751 resultados para Leishmania


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O presente relato tem por objetivo descrever o primeiro caso alóctone de leishmaniose visceral (LV) no município de Campo Mourão, Paraná, Brasil, em um canino, da raça Boxer, apresentando lesões oculares e cutâneas, linfoadenomegalia e esplenomegalia, atendido no Hospital Veterinário da Faculdade Integrado de Campo Mourão, após ter residido na cidade de Campo Grande, Mato Grosso do Sul. O diagnóstico da enfermidade baseou-se na observação direta de formas amastigotas de Leishmania spp., em linfonodos poplíteos, sugerindo ser um caso de LV, uma vez que o animal era proveniente de área endêmica para a enfermidade. A migração de cães infectados de regiões endêmicas para áreas indenes torna-se um problema para a saúde pública, uma vez que poderá permitir a instalação de novos focos, favorecendo a disseminação da doença em todo o país.

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Abstract Background The mitochondrial DNA of kinetoplastid flagellates is distinctive in the eukaryotic world due to its massive size, complex form and large sequence content. Comprised of catenated maxicircles that contain rRNA and protein-coding genes and thousands of heterogeneous minicircles encoding small guide RNAs, the kinetoplast network has evolved along with an extreme form of mRNA processing in the form of uridine insertion and deletion RNA editing. Many maxicircle-encoded mRNAs cannot be translated without this post-transcriptional sequence modification. Results We present the complete sequence and annotation of the Trypanosoma cruzi maxicircles for the CL Brener and Esmeraldo strains. Gene order is syntenic with Trypanosoma brucei and Leishmania tarentolae maxicircles. The non-coding components have strain-specific repetitive regions and a variable region that is unique for each strain with the exception of a conserved sequence element that may serve as an origin of replication, but shows no sequence identity with L. tarentolae or T. brucei. Alternative assemblies of the variable region demonstrate intra-strain heterogeneity of the maxicircle population. The extent of mRNA editing required for particular genes approximates that seen in T. brucei. Extensively edited genes were more divergent among the genera than non-edited and rRNA genes. Esmeraldo contains a unique 236-bp deletion that removes the 5'-ends of ND4 and CR4 and the intergenic region. Esmeraldo shows additional insertions and deletions outside of areas edited in other species in ND5, MURF1, and MURF2, while CL Brener has a distinct insertion in MURF2. Conclusion The CL Brener and Esmeraldo maxicircles represent two of three previously defined maxicircle clades and promise utility as taxonomic markers. Restoration of the disrupted reading frames might be accomplished by strain-specific RNA editing. Elements in the non-coding region may be important for replication, transcription, and anchoring of the maxicircle within the kinetoplast network.

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Abstract Background Sand fly saliva contains potent and complex pharmacologic molecules that are able to modulate the host's hemostatic, inflammatory, and immune systems. In this study, we evaluated the effects of salivary gland sonicate (SGS) of Lutzomyia intermedia, the natural vector of Leishmania braziliensis, on monocytes obtained from the peripheral blood mononuclear cells (PBMC) of healthy volunteers. We investigated the effects of sand fly saliva on cytokine production and surface molecule expression of LPS-stimulated human monocytes uninfected or infected with L. braziliensis. Results Pre-treatment of non-infected human monocytes with L. intermedia SGS followed by LPS-stimulation led to a significant decrease in IL-10 production accompanied by a significant increase in CD86, CD80, and HLA-DR expression. Pre-treatment with SGS followed by LPS stimulation and L. braziliensis infection led to a significant increase in TNF-α, IL-6, and IL-8 production without significant alterations in co-stimulatory molecule expression. However, pre-treatment with L. intermedia SGS did not result in significant changes in the infection rate of human monocytes. Conclusion Our data indicate that L. intermedia saliva is able to modulate monocyte response, and, although this modulation is dissociated from enhanced infection with L. braziliensis, it may be associated with successful parasitism.

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Background ArtinM is a D-mannose-specific lectin from Artocarpus integrifolia seeds that induces neutrophil migration and activation, degranulation of mast cells, acceleration of wound healing, induction of interleukin-12 production by macrophages and dendritic cells, and protective T helper 1 immune response against Leishmania major, Leishmania amazonensis and Paracoccidioides brasiliensis infections. Considering the important biological properties of ArtinM and its therapeutic applicability, this study was designed to produce high-level expression of active recombinant ArtinM (rArtinM) in Escherichia coli system. Results The ArtinM coding region was inserted in pET29a(+) vector and expressed in E. coli BL21(DE3)-Codon Plus-RP. The conditions for overexpression of soluble ArtinM were optimized testing different parameters: temperatures (20, 25, 30 or 37°C) and shaking speeds (130, 200 or 220 rpm) during induction, concentrations of the induction agent IPTG (0.01-4 mM) and periods of induction (1-19 h). BL21-CodonPlus(DE3)-RP cells induced under the optimized conditions (incubation at 20°C, at a shaking speed of 130 rpm, induction with 0.4 mM IPTG for 19 h) resulted in the accumulation of large amounts of soluble rArtinM. The culture provided 22.4 mg/L of rArtinM, which activity was determined by its one-step purification through affinity chromatography on immobilized D-mannose and glycoarray analysis. Gel filtration showed that rArtinM is monomeric, contrasting with the tetrameric form of the plant native protein (jArtinM). The analysis of intact rArtinM by mass spectrometry revealed a 16,099.5 Da molecular mass, and the peptide mass fingerprint and esi-cid-ms/ms of amino acid sequences of peptides from a tryptic digest covered 41% of the total ArtinM amino acid sequence. In addition, circular dichroism and fluorescence spectroscopy of rArtinM indicated that its global fold comprises β-sheet structure. Conclusions Overall, the optimized process to express rArtinM in E. coli provided high amounts of soluble, correctly folded and active recombinant protein, compatible with large scale production of the lectin.

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Abstract Background The study of the distribution and ecology of sandfly species is essential for epidemiological surveillance and estimation of the transmission risk of Leishmania spp. infection. Findings In the present study, sandflies were captured in native fragmented forest areas in Rubião Júnior district, Botucatu municipality, São Paulo state, Brazil, between September 2001 and January 2005. A minimum of two automatic light traps were installed per night from 6 pm to 8 am, in different months, resulting in approximately 900 collecting hours. During this period, 216 sandfly specimens of sixteen species were captured. Pintomyia monticola and Brumptomyia guimaraesi were the most abundant with 56 specimens (25.93%) captured per species, followed by Pintomyia fischeri 28 (12.96%) and Psathyromyia pascalei 18 (8.33%). Other captured species were Lutzomyia amarali, Sciopemyia sordellii, Psathyromyia aragaoi, Nyssomyia whitmani, Migonemyia migonei, Pintomyia bianchigalatiae, Pintomyia misionensis, Brumptomyia carvalheiroi, Brumptomyia cardosoi, Brumptomyia cunhai, Brumptomyia nitzulescui, Brumptomyia brumpti and Brumptomyia spp. represented by 58 (26.85%) specimens. Conclusions Although less frequently found, the presence of Pintomyia fischeri, Nyssomyia whitmani and Migonemyia migonei, known vectors of Leishmania braziliensis, indicates risk of American cutaneous leishmaniasis occurrence. Moreover, the absence of Lutzomyia longipalpis-the main vector of Leishmania infantum chagasi, which is the agent of American visceral leishmaniasis-suggests that there is no risk of introduction and establishment of this disease in the studied area.

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OBJECTIVES: The aim of this study was to describe the pattern of expression of Toll-like receptor 2 (TLR2) and Toll-like receptor 4 (TLR4) in skin biopsies of patients with American tegumentary leishmaniasis (ATL) caused by Leishmania braziliensis. METHODS: This prospective study evaluated 12 patients with ATL caused by Leishmania braziliensis confirmed by polymerase chain reaction. Immunohistochemistry was performed to determine the expression of TLR2 and TLR4. The number of NK cells, dendritic cells and macrophages in the tissue were calculated. The cytokine expression was determined using the anti-TNF-α, anti-IFN-Γ, anti-IL-1 and anti-IL-6. Double immunostaining reactions were used to determine the cell expressing TLR2 and TLR4. RESULTS: The numbers of cells expressing TLR2 and TLR4 were 145.48 ± 82.46 cell/mm² and 3.26 ± 4.11 cell/mm² respectively (p < 0.05). There was no correlation of TLR2 and TLR4 with the amount of cytokines and the number of NK cells, dendritic cells or macrophages. The double immunostaining revealed that TLR2 was expressed by macrophages. CONCLUSION: In human cutaneous leishmaniasis caused by Leishmania braziliensis, TLR2 is the most common TLR expressed during active disease, mainly by macrophages although without correlation with the amount of cytokines and number of cells.

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INTRODUCTION: An epidemiological study was undertaken to identify determinant factors in the occurrence of American cutaneous leishmaniasis in areas under the influence of hydroelectric plants in Paranapanema river, State of Paraná, Brazil. The ecological aspects of the phlebotomine fauna were investigated. METHODS: Sandflies were sampled with automatic light traps from February 2004 to June 2006 at 25 sites in the urban and rural areas of Itambaracá, and in Porto Almeida and São Joaquim do Pontal. RESULTS: A total of 3,187 sandflies of 15 species were captured. Nyssomyia neivai predominated (34.4%), followed by Pintomyia pessoai (32.6%), Migonemyia migonei (11.6%), Nyssomyia whitmani (8.8%), and Pintomyia fischeri (2.7%), all implicated in the transmission of Leishmania. Males predominated for Ny. neivai, and females for the other vector species, with significant statistical differences (p < 0.001). Nyssomyia neivai, Pi. pessoai, Ny. whitmani, Brumptomyia brumpti, Mg. migonei, and Pi. fischeri presented the highest values for the Standardized Species Abundance Index (SSAI). The highest frequencies and diversities were found in the preserved forest in Porto Almeida, followed by forests with degradation in São Joaquim do Pontal and Vila Rural. CONCLUSIONS: Sandflies were captured in all localities, with the five vectors predominating. Ny. neivai had its highest frequencies in nearby peridomestic environments and Pi. pessoai in areas of preserved forests. The highest SSAI values of Ny. neivai and Pi. pessoai reflect their wider dispersion and higher frequencies compared with other species, which seems to indicate that these two species may be transmitting leishmaniasis in the area.

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Ethyl acetate extracts of cultures grown in liquid Czapek and on solid rice media of the fungal endophyte Fusarium oxysporum SS46 isolated from the medicinal plant Smallanthus sonchifolius (Poepp.) H. Rob., Asteraceae, exhibited considerable cytotoxic activity when tested in vitro against human cancer cells. Chromatographic separation yielded anhydrofusarubin (1) and beauvericin (2) that were identified based on their ¹H and 13C NMR data. Compounds 1 and 2 showed the strongest cytotoxic activity against different cancer cell lines. Compound 2 also showed promising activity against Leishmania braziliensis. Hexanic extract of F. oxysporum SS50 grown on solid rice media also afforded a mixture of compounds that displayed cytotoxic activity against different cancer cell lines. Chemical analysis of the mixture of compounds, investigated by gas chromatography-mass spectrometry (GC-MS), showed that there was a predominance of methyl esters of fatty acids and alkanes.

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In vitro evaluation of alkaloidal fractions of twigs, barks and leaves from two Unonopsis species, Unonopsis guatterioides R.E. Fr. and Unonopsis duckei R.E. Fr., Annonaceae, against promastigote forms of Leishmania amazonensis revealed these species as sources of substances with promising leishmanicidal potential. All alkaloidal fractions from twigs, barks and leaves of U. guatterioides were classified as highly active, with IC50 1.07, 1.90, and 2.79 mg/mL, respectively. Only the alkaloidal fraction from the twigs of U. duckei was classified as inactive.

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Este trabalho teve como objetivos determinar a soroprevalência e as variáveis epidemiológicas associadas com a infecção de Leishmania spp. em cães de cinco localidades no Distrito do Tirirical no município de São Luís, Maranhão. Foram visitadas 72 moradias, perfazendo uma amostra de cem cães domiciliados, e aplicados questionários com o objetivo de determinar os fatores que poderiam estar relacionados com a ocorrência da infecção. Utilizaram-se como variáveis: proximidade da moradia com a mata, existência de criação/abrigo de animais de produção e de animais silvestres, sexo, idade, raça, além de exame clínico do animal, com observação da presença de sinais clínicos compatíveis com a doença. A análise sorológica demonstrou que 67 amostras apresentaram-se positivas para Leishmania spp. Os sinais clínicos observados foram linfadenopatia localizada, alopecia, pelo opaco, emagrecimento, úlceras cutâneas, descamação furfurácea, ceratoconjuntivite, e onicogrifose. Animais das localidades Cruzeiro de Santa Bárbara e Cajupari, ambas localizadas próximas de matas, têm 3,4 e 12,0 vezes mais chances de serem soropositivos para Leishmania spp. do que aqueles das outras localidades estudadas. Não se verificou correlação entre as outras variáveis estudadas e soropositividade para Leishmania spp.

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INTRODUCTION: This work was carried out on the purpose of identifying the species of phlebotomine sandflies in the municipality of Monte Negro, state of Rondonia, Brazil, that may have been transmitting the American cutaneous leishmaniasis (ACL), and concisely describe epidemiological aspects of disease. METHODS: The epidemiologic and socioeconomical indicators were obtained from government institutions and the local Municipal Secretary of Health. Phlebotomine sandflies were captured using CDC light traps between July 2006 to July 2008. The total of 1,240 of female sandflies were examined by PCR method directed to k-DNA. RESULTS: There has been a significant decrease in the incidence of ACL of about 50% over the last ten years in the municipality. A total of 1,935 specimens of 53 sandfly species were captured, three of the genus Brumptomyia genus and 50 of the genus Lutzomyia. The predominant species was Lutzomyia acanthopharynx, Lutzomyia whitmani, Lutzomyia geniculata and Lutzomyia davisi. None were positive for Leishmania sp. CONCLUSIONS: Four sandflies species were found in the State of Rondonia for the first time: Brumptomyia brumpti, Lutzomyia tarapacaensis, Lutzomyia melloi and Lutzomyia lenti. The presence of Lutzomyia longipalpis, was also captured. Socioeconomical improvement of Brazilian economy and the increase of environmental surveillance in the last 15 years collaborated in the decrease of people exposed to vectors, reducing the incidence of ACL.

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This study evaluated the applicability of kDNA-PCR as a prospective routine diagnosis method for American tegumentary leishmaniasis (ATL) in patients from the Instituto de Infectologia Emílio Ribas (IIER), a reference center for infectious diseases in São Paulo - SP, Brazil. The kDNA-PCR method detected Leishmania DNA in 87.5% (112/128) of the clinically suspected ATL patients, while the traditional methods demonstrated the following percentages of positivity: 62.8% (49/78) for the Montenegro skin test, 61.8% (47/76) for direct investigation, and 19.3% (22/114) for in vitro culture. The molecular method was able to confirm the disease in samples considered negative or inconclusive by traditional laboratory methods, contributing to the final clinical diagnosis and therapy of ATL in this hospital. Thus, we strongly recommend the inclusion of kDNA-PCR amplification as an alternative diagnostic method for ATL, suggesting a new algorithm routine to be followed to help the diagnosis and treatment of ATL in IIER.

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La leishmaniosi è una malattia protozoaria importante che interessa l’ambito della sanità animale e umana, in relazione al carattere zoonotico dell’infezione. In Italia l’infezione è sostenuta da Leishmania infantum, i cui ceppi viscerotropi sono responsabili della leishmaniosi canina (LCan) e della forma viscerale zoonotica (LVZ), ed i ceppi dermotropi della forma cutanea sporadica nell’uomo (LCS). La trasmissione dell’infezione è sostenuta da femmine ematofaghe di ditteri appartenenti al genere Phlebotomus, che hanno il ruolo di vettori biologici attivi. L’unico serbatoio domestico riconosciuto è il cane. In Italia la LCan è in forte espansione. Fino agli anni ottanta era presente in forma endemica nel centro-sud Italia e nelle isole mentre il nord Italia, fatta eccezione per la Liguria e una piccola parte dell’Emilia-Romagna risultava indenne. A partire dagli anni novanta, parallelamente ad un aumento della consistenza e del numero dei focolai nelle aree storicamente endemiche, sono iniziate, nelle regioni del Nord, le segnalazioni di focolai autoctoni stabili. Le attività del network scientifico LeishMap™, tra il 2002 e il 2005, hanno evidenziato un nuovo quadro epidemiologico in tutte le regioni del nord Italia, confermato anche da indagini successive. Alla riemergenza della leishmaniosi hanno concorso una serie di fattori ecologico-ambientali e umani. Tra i primi si ricorda il cambiamento climatico che ha influito sulla distribuzione e sulla densità della popolazione vettoriale; tra i secondi, ruolo fondamentale ha giocato la maggiore movimentazione di animali, provenienti da aree indenni, in zone interessate dalla malattia. La valutazione di tutti questi aspetti è stato il punto di partenza per la messa a punto di un progetto per la realizzazione della sorveglianza della leishmaniosi in Emilia-Romagna. Parte delle attività previste da tale progetto costituiscono la prima parte della presente tesi. Mediante la realizzazione di una banca dati e, la successiva georeferenziazione, dei casi di leishmaniosi canina (LCan) in cani di proprietà della regione e zone limitrofe (Pesaro-Urbino, Repubblica di San Marino), sono stati evidenziati 538 casi, la maggior parte dei quali nelle province di Bologna e Rimini (235 e 204, rispettivamente). Nelle due province sono stati individuati clusters di aggregazione importanti in base alla densità di casi registrati/km2 (4 nella provincia di Bologna e 3 in quella di Rimini). Nella seconda parte della presente tesi è stato approfondito l’aspetto diagnostico della malattia. Molte sono le metodiche applicabili alla diagnosi di LCan: da quelle dirette, come i metodi parassitologici e molecolari, a quelle indirette, come le tecniche sierologiche. Nella II parte sperimentale della presente tesi, 100 sieri di cane sono stati esaminati in Immunofluorescenza Indiretta (IFI), Enzyme-Linked Immunosorbent Assay (ELISA) e Western Blot (WB), al fine di valutare l’applicazione di queste metodiche a scopi diagnostici ed epidemiologici. L’elaborazione statistica dei risultati ottenuti conferma l’IFI metodica gold standard per la diagnosi della LCan. Inoltre, si è osservato che il grado di concordanza tra l’IFI e le altre due metodiche aumenta quando nell’animale si instaura una risposta anticorpale forte, che, corrisponderebbe ad uno stato di infezione in atto.

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In der murinen kutanen Leishmaniose ist die Ausheilung der Infektion mit dem Auftreten von schützenden CD4+ Th1- sowie CD8+ Tc1-Immunantworten assoziiert. Daher sollte eine wirksame Vakzine beide T-Zell-Populationen induzieren. Im Rahmen dieser Dissertation konnte gezeigt werden, daß mit TAT-LACK Fusionsproteinen effektiv gegen eine progressiv verlaufende Infektion mit Leishmania major in empfindlichen BALB/c sowie resistenten C57BL/6 Mäusen vakziniert werden kann. TAT-LACK konnte hierbei sowohl im DC- als auch im proteinbasierten Ansatz protektive Immunität verleihen. Das TAT-Peptid ist in der Lage, Proteine direkt in das Zytosol von DC zu schleusen und so den für die CD8+ T-Zell-Antworten erforderlichen MHC Klasse I Präsentationsweg einzuschlagen. Stammesspezifische Untersuchungen des inflammatorischen Infiltrates in Läsion und Lymphknoten bestätigten die physiologische Relevanz von DC und CD8+ T-Zellen im Verlauf einer etablierten Leishmania-Infektion in beiden Mausstämmen und rechtfertigten somit den Einsatz einer DC basierten Vakzine, die vermehrt CD8+ T-Zellen induzieren sollte. Tatsächlich konnte mit TAT-LACK transduzierten DC in beiden Mausstämmen effektiv gegen eine progressiv verlaufende Leishmania-Infektion vakziniert werden. Der Vakzinierungserfolg ließ sich anhand verringerter Läsionsvolumina, reduzierter Parasitenlasten und einer Verschiebung des Zytokinprofils in Richtung einer Th1 dominierten Immunantwort bestätigen. In allen Ansätzen war die i.d. Vakzinierung mit TAT-LACK transduzierten DC der Injektion von LACK gepulsten DC überlegen. Experimente mit DC aus IL-12p40 defizienten Mäusen belegten die IL-12 Abhängigkeit der Vakzine. Mit Hilfe von in vitro Restimulierungsexperimenten konnte nachgewiesen werden, daß nach Applikation TAT-LACK transduzierter DC in beiden Mausstämmen vermehrt CD8+ T-Zellen induziert werden. Des weiteren waren TAT-LACK transduzierte DC in Restimulationsexperimenten stärkere Aktivatoren der CD8+ T-Zell-Proliferation als LACK gepulste DC. Depletionsexperimente bestätigten die T-Zell-Abhängigkeit der Vakzine. Weitere in vivo Versuche belegten zudem die protektive Wirkung von TAT-LACK Fusionsproteinen im direkten, proteinbasierten Vakzinierungsansatz. Floreszenzmikroskopische Analysen der Epidermis bestätigten hierbei Aktivierung und Auswanderung von LC nach i.d. TAT-LACK Applikation.

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La leishmaniosi canina (LCan) causata da Leishmania infantum rappresenta un’importante zoonosi in molte aree del mondo ed il cane rappresenta il principale reservoir del parassita per l’uomo. Il tipo di risposta immunitaria che i soggetti colpiti mettono in atto condiziona fortemente la progressione della malattia: animali che non sviluppano un’adeguata risposta immunitaria cellulo-mediata mostrano la sintomatologia clinica nonostante abbiano una forte ma inefficace risposta umorale che contribuisce al peggioramento della sintomatologia clinica. L’obbiettivo dello studio è stato quello valutare da un punto di vista descrittivo il segnalamento, i segni clinici e clinicopatologici dei pazienti affetti da leishmaniosi portati in visita presso il Dipartimento di Scienze Mediche Veterinarie nel periodo compreso da Gennaio 2002 a Marzo 2012 con particolare attenzione sull’impatto della patologia renale e dell’anemia nel quadro clinico della LCan. In base ai risultati ottenuti è stato possibile affermare che la leishmaniosi canina è una patologia relativamente frequente nella nostra realtà clinica universitaria e che presenta caratteristiche cliniche e clinicopatologiche simili a quelle riportate in letteratura. I nostri risultati preliminari suggeriscono che in questa malattia il coinvolgimento renale e le conseguenze sistemiche che ne derivano possono essere predominanti a livello clinico e laboratoristico. La gravità del quadro clinico appare associata in maniera significativa all’entità della risposta umorale e del successivo coinvolgimento glomerulare nel contesto di una risposta infiammatoria sistemica cronica. Successivamente, sono state misurate le concentrazioni di IgG ed IgM in corso di follow-up in alcuni dei soggetti inclusi nello studio e sottoposti a differenti trattamenti anti-leishmania. Dai risultati preliminari ottenuti nel nostro lavoro è stato possibile affermare che in corso di trattamento le concentrazioni di tali immunoglobuline subiscono una riduzione progressiva confermando pertanto l’efficacia del trattamento anti-leishmania non solo nella remissione della sintomatologia clinica ma anche nel ripristino della normale risposta umorale.