Since 2004, when the Long Term Evolution (LTE) was first proposed to be publicly available in the year 2009, a plethora of new characteristics, techniques and applications have been constantly enhancing it since its first release, over the past decade. As a result, the research aims for LTE-Advanced (LTE-A) have been released to create a ubiquitous and supportive network for mobile users. The incorporation of heterogeneous networks (HetNets) has been proposed as one of the main enhancements of LTE-A systems over the existing LTE releases, by proposing the deployment of small-cell applications, such as femtocells, to provide more coverage and quality of service (QoS) within the network, whilst also reducing capital expenditure. These principal advantages can be obtained at the cost of new challenges such as inter-cell interference, which occurs when different network applications share the same frequency channel in the network. In this thesis, the main challenges of HetNets in LTE-A platform have been addressed and novel solutions are proposed by using self-organising network (SON) management approaches, which allows the cooperative cellular systems to observe, decide and amend their ongoing operation based on network conditions. The novel SON algorithms are modelled and simulated in OPNET modeler simulation software for the three processes of resource allocation, mobility management and interference coordination in multi-tier macro-femto networks. Different channel allocation methods based on cooperative transmission, frequency reuse and dynamic spectrum access are investigated and a novel SON sub-channel allocation method is proposed based on hybrid fractional frequency reuse (HFFR) scheme to provide dynamic resource allocation between macrocells and femtocells, while avoiding co-tier and cross-tier interference. Mobility management is also addressed as another important issue in HetNets, especially in hand-ins from macrocell to femtocell base stations. The existing research considers a limited number of methods for handover optimisation, such as signal strength and call admission control (CAC) to avoid unnecessary handovers, while our novel SON handover management method implements a comprehensive algorithm that performs sensing process, as well as resource availability and user residence checks to initiate the handover process at the optimal time. In addition to this, the novel femto over macro priority (FoMP) check in this process also gives the femtocell target nodes priority over the congested macrocells in order to improve the QoS at both the network tiers. Inter-cell interference, as the key challenge of HetNets, is also investigated by research on the existing time-domain, frequency-domain and power control methods. A novel SON interference mitigation algorithm is proposed, which is based on enhanced inter-cell interference coordination (eICIC) with power control process. The 3-phase power control algorithm contains signal to interference plus noise ratio (SINR) measurements, channel quality indicator (CQI) mapping and transmission power amendments to avoid the occurrence of interference due to the effects of high transmission power. The results of this research confirm that if heterogeneous systems are backed-up with SON management strategies, not only can improve the network capacity and QoS, but also the new network challenges such as inter-cell interference can also be mitigated in new releases of LTE-A network.

The thesis systematically investigates the laser interference nanomanufacturing technology taking into account its advantages and abilities to realise various potential applications. The latest progresses have addressed the major issues hampering the cross-scale developments of structural applications, such as cost-ineffective fabrication, limited area, low efficiency and challenging integration. The studies carried out on high-resolution and large-area laser interference nanomanufacturing technology will complement the exploration of modern optical devices and extraordinary functional applications. With respect to classical interference theory and relevant references, there is still a lack of studies providing insight into the effects of polarisation on the multi-beam interference while it is found that the polarisation vector plays a key role in the formation, period and contrast of interfering patterns. Herein, the theory of multi-beam interference is developed through the integration of the polarisation vector and electric field vector. It is worth pointing out that based on the detailed analysis of the four-beam interference with the special polarisation modes, it is demonstrated that the modulation phenomenon in four-beam laser interference is the result of the misalignment of incident angles or unequal incident angles only in the case of the TE-TE-TM-TM mode. In the experiments, a straightforward method of generating various well-defined structures on material surfaces is proposed using the nanosecond laser interference system. The experimental results of two-, three- and four-beam interference show a good correspondence to the theoretical analyses and simulations. Artificial bio-structures are fabricated using the four-beam interference method with the TE-TE-TE-TE polarisation mode and the fabricated microcone structures exhibit excellent properties with both a high contact angle (CA=156.3°) and low omnidirectional reflectance (5.9-15.4%). In order to fabricate high-resolution structures, the 266nm nanosecond laser interference system is employed to treat the organic and metal-film materials. Nanograting structures with feature sizes of sub-100nm width and 2nm height are fabricated on the organic material surface. An attempt is successfully conduced to produce the nanoelectrode arrays by using laser interference lithography and chemical deposition. Finally, the advantages of the developed laser interference technology and contributions of the research are summarised, and recommendations of future work are given.

M.Ing. / In this investigation charge balancing will be investigated from an Electro-Magnetic- Compatibility perspective. The primary sources of common mode Electro-Magnetic- Interference in switching converters are the switching nodes. This is mainly due to the parasitic capacitance between the switching node and the reference earth. Filtering components that are currently used take up a lot of valuable space resulting in the products overall size and cost to increase. Combating common mode current at the source will drastically reduce the size or the need for these large filters. This investigation will focus on a simple method of reducing common mode noise (produced by the switching node), of a two wire system, at the source by making use of a compensating winding which requires very little or no additional space; a buck converter will be used to illustrate the concept. The investigation will start with an overview of Electro-Magnetic-Interference and its components (common and differential mode noise). This investigation will deal with the measurement of common and differential mode noise as well as general Electro-Magnetic-Interference measurement. A design of the buck converter and its drive circuit will also be presented. Reducing the common mode noise by making use of charge balancing using planar inductors will then be presented. This investigation contains the theoretical analysis as well as experimental results to validate the theory. The experiments show encouraging results in using this technique to minimise common mode noise in switched-mode-power-supplies.

Background. Wireless connectivity is simple and convenient for the user. This is the reasons why it is predominantly used today for local networks at home. However the potential drawbacks facing this technology is unknown to many of its users. This study is aimed at examining some of these issues in the context of what is used today.Objectives. This study intends to research what types of security features and frequency settings are being used today. It also aims to evaluate what this means in the context of security and usability effecting the user.Methods. The approach of this study is to gather networks in different geographical areas. To do this a Raspberry Pi with an external antenna is used. When the data collection is completed, the networks are broken down into categories. Results. The results show significant frequency overlap on the most commonly used channels. There are vastly more overlap in areas with apartment buildings compared to other residential areas. The results also show that most networks are using secure encryption settings. Conclusions. Careful selection of channels is required to minimise interference, but methods for doing so is specific for each environment. Security wise there are no big concerns except when it comes to password selection.

In prokaryotes, CRISPR/Cas9 system provides molecular immunity to bacteria and archaea against invading phages, conjugative plasmids and nucleic acids. CRISPR/Cas9 system has been adapted for targeted genome editing across diverse eukaryotic species for a variety of applications in basic and applied research. In this dissertation, I propose to adapt the CRISPR/Cas9 system to function as molecular immunity machinery against plant DNA viruses. Therefore, to test whether the CRISPR/Cas9 system is portable to plants, I produced plants stably over-expressing Cas9 and sgRNAs against single or multiple DNA viruses in Nicotiana benthamiana (N. benthamiana) and tomato (Solanum lycopersicum) plants. sgRNAs targeting the Cas9 endonuclease against different coding and non-coding viral sequences were tested in virus- interference experiments. I explored the possibility of generating robust interference against single and multiple DNA viruses. Subsequently, I studied the possibility of virus evasion of the CRISPR/Cas9 machinery and evolution of the virus escapees. Finally, I produced N. benthamaiana and tomato plants stably expressing the CRISPR/Cas9 machinery for developing durable virus resistance. Furthermore, developing effective viral-interference system in plants will help to understand the molecular underpinning of virus biology and host-defense mechanisms against plant viruses. In conclusion, my research project attempted to establish the efficacy and extend the utility of CRISPR/Cas9 system for viral interference in plants which promise exciting applications including producing engineered plants resistant to multiple viral infection.

A dissertation submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfilment of the requirements for the degree of Master of Science. Johannesburg, 2014. / RNA interference (RNAi) is a highly conserved gene regulatory mechanism triggered by the presence of double-stranded RNAs and results in post-transcriptional and transcriptional gene silencing. RNAi has been demonstrated to have therapeutic potential to treat chronic viral infections including HIV-1. Due to the side effects of and eventual drug resistance to highly active antiretroviral therapy, a novel anti-HIV-1 therapy is required. The most suitable exogenous RNAi triggers to use in anti-HIV-1 RNAi-based therapy are expressed short hairpin RNAs (shRNAs). Despite being highly developed, shRNA systems still pose safety concerns. Highly expressed shRNAs are at risk of over-saturating the endogenous RNAi pathway, inducing an innate immune response or silencing off-target mRNA. The purpose of this study was to minimise shRNA-associated off-target effects and simultaneously maximise the potency and specificity of expressed shRNAs for potential therapeutic application. ShRNAs shorter than 19 base pairs are not recognised by the endonuclease Dicer, which is an important component of the RNAi pathway, but miR-451 is Dicer-independent. Smaller shRNAs that retain their potency would be easier to deliver into a disease model. For this study, 25mers and miR-451-mimicking 19mers were generated. The shRNA pairs exhibited significant knockdown of their respective targets in dual-luciferase assays. The 19mers are more specific gene silencers compared to the 25mers. A 19mer that is more potent than its 25mer counterpart was identified. None of the hairpins induced an innate immune response, caused cytotoxic effects or saturated the endogenous RNAi pathway. This study concludes that the 19mers were processed in a manner similar to miR-451 resulting in a single ~30 nt mature RNA product. We dubbed these miR-451-mimicking 19mers, guide shRNAs. The single RNA strand of mature guide shRNAs abolishes the risk sense strand-associated off-targeting thus improving shRNA specificity. These revolutionary guide shRNAs can be developed into highly potent activators of the RNAi pathway in a therapeutic setting.

ABSTRACT Cassava is currently the second most important source of carbohydrates on the African continent. In the last two decades, cassava crops have been severely affected by outbreaks of cassava mosaic disease (CMD). South African cassava mosaic virus (SACMV) has been associated with CMD outbreaks in the Mpumalanga province. Advances in post-transcriptional gene silencing (PTGS) technology have provided promising new strategies for the engineering of virus resistance in plants. Inverted repeat (IR) constructs are currently the most potent inducers of PTGS, however, these constructs are inherently unstable. The purpose of this study was to develop IR constructs with an improved stability for the efficient induction of PTGS in plants. Two mismatched inverted repeat constructs, one targeting the SACMV BC1 open reading frame, the other targeting the Maize streak virus (MSV) AC1 open reading frame, were successfully created. Sodium bisulfite was used to deaminate cytosine residues on the sense arm of the constructs. The resulting number of GT mismatches was seemingly sufficient to stabilize the linear conformation of the IR constructs, as they were efficiently propagated by E.coli DH5!, and subsequently behaved like linear DNA molecules. Furthermore, it was found that the number of mismatches on the BC1 construct (17.5%) was ideal, as the subsequent stability of the predicted RNA hairpin was not affected. Due to the higher number of mismatches on the AC1 construct (23.5%), it was found that the loop region of the RNA hairpin was marginally destabilized. Despite this, long stretches of stable dsRNA were still produced from the AC1 IR construct, and is likely to induce PTGS. Interestingly, it was observed that the mismatched IR constructs, although still replicated in E.coli, were marginally destabilized in Agrobacterium. Therefore, it was deduced that the stability of a mismatched IR construct may be influenced by the particular intracellular environment of an organism. Due to the recalcitrance of cassava to transformation, a model plant system, Nicotiana benthamiana, was used to screen constructs for toxicity, stability, and efficiency of PTGS induction. Agrobacteriummediated transformation and regeneration of N. benthamiana was optimized, and 86% transformation efficiency was achieved when using leaf disk explants. It was found that the addition of an ethylene scrubber, potassium permanganate, substantially increased the rate of regeneration by reducing the frequency of hyperhydritic plants. Transgene iv integration was confirmed by PCR amplification of the hptII gene in the T-DNA region. Transgene expression was confirmed by screening for GUS and GFP reporter genes. No toxic responses to the transgene have been observed thus far. Studies are currently underway to confirm the stability of the mismatched IR constructs in N. benthamiana. PAGE Northern blotting is being done, as the detection of siRNAs derived from the transgene will confirm that constructs are functional. In addition, infectivity assays are underway to determine the efficacy of BC1 knockdown by a stably integrated construct. Due to the enhanced stability of mismatched IR constructs, they may be an appealing alternative to currently available intron-spliced, or exact matched hairpin systems.

[pt] Dois dos principais fatores que afetam o desempenho dos sistemas de comunicação sem fio são a ocorrência de chuvas ao longo do percurso de transmissão e a existência de interferências externas. Para garantir um desempenho adequado para o enlace, é usual estabelecer limites para as percentagens de tempo durante as quais o desempenho do sistema pode ficar abaixo de alguns níveis pré-estabelecidos. importante que, tanto a degradação de desempenho provocada pela chuva quanto aquela devida às interferências externas sejam tais que as restrições de desempenho sejam atendidas. A degradação devida a chuvas é usualmente considerada no dimensionamento do enlace, uma vez que os modelos matemáticos para a atenuação por chuvas são amplamente conhecidos. No caso de interferências externas, a degradação por elas causada é limitada através do estabelecimento de restrições ao comportamento estatístico das potências dos sinais interferentes. Estas restrições, atualmente em estudo no âmbito da União Internacional de Telecomunicações, devem ser tais que, independentemente das características específicas do sistema interferente considerado, as condições de desempenho requeridas para o enlace sejam satisfeitas. O presente trabalho define um problema de otimização com restrições, cuja solução permite estabelecer as condições a serem impostas ao comportamento estatístico das potências dos sinais interferentes presentes em um enlace. / [en] Two of the main factors that affect the performance of wireless communication systems are fading due to rain and interfering signals that reach the receiver. To guarantee an adequate communication link performance, it is usual to limit the percentages of time during which the system performance may be below certain predefined levels. It is important that performance degradation due to both rain and external interferences be such that these performance constraints are met. Degradation due to rain is usually considered in the communication link design, as mathematical models for rain attenuation are widely known. For external interferences, degradation is usually limited by establishing constraints to the statistical behaviour of the interfering signal power. These constraints should be such that, independently of the specific characteristics of the considered interfering system, link performance objectives can be met. Studies aiming the definition of adequate constraints are currently being developed within the International Telecommunication Union. This dissertation defines a constrained optimization problem that allows for the definition of the constraints to be satisfied by the statistical behaviour of the interfering signal power so that link performance are met.

O antimônio é um elemento encontrado em baixas concentrações no meio ambiente. No entanto, a sua determinação tem despertado grande interesse devido ao conhecimento de sua toxicidade e da crescente aplicação na indústria. A determinação de antimônio tem sido um desafio para os pesquisadores uma vez que o elemento é encontrado em baixas concentrações, o que faz de sua análise uma tarefa difícil. Portanto, embora a análise por ativação de nêutrons (NAA) seja um método adequado para a determinação de vários elementos em diferentes tipos de matriz, no caso de Sb, a análise apresenta algumas dificuldades. A principal dificuldade é devido às interferências espectrais. O objetivo desta pesquisa foi validar o método de NAA para a determinação de Sb em amostras ambientais. Para estabelecer condições adequadas para a determinação de Sb, ensaios preliminares foram realizados para posterior análise de materiais de referência certificados (MRC). O procedimento experimental consistiu em irradiar amostras juntamente com padrão sintético de Sb por períodos de 8 ou 16 horas no reator nuclear de pesquisa IEA-R1, seguido de espectrometria de raios gama. A quantificação de Sb foi realizada pela medição dos radioisótopos de 122Sb e 124Sb. Ensaios preliminares indicaram a presença de Sb em papel de filtro Whatman, utilizado no preparo do padrão, porém em teor muito baixo, podendo ser considerado desprezível. No caso do material plástico utilizado como invólucro para a irradiação da amostra, foi verificado que ele deve ser escolhido cuidadosamente, pois dependendo do plástico, este pode conter Sb. A análise da estabilidade da solução padrão diluída de Sb, dentro do período de oito meses, mostrou que não há alteração significativa na concentração deste elemento. Os resultados obtidos nas análises dos materiais de referência certificados indicaram a formação de radioisótopos de 76As e também de 134Cs e 152Eu, podendo interferir na determinação de Sb pela medição de 122Sb, devido à proximidade de energias dos raios gama emitidos. Além disso, a alta atividade do 24Na pode mascarar o pico do 122Sb e dificultar a sua detecção. As análises dos MRC indicaram que a exatidão e a precisão dos resultados de Sb dependem principalmente do tipo e composição da matriz, da sua concentração na amostra, do radioisotopo medido e do tempo de decaimento utilizado para a medição. A avaliação dos componentes que contribuem para a medição da incerteza da concentração de Sb, mostrou que a maior contribuição da incerteza é dada pela estatística de contagem da amostra. Os resultados da avaliação da incerteza indicaram também que o valor da incerteza padrão combinada depende do radioisótopo medido e do tempo de decaimento utilizado para as contagens. Este estudo mostrou que a NAA é um método bastante adequado na determinação de Sb em amostras ambientais, possibilitando a obtenção de resultados com baixos valores de incerteza e por ser uma técnica puramente instrumental, permite a análise de um grande número de amostras. / Antimony is an element found in low concentrations in the environment. However, its determination has attracted great interest due to the knowledge of its toxicity and increasing application in industry. The determination of antimony has been a challenge for researchers since this element is found in low concentrations which make its analysis a difficult task. Therefore, although neutron activation analysis (NAA) is an appropriate method for the determination of various elements in different types of matrix, in the case of Sb its analysis presents some difficulties, mainly due to spectral interferences. The objective of this research was to validate the NAA method for Sb determination in environmental samples. To establish appropriate conditions for Sb determinations, preliminary assays were carried out for further analysis of certified reference materials (CRM). The experimental procedure was to irradiate samples with a synthetic Sb standard for a period of 8 or 16 hours in the IEA-R1 nuclear research reactor, followed by gamma ray spectrometry. The quantification of Sb was performed by measuring the radioactive isotopes of 122Sb and 124Sb. The results of preliminary assays indicated the presence of Sb in Whatman no 40 filter paper used in the preparation of the synthetic standard, but at very low concentrations, which could be considered negligible. In the case of the plastic material used in bags for the sample irradiation, it should be chosen carefully, because depending on the thickness, they may contain Sb. The analyses of the stability of the diluted Sb standard solution showed no change in the Sb concentration within eight months after its preparation. Results obtained in the analysis of certified reference materials indicated the interference of 76As and also of 134Cs and 152Eu in the Sb determinations by measuring 122Sb, due to the proximity of the gamma ray energies. The high activity of 24Na can also mask the peak of 122Sb hindering its detection. The analysis of CRM indicated that the accuracy and precision of the results depend on the type of matrix analyzed, its concentration in the sample, radioisotope measured and of the decay time used for the measurements. The analysis of the components that contribute to the uncertainty of the Sb concentration indicated that the largest uncertainty contribution is given by statistical counting of the sample. The findings also showed that the value of combined standard uncertainty depends on the radioisotopes of Sb measured and the decay time used for counting. This study showed that NAA is a very adequate method for Sb determinations in environmental samples furnishing results with low uncertainty values.

A raiva é uma zoonose que afeta todos os mamíferos e causa cerca de 55.000 mortes humanas por ano, causada pelo vírus da raiva. O vírus da raiva pertence à Ordem Mononegavirales, Família Rhabdoviridae e o Gênero Lyssavirus. Ultimamente, o Protocolo de Milwaukee é a base do tratamento humano, com indução do paciente ao coma e uso de massiva terapia antiviral. O protocolo, embora tenha sido utilizado duas vezes com sucesso, inclusive em um caso brasileiro, ainda requer aperfeiçoamentos. Neste sentido, a interferência por RNA (RNAi) é uma nova abordagem para terapia de doenças virais. O objetivo deste trabalho foi avaliar a inibição da replicação do vírus da raiva in vitro e in vivo utilizando RNAi. Para este fim, foram utilizados três siRNAs (siRNA 360, siRNA 652, siRNA 649) com a fita antisenso complementar ao mRNA da fosfoproteína (P) e três siRNAs (Le 1, Le 2, Le 3) contra o RNA líder do vírus da raiva. Para o ensaio in vitro foram utilizadas as amostras PV e 4005 (AgV3) do vírus da raiva e as células de BHK-21 (Baby hamster kidney). As monocamadas celulares foram infectadas com as amostras PV ou 4005 e depois de 2 horas de incubação transfectadas com cada um dos siRNAs em combinação com Lipofectamine 2000TM. Depois de 24 e 48 horas as placas teste e controle foram submetidas à imunofluorescência direta (IFD) com conjugado globulina de coelho anti-ribonucleocapsídeo do vírus da raiva/isotiocianato de fluoresceína (Instituto Pasteur de São Paulo). Os resultados revelaram que os siRNAs contra o RNA líder do vírus não foram capazes de inibir a replicação do vírus. A utilização dos siRNAs contra mRNA P resultaram em títulos de 3,625logTCID50/ml, 3,875logTCID50/ml e 4,125logTCID50/ml para os siRNAs 360, 649 e 652, respectivamente, enquanto que, para a placa controle, o título foi 4,0logTCID50/ml nas placas infectadas com PV e período de incubação de 24h. Nas placas infectadas com a amostra 4005 e tratadas com siRNAs, a maior queda de título viral foi na placa tratada com siRNA 360, de 1,0 log, comparando-se com a placa controle de incubação de 24 para a amostra 4005. Nas placas tratadas com siRNA 649 e siRNA 652, também houve a diminuição de título viral, mas em uma escala menor (0,25log e 0,125log, respectivamente) comparando-se com o controle. Nas placas infectadas com PV e incubadas durante 48h, os títulos apresentados foram de 5,625logTCID50/ml, 4,625logTCID50/ml e 4,75logTCID50%/ml para os siRNAs 360, 649 e 652, respectivamente, enquanto que na placa controle o título foi 6,0logTCID50C%/ml. A placa com período de incubação de 48h com a amostra 4005 e tratada com siRNA 360 apresentou a maior queda de título viral entre os três siRNAs, o que resultou em 1,125log de diferença. Nas monocamadas onde foram administrados siRNA 649 e siRNA 652, observou-se também uma pequena queda de título viral igual a 0,875log e 0,295log, respectivamente, comparando-se com a placa não tratada. Para o ensaio in vivo, foram usados camundongos albino suíços de 21 dias com peso entre 11 e 14g, infectados com a cepa PV e AgV3 em 10DL50% via intracerebral. Duas horas depois da infecção, foi inoculada por via intracerebral uma solução do siRNA 360 com Lipofectamine 2000TM. Os animais com paralisia foram eutanasiados e aqueles sobreviventes foram observados até completar 30 dias de observação quando foram, então, eutanasiados. O sistema nervoso central de todos os animas foi recolhido e submetido a IFD. A utilização do siRNA 360 em camundongos resultou em 30% de animais sobreviventes frente amostra 4005, enquanto que a mortalidade nos animais não tratados foi de 90%. Nos animais inoculados com a amostra PV e tratados com este siRNA, a sobrevivência foi de 40%, enquanto que no grupo controle a mortalidade foi de 100%. O resultado do ensaio in vitro demonstra que os siRNAs utilizados são capazes de inibir a replicação do vírus da raiva, com eficiência mais pronunciada para o siRNA 360. In vivo, este siRNA foi capaz de induzir a proteção parcial dos animais inoculados com as duas variantes virais. Estes resultados, ainda que indiquem a necessidade de mais estudos, permitem concluir que a RNAi é uma tecnologia promissora como antiviral contra a raiva / Rabies is a zoonotic disease that affects all mammals and causes more than 55.000 human deaths every year, caused by rabies virus (RABV) a virus of the Mononegavirales order, Family Rhabdoviridae and the Lyssavirus genus. After the onset of the symptoms, the illness has a fast progression and the patients feel intense physical suffering. Currently, human rabies treatment has been based on the Milwaukee Protocol which consists on the induction of coma and massive antiviral therapy. Despite this protocol has been successful in two cases, including a Brazilian one, more studies on antivirals for human rabies treatment are required. RNA interference is a new antiviral approach, which gives hope to the possibility of rabies antiviral treatment. The aim of this study was to assess the decrease in titres of rabies virus in vitro and in vivo using short-interfering RNAs. To this end, three siRNAs (siRNA 360, siRNA 652, and siRNA 649) were used with antisense strands complementary to rabies virus phosphoprotein (P) mRNA and three other (Le 1, Le 2, Le 3) to the leader RNA. Pasteur virus strain (PV) and strain 4005 (AgV3) of rabies virus and BHK-21 cells were used, and the monolayers were transfected with each of the RNAs with Lipofectamine-2000 TM. After 22 hours, the siRNA-treated and the control plates were tested by direct fluorescent antibody test (DFAT) with anti-rabies virus nucleocapsid antibody conjugate with fluorescein isothiocianate (Pasteur Insitutte, Brazil). The plates transfected with siRNA against phosphoprotein mRNA were also incubated for 48 hours and subjected to IFD assay. Virus titres were calculated by the Spearman-Karber method. The results showed that siRNAs against virus leader RNA were not able to inhibit the replication of the virus. The use of siRNAs against P mRNA resulting titres of 3.625logTCID50/ml 3.875logTCID50/ml and 4.125logTCID50/ml for siRNAs 360, 649 and 652, respectively, while, for the control plate, the titre was 4.0logTCID50/ml in plates with PV and 24h incubation period. In plates with strain 4005 and treated with siRNAs, the highest viral titre decrease was obtained with siRNA 360, with a 1.0 log difference compared to the control plate of strain 4005 incubated for 24h. The plates treated with siRNA 649 and siRNA 652 have was also shown a decrease in viral titres, but on a smaller scale (0.25log and 0.125log, respectively) compared to the control. The plates infected with PV and incubated for 48 hours showed titre of 5.625logTCID50/ml, 4.625logTCID50/ml and 4.75logTCID50%/ml for siRNAs 360, 649 and 652, respectively, while for the control plate the titre was 6.0logTCID50C%/ml. The plate with strain 4005 and then treated with siRNA360 and incubated for a total of 48h had the highest viral titre decrease among the three siRNAs, which resulted in a 1.125log difference compared to the control plate. In monolayers treated with siRNA649 and siRNA652 there was also a discrete drop in viral titres (0.875log and 0.295log, respectively) compared to the control plate. For the in vivo assay, 21-day old Swiss albino mice weighing between 11 and 14g were intracerebrally inoculated with PV or 4005 strains (10DL50%). Two hours after inoculation, a solution of siRNA360 with Lipofectamine 2000 TM was also intracerebrally injected. Mice presenting paralysis and those that survived the 30 days of observation were euthanized. The central nervous system of all animals was collected and submitted to IFD. The use of siRNA360 in mice resulted in survival of 30% of animals in the group inoculated with strain 4005, whereas 90% mortality was observed in the control group. In animals inoculated with the PV strain, and treated with siRNA360, the survival rate was 40% and in the control group the mortality was 100%. The results of the in vitro assay demonstrate that the siRNAs used are effective in inhibiting the replication of rabies virus with a more intense inhibition regarding siRNA 360. In vivo, this siRNA was able to induce partial protection of animals infected with both viral variants. These results also indicate that, despite the need for further studies, RNAi is a promising technology as antiviral against rabies