RESUMO
Ruderal species may provide pollen and nectar to maintain the pollinators of crops in periods of floral resource shortage. The knowledge about the floral biology of these plant species and their interaction with insects is important for management strategies of agricultural systems. The study was carried out at an experimental research station in two different periods (August 2010-April 2011 and August 2012-January 2013). Floral biology was studied, and the reproductive system and reproductive efficacy (RE) were analyzed using controlled pollination experiments. Furthermore, floral visitors and pollination were identified and quantified. Reproductive success obtained in the open pollination and cross-pollination experiments was higher than those obtained in spontaneous self, hand self, and wind pollination. Richardia grandiflora bloomed throughout the experimental period, and flowers were visited by Coleoptera, Diptera, Hymenoptera, and Lepidoptera, which were observed foraging for pollen and/or nectar. Among the floral visitors, bees were the richest and most frequent group and often contacted anthers and stigmas during visits. Africanized honeybees touched the floral reproductive structures in all visits, and their frequency may be related to changes in the reproductive efficacy between the study periods. Pollinator species of crops cultivated at the experimental research station were frequent bee visitors of R. grandiflora. We demonstrated that R. grandiflora requires cross-pollination and biotic pollen vectors. Among floral visitors, bees are the main pollinators, especially the Africanized honeybees. R. grandiflora can be considered an important ruderal species for maintaining bee pollinator populations at the study site, providing resources during the period that crops are not blooming.
Assuntos
Abelhas , Polinização , Rubiaceae , Animais , BrasilRESUMO
Down syndrome (DS) is the most common disease due to an autosomal aneuploidy in live born children and also the major known genetic cause of mental retardation. The risk of a DS pregnancy increases substantially with increasing maternal age. However, several women aged less than 35 years at conception have a child with DS. The micronucleus (MN) assay can identify chromosome breakage or chromosome malsegregation and is an ideal biomarker to investigate genomic instability. The aim of the present study was to determine the frequency of peripheral lymphocytes with MN in the parents of DS individuals. The subjects were 17 couples, 1 father and 9 mothers, and 24 couples who had at least one healthy child formed the control group. For each individual we evaluated the frequency of binucleated micronucleated lymphocytes (BNMN%) as number of binucleated lymphocytes containing one or more MN per 1000 binucleated cells. The mean age of DS parents and controls was 32.6 and 29.8 years, respectively. The frequency of MN in DS parents was significantly higher compared to controls. The higher frequency of MN in DS parents suggests a higher predisposition of DS parents to aneuploidy events in this sample.
Assuntos
Adulto , Criança , Feminino , Humanos , Masculino , Síndrome de Down/genética , Linfócitos/ultraestrutura , Micronúcleos com Defeito Cromossômico , Estudos de Casos e Controles , Marcadores Genéticos , Predisposição Genética para Doença , Testes para MicronúcleosRESUMO
Down syndrome (DS) is the most common disease due to an autosomal aneuploidy in live born children and also the major known genetic cause of mental retardation. The risk of a DS pregnancy increases substantially with increasing maternal age. However, several women aged less than 35 years at conception have a child with DS. The micronucleus (MN) assay can identify chromosome breakage or chromosome malsegregation and is an ideal biomarker to investigate genomic instability. The aim of the present study was to determine the frequency of peripheral lymphocytes with MN in the parents of DS individuals. The subjects were 17 couples, 1 father and 9 mothers, and 24 couples who had at least one healthy child formed the control group. For each individual we evaluated the frequency of binucleated micronucleated lymphocytes (BNMN%) as number of binucleated lymphocytes containing one or more MN per 1000 binucleated cells. The mean age of DS parents and controls was 32.6 and 29.8 years, respectively. The frequency of MN in DS parents was significantly higher compared to controls. The higher frequency of MN in DS parents suggests a higher predisposition of DS parents to aneuploidy events in this sample.
Assuntos
Síndrome de Down/genética , Linfócitos/ultraestrutura , Micronúcleos com Defeito Cromossômico , Adulto , Estudos de Casos e Controles , Criança , Feminino , Marcadores Genéticos , Predisposição Genética para Doença , Humanos , Masculino , Testes para MicronúcleosRESUMO
The role played by genetic components in the etiology of the Class III phenotype, a class of dental malocclusion, is not yet understood. Regions that may be related to the development of Class III malocclusion have been suggested previously. The aim of this study was to search for genetic linkage with 6 microsatellite markers (D1S234, D4S3038, D6S1689, D7S503, D10S1483, and D19S566), near previously proposed candidate regions for Class III. We performed a two-point parametric linkage analysis for 42 affected individuals from 10 Brazilian families with a positive Class III malocclusion segregation. Analysis of our data indicated that there was no evidence for linkage of any of the 6 microsatellite markers to a Class III locus at = zero, with data supporting exclusion for 5 of the 6 markers evaluated. The present work reinforces that Class III is likely to demonstrate locus heterogeneity, and there is a dependency of the genetic background of the population in linkage studies.
Assuntos
Má Oclusão Classe III de Angle/genética , Prognatismo/genética , Brasil , Genes Dominantes , Heterogeneidade Genética , Ligação Genética , Loci Gênicos , Mandíbula/anormalidades , Repetições de Microssatélites , LinhagemRESUMO
Cryptococcosis in México is caused by both species of the Cryptococcus species complex i.e., Cryptococcus neoformans and C. gattii. The current study was aimed to determine genetic variability of 72 Mexican clinical isolates using PCR-fingerprinting with the primer M13. PCR fingerprinting revealed 55 VNI, five VNII, three VNIII, one VNIV, two VGI, two VGII, two VGIII and two VGIV isolates among those studied. The results show that most cryptococcosis cases in México are AIDS related and are caused by C. neoformans var. grubii, genotypes VNI and VNII. In addition this study revealed for the first time the presence of genotypes VNIV and VGII among Mexican clinical isolates. The present data show that all genotypes that have been described for the Cryptococcus species complex are found in México, indicating a much wider geographic distribution of genotypes than previously reported. The molecular analysis of Mexican cryptococcal isolates generated PCR-fingerprinting patterns which will provide references for future typing studies to allow the integration of Mexican cryptococcal genotypes into the ongoing global genotyping study of the Cryptococcus species complex.
Assuntos
Cryptococcus gattii/genética , Cryptococcus neoformans/genética , Impressões Digitais de DNA/métodos , Reação em Cadeia da Polimerase/métodos , Adolescente , Adulto , Idoso , Antifúngicos , Criança , Criptococose/epidemiologia , Feminino , Genótipo , Humanos , Masculino , México/epidemiologia , Pessoa de Meia-Idade , Filogenia , Estudos RetrospectivosRESUMO
OBJECTIVES: To investigate the prevalence of human papillomavirus (HPV), and HPV type 16 (HPV16) infection in cervical ectopy, and the presence of anti-HPV16 secretory IgA (sIgA) antibodies. METHODS: DNA from patients with cervical ectopy (n=218), HPV-associated lesions (n=111), and controls without evidence of cervical ectopy or HPV infection (n=93) were analyzed by PCR for the presence of HPV and HPV16. The presence of mucosal sIgA antibodies against HPV16 capsid antigens (VLP) was assayed in cervical mucus by ELISA. RESULTS: Prevalence of HPV DNA was higher in cervical ectopy than in controls (P=0.04; OR=2.06; 95% CI 0.99-4.33). HPV16 was 6.3 times more prevalent in cervical ectopy than in controls. Anti-HPV16 sIgA were detected more frequently in cervical ectopy patients than in controls (P=0.0004). CONCLUSIONS: Cervical ectopy correlates with HPV infection. HPV16 is highly prevalent in cervical ectopy. sIgA antibodies against HPV16 capsids are generated in patients with cervical ectopy.
Assuntos
Colo do Útero/patologia , Papillomaviridae , Infecções por Papillomavirus/patologia , Adulto , Proteínas do Capsídeo/imunologia , Muco do Colo Uterino/imunologia , Colo do Útero/virologia , DNA Viral/análise , Epitélio/patologia , Feminino , Humanos , Imunoglobulina A Secretora/imunologia , Papillomaviridae/genética , Papillomaviridae/imunologia , Infecções por Papillomavirus/imunologia , Fatores de RiscoRESUMO
The transcriptional terminator tI generates the 3'end of the integrase (int) gene transcript that is read from the lambda PI promoter in lambda phage. We have studied the factors that affect transcription termination in vitro and in vivo at the lambda tI terminator. In vitro transcriptional studies showed that tI is about 80% efficient in the presence of purified NusA protein, whereas it is only about 50% efficient in its absence. In vivo studies, where the readthrough transcript of lambda tI was measured by quantitative dot blot analysis, gave about 80% efficiency in wild-type strains, but only 60% in the nusA1 mutant strain at non-permissive temperatures. These results support the idea that termination at lambda tI in vivo involves interaction with the NusA factor.