Alternative PCR protocol using a single primer set for assessing DNA quality in several tissues from a large variety of mammalian species living in areas endemic for leishmaniasis.

The aim of this work was to establish a modified pre-diagnostic polymerase chain reaction (PCR) protocol using a single primer set that enables successful amplification of a highly conserved mammalian sequence in order to determine overall sample DNA quality for multiple mammalian species that inhabit areas endemic for leishmaniasis. The gene encoding interphotoreceptor retinoid-binding protein (IRBP), but not other conserved genes, was efficiently amplified in DNA samples from tail skin, ear skin, bone marrow, liver and spleen from all of the species tested. In tissue samples that were PCR-positive for Leishmania, we found that DNA from 100%, 55% and 22% of the samples tested resulted in a positive PCR reaction for the IRBP, beta-actin and beta-globin genes, respectively. Nucleotide sequencing of an IRBP amplicon resolved any questions regarding the taxonomical classification of a rodent, which was previously based simply on the morphological features of the animal. Therefore, PCR amplification and analysis of the IRBP amplicon are suitable for pre-diagnostically assessing DNA quality and identifying mammalian species living in areas endemic to leishmaniasis and other diseases.

Leishmania presence in bats in areas endemic for leishmaniasis in central-west Brazil.

Leishmaniasis involves the participation of several species of both wild and domestic mammal hosts and sandfly vectors, which demonstrates the eco-epidemiological complexity observed in this disease. Bats are among the most abundant types of mammals and the scarcity of research on Leishmania infection in these animals gives evidence of the importance of new studies that aim to clarify this relationship. This study aimed to detect the Leishmania spp. in bats. 146 bats, representing 16 different species belonging to the Molossidae, Vespertilionidae, and Phyllostomidae families, were received and processed for collection of tissues. Skin samples were collected from 100% of the bats, and liver samples were collected from 87% (n = 127). After evaluating the quality of the DNA extracted by means of PCR directed to the IRBP gene, the samples considered suitable for the Leishmania detection test were submitted for PCR directed to Leishmania kDNA, and to confirm positivity, were tested to the SSUrRNA gene-directed Nested-PCR. The Leishmania presence in the species Molossus pretiosus, Nyctinomops macrotis, and Lasiurus cinereus are the first reports this encounter in these species of bats in Brazil. Furthermore, new species of bats as possible hosts for L. infantum are reported, such as Molossus pretiosus, Myotis nigricans, Nyctinomops laticaudatus, Nyctinomops macrotis, and, for L. braziliensis, Lasiurus cinereus and Cynomops planirostris. These findings in bats in an area endemic for leishmaniasis indicate that these animals may be involved in sustaining the disease cycle in this location.

Influences of cadmium on fine structure and metabolism of Hypnea musciformis (Rhodophyta, Gigartinales) cultivated in vitro.

The in vitro effect of cadmium on apical segments of Hypnea musciformis was examined. Over a period of 7 days, the segments were cultivated with different concentrations of cadmium, ranging from 50 to 300 µM. The samples were processed for microscopic and histochemical analysis of growth rates, content of photosynthetic pigments, and photosynthetic performance. Cadmium treatments increased cell wall thickness and the accumulation of plastoglobuli. Destruction of chloroplast internal organization was observed. Compared to controls, algae exposed to cadmium showed growth rate reduction, depigmentation, and blending in the lateral branches. The content of photosynthetic pigments, including chlorophyll a and phycobiliproteins, decreased after exposure to different concentrations of cadmium. These results agree with the decreased photosynthetic performance and relative electron transport rate observed after exposure of algae to cadmium. Taken together, these findings strongly indicate that cadmium negatively affects the architecture and metabolism of the carragenophyte H. musciformis, thus posing a threat to the economic vitality of this red macroalgae.

Atypical size and location of a right atrial myxoma: a case report.

INTRODUCTION: Primary intracardiac tumors are rare and approximately 50% are myxomas. The majority of myxomas are located in the left atrium and have variable clinical presentation. We report a case of a large myxoma in the right atrium, which is an uncommon location for this type of tumor. CASE PRESENTATION: A 45-year-old Caucasian woman with a history of palpitation had dyspnea on great exertion and discrete weight loss. A cardiac evaluation showed splitting of S1. An echocardiogram showed a large mass in the right atrium, suggesting myxoma; chest computed tomography confirmed the diagnostic hypothesis. Our patient underwent surgical treatment with excision of a 10 cm multilobulated mass. She presented with supraventricular tachycardia during the operation. She was placed in the intensive care unit and her condition improved after the use of amiodarone. The diagnosis of myxoma was confirmed by histopathological study. CONCLUSIONS: In this case report, we emphasize the rarity of large myxomas in the right atrium and the difficulty of differential diagnosis given their dimension and location.

Molecular detection of Leishmania braziliensis in Rattus norvegicus in an area endemic for cutaneous leishmaniasis in Brazil.

Leishmania nested PCR (LnPCR) targeted to the SSUrRNA gene and DNA sequencing were used to analyze 315 tissue samples from 80 Rattus norvegicus specimens trapped in an area endemic for leishmaniasis in Belo Horizonte, Minas Gerais, Brazil. Of the samples analyzed, 17.46% (55/315) of all tissues, 10% (8/80) of skin, 26.92% (21/78) of blood, 30.76% (24/78) of bone marrow and 2.53% (2/79) of spleen were positive for Leishmania. The overall infection prevalence was 36.25% (29/80) The DNA sequencing showed that 65.51% (19/29) of the positive animals were infected by parasites belonging to the Leishmania braziliensis complex. The identification of L. braziliensis DNA in R. norvegicus in an area with a high prevalence of leishmaniasis might imply a zoonotic role of this species. The rodent control programs and health education may represent important measures toward the control of leishmaniasis.

Alternative PCR protocol using a single primer set for assessing DNA quality in several tissues from a large variety of mammalian species living in areas endemic for leishmaniasis

The aim of this work was to establish a modified pre-diagnostic polymerase chain reaction (PCR) protocol using a single primer set that enables successful amplification of a highly conserved mammalian sequence in order to determine overall sample DNA quality for multiple mammalian species that inhabit areas endemic for leishmaniasis. The gene encoding interphotoreceptor retinoid-binding protein (IRBP), but not other conserved genes, was efficiently amplified in DNA samples from tail skin, ear skin, bone marrow, liver and spleen from all of the species tested. In tissue samples that were PCR-positive for Leishmania, we found that DNA from 100 percent, 55 percent and 22 percent of the samples tested resulted in a positive PCR reaction for the IRBP, beta-actin and beta-globin genes, respectively. Nucleotide sequencing of an IRBP amplicon resolved any questions regarding the taxonomical classification of a rodent, which was previously based simply on the morphological features of the animal. Therefore, PCR amplification and analysis of the IRBP amplicon are suitable for pre-diagnostically assessing DNA quality and identifying mammalian species living in areas endemic to leishmaniasis and other diseases.

Estatus da metilação da caderina-E em tecido tireóideo normal, bócio e câncer papilar de tireóide / E-Cadherin methylation status in normal thyroid tissue, goiter and papillary thyroid cancer

A descoberta de marcadores moleculares que possam predizer transformação maligna em lesões tireoidianas é de fundamental importância na prática clínica. A inativação da caderina-E é um evento inicial observado em muitas lesões epiteliais cancerígenas. Objetivo: Verificar o possível papel da metilação do gene da caderina-E na transformação maligna do tecido tireóideo. Método: A metilação do gene da caderina-E foi determinado por PCR-MS após a extração do DNA usando a técnica com bissulfato de sódio. As linhagens celulares leucêmicas MV411 e BV173 foram usadas como controles positivos. Dez amostras do sangue periférico, tecido tireóideo normal e carcinoma papilar de tireóide foram testados. Resultados: Células MV411 e BV173 mostraram apenas padrão metilado. Todas as amostras de sangue periférico, tecido tireóideo normal e carcinoma papilar de tireóide mostraram apenas padrão não metilado. Conclusão: Esses dados sugerem que a falta do padrão metilado tanto no tecido tireóideo normal como no carcinoma papilar indicam que a metilação da caderina-E não tem significância na carcinogênese dos tumores papilares de tireóide

The discovery of a molecular marker able to predict malignant transformation of thyroid lesions would be of up most importance in clinical practice. E-cadherin inactivation is an early event observed in many cancerous epithelial lesions. Objective: To verify the possible role of the E-cadherin gene methylation in malignant transformation of the thyroid tissue. Method: The methylation of the E-cadherin gene was assessed by MS-PCR after DNA extraction by using sodiumbisulphate technique. The leukemia-MV411 and BV173 cell lines were used as positive controls. Ten samples of peripheral blood, normal thyroid tissue, and papillary thyroid carcinomas were tested. Results: MV411 and BV173 cell lines showed only methylated pattern. All the samples of peripheral blood, normal thyroid tissue or papillary carcinomas showed only non-methylated pattern. Conclusion: These data suggest that the lack of methylated pattern for both normal thyroid tissue and papillary carcinomas indicates that methylation of the E-cadherin has no significance in thyroid papillary carcinogenesis