Call number: LD2668 .T4 1984 A4 / Master of Science

Thesis (PhD)--Stellenbosch University, 2015. / ENGLISH ABSTRACT: Bovine tuberculosis (BTB), caused by bacteria of the Mycobacterium tuberculosis complex is reported to cause economic and public health negative impact in countries where it is prevalent. The control of the disease has been a difficult task worldwide. The main object of this thesis was to use molecular tools to generate useful information to contribute to the design of appropriate BTB control measures in Mozambique. To do so we considered a deep knowledge of the BTB history in Mozambique to be essential. The search was largely based on the reports produced annually by the Veterinary Services and other available information. We found reports of BTB in Mozambique as early as 1940. These cases were mainly identified as a result of post-mortem meat inspection. The higher numbers of cases reported were from 8 locations, namely Maputo, Magude, Vilanculos, Beira, Chimoio, Tete, Quelimane and Nampula, and served as a basis to decide the locations to perform prevalence and molecular epidemiologic studies. Prevalence studies were done in 10 districts selected based on the history of a high number of BTB case reports (intentionally biased towards locations presumably with higher prevalence), a high cattle density, but also to represent districts from the south, centre and north of Mozambique. A representative sample was defined, based on all livestock areas or villages in Massingir and Govuro Districts or by randomly selecting small-scale and commercial herds in 8 districts, specifically Manhiça, Chibuto, Buzi, Gondola, Mutarara, Mogovolas, Angoche and Mecanhelas. Results were obtained from 6983 cattle tested using tuberculin testing. Apparent prevalence varied from 0.98% in Massingir to 39.6% in the Govuro, with prevalence as high as 71.4% in some livestock areas/herds. The analysis of risk factors showed no noteworthy difference with respect to the sex of the animal. Younger age had significantly lower odds of infection compared to the older age class. There was a tendency of cattle from small-scale herds to have lower prevalence when compared to the commercial herds. From the prevalence studies, 187 tissue and 41 milk samples from BTB reactors were collected. Additionally 220 tissue samples were obtained from the Central Veterinary Laboratory routine diagnostic work. Samples were subject to bacteriological culture and a collection of 170 M. bovis isolates were obtained. Eight additional isolates were supplied from another study. All isolates were subjected to molecular typing using spoligotyping, and a sub-sample using MIRU-VNTR and regions of difference (RD) analysis. Fifteen different spoligotype patterns were identified of which 8 were not previously registered in the Mbovis.org database. The pattern SB0961 accounted for 61% of the isolates and was found in all areas of the country investigated. We hypothesize that this was one of the first clones to be introduced in Mozambique. Twenty-nine isolates had the pattern SB0140, which is specific for the European 1 (Eu1) clonal complex. Eleven isolates with this spoligotype were subjected to RD analysis, and all isolates had the Eu1 specific deletion. These were all isolated from cattle from the south of Mozambique and the majority from commercial farms that imported cattle, mainly from South Africa, where the Eu1 clonal complex is common. There were no isolates of the African 1 (Af1) or African 2 (Af2) clonal complexes that are frequent in Central-West Africa and East Africa, respectively. The clones identified from different farms and districts, strongly suggest routes of transmission and/or common source of infection. In conclusion, our results show a potential increase in the prevalence of BTB in Mozambique even taking into consideration i) that the selection of locations in our study was biased towards locations with a history of higher BTB prevalence and ii) the use of a more sensitive technique i.e. the testing in the middle neck region as opposed to the testing in the caudal fold as used in previous studies. Even if no cattle to human transmission was found in studies done in Mozambique so far, the evidence of M. bovis shedding through milk and the lack of correct practices to prevent animal to human transmission (consumption of raw milk), strongly suggests that there is zoonotic risk; a subject that needs to be investigated. The results presented in this work also strengthen the need to reinforce the current regulations that require a negative BTB test result before cattle importation. The same should be enforced for the internal movements, as the frequency of shared genotypes (Spoligotype and MIRU) from cattle originating from different parts of the country strongly suggest intra-contry transmission of BTB. / AFRIKAANSE OPSOMMING: Beestering (BTB), wat veroorsaak word deur bakterieë van die Mycobacterium tuberculosis kompleks, het ‘n negatiewe impak op die ekonomiese en publike gesondheid in lande waar dit voorkom. Die beheer van die siekte is ‘n moeilike taak wêreldwyd. Die hoofdoel van hierdie tesis was om molekulêre toetse te gebruik om nuttige inligting te genereer wat sal bydra tot die ontwikkeling van toepaslike BTB beheermaatrëels in Mosambiek. Om dit te kon doen, was dit noodsaaklik om ‘n indiepte kennies te hê van BTB geskiedenis in Mosambiek. Die soektog was gebaseer op jaarlikse verslae van Veearts Dienste en ander beskikbare inligting. Ons het verslae gevind van BTB in Mosambiek so vroeg as 1940. Hierdie gevalle is hoofsaaklik geïdentifiseer as gevolg van roetine na-doodse inspeksie van vleis. Hoër getalle van sulke gevalle is geïdentifiseer in 8 distrikte, naamlik Maputo, Magude, Vilanculos, Beira, Chimoio, Tete, Quelimane en Nampula; en het gedien as ‘n basis vir die seleksie van studieareas vir die voorkoms studies. Voorkoms studies is uitgevoer in 10 distrikte gekies op grond van die geskiedenis van 'n hoër aantal BTB gevalle in hierdie areas (doelbewus bevooroordeeld teenoor plekke vermoedelik met 'n hoër voorkoms), asook‘n hoë digtheid beeste, maar ook om distrikte in die suide, middel en noorde van Mosambiek te verteenwoordig. ‘n Verteenwoordigende steekproef is geïdentifiseer gebaseer op al die vee-gebiede of dorpe in Massingir and Govuro distrikte óf deur kleinskaalse en kommersiële kuddes lukraak te kies in 8 distrikte, spesifiek Manhica, Chibuto, Busi, Gondola, Mutarara, Mogovolas, Angoche en Mecanhelas. Resultate is verkry deur 6983 beeste te toets met behulp van die tuberkulien vel toets. Skynbare voorkoms het gewissel van 0,98 % in Massingir tot 39,6 % in Govuro, met voorkoms so hoog as 71,4 % in sommige vee gebiede/ kuddes. Die ontleding van risiko faktore het geen noemenswaardige verskil met betrekking tot die geslag van die dier gewys nie. Jonger ouderdom diere het ‘n aansienlike laer kans van infeksie gehad in vergelyking met die ouer ouderdom klas. Daar was 'n neiging van beeste van kleinskaalse kuddes om ‘n laer voorkoms te hê in vergelyking met die kommersiële kuddes. Van die voorkoms studies, is 187 weefsel- en 41 melkmonsters van BTB reaktors ingesamel. ‘n Addisionele 220 weefselmonsters is verkry vanaf die Sentrale Veterinêre Laboratorium se roetine diagnostiese werk. Monsters was onderhewig aan bakteriologiese kweking en 'n versameling van 170 M. bovis isolate is verkry. Agt bykomende isolate is voorsien deur 'n ander studie. Alle isolate was onderhewig aan molekulêre-tipering met behulp van spoligotipering en ‘n subgroep met behulp van MIRU-VNTR en analise van genomies diverse areas. Vyftien verskillende spoligotipering patrone is geïdentifiseer, waarvan 8 nie voorheen in die Mbovis.org databasis geregistreer is nie. Die SB0961 patroon is geïdentifiseer vir 61% van die isolate en gevind in alle dele van die land wat ondersoek was. Ons hipotese is dat hierdie een van die eerste klone was wat voorgestel is in Mosambiek. Nege en twintig isolate het die SB0140 patroon gehad wat spesifiek is aan die Europese 1 (EU1) klonale kompleks. Elf isolate met hierdie spoligotipering patroon is verder geanaliseer om genomies diverse areas te identifiseer, waarvan almal die Eu1 spesifieke delesie getoon het. Hierdie isolate is almal geïsoleer uit beeste van die suide van Mosambiek, asook beeste gevind op kommersiele plase wat hoofsaaklik vanuit Suid Afrika invoer- waar die EU1 klonale kompleks algemeen is. Daar is geen isolate van die Afrikaans 1 (AF1) of Afrikaans 2 (AF2) klonale komplekse nie, dikwels gevind in onderskeidelik Sentraal-Wes-Afrika en Oos- Afrika. Isolate wat in verskillende plase en distrikte geïdentifiser is dui roetes van transmissie en/ of a gemeenskaplike bron van infeksie aan. Ten slotte, ons resultate dui op 'n moontlike toename in die voorkoms van BTB in Mosambiek, selfs met inagneming dat i) die keuse van areas in ons studie is bevooroordeeld teenoor areas met 'n geskiedenis van hoër BTB voorkoms en ii) die gebruik van 'n meer sensitiewe tegniek d.w.s. toetsing in die middel nekgebied i.p.v. toetsing in die stert vou soos gebruik in vorige studies. Selfs al is geen bees-na-mens-oordrag gevind nie, is die bewys van M. bovis oordrag deur melk en die gebrek aan korrekte prosedures om dier-na-mens-oordrag te voorkom (verbruik van nie-gepasturiseerde melk), ‘n sterk bewys van die soönotiese risiko; ‘n onderwerp wat ondersoek moet word. Die resultate van hierdie ondersoek beklemtoon die behoefte om die huidige regulasies wat ‘n negatiewe BTB toetsuitslag vereis voor beeste ingevoer word, te versterk. Dieselfde maatreëls moet ingestel word vir interne beweging van beeste, omdat die frekwensie van gedeelde genotipes (Spoligotipering en MIRU) tussen beeste met oorsprong uit verskillende dele van die land aandui dat interne oordrag van BTB plaasvind.

Earthworms, Lumbricus terrestris, were challenged orally and intracoelomically with two bacterial species, Aeromonas hydrophila and Pseudomonas aeruginosa, and mortality rates were observed. Neither were found to be particularly pathogenic at injected doses of up to 108 bacteria per earthworm. The influence of Cu++ (as CuSO4) on the earthworm's response to bacterial challenge was investigated by exposing earthworms to sublethal levels of Cu++ prior to bacterial challenge. Exposure at sublethal concentrations up to 3 m g/cm2 did not have a pronounced influence on host resistance to challenge as measured by earthworm mortality. Cu++ increased the earthworm's ability to agglutinate rabbit erythrocytes, indicating that Cu++ exposure caused coelomocyte death, autolysis and release of agglutinins into the coelom, possibly explaining resistance to bacterial challenge.

Aquaculture is being seriously considered as a promising sustainable industry in the Sultanate of Oman. Fish farming commenced in Oman in 1986, but it was only in 2011 that it became a more commercially driven sector. While worldwide aquaculture production is expected to rise to meet the shortage in capture fisheries, there is a parallel requirement to identify potential threats to the health and welfare of existing aquatic farmed stocks and to take appropriate steps to mitigate them. As aquaculture in Oman is in an early stage of development, it is important to acquire baseline data on the existence and prevalence of aquatic diseases and pathogens to help the Government make policy decisions to develop health management regimes applicable for Omani aquaculture. Therefore, this study was conducted to evaluate current farming practices of tilapia in Oman, to investigate the bacterial species composition and distribution from different sites in some of the economically important fish species, and to study the characteristics and pathogenicity of Aeromonas species. The current practices were studied for 9 Nile tilapia (Oreochromis niloticus) farms from four areas (Al Batinah, Ad Dhahirah, Ad Dakhiliyah and Ash Sharqiyah North) during the period of September to November 2012 by using questionnaires and interviews with the farm owners and staff. In total 417 fish representing 5 target species were chosen on the basis of the commercial importance and their potential for aquaculture in Oman, including red spot emperor (Lethrinus lentjan), king soldier bream (Argyrops spinifer), white spotted rabbit fish (Siganus canaliculatus), abalone (Haliotis mariae) and tilapia (Oreochromis niloticus). The fish were collected from 5 main sampling areas in Oman (Muscat, Mudhaibi, Manah, Sohar and Salalah) based on the Atlas of suitable sites for aquaculture in Oman to investigate the bacterial species composition and distribution. The animals were examined for clinical signs of disease prior to routine bacteriology. Bacterial isolates were recovered using traditional methods and identified to species level using phenotypic and molecular approaches using 16S rDNA, 16S rDNA RFLP and 16S rDNA sequencing. Experimental fish challenge studies were also conducted using both live bacterial cells and ECP protein to investigate the pathogenicity of Aeromonas isolates. In addition, the presence of some virulence factors was investigated using both phenotypic and genotypic methods. The results of this study showed that, the most farms in the Oman follow very similar farming practices. The major proportion of the tilapia is consumed within the local communities. A number of farmers have experienced mortalities, which were considered to be attributable to poor water quality, overcrowding or due to excessive feeding. Farmers facing fish mortalities tended not to record the problems due to a lack of understanding of the concept of fish farm management. There is a regulation about aquaculture and related quality control, but it has not yet been implemented in an appropriate manner in Oman. From the diverse group of bacteria recovered from wild and farmed fish, 83% of the total isolates comprised Gram negative, rod-shaped bacteria. The most frequently isolated groups from marine and cultured fish were Aeromonas spp., Vibrio spp., Sphingobacterium spp., Micrococcus spp. and Staphylococcus spp., with Aeromonas spp. being the predominant group representing 25% of the isolates recovered in this study. Identification of the Aeromonas spp. showed 57% agreement between the results of phenotypic and genotypic methodologies, and determined 6 species as the dominant organisms, i.e. A. veronii, A. jandaei, A. caviae, A. trota, A. encheleia and A. salmonicida. 65% of the iso-lates shared 99% 16S rDNA sequence similarity with the closest sequences in GenBank, and the dominant species was A. veronii. In conclusion, the Aeromonas isolates recovered from fish with clinical signs of disease showed heterogeneity in their identification profiles and their pathogenicity.

A dificuldade na detecção precoce de focos infecciosos específicos causados por bactérias tem aumentado a necessidade de pesquisar novas técnicas para este fim, uma vez que estes focos necessitam de tratamento prolongado com antibióticos e, em alguns casos, até mesmo drenagem ou, se for o caso, a remoção de próteses ou enxertos. A detecção de infecções bacterianas por cintilografia teria a vantagem de uma imagem de corpo inteiro, desde que traçadores específicos estejam disponíveis. Esse estudo visa a obtenção de aptâmeros específicos para identificação de bactérias para uso futuro como radiofármaco. A metodologia SELEX (do inglês Systematic Evolution of Ligands by Exponential Enrichment) pode gerar oligonucleotídeos (aptâmeros) que são capazes de se ligar com alta afinidade e especificidade a alvos específicos, desde pequenas moléculas até proteínas complexas, usando ciclos de enriquecimento e amplificação. Aptâmeros podem ser marcados com diferentes radionuclídeos tais como 99mTc, 18F e 32P. Aptâmeros anti-peptideoglicano, o principal componente da parede celular externa bacteriana, foram obtidos através da SELEX. Células inteiras de Staphylococcus aureus também foram utilizadas para a realização da SELEX para células (cell-SELEX). A seleção dos aptâmeros foi realizada por meio de dois procedimentos distintos. Esses foram o processo A em que foram realizados 15 ciclos da SELEX nos quais a separação dos oligonucleotídeos ligados ao peptideoglicano dos não ligados foi efetuada por filtração e o processo B em que foram realizados 15 ciclos com a separação realizada por centrifugação, seguidos de 5 ciclos de cell-SELEX. A SELEX teve início com um pool de ssDNA (DNA de fita simples). Para o processo A, inicialmente a biblioteca de ssDNA foi incubada com o peptideoglicano e a amplificação dos oligonucleotídeos que foram capazes de se ligar ao peptideoglicano foi realizada por PCR (Polymerase Chain Reaction). Os oligonucleotídeos amplificados foram novamente incubados com o peptideoglicano, amplificados e purificados. Ao fim de 15 ciclos de seleção, os oligonucleotídeos selecionados foram clonados. O produto de recombinação foi utilizado para transformar a bactéria Escherichia coli Top10F. O DNA plasmidial de 40 colônias selecionadas foram extraídos e quantificados. Os plasmídeos foram sequenciados, duas sequências diferentes (Antibac1 e Antibac2) foram obtidas e as estruturas secundárias determinadas. Os aptâmeros obtidos foram sintetizados e marcados com 32P. Os aptâmeros marcados foram incubados com células de S. aureus e a quantidade de ssDNA ligado às bactérias foi determinado por espectrometria de cintilação líquida. A biblioteca de oligonucleotídeos marcada com 32P foi usada como controle. Para o aptâmero Antibac1 a radiação foi 28 vezes maior do que a obtida com o controle e para o aptâmero Antibac2 22 vezes. Um ensaio de especificidade foi conduzido com os aptâmeros marcados utilizando-se células de S. aureus, E.coli, Candida albicans e fibroblastos humanos. Para os dois aptâmeros (Antibac1 e Antibac2) a ligação às células bacterianas foi significativamente superior à verificada para C. albicans e fibroblastos, demonstrando a especificidade dos mesmos para identificação de bactérias. Para o processo B após os 15 ciclos da SELEX foi realizada a cell-SELEX que começou com o produto do 15o ciclo sendo incubado com células de S.aureus. Ao fim de 5 ciclos de seleção, os oligonucleotídeos selecionados foram clonados e sequenciados como no processo A. Onze diferentes sequências foram obtidas de 21 clones e as estruturas secundárias foram determinadas. Os aptâmeros obtidos pelo processo A apresentaram alta afinidade e especificidade para bactérias. Os aptâmeros obtidos pelo processo B serão avaliados quanto a estes parâmetros em trabalhos futuros. / The difficulty in early detection of specific foci caused by bacteria in the bacterial infection has raised the need to search for new techniques for this purpose, since these foci require prolonged treatment with antibiotics and in some cases even drainage or, if applicable, removal of prostheses or grafts. Detection of bacterial infections by scintigraphy had the advantage that a whole body image could be obtained, since specific tracers were available. This study aims to obtain aptamers specific for bacteria identification for future use as radiopharmaceutical. The SELEX (Systematic Evolution of Ligands by Exponential Enrichment) methodology can generate oligonucleotides (aptamers) that are able to bind with high affinity and specificity to a specific target, from small molecules to complex proteins, by using rounds of enrichment and amplification. Aptamers can be labeled with different radionucleotides such as 99mTc, 18F and 32P. In this study, aptamers anti-peptidoglycan, the main component of the bacterial outer cell wall, were obtained through SELEX. Whole cells of Staphylococcus aureus were also used to perform the SELEX to cells (cell-SELEX). The selection of aptamers was performed by two different procedures (A and B). The A process has been accomplished by 15 SELEX rounds in which the separation of the oligonucleotides bound to the peptidoglycan of unbound ones was performed by filtration. In the B process 15 SELEX rounds were performed using the centrifugation for this separation, followed by 5 rounds cell-SELEX. The SELEX started with a pool of ssDNA (single stranded DNA). For A process, initially a library of ssDNA was incubated with peptidoglycan and the amplification of oligonucelotides that were able to bind to peptidoglycan was performed by PCR (Polymerase Chain Reation). The amplified oligonucleotides were again incubated with peptidoglycan, amplified and purified. At the end of 15 selection rounds the selected oligonucleotides were cloned. The product of recombination was used to transform Escherichia coli Top10F. The plasmid DNA from 40 selected colonies were extracted and quantified. The plasmids were sequenced, two different sequences (Antibac1 and Antibac2) were obtained and their secondary structures determined. The aptamers obtained were synthesized and labeled with 32P. The labeled aptamers were incubated with S. aureus cells and the amount of radiolabeled ssDNA was determined by liquid scintillation spectrometry.

A study to assess the potentials of some commensal bacteria that belong to Staphylococcus, Acinetobacter and Stenotrophomonas genera as reservoirs of antibiotic resistance determinants in the environment of Nkonkobe Municipality of the Eastern Cape Province, South Africa, was carried out using standard microbiological and molecular techniques. A total of 120 Staphylococcus isolates which consisted of Staphylococcus haemolyticus (30%), Staphylococcus aureus (23.3%) from pig; Staphylococcus capitis (15%) from goat; Staphylococcus heamolyticus (5%) and Staphylococcus xylosus (15%) from cattle and other Staphylococci (11%) from dead chicken and pigs were isolated. About 23.3% of these isolates were coagulase positive and 76.7% were coagulase negative. This difference in prevalence along coagulase production divide was statistically significant (p < 0.05). Eighty-six Acinetobacter species (Acinetobacter baumannii/calcoaceticus and Acinetobacter haemolyticus) were also isolated from Alice and Fort Beaufort towns samples, while 125 Stenotrophomonas maltophilia isolates were from grass root rhizosphere (96%) and soil butternut root rhizosphere (4%). Between 75-100% of the Staphylococccus species were resistant to Penicillin G, tetracycline, sulphamethaxole and nalidixic acid; about 38 % were methicillin resistant, consisting of 12.6% methicillin resistant Staphylococcus aureus (MRSA) from pig and a total of 12% vancomycin resistant were observed. Also, 12% of the isolates were erythromycin resistant while 40.2 % were resistant to the third generation cephalosporin, ceftazidime. The antibiotic resistance genes vanA, VanB, eryA, eryB, eryC were not detected in all the phenotypically resistant Staphylococccus species, but mec A gene and mph genes were detected. In the Acinetobacter species, a wide range of 30-100% resistance to penicillin G, ceftriazone, nitrofurantoin, erythromycin, and augmentin was observed. Polymerase chain reaction (PCR) revealed the presence of Tet(B) and Tet(39) genes in these species, while Tet (A), Tet(M) and Tet(H) were absent. Also, 9.3% of the Acinetobacter species showed phenotypic production of extended spectrum beta lactamases (ESBLs) while 3.5% were positive for the presence of blaCTX-M-1 genes. The Stenotrophomonas maltophilia isolates showed varying resistance to meropenem (8.9%), cefuroxime (95.6 %), ampicillin-sulbactam (53.9%), ceftazidime (10.7%), cefepime (29.3 %), minocycline (2.2%), kanamycin (56.9%), ofloxacin (2.9%), levofloxacin (1.3%), moxifloxacin (2.8%), ciprofloxacin (24.3%), gatifloxacin (1.3%), polymyxin B (2.9 %), cotrimoxazole (26.1%), trimethoprim (98.6%), aztreonam(58%) and Polymyxin B (2.9 %). The isolates exhibited significant susceptibility to the fluoroquinolones (74.3-94.7 %), polymycin (97.1%) and meropenem (88.1%). Only sul3 genes were the only sulphonamide resistance gene detected among the trimethoprim-sulphamethoxazole resistant isolates. The observed multiple antibiotic resistance indeces (MARI) of >2 for Staphylococcus species, Acinetobacter species and Stenotrophomonas maltophilia suggest that they have arisen from high-risk sources where antibiotics are in constant arbitrary use resulting in high selective pressure. The presence of tetracycline resistance genes in Acinetobacter species justifies the observed phenotypic resistance to oxytetracycline and intermediate resistance to minocycline. High phenotypic resistance and the presence of some resistance genes in Staphylococcus species is a possible threat to public health and suggests animals to be important reservoirs of antibiotic resistance determinants in the environment. Indiscriminate use of antibiotics induces this kind of antibiotic resistance and should be discouraged. Personal hygiene is encouraged as it reduces the load of Acinetobacter species contacted from the environment that may be difficult to control. Commensal Stenotrophomonas maltophilia are as important as their clinical counterparts due to their roles in opportunistic infection, antibiotic resistance and their associated genes, especially sul gene. Personal hygiene is hereby advocated especially when in contact with soil, plants and plants’ rhizospheric soil

Piscine francisellosis, caused by Francisella noatuenensis subsp orientalis (Fno), is an emerging infectious disease in the tilapia industry, but no effective commercial treatments or vaccines are available. The use of immunostimulants is a promising method to control diseases in aquaculture, and various algae and algal-derived compounds are potent immunostimulants for improving immune status. Algae produce a great variety of secondary metabolites that exert a broad spectrum of biological activities. The aim of this thesis was to evaluate the effectiveness of algal compounds against Fno in vitro and in vivo and determine their potential to control francisellosis infection in Nile tilapia Oreochromis niloticus L. under experimental conditions, and in an alternative host, namely the greater wax moth Galeria mellonella. Some of the algae and their compounds (Chlorella sp., alginic acid, and ß-glucan) exerted antimicrobial activity in vitro against Fno, Aeromonas hydrophila and Streptococcus agalactiae and stimulated responses of Nile tilapia macrophages (Chapter 2). An immersion challenge model for Fno STIR-GUS-F2f7 was developed in two genetic groups of Nile tilapia, and the homo gold strain was more susceptible to infection than wild type (Chapter 3). In vivo trials were conducted in Nile tilapia homo gold where fish were fed diets supplemented with 10% Scenedesmus quaricauda, 10% Haematococcus pluvialis, and 0.1% or 0.2% alginic acid or ß-glucan, and then challenged with Fno and co-infected with S. agalactiae (Chapter 4). The Fno challenge failed to produce mortality; however, co-infection resulted in high mortalities in all groups. As the in vivo trial in tilapia could not be to repeated, a G. mellonella model for Fno was validated. Fno doses between 0.7–1.7 x 108 CFU mL-1 killed G. mellonella, while tetracycline, alginic acid and ß-glucan rescued the wax moth from lethal doses of bacteria (Chapter 5).

Thesis (Ph. D.)--Rutgers University, 2008. / "Graduate Program in Entomology." Includes bibliographical references (p. 132-139).

No description available.

No abstract available. / Thesis (Ph.D.)-University of Natal, Pietermaritzburg, 1975.