Postembrionic development and reproductive parameters of the grasshopper pest Borellia bruneri (Acrididae: Gomphocerinae) under controlled conditions

Abstract Borellia bruneri, a common grasshopper in much of the grasslands of Argentina and Uruguay, is considered, according to the categories widely accepted for defining the pest status of grasshopper species, a "Frequent plague of importance". In order to determine fundamental aspects of its biology and reproduction, three cohorts of B. bruneri were monitored under controlled conditions (30º C, 14L: 10D, 40% RH). The total duration of nymphal development was 50.6 days, both males and females having five nymphal instars. There was a significant difference in the duration of the different stages within each cohort. In the three cohorts, the first instar duration (12.87 days) was longer than the rest, approximately 5.6 days more than the second that was the shortest (7.26 days). The average longevity of female adults was 56.6 days, and in males, 54.4 days. The number of egg-pods per female was 3.5 and the amount of eggs per egg-pod was 10.8. Mean fecundity was 37.9 eggs per female with an oviposition rate of 1.20 eggs/female/day. Finally, knowing the life cycle of B. bruneri is relevant in order to optimize the control measures for this species.

Plantas medicinais utilizadas por idosos com diagnóstico de Diabetes mellitus no tratamento dos sintomas da doença / Medicinal plants used by elderly people with Diabetes mellitus in the treatment of the disease symptoms

Este trabalho teve como objetivo investigar as plantas medicinais utilizadas por idosos assistidos em uma Unidade Básica de Saúde de Pelotas-RS, com diagnóstico de Diabetes mellitus, como terapia complementar no tratamento dos sintomas da doença. Caracterizou-se por pesquisa qualitativa, realizada em julho de 2009, no município de Pelotas-RS. Foram entrevistados 18 idosos com idade entre 60 e 77 anos, sendo 14 do sexo feminino. Os participantes citaram 20 plantas medicinais utilizadas como terapia complementar no tratamento do Diabetes mellitus. Entre estas, as mais citadas utilizadas para diminuir os níveis de glicose no sangue foram Sphagneticola trilobata, Bauhinia spp. e Syzygium cumini, sendo que para as duas últimas há comprovação científica do efeito hipoglicemiante. A infusão foi a forma de preparo predominante. Considera-se importante a realização de estudos farmacológicos que investiguem os efeitos das plantas utilizadas pela população, a fim de que o uso proporcione os benefícios desejados e não cause danos à saúde.

This study aimed to investigate medicinal plants used as complementary therapy by the elderly with diabetes mellitus, assisted by a Health Basic Unit in Pelotas (RS, Brazil). This qualitative research was conducted in July 2009. Eighteen 60 to 77 years old elderly (14 of them female) were interviewed. The participants identified 20 medicinal plants used as complementary therapies in the treatment of diabetes mellitus. Among these, the most used ones to reduce the levels of glucose in the blood were Sphagneticola trilobata, Bauhinia spp. and Syzygium cumini. For the last two plants, there are scientific proofs of hypoglycemic effects. The infusion was the predominant form of preparation. Studies to investigate the pharmacological effects of plants used by the population have become very important, for providing scientific information on their possible health benefits and side effects.

Detecção de Listeria monocytogenes pela técnica de PCR em leite contaminado artificialmente / Detection of Listeria monocytogenes by PCR in artificially contaminated milk samples

Avaliou-se a técnica de PCR como opção para reduzir o tempo de detecção de Listeria monocytogenes no leite. Para tanto, amostras de leite desnatado esterilizado e de leite cru integral - com baixa, média e alta contagem de microrganismos aeróbios mesófilos - foram inoculadas experimentalmente com diversas concentrações de L. monocytogenes. Os resultados da reação de PCR foram comparados com os da cultura da amostra empregando-se metodologia padronizada tradicional. Não se detectou L. monocytogenes pela reação de PCR quando esta foi realizada a partir do caldo de enriquecimento de Listeria (LEB) após 24 horas de incubação, nem no leite desnatado esterilizado, nem no leite cru integral. Após 48 horas de enriquecimento em LEB, a bactéria foi detectada por PCR nas amostras de leite desnatado esterilizado, com a sensibilidade de 1UFC/mL, mas não nas amostras de leite cru integral. Pela metodologia tradicional, a bactéria foi recuperada de todos os ensaios. Entretanto, nas amostras de leite cru com altas contagens de aeróbios mesófilos, a sensibilidade da metodologia tradicional foi reduzida (a partir de 7UFC/mL). Melhores resultados foram obtidos quando a reação de PCR foi feita utilizando-se DNA obtido diretamente da colônia suspeita em meio sólido (Oxford e Palcam). Foi possível substituir os testes fenotípicos de identificação de L. monocytogenes pela técnica de PCR reduzindo-se o tempo de identificação da bactéria de vários dias para algumas horas.

The polymerase chain reaction (PCR) was used to detect Listeria monocytogenes in inoculated milk samples after selective enrichment. Samples of sterile skim milk and raw whole milk (with low, intermediate, and high counts of aerobic mesophilic microorganisms) were inoculated with several concentrations of L. monocytogenes. The results of PCR assays were compared to the results of culturing the samples using a standardized traditional method for isolation of L. monocytogenes. The pathogen was detected by PCR in Listeria Enrichment Broth (LEB) after 48h-incubation (sensitivity of 1CFU/mL) but not after 24h-incubation from the samples prepared with sterile skim milk. L. monocytogenes was not detected by PCR in LEB after 24 and 48h-incubation from the samples prepared with raw whole milk. Using the traditional method, the pathogen was detected in all experiments. However, sensitivity decreased in raw whole milk with high counts of aerobic mesophilic microorganisms (up to 7CFU/mL). Best results were obtained when PCR was done to identify presumptive L. monocytogenes colonies directly from Palcam and Oxford media, after the enrichment step. This procedure allowed reducing to a few hours the period of several days usually needed to obtain the final identification of L. monocytogenes using phenotypic tests.

Detecção de Escherichia coli O157: H7 inoculada experimentalmente em amostras de leite cru por método convencional e PCR multiplex / Detection of E. coli O157: H7 experimentally inoculated in raw milk samples by conventional method and multiplex PCR

Padronizou-se um método de reação em cadeia da polimerase (PCR) multiplex para detecção de Escherichia coli O157:H7 e avaliou-se a eficiência da PCR e de um método de cultivo convencional em placas na detecção desse patógeno experimentalmente adicionado em leite estéril e em leite cru com baixa contagem bacteriana total (média de 4,01 x 10³ UFC/ml) e com alta contagem bacteriana (média de 2,10 x 10(6) UFC/ml). Foram padronizadas duas reações de PCR com o uso dos primers: "A" (RfbF; RfbR e FLICh7F/FLICh7R) e "B" (SLT-IF/SLTIR e SLT-IIF/SLT-IIR). A detecção de E. coli O157:H7 (1UFC/ml) a partir do leite estéril e do leite cru com baixa contaminação bacteriana foi possível quando se utilizou o método de contagem em placas e a PCR. A sensibilidade dos dois métodos foi menor quando se testou o leite cru com alta contaminação microbiana, sendo o método convencional mais sensível. Os resultados indicam que a presença de outros microrganismos, em alta quantidade no leite, dificulta a detecção de E. coli O157:H7 pelos métodos utilizados.

This experiment was carried out in order to evaluate the effect of the raw milk bacterial count on the efficiency of a multiplex polymerase chain reaction and a conventional plate count method for detection of Escherichia coli O157:H7. This pathogen was experimentally inoculated into sterile milk, raw milk with low bacterial count (count mean of 4.01 x 10³ cfu/ml) and, raw milk with high bacterial count (mean 2.10 x 10(6) cfu/ml). Two protocols of PCR were standardized using primers "A" (Rfbf and Rfbr and FLICh7F/FLICh7R) and "B" (SLT-IF/SLTIR and SLT-IIF/SLT-IIR). Both conventional plate count and PCR methods were able to detect the presence of E. coli O157:H7 in either sterile milk or raw milk with low bacterial count initially inoculated with 1cfu of E. coli O157:H7 per ml. The sensibility of both methods for high-contaminated raw milk samples was lower, being the conventional approach more sensitive. These results indicate that high bacterial count in raw milk can affect E. coli O157:H7 detection.

Contagem de células somáticas e isolamento de agentes causadores de mastite em búfalas (Bubalus bubalis) / Somatic cell count and mastitis causing pathogens isolation in water buffaloes (Bubalus bubalis)

The research was accomplished in eight dairy water buffalo herds, randomically choosen in Região do Alto São Francisco, State of Minas Gerais, Brazil. Information was collected from March to November, 2003 during 270 days of observation. In order to determine the somatic cell count (SCC) in presence or absence of microbial isolation, 1,393 samples were collected from 285 lactating females and microbiological exams and SCC were done. Samples obtained from udders without evidence of clinical or subclinical inflammation showed infection for a great variety of microbial mastitis pathogens. The low SCC did not necessarily indicate the absence of intramammary infection, suggesting that SCC patterns used for bovine cannot be appropriate in order to control mastitis in buffalo herds.