Made available in DSpace on 2014-06-12T15:04:58Z (GMT). No. of bitstreams: 2 arquivo1766_1.pdf: 916614 bytes, checksum: d16125fdbdb2b99a4f6d33952c69a16b (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) Previous issue date: 2006 / O bicudo do algodoeiro, Anthonomus grandis Boheman, é considerado a maior praga da cotonicultura mundial, ocasionando danos que repercutem principalmente na produtividade, qualidade do algodão colhido e gasto com medidas de controle. Neste estudo foi realizada pela primeira vez, uma análise da diversidade e estrutura genética das populações naturais de A. grandis do Brasil. Doze populações coletadas em seis estados brasileiros (Paraíba, Ceará, Bahia, Pará, Mato Grosso e Goiás) em áreas onde são praticadas a agricultura em escala empresarial e agricultura familiar, foram avaliadas pelas técnicas de Polimorfismo do DNA Amplificado Randomicamente (RAPD), Isoenzimas e Microssatélite. Os resultados obtidos em seis populações pela técnica de RAPD baseados em 25 loci, revelaram uma heterozigosidade média de 0,262, com polimorfismo (P) variando de 52 a 84%. A diferenciação genética entre as populações foi extremamente elevada e significativa (GST = 0,258; p < 0,05), refletindo a existência de baixo fluxo gênico entre as mesmas (Nm = 0,72). A análise de cinco populações com 6 loci alozímicos mostrou uma heterozigosidade média de 0,212 e polimorfismo (P) variando entre 25 e 100%. O índice de diferenciação genética FST obtido por este marcador entre as populações correspondeu a 0,544 (p < 0,05), sugerindo a ocorrência de baixo fluxo gênico (Nm = 0,210) entre as populações. A heterozigosidade e o polimorfismo (P) observados em onze populações pela análise de 8 loci de microssatélites variaram entre 0,038 e 0,224 e de 37,5 a 75%, respectivamente. O FST entre as populações correspondeu a 0,220, produzindo um Nm de 0,8. Os três marcadores moleculares utilizados revelaram que as populações de A. grandis dos estados brasileiros avaliados apresentam baixa diversidade genética, em comparação às populações dos Estados Unidos, México e demais países da América do Sul, sugerindo que a colonização deste inseto ocorreu em uma ou poucas áreas. Os resultados obtidos relativos à diversidade genética também permitiram distinguir populações oriundas de regiões onde é praticada a agricultura em escala empresarial das áreas de agricultura familiar, assim como mostrou que as populações do nordeste podem estar servindo de fonte para colonização de novas áreas e de áreas já tratadas

The bromeliad family comprises about 3,000 species distributed in 58 genera and 3 subfamilies: Pitcarnioideae, Bromelioideae and Tillandsioideae. The increasing demand of the market has been responsible for increasing the production and sale of bromeliads. However the illegal extraction is still dramatically reducing existing species. This fact, coupled with the devastation of Brazilian ecosystems, has caused irreparable losses in diversity. Considering this fact, have a basis with stored genetic material for future studies is very important. The main reason for the establishment and maintenance of a germplasm bank is to store and make available germplasm and provide information regarding certain accessions. The aim of the work was to perform the molecular characterization of accessions of native bromeliads prospected in Sergipe State, using tools such as RAPD and ISSR molecular markers and flow cytometry. The collections were performed in four counties of the Sergipe state (Itabaiana, Frei Paulo, Simão Dias e Poço Redondo), whose locations were mapped with the use of a GPS and the individuals were kept in a greenhouse, composing a Active Germplasm Bank (AGB). For molecular analyzes young leaves were collected and used for DNA extraction. Eleven ISSR primers and 13 RAPD primers were used to characterize the prospected accessions. Analyses by flow cytometry were performed for the determination of DNA content, using young leaves and extraction of nuclei was performed following the method of Dolezel. ISSR and RAPD markers detected large genetic variability among the accessions of the AGB. The estimation of the DNA content obtained by flow cytometry of the bromeliad accessions collected in four municipalities of Sergipe State allowed the distinction of two groups (group 1 = 1,59 pg and group 2 = 1,057 pg). / A família bromeliácea compreende aproximadamente 3.000 especies, distribuídas em 58 gêneros e 3 subfamílias: Pitcarnioideae, Bromelioideae e Tillandsioideae. A crescente demanda de mercado tem sido responsável pelo aumento da produção e comercialização das bromélias. No entanto o extrativismo ilegal ainda existente está reduzindo drasticamente as espécies. Esse fato, somado à devastação dos ecossistemas brasileiros, tem causado perdas irreparáveis na diversidade. Diante desse fato, ter uma base com material genético guardado para futuros estudos é muito importante. A principal razão para o estabelecimento e a manutenção de um banco de germoplasma é armazenar e disponibilizar germoplasma e prover informações a respeito de determinado acesso. O objetivo do trabalho foi realizar a caracterização molecular dos acessos de bromélias nativas prospectadas no Estado de Sergipe, empregando ferramentas como marcadores moleculares RAPD, ISSR e citometria de fluxo. As coletas foram realizadas em quatro municípios do Estado de Sergipe (Itabaiana, Frei Paulo, Simão Dias e Poço Redondo), cujos locais foram mapeados com o auxílio de GPS e os indivíduos foram conservados em casa de vegetação, compondo um Banco Ativo de Germoplasma (BAG). Para as análises moleculares folhas jovens foram coletadas e utilizadas para a extração do DNA. Onze iniciadores ISSR e 13 iniciadores RAPD foram utilizados para a caracterização dos acessos prospectados. As análises por citometria de fluxo foram realizadas para a determinação do conteúdo de DNA, usando folhas jovens e as extrações dos núcleos foram realizadas seguindo o método de Dolezel. Os marcadores ISSR e RAPD detectaram ampla variabilidade genética entre os acessos do BAG. A estimativa do conteúdo de DNA obtido pela citometria de fluxo dos acessos de bromélias coletados nos quatro municípios de Sergipe possibilitou a distinção de dois grupos (grupo 1 = 1,59 pg e grupo 2 = 1,057 pg).

O setor agropecuário responde atualmente por cerca de 9,2% do Produto interno bruto (PIB) brasileiro, sendo que a cana-de-açúcar ocupa cerca de 9% da área cultivada, fato que lhe confere especial relevância com relação ao desenvolvimento nacional. Os dois produtos mais importantes desta cultura são o açúcar e o álcool etílico produzido por fermentação com leveduras. Durante o processo de fermentação alcoólica, o fermento sofre inúmeras reciclagens e interferências externas advindas do caldo, do ambiente e de outras fontes, tornando-se vulnerável à contaminação por outros microrganismos e mesmo leveduras indesejáveis. Métodos de monitoramento microbiológico que possibilitem a discriminação das linhagens de forma rápida e inequívoca, além de baratos, são altamente desejáveis. A utilização de meios diferenciais e seletivos, métodos bioquímicos e análise molecular tem se mostrado eficientes, porém são demorados e dispendiosos. A reação ‘killer’ é um fenômeno descoberto há 40 anos em S. cerevisiae, e resultados satisfatórios já foram obtidos na caracterização de leveduras, considerando-se o perfil de sensibilidade ‘killer’. O padrão de sensibilidade às toxinas killer foi utilizado nesse projeto em leveduras industriais (isoladas de processo fermentativo para produção de etanol). Os dados gerados com os testes de sensibilidade às toxinas Killer geraram polimorfismos entre as linhagens, mesmo em nível intra-específico, validando a metodologia na biotipagem das leveduras. As informações obtidas subsidiam o desenvolvimento de uma metodologia de biotipagem aplicável para o monitoramento microbiológico na indústria sucro-alcooleira, com a seleção de nove leveduras killer contra as quais as leveduras industriais apresentaram um perfil característico de sensibilidade, dependendo do grupo ao qual pertencem (S. cerevisiae ou não Saccharomyces). Finalmente, vale citar que os testes foram corroborados pelos resultados obtidos com a taxonomia clássica e pelos métodos de biologia molecular com reações de PCR (Polymerase Chain Reaction) e RAPD (Random Amplified Polimorphism DNA). / Agriculture is an important sector in the economy of Brazil. The sugar cane occupies 9% of the cultivated area in this country. The most important products from the sugar cane industry are sugar and alcohol, the latest produced by fermentative process by yeasts. During the fermentation the yeast population changes due to the interferences coming from the sugar cane juice or other sources, turning the process susceptible to undesirable contaminations. In this way, fast, reliable and cheap methods for microbiological monitoring can be helpful. Selective culture media, biochemical tests and molecular analyses have been used but they are time-consuming or expensive. The killer phenomenon discovered initially in Saccharomyces cerevisiae have shown interesting results to yeast biotyping. The sensibility pattern to different killer toxins was used to make a “fingerprinting” and successfully separate different strains of yeasts. This method was corroborated by classical taxonomy and molecular biology results (PCR and RAPD-PCR). The results obtained gives support to development of a methodology useful on fermenting microbiologic monitoring with the selection of nine strains of killers yeasts with highly discrimination between industrial bakker yeasts and contaminants of the fermentation process.

Zvýšená konzumace fermentovaných mléčných výrobků v posledních letech vede k zavádění nových výrobků na trh. Funkční a probiotické produkty jsou v dnešní době také hojně rozšířeny. Cílem diplomové práce bylo posoudit mikrobiální kvalitu komerčních jogurtů a nefarmakologických probiotických výrobků. Bylo zkoumáno 24 vzorků jogurtů a 8 vzorků probiotických mléčných výrobků. Pozornornost byla zaměřena zvláště na kvantifikaci mikroorganismů v jednotlivých výrobcích a na sledování viability buněk. Většina mléčných produktů obsahovala počty odpovídající minimální požadované hodnotě 1x107cfu/ml. Nicméně byly objeveny produkty, které neobsahovaly živé bakterie nebo obsahovaly jen jejich menší množství. To platí zejména pro běžné jogurty. Probiotické mléčné výrobky v zásadě obsahovaly větší množství bakterií než jogurty, protože je u nich navíc požadováno 1x106cfu/ml minimálního množství specifických bakterií jiných než jogurtových startovacích kultur. Isoláty z fermentovaných mléčných výrobků byly identifikovány jako Streptococcus thermophilus and Lactobacillus spp. Isoláty byly poté rozlišeny na jednotlivé kmeny pomocí RAPD použitím tří různých primerů. Byla zjištěna velká různorodost mezi kmeny rodu Lactobacillus spp. používaných různými podniky.

No description available.

La fusariose vasculaire du cyclamen est une maladie causée par le champignon tellurique Fusarium oxysporum f. sp. cyclaminis. Elle est considérée comme l’une des maladies les plus graves du cyclamen et se traduit par des pertes atteignant jusqu’à 50 % de la production. Actuellement, les moyens de lutte ne permettent pas de contrôler la maladie. Dans ce contexte, une collaboration s’est engagée entre l’institut technique de l’horticulture, Astredhor, représentant les producteurs, l’INRA de Dijon pour son expertise sur F. oxysporum et la société Agrene pour son expertise en lutte biologique. Les objectifs de cette collaboration étaient doubles : i) identifier un marqueur spécifique de la forme spéciale cyclaminis et développer un outil de détection de l’agent pathogène permettant de mettre en place des méthodes de lutte appropriées ; ii) identifier un agent de lutte biologique efficace contre le pathogène. Le travail s’est donc structuré autour de ces deux objectifs.Une collection de souches représentatives de la diversité des populations de F. oxysporum f. sp. cyclaminis a été constituée. Elle regroupe des souches provenant de collections internationales et des isolats obtenus de cyclamens symptomatiques ou non. L’analyse moléculaire de cette collection a permis de caractériser son importante diversité génétique et a mis en exergue la difficulté d’identifier un marqueur moléculaire spécifique. Néanmoins, un fragment d’ADN spécifique de l’agent pathogène a pu être mis en évidence par amplification aléatoire d’ADN polymorphe. A partir de ce fragment, un couple d’amorces spécifiques a été dessiné et un outil moléculaire a été développé. Ce dernier permet une détection du champignon in planta en PCR conventionnelle et en PCR en temps réel.Parallèlement, une étude bibliographique approfondie relative aux méthodes de lutte biologique contre les fusarioses induites par F. oxysporum sur les plantes ornementales a été effectuée. Cette revue a souligné la possibilité d’utiliser des ressources d’origine microbienne et d’origine végétale pour contrôler F. oxysporum, mais cette stratégie impliquant une étape de sélection nous est apparue lourde et laborieuse. Nous avons opté pour une autre démarche visant à identifier, parmi des produits déjà sur le marché, ceux susceptibles de réduire significativement la gravité de la maladie. Des bioessais ont été conduits en serre, dans des conditions proches de celles de la production pour tester sept produits reposant sur la formulation de bactéries, de champignons ou de combinaisons de ces microorganismes. Les produits les moins performants ont été éliminés à l’issue d’un premier essai. Des bioessais ont été conduits à nouveau avec trois produits. Un seul de ces produits donne satisfaction mais son efficacité devra être validée en conditions de production réelles.En conclusion, l’outil de détection spécifique permettra aux producteurs de s’assurer de la qualité sanitaire de la culture et des supports de culture. L’agent de lutte biologique retenu à l’issue de nos essais permettra dans un premier temps aux producteurs de prévenir le risque d’activité infectieuse de F. oxysporum f. sp. cyclaminis. Cependant, un travail de recherche d’un agent de lutte plus performant s’avère nécessaire. Des pistes sont proposées. / Fusarium wilt of cyclamen is one of the most damaging diseases of cyclamen. The causal agent, Fusarium oxysporum f. sp. cyclaminis, is a soil-borne fungus. Losses can reach more than 50 % of the production. Several methods of control are available, but none of them offer an efficient and environmentally friendly solution. In this context, a project was developed in collaboration with the French institute of horticulture, Astredhor, which represents the producers, the INRA of Dijon, for its expertise on F. oxysporum and the company Agrene for its expertise in biological control. The project has two goals: i) design a molecular marker specific of Fusarium oxysporum f. sp. cyclaminis allowing a better management of the disease, ii) identify one or several efficient biological control agents.A collection of strains representative of the diversity of F. oxysporum f. sp. cyclaminis populations was made up with strains from international collections and isolates collected from symptomatic and asymptomatic cyclamens. A molecular study of the collection demonstrated the high genetic diversity of the forma specialis, which makes the identification of a specific molecular marker more complicated. However, a specific DNA fragment was identified by random amplified polymorphic DNA. A primer pairs was designed and a specific tool of detection was developed. Thanks to this tool, it is now possible to detect the fungus in planta by conventional and real-time PCR.Simultaneously, a broad literature analysis on the biocontrol of ornamental plant diseases caused by F. oxysporum was performed. The review emphasized that biocontrol of F. oxysporum encompassed both microbial biocontrol agents and botanicals. To avoid the laborious and time-consuming screening step, we decided to assess the antagonistic activity of seven commercial products containing bacteria, fungi or a combination of both microorganisms. Greenhouse trials were performed under conditions similar to those of the production. First trial led to the exclusion of the less efficient products. Other trials were conducted with the three remaining products. Disease reduction was obtained with one of these products although it must be validated in production.Finally, the molecular tool of detection will allow producers to insure the health status of the culture. In addition, the efficient biocontrol agent identified will prevent the disease progress for a while but more investigations are needed to obtain reliable, efficient and sustainable biocontrol agents. Proposals to improve Fusarium wilt control are discussed.

Τρεις ευρέως χρησιμοποιούμενες μέθοδοι τυποποίησης, μια βιοχημική (API20NE), μια φαινοτυπική (SDS-PAGE) και μια μοριακή (RAPD) χρησιμοποιήθηκαν για την ταυτοποίηση και ταξινόμηση 160 περιβαλλοντικών ψευδομονάδων που απομονώθηκαν από το υδάτινο περιβάλλον της Νοτιοδυτικής Ελλάδας και συγκεκριμένα από εμφιαλωμένα νερά (46%), νερά δικτύου ύδρευσης (16%), κολυμβητικών δεξαμενών (9%) και θαλασσών (29%). Οι ψευδομονάδες ταυτοποιήθηκαν με βάση το βιοχημικό τους αποτύπωμα δια μέσου του συστήματος ΑΡΙ20ΝΕ, και στη συνέχεια υποβλήθηκαν σε ηλεκτροφόρηση των ολικών πρωτεϊνών τους (SDS-PAGE) και σε ανάλυση του γενετικού τους υλικού με τη μέθοδο RAPD (Random Amplified Polymorphic DNAs) με χρήση δύο διαφορετικών δεκαμερών εκκινητών (primers). Το σύστημα API20NE ταυτοποίησε το 88% των στελεχών διακρίνοντας 14 ομάδες-είδη, ενώ η SDS-PAGE ταξινόμησε το 98.1% σε 20 ομάδες και η RAPD το 94% των στελεχών σε 22 και 34 ομάδες, με εκκινητή τον OPA-13 και τον OPD-13 αντίστοιχα. Η ταξινόμηση προέκυψε με εφαρμογή της ανάλυσης κατά συστάδες (cluster analysis) των αποτυπωμάτων (πρωτεϊνικών και γενετικών) που παρήγαγαν τα στελέχη. Τα 20 στελέχη που δεν ταυτοποιήθηκαν σε επίπεδο είδους με το API20NE, ταξινομήθηκαν με την SDS-PAGE σε ποσοστό 100%, ενώ με την RAPD σε ποσοστό 90%. Οι τρεις μέθοδοι συγκρίθηκαν ως προς την επαναληψιμότητα (reproducibility), την ικανότητα τυποποίησης (typeability) και τη διακριτική ικανότητα (discriminatory power). Την μεγαλύτερη επαναληψιμότητα έδωσαν το API20NE και η RAPD με τον εκκινητή OPA-13, την μεγαλύτερη ικανότητα τυποποίησης η SDS-PAGE, ενώ τη μεγαλύτερη διακριτική ικανότητα έδωσε η RAPD με τον εκκινητή OPD-13. Η πλέον σωστή ταξινόμηση, όπως προέκυψε από τη διακριτή ανάλυση, επιτεύχθη με τη μέθοδο SDS-PAGE. Η παρούσα εργασία αποδεικνύει ότι τα βιοχημικά συστήματα ταυτοποίησης (όπως το API20NE) μπορούν να χρησιμοποιηθούν με αξιοπιστία μόνο για αδρή αναγνώριση των περιβαλλοντικών ψευδομονάδων. Πληροφορίες σε βάθος για την ταυτότητα και τη φύση τους μπορούν να εξαχθούν με τη περαιτέρω εφαρμογή ηλεκτροφορητικών και μοριακών μεθόδων. Δεδομένης της ευρείας διασποράς, της ετερογένειας και της, έστω και δυνητικής, παθογόνου δράσης των ψευδομονάδων, είναι σημαντικό, από πλευράς δημόσιας υγείας, ο προσδιορισμός της ταυτότητάς τους να γίνεται με συνδυασμένη εφαρμογή βιοχημικών, ηλεκτροφορητικών και μοριακών μεθόδων ώστε να καθίσταται δυνατή η αναγνώριση στελεχών που μπορούν να αποτελέσουν αιτιολογικούς παράγοντες ασθενειών, ιδιαίτερα σε ομάδες υψηλού κινδύνου. / Three broadly used typing techniques, one biochemical (API20NE), one phenotypic (SDS-PAGE) and one molecular (RAPD), were employed for the identification and taxonomy of 160 environmental pseudomonas isolated from the aquatic environment in Southwestern Greece. In particular, the isolates were obtained from bottled waters (46%), potable waters (16%), waters from swimming pools (9%) and seawaters (29%). The isolates were identified by the system API20NE and then subjected to whole-cell protein electrophoresis (SDS-PAGE) and Random Amplified Polymorphic DNAs (RAPD) using two 10-mer primers. The API20NE system identified 88% of the whole bacterial population and classified them in 14 species, while SDS-PAGE classified 98.1% of the isolates in 20 groups and RAPD classified 94% of the strains in 22 groups using the primer OPA-13 and 34 groups using the primer OPD-13. The classification was achieved by applying cluster analysis in the protein or RAPD fingerprints of the isolates. Twenty isolates that could not be identified by the API20NE system, at least to the species level, were classified by the SDS-PAGE and the RAPD in a percentage of 100% and 90%, respectively. The reproducibility, typeability and discriminatory power of the three methods were compared to evaluate their application. The API20NE and the RAPD assay with primer OPA-13 showed better reproducibility in comparison with the other methods; the higher typeability was achieved by the SDS-PAGE assay while the higher discriminatory power was that obtained by the RAPD method with the primer OPD-13. The SDS-PAGE gave the higher percentage of “correctly classified” isolates, as it was assessed by discriminant analysis. This study shows that the rapid identification systems, such as the API20NE, may be reliable only for a rough characterization of environmental Pseudomonas. In order to acquire further information about their identities, other phenotypic and molecular techniques have to be applied. Given the ubiquity, heterogeneity and pathogenicity, either established or potential, of the environmental pseudomonas it is important, from a public health point of view, to monitor the identities of environmental Pseudomonas isolates using the combination of specific methods, so as to be possible for strains, which can serve as causative agents of diseases, especially in high risk population, to be recognizable.

In many countries, the authorities face extreme difficulties in monitoring and ensuring that food sold on the street is safe, that is, fit for human consumption. This is particularly the case in urban areas, where people buy food on the street because it is readily available and relatively inexpensive. The objective of this study was to determine the food safety knowledge and microbial hazard awareness of street food consumers, and to assess the bacteriological quality of selected ready-to-eat foods sold by street vendors in the Johannesburg municipality. A cross-sectional survey study was conducted and a total of 402 respondents who buy and consume street-vended foods were randomly selected at various street food vending locations. A total of 315 various street-vended samples were purchased from randomly selected street food vendors at different vending locations in Johannesburg metropolis, in order to investigate the bacteriological quality of street-vended foods. Results of the bacteriological analysis revealed that total aerobic counts ranged from 0.3*102 - 0.4*105 cfu/g in cereals and grain-based foods; 0.4*102 - 0.5*105 cfu/g in meat-, dairy- and fish-based foods and 0.7*102 - 0.9*104 cfu/g in fruit- and vegetable-based foods. None of the food samples tested positive for Salmonella spp and Staphylococcus aureus. Results of the survey showed that the majority of respondents were black males younger than 35 years. Individuals of different gender, race, level of education and monthly income groups significantly (p<0.05) differed in their responses regarding the frequency of purchasing and confidence in the safety of street-vended food. Better taste followed closely by affordability and accessibility were the most cited reasons for purchasing street-vended food / Life and Consumer Sciences / M. Sc. (Life Sciences)