Trichophoromyia auraensis is a putative vector

The sandfly Trichophoromyia auraensis has recently evolved as a proven vector of Leishmania (Viannia) endemic to state of Acre in the north of Brazil. This note is intended to propose a correction in the report of the first occurrence of natural infection of Leishmania (Viannia) in this species. We and the other scientific groups reinforced that Tr. auraensis is a possible vector involved in the transmission of American cutaneous leishmaniasis in Acre, Brazil.

First description of Leishmania (Viannia) infection in Evandromyia saulensis, Pressatia sp. and Trichophoromyia auraensis (Psychodidae: Phlebotominae) in a transmission area of cutaneous leishmaniasis in Acre state, Amazon Basin, Brazil

Studies on the sandfly fauna to evaluate natural infection indexes are still limited in the Brazilian Amazon, a region with an increasing incidence of cutaneous leishmaniasis. Here, by using a multiplex polymerase chain reaction directed to Leishmania kDNA and hybridisation, we were able to identify L. (Viannia) subgenus in 12 out of 173 sandflies captured in the municipality of Rio Branco, Acre state, revealing a positivity of 6.94%. By sequencing the Leishmania 234 bp-hsp70 amplified products from positive samples, infection by L. (V.) braziliensis was confirmed in five sandflies: one Evandromyia saulensis, three Trichophoromyia auraensis and one Pressatia sp. The finding of L. (Viannia) DNA in two Ev. saulensis corresponds to the first record of possible infection associated with this sandfly. Moreover, our study reveals for the first time in Brazil, Th. auraensis and Pressatia sp. infected by L. (Viannia) parasites.

Hepatozoon canis and Leishmania spp. coinfection in dogs diagnosed with visceral leishmaniasis / Coinfecção com Hepatozoon canis e Leishmania spp. em cães diagnosticados com leishmaniose visceral

Abstract This study describes the occurrence of dogs naturally co-infected with Hepatozoon canis and two Leishmania species: L. infantum or L. braziliensis. Four dogs serologically diagnosed with Visceral Leishmaniasis were euthanized. Liver and spleen samples were collected for histopathological analysis and DNA isolation. H. canis meronts were observed in tissues from all four dogs. H. canis infection was confirmed by PCR followed by sequencing of a fragment of 18S rRNA gene. Leishmania detection and typing was confirmed by ITS1' PCR-RFLP and parasite burden was calculated using ssrRNA quantitative qPCR. A DPP - Dual Path platform test was performed. One out (Dog #2) of four animals was asymptomatic. Dogs #1 and #4 were infected by L. infantum and were DPP test positive. Dogs #2 and #3 were infected by L. braziliensis and were DPP test negative. Furthermore, visceral dissemination was observed in Dogs #2 and #3, since L. braziliensis was detected in liver and spleen samples. The visceral dissemination of L. braziliensis associated with systemic signs suggested that this co-infection could influence the parasite burden and disease progression.

Resumo O presente estudo descreve a ocorrência de coinfecção com Hepatozoon canis e duas espécies de Leishmania (L. infantum ou L. braziliensis) em cães. Quatro cães sorologicamente diagnosticados com leishmaniose visceral foram eutanasiados. Amostras do baço e fígado foram submetidas à histopatologia e extração de DNA. Merontes de H. canis foram observados nos quatro cães. A infecção por H. canis foi confirmada por PCR e sequenciamento de um fragmento do gene 18S rRNA. A infecção por Leishmania e tipagem foram realizadas por PCR-RFLP do região intergênica ITS1. A carga parasitária foi calculada pela qPCR quantitativa baseada no gene ssrRNA. O teste DPP - Dual Path platform foi realizado. Apenas o Cão #2 era assintomático. Os cães #1 e #4 estavam infectados com L. infantum e foram positivos no DPP. Os cães #2 e #3 estavam infectados com L. braziliensis e foram negativos no DPP. Além disso, visceralização foi observada nos cães #2 e #3, nos quais L. braziliensis foi detectada em amostras de baço e fígado. A visceralização da L. braziliensis associada a sinais clínicos sistêmicos sugerem que esta coinfecção pode ter influenciado na carga parasitária e progressão da doença.

Expression of annexin A1 in Leishmania-infected skin and its correlation with histopathological features

ABSTRACTINTRODUCTION:The aim of this study was quantify annexin A1 expression in macrophages and cluster of differentiation 4 (CD4) + and cluster of differentiation 8 (CD8)+ T cells from the skin of patients with cutaneous leishmaniasis (n=55) and correlate with histopathological aspects.METHODS:Infecting species were identified by polymerase chain reaction-restriction fragment length polymorphism, and expression of annexin A1 was analyzed by immunofluorescence.RESULTS:All patients (n = 55) were infected with Leishmania braziliensis . Annexin A1 was expressed more abundantly in CD163 + macrophages in infected skin (p < 0.0001) than in uninfected skin. In addition, macrophages in necrotic exudative reaction lesions expressed annexin A1 at higher levels than those observed in granulomatous (p < 0.01) and cellular lesions p < 0.05). This difference might be due to the need to clear both parasites and necrotic tissue from necrotic lesions. CD4 + cells in cellular lesions expressed annexin A1 more abundantly than did those in necrotic (p < 0.05) and granulomatous lesions (p < 0.01). Expression in CD8 + T cells followed the same trend. These differences might be due to the pervasiveness of lymphohistiocytic and plasmacytic infiltrate in cellular lesions.CONCLUSIONS:Annexin A1 is differentially expressed in CD163 + macrophages and T cells depending on the histopathological features of Leishmania -infected skin, which might affect cell activation.

Desenvolvimento e aplicação de marcadores moleculares para estudos taxonômicos, genéticos e epidemiológicos em Leishmania (Viannia) / Development and application of molecular markers for taxonomic, genetic and epidemiological studies in Leishmania (Viannia)

Métodos moleculares estão sendo cada vez mais empregados para diagnóstico, estudos taxonômicos, filogenéticos e epidemiológicos envolvendo este parasita. [...] O principal objetivo deste trabalho foi desenvolver marcadores multilocus para Leishmania (Viannia) e avaliar sua aplicabilidade em estudos epidemiológicos. Os objetivos específicos incluíram: i) o desenvolvimento de um painel multi locus sequence analisys (MLSA) para cepas de Leishmania (Viannia) que circulam no Brasil que permita, concomitantemente, a identificação de isolados e a realização de estudos filogenéticos; ii) o estudo da estrutura da população de cepas de Leishmania (Viannia) quanto à clonalidade e ocorrência de eventos de recombinação pela determinação de perfis de microssatélites; iii) avaliação da aplicabilidade do painel MLSA como ferramenta epidemiológica para as leishmanioses; iv) a descrição de eventos moleculares em leishmânia que podem interferir nos resultados obtidos a partir de marcadores moleculares empregados...

Molecular methods have been often applied for diagnosis, studies oftaxonomy, phylogeny and epidemiology. [...] The main objective ofthis study was to develop multi locus markers for Leishmania (Viannia) and to evaluate its applicability in epidemiological studies. The specific objectives were: i) to develop a multi locus sequence analyses (MLSA) panel with Leishmania (Viannia) strains from Brazil that allows the species identification and phylogenetic inferences to be performed; ii) to execute a population structure study through microsatellites profiles (MLMT); iii) to evaluate the MLSA panel as anepidemiological tool; iv) to describe molecular events that may interfere in the results obtained by the molecular markers employed. After MLSA and MLMT, the results could be compared. MLMT defined two main populations, one comprising L. (V.) guyanensis and other L. (V.) braziliensis strainsfrom the Atlantic coast; recombination signs were detected for both. A third group, quite heterogeneous, included L. (V.) braziliensis strains from northern Brazil and the other species L. (V.)shawi, L. (V.) naiffi, and L. (V.) lainson...

Comparative analyses of classical phenotypic method and ribosomal RNA gene sequencing for identification of medically relevant Candida species

As the distribution of Candida species and their susceptibility to antifungal agents have changed, a new means of accurately and rapidly identifying these species is necessary for the successful early resolution of infection and the subsequent reduction of morbidity and mortality. The current work aimed to evaluate ribosomal RNA gene sequencing for the identification of medically relevant Candida species in comparison with a standard phenotypic method. Eighteen reference strains (RSs), 69 phenotypically identified isolates and 20 inconclusively identified isolates were examined. Internal transcribed spaces (ITSs) and D1/D2 of the 26S ribosomal RNA gene regions were used as targets for sequencing. Additionally, the sequences of the ITS regions were used to establish evolutionary relationships. The sequencing of the ITS regions was successful for 88% (94/107) of the RS and isolates, whereas 100% of the remaining 12% (13/107) of the samples were successfully analysed by sequencing the D1/D2 region. Similarly, genotypic analysis identified all of the RS and isolates, including the 20 isolates that were not phenotypically identified. Phenotypic analysis, however, misidentified 10% (7/69) of the isolates. Phylogenetic analysis allowed the confirmation of the relationships between evolutionarily close species. Currently, the use of genotypic methods is necessary for the correct identification of Candida species.

Development and validation of PCR-based assays for diagnosis of American cutaneous leishmaniasis and identificatio nof the parasite species

In this study, PCR assays targeting different Leishmania heat-shock protein 70 gene (hsp70) regions, producing fragments ranging in size from 230-390 bp were developed and evaluated to determine their potential as a tool for the specific molecular diagnosis of cutaneous leishmaniasis (CL). A total of 70 Leishmania strains were analysed, including seven reference strains (RS) and 63 previously typed strains. Analysis of the RS indicated a specific region of 234 bp in the hsp70 gene as a valid target that was highly sensitive for detection of Leishmania species DNA with capacity of distinguishing all analyzed species, after polymerase chain reaction-restriction fragment length polymorfism (PCR-RFLP). This PCR assay was compared with other PCR targets used for the molecular diagnosis of leishmaniasis: hsp70 (1400-bp region), internal transcribed spacer (ITS)1 and glucose-6-phosphate dehydrogenase (G6pd). A good agreement among the methods was observed concerning the Leishmania species identification. Moreover, to evaluate the potential for molecular diagnosis, we compared the PCR targets hsp70-234 bp, ITS1, G6pd and mkDNA using a panel of 99 DNA samples from tissue fragments collected from patients with confirmed CL. Both PCR-hsp70-234 bp and PCR-ITS1 detected Leishmania DNA in more than 70% of the samples. However, using hsp70-234 bp PCR-RFLP, identification of all of the Leishmania species associated with CL in Brazil can be achieved employing a simpler and cheaper electrophoresis protocol.

Comparação de diferentes técnicas de sincronização da emergência da onda folicular visando a superovulação em bovinos / Comparative technics of follicular wave emergence synchronization in the cattle superovulation

Foram avaliadas quatro técnicas de sincronização da onda folicular em protocolos de superovulação. Para tal, foram utilizadas 112 vacas doadoras, das raças Simental, Limousin e Red Angus, com escore corporal médio de 3,0. Os animais foram divididos aleatoriamente em cinco grupos experimentais de acordo com o método de sincronização da emergência da onda folicular. Foram realizadas 30 superovulações em cada grupo, considerando os seguintes protocolos: GI - grupo controle – animais superovulados entre o 8o e o 12o dia do ciclo estral (dia zero = estro); GII – animais que sofreram punção folicular no 9o dia (dia 0 = estro) e início do tratamento superovulatório no 11o dia; GIII – animais que sofreram punção folicular em fase não conhecida do ciclo estral, associada ao uso de um dispositivo intravaginal contendo progesterona (P4) e tratamento superovulatório iniciado 48h após a punção, GIV – animais que utilizaram implante intravaginal de progesterona colocadoem fase aleatória do ciclo estral, mantido por nove dias, associado à administração de 50 mg de P4 e de 2mg de benzoato de estradiol, sendo o tratamento superovulatório iniciado cinco dias após a colocação do dispositivo e GV – animais que receberam implante intravaginal de P4 colocado em fase aleatória do ciclo estral e mantido por oito dias, associado à administração de 50mg de P4 e 2mg de 17â-estradiol, sendo o tratamento superovulatório iniciado quatro dias após a colocação do dispositivo. Nos grupos I, II, III, IV e V o total de estruturas coletadas e de embriões viáveis foram, respectivamente (13,53±9,23 vs 13,87 ± 7,85 vs 18,70 ± 10,88 vs 9,03 ± 4,97 vs 13,60 ± 8,39) e (8,43±5,68 vs 8,27 ± 7,06 vs 10,47 ± 8,19 vs 5,37 ± 2,92 vs 7,23 ± 5,30). Os resultados observados no GIII foram superiores ao GI, GII, GIV e GV (P 0,05), enquanto o desempenho de GIV foi inferior (P<0,05). Os resultados permitem concluir que é possível sincronizar a emergência da onda folicular de vacas doadoras, com início da superovulação em qualquer momento do ciclo estral, e que o tratamento progestágeno associado à punção folicular oferece os melhores resultados.

We evaluated four different techniques of follicular wave synchronization by comparing total number of structures recovery, number of viable and degenerated embryos, number of oocytes recovery and cost of uterine flushing. One hundred twelve Simental, Limousin and Red Angus donators were randomly allocated in five treatment groups according to protocol used for follicular wave emergence synchronization. Thirty superovulations were performed in each group, the programs were: G1- Control, superovulation treatment between days 8 and 12 of the estrous cycle; G2- follicle aspiration on day 9 of the estrous cycle; G3- follicle aspiration plus intravaginal progesterone implant; G4- intravaginal progesterone implant plus estradiol benzoate and G5- intravaginal progesterone implant plus estradiol-17â. Artificial insemination was performed twice, 12 and 24 hours after detection of behavioral estrus. Embryo collection was performed on day 7 after inseminations. Total number of recovered structures (18,70 ± 10,88 vs 13,53 ± 9,23) and viable embryos (10,47 ± 8,19 vs 8,43 ± 5,68) were higher (P0,05) were detected amongst groups 2, 5 and 1, while performance of G4 was the lowest (P<0,05). Results demonstrate to be possible synchronize follicular wave emergence by initiating superstimulation at any time of the estrous cycle. Additionally we verified that the program using progesterone associated to follicular ablation had the best results in synchronizing follicular wave emergence aiming superstimulation in cattle.