Animal Science. Brasilia, DF, Brazil / University of Brasília. Veterinary Pathology Laboratory. Brasília, DF, BrazilUniversity of Brasília. Graduate Program in Animal Science. Brasilia, DF, Brazil / University of Brasília. Veterinary Pathology Laboratory. Brasília, DF, BrazilUniversity of Brasília. Graduate Program in Animal Science. Brasilia, DF, Brazil / University of Brasília. Veterinary Pathology Laboratory. Brasília, DF, BrazilUniversity of Brasília. Graduate Program in Animal Science. Brasilia, DF, BrazilUniversity of Brasília. Graduate Program in Animal Science. Brasilia, DF, Brazil / University of Brasília. Veterinary Pathology Laboratory. Brasília, DF, BrazilThe early detection and diagnosis of deaths in free-ranging non-human primates (NHPs) are key points for the surveillance of Yellow Fever (YF) in Brazil. The histopathological identification of infectious diseases remains very useful and reliable in the screening and detection of emerging zoonotic diseases such as YF. We surveyed data records and liver slides stained with hematoxylin and eosin from the Epizootics Surveillance Network to control YF, Ministry of Health of Brazil, to evaluate histopathological hallmarks for the diagnosis of the YF virus infection. We selected natural fatal cases in NHPs from the genera Alouatta spp., Callithrix spp., and Sapajus spp. with a positive immunohistochemical assay for YF in liver samples. Our findings showed the full-spectrum YF-associated hepatic lesions in all NHPs, but some histopathological findings differed in the distribution and intensity between the three genera. In our study, South American NHPs showed significant differences in the YF-associated hepatic histopathological features compared to fatal cases reported in humans
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