No description available.

No description available.

Pumkin seedlings (Cucurbita maxima) were inoculated with the fungus Sclerotinia sclerotiorum (Lib.) de Bary. Center regions of non-infected and infected cotyledons of various lengths were cut into 1 x 2 mm strips and processed for ultrastructural investigations. Complementary portions of opposing non-infected cotyledons were also processed as control tissue, and contained fewer storage products in cells than cotyledons of comparable size from non-infected plants. Young non-infected cells contained distinct lipid bodies, protein bodies and electron dense inlusions which were translocated out of older cells by abundant plasmodesmata. Initally, infected cells became plasmolyzed, followed by breakdown of the cytoplasm. Host cells were generally affected only 4-6 cells from the infection front. Many infected cells had abundant rough endoplasmic reticulum and all organells were eventually completely disrupted. Action of enzymes from fungal cells did not appear to be limited to the area immediatedly adjacent to hyphal cells.

No description available.

No description available.

Mistletoes are a group of hemiparasitic plants that grow on a wide variety of host trees and differ in their degree of host specificity, ranging from specialists to generalists. Mistletoes can also be locally host specific where host preference varies geographically, i.e. at a given location a mistletoe species may infect only part of its overall host set. The mistletoe Agelanthus natalitius parasitises at least 11 tree genera distributed throughout South Africa. However, there is geographic variation in infection patterns over the parasite’s range, suggesting that A. natalitius may be locally host specific. We quantified the degree of host specificity and tested the mechanisms that direct host specialisation in two distinct mistletoe populations at Highover and Mtontwane (about 110 km apart) in KwaZulu-Natal, South Africa. We investigated the distribution, abundance and community composition of woody species that host the mistletoe. We also assessed the effect of light on germination and early survival of the mistletoes in a greenhouse experiment. We conducted field reciprocal transplant experiments at both sites to investigate the compatibility of these mistletoes with their hosts Acacia karroo and A. caffra during early development. We then analysed the nutrient and water contents of the mistletoe-host pairs to investigate the role of nutrient and water status in directing host specificity in mistletoes. We further studied avian dispersal in the field and in captivity to investigate optimal dispersal distance and germination success, and evaluated their role in determining mistletoe host specificity. At both study sites, five host species were recorded as being parasitised by the mistletoe A. natalitius. A. karroo and A. caffra appear to be the two most common host species in the region; both grow abundantly at the study sites and were recorded with high infection by A. natalitius. However, A. karroo is the most abundant host species and the mistletoe showed a high degree of host specificity on A. karroo. Infection by mistletoes was positively correlated with tree size, and was highly aggregated, both individually and locally. Field observations and greenhouse shade experiments showed that light can influence mistletoe distribution. Germination of mistletoe seeds was independent of host species and site. However, hypocotyls (the structures that develop into haustoria) grew longer when placed on their source host species within their locality. Additionally, they showed preference for the most abundant host species, A. karroo. Water and nutrient status of the host species A. karroo and A. caffra had no significant effect. Thus, host nutrient and water content may not account for host specificity in this mistletoe species. Mistletoes accumulated more nutrients and maintained more negative than their host trees. We also investigated the mistletoes’ use of passive nutrient uptake (from host xylem) and active nutrient uptake (from host phloem) by using the N:Ca ratio as an index of nutrient access. Mistletoes growing on A. caffra had a ratio > 1, i.e. the mistletoe actively accessed nutrients from the phloem of host trees. However, mistletoes on A. karroo had a N:Ca ratio < 1, which implies that they passively accessed nutrients from the xylem. The difference in mechanism of nutrient acquisition on different host species may reflect the level of compatibility between mistletoe and host. Several bird species were frequently observed to feed on mistletoes, many of which were used in our captivity studies. Although birds did not consume mistletoe fruits in captivity as they do in the field, they were effective in removing the pulp cover of mistletoe fruits and exposing seeds in germinable condition. In captivity, the Red-winged Starling ingested whole fruits and regurgitated seeds, deliberately wiping their bills on twigs to remove the sticky seeds. As a result, germination success of mistletoes processed by Red-winged Starlings was higher than any other bird species tested in captivity. Overall, there appears to be host specificity in morphologically identical mistletoes. Understanding the mechanisms that result in host race evolution are potentially important to the process of speciation in hemiparasitic mistletoes. We need to take into account genotypic matching in conserving these different forms of mistletoes and their host Acacia genotypes. Further research into the mechanisms of host specificity and patterns of genotypic matching is warranted. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2009.

Call number: LD2668 .T4 1979 C66 / Master of Science

The ectoparasitic monogenean fluke, Gyrodactylus salaris, is a parasite known to be highly pathogenic to Atlantic salmon (Salmo salar). Although present in the environment of several neighbouring European countries, the UK is thought to be G. salaris-free, but, if national contingency plans to control this parasite are to be effective, it is vital that we understand the factors underlying its transmission from host to host. This study demonstrates that the majority of parasites transferring to new hosts are mature parasites that have reproduced at least once. Since, exploration and host transfer strategies pose a risk to survival; the parasite will endeavour to pass on its genes before attempting to transfer from one host to another. This study has also shown that when pregnant parasites are forced to leave their hosts, their offspring are aborted prematurely to ensure the survival of the mature parasite. Gyrodactylids do not possess a free-swimming stage in their life cycle, which allows for their migration between hosts. In spite of this, they are able to rapidly colonise naïve hosts, even in non-shoaling populations of fish. This study investigates the transmission strategies employed by detached parasites in the colonisation of new hosts. Observations of gyrodactylids collected from 3-spine sticklebacks, Gasterosteus acuelatus, suggest that their activity increases as a stickleback approaches, alerting the host to its presence. The parasite is then ingested directly by the prospective host. A time series of experimental exposures and specimens prepared for Scanning Electron Microscopy (SEM) suggest that once ingested, the parasites attach to the lining of the buccal cavity and then migrate out to their preferred colonisation site on the outer surface of the fish. It is proposed that this may be an alternative route for host infection. Similarly, direct ingestion by the scavenging on infected hosts by 3-spine sticklebacks suggests another route of infection of new hosts. Although these routes of transmission may be of lesser significance, infections in the buccal cavity may be an important indicator for detection of infection and those personnel involved in screening fish for gyrodactylids should be aware that this is an area in which infections can occur. This study also demonstrated that the use of the anaesthetic 2-phenoxyethanol does not affect the number of gyrodactylids which leave the host to colonise a new host. Additionally, observations of the transmission process suggest that turbulence produced by the movement of the fish’s fins may facilitate the transfer of detached parasites from the substrate. While this hypothesis appears to be supported by video evidence and photographic stills gathered throughout the duration of this study, further work should be conducted using particle tracking techniques to determine the efficacy of using a vortex effect as a means of colonising new hosts. Field sampling processes may have an effect on this type of research, giving rise to problems with the accurate diagnosis, management and control of gyrodactylids in a variety of fish. Gyrodactylus infected specimens of 3-spine stickleback (Gasterosteus aculeatus L.), minnows (Phoxinus phoxinus L.) and stone loach (Barbatula barbatula L.) from one Scottish river were cohabited. The study found that small numbers of Gyrodactylus do transfer to atypical hosts. This study highlights that personnel involved in fish disease surveillance programmes should be aware of the consequences of transporting multiple species in the same transport vessel as gyrodactylids may infect species previously thought to be resistant. Equally, diagnosticians should be aware of the fact that atypical species may act as temporary hosts and that their gyrodactylid fauna should not be assumed. Non-feeding life-cycle stages, such as the dispersal stages of parasites, are dependant for survival upon finite energy reserves gathered during feeding phases. Thus, those individuals with more limited reserves will die sooner and consequently have less time available to find a new host once detached. At this stage, the principal energy reserves in gyrodactylids are stored as large lipids droplets. Confocal laser scanning microscopy (CLSM) has been used to investigate the distribution of lipid droplets in Gyrodactylus, which have migrated off their fish host, testing the hypothesis that these droplets function as a proxy for the nutritional state. This study, demonstrated that the lipid droplets were particularly associated with the gut and that there is a significant variability in the volume of stored lipid carried out by each individual. Transmission Electron Microscopy (TEM) showed that gyrodactylids carry lipid droplets at all stages of their life cycle, including at release from the birth pore. It is likely that transferring worms require stored energy reserves to survive in the event of failure to establish contact with a new host. These reserves could allow the parasite to survive without a host for several days. As gyrodactylids appear to respond to a range of stimuli including vibration and chemicals released from the host, the presence or absence of such cues may have consequences on the rates of Gyrodactylus transmission. If these chemical stimuli can be identified and then mimicked or blocked, then this may offer potential opportunities for the control of gyrodactylid behaviour and for disrupting their transmission to new hosts. Baseline gyrodactylid behaviour, in the absence of a host, was determined under white light and infrared. This was achieved using a specially constructed arena and purpose written image analysis software to analyse parasite movement under different lighting conditions. The study found that gyrodactylids were more active in the dark than in light conditions, typically displaying longer, more sinuous tracks under red light than under white light. To begin investigating the effect of chemical presence on gyrodactylid behaviour, the activity of octopaminergic agonists and antagonist which bind to muscle receptors and alter muscle activity, were assessed. The impact of octopamine hydrochloride, clonidine hydrochloride, amitraz and, a toxic reference, chlordimeform, over a range of concentrations (0.2 to 3.2µM/L) were assessed on gyrodactylid behaviour. All of the four chemicals affected Gyrodactylus and produced muscle tetanus, causing muscle spasms when extension was attempted. Prolonged exposure resulted in death. Only the highest concentration of chlordimeform, the toxic reference, affected 100% of Gyrodactylus after 24 hours. After 48 hours, all of the Gyrodactylus treated with chlordimeform were either affected, moribund or dead. Amitraz was more toxic than chlordimeform with 80% of Gyrodactylus being dead after 24 hours at the highest concentration. After 48 hours 100% of Gyrodactylus exposed to 3.2 µm/L amitraz were dead, and up to 80% were dead in those exposed to lower concentrations; with no parasites being left unaffected. Although these particular compounds are toxic to fish, the effect of these agonistic chemicals on Gyrodactylus behaviour and survival is interesting and suggests that a closely related compound that is safe for use against fish may offer a potential treatment for the control of G. salaris infections in rivers. An ultrastructure study was undertaken to contribute to the current understanding of gyrodactylid ultrastructure. The findings of this research require broad understanding of gyrodactylid behaviour for their interpretation. Photographic evidence was gathered using transmission and electron microscopy. From these results, it is clear that Gyrodactylus gasterostei on a three-spine stickleback host will respond to a range of stimuli (i.e. vibration or chemical cues released from the host) in their assessment of host suitability.

Fragmentation can drive local populations to become smaller and more isolated, and consequently more susceptible to extinction. Movement between patches, however, can interconnect such populations so that they effectively behave as larger and more stable metapopulations. Over the past two decades metapopulations have been used to shed light on the complex interactions that occur between hosts and parasites. Effectively every host can be considered as a discrete habitat patch from the perspective of a parasite. As such, host-parasite interactions naturally lend themselves to being examined within the metapopulation paradigm. In this thesis I examine empirically how various aspects of metapopulation structure, such as local host population size and landscape isolation/connectivity, combine to determine the extinction and recolonization dynamics of parasites in the landscape. Using a naturally fragmented water vole (Arvicola amphibious) metapopulation, I describe the spatial and temporal variation in parasite infection prevalence or burden in a Scottish landscape. I specifically address the spatial and temporal dynamics of both ectoparasites, and vectortransmitted microparasites, since these are two groups of parasites commonly found in natural systems yet often overlooked in the host-parasite metapopulation literature. In addition, I attempt to understand how specific parasite characteristics, such as transmission mode and infectious period, can influence how parasites respond to host population structure. In the final chapter, I bring together a number of parasite groups to examine the impact of metapopulation dynamics on parasite communities as a whole by investigating its impact of parasite community richness. Overall the findings of my study indicate that host spatial structure and the level of connectivity between patches are important factors that affect parasite dynamics and community richness. However, the exact level of connectivity required to sustain a parasite population locally depended on specific parasite characteristics. In contrast, local effects host/vector population size and patch infection history) had no discernible impact on most parasite groups.

published_or_final_version / Zoology / Master / Master of Philosophy