Contribuição ao estudo morfológico de ovos e ninfas de Triatoma brasiliensis neiva, 1911 (hemiptera, reduviidae, triatominae)

Foi feito um estudo da estrutura dos ovos e morfologia das ninfas, através da microscopia ótica e eletrônica de varredura, na procura de estabelecer novos parãmetros de identificação. Em microscopia ótica (MO) os ovos apresentam a superfície exocorial dividida em áreas poligonais. O exocório do corpo possui polígonos maiores do que os do opérculo, porém ambos são lisos. Em microscopia eletrõnica de varredura (MEV) o exocório do opérculo apresenta áreas poligonais de superfície estofada em pequenos sulcos irregulares e perfurações distribuídas aleatoriamente. O exocório do corpo possui áreas pouco acolchoadas com perfurações na superfície e nos bordos. Nas ninfas o sulco estridulatório apresenta características próprias para cada estádio.

Alterações biomorfogênicas causadas pela aplicação de precoceno II em ninfas de Triatoma infestans (Klug, 1834) (Hemiptera, reduviidae, triatominae)

O precoceno II aplicado topicamente em ninfas de 4ª estádio, nas dosagens de 200, 300 e 400 micron-grama/1 micron-litro de acetona, proporcionou o aparecimento de adultóides, em diferentes percentagens com as seguintes características: tegumento alterado, aparelho bucal deformado, asas braquípteras, tarsos trímeros, ocelos, evidentes e genitália externa com estruturas desenvolvidas e deformadas; genitália interna em estágio intermediário entre ninfas de 4§ e 5§ estádios. Os adultóides apresentaram um período de sobrevivência inversamente proporcional à dosagem aplicada, variando de 3 a 22 dias, não tendo se alimentado devido as alterações.

A genitália externa dos machos de sete espécies de Triatoma Laporte, 1832 da região Neártica (Hemiptera, Reduviidae, Triatominae)

Sete espécies da região neártica: Triatoma barberi Usinger, 1939; T. rubida (Uhler, 1894); T. gertaeckeri (Stal, 1859); T. lecticularia (Stal, 1859); T. protracta (Uhler, 1894); T. recurva (Stal, 1868) e T. sanguisuga (Leconte, 1855) foram analisadas comparativamente, tendo como enfoque as estruturas da genitália do macho: falosoma (Ph), suporte do falosoma (SPh), processo do endosoma (PrEn), vesica (V) e aparelho articular (Apb). As estruturas fálicas se mostraram capazes de serem usadas como critério morfológico suplementar aos padrões atualmente usados, em taxonomia. Estas espécies silvestres são encontradas nos Estados Unidos e México, naturalmente infectadas pelo T. cruzi; algumas vivem no perdomicílio e outras eventualmente no domicílio, sem contudo colonizá-lo.

Biologia do triatoma vitticeps (Stal, 1859) em condiçoes de laboratórios (Hemiptera: Reduvidae: Triatominae) I. Ciclo evolutivo

Foram feitas observações do ciclo evolutivo do Triatoma vitticeps com alimentação semanal em camundongo, em condições de laboratório. De quatro casais virgens obtiveram-se 435 ovos, sendo que 149 destinaram-se ao ciclo evolutivo e 286 ao estudo da resistência ao jejum, o que constituirá a segunda etapa deste trabalho. Apenas 50 exemplares atingiram a fase adulta num período X (S) = 270 ± 45 dias. Quanto ao tempo de incubação, o 1° e o 2° estádios foram realizados, cada um, em menos de um mês, enquanto que os 3º, 4º e 5º estádios requereram cerca de um, dois e três meses, respectivamente. A procura pelo 1º repasto ocorreu de forma sensível no 3º, 6º e 10º dias. Em todos os estádios, mais de 50% dos exemplares realizaram apenas um repasto, com exceção do 5º, onde foram necessários dois. No que diz respeito ao intervalo de tempo entre o oferecimento do repasto, o ato de picar, e a duração do repasto, observou-se que estes aumentaram gradativamente de acordo com o estádio. Dos 423 repastos realizados, 390 não foram seguidos de defecação no prazo de 10 min. Sob este aspecto parece que o T. vitticeps não é um bom transmissor do T. cruzi. O experimento teve a duração de 13 meses e neste período as temperaturas máximas e mínimas e a umidade relativa do ar variaram em média de 28 ± 2°C a 25 ± 2°C e 80 ± 2%, respectivamente. O material é proveniente da criação mantida no Departamento de entomologia do Instituto Oswaldo Cruz.

Biologia do Triatoma vitticeps (Stal, 1859) em condições de laboratório (Hemiptera: Reduviidae: Triatominae): II. Resistência ao jejum

Em prosseguimento ao estudo da biologia do Triatoma vitticeps (Gonçalves et al., 1988), foram feitas observações sobre a sua resistência ao jejum. Dos 286 ovos obtidos, apenas 201 eclodiram e atingiram o estádio pretendido para as observações. Os demais não eclodiram, não completaram a muda ou morreram sem motivo aparente. As ninfas foram acondicionadas, individualmente em frascos de Borrel, devidamente registrados. Para a alimentação foram utilizados camundongos e a medida que as ninfas atingiam o estágio pretendido a alimentação era suspensa até ocorrer a morte. A avaliação da resistência ao jejum foi feita da seguinte forma: o intervalo de dias entre o último repasto e a morte e entre a muda e a morte. Verificou-se que a resistência está diretamente relacionada com a fase de desenvolvimento. Para os parâmetros último repasto/morte e muda/morte, ambos os sexos foram menos resistentes do que as ninfas de 3º e 2º estádios, respectivamente. O experimento teve duração de 15 meses e neste período as temperaturas máxima e mínima e a umidade relativa do ar variaram em média de 25 ± 2ºC e 81 ± 3% UR, respectivamente. O material foi proveniente da criação de triatomíneos mantida no Departamento de Entomologia do Instituto Oswaldo Cruz.

Estudos sobre a resistência ao jejum e aspectos nutricionais de Triatoma lecticularia (Stal, 1859) (Hemiptera, Reduviidae, Triatominae)

Foi feito um estudo sobre a resistência ao jejum em todas as fases evolutivas e pesagens em diferentes situações nutricionais de Triatoma lecticularia (alimentado; não alimentado; na morte após o jejum) com temperatura e umidade registradas. Observou-se que os períodos de resistência das fases ninfais apresentaram médias (dias) crescentes: 1º: 45,84; 2º: 61; 3º: 88,74; 4º: 123,47; 5º 162,30. Na fase adulta as médias foram aproximadas à do 3º estádio (para os machos 88,94 e para as fêmeas 83,66). O procedimento de pesagens permitiu registrar a quantidade de sangue ingerido, a perda de peso durante o jejum e o respectivo percentual em relação ao peso inicial. Esta espécie tem assinalada sua distribuição geográfica na região Neártica, onde tem sido encontrda infectada com Trypanosoma cruzi associada a Neotoma micropus Baird e Spermophilus variagatus (Erxeleben).

Fonte alimentar e potencial vetorial de Triatoma vitticeps (Stal, 1859) com relação à doença de Chagas humana no estado do Espírito Santo, Brasil (Hemiptera, Reduviidae)

In paralel with several other epidemiologic and entomologic data of 19 Municipalities of Espírito Santo State, Brazil, the feeding pattern of 222 Triatoma vitticeps is studied through precipitin tests. Very high levels of natural infection with Trypanosoma cruzi are observed in adult insects, in contrast with the abscence or minimum degrees of infection among nymphs and human individuals. The precipitin tests showed the contact of the insects with multiple blood sources, chiefly human and birds, followed by rodents and marsupials. The data suggest that T. vitticeps in spite of being highly antropophilic, become infected by T. cruzi in sylvatic ambient and occasionally invade houses. The species doesn't seem to be - at least until now - a good vector in the domestic cycle of Chagas' disease. Several factors seem to be involved in this conclusion, mainly the low density of the insect in the houses, its hardness to coloniza them, its slowness concerning to suction and defecation and possibly its low susceptibility to different T. cruzi strains.

Origine des populations de rainette verte (Hyla spp.) de l'ouest de la Suisse

DNA-based techniques are important tools for species assignment, in particular when identification with morphological criteria is difficult. The aim of this study was to genetically determine the species identity of tree frogs (Hyla spp.) populations from western and northern Switzerland (Swiss Plateau), this area being frequently subjected to introductions of species or sub-species from south of the Alps. We sequenced 261 base pairs of the mitochondrial DNA cytochrome b gene from 24 samples of tree frogs from the Swiss Plateau, Ticino (southern Switzerland) and the Dombes region (Ain, France), and compared them with homologous sequences retrieved from DNA databases. The phylogenetic analyses revealed two distinct clades. The first one is represented by samples of Green tree frog (Hyla arborea) from the Swiss Plateau, France, Germany and Greece, confirming the current knowledge about the species' distribution. The second clade includes samples belonging to the Italian tree frog (Hyla intermedia) from south of the Alps (Ticino and Italy), and unexpectedly from the Grangettes site in western Switzerland. These results suggest the introduction of the Italian tree frog H. intermedia north of the Alps, and raise questions about the management of the Grangettes protected area.

The distribution of agglutinins and lytic activity against Trypanosoma rangeli and erythrocytes in Rhodnius prolixus and Triatoma infestans tissue extracts and haemolymph

Haemolymph, heads, salivary glands, crops, midguts, hindguts, and Malpighian tubules from Rhodnius prolixus and Triatoma infestans were extracted in phosphate or Tris buffer saline with calcium, and tested for agglutination and lytic activities by microtitration against both vertebrateerythrocytes and cultured epimatigote forms of Trypanosoma rangeli. Haemagglutination activity against rabbit erythrocytes was found in the crop, midgut and hindgut extracts of T. infestans but only in the haemolymph of R. prolixus. Higher titres of parasite agglutinins were found in R. prolixus haemolymph than T. infestans, whilst the converse occurred for the tissue extracts. In addition, the extracts of T. infestans salivary glands, but not those of R. prolixus, showed a trypanolytic activity that was heat-inactivated and was not abolished by pre-incubation with any of the sugars or glycoproteins tested. T. infestans, which is refractory to infection by T. rangeli, thus appears to contain a much wider distribution of agglutinating and trypanolytic factors in its tissues than the more susceptible species, R. prolixus

Redescription of Nomimoscolex piraeeba Woodland, 1934 (Cestoda, Proteocephalidea), from the Amazon catfishes, Brachyplatystoma spp. with proposal of synonyms and invalidation of Endorchiinae and Endorchis

The proteocephalid species Nomimoscolex piraeeba Woodland, 1934, N. dorad (Woodland, 1935) and Endorchis piraeeba Woodland, 1934, from Brachyplatystoma spp., South American silurid fishes, are critically revised. It is concluded that they concern to one species, N. piraeeba. The Endorchiinae, a subfamily of Monticelliidae, and genus Endorchis are invalidated herein. The valid species of Endorchiinae, belonging to genus Muzophorus, M. admonticellia Woodland, 1934, M. pirarara Woodland, 1934 and M. woodlandi Rego, 1984, are transferred provisionally to Zygobothriinae.

Are dead Triatoma infestans a competent vector of Trypanosoma cruzi?

After Triatoma infestans death, Trypanosoma cruzi survived several days, maintaining the ability to infect a vertebrate host. Dead bugs from an endemic area collected during an official spraying comapign showed mobile rectal tripanosomes up to 14 days after vector death. Two days after vector death2, 760 tripomastigotes were found alive in its rectal material. However, the number of mobile tripomastigotes decreased significantly from the 5th day after death. Laboratory proofs with third and fifth nymphal stage showed similar results. Living tripanosomes were found in their rectal material at 10 days in third stage and even at 30 days in fifth nymphal stage. The mean number of tripomastigotes had no changes up to 10 days in third nymphal stage and increased significantly from 1 to 10 days in the fifth stage. Conjuctival instillation as well as intraperitoneal innoculation to mice, of metacyclic forms from dead T. infestans produced infection in the vertebrate host. Present results show that human contact with dead vector highly probable in summer and living and infective T. cruzi are available for transmision in the vector.

Cardenolides, induced responses, and interactions between above- and belowground herbivores of milkweed (Asclepias spp.).

Theory has long predicted allocation patterns for plant defense against herbivory, but only recently have both above- and belowground plant defenses been considered simultaneously. Milkweeds in the genus Asclepias are a classic chemically defended clade of plants with toxic cardenolides (cardiac glycosides) and pressurized latex employed as anti-herbivore weapons. Here we combine a comparative approach to investigate broadscale patterns in allocation to root vs. shoot defenses across species with a species-specific experimental approach to identify the consequences of defense allocational shifts on a specialist herbivore. Our results show phylogenetic conservatism for inducibility of shoot cardenolides by an aboveground herbivore, with only four closely related tropical species showing significant induction; the eight temperate species examined were not inducible. Allocation to root and shoot cardenolides was positively correlated across species, and this relationship was maintained after accounting for phylogenetic nonindependence. In contrast to long-standing theoretical predictions, we found no evidence for a trade-off between constitutive and induced cardenolides; indeed the two were positively correlated across species in both roots and shoots. Finally, specialist root and shoot herbivores of common milkweed (A. syriaca) had opposing effects on latex production, and these effects had consequences for caterpillar growth consistent with latex providing resistance. Although cardenolides were not affected by our treatments, A. syriaca allocated 40% more cardenolides to shoots over roots. We conclude that constitutive and inducible defenses are not trading off across plant species, and shoots of Asclepias are more inducible than roots. Phylogenetic conservatism cannot explain the observed patterns of cardenolide levels across species, but inducibility per se was conserved in a tropical clade. Finally, given that above- and belowground herbivores can systemically alter the defensive phenotype of plants, we concur with recent calls for a whole-plant perspective in testing models of plant defense allocation.

Influence of mating on ovarian follicle development in Triatoma infestans (Klug, 1834)

This works examines the influence of mating on ovarian follicle development in Triatoma infestans. The observations were carried out on both virgin and mated females, wich were killed at various times after their emergence. There was no difference in the ovarian development of both experimental groups during the first gonadotrofic cycle. By the 7th day mated females as well as virgn females showed vitellogenic oocytes. The coriogenesis and ovulation process began on the 13th day after imaginal moulting. However we could observe that egg-laying was dependent on mating. Mated females laid eggs whereas virgin females did not lay eggs. However ovarian production was significantly greater in the mated females. It is suggested that in T. infestans mating stimulates egg-laying but it does not influence the oogenesis and ovulation process.

ESCMID* guideline for the diagnosis and management of Candida diseases 2012: prevention and management of invasive infections in neonates and children caused by Candida spp.

Invasive candidiasis (IC) is a relatively common syndrome in neonates and children and is associated with significant morbidity and mortality. These guidelines provide recommendations for the prevention and treatment of IC in neonates and children. Appropriate agents for the prevention of IC in neonates at high risk include fluconazole (A-I), nystatin (B-II) or lactoferrin ± Lactobacillus (B-II). The treatment of IC in neonates is complicated by the high likelihood of disseminated disease, including the possibility of infection within the central nervous system. Amphotericin B deoxycholate (B-II), liposomal amphotericin B (B-II), amphotericin B lipid complex (ABLC) (C-II), fluconazole (B-II), micafungin (B-II) and caspofungin (C-II) can all be potentially used. Recommendations for the prevention of IC in children are largely extrapolated from studies performed in adults with concomitant pharmacokinetic data and models in children. For allogeneic HSCT recipients, fluconazole (A-I), voriconazole (A-I), micafungin (A-I), itraconazole (B-II) and posaconazole (B-II) can all be used. Similar recommendations are made for the prevention of IC in children in other risk groups. With several exceptions, recommendations for the treatment of IC in children are extrapolated from adult studies, with concomitant pharmacokinetic studies. Amphotericin B deoxycholate (C-I), liposomal amphotericin B (A-I), ABLC (B-II), micafungin (A-I), caspofungin (A-I), anidulafungin (B-II), fluconazole (B-I) and voriconazole (B-I) can all be used.