Ineffective biological control of the Eucalyptus pest Paropsis charybdis Stål (Coleoptera: Chrysomelidae: Paropsini) in cold areas of New Zealand was believed to be caused a climatic mismatch of the egg parasitoid Enoggera nassaui Girault (Hymenoptera: Pteromalidae). Two Tasmanian strains of the parasitoid were introduced to test climate-matching theory in 2000, with approximately 7000 wasps released. Establishment of the Florentine Valley strain was detected in 2002 using the Mitochondrial (mtDNA) gene Cytochrome Oxidase I (COI) as a strain specific marker. The hyperparasitoid Baeoanusia albifunicle Girault (Hymenoptera: Encyrtidae) and primary parasitoid Neopolycystus insectifurax Girault (Hymenoptera: Pteromalidae) were detected for the first time in New Zealand.
As paropsines have proven highly invasive internationally, a risk assessment of the paropsine threat to New Zealand was undertaken by evaluating the host range of E. nassaui and a reproductive assessment of 23 paropsine species in the genera Dicranosterna Motschulsky, Chrysophtharta Weise, Paropsis Olivier, Paropsisterna Motschulsky and Trachymela Weise. Enoggera nassaui proved polyphagous, but bioassay results proved that Paropsis species were significantly more susceptible to the egg parasitoid than Chrysophtharta species. Resistance within Chrysophtharta was attributed to spine-like chorion modifications. A COI derived Chrysophtharta phylogeny divided the genus into two distinct groupings, which was supported by chorion morphology.
Paropsine reproductive output was tested for key parameters indicating pest potential. Pest species displayed fecundity exceeding 600 eggs at an oviposition rate above 10 eggs per day⁻¹. Several non-pest species were identified as potential pests based on these parameters. The Chrysophtharta phylogeny suggested a moderate relationship between genetic relatedness and reproductive output. The Acacia defoliating paropsine Dicranosterna semipunctata (Chapuis) was evaluated for its susceptibility to E. nassaui and reproductive output. Egg parasitism occurring in bioassay did not translate into biological suppression following a specifically targeted release of E. nassaui, and the fecundity and oviposition rates fell below the thresholds predicted for a pest paropsine species.
Despite establishment of Tasmanian E. nassaui, hyperparasitism has now rendered this control agent ineffective in New Zealand. Neopolycystus insectifurax offers the best hope for future biological control of paropsine species in New Zealand.

The tumor suppressor p53 has a close relation with reactive oxygen species (ROS). As an indispensable component of the cellular redox system, ROS not only have been established to be involved in p53-dependent apoptosis, but also regulate p53 activity. Recent studies revealed several novel actions of p53, such as transactivation of antioxidative proteins, mitochondria translocation and inhibition of glycolysis. The fate of cells where p53 signaling pathways are initiated is either survival or death. In this review, we examine the hypothesis that ROS regulate cell fate through p53, in a way that physiological ROS levels trigger the protective pathways, while p53 behaves more like a cell killer under cytotoxic oxidative stress.

Inconsistent seed germination poses a problem for efficient seedling production of Echinacea species. Evidence suggests that ethylene can be effective for improving germination in Echinacea species. The objectives of this research were: to develop an ethylene pre-germination treatment that enhances germination in Echinacea species that is retained following drying and storage, and to determine if the ethylene effect on enhanced germination was an important mode of action for dormancy release. Four species of Echinacea (E. purpurea, E. tennesseensis, E. angustifolia and E. simulata) treated with 1-aminocyclopropane-1-carboxylic acid (ACC) or ethephon resulted in faster and generally higher germination. Pre-treatment of seeds with ACC or ethephon followed by drying was as effective as chilling stratification for enhancing germination depending on the species. While ethylene pretreatments did increase germination to some extent depending on species, it was concluded that 60-day stratification alone was a more commercially-viable treatment. Ethylene production or perception was not necessary for germination in untreated or stratified seeds as shown by aminoethoxyvinylglycine (AVG), silver thiosulfate (STS), and 1-methylcyclopropene (MCP) treatments. Both stratification and ACC treatment reduced Echinacea seed sensitivity to ABA and could be a common mechanism for enhanced germination. However, it does not appear that the increased germination seen after stratification was mediated through ethylene production because final germination percentages were generally unchanged following inhibition of ethylene production or action. In contrast, inhibition of ethylene production and perception reduced early 3-day germination suggesting that ethylene was more involved in seed vigor than final germination. It was determined that there is no physiological significance of ethylene for dormancy release in these Echinacea species.

The analysis of diverse data sets can yield different phylogenetic estimates that challenge systematists to explain the source of discordance. The Ambystomatidae are a classic example of this phylogenetic conflict. Previous attempts to resolve the ambystomatid species tree using allozymic, morphological, and mitochondrial sequence data have yielded different estimates, making it unclear which data source best approximates ambystomatid phylogeny. We present the first multi-locus DNA sequencebased phylogenetic study of the Ambystomatidae. Because independent loci can contain discordant gene tree histories, concatenating unlinked loci into a single data matrix can lead to strongly supported and erroneous results. Therefore, we utilized a range of analyses, including coalescent-based methods of phylogenetic estimation that account for incomplete lineage sorting and concordance-based methods that estimate the proportion of sampled loci that support a particular clade. We repeated these analyses with the removal of individual loci to determine if any locus has a disproportionate effect on our phylogenetic results. Many deep and relatively shallow clades within Ambystoma were robustly resolved. Analyses that excluded loci produced overlapping posterior distributions, suggesting no disproportionate influence of any particular locus. Our estimates differ from previous hypotheses, although there was greater similarity with previous molecular estimates, relative to morphological estimates.

Poison hemlock, Conium maculatum (Apiaceae), is an invasive plant in North America with a unique toxic chemistry. Previous research on this plant has focused on identifying herbivores as potential biological control agents or describing the toxic plant alkaloids. However, none have examined the role of higher trophic levels in the food web surrounding poison hemlock. Generalist predators and food web interactions are an important component of studies investigating invasion effects, as plant or animal introductions can alter ecosystem functioning. In this study, predators in poison hemlock were sampled at the foliar and epigeal levels, resulting in 956 Carabidae and 321 Coccinellidae being collected. Predator connectedness to plant resources was quantified using molecular gut-content and chemical analyses. Foliar Harmonia axyridis (Coccinellidae) contained aphid DNA and plant chemicals, while Harpalus pensylvanicus (Carabidae) only contained alkaloids, suggesting that the ground predators were obtaining plant chemicals via alternative prey. Feeding trials between H. axyridis and their potentially toxic prey, Hyadaphis foeniculi (Aphididae), revealed that the exotic predator shows faster development when consuming aphids from poison hemlock compared to alternative diets. This study reveals that three Eurasian species may be facilitating one another, illustrating the importance of continued examination of invasive species interactions.

Candida species are ubiquitous, ranging from pure saprobes through endo-symbionts of animals, to pathogens in many animals including humans. Some of the pathogenic species are of medical importance, especially Candida albicans. However, the prevalence of other non-albicans Candida species as human pathogens has been increasing worldwide. The aim of this study was to use conventional phenotypic tests and molecular methods to isolate, identify and characterise 600 Candida isolates from three teaching hospitals in Ghana, namely Korle Bu, Komfo Anokye and Tamale from mid-January to April, 2012. The prevalence of these species in cases of genitourinary candidiasis and pelvic inflammatory disease was investigated. Preliminary identification and characterisation of Candida isolates using four conventional phenotypic tests showed that C. albicans was the most common species, which constituted 41% of the isolates whereas non-albicans Candida species constituted 59% of the total number of Candida isolates. In patients presenting with vulvovaginal candidiasis (VVC) for at least two or more times, chi-square analysis indicates that the frequency of Candida species isolated were not statistically different from patients presenting for the first time with VVC. Candida albicans was the most common species in vaginal swabs from patients presenting with vulvovaginal candidiasis (VVC) for the first time in each of the three locations, present in 53.4% of the total swabs. The other species that were present were C. glabrata (21.6%), C. parapsilosis (15.5%), C. tropicalis (4.7%) and C. krusei (4.7%). Similar Candida species distributions were found in swabs taken from patients presenting with suspected pelvic inflammatory disease (PID). Across the three locations, however, there was a significant difference in the frequency of C. albicans, which was present in 68 and 69.6% of patients from Komfo Anokye and Tamale, but only 26.7% of patients from Korle Bu. Urine samples were taken in two of the locations, Korle Bu and Tamale, from female patients presenting with candiduria. Statistical analysis indicated a significant difference in the frequency of Candida isolates in cases of candiduria between the two locations. In Korle Bu, C. glabrata was the most prominent species (37.8%) followed by C. albicans (22.4%), C. parapsilosis (21.7%), C. tropicalis (10.5%), C. krusei (7%) and C. lusitaniae (0.7%). In Tamale, the species distribution was C. albicans (60.9%), C. glabrata (21.7%), C. parapsilosis (13%) and C. krusei (4.3%). The data highlight the prevalence of species other than C. albicans in case of candidiasis in Ghana. Delineation of C. albicans strains using the 25S rDNA to investigate the genotypic variation among C. albicans isolates showed that genotype A constituted about 95% of the Ghanaian C. albicans isolates, genotypes B and C constituted 2.5% each respectively. The general-purpose genotype (GPG) which corresponds to clade 1 among C. albicans was also investigated to know the prevalence of clade 1 among the C. albicans isolates investigated. The presence or absence of general-purpose genotype (GPG) gene was used to categorise the 240 C. albicans to clade 1 or other clade. The test revealed that 64.2% had the GPG genotype which corresponds to clade 1 and the remaining 35.8% were of non-GPG genotype; thus belongs to other clades. The population structure of C. albicans from the three teaching hospitals indicates a mainly clonal and homogeneous population across the three sampling locations from Ghana. Molecular analyses of the transposable group 1 intron in the ITS1-5.8S-ITS2 region using universal primer pair ITS1 and ITS4 revealed the presence of two rare Candida species; Candida rugosa and Candida mesorugosa. To the best of my knowledge this is the first report of either of these in Africa. Antifungal susceptibility tests among Candida isolates recovered from patients presenting with clinically suspected or symptomatic candidal vaginitis for the first time and patients presenting with candidal vaginitis on two or more occasions revealed a high percentage of Fluconazole-resistant C. albicans. This study highlights the prevalence of species other than C. albicans in cases of candidiasis in Ghana. Furthermore, this study has also demonstrated that no single conventional phenotypic test has been highly efficient to delineate Candida species into their respective species type. Thus, development of an identification scheme, which can discriminate between Candida isolates both at species and strain levels, will have prognostic and therapeutic significance for effective patient management.

Methylmercury (MeHg) is an environmental toxin to which we are exposed through the consumption of seafood. Reactive oxygen species (ROS) have been implicated in the mechanism of toxicity, and in vitro studies in our laboratory have implicated DNA oxidation, particularly the DNA repair enzyme oxoguanine glycosylase 1 (OGG1). My studies determined the effects of in utero exposure to MeHg on fetal brain DNA oxidation and postnatal neurodevelopmental deficits, and the role of ROS-mediated oxidative DNA damage using the free radical spin trap, α-phenyl-N-tert-butylnitrone (PBN), and DNA repair-deficient ogg1 knockout mice. While neither MeHg nor PBN altered DNA oxidation in fetal brain, MeHg caused cognitive deficits in passive avoidance and novel object recognition, the latter of which was blocked by PBN pretreatment, suggesting ROS involvement. Preliminary longevity studies following one litter from each treatment group to 16 months suggest that in utero MeHg treatment may shorten lifespan. Endogenous DNA oxidation was increased in the brains of ogg1 knockout fetuses compared to wild-type littermates, although this was not enhanced by MeHg. However, OGG1-deficient animals exhibited cognitive deficits in passive avoidance after MeHg treatment, suggesting a role for DNA damage. Furthermore, ogg1 knockout female mice exhibited a passive avoidance deficit compared to wild-type females regardless of treatment, corroborating a role for oxidative DNA damage in neurodevelopmental deficits. MeHg increased apoptosis in the hippocampal region of fetal brain, and may cause DNA double-strand breaks (DSBs), evidenced by enhanced phosphorylation of histone 2AX (γH2AX). Ogg1 knockout progeny exhibited increased cellular proliferation or migration in the developing hippocampal region, which was blocked by MeHg. My results provide the first evidence that: (1) MeHg may decrease lifespan; (2) PBN protects against some postnatal neurodevelopmental deficits caused by in utero exposure to MeHg; and (3) DNA repair-deficient progeny are more susceptible to postnatal cognitive deficits caused by in utero MeHg exposure, suggesting that ROS-mediated DNA oxidation plays a role in MeHg-initiated neurodevelopmental deficits.

Proteinaceous infectious particles, termed 'prions' are self-perpetuating protein isoforms that transmit neurodegenerative diseases in mammals and phenotypic traits in yeast. Each conformational variant of a prion protein is faithfully propagated to a homologous protein in the same cell environment. However, a reduction in the efficiency of prion transmission between different species is often observed and is termed "species barrier". Prion transmission to a heterologous protein may, in some cases, permanently change the structure of the prion variant, and divergent proteins may interfere with prion propagation in a species-specific manner. To identify the importance of both protein sequence and the cell environment on prion interference and cross-species transmission, we employed heterologous Sup35 proteins from three Saccharomyces sensu stricto species: Saccharomyces cerevisiae (Sc), Saccharomyces paradoxus (Sp), and Saccharomyces bayanus (Sb). We performed our experiments in two different cell environments (Sc and Sp). Our data show that Sup35 from one species can form a prion in another, and we employed a transfection procedure to perform cross-species transfer of the prion. Using a shuffle procedure, we demonstrate that the specificity of prion transmission is determined by the protein itself rather than the cell environment. Interestingly, we noted that variant-specific prion patterns can be altered irreversibly during cross-species transmission through S. bayanus module II. We further show that prion interference does not always correlate with cross-species prion transmission, and the identity of particular regions or even a specific amino acid, rather than the overall level of PrD homology is crucial for determining cross-species transmission and interference. Lastly we provide evidence to suggest that prion interference is specific to the cell environment.

Pennisetum Rich, is one of the most important genera in the family Poaceae because it includes forage and crop species such as Pennisetum purpureum Schumach. and Pennisetum glaucum (L.) R. Br. Both P. purpureum and P. glaucum have a number of cultivars and varieties arising due to natural crossing which are very difficult to distinguish morphologically. P. purpureum and P. glaucum also hybridize naturally because they are protogynous and cross pollinated. The resulting hybrids are highly sterile and resemble P. purpureum. Lepidopteran stem borers cause great yield loss in maize produced by resource-poor farmers in Africa and are managed by habitat management or push-pull strategies, in which P. purpureum cultivars and hybrids are used as a trap crop. The aims of this project were to genotype different P. purpureum cultivars and hybrids using Amplified Fragment Length Polymorphism (AFLP) as well as Random Amplified Polymorphic DNA (RAPD) in order to identify cultivars and hybrids and possible misidentifications, assess the congruency of results between AFLPs and RAPDs and to attempt to relate these results to the oviposition preference of Chilo partellus for different P. purpureum cultivars. The individuals to be fingerprinted were collected from several countries in sub-Saharan Africa, a few from the USA and one from China. The AFLP analysis of these individuals were done with primer combinations EcoRI/MseI and Mlul/Msel on polyacrylamide gels and an ABI 3130 xl Genetic Analyzer respectively. The automated sequencer visualized more bands than the polyacrylamide gels. The RAPD technology was not developed any further after 17 primers were tested and no polymorphic bands detected. Overall results indicated that cultivars did not cluster according to geographical origin, and cultivars known by popular names did not always cluster together, indicating diversity within the cultivar or misidentifications. An example of a misidentification is the cultivar Green Gold being no other than cultivar Harare, or cultivar Swaziland 3 being cultivar Sanitas. Proper management by nursery managers cannot be stressed enough, as this will prevent plants getting mixed up, causing confusion. There was no relationship between the relatedness of cultivars and moth oviposition preference. The AFLP technology could be a powerful tool for the DNA fingerprinting and molecular characterization of this grass species, but poor germ plasm management negates its application. / Thesis (M. Environmental Science)--North-West University, Potchefstroom Campus, 2008.

Ischemic stroke is characterized by a disruption of blood supply to a part of the brain tissue, which leads to a focal ischemic infarct. The expression and activity of MMP-9 is increased in ischemic stroke and is considered to be one of the main factors responsible for damages to the cerebral vasculature, resulting in compromised blood-brain barrier (BBB) integrity. However, the regulatory mechanisms of MMP-9 expression and activity are not well established in ischemic stroke. Since hypoxia/ischemia and reperfusion generates reactive oxygen species (ROS), I hypothesize that ROS is one of factors involved in up-regulation of MMP-9 expression in brain cells and ROS-mediated effect may occur via MAPK signaling pathway. My study has provided the evidence that ROS is responsible for an increase in MMP-9 expression in astrocytes mediated via MAPK-AP1 signaling pathway. Preliminary studies with an in vitro model of the BBB suggest that inhibition of MMP-9 is a critical component of reducing ROS-induced BBB permeability.