Made available in DSpace on 2016-12-08T16:24:19Z (GMT). No. of bitstreams: 1 PGCA14MA143.pdf: 660934 bytes, checksum: 322caf24b166ea109317557fea920473 (MD5) Previous issue date: 2014-02-24 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / The forage intake is determinant on animal performance and can be changed when more than one type of forage are used. The aim of this work was to assess the effects of corn silage supplementation + soybean meal (9:1 as DM basis) fed as a proportion of 10 g DM kg-1 LW, to wethers receiving ryegrass (Lolium multiflorum Lam.) haylage with two forage offers: ad libitum or restrict amount, (60% of ad libitum DM intake). Eight wethers (average 31.5±2.2 kg of body live weight, LW) were used in a replicated 4 × 4 Latin Square design. Each experimental period conducted over 19 d, with a 14 of adaptation and 5 of measurements. Animals were fed three times a day (08:00h, 11:30h and 16:30h). Supplemented animals received corn silage at 08:00h and ryegrass haylage at 11:30h and 16:30h. The substitution rate was 0.93 in supplemented group ad libitum and zero in animal receiving restricted amount of ryegrass haylage. The digestible OM intake and N retention were similar in animals receiving ryegrass haylage ad libitum, but increased when ryegrass haylage was restricted. However, even with the supplementation animals receiving restricted amount of ryegrass haylage showed lower OM digestible intake and N retention compared to animals average of receiving ryegrass ad libitum. The OM digestibility and efficiency of rumen microbial protein synthesis were not affected by treatments, but the NDF and ADF digestibility were lower in supplemented animals compared to unsupplemented ones and in restricted compared to ad libitum diets. The corn silage supplementation could not be enough to avoid reductions on OM digestible intake and N retention to wethers receiving restrict amounts of ryegrass haylage / O consumo é determinante no processo produtivo, e pode ser modificado, quando é fornecido mais de um tipo de forragem na dieta. O objetivo deste trabalho foi avaliar os efeitos da suplementação com silagem de milho + farelo de soja (9:1 com base na MS) na proporção de 10 g de MS/kg PV, para cordeiros recebendo silagem pré-secada de azevém (Lolium multiflorum Lam) em duas ofertas de forragem: à vontade ou restrito (60% do consumo à vontade). Oito ovinos machos castrados cruza Texel × Crioula (média de 31,5 ± 2,2 kg de peso vivo, PV) foram usados em um delineamento experimental em Quadrado Latino 4 × 4. Cada período experimental foi realizado durante 19 dias, com 14 de adaptação e 5 de medidas. Os animais foram alimentados três vezes ao dia (08:00 h, 11:30 h e 16:30 h). Animais suplementados receberam silagem de milho às 08:00 h e silagem pré-secada de azevém às 11:30 h e às 16:30 h. As taxas de substituição foram 0,93 nos animais com oferta de azevém à vontade e zero nos que recebiam o mesmo em quantidade restrita. O consumo de MO digestível e a retenção nitrogenada não variaram com a suplementação nos animais que receberam o azevém à vontade, mas aumentaram nos animais com oferta restrita. Contudo, os animais com oferta restrita e suplementados tiveram menor consumo de MOD e retenção nitrogenada que a média dos que receberam azevém à vontade. A digestibilidade da MO e a eficiência de síntese de proteína microbiana não foram afetadas pelos tratamentos, mas a digestibilidade do FDN e FDA foi menor nos animais suplementados em comparação aos não suplementados e nos de oferta restrita em comparação a oferta à vontade. Mesmo com a suplementação, a restrição alimentar da forragem de base pode limitar a ingestão diária de MO digestível e a retenção diária de N em ovinos

Made available in DSpace on 2016-12-08T16:24:15Z (GMT). No. of bitstreams: 1 PGCA13MA109.pdf: 718774 bytes, checksum: 4cfe5eddf591c6526406aa72f7218dfb (MD5) Previous issue date: 2013-08-02 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / The ingestive and digestive interactions when diets with more than one type of forage are used have not been sufficiently studied. Thus, the aim of this study was to assess the effects of maize silage supplementation to weathers receiving ryegrass haylage on feed value of diet. The four treatments consisted of ryegrass haylage (RH, Lolium multiflorum Lam.) offered ad libitum without supplementation (WS) or supplemented with maize silage + soybean meal (9:1 on DM basis) in proportion of 5 (MS5), 10 (MS10) or 15 g (MS15) of DM/kg of live weight. Eight castrated male sheep (27.6 ± 3.5 kg live weight) were assigned in a 4 × 4 Latin square design with four periods of 18 days, with a 12 days of adaptation and 6 days of measurements. The total DM intake was not affected by treatments, but ryegrass DM intake decreased in animals receiving maize silage compared with animals without supplementation. The substitution rate was 1.6, 1.1 and 0.87 in animals receiving 5, 10 and 15 g/kg LW of supplement, respectively. The OM digestibility was not affected by supplementation, but the metabolisable energy intake and daily N retention were lower in animals receiving treatment MS5 compared with average of animals receiving treatments MS10 and MS15. The duodenal flow of microbial N increased with the level of supplementation, but duodenal flow of non-amonia N was similar between treatments. The lower level of maize silage supplement distributed during a single meal can negatively affect the energy intake and N retention / As interações ingestivas e digestivas decorrentes do fornecimento de dietas com mais de um tipo de forragem não têm sido suficientemente estudadas. Objetivou-se neste trabalho determinar a influência da inclusão de diferentes níveis de silagem de milho (Zea mays) para ovinos recebendo silagem pré-secada de azevém (Lolium multiflorium Lam.), sobre o valor alimentar da dieta. Os tratamentos experimentais consistiram de silagem pré-secada de azevém sem suplementação ou com suplementação de silagem de milho + farelo de soja (9:1 na MS) em níveis de 5 (SM5), 10 (SM10) ou 15 (SM15) g de MS/kg PV. Oito ovinos mestiços Texel × Ile de France, machos, castrados, com idade de aproximadamente 10 meses e peso vivo médio inicial de 27,6 ± 3,5 kg, foram distribuídos em um delineamento experimental em quadrado latino 4×4, com quatro períodos de 18 dias (12 de adaptação e 6 de coleta). O consumo total de MS não foi afetado pelos tratamentos, mas o consumo de azevém diminuiu nos animais suplementados em comparação aos não suplementados. As taxas de substituição de silagem pré-secada de azevém pelo suplemento foram 1,6, 1,1 e 0,86 nos tratamentos SM5, SM10 e SM15, respectivamente. A digestibilidade aparente da matéria orgânica não foi afetada pela suplementação, mas o consumo de energia metabolizável e a retenção diária de N foram inferiores no tratamento SM5 em comparação às médias dos tratamentos SM10 e SM15. O fluxo duodenal de nitrogênio proveniente de origem microbiana aumentou com o nível de suplementação, mas fluxo duodenal de N não amoniacal foi semelhante entre tratamentos. O fornecimento de forragem suplementar em quantidades inferiores a 10 g de MS/kg PV associada a redução do tempo de acesso ao suplemento em uma refeição principal pode diminuir o consumo de energia metabolizável e a retenção diária de nitrogênio

Porcine parvovirus (PPV) is considered to be one of the most important causes of reproductive failure in swine. Fetal death, mummification, stillbirths and delayed return to estrus are some of the clinical signs commonly associated with PPV infection in a herd. The virus genome is considered to be conservative, with substitution rates near to that of their host. However, it has been shown that some parvoviruses exhibit a substitution rate close to that commonly determined for RNA viruses. In this scenario, new PPV phenotypes may reduce the effectiveness of the currently used vaccines, recommending the continuous monitoring of the currently prevalent PPV strains. In addition, a number of novel porcine parvoviruses have been described during the last decade, but the importance and characteristics of these viruses remain unknown. In the present dissertation, three studies were performed to address the PPV genetic variability, to monitor the emergence of new PPV strains and the prevalence of novel parvoviruses. In the first study, recent PPV field isolates from Austria, Brazil, Germany and Switzerland were sequenced and analyzed. These samples, together with sequences retrieved from GenBank, were included in three datasets (viral protein complete gene, viral protein partial gene and non-structural protein complete gene). For each dataset, the nucleotide substitution rate was determined and a molecular clock estimated. The analysis revealed that for the new strains, the amino acids substitutions were located mainly in the viral capsid loops. Only the capsid protein datasets present the higher suitability for phylogenetic analysis. In them, a higher divergence was found, with three well defined clusters. By inferring the evolutionary dynamics of the PPV sequences, a nucleotide substitution rate of approximately 10 -4 substitutions per site per year was found for these datasets. An association of the phylogenetic tree with the molecular clock revealed that the main divergence of the PPV strains for the viral protein ocurred in the last 30 years. In the second study, the population dynamic of PPV isolates from swine herds was analyzed using PPV complete protein gene and partial sequences deposited in GenBank. The population dynamic of the virus was calculated using a Bayesian approach with a Bayesian skyline coalescent model. Additionally, an in vitro model was performed by twenty-one consecutives passages of the Challenge strain (a virulent field strain) and NADL2 strain (a vaccine strain) in PK15 cell-line supplemented with polyclonal antibodies raised against the vaccine strain (negative control was not supplemented). The Bayesian analysis indicated a decrease in the population diversity over the years and the predominance of some PPV strains. In agreement, the in vitro study revealed that a lower number of mutations appeared for both viruses in the presence of anti-PPV antibodies in comparison with the control passages without antibodies. In the third study, tonsils and hearts from 100 pigs were collected in a German slaughterhouse in 2010 and tested for PPV, porcine parvovirus 2 (PPV2), porcine parvovirus 3 (PPV3) and porcine parvovirus 4 (PPV4). Positive samples of PPV, PPV2 and PPV3 were sequenced. PPV was observed in 60/100 hearts and 61/100 tonsils and PPV2 in 55/100 hearts and 78/100 tonsils. PPV3 and PPV4 could not be detected in the heart samples but 20/100 and 7/100, respectively, of the tonsils were tested positive. The phylogenetic analysis of the PPV, PPV2 and PPV3 sequences revealed that the German samples could be divided in at least two clusters or clades for each virus. Altogether, it can be concluded that PPV is continuously evolving. Apparently, PPV vaccines largely used in the last 30 years probably have reduced the genetic diversity of the virus and induced the predominance of strains with distinct capsid profile from the original vaccine-based strain. Moreover, the high prevalence of the PPV, PPV2 and PPV3 and their genetic diversity highlight the importance of the continuous monitoring of these viruses.

The placement of genetic information within bacterial genomes is intentionally organized, creates predictable gradients of molecular properties along the origin-terminus of replication axis. Previous studies have reported that genes located near the origin of replication generally have a higher expression level, increased dosage, and are more conserved than genes located near the terminus of replication. Additionally, substitution rates usually increases with increasing distance from the origin of replication. However, the constant reorganization of genetic information is often overlooked when considering spatial molecular trends. Here, we explore the interplay of genomic reorganization along the origin and terminus of replication axis of gene expression and substitutions in Escherichia coli, Bacillus subtilis, Streptomyces, and Sinorhizobium meliloti. Using ancestral reconstruction to account for genome reorganization, we demonstrated that the correlation between the number of substitutions and distance from the origin of replication is significant but small and inconsistent in direction. In another study, we looked at the overall expression levels of all genes from the same bacteria, and confirmed that gene expression tends to decrease when moving away from the origin of replication. We looked specifically at how inversions - one type of genomic reorganization - impact gene expression between closely related strains of E. coli. Some inversions cause significant differences in gene expression compared to non-inverted regions, however, the variation in expression does not significantly differ between inverted and non-inverted regions. This change in gene expression may be due to the expression regulation properties of two nucleoid proteins, Histone-like Nucleoid-Structuring (H-NS) and Factor for inversion stimulation (Fis), who’s binding sites had a significant positive correlation with inverted regions. In conclusion, we highlight the impact that genomic rearrangements and location have on molecular trends in bacteria, illustrating the importance of considering spatial trends in molecular evolutionary analysis, and to ensure accurate generalization of previously determined trends. Assuming that molecular trends are exclusively in one direction can be problematic. / Dissertation / Doctor of Philosophy (PhD)

La donnée de séquences nucléotidiques permet d'inférer des arbres phylogénétiques, ou phylogénies, qui décrivent leur lien de parenté au cours de l'évolution. Associer à ces séquences leur date de prélèvement ou leur pays de collecte, permet d'inférer la localisation temporelle ou spatiale de leurs ancêtres communs. Ces données et procédures sont très utilisées pour les séquences de virus et, notamment, celles du virus de l'immunodéficience humaine (VIH), afin d'en retracer l'histoire épidémique à la surface du globe et au cours du temps. L'utilisation de séquences échantillonnées à des moments différents (ou hétérochrones) sert aussi à estimer leur taux de substitution, qui caractérise la vitesse à laquelle elles évoluent.Les méthodes les plus couramment utilisées pour ces différentes tâches sont précises, mais lourdes en temps de calcul car basées sur des modèles complexes, et ne peuvent traiter que quelques centaines de séquences. Devant le nombre croissant de séquences disponibles dans les bases de données, souvent plusieurs milliers pour une étude donnée, le développement de méthodes rapides et efficaces devient indispensable. Nous présentons une méthode de distances, Ultrametric Least Squares, basée sur le principe des moindres carrés, souvent utilisé en phylogénie, qui permet d'estimer le taux de substitution d'un ensemble de séquences hétérochrones, dont on déduit ensuite facilement les dates des spéciations ancestrales. Nous montrons que le critère à optimiser est parabolique par morceaux et proposons un algorithme efficace pour trouver l'optimum global.L'utilisation de séquences échantillonnées en des lieux différents permet aussi de retracer les chaînes de transmission d'une épidémie. Dans ce cadre, nous utilisons la totalité des séquences disponibles (~3 500) du sous-type C du VIH-1 (VIH de type 1), responsable de près de 50% des infections mondiales au VIH-1, pour estimer ses principaux flux migratoires à l'échelle mondiale, ainsi que son origine géographique. Des outils novateurs, basés sur le principe de parcimonie combiné avec différents critères statistiques, sont utilisés afin de synthétiser et interpréter l'information contenue dans une grande phylogénie représentant l'ensemble des séquences étudiées. Enfin, l'origine géographique et temporelle de ce variant (VIH-1 C) au Sénégal est précisément explorée lors d'une seconde étude, portant notamment sur les hommes ayant des rapports sexuels avec des hommes. / Nucleotide sequences data enable the inference of phylogenetic trees, or phylogenies, describing their evolutionary re-lationships during evolution. Combining these sequences with their sampling date or country of origin, allows inferring the temporal or spatial localization of their common ancestors. These data and methods are widely used with viral sequences, and particularly with human immunodeficiency virus (HIV), to trace the viral epidemic history over time and throughout the globe. Using sequences sampled at different points in time (or heterochronous) is also a mean to estimate their substitution rate, which characterizes the speed of evolution. The most commonly used methods to achieve these tasks are accurate, but are computationally heavy since they are based on complex models, and can only handle few hundreds of sequences. With an increasing number of sequences avail-able in the databases, often several thousand for a given study, the development of fast and accurate methods becomes essential. Here, we present a new distance-based method, named Ultrametric Least Squares, which is based on the princi-ple of least squares (very popular in phylogenetics) to estimate the substitution rate of a set of heterochronous sequences and the dates of their most recent common ancestors. We demonstrate that the criterion to be optimized is piecewise parabolic, and provide an efficient algorithm to find the global minimum.Using sequences sampled at different locations also helps to trace transmission chains of an epidemic. In this respect, we used all available sequences (~3,500) of HIV-1 subtype C, responsible for nearly 50% of global HIV-1 infections, to estimate its major migratory flows on a worldwide scale and its geographic origin. Innovative tools, based on the principle of parsimony, combined with several statistical criteria were used to synthesize and interpret information in a large phylogeny representing all the studied sequences. Finally, the temporal and geographical origins of the HIV-1 subtype C in Senegal were further explored and more specifically for men who have sex with men.

Reverse genetics is an innovative molecular biology tool that enables the manipulation of viral genomes at the cDNA level in order to generate particular mutants or artificial viruses. The reverse genetics system for the influenza virus is arguably one of the best illustrations of the potential power of this technology. This reverse genetics system is the basis for the ability to regularly adapt influenza vaccines strains. Today, reverse genetic systems have been developed for many animal RNA viruses. Selection-free reverse genetics systems have been developed for the members of the Reoviridae family including, African horsesickness virus, bluetongue virus and orthoreovirus. This ground-breaking technology has led to the generation of valuable evidence regarding the replication and pathogenesis of these viruses. Unfortunately, extrapolating either the plasmid-based or transcript-based reverse genetics systems to rotavirus has not yet been successful. The development of a selection-free rotavirus reverse genetics system will enable the systematic investigation of poorly understood aspects of the rotavirus replication cycle and aid the development of more effective vaccines, amongst other research avenues. This study investigated the importance of co-expressed rotavirus proteins in the development of a selection-free rotavirus reverse genetics system. The consensus sequences of the rotavirus strains Wa (RVA/Human-tc/USA/WaCS/1974/G1P[8]) and SA11 (RVA/Simian-tc/ZAF/SA11/1958/G3P[2]) where used to design rotavirus expression plasmids. The consensus nucleotide sequence of a human rotavirus Wa strain was determined by sequence-independent cDNA synthesis and amplification combined with next-generation 454® pyrosequencing. A total of 4 novel nucleotide changes, which also resulted in amino acid changes, were detected in genome segment 7 (NSP3), genome segment 9 (VP7) and genome segment 10 (NSP4). In silico analysis indicated that none of the detected nucleotide changes, and consequent amino acid variations, had any significant effect on viral structure. Evolutionary analysis indicated that the sequenced rotavirus WaCS was closely related to the ParWa and VirWa variants, which were derived from the original 1974 Wa isolate. Despite serial passaging in animals, as well as cell cultures, the Wa genome seems to be stable. Considering that the current reference sequence for the Wa strain is a composite sequence of various Wa variants, the rotavirus WaCS may be a more appropriate reference sequence. The rotavirus Wa and SA11 strains were selected for plasmid-based expression of rotavirus proteins, under control of a T7 promoter sequence, due to the fact that they propagate well in MA104 cells and the availability of their consensus sequences. The T7 RNA polymerase was provided by a recombinant fowlpox virus. After extensive transfection optimisation on a variety of mammalian cell lines, MA104 cells proved to be the best suited for the expression rotavirus proteins from plasmids. The expression of rotavirus Wa and SA11 VP1, VP6, NSP2 and NSP5 could be confirmed with immunostaining in MA104 and HEK 293H cells. Another approach involved the codon-optimised expression of the rotavirus replication complex scaffold in MA104 cells under the control of a CMV promoter sequence. This system was independent from the recombinant fowlpox virus. All three plasmid expression sets were designed to be used in combination with the transcript-based reverse genetics system in order to improve the odds of developing a successful rotavirus reverse genetics system. Rotavirus transcripts were generated using transcriptively active rotavirus SA11 double layered particles (DLPs). MA104 and HEK293H cells proved to be the best suited for the expression of rotavirus transcripts although expression of rotavirus VP6 could be demonstrated in all cell cultures examined (MA104, HEK 293H, BSR and COS-7) using immunostaining. In addition, the expression of transcript derived rotavirus VP1, NSP2 and NSP5 could be confirmed with immunofluorescence in MA104 and HEK 293H cells. This is the first report of rotavirus transcripts being translated in cultured cells. A peculiar cell death pattern was observed within 24 hours in response to transfection of rotavirus transcripts. This observed cell death, however does not seem to be related to normal viral cytopathic effect as no viable rotavirus could be recovered. In an effort to combine the transcript- and plasmid systems, a dual transfection strategy was followed where plasmids encoding rotavirus proteins were transfected first followed, 12 hours later, by the transfection of rotavirus SA11 transcripts. The codon- optimised plasmid system was designed as it was postulated that expression of the DLP-complex (VP1, VP2, VP3 and VP6), the rotavirus replication complex would form and assist with replication and/or packaging. Transfecting codon- optimized plasmids first noticeably delayed the mass cell death observed when transfecting rotavirus transcripts on their own. None of the examined coexpression systems were able to produce a viable rotavirus. Finally, the innate immune responses elicited by rotavirus transcripts and plasmid-derived rotavirus Wa and SA11 proteins were investigated. Quantitative RT-PCR (qRT-PCR) experiments indicated that rotavirus transcripts induced high levels of the expression of the cytokines IFN- α1, IFN-1β, IFN-λ1 and CXCL10. The expression of certain viral proteins from plasmids (VP3, VP7 and NSP5/6) was more likely to stimulate specific interferon responses, while other viral proteins (VP1, VP2, VP4 and NSP1) seem to be able to actively suppress the expression of certain cytokines. In the light of these suppression results, specific rotavirus proteins were expressed from transfected plasmids to investigate their potential in supressing the interferon responses provoked by rotavirus transcripts. qRT-PCR results indicated that cells transfected with the plasmids encoding NSP1, NSP2 or a combination of NSP2 and NSP5 significantly reduced the expression of specific cytokines induced by rotavirus transcripts. These findings point to other possible viral innate suppression mechanisms in addition to the degradation of interferon regulatory factors by NSP1. The suppression of the strong innate immune response elicited by rotavirus transcripts might well prove to be vital in the quest to better understand the replication cycle of this virus and eventually lead to the development of a selection-free reverse genetics system for rotavirus. / PhD (Biochemistry), North-West University, Potchefstroom Campus, 2014

Reverse genetics is an innovative molecular biology tool that enables the manipulation of viral genomes at the cDNA level in order to generate particular mutants or artificial viruses. The reverse genetics system for the influenza virus is arguably one of the best illustrations of the potential power of this technology. This reverse genetics system is the basis for the ability to regularly adapt influenza vaccines strains. Today, reverse genetic systems have been developed for many animal RNA viruses. Selection-free reverse genetics systems have been developed for the members of the Reoviridae family including, African horsesickness virus, bluetongue virus and orthoreovirus. This ground-breaking technology has led to the generation of valuable evidence regarding the replication and pathogenesis of these viruses. Unfortunately, extrapolating either the plasmid-based or transcript-based reverse genetics systems to rotavirus has not yet been successful. The development of a selection-free rotavirus reverse genetics system will enable the systematic investigation of poorly understood aspects of the rotavirus replication cycle and aid the development of more effective vaccines, amongst other research avenues. This study investigated the importance of co-expressed rotavirus proteins in the development of a selection-free rotavirus reverse genetics system. The consensus sequences of the rotavirus strains Wa (RVA/Human-tc/USA/WaCS/1974/G1P[8]) and SA11 (RVA/Simian-tc/ZAF/SA11/1958/G3P[2]) where used to design rotavirus expression plasmids. The consensus nucleotide sequence of a human rotavirus Wa strain was determined by sequence-independent cDNA synthesis and amplification combined with next-generation 454® pyrosequencing. A total of 4 novel nucleotide changes, which also resulted in amino acid changes, were detected in genome segment 7 (NSP3), genome segment 9 (VP7) and genome segment 10 (NSP4). In silico analysis indicated that none of the detected nucleotide changes, and consequent amino acid variations, had any significant effect on viral structure. Evolutionary analysis indicated that the sequenced rotavirus WaCS was closely related to the ParWa and VirWa variants, which were derived from the original 1974 Wa isolate. Despite serial passaging in animals, as well as cell cultures, the Wa genome seems to be stable. Considering that the current reference sequence for the Wa strain is a composite sequence of various Wa variants, the rotavirus WaCS may be a more appropriate reference sequence. The rotavirus Wa and SA11 strains were selected for plasmid-based expression of rotavirus proteins, under control of a T7 promoter sequence, due to the fact that they propagate well in MA104 cells and the availability of their consensus sequences. The T7 RNA polymerase was provided by a recombinant fowlpox virus. After extensive transfection optimisation on a variety of mammalian cell lines, MA104 cells proved to be the best suited for the expression rotavirus proteins from plasmids. The expression of rotavirus Wa and SA11 VP1, VP6, NSP2 and NSP5 could be confirmed with immunostaining in MA104 and HEK 293H cells. Another approach involved the codon-optimised expression of the rotavirus replication complex scaffold in MA104 cells under the control of a CMV promoter sequence. This system was independent from the recombinant fowlpox virus. All three plasmid expression sets were designed to be used in combination with the transcript-based reverse genetics system in order to improve the odds of developing a successful rotavirus reverse genetics system. Rotavirus transcripts were generated using transcriptively active rotavirus SA11 double layered particles (DLPs). MA104 and HEK293H cells proved to be the best suited for the expression of rotavirus transcripts although expression of rotavirus VP6 could be demonstrated in all cell cultures examined (MA104, HEK 293H, BSR and COS-7) using immunostaining. In addition, the expression of transcript derived rotavirus VP1, NSP2 and NSP5 could be confirmed with immunofluorescence in MA104 and HEK 293H cells. This is the first report of rotavirus transcripts being translated in cultured cells. A peculiar cell death pattern was observed within 24 hours in response to transfection of rotavirus transcripts. This observed cell death, however does not seem to be related to normal viral cytopathic effect as no viable rotavirus could be recovered. In an effort to combine the transcript- and plasmid systems, a dual transfection strategy was followed where plasmids encoding rotavirus proteins were transfected first followed, 12 hours later, by the transfection of rotavirus SA11 transcripts. The codon- optimised plasmid system was designed as it was postulated that expression of the DLP-complex (VP1, VP2, VP3 and VP6), the rotavirus replication complex would form and assist with replication and/or packaging. Transfecting codon- optimized plasmids first noticeably delayed the mass cell death observed when transfecting rotavirus transcripts on their own. None of the examined coexpression systems were able to produce a viable rotavirus. Finally, the innate immune responses elicited by rotavirus transcripts and plasmid-derived rotavirus Wa and SA11 proteins were investigated. Quantitative RT-PCR (qRT-PCR) experiments indicated that rotavirus transcripts induced high levels of the expression of the cytokines IFN- α1, IFN-1β, IFN-λ1 and CXCL10. The expression of certain viral proteins from plasmids (VP3, VP7 and NSP5/6) was more likely to stimulate specific interferon responses, while other viral proteins (VP1, VP2, VP4 and NSP1) seem to be able to actively suppress the expression of certain cytokines. In the light of these suppression results, specific rotavirus proteins were expressed from transfected plasmids to investigate their potential in supressing the interferon responses provoked by rotavirus transcripts. qRT-PCR results indicated that cells transfected with the plasmids encoding NSP1, NSP2 or a combination of NSP2 and NSP5 significantly reduced the expression of specific cytokines induced by rotavirus transcripts. These findings point to other possible viral innate suppression mechanisms in addition to the degradation of interferon regulatory factors by NSP1. The suppression of the strong innate immune response elicited by rotavirus transcripts might well prove to be vital in the quest to better understand the replication cycle of this virus and eventually lead to the development of a selection-free reverse genetics system for rotavirus. / PhD (Biochemistry), North-West University, Potchefstroom Campus, 2014