RESUMO
Diacrodon is a monotypic genus of the tribe Spermacoceae (Rubiaceae), endemic to northeastern Brazil. Diacrodon compressus is frequently misidentified with a two lobed calyx species of Borreria, B. verticillata. Traditionally, in Spermacoceae the fruit type was considered a diagnostic character among the genera. In this sense, D. compressus presents a strongly compressed, one seeded and indehiscent fruit (vs. globose, two seeded and dehiscent fruit in B. verticillata). In this work, we address two objectives: evaluate the systematic position and determine the identity of Diacrodon in respect to other taxa. Molecular analyses using ITS and ETS indicate that D. compressus is strongly related to other species of Borreria. The morphological results revealed that D. compressus, despite of its type of fruit, is identical to Borreria in floral and palynological features. As conclusion, the new combination Borreria diacrodonta is made and a lectotype is designated. An updated description of the species and a key to the Borreria species with a two lobed calyx are provided. The distribution of B. diacrodonta is extended to Brazilian states Goiás and Minas Gerais, and Paraguay. By this taxonomical change it has become clear that the dehiscence of the fruits lack taxonomic value in the delimitation of Borreria.
Assuntos
Flores/genética , Frutas/genética , Rubiaceae/genética , Brasil , Flores/classificação , Frutas/classificação , Especiação Genética , Filogenia , Filogeografia , Dispersão Vegetal , Rubiaceae/classificação , Análise de Sequência de DNARESUMO
El diagnóstico inmunológico y parasitológico de la leishmaniasis tegumentaria (LT) y visceral (LV)continúa siendo un desafío ya que una limitante es la demostración etiológica mediante extendidos coloreados, histopatología, cultivos, inoculación en animales de laboratorio, xenodiagnósticos. El procedimiento de PCR incrementa la sensibilidad del diagnóstico microscópico directo considerándola actualmente una herramienta muy valorable en la identificación y caracterización de las diferentes especies de Leishmania. En el presente trabajo se evalúan dos métodos de extracción de ADN en diferentes tejidos de hámster (Mesocricetus auratus) experimentalmente infectado con Leishmania (Viannia) braziliensis con material de un enfermo con LT con confirmación parasitológica. Los ADN obtenidos fueron sometidos a una técnica de PCR específica para Le. braziliensis. Se consideró positiva a toda muestra que evidenciara un amplicón de 126 pb en electroferograma de agarosa al 2%.Se realizaron otros métodos como el xenodiagnóstico y técnicas microscópicas directas para comparar la sensibilidad con la PCR. Todas las muestras del roedor infectado evidenciaron el amplicón correspondiente a Le. braziliensis. En este trabajo se demuestra que el detergente CTAB es adecuado para obtener una ADN óptimo para una amplificación específica y que PCR es el método más sensible ensayado (AU)
The etiologic diagnostic of Tegumentary Leishmaniasis (TL) and Visceral Leishmaniasis (VL) is performed by microscopic examination of stained smears of skin lesions, by histopathology, by culture, inoculation in animals or by xenodiagnostic. PCR procedure is currently considered as one promisory diagnostic tool due to its sensitivity, being usually used in identification and characteristization of Leishmania genus.In this work two DNA extraction methods using different golden hamsters (Mesocricetus auratus)tissues experimentaly infected with Leishmania (Viannia) braziliensis from a patient with parasitologic confirmation of TL are evaluated. DNA obtained were put through specific L. braziliensis PCR, considering positive every sample showing an amplicon of 126 pb in the electroferogram of agarose 2%.PCR sensitivity was compared with xenodiagnostic and direct microscopic examination. All infected mices samples showed the corresponding amplicon to L. braziliensis, demonstrating that CTAB use is adecuated to obtain a top quality DNA and that, in these conditions, PCR is the highest sensitivity method (AU)
